Every year for 17 years I have supported Cystic Fibrosis Foundation in honor of my grandson, Levi Kelley who was born with CF.
The Cystic Fibrosis Foundation is celebrating 68 years of research, support and treatments that have greatly benefited Levi and others who have this life-threatening disease.
The recent new treatment, Trikafta, has greatly benefited Levi. He has gained weight and no longer needs a feeding tube. He continues to take his breathing treatments and the enzymes meds. He is a very mature and responsible young man as he knows and understands what he needs to live a full and productive life.
These treatments, support, and education are the direct result of all the donations received from family and friends but we still need to fund the CF Foundation until CF stands for CURE FOUND!
Levi continues to battle this disease and along with his parents, my daughter Beth and Son-in-law, Todd and brother, Logan and all of his extended family, we will always be grateful to everyone who gives to help him. He does very well in school with a GPA 4.0.
He continues playing soccer again this year and enjoys it and it is great exercise for his lungs. The Cystic Fibrosis Foundation’s unrelenting work and research to find a cure is ongoing and that takes money. 90 cents of every dollar donated goes to research, education and support. And your donation is 100% tax deductible.
You can donate by check made payable to CYSTIC FIBROSIS FOUNDATION and mail to me at Suzanne Rukes 10418 S US Highway 41 Rosedale IN 47874 or just click on the donate button on here.
I will also provide a link on my Facebook page. All online donations are secure.
The Cystic Fibrosis Foundation funds all research solely by donations from me and you. We must continue to donate so we can give HOPE to all those that have this life threating disease. Levi has benefited greatly from the Foundation and we must continue to add tomorrows for him too.
Levi and I thank you for your generous consideration