THE EVOLUTION OF CARE
Discover the new ways we’re supporting children and youth in the region with physical, developmental and communicative delays.
Discover the new ways we’re supporting children and youth in the region with physical, developmental and communicative delays.
In a year where the pandemic continued to be a significant disruptor affecting our services, families and our employees, new opportunities for growth and innovation gave us reason to look towards the future with optimism.
Throughout this report, you’ll discover stories that reflect an overarching theme for Niagara Children’s Centre, specifically “an evolution care”. That theme, highlighted by the implementation of several programs and initiatives in the past year, marked a new way for us to support children and youth in the region with physical, developmental and communicative delays.
For the first time in many years, we received a funding increase from the provincial government. While the funding will not fully meet the high demand for our Centre services, we were able to hire additional employees which, in turn, increased our ability to serve more children and families.
We found innovative ways to overcome operational challenges resulting from the prolonged pandemic. We expanded our capacity to provide in-person services. We continued to offer virtual care, webinars and parent education programs, where this was the preference of the families. We implemented new ways to support children and families with virtual care, including improved therapeutic interventions and
activities, equipment loans to families and technical supports for families who needed them. Virtual care was no longer viewed as a necessary alternative, but as an effective model of service delivery by many families and therapists.
Niagara Children’s Centre became a Regional Partner, delivering two early intervention programs under the Ministry’s new Ontario Autism Program. These included an entry-to-school program and a caregiver-mediated early years program, where we focus on a specific play-based, child-led model known as ESI/SCERTS.
We expanded our Family-to-Family Support program thanks to support from a number
of grants and donations. The Centre launched a Peer Mentorship program based on best practices, where caregivers are trained as mentors and then matched with families that are new to the Centre community as mentees.
A new partnership between our recreation therapy program and Broken Spoke enabled dozens of Centre children to benefit from low-cost adapted bikes. The program, run out of Port Colborne High School by Aubrey Foley, teaches students the understanding and benefits of refurbishing bicycles.
Our facility went through a number of upgrades. From ensuring our spaces were supporting safe care from an infection control perspective, to supporting the return of an expanded workforce on-site, numerous areas were renovated, repurposed and re-furnished. A major roof repair and replacement was also undertaken thanks to an infrastructure investment from the Ministry of Children, Community and Social Services.
Fundraising once again had a very successful year, with the return of many popular events to an in-person setting. The Superhero Run achieved record results and, for the first time in many years, we were selected as a beneficiary of Tim Hortons Smile Cookies campaign. We are incredibly grateful for the generous support from the community. Donations, grants and fundraisers allow us to support more children and families in our community and to deliver important programs that are not funded through government funding.
Looking towards the year ahead, we are hoping to see an end to the pandemic and, as a result, greater stability in our day-today operations. We will be focused on continuing to provide high-quality and innovative services, the launch of a new strategic plan and the implementation of the new SmartStart Hub initiative.
We end with a note of gratitude. We are privileged to work with an amazing group of children and families. We are incredibly grateful to our employees who continued to deliver quality services under very challenging circumstances. A final note of gratitude to our volunteer Directors, community partners, donors and funders who supported us to do the work we love to do.
we will realize our vision of “Niagara’s children and youth at their best”.
Mr. Mathew Siscoe, Chair
Ms. Lois Ouellette, Vice-Chair
Ms. Shirley Cordiner, Director
Ms. Angela Davidson, Director
Ms. Dolores Fabiano, Director
Mr. Lorne Gretsinger, Director
Mr. Ken Janzen, Director
Mr. Larry Kent, Director
Mr. Vic Kerschl, Director
Mr. Frank Ruberto, Director
Mr. Don Thorpe, Director
Oksana Fisher,
Chief Executive Officer Dorothy Harvey, Director of Clinical Services
April 2021 to March 2022 Kathy Bell, Director of Clinical Services
January 2022 to present Tammy Davey-Wiebe, Director of Corporate Services and Finance Marla Smith, Director of Development Kristen Groom, Human Resources Manager
From not leaving your home, to worrying about finding childcare or the difficulty of navigating transportation to and from an
appointment, the pandemic changed the way we approached daily tasks.
In the first year of the pandemic, virtual therapy was the only service delivery option for most families. In the second year of the pandemic, the Centre returned to in-person services, but continued to support virtual offerings where this was the preference of families. Many parents started to truly
value the adaptation of services to virtual offerings and embraced them as a new way forward. This past year, approximately fifty per cent of the nearly 48,000 visits were delivered virtually. This included assessments, therapy visits, child groups, as well as parent education and support groups.
For Niagara Children’s Centre, it marked an evolution of care – an additional way to support children and youth in the region with physical, developmental and communicative delays.
A survey conducted by the Children’s Centre indicated that eighty-three per cent of families were satisfied with the services provided by virtual care with forty-one per cent suggesting it was better than expected. The medium provided new opportunities for interactive games and activities with families during the sessions, while the technology made it possible for parents to join their child and significant other if they were unable to make the physical commute from home or work.
Virtual appointments can be a benefit for therapists as well. The ability to see the child and family in their natural home environment can provide additional insight for therapists and allow them to better individualize their recommendations and treatment approaches. While many forms of treatment still benefit from an in-person visit, a survey sent to Niagara Children’s Centre therapists indicated that seventy three per cent of staff felt that future services should continue to be a mix of both offerings.
This past year, the Centre was able to improve some of the early challenges experienced with virtual care. Therapists learned what services and programs could be delivered well virtually, which types of clients and families benefitted from virtual care, and families were offered technical support and equipment loans, where needed. Niagara Children’s Centre also modified many of our therapeutic activities for a virtual platform.
While the advent of virtual has been a learning curve for all involved, virtual appointments have found a place in the Centre and will continue to play a role in the way services are delivered.
The new program pairs trained parents or caregivers as mentors with families that are new to the Centre community as mentees.
“We talked about acceptance, how to make it okay to be around neurotypical children and the best way to include our kiddos in different activities,” said De Lima Pinto.
The mentors share their lived experience, provide a working knowledge of community resources and Centre services while offering emotional support to new families.
“Communication skills are key but, more importantly, it’s listening skills,” Sabrina Elliott Vergara, Family Mentor Coach at Niagara Children’s Centre. “Many parents are not looking for answers, they’re looking for someone who gets it to have a listening ear.”
The programs also allows mentors and mentees to set their own schedules and connect when it’s convenient for them. Families can be matched based on their child’s diagnosis, specific resource / expertise, similar situations and a number of other factors.
Having someone to talk to made all the difference for Dyane De Lima Pinto.
After moving to the region with her family and starting treatment for her daughter, Joannah, at Niagara Children’s Centre, all she was looking for was a friendly ear.
“I wanted to speak to someone that was already involved in the community and knew different inclusive activities that we could take part in,” said De Lima Pinto.
She signed up for the family mentor program, an initiative started by the Children’s Centre over the past year.
“To learn that there’s another parent out there that has gone through everything you are going through right now, and understands your feelings – it means a lot,” said De Lima Pinto.
While the program is still in its early development stages, the Centre anticipates to move into the next phase in the upcoming year, which aims to recruit more volunteer mentors to support the growing demand from families.
“When parents and caregivers are supported and have the opportunity to find community, connection and resources, it’s a win for all involved,” said Elliott Vergara.
The mentorship program is part of the Children’s Centre’s family partnership program.
Launched in 2014, the program was co-designed with families connected to the Centre’s services and embodies the organization’s philosophy of family-centred care. It’s built upon four pillars that include families as advisors, family-to-family support, families as informed consumers and families as educators and ambassadors.
The Family Advisory Network (FAN), a group of 15 parents and caregivers, meet monthly with management to discuss initiatives. Over the past year, they’ve provided input on intake messaging and scripts, the Clinical Services Information Guide, along with Ontario’s new Autism program and SmartStart Hub.
Family-to-family support includes a number of initiatives designed to encourage parents and caregivers to talk about their shared experiences and connect with the Centre community.
A monthly Parent Talk support group meets virtually, and in-person, throughout the year. Each of the 10 sessions held this year were based on a theme that parents and caregivers can relate to, such as consistency amongst the chaos,
Pictured right:
Sabrina Elliott Vergara, Family Mentor Coach at Niagara Children’s Centre.
transitioning to school, the power of play and balancing relationships.
Helping families be informed is another important aspect of the family partnership program. This past year, the Centre hosted its 3rd annual Parent & Caregiver Conference on April 27 virtually to a group of 32 participants. Themed around the power of a personal story, special guests Mike Lang and Sue Robbins shared insights on how to find meaningful moments and create meaningful change in the home and the places we go.
Family advisors also shared their ideas about the future redesign of the Centre’s website to make it more informative and user-friendly.
Families also play an important role as educators and ambassadors in the community. This past year, 16 families served as ambassadors for our annual Help Kids Shine fundraising and public awareness campaign. Throughout the month of May, families shared their personal stories at speaking engagements, online and through media interviews to educate the Niagara community about the therapy and support services the Centre provides.
We are grateful for the financial contribution received by the Niagara Community Foundation and TD Bank towards the family partnership program, which provided our organization with the capacity to expand our support and develop the mentorship program.
He’s a cutie. He’s very smiley,” says Jillian Janzen.
He’s Paddy — baby Patrick Janzen
— just turned one year old, and soon one of the faces of Niagara Children’s Centre’s Help Kids Shine campaign that starts in May.
Four months into her pregnancy, Jillian and her husband Tom learned Paddy would be born with Down syndrome, meaning he had an extra, 21st chromosome.
It occurs in about one in 800 live births worldwide, usually causing varying degrees of intellectual or physical disability, and in some cases other medical issues.
Getting the diagnosis early was good but worrying, Jillian Janzen says.
“It’s like, you have time to digest it. But you also have a lot of time to think about it before he’s born.”
“For us, receiving that diagnosis, I kind of felt a little bit alone … when you get a diagnosis, it’s very clinical and medical. They kind of red flag some things that might be there related to the diagnosis.”
By taking part in the Help Kids Shine campaign, she hopes other parents in her situation will realize they’re not alone.
“I hope if there is a parent with a prenatal diagnosis or that just received a diagnosis, whether that’s of Down syndrome or cerebral palsy or any birth diagnosis, they can see, ‘All right , I’m going to be OK. There is support in my community, and there are resources there.”
Janzen says Paddy is in an infant development program there: “He has, immediately, a team of a social worker, an occupational therapist, a physiotherapist and a speech language pathologist.
“They kind of give you space — you know, you just had a baby … in terms of getting connected with your team, that usually happens in the first month or so.”
Janzen has a family member with Down syndrome as well as a background in teaching and working with kids and adults with special needs.
Even so, she says, the diagnosis can be hard to take.
Her biggest concern was that Paddy might have one of the medical issues that can come with Down syndrome.
In a small number of cases, babies can experience epileptic seizures. Thyroid problems are more common in children with Down syndrome, and about half of kids born with it will have a heart defect, according to Down Syndrome International.
Janzen says Paddy has a small hole in his heart, but doctors believe it will close on its own.
Paddy’s sister, who is two and a half years old, was not born with Down syndrome.
“To be honest, a baby is a baby is a baby …” says Janzen.
“Yes, they might have special needs. But he loves to play, he loves to smile, he loves to say Momma and Dadda and stuff like that. He loves interacting with other kids and looking at them.”
She says Paddy’s team at the Centre works with him in areas like feeding and improving his motor skills. They gave her exercises she and her husband can do with Paddy to help him progress.
“For example, Paddy is learning to stay in a standing position by holding onto an object in front of him, or a table,” she says.
“(The occupational therapist) will show me techniques of how to move his body to help him develop that skill. Or for reaching for objects.
“Right now, we’re working on him sitting alone, so supporting his hips. Things like that.”
He can crawl army-style and put food into his mouth, learning it through therapy and by just being a baby.
“He’s doing things a baby would normally learn, sometimes he just needs a little extra help or it’s just a little bit later,” Janzen says.
“Your typical child will maybe walk by a certain age, whereas in Down syndrome it’s a large range so that it could be 15 months, it could be three years,” she says.
“That’s something the occupational therapist works with in terms of focusing on where he is.
“So we don’t really track whether he’s behind or ahead, he’s just where he needs to be and he will do it at his own time.”
Usually when a baby is born with special needs, the doctor will refer the parents to Niagara Children’s Centre, Janzen says.
“But it’s nice to hear stories of, ‘Oh, that kid’s doing OK. I’m going to be OK,’” says Janzen. “I hope that Paddy’s story shows that.”
Reprinted with the permission of Metroland Media. To read the full article, visit stcatharinesstandard.ca.
Jillian and Tom Janzen with baby Paddy, who was born with Down syndrome, and daughter Morgan. Photo credit: Bob Tymczyszyn (TORSTAR).What are your hands doing that your child’s hand could? It’s often the first question posed by Savanna Bond and Jocelyn
Fedyczko to parents when meeting for their virtual therapy sessions.
As Speech Language Pathologists for Niagara Children’s Centre, it’s an important discussion topic to have with families new to a diagnosis of Autism Spectrum Disorder (ASD).
Bond and Fedyczko are responsible for delivering a new initiative under the Ontario Autism Program (OAP), known as the caregiver-mediated early years program. Within the program, there are six available models for families to learn therapeutic strategies and specific techniques from professionals based on their child’s individual needs.
Bond and Fedyczko focus on a specific play-based, child-led model, known as the
“It empowers the parents to see how much they can do with their child,” said Fedyczko.
Based on an evidence-based approach to treatment from Florida State University, the model targets Autism’s core features, communication, social interaction and
Jocelyn Fedyczko and Savanna Bond, Speech-Language Pathologists at the Centre, deliver a specific play-based, child-led model, under the Ontario Autism Program (OAP).repetitive patterns of behaviors or interests. To enroll, the child must have a diagnosis of ASD, be 12 to 36 months at the start of intervention, and be registered with the OAP. The program is fully funded by the provincial government and is available to families for six months with sessions occurring twice weekly.
In ESI/SCERTS, families receive virtual coaching and support to develop their child’s social communication skills within everyday and social activities, such as games, meals and snacks, caregiving activities, play with toys, family chores, books and transitions from one activity to another.
“We’ve done a lot of laundry during our sessions,” said Bond. “The model provides families with ideas for embedding supports and strategies that their child needs to be successful across an endless amount of activities.”
A typical session has Bond and Fedyczko review priorities with the parent or caregiver followed by a selection of three to five activities. During the activities, they provide encouragement, positive feedback and coaching strategies to work on at home. After the activities, they reflect and discuss any feedback with the family before planning for the next session.
“The opportunities for embedding those strategies are endless,” said Bond. “It’s really cool to see the activities the families come up with.”
Bond and Fedyczko also guide and support them throughout the program, helping parents and caregivers engage their child by following their focus of interest and by keeping activities predictable.
“One of the biggest challenges with Autism is gaze shifting,” said Bond. “All we want to do is get their attention. They’re not learning from experiences of things around them unless they’re embedded in their routine as an active participant.”
Research from the ESI/SCERTS model suggests that children with ASD should spend at least 25 hours per week actively engaged to improve outcomes.
“The key to keeping a child actively engaged is finding their interest and building on that as a learning opportunity,” said Fedyczko. “The best part is that it can occur in any activity that your family already spends time doing.”
From games to preparing snacks, family chores to reading books, the model encourages parents to look at a variety of activities spread across the day to support their child’s development.
Clear signs that a child is actively engaged are evident when they are well regulated, productive, socially connected, looks at another person’s face often, responds to voices and words and communicates directly with their parent or caregiver.
Some of the biggest progress that Bond and Fedyczko have seen since the start of the program has been with the parents.
“We’ve watched parents blossom and grow into very confident support systems for their children,” said Fedyczko. “They become completely different people over the course of six months.”
Bond and Fedyczko joke that the ultimate goal of the program is to work themselves out of job.
“We are building fidelity in parents so that they can continue the intervention themselves,” said Bond.
Preparation for delivering the ESI/SCERTS model began more than two-and-half years ago.
Bond and Fedyczko were enrolled in a rigorous training program. They’re two of a handful of therapists in the province of Ontario to have completed tier three program certification. Now they support families from across the golden horseshoe including Cambridge, Milton and Stoney Creek.
Their efforts were recognized by the Centre at this year’s Employee Recognition Dinner when they were presented with an award for Innovation & Excellence. The award recognizes employees who demonstrates a commitment to and/or achievement in activities that support innovation and excellence in the workplace.
As the Centre moves into year two of the program, Bond will continue to work with families enrolled in the program while Fedyczko will also work towards tier 4 certification in the program. Upon completion, Fedyczko will become a regional trainer to educate additional clinicians in the model.
When Kimberly Melville and her daughter Amelia started going to Niagara Children’s Centre, it was just a place they went.
Like going to the doctor.
But as Amelia got older, requiring more and more of its services, the centre became “embedded” into their lives in ways Melville never saw coming.
“I thought we would go in there, maybe have a couple of therapy sessions and that would be it,” she said. “Now, nine years later, it’s very much a part of us, a part of
our family. We’ve gotten to know a lot of the staff up there, we have gotten to know a lot of families.”
Amelia, who has a rare condition called Zellweger spectrum disorder, first started at the centre when she was eight months old, delayed in her gross, motor and fine motor skills. The St. Catharines family was referred to the Centre, without a diagnosis, after a stint at McMaster Children’s Hospital in Hamilton.
Melville recalled being a “nervous wreck of a parent,” not knowing what to expect.
“I remember when I first got the call from the Children’s Centre to do the intake, and the social worker telling me that she’s here to help and guide us through it,” she said.
“I spent eight months struggling, trying to figure out what I was doing. I was just calling people and showing up at doctors. So to have somebody that can help you navigate that and understand and support— I honestly don’t know how we would have gotten through … without having that.”
Through Niagara Children’s Centre — it helps about 5,800 Niagara children and
Niagara Children’s Centre has become embedded into the lives of Kimberly Melville and her nine-year-old daughter Amelia. Photo credit: Julie Jocsak (TORSTAR).youths with physical, developmental and communicative delays each year — Amelia has accessed services including physiotherapy, occupational therapy, speech-language pathology, augmentative communication (allowing Amelia to use a tablet to communicate) and its gait clinic.
Now, at nine years old, Amelia is “doing really well.”
“She’s exceeding all expectations. It’s very unusual for a child like her, with her diagnosis, to live until nine,” said Melville.
“To be as healthy as she is still right now, very vibrant, energetic, super social, fun, so smart — she’s learning Braille and ASL (American Sign Language). She’s doing great.”
Amelia — as well as her mom and dad, Todd — participated as Team Unicorn at the Niagara Children’s Centre Plasma Car Race, a relay-style event that marked the end of the centre’s monthlong community fundraising campaign, Help Kids Shine.
Melville has been a part of the Centre’s family advisory network since its inception, providing upper management with personal perspective on how best to engage families and help those who directly use its services.
She knows personally the feeling of needing help, but not being able to access it due to long wait lists. Melville hopes the centre’s campaign will increase staff and available programming, and get children, and families, the support they need.
“When you’re a family and you’re waiting for help for your children, it is one of the hardest things,” she said.
“It’s more than just your rehabilitative supports, it’s the whole system … (the centre) made it relatable, gave us people that understood us. It’s an isolating life if you don’t have people that you can connect to or that understand what you’re going through.”
Reprinted with the permission of Metroland Media. To read the full article, visit stcatharinesstandard.ca.
Team Unicorn, comprised of Todd, Amelia and Kimberly Melville, along with Lauren Skeoch and Rhonda Silwa, raised
for the Centre through the Plasma Car Race.
The Niagara Regional Chair was unanimously selected as the recipient of the 2021 Dr. Orr Tribute Award.
The award, which honours the legacy of the Centre’s founding medical director, recognized Chair Bradley’s outstanding dedication to supporting the mission and vision of Niagara Children’s Centre and positively impacting the quality of life of children and youth with disabilities.
Chair Bradley has not only been a supporter and influencer through his various educational and political roles but, on a personal level, he has been a strong ambassador, advocate and supporter of the Centre. He has seen the evolution of the Children’s Centre over the course of his
political career and has always taken the time to support the Centre and the children and families we serve.
“Chair Bradley is well respected across our region and by people across the political spectrum,” says Oksana Fisher, CEO, Niagara Children’s Centre. “Having an advocate like Chair Bradley in our corner has opened many doors and conversations, always to the benefit of children with delays and disabilities.”
Never one to shy away from an opportunity to connect, Chair Bradley has visited the Centre on numerous occasions over the years. He came to the Centre to announce provincial infrastructure grants to support much-needed improvements to the
building, facilitated meetings and site visits with then Minister of Children and Youth and regularly attended the launch of our annual Help Kids Shine campaigns and Superhero Runs.
Community support is at the heart of Chair Bradley’s public service. Through his public service, he has demonstrated a commitment to positively impacting the lives of children with disabilities and their families.
Fisher added that the organization is so proud to present Chair Bradley this award and we hope that it reminds him that his impact and legacy are seen and celebrated.
RECREATION THERAPY AT A GLANCE
Adapted bikes have been donated to the Centre.
Participants at the Centre
The feeling of freedom and independence created with a bicycle can bring back fond childhood memories.
Many children, however, are unable to experience this feeling due to physical limitations that make it difficult or impossible to ride a traditional bicycle.
Specialized mobility bikes offer a solution, but with costs ranging from $600 to $4,000, they’re inaccessible for many families.
Aubrey Foley, founder of the Broken Spoke program, found a solution. The program, run out of Port Colborne High School,
teaches students the understanding and benefits of refurbishing bicycles to provide enjoyment and transportation for themselves and others.
The program has partnered with Niagara Region Waste Management to divert bikes, wheelchairs and walkers from landfills and, to date, has donated more than 15,000 bikes to people in need. To date, this includes more than 30 specialized mobility bikes to families at Niagara Children’s Centre.
Jaymieson O’Neill, Recreation Therapist at Niagara Children’s Centre, said the partnership has completely changed how
the Centre runs its bike program.
“Families could wait for up to two years for funding for a bike,” said O’Neill. “Now, I can do an assessment and, without any financial obligation, get them a bike that suits them 95 per cent of the time within one or two weeks.”
The program will provide countless children with the opportunity to participate in biking with family and friends, build confidence and strengthen muscles.
“It’s incredible to see the reaction,” said O’Neill, “when they see the bike is something they get to take home and keep.”
Quality Client Services
the exception of wait times for assessment and treatment.
performance
historical challenge, rooted in the demand for services exceeding the Centre’s financial resources, therefore limiting our capacity to meet the demand. Numerous disruptions arising from the pandemic, further increased
Centre continues to look at strategies
wait times.
reduce wait times.
Ministry of Children, Community and Social Services
Community-Based Rehabilitation
School-Based Rehabilitation
Preschool Speech and Language
SSAH, SCS
Regional Municipality of Niagara
Home & Community Care Support Services
Other Income
Amortization of Deferred Capital Contributions
Total 2022
$4,952,350 $2,329,933 $1,647,523 $1,122,408 $309,697 $106,007 $583,110 $102,358 $11,153,386
Total 2021
Salaries and Benefits
Building Services
$4,132,679 $1,833,697 $1,439,145 $1,163,519 $314,166 $90,794 $656,845 $110,726 $9,741,571
Contracted Services
Operating
Amortization of Property and Equipment
DEFICIENCY
Excess of Operating Revenues over Expenses for the year
FUNDRAISING Contributions Salaries and Expenses
Excess of fundraising revenues over expenses
Total 2022
$8,220,824 $936,516 $1,228,504 $929,141 $102,358 $11,417,343 (263,957)
Total 2021
$7,402,022 $260,641 $1,407,079 $770,203 $110,794 $9,950,739 (209,168)
Thank you to our funders:
Community Based Rehabilitation
School Based Rehabilitation
Preschool Speech and Language
SSAH, SCS
Donations
Other Income
Regional Municipality of Niagara
Home and Community Care Support Services
Amortization of Deferred Capital Contributions
EXCESS (deficiency) of Revenues over Expenses for the yea
$1,070,379 ($359,135)
$711,244 $447,287
$876,869 ($272,409)
$604,460 $395,292
Auditors: Grant Thornton LLP, St. Catharines. A complete set of audited financial statements is available upon request.
Salaries and Benefits
Building Services
Contracted Services
Centre operating
Amortization of Property and Equipment
Fundraising Expenses
Through
very
Marcella
Niagara Children’s
Hortons
need
become
“Hearing about the families who have found
for their children at the Centre through
interviews with parents during the
Kids Shine
knowing
motivated me to
was a
Lillian
Cotton Construction Golf Tournament
Joseph Olascki Trust Fund at the Niagara Community Foundation
Niagara Catholic District School Board
Niagara Home Builders Association
Regional Chair’s Charity Golf Tournament
Sansom
Stamford Kiwanis Club
The Viola-Salter Group
-
$5,000 - $9,999 continued
Alectra Utilities
BrokerLink-Sheehan & Rosie Ltd
CIBC Wood Gundy, St. Catharines Team
Cla-Val Canada Corp
Cooper Wealth Management of RBC Dominion Securities
Dr. William Orr Foundation
F.K. Morrow Foundation
MNP Ltd.
Nickolas & Barbara Sacco Charitable Foundation
Pen Financial Credit Union
Rona Inc.
Scotia Wealth Management Shaw Communications Inc.
Oksana & Bob Fisher
Barbara Jeffery Gibson
Roman Groch
Dorothy & Geoff Harvey
Heavy Construction Association
of Regional Niagara (HCARN)
Bryan & Nancy Hermans
Intact Insurance
Yvonne Kala
Kelly Jones - Desjardins Insurance
Moksha Indian Bistro
Susan Mull
Niagara Brewery Collectibles Club
Niagara Dairy Producers
O’Hara Trucking & Excavating Inc
Robert Orr
Scotiabank
“As an association, which collectively employs over 5,000 people, we realize the importance of giving back to Niagara by supporting local initiatives that benefits families.”
Jim Phibbs, President, Heavy Construction Association of Regional Niagara (HCARN)
Dr. Karl & Julie Stobbe
David & Susan Siscoe
Vyadom Group Walker Industries
$2,500 - $4,999
Air Canada
Bayshore Masonry Limited
Estate Of Muriel Jean Etsell
Lou Biagi
Billyard Insurance Group
Bill & April Janzen
Boldt Realty Inc.
Estate of Alice Bundzeak
Clench House Foundation
Club Richelieu
Credit Bureau Services Canada
Cruising On The Q
Darcy Richardson Real Estate Group
Gerald Ducharme
Evans Heating & Cooling
Fidelity Investments
John & Lynda Gammage
Georges Greek Village
Grant Thornton LLP
Grantham Lioness Club
Bob & Lorraine Hand
Darren Hendriks
Homes by Hendriks
Susan Howlett
In The Event by Maria Ken & Donna Janzen
Karyn Langendoen
Link Charity Canada Inc.
The May Court Club of St. Catharines
Modern Landfill
Niagara Corvette Club
Parkside Custom Homes Inc
PBO Group
Sherrard Kuzz LLP
Johannes & Marga Thiessen
Wormald Masse Keen Lopinski LLP
$1,000 - $2,499
1832 Asset Management LP
Aqua-Don Pool Service & Supplies
Tom McConnell
Jeanette McGinty
Cindy & Derek Mewhinney
Jessica Millar
Rob Mills
Todd Morgan Rob & Patricia Neill
Brian McKeown & Gail Norris
Ridley College
Jerry & Joanie Rinaldi
Robert A. Lavelle Memorial Foundation
Grant at the Niagara Community Foundation
Grierson Salter
Sandtrap Pub & Grill
SunOpta Inc
Cheryl & Doug Smith
Marla & Adam Smith
Greg Sykes
Joseph Viola
Diane Watson
Margaret Webster
Alfred Wiens
Wills Family Foundation at the Niagara Community Foundation
Anonymous - 2
$500 - $999
Aristocrat Floors
Sandra Arkison
Aurora Tancock Financial Services
Karen Bader
Anne Balanowski
Laura-Jane Benoit
Adam Bosak
Brock Ford Lincoln
Paul Brodeur
Ken Burch
Carson’s Pizzeria
Lenore Cardiff-Hinchliffe
Don Chambers
Joel & Brenda Chatterton
Chippawa Volunteer Firefighters Assoc.
Club Sardegna Nel Niagara Inc Court Holdings Limited
CR Smith Financial
Tammy Davey-Wiebe
Terry & Diane Dick
Donnelly’s Irish Pub
Mario Durand
Julia Frei
Don & Lois Fretz
Derek Gareau
Greg Frewin Theatre
Handlebar Hank’s Roadhouse
Joan Jamison
Jackpot Flowers
Craig Janzen
Mary Kala
Larry & Eleanor Kent
Vic & Farida Kerschl
Art Klassen
Kurt Klein
Ivana Komljenovic Metcalf
KPMG
Bill & Beth Lamb
Lancaster Brooks & Welch LLP
Lions Club of Chippawa
Lions Club of Port Dalhousie
LJM Developments Grimsby Inc.
Robert & Judy Mansfield
Manulife
Mark’s No Frills
Mathnasium Math Learning Centre
Colin McDougall
Chuck McShane
Midas Auto Service
Mountainview Homes
Niagara Region Police Association
Donald Pearson
Bernice Perusse
Picton Mahoney Asset Management
Brent Pym
Rankin Construction Inc.
Revel Realty Inc Brokerage
Keith Robinson
Silvergate Homes
Don & Karen Smith
Solaris Tint
Stamford Centre Volunteer
Firemen’s Association
Allison Suk
Sullivan Injury Law P.C.
TD Volunteer Grant Program
John & Heidi TeBrake
Upper Canada Consultants
“I believe that the strength of our children and our community plays a vital role in our future so making a donation to Niagara Children’s Centre was an easy decision for me.”
Angela Davidson, Board Member, Niagara Children’s Centre
Vanderzalm Construction
Walter Hiltebrand Marine Services
Darrell Weber
Eric & Darci Weinert
Joy Vongphachanh
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$250 - $499
Leanne Abramovitz
Sarah Ane
Anthony Petti Real Estate
A-Plus Air
Robert Beach
Beatties
Gary Benson
Bocchinfuso Funeral Home
Sandra Bolibruck
Boston Pizza - Pen Centre
Jim Bradley
Claudia Brema
Brooker Homes
John Cardillo
CI Investments
Tony & Leslie Cirasuolo
The Cirone Family
Marilyn Coull
Graham Coveney
Mackenzie Cullip
Ed & Anita Curran
Michelle Czaplicki
Angela Davidson
Jason Dell
Ryan Denhollander
Whitney Dillon
Danny DiPardo
Audrey Doran
Kristine Douglas
Holly Krys
Ladies Auxiliary - Canadian Corps Unit 44
Gregory Lavelle
Charles LeGuerrier
Sandy & Frank Leslie
Joe Link
Lions Club of Port Colborne
Brent Longmoore
Kerry MacCarron
The Mackenzie Group Nadeen MacNeil
Jenna MacPherson
Mark Malinowski Right At Home Realty
John & Linda Reiter
Jessie Ritchie
Jeff Robichaud
Rockway Presbyterian Church Women
Grandma & Grandpa Sanders
Michaela Shaw Doug Smith
Kathy Smith
St. Andrews School
St. Catharines Nissan
Matt & Lauren Swindley
Howard Staynes
David Staynes
Darryl & Lisa Strum
“Being a parent, it is comforting to know that should our children need special care, we can access it in our own backyard. Supporting such an amazing Centre in Niagara means that we are, in a small way, helping to provide that comfort to families across our region.”
Matt & Lisa Vinc Community members
Mike & Ashley McCormick
Niagara Caulking & Firestopping
Jaymieson O’Neill
Sebastian Oort
David Orr
Orangetheory Fitness
Pelham Street Grille
Debra Pollice
Marney Portugaise
Rod Portugaise
Richard & Helen Predovich
Pete’s Pizza
Vaino Raun
Meghan Reichheld
Nancy Taylor
Judith Thiessen
Pamela Turnbull
Don & Debbie Thorpe
Lisa Vinc
Walker’s Country Market
Hilda Wiley
Kate Wiley
Leah Williams
Evan & Beth Williamson
Joel Willms
Willoughby Volunteer Fire Department
Madeline Woodhead
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