Post
by zenhead1 » Tue Oct 25, 2011 4:40 am
i don't do too much walking - with a walker and only when my electric chair is recharging - but i am fairly certain ampyra does what it is supposed to do. days when i have missed taking it, i notice a definite difference. i have not started LDN, seeing my neuro in about a month, and will see how much convincing she needs. sorry, not cytoxin, it's cellcept i'm taking, and i'm not sure it's doing any good. i like the idea of LDN as it is the ONLY treatment i've found the even suggests improvement. everything else, like cellcept, only suggest that they might slow the disease process, and i have a feeling that in later stages, like SPMS, it is ineffective. i am cautiously optimistic about the LDN (hard not to be wildly optimistic!)