Remembering Ryan Scott Ride
Once again, we will be biking the 5 boroughs of NYC in the hopes of raising awareness as well as raising money for a great cause.
The Dystrophic Epidermolysis Bullosa Research Association of America (debra of America) provides all-inclusive support to the EB Community, through funding research for a cure and by providing free programs and services for those with EB.
Ryan David Scott was born December 26, 2009 and adopted by Craig and Mary Ellen Scott just a few days later. Soon after joining their family Ryan was diagnosed with a rare and deadly form of EB called Junction Herlitz. Ryan lived most of his 80 days in the arms of his mom and dad and changed their hearts forever.