David Foster Foundation Summer Newsletter

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CELEBRATE

the Gift of Life

B e ll

a an

d Ky l a Th

oms

on w al k in

g th e

purple

carpet

at A Nig ht on Bro a

dway!

SUMMER 2022 | VOLUME 37 Bella's Transplant Journey

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Message from the Chairman

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Message from the CEO

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Bella’s Transplant Journey August 2022 will mark two full years of waiting for the Thomson family. It will mark two years

Bella TRANSPLANT NEEDED: BOWEL

Message from the SVP, Fund Development

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Message from the Director of Family Relations

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Bella's Transplant Journey Continued

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Gold Mining with Avenue Family Dental

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Sharing Smiles this Summer

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A Night On Broadway Raises Record-breaking $11.2 Million!

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2022 Visionary Award Winners

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Partner Spotlight: The Simon Keith Foundation

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Thank You to All Our Partners

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medical team hoped would improve her quality of life. Unfortunately,

Thank You! A Night On Broadway in Partnership with Hotel X Toronto

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the procedure did not work, and Bella would remain in the hospital for

of hearing the phone ring and wondering if it is a medical professional calling to say that they have matched Bella to a bowel donor who

HOME: SWIFT CURRENT, SK

will save her life. Two years of always trying to remain positive but always having the “what-ifs” at the back of their mind. Bella was born in 2013 and Kyla and Lyle were overjoyed to welcome their first child. At only three days old, Bella was air ambulanced to the Royal University Hospital in Saskatoon, SK as she was continuously vomiting and obviously suffering from painful distension. Bella was diagnosed with Hirschsprung’s disease, which is a disease that affects an infant’s intestines and makes it impossible for them to have bowel movements. She was rushed into an emergency surgery that the

the first two years of her life. During these two years, Kyla and Lyle also learned that Bella was

212 HENRY ST., VICTORIA, BC V9A 3H9 OFFICE: 250.475.1223 FAX: 250.475.1193 TOLL FREE: 1.877.777.7675

born with severe combined immunodeficiency (SCID) and a form of

DAVIDFOSTERFOUNDATION.COM

old due to her SCID diagnosis.

dwarfism called cartilage hair hypoplasia. On top of all of this, she needed to have a bone marrow transplant when she was just a year

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