This was My Bill

This was something I wrote while my husband was still at home. It was therapeutic for me to express what was going on in my life. Thank you. Bill’s Story I have thought long and hard about documenting the part of my life living with someone who is ‘physically...
Carol’s story

Carol’s story

I’ve been with the ataxia foundation a year now so I’m still getting my feet wet. The correspondence has been great, no doubt it’s helping lots of people!. I take note of all the activities offered. I was able to attend my first walk in September. My takeaway was...

Ataxia and Me

I was diagnosed in 2017 after talking to a co-worker and out of nowhere I just fell back like a tree. My doctor referred me to a neurologist who after an MRI diagnosed me with Cerabellar Ataxia. After getting referred to a new neurologist who did a DNA test found that...
Life is Full of Ups and Downs!

Life is Full of Ups and Downs!

My storyline was a priceless one! As I reacted to posts on the NAF Facebook , I came across a lady, Amy Draves, that lived about 30 minutes from me. We agreed to meet halfway and talk! We met and we could not believe how we viewed life with Ataxia! Then we decided to...
Struggle and endurance

Struggle and endurance

Your friend and supporter / Walid Affas Hammoud Al-Mutairi from Saudi Arabia Hello my warrior friends I am really proud to join with you and have the same disease I really have unfortunately Frederick stutter but I still hold on to God and my strength and inevitably I...