I was in contact with an acquaintance who has had MS for 14 years and has been on "an alternative therapy". She seems great.
I've agreed to go on to a clinical trial in June. I have some worries about it. Especially when she said she was on alternative therapy...
do all of you get confused by what your neuro recommends?
I feel as if I'm in a sea of molasses...trying to figure out the best course for me...