My Great Strides Story
Suzanne Nolan
Fundraising for Baltimore Great Strides
Suzanne Nolan
This is my 30th year as a Development Director for the Cystic Fibrosis Foundation - in that time I have seen babies grow up, graduate from College, get married, have careers and start families of their own! When I started the life expectancy was 12 years old. NOW it is 50's 60's and beyond. We are on the verge of a cure for CF with may lifesaving drugs making life easier for all of our patients!
Your donations over the years have truly made a difference in this world - and for that I thank YOU!
There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality. We have made a lot of progress from 1995 when I started at CF to this year 2025!
This year as I walk and ask you to JOIN ME at the Zoo on May 15, 2025 for food, fun, exercise and ice cream! It's going to be the best celebration ever. I am walking for Henry this year a vivacious 10 year with CF! He is into sports, has a younger brother, Ollie and a loving Mom and Dad. If you can't be there please donate to my team to help cure CF for Henry and all of those with CF.
CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.
Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.
Will you help us end cystic fibrosis?
Thanks for all you have done in the past to help CF stand for Cure (almost) Found. Sue
Your donations over the years have truly made a difference in this world - and for that I thank YOU!
There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality. We have made a lot of progress from 1995 when I started at CF to this year 2025!
This year as I walk and ask you to JOIN ME at the Zoo on May 15, 2025 for food, fun, exercise and ice cream! It's going to be the best celebration ever. I am walking for Henry this year a vivacious 10 year with CF! He is into sports, has a younger brother, Ollie and a loving Mom and Dad. If you can't be there please donate to my team to help cure CF for Henry and all of those with CF.
CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.
Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.
Will you help us end cystic fibrosis?
Thanks for all you have done in the past to help CF stand for Cure (almost) Found. Sue
MAY
10
10
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