I am Karen Stewart
a family member of someone living with ALS
Ohio
No one should have to feel this way that there is not hope.
Visited my son last evening. He’s two years from diagnosis of ALS. He is totally wheelchair bound. Last night he said even if NurOwn was given to him last night, he didn’t think it would change anything as he has progressed too far. No one should have to feel this way that there is not hope.
