Clarke Walk For Pulmonary Fibrosis
Canadian Pulmonary Fibrosis Foundation
Clarke Walk for Pulmonary Fibrosis in support of Canadian Pulmonary Fibrosis Foundation (CPFF). Walk and stay for the BBQ!
Sunday September 15, 2019
In 2007 Abigayle Clarke’s grandpa Chris passed away from a disease called Pulmonary Fibrosis. In the past 12 years, Abbie has lost several other family members, including her Auntie Cathy and cousin Johnny Clarke who all died from Pulmonary Fibrosis. Abbie also has a cousin Rayyan who was diagnosed with pulmonary fibrosis at the age of one and has been battling the disease for the last 9 years and is on oxygen 24/7. Shortly after the passing of Cathy, Abbie’s Auntie Shelley (Rayyan’s mother) got sick with pulmonary fibrosis, which led to a lung transplant in March 2017. All of this made Abbie really scared and sad, as she didn’t quite understand what was going on. Her mother, Amanda Clarke explained everything, but Abbie still didn’t understand. She asked lots of questions and that helped her learn more. Then Abbie discovered that there were a lot of other people who did not know about Pulmonary Fibrosis. Abbie decided to do something about this terrible disease by organizing a run/walk to help Canadian Pulmonary Fibrosis Foundation (CPFF) to raise awareness and funds to hopefully find a cure.
Please join Abbie and her family on Sunday September 15, 2019 to help raise awareness and funds to continue our work. Click here https://cpff.ca/donations/clarke-family-walk-for-pf/
Individual is $10 per person
Family of 4 (2 adults & 2 children, 17 & under) is $25
4th Annual Clarke Walk for Pulmonary Fibrosis
Sunday, September 15, 2019 at 11:30 am
Edworthy Park https://goo.gl/maps/Th8XcSCk6Z4qr2z6A
5050 Spruce Drive
Calgary, AB T3C 3B2
In support of Canadian Pulmonary Fibrosis Foundation (CPFF) Charitable# 850554858 RR0001
The Canadian Pulmonary Fibrosis Foundation (CPFF) provides support for all people affected by pulmonary fibrosis (PF), and is the voice of patients living with PF.
Our four pillars of focus:
1. Educate and raise awareness about PF among Canadians;
2. Support PF patients and caregivers;
3. Raise funds to finance research and;
4. Give a voice to PF patients and caregivers.
Our mission is to raise funds to finance research to better understand, develop treatment and find a cure for pulmonary fibrosis.
Our vision is make lung transplants the LAST resort not the ONLY resort for people with pulmonary fibrosis.