Isaiah was diagnosed with Cystic Fibrosis when he was just a week old at Albany Med after he was admitted there for not breathing after he was born.
He was also admitted into the hospital when he was just a month and a half old for he stopped breathing at home and had his first helicopter ride in life he had the virus and four bacterial infections.
Isaiah is 6 years old and now a 1st grader. He continues to be in a special educational class due to him also being Autistic. He still has his therapies which are occupational, Speech, and physical therapy at school. He continues to change and grow it’s amazing to watch just alone his communication has gotten so much better. He has made great friendships in school and his teachers absolutely adore him.
Isaiah is a very happy boy, has an amazing personality, sensitive, loves his family, his dog Emma, absolutely loves animals and loves being at the ocean.
We are so excited that he gets his make a wish this year!
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. Will you join me and support my fundraising goal?
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.