Will be in Washington D.C. on Sunday through Tuesday. We are going there for Lou Gehring’s Disease “ALS” to meet with people of the Senate and Congress to tell our stories and hope in order to help people with this disease. There will be ALS caregivers and families that went through this or are going through it now. They will make you cry and at the same time will make you laugh! These people have HEART!
I lost my father to ALS. I wish I could go back and have a catch with him. So now I don’t want anyone to ever have that happen to them, and that’s why I go each year.