MMS and MS - My experience

[Guest guest]

I have been on MMS and StemEnhance for about 5 weeks now and I must say that I

am starting to notice slight improvements. When I am facing one direction I can

turn around slowly without holding on. I can lift my left leg without using my

hands to put on my jeans. My brain is clearing. I have more energy. My balance

with walking is pretty much the same but I think that because as my legs are

strengthening my body is readjusting and that is why my balance has not improved

much. Once the legs have come completely right then I think that the balance

will improve. I am also on LDN and have been for 7 months but I think that the

MMS and StemEnhance are responsible for the immprovements. LDN is still great

because it is stopping relapses but it hasn't done much for improvements for me

but all together they seem to work really well.

I am currently taking 13 drops. I tried to up to 14 a few days ago but threw up

(not my favourite pastime - except I feel great afterwards). I will try again in

another day or two to go to 14 drops. I threw up at 8 drops for the first time

and again when I first tried 13 drops. I take the MMS twice a day except when I

throw up then I miss one dose.

I would love to hear experiences of others with MS that are using MMS.