My Great Strides Story
Jenna Williams
Fundraising for Middle Tennessee Great Strides
Jenna Williams
Cystic fibrosis was a diagnosis I was not familiar with until we got the call telling us Laine's newborn screen had come back abnormal and we would need to come in for further testing. Through lots of tears I started researching as much as I could on what this meant for us and for Laine's future. Coming from the non profit world I quickly discovered the cystic fibrosis foundation and boy was that a relief! I immediately felt hope during a very scary time. This foundation is changing the lives of those with cystic fibrosis by funding research and developing modulators to help people with cf live normal lives. To say the work they have already accomplished is astounding is an understatement. Join me today in donating and help this incredible organization fulfill their mission - let's end CF!
There is currently no cure for cystic fibrosis and too many people with CF die young. I'm walking to help change that reality.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?
By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward - a cure for everyone with CF.
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