nine months on LDN

[Guest guest]

My daughter has been on LDN for just nine months. I posted

after a couple of months to tell you how wonderful it was. She is

SPMS, has not been able to walk more than a few feet for a couple

of years now and before LDN was always sick, dizzy, unhappy, weak,

slept almost all the time - in short, terrible. She has gotten

progressively better, slowly but surely. Her walking is still

difficult but she can do a couple of trips up and down the hall

holding the rails. She is always quite happy (on her 41st birthday

when she blew out the candles she said she couldn't think of

anything to wish for because she had everything!) (Lots of tears

from me that day) Last visit to neuro - her " jumpy " eyes much

better, he admitted quite a difference. She can now read novels as

long as the print is not tiny - to make this long post short - I

couldn't possibly list all the good changes. And no exacerbations

or regression at all. To everyone, keep on the LDN. As was said

before, it works slowly, but it works. Much thanks to you, Joyce,

for turning us on to it. I don't think would be living at

home now without it.