Monday, May 04, 2009

It's Friedreich's Ataxia

Neuro just called and life just turned upside down.

11 comments:

Beth said...

It's not fair. I'm at a loss for words. I'll keep praying for Hannah, you, and Jason.

Marcia said...

thinking of you

Kathy said...

YOU HAVE MY LOVE AND PRAYERS. WISH I COULD GIVE YOU ALL A GREAT BIG HUG.

Melisa said...

Angel Blessings for Hannah and your family!

Anonymous said...

Candy, I don't know what to say except I love all of you and am continuing to pray for you.My heart hurts with you. I am so very sorry.
Love to all - Sarita

Jenny said...

Candy I'm so sorry. I was hoping for much better news for you. Sending lots of hugs!

Sarah Ann said...

I help manage an online support community for people affected with Ataxia. If you have come across this site in search of support and kind words from others like you, please stop by: http://www.livingwithataxia.org

Tracy Batchelder said...

I am so sorry that it turned out to be this.

knitalittle said...

My dear I wish I could just give you a hug and tell you everything was going to be alright but I can't. I wish I didn't know the road you are starting down but wish don't change the road you are on. My heart and prayers are with you.

Catherine said...

I've been offline for a few days. Please know I'm thinking of you all. {{{hugs}}}

Unknown said...

I also have FA. My advise for you will be to keep your little girl as active as possible. Exersice is not cure but a great way to slow it's progress.