Join me in raising funds for The Flanigan Lab to help the Kasners Kick Duchenne!
We are determined to help Caleb and Dunky live longer and better lives than currently projected. Duchenne Muscular Dystrophy is an awful disease that affects Caleb (8) and Dunky (6) and many other boys. But the care at Nationwide is top notch. We feel lucky to have Dr. Flanigan as the boys Neurologist and will do anything to help his lab find treatments for Duchenne. Caleb and Dunky not only have a rare disease, but they have a rare mutation of this disease to make it more complicated. The Flanigan Lab has cutting edge research in the works to help boys like Caleb and Dunky.
Please consider supporting The Flanigan Lab and Caleb and Dunky by making a donation today. All donations go directly to helping Duchenne Muscular Dystrophy.
All donations are tax-deductible and will be acknowledged by Nationwide Children's Foundation.
On behalf of Caleb and Dunky and all other families affected by this disease, thank you for your support!