Liam Fabrizi is a 7-month-old boy who is battling a type 1 genetic disorder.
Spinal Muscular Atrophy affects and weakens muscles to the point where Liam will need help just to sit up.
There is no cure for the disease and throughout the United States, there is only one treatment center and it's located in Rochester New York.
Liam's family and friends spent Sunday morning at Topper Saloon and Eatery in Endicott, enjoying one another's company and helping raise money for medical and travel expenses.
Over 60 baskets were donated and raffled off.
Liam's mother Meghan Fabrizi said, "all of this has truly shown us what community means, we're baffled by the amount of kindness and generosity, the support the prayers there's honestly no words".
For more information about SMA click here