the sun never sets on our research
fara - Friedreich's Ataxia Research Alliance
Katelyn's Story

This is Katelyn. My name is Katelyn and I live in New York I am a 17 year-old in my last year in high school. I too have FA. It has been hard to live with and I get very frustrated at times to where I just want to give up.

All my family and love ones encourage me to keep going and stay strong so I do not for me but for them. I started noticing there was something wrong with my coordination when I was 10. I was first sent to an ENT doctor and then I was sent to a neurologist and that's when I found out that I have FA. Both my family and I were devastated, however we do our best to stay strong. I am not yet in a wheelchair; however I know I will be soon. I just accept everything that is going to happen. I live life to the fullest because you only live one and this is the life God gave me.

[ ^ jump to top ]  
fara dancing people - jump to the home page DONATE TODAY | Patient Registry Sign In | Apply for Grants

Copyright © 2001 - 2008. All Rights Reserved.
FARA — Friedreich's Ataxia Research Alliance

P.O. Box 1537, Springfield, VA 22151 | (703) 426-1576
fara@CureFA.org | www.CureFA.org