Hello and Welcome!!

Friedreich's Ataxia is a debilitating, damaging, genetically concealable, very rare, and life-shortening disease that currently has no cure. You are now a part of the journey and battle to raise awareness for, treat, and eventually cure FA! This website was originally started for the fundraiser that will take place in the Spring of 2018. Details will soon be released in the "Events" page about how you can donate in conjunction with, reserve tickets for, and attend the fundraiser. Proceeds raised will go to the Friedreich's Ataxia Research Alliance (FARA). Take a look at our site to find out more about Friedreich's Ataxia, check out how much money FTCFA has raised, read stories from the FA community, learn about future events (soon), and contact us!!