Re: nine months on LDN

[Guest guest]

Your story about a mother and her daughter's improvements touched me

as my mother is the same about me. She is happy and hopeful and

proud, and LDN does improve our outlook and behaviour in such a way

that it makes our families breathe a sigh of relief - slowly but

surely, the strength and balance, sleep and bladder improve to a

degree that nothing else has given us to date. Im very happy that

's condition is definitely not regressing, and while most of

us notice subtle changes, those changes must be appreciated and

greeted with enthusiasm as we wouldn't have had them before. You're

a terrific mum, just like mine. regards to from us all.

Friday

--- In low dose naltrexone , " paatti1 " <b_hammel@h...>

wrote:

> 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.