Sue Falcone
May 18th, we are walking to raise awareness and funds to cure Cystic Fibrosis. This disease has profoundly affected our family, and way too many others. Research has changed CF immensely since our first diagnosis in 1988 of Nicholas. CF has relentlessly taken too many young lives far too soon, including two of the Falcone four, Samantha Reid, and Nicholas Falcone. Gabby Lauer and Nathan still face CF everyday, with hope of more and better treatments to end CF. You have the power to advance the research and science needed to drive our shared dream forward - a cure for everyone with CF. If you are able, PLEASE PLEASE help us end Cystic Fibrosis! #Breathelove #FalconeFour
We gratefully thank you for every dollar raised!
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