Celebration of Life

Celebration of Life

An eternal thanks to our MS Heroes

Table of Contents

Our eternal thanks to our MS Heroes

Introducing the MS Callistemon League

Meet our loving Benefactors

Remember our loving Benefactors

“Celebration of Life”

an eternal thanks to our MS Heroes

People living with multiple sclerosis (MS) have been blessed by the generosity of so many individuals, our MS Heroes. They spoke with their heart and left a statement of their love for people with MS through a gift in their Will. These gifts will not only fast–track to a cure but they will also provide care until we’re there. Protecting future generations from MS.

Together we can empower people living with MS, to live their best life

Many of our amazing Benefactors know, either firsthand or through friends and family, how difficult it is for someone to traverse the MS journey on their own.

They all understand how important it is having people surrounding you who understand you. People who will extend a caring and loving hand. They all wanted to be that “special person”, who beyond their own lifetime, makes a difference in the lives of others.

With their hearts, they left behind one of the most loving legacies of their values. All gifts, big or small can be transformational. We extend our eternal gratitude to all these heroes for their selfless decision to leave a gift in their Will.

By giving the “Ultimate Gift” they are empowering people living with MS to live their best life.

To their families, we provide a space for you to remember and recognise their intentions, their life, their amazing legacy! This is just one small way of showing our eternal gratitude – to our amazing Benefactors!

We are all together on the MS journey to help break down barriers, achieve goals and live well. It is this aspiration and our values which have inspired them to leave a gift, their most significant one. An ultimate gift that speaks of what was important to them and how they may want to be remembered.

Today, we ask that you spend a few minutes thinking about these loving and kind individuals. They have already made such an enormous difference to both the lives of those living with MS and to our own lives.

They thought “with their heads and then with their hearts” … thus we can all continue to work to stop MS and make this a better place for those living with MS.

Would you like to ensure that people with multiple sclerosis can face the challenges and know the joy of following their dreams? Would you like to be part of the team that will help fast track a cure to stop MS?

Consider joining our generous group of supporters: the MS Callistemon League. These supporters want to stop MS and ensure people don’t face MS alone. They are here with them, every step of the way, while the search for a cure continues.

Every gift, large or small matters. Many supporters leave 1% or 2% after including family and friends. These ‘ultimate’ gifts will provide vital support for people living with multiple sclerosis. You too can leave a legacy of your values!

To find out how, please call our Gift in Will Team

Call Laura or Rebecca on 1800 443 867

Email futureplanning@ms.org.au or visit www.mymslegacy.org.au

Introducing the MS Callistemon League

Callistemon Phoeniceus is the emblem chosen for the MS Callistemon League. It has been selected for three reasons:

• The callistemon or bottlebrush is an Australian native shrub symbolising healing and joy.

• The structure of the flower with its filaments emerging from a central stem, mirrors the central nervous system –the part of the human anatomy most profoundly affected by multiple sclerosis.

• This native flower blooms a striking red, the very same colour as the MS logo.

We recognise remarkable individuals like you who have made a legacy gift commitment to the MS organisation with membership in the MS Callistemon League. Through your commitment, you will be there, along the journey, helping people with multiple sclerosis to live the best life that they can. Our heartfelt thanks for your loving and thoughtful support.

If you’ve already named MS Plus in your Will or trust, please let us know. We would appreciate the opportunity to recognise you for your generosity. If you prefer to remain anonymous, we will honour your wishes, but we would like to thank you privately.

Benefits of joining the MS Callistemon League

As a valued member of the MS Callistemon League, you will:

• Be included in our Celebration of Life book – including words of your choice which will live on forever

• Be individually acknowledged in newsletters, promotional material and on the MS website – with your permission

• Receive regular newsletters

• Receive VIP invitations to special events

Perhaps the greatest reward you will gain is the knowledge that your commitment to MS through your gift in Will will serve to improve quality of life for countless Australians affected by multiple sclerosis, for generations to come.

Please don’t hesitate to get in touch if you have any questions about setting up your legacy gift or if you need more information.

“My name is Laura. I head up the Gifts in Wills team here at MS Plus. I have met so many people diagnosed with MS, heard their stories, understood their struggles.”

That’s why I’m leaving a gift in my Will, so that I can help to fast track a cure for MS. And until a cure is discovered, I can be there for every Australian with a multiple sclerosis diagnosis, forever.

A gift in your Will can offer the same.

By allowing MS Plus to plan into the future with a gift in your Will, you will help them to power essential research and provide support for all diagnosed.

Anyone who has had anything to do with MS – friends, family, carers and people with MS alike – knows how devastating the disease can be. It’s not only devastating but isolating, as it also places ever–greater pressures on intimate relationships, family, social life and career.

As the condition advances and people’s nervous systems degenerate, they need increasingly specialist help and support. More than anything, every person living with MS needs a cure.

That’s why our MS entities have been there for more than 60 years as a committed leader in treatment, medication, support and research – trying to discover a cure for MS and being a constant presence for people with MS and their families. Because MS is too hard to do alone.

Your thoughtful, caring gesture will help ensure you’re there, not only doing the day–to–day, but a constant presence driving advances in care like our new Wellness Centers.

These are specialist hubs that focus on holistic wellbeing, helping people with MS navigate the NDIS, advising and providing equipment for therapeutic exercise, supporting mental health, and so much more.

You’ll be there for those you care about, driving a new, greater national focus on clinical research, striving for greater understanding into the causes of MS, looking for new treatments that ease and delay the advance of the condition, and yes – ultimately – looking for a cure.

But most of all, you’ll be giving people with MS something even greater – the sure knowledge that no matter how hard the condition is, they’re not alone. That’s why I’m leaving a gift in my Will. I hope you will too.

Then you’ll know that there’s someone on the side of every person diagnosed with MS, working to make it better.

Meet our loving Benefactors

A LIVING CELEBRATION

Susan Abbey

“A story from an unsung hero… one of indefatigable love”

It was over 15 years ago when Susan had to face a stark reality. She was working at Woolworths and was looking forward to starting a family with the love of her life, Tim. But, the reality of her health situation somewhat changed this course. She was diagnosed with multiple sclerosis.

Susan has always been known to be full of life, with infectious laughter and a joy for living! It did not take her long to check how she could best face this new challenge. She found it with the help of her family, friends and MS Plus (formerly Multiple Sclerosis Limited).

As the disease progressed, she had to abandon her job at Woolworths. However, she was determined to continue to be ‘independent and useful’. As well as her dream of a family. This came through in 2009 when Rowan, her son, was born.

Susan was on a courageous and determined path. She dedicated herself to learn more about multiple sclerosis. She also investigated how she could help others in a similar situation to herself. “I find that in life if you help others, you get much more returned to you.” Susan became a proud MS Peer Support Volunteer.

Having recently completed an 8–week course: Women with a Disability, she is looking forward to doing a “Certificate III in Community Care”.

Nowadays Susan must rely

80% of her time on the use of a wheelchair, as her physical ability is limited. ‘However, I can use my voice to help others and with the training I am doing, I should be able to further this help.”

Susan tells us that she has benefitted from many of the services that MS provides. She has accessed expert advice and support for herself and her family. Additionally, the opportunity that MS offers to help others is something that empowers her and keeps her strong.

She also decided to leave a legacy of love to MS via a Gift in her Will.

Susan tells us that she has benefitted from many of the services that MS provides. She has accessed expert advice and support for herself and her family. MS offers the opportunity to help others. This is something that empowers her and keeps her strong. “I don’t feel alone… I know MS and my family are behind me all the way.”

Susan is indefatigable. She has instigated local events and has participated in many others. “I have an extremely supportive group of family (especially my husband Tim and my son Rowan). Also, many dear friends that come from afar to take part in fundraising activities. They are my rock.”

“I used to be an ‘MS Angel” too for the MS Readathon, so I was delighted when I was able to support its re–launch in 2019.”

“I have an extremely supportive group of family (especially my husband Tim and my son Rowan) and many dear friends that come from afar to participate in fundraising activities with me. They are my rock.

My family and I have attended a couple of MS family camps. This is the kind of support that makes a great difference to our lives.

Some time ago I decided to leave a legacy of love in my Will to MS Plus (then Multiple Sclerosis Ltd).

I wanted to be part of the future of MS and contribute so they will have the resources to continue to help and support people with MS. I believe it is very important that ‘no one has to face MS alone, now or in the future’.

I am thrilled that I am giving my money to a worthy cause and leaving a legacy that will help others with MS. This was a very easy decision as it is one more way that I can be useful and give back to my community.

“I would encourage others to do so. I personally believe in doing what you can to help others. It is my life quest to provide support where I can especially in relation to MS which is a life changing illness.”

A LIVING CELEBRATION

Nigel Caswell

“Engineering a way to help others with MS”

Nigel Caswell wasn’t keen on attending his first multiple sclerosis (MS) conference. Diagnosed with progressive MS in 1993, he admitted he was afraid. “I didn’t know what I’d see or what my future held,” recalled Nigel. But going turned out to be a good decision.

While at the conference, he noticed an ambassador’s stall and spoke to the people running it.

“They were recruiting people willing to talk to community groups about MS. I enjoy public speaking, and I’m a blue sky sort of person, so I thought: why not help?”

It changed his life for the better.

Nigel has been a volunteer and advocate in the MS community for over 20 years. For MS Plus, he speaks to groups and schools about living with MS. For MS Australia, Nigel

lobbies politicians about the MS community’s concerns.

In 2022, the 78–year–old Bentleigh resident received MS Australia’s John Studdy Award. The award recognised his service to others living with the condition.

“Volunteering has helped me to live with MS. It’s turned something that might seem like bad luck into an advantage.

I’m sure I get more attention because people don’t expect someone in a wheelchair to make intelligent remarks.”

Nigel doesn’t consider himself an invalid.

“I’m a healthy person who happens to have MS,” he said.

MS likely started in his teens

After emigrating to Australia from England for work in 1972, Nigel fell in love with the country’s outdoor lifestyle. He enjoyed camping, bushwalking and skiing with his wife Stevie and their two sons.

But by the late 1980s, he started to have problems with his legs and had to curb his activities.

Like many with MS, it took years for Nigel to get the correct diagnosis. He underwent unpleasant tests and a complex operation that didn’t help.

It took five more years and an MRI scan before Nigel learned he had MS.

Doctors told Nigel he likely had the disease since the mid–1970s. Nigel thought it might have been earlier.

“MS may have been why I failed my air force physical when I was 19. The doctor said I had trouble coordinating my hands and feet,” he recalled.

He thinks there might be a genetic component: a second cousin also has MS.

Getting his diagnosis was a relief because at least he knew what he was dealing with. He could also access proper treatment and support.

Nigel was lucky in his workplace. Thanks to understanding supervisors and colleagues, he continued working as an engineer.

He later worked as general manager at Parks Victoria for several years. He even had a second career as a marriage and funeral celebrant.

“Unfortunately, many others with MS don’t have support in the workplace,” he said.

He wishes the wider community was more understanding of those living with MS.

“While awareness of the capabilities of people with disabilities has increased a lot, some employers still have a way to go.

Many people with MS become unemployed. It’s an enormous waste of their talent and contributions.”

Now retired, Nigel likes caravan touring with Stevie. He enjoys spending time with his four granddaughters. He’s also taken up watercolour painting as a hobby.

Nowadays, he uses a walker at home and a wheelchair when he goes out. But he said he feels lucky.

And he continues volunteering.

In addition to his work with MS Plus and MS Australia, Nigel is president of People with MS (PwMS) Victoria. He’s also the former chair of MS Plus’s community engagement committee.

He’s chaired the Victorian branch of the Institution of Civil Engineers and the Civil Celebrants Graduate Association. He’s sat on several hospital advisory bodies and Victorian government committees.

Nigel’s also given time as secretary of his local Scout group and organised ANZAC Day and Remembrance Day ceremonies.

“I’m not the sort to let the grass grow under my feet,” he said.

For his many endeavours, Nigel received an OAM (Medal of the Order of Australia) in 2013.

Letting his volunteer work live on

Being an ambassador and donor are two ways Nigel has thanked MS Plus for its support and professionalism.

Now, he’s picked a third way: Nigel’s leaving the charity a generous gift in his Will.

“A bequest is a logical extension of my MS ambassador role. It will help keep my work going after I’m gone.

It’s vital to help fund research that will lead to better treatments. The current drugs have unpleasant side effects. It would be great to have better ones available.”

He encourages others to follow his lead.

“If more of us do this, there will be better treatments to help people with MS lead more fulfilling lives.

It would be marvellous if we could tell people ‘yes, you have MS, but we’ve got treatments to ensure it won’t get worse.’”

But a cure would be even better.

“It might not be there in time to help me, but if my gift can help others receive a cure, that’s a good thing in my book,” said Nigel.

You can help fast–track a cure as well.

You can fund more brilliant research, and make sure services and support continue to give people like Nigel the best possible quality of life — by leaving a gift in your Will. Even 1% or 2% of what is left after gifts to family and friends can make a huge difference. It costs nothing now, but changes so many lives into the future.

A LIVING CELEBRATION

Ken & Marilyn Collins

“Stay positive because today could be the best day of your life”

“I am living my second life” says Ken, with the determination of a newborn. He is ready to face any challenges with optimism and determination.

Ken was born in Goondiwindi, Queensland, and moved to New Zealand to work and study. Here he learnt to fly and obtained his private pilot licence. Upon returning to Australia, when in Dubbo, he met Marilyn, the love of his life. They married and have been together for over 45 years.

Ken was only diagnosed with multiple sclerosis in 2005. However, his symptoms had baffled the medical community for years. At that time, he was referred to a neurologist and after many tests an MRI finally confirmed what was really confronting him.

Being global, via the computer, Ken continues his involvement with the MS community. This is his life quest: to continue to make people aware of what is multiple sclerosis and the importance of maintaining a very positive attitude. https://www.facebook.com/ mspositives/

Ken and Marilyn’s life legacy and positive attitude have been formalised via a gift in their Will to MS Plus (formerly Multiple Sclerosis Ltd). As members of the “MS Callistemon League”, they are part of a most loving group of Benefactors. They want to continue to support people living with multiple sclerosis. They do not want them to face it alone. They too will be there with them, every step of the way.

A LIVING CELEBRATION

Glenys Fitzpatrick

“How a Friend’s Diagnosis Changed My Life for the Better”

Multiple sclerosis! This was the announcement that greeted me when I went to see my dear friend Katie. She and her daughter had just returned from a visit to the doctor. We were both devastated at the news.

As a pharmacist, I understood well what this diagnosis meant. I had seen many people living with MS coming into the pharmacy. I knew very well what impact this could have on her life. We were both very shaken at the news. Fortunately, as it was to be, further investigation confirmed her daughter did not have MS. But that diagnosis had a big impact on me.

I want to share with you today because I was shaken by the possibility of my friend’s daughter being diagnosed with MS. Thus, I decided to do something positive about it.

I have put MS Plus (then Multiple Sclerosis Ltd) in my Will. And here’s why ...

This gives me a lot of satisfaction. It’s something you might consider too.

As you and I know, the only thing that’s certain about MS is that nothing is certain.

While one person might live out their life with nothing more than a little muscle weakness, another might lose their ability to walk, to talk or swallow within the year. Understandably, this can be terrifying and totally shocking.

My own life has been so blessed… I have been given the good fortune to have grown within a loving family. My parents taught me to share my good fortune with others.

My journey through life has given me two beautiful daughters and a supportive partner. I love to travel the world. I recently went on a trip to the legendary Silk Road, the islands of Sardinia and Corsica and Venice and Tuscany. Now, I would dearly want others to be able to enjoy life too.

I’m telling you all this because I know you fully understand that fighting multiple sclerosis is the battle of a lifetime. You also know that the best way to fight it is to stay active ... and fight it together!

And that’s where my decision to put a gift to MS in my Will comes in. This is an expression of my values. I have also been thinking about my long–term legacy, what I’m going to leave behind. We hope we make the world a better place because we’ve been here.

Of course, that means two great daughters who will continue to be loving and caring women with families of their own. It also means no one needs to face MS alone, now or in the future, through a gift in my Will.

My daughters know well that I want to do this.

They’re very happy and support my decision.

Many of MS supporters like to include a gift in their Wills. You have supported the fight against MS before. By leaving a gift in your Will is a way to continue this support. It is about the values we share and that you hold dear in your heart.

Every time you think about the gift you will make, you will get a warm, happy feeling. Every gift, no matter what size, will make a difference. Because you’ll know you will be helping a person living with MS have a better life.

Thank you for reading this, and I hope things are going well for you.

A LIVING CELEBRATION

Laura Henschke

“How I Have Made My Blessed Life Even Better”

Many people I talk to have multiple sclerosis (MS). They have shared their stories of struggle and at times, despair. Theirs is not an easy journey. It has made me wonder what else can I do to help.

Until a few years ago, I did not know much about this devastating condition. But I have seen how nothing is certain when someone receives this frightening diagnosis.

I am sharing my story with you today because you also have a personal connection with MS. I want to share with you something that has given me great joy. It is something you might consider too.

I have put MS Plus (formerly Multiple Sclerosis Ltd) in my Will. And here’s why…

I know from personal experience how important it is not to be alone. I know you do too. I was born in Lima, Peru. My family was very loving and caring. I was very lucky. I came

from an affluent part of society. My parents always taught us to treat everyone with dignity and respect. Father insisted, through his example, that we share with those that did not have as much.

When I came to Australia, I left behind the support of a large family. But I was soon made to feel at home, through my church and school. You know, the kind of personal support you need when facing a life–threatening diagnosis. As a cancer survivor, I have a close understanding of how important information and support are. It can make the world of difference on how you can face it!

I have for many years worked in both corporate and in not–for–profit organisations. Like you, I have seen plenty of acts of generosity first–hand, whether it was from donations or from time or expertise given by volunteers. When I joined the team at MS, I was impressed by the dedication of its staff to live up to their mission. Here everyone strives to ensure ‘no one faces MS alone.’

And this is where I made my decision to leave a gift to MS in my Will.

Having experienced the love and help from people in my time of need, I understand why this is crucial. I have now, like you, been touched in my life from the stories of people living with MS. Now I want to do something beyond my current support.

This is an expression of my values. As you and I know, having people standing with us is critical. So, I have been thinking of my long–term legacy and the example I will be leaving behind for my children.

Like you, I am very proud now that I can do my part to make this a better world for those living with MS. I want to be part of this mission, even when I am no longer here. As my Greek friends would say, “Philotimo’! I know this word captures well what my parents taught me. (‘Philo’ means friend and ‘timi’ means doing something honourable, something good.)

I encourage you to think about leaving a gift in your Will to MS too. It’s not a difficult thing to do and it will give you a deep sense of satisfaction.

You too can be part of the fight against MS, by helping people with MS live the best life they can.

Many MS supporters like to include a gift in their Wills. You have supported the fight against MS before. By leaving a gift in your Will, this is a wonderful way to continue your support. It is about the values we share and those that you hold dear in your heart.

Thank you for your time and for reading my story.

A LIVING CELEBRATION Ben Holgate

“Celebrating the will to help out at work”

MS Plus employee Ben Holgate says he wants to give something back to the charity where he’s worked for the past five years.

“It’s the clients and people I work with that make it a special place,” said Ben, executive manager of strategic fundraising.

“Before I came to work here, I didn’t know many people living with MS. Since then, I’ve met plenty of wonderful men and women living with the condition. Our clients are remarkable people doing amazing things despite the massive challenges they often face daily.

What also impresses me is the community around MS and how people living challenging symptoms find the energy to help with the fundraising at the front line. I find that incredibly moving.”

Ben said MS Plus was doing exceptional work through support services to help people cope, as well as funding research to find new treatments and ultimately, a cure. It was another reason he was planning to leave a gift in his will to his employer.

Ben didn’t always work for the non–profit sector. Born in the UK, he had a successful career in advertising agencies. He arrived in Australia in 1996, taking on increasingly senior corporate marketing positions until he took a social marketing role for a government agency. He soon found he preferred work that had a social benefit.

He later worked as director of fundraising and marketing at Plan International for six years before joining MS Plus in 2017. Ben has also volunteered on charity boards like Circus Oz and The Wilderness Society, feeling the need to contribute to society in other ways besides paid work. In his spare time, he’s also a practising artist who has exhibited his work around Australia.

When he started working for MS Plus, Ben was surprised to learn that multiple sclerosis was the most common acquired chronic neurological disease affecting young adults, often diagnosed between the ages of 20 to 40. This made him think about how he could do more to help.

He did what he could on the job front. He helped hone fundraising events like the well–loved MS Sydney to the Gong bike ride and launched the charity’s lottery program to help keep dollars rolling in. The much–loved MS Readathon was relaunched and won the Fundraising Institute Australia Award for the Most Outstanding Fundraising Campaign in 2020.

In his own time, Ben participated in the “Conquer Cradle Mountain to Beat MS” challenge in Tasmania, where he raised over $3,000 through peer–to–peer fundraising.

Then he got another idea from his future strategic planning manager.

Laura Henschke, originally from Peru, told him about her plan to leave a gift in her will to MS Plus as a thank you for a great life in Australia. After thinking about it, Ben decided he would do the same.

When he turned 61, he went to a lawyer to update his Will and, after making provisions for his family, included a gift to MS Plus.

“I’m committed to helping the cause,” he said. He thinks other board members, executives and senior managers should also consider doing the same for their charitable organisations or causes they love.

“It doesn’t have to be a lot of money. It’s what you can afford to do. But it’s important to put a stake in the ground and show your commitment to your charity monetarily,” he said.

Wants to help keep the lights on

As for where Ben would like his gift to go, he’s thinking outside the box.

“So many people want to put a gift in their will towards research to find a cure for MS. I totally understand why they would do that. But I’m going to do something different. It’s important to leave something in the general pot to help the organisation keep the lights on. Also to pay bills and staff. All charities need offices, furniture, accountants, program managers and IT people to function,” he said.

“I know people often grumble about admin costs, but they can help a charity have real impact and do more great work. If a charity is well run, I know I can trust them to do the right thing with my gift,” he said.

He said his wife was supportive of his legacy plan, and has made plans of her own to support her preferred causes too.

A gift in your Will costs nothing right now, but will have a profound impact on the future for people who live with MS. Like Ben, you can leave a legacy of care and lifechanging kindness.

A LIVING CELEBRATION Simon Inwards

“The beat goes on! Life and love of music after MS”

The power of music, and the pursuit of a passion, have helped Simon stay positive while learning to live with his MS.

When he started having symptoms in 2003, Simon was diagnosed with a number of conditions including repetitive strain injuries and carpal tunnel syndrome. The possibility he had Multiple Sclerosis (MS) didn’t even come up.

It took three years to be accurately diagnosed. Then Simon faced medical retirement at just 49. He struggled to process this sudden end to his computer software career. “I resisted and tried to continue working, only to have a nervous breakdown at work,” Simon says.

Over the next 18 months he regained control of his life.

Simon has always loved music. While growing up in The Netherlands, he played bass in a high–school rock band called Anacrusis. As he came to terms with having MS, Simon decided

to reconnect with his creative side. He was bringing Anacrusis back!

It was hard to play instruments because of MS, so Simon learned to make music with software instead. He set up a studio at his home in Canberra and began to experiment with digital art.

Simon is now a recording artist.

He moved to Thailand in 2019 with his partner Nan, and two dogs Clem and Mi. He is mixing, mastering and recording tracks at his second home studio. He released his first

EP, and within months he’d made a whole album, Sounds from Many Scars. You can hear Simon’s music online (https://soundcloud. com/user–16161145).

These days, Simon sees his MS in a positive light, because it gave him time to focus on music. His new motto, Think Positive, is tattooed on his arm. But he acknowledges the journey’s been hard.

He’s grateful for the care and support of the MS community. After his diagnosis, Simon’s neurologist suggested he visit a nearby MS Plus branch. He learned how to administer injectable treatments, but he also connected with a wonderful counsellor who he says saved him.

“The counsellor helped me learn to live with an incurable illness and accept my new normal.” He says it was also helpful and

uplifting to get regular updates about MS research that was being funded by the MS community.

Now Simon is paying it forward.

Simon’s mother, Brenda, included MS Plus in her Will, and inspired Simon to do the same. He says the process itself was very straightforward. He talked about his gift with his adult children — who fully support his decision — and gave his instructions to the solicitor. That’s it.

Most importantly, including a gift in his Will to MS Plus has given Simon a great sense of satisfaction. He says, “If my gift can help current and future people living with MS, in some small way to better manage their condition, I’ll be happy.”

A LIVING CELEBRATION

Marjorie Jones

Marjorie remembers her husband John

John, my first husband was diagnosed with multiple sclerosis in the 1960’s… I did not receive any financial help or other assistance, though I wish I had. That was government policy at the time.’ Those were very, very tough times for John and Marjorie.

‘In the 60’s the role of the then ‘Multiple Sclerosis Society of NSW’ was not so well known, and we had little contact. However, family and friends were of tremendous help. Eventually I was able to take six months long service leave to be with him. I am so grateful that at was with him at the time of his death in 1972.’

Living through that difficult time gave Marjorie a first–hand understanding of the challenges people living with multiple sclerosis face. ‘I learnt how informed, caring and expert support can make a huge difference to the whole family.’

Marjorie has seen the impact that multiple sclerosis has on everyone. As a social worker, she also saw it with her clients. This personal experience aided her decision to support MS Plus (then known as Multiple Sclerosis Ltd (MSL)). She decided to help now and for well into the future.

She has joined the ‘MS Callistemon League’. She is leaving a legacy of her love via a gift in her Will to MS Plus.

“I have lived through it... so MS is a cause close to my heart.”

Marjorie comments on how critical support from MS also extends into regional areas. As it is the case with Marjorie’s niece, who lives in Armidale. She has multiple sclerosis and is benefitting from the services that MS offers.

Marjorie’s decision to leave a legacy gift is a very strong statement of her values. She supports the rights of those facing health and other challenges. Marjorie stands for human rights for all. She doesn’t want anyone to face MS alone.

Marjorie’s legacy will serve as an example for her stepchildren and step–grandchildren. Encouraging them to also live by these caring and supportive values.

She tells us: ‘I have lived through it… so MS is a cause close to my heart”.

Marjorie encourages others to join her in her quest to ensure ‘no one needs to face MS alone.’

A LIVING CELEBRATION

Elizabeth Meredith

Remembering Bill and Celebrating Meredith’s life

Making life better for others has been one of the major aims of Elizabeth Meredith’s life in her career as a scientist and educator. In turn, her four children, two step–children and nine grandchildren are continuing along this path.

Having been touched by multiple sclerosis (MS) when her daughter was diagnosed, she knows the challenges that living with MS can pose, and appreciates how the loving support of family, especially that of her late husband, can positively affect the lives of those with the illness.

Her ongoing involvement includes supporting the ‘Go for Gold Meredith Scholarship’ which has been awarded continuously since 2004. It was created in memory of Bill, her late husband. Bill volunteered at MS for

many years and the generous collection at his funeral was the beginning of this loving tribute.

Elizabeth will also be continuing her support for people living with MS by leaving a gift in her Will. However, she hopes that through ongoing financial support and research MS will eventually be eradicated.

To ensure that she can leave a legacy gift, Elizabeth puts aside a small sum each month just for this purpose, knowing that even a modest amount can make a difference. She hopes that such actions will inspire others to do the same.

A LIVING CELEBRATION

Rod & Lynette Miller

An Enduring Love

In his early 30s, Rod Miller had just about given up on the dating scene when his flatmate organised a dinner party for six. It was there he met a jolly, lively brunette called Lynette Leber, and he was smitten. To his delight, so was she.

When they got married in 1993, the future looked bright. The couple looked forward to setting up a home together in Queensland after months of commuting between Brisbane, where Rod worked in IT, and Melbourne, Lynette’s hometown.

But three years into the marriage, Rod was worried about his wife. Lynette, a highly qualified accountant, kept getting fired from jobs. She said Queensland was the problem and insisted they move to Sydney for a fresh start. Rod, wanting her to be happy, agreed.

Met with a wall of silence

But things didn’t get better for Lynette in Sydney.

“She would go in, do a great interview, get the job. She’d do a day’s work; then, on day two, they’d let her go. No one would say why — there was a wall of silence. Because she

was so likeable and good on paper, she’d get another role. But it would happen again. It was devastating for us,” Rod recalled.

“She would cut out job ads and have them lying all over the floor. She kept trying.”

Rod noticed Lynette was “going haywire” at home too. She’d forget the groceries, lose house keys, had trouble with stairs.

He often had to dash back from his IT job in Parramatta to the flat in North Sydney to sort out the latest crisis.

Another time he noticed she gripped a handrail as she tried to walk down two steps at a hotel. He remembered thinking this was odd. Friends reported she fell over while bushwalking, which they found strange as she was a confident hiker.

But another set of friends told Lynette it was other people being awful, and there was nothing wrong with her. Reassured, she didn’t see a doctor.

Once lively and fun–loving, Lynette sank into a depression. Rod wondered if she had a mental health issue brewing. She ended up seeing four psychiatrists in quick succession. One suggested the couple split up as they were “clearly not compatible.”

“That was not right at all, and it hurt us,” said Rod.

The couple did split up briefly, and Lynette moved back to Melbourne. But they soon reconciled, with Rod regularly commuting to Victoria so they could work on the marriage.

Fired from 17 jobs

In Melbourne, the job woes continued. A friend who’d arranged a bookkeeping job for Lynette told Rod she’d been fired for incompetence. The friend said he couldn’t believe it. It wasn’t the Lynette he knew.

All up, Lynette got fired from 17 jobs. Unemployed and unemployable, she had a nervous breakdown.

While hospitalised, she saw a neurologist who suspected Lynette might have multiple sclerosis. An MRI found lesions and damage to parts of her brain. It was an immune system attack, consistent with MS.

After three stressful years, they knew why Lynette was having cognitive issues. But other challenges awaited.

“We had no idea Lynette had MS. Her presentation was unusual. Often, it attacks the legs first. But she had cognitive impairment,” said Rod.

“I didn’t know much about MS,” he admitted.

“We missed clues like when she was having trouble with the steps at the hotel or when she fell over bushwalking. We realise now these were balance issues, a common MS symptom.”

He is still angry at the friends who said there was nothing wrong with Lynette.

“We wasted precious time. The earlier you start treatment, the better your chance of slowing the disease’s progression,” he said.

Getting help

Besides getting Lynette the medical help she needed, the neurologist put the couple in touch with MS Plus (then MS Limited).

“We went to their presentations and events. The staff were so compassionate,” he said.

The couple benefitted from many of the services MS Plus provides. They received emotional support and expert advice on living with the condition. Later, Lynette would live in one of their residences.

Fortunately, Lynette had income protection insurance. Once she was diagnosed with MS, her insurance firm paid up, and she didn’t have to try to work. Rod had a good job as a trainer with IBM, so there were no financial worries.

Lynette and Rod decided to live for the moment. They went to South Africa, travelling the famous Garden Route and going on safari. They often visited friends and family in Queensland and Western Australia.

They saw plays and movies, enjoyed dinners out, went on picnics with friends. Rod kept a

list going back 20 years of all the fun things they did together as a reminder to both of them of the good things in life.

Bought a house on the same street as the MS residence

But two years after her diagnosis, Lynette developed epilepsy, which sometimes happens with MS. The seizures resulted in Todd’s paresis, a syndrome associated with weakness or paralysis in part or all of the body. Lynette had to stay in a rehab hospital for a week each time to recover.

Soon, she couldn’t live at home anymore. At 40, she moved into MS Plus’ long–term care residence in Williamstown, a seaside suburb of Melbourne. Now 62, she’s been there for 22 years.

To keep close to Lynette, Rod bought a house on the same street. He now runs a software consulting firm from home and visits Lynette every day.

Once a week, Lynette comes over for dinner, and they watch TV together.

For many years, Lynette learned piano and took part in other programs offered by MS. She used to help in Rod’s garden, looking after

the profusion of white roses that bloomed there every year. She also worked in the MS residence garden.

But sadly, she can’t garden anymore. She has developed dementia, type one diabetes, and neuralgia in recent years, making her health care needs more complicated. Her balance has deteriorated, and she uses a walker to get around.

“Lynette’s resistant to the wheelchair because she knows it’s better to keep walking. She also works hard to feed herself because she wants to maintain some independence,” said Rod.

The couple never had children. So, when Rod, now 72, started thinking about his Will, he decided 50 per cent of his estate would go to their respective nieces and nephews. MS Plus would get the other half as a symbol of the couple’s gratitude.

He is happy for his gift to go to research or enhanced support services, wherever it can be helpful.

“I would like to contribute to the future of the organisation. MS’s work is vital to help people like Lynette have a better quality of life. They help partners and families too,” he said.

He remains optimistic about the future.

“One day, there will be a cure, I’m sure of it. In the meantime, I’m happy to leave MS Plus a legacy so they can continue their work and help others,” he said.

Rod said he’d like other people to have an easier time than they did — especially to know more about MS and what signs to look for.

While life hasn’t dealt Lynette a great hand, Rod said she’ll always have his love and support and that of friends and family.

“Some people in the home don’t have family and friends coming to visit, which is sad. Fortunately for Lynette, friends and family visit often, so she’s not lonely.”

“For me, she’s my reason for living, and we’re closer than ever,” he said.

A LIVING CELEBRATION

Wendy Oliver

“I know the struggle and I wish to help others in their journey”

Wendy Oliver was born in October of 1949 in Geelong, the middle child of Roy and Vera Oliver. When her mother passed away, Wendy took on most home responsibilities, aged just 10. Upon leaving home at 19, Wendy joined the Salvation Army as a Minister and later moved around Tasmania and Victoria doing social work before relocating to Brazil in 1980, as a Missionary, to continue helping others.

In Brazil, Wendy started the Salvation Army’s social work in the North–East of the country, helping people affected by poverty, drought, and prostitution. She also adopted a girl named Cristiana (Cris), who was a street child before meeting Wendy.

Due to illness, Wendy returned to Australia in December 1989 and was diagnosed with multiple sclerosis (MS) in 2002.

“At that time, I knew nothing about MS and the diagnosis came as a shock to me.”

Following the diagnosis, Wendy chose to pursue adventure by going scuba diving, kayaking and climbing the Harbour Bridge, to name a few.

“I knew that within too long, I wouldn’t be able to achieve these experiences.”

Despite being sick, Wendy was determined to continue her work with the Salvation Army. When support was needed, Wendy used MS Plus (formerly known as MS Ltd) services and her friend Glenda kindly became her carer. This helped Wendy continue to work until her retirement in 2014, aged 65.

“I have had an amazing career and am grateful for all the experiences I had during that time. Although I am now retired, I continue to still be active, assisting each week at a local Salvation Army centre providing meals for disadvantaged people.”

Alongside her career, Wendy has also made a huge contribution to MS Plus.

“Each year I enjoy taking part in fundraising events, including the Swimathon and Walk and Fun Run, where I am supported and joined by my family. I have also volunteered for the MS Peer Support Program, and won the MS Go for Gold Scholarship in 2004. This allowed me to achieve my dream of travelling to Cape York and stepping on the tip of Australia, which I achieved using walking sticks. This was truly a wonderful experience and I would not have been able to do it without the award.”

Wendy is part of our community of supporters who have generously decided to leave a gift in their Will to MS.

“I have included a gift in my Will for MS Plus as I am so grateful for the assistance provided to me. I am also passionate about supporting the goal of providing resources and options which help people living with MS live meaningful lives.”

A LIVING CELEBRATION

Peter O’Reilly

“In honour of Amanda and a living Celebration of will–power”

Amanda, Peter’s first wife, had multiple sclerosis (MS). She was someone who did not allow the disease to define or limit her life. Peter wants to tell Amanda’s story as a tribute to the person that she was.

Amanda was diagnosed with MS in 1990 and since then, MS Ltd (now MS Plus) has been close to his heart.

Peter O’Reilly was born in Nhill, Victoria where he grew up on a farm until the age of 10 until his family moved to Frankston, Victoria. His parents worked hard to give him an education and all the things he needed growing up. He later went to University to pursue a career in finance and continued to work in this industry for 40 years

Peter always admired Amanda’s strength and willpower to minimise the effect MS had on her life.

“She fought the illness and was determined not to let it define her or limit her life.”

“I chose MS because it chose Amanda.”

There were some days however that the difficulties of MS would overcome her, making Peter aware of how unfair MS can be.

“Sometimes it did limit her, which caused immense frustration.”

Amanda passed away over a decade ago due to an unfortunate car accident. But knowing that life can’t always be predictable, Peter was motivated to was continue her legacy. Her determination inspired Peter to help others with multiple sclerosis to also live their lives with the assistance they need.

“I see it as a dedication to Amanda. There are so many fine causes which seek to improve the life of others. I choose MS, because it chose Amanda.”

Now retired, Peter volunteers at a regional hospital and enjoys spending his time with

his wife, Margaret. They both live on a farm, which is home to many animals, some are pets, others are working animals. However, of all the animals he has owned past and present, it is a horse named Astro he regards so highly. Astro once belonged to his late wife, Amanda.

Peter’s decision to leave a gift in his will to MS Plus is something that gives him peace of mind that Amanda’s memory can live on.

Peter believes it is essential to talk to family members about gifts in wills. A few years ago, he married again and his wife Margaret is ‘most understanding of his wish’ to leave a bequest in Amanda’s memory to help others struggling with the disease.

“Multiple sclerosis can be an unfair disease, and it could cause Amanda immense frustration when she felt tired and limited by the condition. I want to ensure that people with multiple sclerosis can better face their challenges and retain their dreams through my bequest.”

A LIVING CELEBRATION

Lindsay West

“Celebrating a decision that made him very happy”

Kentucky south is a very small country town in NSW. Located 21 km from the larger Uralla. In the 1950’s it only had a post office, a railroad shed and a bus shelter.

This is where Lindsay was born. As the third youngest from a family of ten children, Lindsay grew up within a close–knit family group. He especially recalls the affection and closeness with his aunt and uncle.

It was not long before Lindsay had to go further away, to the town of Barraba, to find work. He found employment in the mines. Here he drove 80 tonne dump trucks.

Now retired Lindsay feels a strong connection with people living with multiple sclerosis. Even though he has never met someone with this condition. Through his contact with MS Plus (formerly known as Multiple Sclerosis Limited), he has learned much about the work MS Plus does.

He now wanted to leave behind a testament of his values and continued support. Thus, he has decided to leave a gift in his Will to MS Plus. The organisation that looks after the wellbeing of people living with multiple sclerosis.

Through communications with MS Plus he finds out about the work that MS entities do. Lindsay knows that he is supporting a charity that he trusts. It is the one that is ensuring people with multiple sclerosis do not have to face it alone, now or in the future.

Lindsay was very excited when he called us to let us know that he has included MS Plus in his Will. This decision made him feel very happy.

“Lindsay knows that he is supporting a charity that he trusts. It is the one that is ensuring people with multiple sclerosis do not have to face it alone, now or in the future”

A LIVING CELEBRATION

Bob Webb – in honour of Judith “Celebrating a legacy of compassion and courage”

Judith Webb was a much–loved primary school teacher, volunteer, wife and mother. Bob, her husband, remembers she was always putting others before herself.

“Judith loved helping people. When we lived in Canberra, she ran a popular church kids’ club, organised a drop–in centre and food parcels for needy people, and participated in pastoral visits to local aged care homes. And while we were in London, she would cook Christmas dinner for the homeless people sleeping in shop doorways,” recalled Bob.

Bob and Judith first met in 1966 at a youth hostel in Wales. Judith’s sense of fun and desire to help others quickly impressed Bob. But he admits Judith’s flaming red hair and ‘terrific smile’ also got his attention!

“We were hitchhiking as we did back then. Judith was holidaying around the UK and Europe. I was on a mission to walk up the highest mountains in Wales, England and

Scotland in the one holiday. I’m sure Judith thought I was a bit crazy,” he laughed. Apparently not. The two talked non–stop while peeling potatoes and washing dishes in the hostel’s communal kitchen. Later they went for a long walk. Bob learned Judith was a teacher from Newcastle, NSW, and she discovered the easy–going Englishman from Gosport, a town on the south coast of England, was studying physics at London University. He liked sport; she didn’t. “Fortunately, she didn’t hold it against me,” he said.

Though they parted to pursue their individual travel goals, they agreed to meet up later in London. A year later, they got married there. Bob was happy to follow Judith back to Australia, where she resumed her teaching career. The couple settled near Bossley Park, Sydney, where Judith was teaching, and Bob pursued a PhD in astrophysics at Sydney University.

While Judith taught, co–parented with

Bob and got involved in charity work, Bob finished his science studies and went on to senior leadership positions in large and diversified organisations, including CSR Ltd, the Australian Trade Commission and the Australian Taxation Office. On retirement, he joined the Australian National University’s Climate Change Institute and Fenner School of Environment and Society part time, where he still participates in climate change and sustainability research.

The couple had two children, Andrew and Kate, and lived in Sydney, Adelaide, London and Canberra during their 54 years together.

“Judith was a wonderful wife and mother. As well as teaching, she did an impressive amount of community work for people of all ages and needs. She was always concerned for others, never herself,” recalled Bob.

In Canberra, the couple attended the local Anglican Church, and Judith started a church–run kids’ club that was tremendously popular, growing to around 90 kids enrolled. She also became the co–leader of a drop–in grocery distribution service, organising a place for tea, coffee, a sandwich and a chat as well as

food parcels for people struggling for whatever reason. In her spare time, she liked to garden and read.

As they entered their 60s, Bob and Judith looked forward to retirement. But in 2007, Judith started having unexpected falls. She underwent a battery of tests, but it wasn’t until two years later that Judith learned she had late onset primary–progressive multiple sclerosis (PPMS), a relatively unusual form of the disease. She was 66.

“As a teacher, Judith had encouraged her students to do the MS Walkathons and Readathons to raise funds to support people with MS. Otherwise, we knew little about the disease. There wasn’t a history of MS in her family, and we didn’t know anyone else who had it,” explained Bob.

The couple turned to Gloria McKerrow House, an MS support and service centre in Canberra, for advice. Supportive staff provided practical tips on managing the condition, and Judith also went there for exercise classes tailored to MS patients. Bob retired from his job with the Commonwealth Government in anticipation of Judith needing more support.

At first, Judith didn’t feel too bad. But a few years after her diagnosis, the symptoms became more obvious and within a few more years she had lost all mobility in her legs, was losing the use of her arms and hands, and her eyesight was deteriorating. For the last years of her life, she was confined to bed, a special chair or a wheelchair.

“We were told early on that there were no treatments for PPMS. Judith was brave and uncomplaining throughout, although I know she found it especially difficult to rely on me and others for everything when she had always been the one to help others. Yet she stayed positive,” said Bob.

Despite a valiant 10–year fight, Judith died in 2020 from complications associated with MS.

“I told her she was my hero because she was. All in all, I was a lucky man to have had such a fabulous and long marriage. The last years were hard, but we did have a good run of health for a long time,” he recalled.

As a tribute to Judith’s generosity and courage, Bob has decided to leave a portion of his will to the research arm of MS Plus.

“Before she died, Judith and I talked about leaving gifts in our will. After providing for the family, we decided we would give money to an overseas humanitarian charity and to MS Plus because they had helped us navigate the world of MS, and we wanted to see more treatments for all forms of MS,” he said.

Their daughter Kate approves of their charitable intentions, and Bob proudly notes Kate is a rock to her family and a helper to others, like Judith.

“Judith had a big influence on Kate’s values,” he said.

Bob believes their son Andrew, who sadly passed away in 2016, would also have been supportive.

Today Bob keeps abreast of PPMS research developments, including those by MS Plus in a collaborative international effort. He’s happy that the first–ever treatment for PPMS has now been medically approved.

“It was too late to help Judith, but it should give hope to others diagnosed,” he said.

“I hope further research will improve MS treatments and maybe even reverse this mean disease. That’s why part of my will is going to MS Plus for research — to remember a brave and loving woman and all the people she would have wanted to help.”

Could you be like Bob and support people with MS?

A LIVING CELEBRATION

Lin Wong – in honour of Deirdre

“Celebrating Deidre’s legacy”

When Lin Wong proposed to his girlfriend Deidre Gaudion in 1987, she looked at him thoughtfully and said: “I have something to tell you. I have MS. That’s your way out if you don’t want to marry me now.”

“I told her that didn’t worry me at all. I was so in love with her,” recalled Lin, 69.

The Melbourne couple, who would be married for 38 years, first met at a friend’s party in the early 1980s. Lin, who worked in retail and later in the transport industry, was captivated by the “intelligent, eloquent and astute” young woman. They soon swapped phone numbers.

“Deidre had certificates in commerce and business studies. She went to England for a few years to work as a PA in various companies. When she returned to Australia, she decided to become a teacher. Deidre could have done anything, she was that bright,” recalled Lin.

For many years, Deidre taught business studies at St Columba’s College, a Catholic girls’ school in Essendon. She later became the career counsellor, helping the girls decide what they should do for a living.

Deidre first started showing symptoms of MS while she was in England. Back in the 1980s, it often took a long time to get a diagnosis. But eventually, she was diagnosed with secondary progressive MS, a stage of the disease which comes after the relapsing form of MS. With secondary progressive MS, one’s disability worsens over time, and there is less likelihood of relapses when symptoms get worse, then better.

“It took a long time for things to get bad. Meanwhile, Deidre just carried on. She didn’t want to let the principal or her students down. She would walk into the school and work. When that got too hard, she used a walker. When she had to retire, she started using a wheelchair,” recalled Lin.

In her spare time, Deidre loved going to the art gallery or theatre with Lin or her girlfriends. The couple also enjoyed downtime at their Coburg home. They decided not to have children, opting for a dog and three cats instead. And Deidre certainly cherished those ‘fur babies.’

Deidre also collected over 200 porcelain dolls and an impressive array of dollhouse miniatures in her lifetime. She would spend hours painting dollhouse furniture and rearranging her collection to her satisfaction. Most years, Lin would take her to the annual dollhouse and miniatures exhibition in Melbourne so she could browse the stalls and add to her collection.

Helped others with MS and other illnesses to cope

When she retired, Deidre said she didn’t want to be stuck at home doing nothing. She told Lin she wanted to become a volunteer counsellor. Deidre first volunteered at the Royal Free Masons Gregory Lodge in Flemington, where she’d been a patient. Later she had the opportunity to volunteer more regularly at Royal Melbourne Hospital’s rehab unit, where she also received medical care.

For four years, Lin drove her three days a week to the hospital, where she would go around in her wheelchair, chatting with patients in various stages of their disability journey.

“Deidre would talk to all kinds of patients ––people with MS, motor neurone disease and diabetics who had had their limbs amputated. She would offer advice on how to manage certain issues or be a sympathetic ear if they needed to unload. Her career counselling training made her a great listener. People responded well to what she had to say. She knew all the nurses and could report on how the patients were going,” said Lin.

But Deidre’s health soon declined, and Lin quit his job to care for her full time. Seven years later, she went into palliative care at the hospital where she’d been such a popular volunteer.

In 2020, Deidre died, aged 69. Tragically, due to Melbourne’s long pandemic lockdown, only 10 people could attend her funeral. But her legacy will now live on.

Twenty years before her death, Deidre sat down with Lin to discuss estate planning.

“Deidre didn’t know how much time she had left, and she wanted to plan for the future. Since we didn’t have children, she suggested we might give most of our money to charity. She wanted to help a pet charity as she loved her animals, but mostly she wanted to give back to MS Plus for their support,” said Lin.

“It’s a great idea. At this stage, I don’t know whether I would like our gift to go for research because while Deidre was keen on finding a cure, so many people with MS need services right now. Most likely our gift will be a combination to help with research and patient services. I have to think about it more while I get my affairs in order with my solicitor,” he concluded.

Remembering our loving Benefactors

In memory of the life of a Benefactor

Waybrett “Brett” James Avery

Brett was born in 1914 and grew up in Loxton, South Australia. He served as a Private in the Citizen Military Forces within Australia between 1941 and 1942. On his discharge, he joined the volunteer Defense Corps in part–time war service until 1945.

Brett continued to work on his father’s farm in Loxton before his own farm in Mount Benson, South Australia. He won an Agricultural “Best improved pasture award” among other agricultural awards. He moved to NSW in 1975, where he purchased a farm that led to meeting his late wife, Marian. In January 1977 (aged 63 years), Brett married Marian. They were married for 30 happy years before her passing in 2006.

Both Brett & Marian had a shared a love for gardening. He continued to enjoy being outdoors and gardening throughout his life, up until he could no longer use his secateurs! When he moved into a self–care village, he took care of their gardens and received the gardener of the year award for his work in 1999 (aged 85 years).

Prior to marrying Marian, Brett had only travelled overseas once; in 1974 he travelled to Papua New Guinea. Marian loved to travel and together they took many trips throughout Australia and around the world. The pair had planned a trip to Canada, however due to the

passing of Marian, Brett continued with the trip alone at the age of 94. Age did not stop him from following his passion for travel; on his 95th birthday he drove to Adelaide and then when some of his family rang him on his 96th birthday, they were surprised to be told that he was driving to Queensland!

Brett was frequently described as a true gentleman by all whom met him, who tried to do good and cause no harm. He was strong and purposeful, as well as generous to the needs of others. He believed he was blessed to have lived a fulfilled life up right up until the age of 99. After supporting MS Plus for a number of years, Brett chose to also leave a gift in his Will as he wanted to share his good fortune from his hard work. Thus, continuing his legacy by how he lived his life, helping to ensure others can live a life as full as his.

Kathy & Vic Bilbrough

Celebration of Life an enduring love

In 1986, while working at the Department of Veterans’ Affairs in Melbourne, Vic Bilbrough met Kathy Adamson. The gregarious supervisor, known for his guitar licks and good time persona, was captivated by the quietly confident assistant research officer.

And the feeling was mutual.

“Vic often joked that he was lucky Kathy stuck by him, especially after meeting our extended clan,” recalled his younger brother, David.

It was a love that endured beyond 1998— the year that Kathy, 41, tragically died from complications arising from multiple sclerosis. Vic never recovered from her death. He died, aged 68, in 2020.

At a gathering in Vic’s memory in 2021, people remembered the couple’s enduring love and many accomplishments.

Kathy grew up in a loving, close–knit family in Melbourne. Her sister Lynne Adamson remembers her as an ‘all–rounder’ at Glen Waverley Secondary College, which the girls and their brother Ron attended.

“Kathy excelled at violin, piano and singing, played softball and netball and won many honours and academic awards. When she died, I received a box from Vic’s family with Kathy’s things. It contained memorabilia like her Euro Rail pass and her school awards. There were also glowing letters from teachers, students, and employers,” she said.

After high school, Kathy studied arts at Monash University, specialising in German. She spent a year perfecting her language skills in Cologne, where she also forged lifelong friendships. She later undertook teacher training in Melbourne. Kathy then taught German at Cato College (now Wesley College Elsternwick) before heading back overseas to teach in Hamburg.

When Kathy returned to Melbourne, she changed careers, opting for a research officer role in the Department of Community Services. She later moved to Veterans Affairs. Ultimately, Kathy decided the life of a public servant wasn’t for her and returned to teaching. She taught German at Caulfield Grammar School until her early retirement.

Born in Gateshead, England, Vic moved to Australia with his parents and two elder brothers as part of the post–war migration scheme. (His brother David and a sister were born in Australia). They settled in Koetong, a community in northeast Victoria.

David noted that Vic was sporty, playing footy and cricket. He also liked fishing, snooker, and golf, although Vic often joked to others that he wasn’t much chop at golf!

“Vic was clever, witty, and talented. I marvelled at his general knowledge and how good he was at cryptic crosswords. He was also wonderful at woodwork. One time, he made the most beautiful wooden guitar,” said Lynne.

Vic was also a good singer and guitar player. At 12, he entered and won a local talent competition with his rendition of Purple People Eater. In his teens, he formed a band called The Firebirds with his brother Stan and friend Steve Miller. The boys even gave a prime–time performance on their local TV station.

“Vic was often at the centre of many musical evenings in the family kitchen,” recalled David.

After high school, Vic clerked in the accounts department at Bunges Flour Mill in Albury and studied accounting. He then moved to Melbourne in the mid–1970s to work for the ATO. Vic later worked in home renovations

with brother Sid before returning to government in the mid–1980s. He then took on a supervisory role at Veterans’ Affairs where he soon met Kathy.

Kathy and Vic married in 1991. They bought a house in Forest Hill and planted a large garden together. They also attended concerts. Kathy also loved visiting Vic’s childhood home in northeast Victoria, and they enjoyed camping.

But trouble was brewing. While teaching in Germany, Kathy experienced vision problems (optic neuritis). She also broke her arm in a fall. Two years into the marriage, she started having more health issues.

It took time to get answers, but Kathy eventually learned she had an aggressive form of multiple sclerosis.

Wanting to spend as much quality time together as possible, Kathy and Vic travelled around Europe and the UK. They enjoyed pints with the Bilbrough relatives in northern England. Later they visited Scotland, France and Germany, where Kathy had many friends from her university and teaching days. “Vic often reminisced about that trip. It was one of the highlights of their life together,” said David.

David and Lynne say Kathy faced her illness with grace and courage. While it must have been a gruelling battle, they said Kathy and Vic didn’t often discuss it.

“Kathy didn’t want to be labelled with the disability

tag, instead concentrating on what she could manage,” said Lynne.

“They were private about it. You’d go there for dinner, and everything was as normal as possible, even when Kathy had to start using a wheelchair. She didn’t want special treatment,” added David.

Kathy worked until the classroom demands became too much. She and Vic turned to their local MS Society (now MS Plus) for support in managing her illness. As her condition deteriorated, Kathy’s parents assisted with her care, and Vic also quit his job to become a full–time carer.

The family thinks Vic mourned Kathy for the rest of his life. While he sought a more positive life path, he was hospitalised several times and died in 2020.

“I remember Vic as a positive person, discussing kitchen renovations, the garden, music, art, food and cooking. He was someone who did his best in the face of great personal challenges, caring for someone who faced a cruel version of MS. With Kathy’s death, we all lost part of ourselves. Victor, I know, lost a huge part of himself and the future they had planned,” said Lynne.

The family soon realised Vic hadn’t left a Will. But David, as Vic’s Administrator, had an inkling of his last wishes.

“Vic mentioned a few times he and Kathy wanted to leave a generous gift in his will to MS Plus as a thank you for their support. He also wanted to help another charity and his siblings. We liked the idea of helping the MS cause,” said David.

“By leaving this gift in their names, we hope that others will be supported with their MS challenges when they need help,” he added.

Today, family members think of Kathy as a bright star in the family firmament. An all–rounder and quiet achiever who refused to let her illness define her.

“Vic was a great bloke who gave it all a fair crack,” was how elder brother Stan summed up Vic’s legacy. A man lovingly remembered for carrying the torch for his wife, his wit, generosity and always being ready for good times.

Thanks to Vic and Kathy, MS Plus can continue its mission to provide support and services to people living with multiple sclerosis. Their legacy to those living with the condition may be a world where MS no longer has the power to devastate families and take away loved ones too early.

Even 1% or 2% of what is left after gifts to

family and friends can make a huge difference. It costs nothing now, but changes so many lives into the future.

If you want to know more about leaving a gift in your will to MS Plus, ring Laura or Rebecca on 1800 443 867, email futureplanning@ ms.org.au, or visit www.mymslegacy.org.au.

Geoff Burfoot

Geoffrey Robert Burfoot left a generous footprint behind him.

The former patrol officer, nicknamed “Barefoot Boy, Burfoot,” left bequests to a staggering 52 charities, including MS Plus. While the reasons for his gift to MS remain a mystery, Geoff’s friends say he was always generous and kind.

Reverend Graeme Hodgkinson, who delivered the eulogy at Geoff’s funeral, said Geoff often helped people who had financial problems and supported many charities in his lifetime.

People in Tyalgum, NSW, remember his community–minded spirit when he helped finance a new roof for St John’s Anglican Church.

Born in 1923 to Bob and Gladys Burfoot, Geoff spent his childhood in Roseville, Sydney. His father had suffered during the Great War, and his issues affected the early life of Geoff and his younger sister, Joyce.

Geoff had poor health as a young man, and his doctor recommended a move to a tropical location. In 1946, he became a patrol officer

in the then Australian Protectorate of New Guinea (now Papua New Guinea). He quickly took to the lifestyle and would spend 29 years working there.

After an initial stint in Port Moresby, he served briefly in Lae, Karapit and Hingaturu before heading to Tufi for 17 months and later Iona as officer–in–charge. He also spent nine months assisting locals after the 1951 Mount Lamington volcano eruption, leading patrols into the disaster zone and assisting with the burials of those who had been killed.

In an article written by a fellow patrol officer, Geoff was referred to as “Barefoot Boy, Burfoot” because he liked going around without shoes, even in the jungle!

After his promotion to assistant district officer, Geoff worked in Artape, Wewak, Goroka and several other communities across New Guinea.

Principled…but fun

Geoff made many friends among his fellow officers. While they remembered him as someone who was highly principled, they also noted he was different from the “run of the mill officers.”

One of Geoff’s bosses recalled: “Our kids loved it when Geoff visited. He learned all the native dances, and he loved to perform them with great gusto in front of anyone interested in watching. Once I called on him and found him hanging from the rafters by his ankles with his arms crossed over his chest doing some Oriental exercises. As an entertainer, Geoff had no equal.”

Whenever he was on leave, Geoff would return to his parent’s home in Sydney and use the shed behind the house as a special retreat. He became legendary among his friends for his beer–making, and it was considered a privilege to be invited over for a taste!

When New Guinea declared independence in 1975, Geoff returned to Australia permanently. He settled near Tyalgum, a rural village in north–eastern NSW. Another friend of Geoff’s, now living in Melbourne, said that Geoff missed the island very much. It’s possible the green hills around Tyalgum reminded Geoff of PNG.

In Tyalgum, Geoff quickly learned how to take care of his country property, helped by local farmers who became his friends. Although, as was wryly noted at his funeral, he still liked to do things his way!

When he wasn’t working the land, Geoff would concoct natural therapy remedies, having picked up those skills from the Australian Natural Therapy College in St Leonards, Sydney. He was also associated with the Southern Cross Herbal School.

Reverend Hodgkinson recalled that Geoff was always making natural remedies to protect himself against illness, preferring them to prescription drugs. While he was personally sceptical of their efficacy, he admitted that Geoff was healthy right up until he passed away!

Geoff kept in shape with daily exercise and was a regular at the Murwillumbah Rifle Club. He collected antique handguns, including a Colt 45. He also liked going to church.

He was a passionate cook who could turn out a variety of delicious German, English and Asian dishes. He often entertained friends and his sister Joy when she visited from Sydney. He kept a detailed diary, and most days, he liked to eat at Flutterbies, a local restaurant. Woe betide management if his favourite table was not available!

You knew when he was in town

Later, a dodgy hip made it difficult for Geoff to drive. But he had many friends in Tyalgum who volunteered to chauffeur him around to get his groceries or attend medical appointments. This included some of the staff at Flutterbies.

And everyone in town knew when Geoff was picking up his mail! When they arrived at the post office, his driver of the day would blast the horn three times and the postmaster and shop assistant would come running out with Geoff’s mail and newspapers. On these runs, he would treat his driver to lunch at a local Chinese restaurant.

Even though he was comfortably well off, Geoff was meticulous in keeping track of his expenses. He filed everything, but at one point, he couldn’t find the paper with the combination to his safe. He spent days looking everywhere for it, finally finding it hidden under the carpet in his study!

Three years ago, at the age of 94, Geoff passed away unexpectedly. “Barefoot Boy, Burfoot” will long be remembered for his colourful ways and generosity to friends and worthy causes.

Elena Franca Canu

“Elena always wanted to help others”

Born in September 1949, Elena Canu grew up in Northern NSW. A much loved daughter to parents who had migrated from Sardinia, Italy, Elena enjoyed a very happy childhood spent outdoors.

As a young woman, she went on to build her career in the Australian television industry, which included roles as a film librarian, a studio director and a producer. Many of her colleagues will remember her as “Paddles”, a nickname Elena developed whilst working at Channel Nine, Sydney. This affection shown by her colleagues reflects the deep care Elena had for her friends and family throughout her life.

“By leaving a gift in her Will to MS, Elena’s caring nature continues” say her sisters Rina and Antonietta, and brothers Mario and Frank.

Elena was very grateful for the support she received from the MS organisation, having lived with multiple sclerosis for 30 years. She was long aware of multiple sclerosis, due to its prevalence in Sardinia where the existence of

multiple sclerosis is significantly higher than in neighbouring Mediterranean regions.

When writing her Will, she found it very easy to help a cause that was so close to her heart. MS helped her greatly on her difficult journey with multiple sclerosis and she was very appreciative of the difference it made in her life. As a legacy she thoughtfully wanted to help others in the same caring way that she was helped.

Elena’s life was cut short, however she continues to live on via this loving legacy. This very generous gift will help fund crucial research and lead to better lives for those living with multiple sclerosis.

Elena knew that you don’t have to be super wealthy to leave a gift in your Will, and that nothing could be further from the truth. After taking care of family and friends, she understood how that one final gift, no matter how big or small, can make a difference.

Today, Elena continues her life legacy and is standing together with those whose journey she well understood, ensuring they do not face multiple sclerosis alone.

Judith Ann Carlson

Judith Ann Carlson, or “Judy”, or “Jude”, was born in San Francisco in 1948 and was raised by Ralph and Eugene Carlson.

She grew up in Sunnyvale California with a younger sister and a younger brother, and had a lovely childhood with friends, church and school. She also excelled academically when she attended Buchser High School, earning prizes, learning the string bass and playing in the orchestra. It was clear she developed a love for music and would have loved to have majored in it, but unfortunately did not get that opportunity when graduating and instead studied Teaching at San Jose University. She majored in English, History and French.

In 1969–1970 she travelled to France and enjoyed travelling and exploration of Europe. She later returned to California, but there was no work there at the time for a teacher. She discovered an advertisement looking for teachers to come to Australia, and with that sense of adventure she applied and came to Australia at 23 years of age in 1971.

She taught at Mitcham Highschool, now known as Mullauna Secondary College, teaching English, History, Social Studies, and Drama. She developed a strong friendship with the headmistress, Edna Usher, who she saw like a second mother. But this would only continue until 1990, when Multiple Sclerosis forced her to retire and put an end to her career. She was teaching with the diagnosis of the disease since 1982, but slowly the terrible disease crippled her nerves and subsequently her body and becoming a patient, her life was changed.

Judy entered a nursing home in 1991 when she was no longer able to cope in her own home. She found the three years there difficult, being she was 43 and the facility was tailored to elderly care. Her life improved when she was transferred to a specialised facility for MS patients in Keilor Victoria, with new friends, and an emphasis on socialization. But this would change over the years. Friends passed away, and Judy’s care needs became greater. Judy remained in Keilor until 2013, when she was accepted as a resident at Karana Nursing Home Yarrawonga.

Judy was a kind–hearted, intelligent, talented and gifted person. She is remembered by her friends as “the person who spread happiness wherever she went”, a good friend appreciated by many. She was born American but gained citizenship in 1996 in Australia.

Judy, like many people who were affected by MS, looked towards a future where this disease is no more. She made the decision to include MS Plus (then MS Limited) in her will, not just as a donation for a cause but as hope for the day when this disease and its affects won’t hurt another gentle soul.

Allan Collier was an inspirational man, a caring father, and a loving husband. His son, David, has shared with us a bit of the person his father was, and to us he seemed like a strong figure to look up to.

When David’s mother, Margaret Collier, was diagnosed with MS, Allan stood by her side and cared for her for years, working tirelessly to ensure she could stay at home for as long as possible. Margaret battled the degenerative disease for ten years, and with her son and husband they fought through its hardships together. The MS society provided its support and assistance, but we doubt that anything is comparable to the love and care Allan and David would have shown.

Allan also endured his own medical complications, including his diabetic condition leading to a leg amputation. Yet throughout the years he remained “positive, independent, and active”. David provides an

Allan William Collier

example of when he was sailing a small yacht, practicing his skills in preparation for a sailing program for other people with disabilities. Another example is when he resumed driving after having his car modified for his medical condition.

Allan will be remembered as an admirable, generous, and a strong person. He has kindly donated to MS Plus (then known as MS Limited), to support the work that we have done for his wife, and for the work we have been inspired to continue delivering for people with MS, and for those like Allan who are willing to stand strongly with those with MS.

James Douglas East

James Douglas East will be remembered as a good humoured and joyful gentleman, willing to provide advice and assistance to those in need.

He was born in rural Kyneton Victoria and lived in Melbourne, experiencing a great deal of hardship along his journey in life. And yet it would seem he still appreciated the goodness in life and wanted to ensure it through supporting the community and organisation working to provide that quality of life.

At the age of three he lost his mother after she battled an illness and took responsibility of helping with the work of running a farm at a young age. He was still in Kyneton at the time, and he and his father recall the return of his uncles with disabilities from their struggles during WWI. But life moved on, and during the Great Depression he came to Melbourne to work and study at night. He lived with his uncle and aunt for many years, and they appreciated James assistance for his Uncle

who was diagnosed with Parkinson’s disease, a condition that worsened his uncle’s health over the years.

In all his life while facing hardship, James’ priority was to help others in need in his community. Perhaps that’s why he decided to support the Multiple Sclerosis society of Victoria – so that even in his passing he would still be contributing to others less fortunate, and making a large impact on the wider community.

During the second world war, he enlisted in the Army, and when he came back he made a career as an accountant in Melbourne in the private sector. James is an example of the diverse people who come from all walks of life but share the common desire of helping charities like MS Plus (then known as MS Limited). He appreciated the significance of medical advances and the importance of helping people, and his legacy will continue on with his donation.

Judith Florence Forman

Felicity describes her mother Judith as very giving and would be truly touched to know that people would be reading about her!

One of the big issues that moved my mother Judith, was mental health. She had a friend who suffered greatly from depression and so Mum was always there to help her in her darkest moments. A fond memory I have of Mum is that she counted everything. She told me that one wet night, while waiting for a mental health group to start, she counted the number of snails she stamped on in the wet! Mum counted everything, cracks in the footpath, people at the bus stop – everything!

Mum had the ability to get along with everyone and anyone. Together with my father they ran a periodical subscription agency which sourced journals from all around the world for libraries, hospitals other large organisations. My father died when I was only eight and after his passing Mum ran the business herself from home. She could talk to anyone. She was well–liked and people naturally gravitated to her.

Due to her father’s job with State Rail, Mum attended 9 schools in 11 years. This gave her lots of opportunities to meet new people from Bondi to South Australia and all points in between. In later life she loved travelling and even got herself really fit for an expedition to Nepal only to break her ankle two days into the trek and had to be airlifted home!

Mum was very compassionate, if she saw a need she really wanted to help, from community help programs to charity Christmas card sales. Even though she had no direct connection to anyone with MS, she was all for the underdog, helping wherever she could. I know Mum would be happy to know her gift was helping those with MS lead more comfortable lives.

(from her daughter Felicity Enriquez)

Jean Fraser

“Kindness was indeed Jean’s legacy”

The Dalai Lama once said “My religion is very simple. My religion is kindness.” He could have been thinking of people like Jean Fraser.

Jean spent all her life living quietly and modestly on the family farm. She was always kind and thoughtful towards those less fortunate than herself. She faced many challenges and misfortunes in her long life. At the age of 16 she lost her mother. In order to help on the farm and look after her father and younger polio afflicted brother, she had to leave school.

Tragedy struck again in 1939 when the family house, farm and animals were destroyed in the terrible Victorian bushfires. This further blow would break many but instead Jean courageously helped rebuild the home and farm. Care of her brother and father continued through, and after, the second world war. Having experienced hardship and loss early in her life, and caring first–hand for her brother, stricken with the paralysis of polio, gave her an insight into the many challenges of multiple sclerosis. Jean never forgot those

less fortunate, and, many years later wanted to help those challenged by MS. She believed people living with MS deserve to have access to care, support and advice. To this end she bequested a gift in her will to MS for MS research.

Jean is no longer with us, but her kindness and thoughtfulness are remembered proudly by her family and friends. She wanted those living with MS to be enabled through her gift, to live a life of possibilities with the care and support of MS for MS research. Kindness was indeed Jean’s legacy.

Robert Wemyss Frewin

“Our family are delighted for your acknowledgement of our wonderful father’s donation left in his Will to the MS Society (an earlier name for MS Plus). Hopefully the gift can help with the continuing research & treatment into MS & benefit other

Margaretha Kuipers

“Wartime experiences shaped Margaretha’s generosity”

Years ago, Margaretha Kuiper’s family ran a small hotel on Amsterdam’s Herengracht canal. During World War II, a Jewish family lived with them. One day Nazi soldiers came looking for the family. Margaretha’s grandmother distracted them with coffee while the family escaped through a trapdoor in the roof.

Meanwhile, Margaretha’s uncle was secretly hiding Jews and funnelling them out of Amsterdam to safety. He would later make the history books.

During the Dutch famine (hongerwinter) of 1944–45, there was no firewood, and people dismantled wooden houses and furniture to provide fuel for heating. Margaretha and her sister Clasina scrounged around Amsterdam’s tram lines, pulling up wooden blocks to take home to burn.

One day, a German soldier caught the girls and threatened to shoot them. Several brave women surrounded the girls and yelled at the soldier to leave them alone. To everyone’s relief, he walked away.

These wartime acts of courage and kindness made Margaretha aware of the need to be generous and help others wherever possible. In the future, she would channel her particular brand of generosity into helping her family and favourite causes.

Margaretha would also extend her philanthropy beyond her lifetime. She left gifts in her Will to several charities, including MS Plus (when it was known as MS Limited).

But this would come later. Meanwhile, the hongerwinter dragged on. Margaretha was evacuated to the countryside like thousands of other Dutch kids as families sought to spare their children from the ensuing famine. While staying on a farm north of Amsterdam, Margaretha met Willem Kuipers, whose parents were hosting her sister. They quickly became friends.

A few years after the war, they became pen pals when Willem went to work in Indonesia as an aeroplane mechanic.

When he returned to the Netherlands two and a half years later, Willem would often bike from his village to Amsterdam to see Margaretha. Friendship turned to love, and they got married.

In 1955, Margaretha and Willem immigrated to Australia in search of a better life. They went to Melbourne, where they bought a plot of land in Noble Park, a suburb southeast of the CBD. Willem worked as a toolmaker, and Margaretha took in sewing as she enjoyed making clothes.

The couple built their home, adopted two girls and had two more daughters. Daughter Brenda White said her parents took their time with the family home, wanting it to be perfect.

The local council told them to hurry up. They lived for years in a sort of shed. Eventually, it became the garage,” recalled Brenda.

Over the years, the close–knit family expanded. Today it includes four sons–in–law, three grandsons, six granddaughters and three great–granddaughters.

After Willem passed away in 1989, Margaretha continued to live in the house they built together until she died unexpectedly in 2019.

“Mum loved her family above all and relished extended family events. While often a straight talker, she appreciated a good laugh and loved telling jokes. She would have given anything to spend more time with her loved ones,” said Brenda.

Margaretha was frugal and careful with money all her life. Brenda believes this trait was a holdover from growing up in the Great Depression and World War II. But at the same time, her mother was generous and fair to all her children.

“If one of us received some money from mum, she would make sure the others got the same amount,” said Brenda.

Brenda noted her mother was also generous to charities she considered worthwhile.

Margaretha first became interested in MS Plus because Brenda had developed multiple sclerosis at the age of 33. She was also pregnant with her second child.

Brenda had relapses that left her exhausted, numb and with the “pins and needles” that often plague those living with the condition.

Margaretha was devastated about Brenda’s illness. She told her daughter she felt “useless” about making the diagnosis easier. But she would come over to Brenda’s house to fold laundry and look after her grandchildren so her daughter could rest.

When she died, Margaretha provided generously for her family. But the full extent of her generosity became apparent when her daughters realised Margaretha had left gifts in her Will to charities that were close to her heart. These were charities focused on conditions family members had, including diabetes, epilepsy and Brenda’s MS.

“During her life, Mum supported some of the MS Run and Ride Festivals. In her Will, she decided to support MS further. She wanted more research conducted that would help people with MS live better lives. It’s a wonderful legacy,” said Brenda.

Ruth Uriel Leggett

I’d like to share with you the story of my loving sister Ruth.

Born in 1922, Ruth was one of six kids in our family who grew up during the harsh years of the Depression. Our mother and father were terrific examples to all their children. Dad was never out of work, and for that the whole family was very grateful. Mum was a truly charitable woman giving vegetables and money to those in need and was also known to take in homeless people.

Despite the hardship of growing up during the Depression our parent’s work ethic, kindness and boundless generosity instilled in Ruth a strong responsibility to “give back”. Her practical way of doing this was to donate to charity and engage in volunteer work that she felt benefitted the community.

In 1941 Ruth joined the WAAF. She was a true–blue Aussie. After the war she married, had her daughter Annette, worked in a volunteer capacity at Dalwood Children’s Home and with the Seaforth Returned Services League. Later as a single mum, Ruth supported her family by working for MBF and through her community spirit and

tireless volunteering she came to know almost everyone who lived in the Manly area! Her daughter Annette was also strongly connected to the local community though her position as a High School Teacher in the Northern Beaches area of Sydney.

Ruth and Anette loved to travel and together shared many journeys overseas. Sadly, Annette died several years ago from bowel cancer. With her daughter’s passing Ruth’s passion became her garden. Like our mother, almost everything Ruth touched grew and grew well. Ruth learned a lot from Mum and always looked up to her. Ruth loved children and was always very generous to her family and friends. One of her sorrows however was she didn’t have any grandchildren but the love she would have had for them she gave to my children. I am very proud of Ruth’s decision, in discussion with her solicitor, to donate in her will to MS and other charities, as I believe it was based on her values and bountiful love for others, always wanting to give back to the community.

I miss Ruth greatly, but she continues to have an impact on many lives through her generous legacy, making this world a better place for people living with MS.

Story by Ruth’s sister Patricia Wilson O’Connell.

Maxwell Arthur Thomas Mawson

Quiet achieving farmer leaves generous legacy to MS.

A farmer from southwest Victoria has left a generous gift in his Will to MS for research. A tribute to a niece who has the condition.

Descended from a long line of Victorian farmers, Maxwell Arthur Thomas Mawson owned a farm at Wensleydale. This is a small rural community at the foothills of the Otway Ranges. Max passed away in 2020 at the age of 83.

For about a hundred years, the fertile soil had enabled the Maxwell family to grow peas and potatoes. He was also able to raise fat lambs and cattle on the hilly slopes at Wensleydale. At one point, the family purchased a large acreage of bushland. Here they felled timber for firewood later sent to Geelong by train. Max took over the family farm in the 1960s.

“It was mixed farming at its best. The work was hard and the days long,” recalled Kim Johnson, Max’s niece. Kim is a merchandiser who also raises horses on a farm–let about 10 minutes from her uncle’s former home.

But it wasn’t all work for Max. As a young man, he played cricket and football for Modewarre. Max was also a regular at the popular Saturday night local dances and suppers. As a member of the Wurdale Rural Fire Brigade for 45 years Max fought many fires in the foothills of the Otways. This included the 1983 Ash Wednesday bushfires. This was one of Australia’s most destructive bushfire events.

Kim remembers her uncle as a kind–hearted man. As a life–long bachelor who lived frugally and was always busy around the farm.

“Max never did find that someone special, but he was highly regarded and liked by everyone who knew him,” she said.

Kim’s mother, June (Max’s sister), kept an eye on Max over the years. But when she died suddenly in 2019, Kim took on the role of Max’s carer until he passed away in 2020.

“So, for the last two years of Max’s life, I got to know this lovely quiet man. He had retired on his farm and left the world on his terms,” she said.

Max was also a generous man who, upon his passing, bequeathed money to many charities. But the one closest to his heart was MS, which was very poignant for Kim, who has MS.

Max requested that his gift be used to support the MS community and fund more research into the disease.

“I didn’t know Max was going to leave a gift to MS. I think he discussed it with my mum. So, when I found out at the Will–reading, I was over the moon that he wanted to help the cause. To me, in his quiet way, he was saying he wanted to help me,” she said.

Kim developed MS at 33, after the birth of her second child. Thankfully, her MS journey for the last 20 years has been a relatively uneventful one. However, she admits she lives with fatigue, balance, and coordination issues.

“I like to think the money my uncle has left for MS will allow researchers to do more work to discover better drugs or a cure. It would be wonderful to think Max made that vital difference through his gift. Thanks, Uncle Max!”

Luigi Renato Mazzotti

Grand designs: builder’s bequest a boost for people with MS

Luigi Mazzotti was a familiar sight to people in the Melbourne suburb of Lilydale. Rain or shine, Luigi would don his black bomber jacket, climb on his motorised scooter and cruise down the footpath to the Degani Café in the Lilydale Marketplace.

During the daily 10–minute trip from his nursing home to the café, Luigi would smile and call out greetings to passersby. And Lilydale residents would warmly respond to the jovial Luigi as he tootled past.

But the staff at MS Plus (then known as MS Limited) didn’t know Luigi. The first they heard of him was when he passed away in June 2020, aged 88. The retired Melbourne builder had mysteriously left them a generous gift in his Will.

“Many people have a connection to multiple sclerosis. They know someone with the disease or have it themselves, which is why they give. But sometimes we receive charitable gifts out of the blue,” said Laura Henschke, MS Plus’ strategic future planning manager.

“We don’t know why Luigi was so generous to our cause. But we’re grateful to him for making a difference to people living with MS,” she said.

Luigi was born in 1932 in Coreglia Antelminelli, a mountain town in Tuscany, Italy. He was the only child of Mario and Gida Mazzotti. At 18, Luigi undertook his two years of compulsory military service.

When he turned 20 in 1952, he followed the path of many Italians before him and immigrated to Australia. He settled in Lilydale, an outer suburb of Melbourne in the Yarra Valley. Six years later, he became an Australian citizen.

As a young man, he studied English at TAFE and quickly became fluent. He also studied German to an advanced level.

A talented cabinet maker, Luigi spent his first years in Melbourne making and repairing furniture. He later worked as a payroll escort at Victorian Railways. He then moved into developing and building, where he spent the rest of his working life. Luigi built many houses, including his own, across the eastern suburbs of Melbourne. He later moved to a unit.

Luigi did not marry or have children. But he had lots of friends, and he brought his parents over to live in Australia. He enjoyed fixing cars and motorbikes, cooking, woodworking, gardening and photography during his long life.

Luigi also frequented the Veneto Club in Bulleen. There he played bocce (Italian lawn bowls) and conversed with his Italian friends. He often spoke fondly of the club and the happy times he had there.

In the last seven years of his life, he became friends with Jade Grbac, 26, and her boyfriend, Marlon Morabito, 28. Jade, a former barista and server at the Degani Café, often took his daily coffee order.

“It was a latte with a half shot and one sugar,” she recalled.

When Jade left the café for another job, she ensured the other baristas knew how to make Luigi’s coffee the way he liked it. He was popular with café staff and the retailers in the Lilydale Marketplace, she said.

“I have a soft spot for older people. Luigi was so cute, and he had the sweetest smile. He was always patient and kind, even the time I forgot to place his order,” said Jade.

“He loved to have chats with me about his bocce or whatever he was doing that day. It became a wonderful friendship,” she added.

Jade introduced Luigi to Marlon because she knew they would click. At the time, Marlon was studying construction and project management at university.

“I respect older people for their wisdom and experience. Luigi and I had much in common, like our Italian heritage and careers in the building industry. I understood his immigration story because it was like my family’s journey,” he said.

The three of them would enjoy many coffees and conversations over the years.

Luigi had an accident at one point, and the resulting injuries made it difficult for him to walk and stay in his unit. He later moved into Lilydale Aged Care. Luigi was a devout Catholic, attending St Patrick’s Church in Lilydale.

Debbie Edwards, the pastoral worker at St Patrick’s, often spoke with Luigi when he came to mass or when she visited the residents at Lilydale Aged Care.

“Luigi was such a lovely, faithful man with a huge smile and a huge heart,” she recalled.

“I first knew him when he would come to the church using his walker, and then he progressed to riding on his scooter. He used that scooter to maintain his independence when he moved into Lilydale Aged Care.

“I visited the nursing home regularly. But Luigi was often ‘absent on leave,’ riding his scooter to Lilydale Marketplace as often as he could. He had many friends there, especially at the coffee shop,” she added.

Sadly, Luigi died during the lengthy COVID–19 lockdown in Melbourne in 2020.

“We rang one day and learned he had recently passed away. It took us off guard because we didn’t expect it. We were also upset because we weren’t able to visit him during the lockdown,” said Marlon.

Marlon delivered the eulogy at Luigi’s funeral. He said Luigi had made a good life in Australia for himself and was always “humble and kind.”

Luigi left Jade and Marlon two of his intricately carved wooden boxes, photographs and his mother’s wedding ring.

“I’ll always treasure these things. Luigi wanted to leave us money in his Will, but we said no, you mustn’t. We’re fine; you should give your money to those who need it,” said Jade.

”We told him to do what makes him happy. As long as he was happy, we would be happy too,” added Marlon.

Indeed, Luigi wanted to ensure his legacy would be worthwhile. In the end, he left a generous gift to MS Ltd (now “MS Plus”) to help people affected by multiple sclerosis.

“It must have been something that he really wanted to do. It was so like him to want to help people,” said Marlon.

Why Luigi chose this cause will forever remain a mystery. But the charity is grateful the retired builder had grand designs to fund services to support those living with MS.

Molly Louvain McTaggart

Molly Louvain was born in Loria, in the West Tamar region of Tasmania in 1916. In her early years Molly worked at the historic Cadbury’s Chocolate Factory and lived in the mining town of Beaconsfield until moving to Melbourne in 1939.

In 1942 Molly married her husband, Bill McTaggart. Bill was a butcher and Molly worked in the shop with him. They lived in Burwood, Victoria for 63 years, had one daughter Margaret and a grandson, Craig. Margaret tells us her mother was gifted with her hands. Molly loved doing craft projects.

She spent over 30 years helping the Country Women’s Association in Melbourne. They help the disadvantaged and vulnerable women, children and families in need.

Bill passed away in 1990 and Molly returned to Tasmania in early 2007 aged 91. She then bought a house and lived on her own until she passed away in 2018 aged 102 and 4 months.

People living with Multiple Sclerosis benefited from Molly’s forethought and loving care. MS received a gracious and caring gift in her will.

Molly’s story is shared by her daughter Margaret Peters.

Eric Joseph Olsen

Eric Joseph Olsen lived a “fiercely independent” life in his later years, but one deeply involved with his local Orana community.

Also known as Aircraftman Eric Jospeph Olsen (Retired), Eric was a surviving veteran of World War 2. As part of his service, he was a RAAF Aircrew defender helping in the Battle of Kokoda, New Guinea. Eric served gallantly using his prior private flight experience gained from farming life in the late 1930’s.

On his return from service, Eric settled back into farming life in the Orana area. Eric married his beloved Norma and together bought a small property he called “Eureka” near Dubbo. While Eric and Norma did not have any children, Eric had a very loyal pet dog.

His war experiences changed him and Eric made a life–long decision to help others in need. After Norma passed, Eric left his estate to benefit many charities, one of which was MS.

Thank you Eric, your decision to leave such a generous gift in your Will, ensures our work can continue. Caring with people living with MS, now and into the future, continues with legacies like Eric’s.

A

Alice Robinson

tribute by her son Neil Robinson

I’d like to share with you the story of my mother Alice who was born in Cowes, a small community on Phillip Island, isolated from the Victorian mainland until the first suspension bridge was built in 1940.

Alice’s childhood years were the hard times of Depression and War. In her small, isolated community everyone had to pull together to get by. That spirit of belonging, caring and serving became my mother’s guiding light for her whole life.

In 1946 Alice met Jack Robinson, a handsome young PMG linesman who had been posted to Philip Island. They subsequently married in 1949 and had three children Neil, Barbara and Stuart. Mum and Dad remained together for forty–four years.

Dad’s work took the family to Melbourne where, along with raising myself, Barbara and Stuart, Mum became involved in new communities. She was involved in the

Mother’s Club at the local church, was active on the parents’ committees at our schools, as well as being the canteen manager.

Education was very important to our parents. They both did all they could to provide support for us during our school years. We were always well fed and cared for so we could be the best we could possibly be. She was immensely proud of our achievements later in life.

Alice did have her challenges in life. Jack developed crippling arthritis and died way too soon in 1993. At about the same time my brother Stuart was diagnosed with MS.

Mum cared for her loved ones without complaint. She was a quiet achiever – just did what had to be done, accepted the cards that were dealt and got on with it. Together with wonderful support and respite care provided by the Multiple Sclerosis Society (now MS Plus), Mum was able to look after Stuart at home until she was well into her 70s. After Mum couldn’t continue to look after Stuart at home MS provided a home away from home for him in their accommodation unit at Williamstown in Victoria.

Sadly, Mum died in 2019. She will always be remembered for her life of service to others and even though she’s gone, her concern for others is still being expressed through her generous gift in her Will to MS.

Our family has always been very grateful for the support and kindness of the MS and the staff at Williamstown and now Mum’s donation towards the ongoing care for people living with MS will help to ensure that no–one needs to face this crippling disease alone.

Janis Salisbury

Jan Salisbury cared about others.

In life, she generously supported numerous charities but her philanthropy, and that of her family, extended beyond that: in a case of people’s homes having been destroyed by bushfire, she and her mother drove to the devastated area and provided cash to those who had lost everything; in the case of a teenager, of whom she learned that her parents could no longer afford to send her to her accustomed school, Jan paid the fees for the rest of the girl’s secondary education.

Jan loved children and animals: she supported Bear Cottage and Taronga Zoo, among many others.

Jan’s driving philosophy was to help where she could, and where there was a need – a

philosophy inherited from her parents who had been successful in business and investment: she was particularly concerned to help others including those living with MS for which she had a very high regard.

In her circumstances, and without children of her own, there was no imperative for Jan to work; yet she trained and qualified as a registered nurse and practised in that capacity for many years.

Although she did not neglect her friends, Jan’s ethos was to help others who were less fortunate than she was.

Many, many people will miss Janis Salisbury.

Betty Stewart

The inspirational life story of Betty Stewart is not a short one. She died aged 99 after living her life to the fullest she could. She accomplished many of her dreams and forged a pathway for women after her.

Betty was raised by a caring, devoted mother who guided her through her early years. “Mother taught me that to achieve success in my life and career, I would have to work hard”. She credits her mother for her ambition and drive that led to her many years in a successful career, working right up into her late 70s.

“She was born before her time” states Betty’s cousin, Barbara. Betty proved that nothing would get in the way of achieving her dreams. Starting off as a humble temp at 3AW Radio Station, she battled years of gender adversity, and later fulfilled her wildest dreams of having her own PR business. Betty became one of the first women in Australian show business to have their own company.

Over her lifetime, she worked with many world–renowned stars such as The Trapp Family, Shirley Bassey, Jane Russel and most notably, The Beatles.

In 1992, Betty made the decision to retire so she could “Smell the flowers” so to speak

and enjoy the many years to come with her Husband, Ray. During her retirement, Betty embarked on her memoirs, recounting her 60–year career. In 2000, Betty self–published her autobiography titled ‘A Survivor in a Star Spangled World’.

Barbara, lovingly describes Betty as “a very caring and generous person”.

Betty was very giving throughout her life and passionate about helping those in need. She wanted to provide a lasting legacy by doing something special and leaving a gift in her will to MS Plus. MS became close to her heart when a beloved family member of hers was diagnosed with MS over 20 years ago.

Patrick Stewart

Patrick arrived from Scotland in the 1930s and made his way to Richmond, New South Wales.

He established a retail clothing shop and indulged his keen eye for property, creating and building up an impressive portfolio of properties, of which those who live with multiple sclerosis were to benefit from. A testament to his compassion for those dealing with tougher challenges of life.

Patrick lived quietly, keeping to himself and whose only indulgence was in property investment and walking about the streets

of Richmond. And yet through his generous spending, Patrick fostered a connection with the MS society, funding for a supportive community that helps those with MS in need. It is because of people like Patrick that MS patients don’t have to endure their challenges alone, or without joy.

Patrick is just an example of the diverse group of Benefactors who come from all walks of life, but share a desire to ensure that MS Limited will be there to help people face MS together. Whilst Patrick is no longer with us, we will know him through years to come from his incredible legacy he leaves behind.

Arthur Mervyn Sheriff

A Tribute by his niece Lynne Moseley

My name is Lynne Mosely. I was diagnosed with remitting relapsing MS about 15 years ago.

Lucky for me I am doing very well with limited deterioration. I had no idea, until I read my Uncle’s Will, that he had bequeathed a sum for MS Plus (then called MS Limited).

I like to think he did so in honour of me and this thought warms my heart. My Uncle was a very quiet man and one of nature’s true gentlemen. He never married and kept his cards very close to his chest. I miss him terribly.

Agnes Martha Wakefield

A Tribute by Verna Wakefield

Verna Wakefield fondly remembers, and describes her mother Agnes, as being the salt of the earth.

My mother Agnes was born in Melbourne and lived all her early years there. With the onset of World War 2 she joined the army, spending most of the war in New Guinea, where she met my father, Roy Wakefield. Dad was a farmer from the Mallee district in North Western Victoria.

After the war they married, and Mum created a new life in the hot, dry, harsh farming lands of the Mallee – a very different place to where she grew up. As I look back now as an adult, (as a kid you really didn’t know anything different), but I think, wow, that was a big ask to move to the Mallee – I take my hat off to her.

Mum was strict but there was always lots–of–love in the family. She had her firm rules and regulations about how her four children were brought up, which instilled in us good morals,

correct behaviour, everything that helps and influences my life now.

Life in the Mallee was tough for Mum, but I never heard her complain. It was hot and it was lonely at times, as Dad was away most of the day out working on the farm. The closest town was small, with only a couple of hundred people. Mum was always helping with the local fundraising efforts for the school, the football club, Red Cross and the annual Anzac Day appeal. It’s just what everyone did. The cake stalls were always fully stocked with Agnes’s fantastic baked goods, she loved cooking, even in 40–degree heat with a wood fired oven!

Mum grew up with three brothers and she was very close to her brother Fred. He and his wife had only one child, a daughter Mavis, who tragically developed MS.

Every year Fred and his family would visit the farm and Mum saw first–hand the devastating impact MS had on Mavis and those close to her.

Mavis’s condition deteriorated rapidly, and the

debilitating effects of the disease became very noticeable. It was very hard to watch because she was very outgoing, the life of the party. Mavis was married with two children and her husband Graeme supported her enormously with help from the MS. Her children were young teenagers when she was diagnosed and just young adults when she passed away.

This first–hand experience of someone living with MS, whom she cared deeply about, led Mum to make a bequest in her will. She saw a real need to help others lead better lives, on their often very difficult journeys with Multiple Sclerosis.

My mother Agnes died in November 2018 but I know her legacy lives on.

Margery Stewart Rix

“I have been fortunate to have a healthy and vibrant life and still enjoy getting out to do the things I love most and connect with communities that fulfill me.

I am eternally grateful for my life which is why I am motivated to give back to those who have been less fortunate than me. It breaks my heart to see people living with multiple sclerosis being isolated because they don’t have the support they need.

I believe in my heart that everyone deserves the opportunity to live the best life possible and that is what a gift in my Will to MS will do. I am delighted to know that my special gift will make sure that people diagnosed with multiple sclerosis don’t have to face it alone.”

Gwenneth Gray

A Celebration of Life

As a pioneering mechanical engineer Gwen Gray was a visionary. Her kindness continues to have an impact beyond her years

Gwen understood the power of science, research and determination. She used it to solve our most intractable problems. She included a gift in her Will to MS. She wanted for people living with multiple sclerosis (MS) to continue to get the support they need. Thus, they can live well while the search for a cure continues.

Her nephew, Geoff, isn’t quite sure about his aunt’s connection to MS. He says the kind–hearted gift in her Will comes as no surprise. “Nobody could deny Gwen’s generosity,” he says.

Gwen’s life story is interesting and inspiring. She was a celebrated mechanical engineer who shattered a string of glass ceilings.

Gwen entered the workforce with the Government Aircraft Factories during World War Two. Later, she took a job with W.E Bassets. She also started to study mechanical and marine engineering at Footscray Technical College. When she left W.E Bassets four decades later, she was a Company Associate.

During her career, Gwen was involved in the construction of several of Melbourne’s most iconic buildings. This includes the Royal Women’s and Children’s hospitals, and the Arts and Hamer Hall complexes.

Gwen designed courses for RMIT university, where she worked as a lecturer. And in 2006, she was named as one of only 90 Legends of Victoria University.

Gwen leaves a lasting impact not only in her chosen field, but also for people who live with MS.

Geoff is glad that his aunty Gwen’s kind and positive influence will continue. He remembers her fond dedication to family, and many weekends away with her before she passed at 95.

“We had an ongoing $2.50 bet as to whether she would make a hundred.

I remembered visiting her at the rehab hospital. It was when she suffered pneumonia a couple of years ago. She looked terrible. I asked how she was feeling. She leaned over slowly and said, “Shithouse. I feel about $1.20!”

Gwen’s gift in her Will means she continues to influence the world in a positive way. This also expresses her values in perpetuity. It will be driving transformative change even after she’s passed.

This is why we honour her with a special place in our hearts, and membership in the MS Callistemon League.

A gift in your Will costs nothing right now, but will have a profound impact on the future for people who live with MS. Like Gwen, you can leave a legacy of care and lifechanging kindness.

Dr Zula Nittim

Marie Pearl White

Trevor Joseph Nolan

Winsome Aboud

Dudley Adams

“The Baldy Trust Fund”

Emma Baybara

Janet Brumley

Olive Buzacott

Marion Aileen Carmichael

Patrick Corbett

Samuel Courtnay

Constance Crerar

Flaviano Di Blasio

Nance Ebery

Ethel “Florence” Felstead

Marjorie Ford

Lois Hagin

Alison Hale

Patience Harris

Jennifer Hiatt

Colin Hoffman

Malcolm Howard

Noel John Hutchinson

Margot Hyslop

Jennifer Anne Hiatt

Ellen Jones

Elsie May Joyce

Nancy Jury

Wilma Keir

Lydia MacMichael

Tatiana Madatow

Norma Martens

Edna Mathews

Margaret Merrifield

George Miller

Ethel Murray

Nancy Kathleen Newton

Nancy Newton

Ian John Norman

Josie Patterson Trust

“Heather Margaret Ryan

Charitable Trust”

David Sullivan

Catherine Clare Taylor

Margaret Tutton

Lorna Watson

Margaret White

Andrew Wilson

Walter Bien Ziemba

Isabel Sly

People recognised in our Celebration of Life book in alphabetical order

Index of our loving Benefactors

A

Abbey, Susan – Susan Abbey

Aboud, Winsome – Winsome Aboud

Adams, Dudley – Dudley Adams

Avery, Waybrett – “Brett” Avery

BBaldy, Lindsay James – “The Baldy Trust Fund”

Baybara, Emma – Emma Baybara

Bilbrough, Kathy & Vic – Kathy & Vic

Bilbrough

Brumley, Janet – Janet Brumley

Burfoot, Geoff – Geoff Burfoot

Buzacott, Olive – Olive Buzacott

C

Canu, Elena – Elena Canu

Carlson, Judith – Judith Carlson

Carmichael, Marion – Marion Carmichael

Castles, Patricia – Patricia Castles

Caswell, Nigel – Nigel Caswell

Collier, Allan William – Allan William Collier

Collins, Ken & Marilyn – Ken & Marilyn

Collins

Corbett, Patrick – Patrick Corbett

Courtnay, Samuel – Samuel Courtnay

Crerar, Constance – Constance Crerar

DDi Blasio, Flaviano – Flaviano Di Blasio

EEast, James – James East

Ebery, Nance – Nance Ebery

F

Felstead, Ethel Florence – Ethel Felstead

Fitzpatrick, Glenys – Glenys Fitzpatrick

Ford, Marjorie – Marjorie Ford

Forman, Judith – Judith Forman

Fraser, Jean – Jean Fraser

Frewin, Robert – Robert Frewin

GGray, Gwenneth – Gwenneth Gray

HHagin, Lois – Lois Hagin

Hale, Alison – Alison Hale

Harris, Patience – Patience Harris

Henschke, Laura – Laura Henschke

Hiatt, Jennifer – Jennifer Hiatt

Hoffman, Colin – Colin Hoffman

Holgate, Ben – Ben Holgate

Howard, Malcolm – Malcolm Howard

Hutchinson, Noel – Noel Hutchinson

Hyslop, Margot – Margot Hyslop

I

Inwards, Simon – Simon Inwards

JJennifer, Hiatt – Hiatt Jennifer

Jones, Ellen – Ellen Jones

Jones, Ivan – Ivan Jones

Jones, Marjorie – Marjorie Jones

Jowett, Ian – Ian Jowett

Joyce, Elsie – Elsie Joyce

Jury, Nancy – Nancy Jury

KKeir, Wilma – Wilma Keir

Kuipers, Margaretha – Margaretha Kuipers

LLeggett, Ruth – Ruth Leggett

Littlejohn, Adell – Adell Littlejohn

MMacMichael, Lydia – Lydia MacMichael

Madatow, Tatiana – Tatiana Madatow

Martens, Norma – Norma Martens

Mathews, Edna – Edna Mathews

Mawson, Maxwell – Maxwell Mawson

Mazzotti, Luigi – Luigi Mazzotti

McTaggart, Molly – Molly McTaggart

Meredith, Elizabeth – Elizabeth Meredith

Merrifield, Margaret – Margaret Merrifield

Miller, George – George Miller

Miller, Rod – Rod Miller

Murray, Ethel – Ethel Murray

NNewton, Nancy – Nancy, Newton –

Newton, Nancy – Nancy Newton

Nittim, Zula (Dr) – Dr Zula Nittim

Nolan, Trevor – Trevor Nolan

Norman, Ian John – Ian John Norman

OO’Reilly, Peter – in honour of Amanda

O’Reilly

Oliver, Wendy – Wendy Oliver

Olsen, Eric – Eric Olsen

Patterson, Josie – “Josie Patterson Trust”

Ralston, Margaret – Margaret Ralston

RRix, Margery – Margery Rix

Robinson, Alice – Alice Robinson

Ryan, Heather – Heather Ryan

S

Salisbury, Janis – Janis Salisbury

Sherrif, Arthur – Arthur Sherrif

Sly, Isabel – Isabel Sly

Stewart, Betty – Betty Stewart

Stewart, Patrick – Patrick Stewart

Sullivan, David – David Sullivan

TTaylor, Catherine – Catherine Taylor

Tutton, Margaret – Margaret Tutton

WWakefield, Agnes – Agnes Wakefield

Watson, Lorna – Lorna Watson

Webb, Bob – Bob Webb

West, Lindsay – Lindsay West

White, Margaret – Margaret White

White, Marie – Marie White

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These stories are of incredible people dedicated to fast–tracking a cure for multiple sclerosis and providing care until we’re there. Will you add your story by leaving a gift in your Will?

Our friendly Gifts in Wills team is here to answer any questions or concerns you may have.

Please don’t hesitate to get in touch on: 1–800–GIFT–MS (1800 443 867)

By email: futureplanning@ms.org.au or find us online at: www.mymslegacy.org.au

If you wanted to honour a loved one with an online donation and tribute please find us at msinmemory.org.au

MS Plus ABN: 66 004 942 287

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