to all MS sufferers: maybe doctors can convince

[Guest guest]

I find it unacceptable that my GP and my neurologist are unwilling

to prescribe LDN when many in the medical community are.

I think it is because they do not think it has a chance of working,

and because they think I am not qualified to judge, and because I

heard about it on the internet, which has an often deserved bad

reputation.

So: if *your* personal, regular GP and/or neurologist have prescribed

LDN therapy for you, and it has helped yoour MS, in *any* way, I am

asking *you* to ask *them* to write or FAX *my* GP and/or *my*

neurologist, describing the benefit you encountered. I am willing to

pay both you and your doctor for the time and expense this incurs.

If you trust me in this, please discuss it with your doctor(s) and

let me know by private email, if you are both willing to help. If

you are, I will tell you the addresses and phone numbers to contact,

and we will get started.

Thanks very much and I hope this convinces them (and maybe others).

-Sullivan