Supporting the PALS SkyHope Rare Diseases Fund helps patients like
Quinlee
MAINE
Quinlee was born with a rare disease that left so much uncertainty for her future. Doctors didn’t know if she would be able to walk or talk. When she was 2 months old, Quinlee began regular specialized treatments, but they were an 11-hour car ride away. That’s when her mom learned about PALS SkyHope. With her regular trips shortened to a quick plane ride away, Quinlee has gone way beyond what most people thought she would.
