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David Foster Foundation 2022 Winter Newsletter

Page 1

CELEBRATE

Photo credit: Flytographer

the Gift of Life

Calvin

with h

i s dad

, Loyd,

an d his

mom, Ch

ristine.

Calvin’s Transplant Story

WINTER 2022 | VOLUME 39

A transplant story through the eyes of a mother:

Calvin's Transplant Story

1

Message from the Chairman

2

Message from the CEO

2

Message from the SVP, Fund Development

3

Message from the Director of Family Relations

3

Calvin's Transplant Journey Continued

4

Celebrating with Oak Bay Beach Hotel's Oliver Bear

6

A Story of Perserverance, Thanks and Survival

7

A Review of Spectacular 2022

8

Ways to Give

10

Thank You to All Our Partners

11

Organ Donation Facts

12

Just

over

four

years

ago,

our

world

turned upside down the Saturday before Thanksgiving. My husband and I rushed our son to the Alberta Children’s Hospital as he had been sick on and off for two weeks with

Calvin TRANSPLANT NEEDED: KIDNEY HOME: CALGARY, AB

a cough and after numerous visits to clinics his condition had gotten worse. Five minutes into the ACH emergency triage the trauma team was called and we knew something serious was going on. Numerous blood tests were done and the fear of the unknown finally came to a halt when we were advised that our precious son’s kidneys were failing and he would need to be put on dialysis. That feeling of wanting to pause the moment and digest everything is so real. So many questions came crashing into our minds, the biggest of which was “why?”. We were scared to death, but we knew we had to remain strong. The only words that I could manage formed a question, will my son still live? We were assured that they would do everything to keep him alive and do the best they can. We were rushed to the ICU, I was hugging my son telling him that he was a strong brave

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

boy and he would make it through. He was later diagnosed with

DAVIDFOSTERFOUNDATION.COM

Alberta Children’s Hospital was our home for almost two months.

Infantile Nephronophthisis, a rare genetic condition which can cause childhood kidney failure and was put on peritoneal dialysis. The

CONTINUES ON PAGE 4


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