Re: MS Society program

[Guest guest]

Leatha,

Wow that is great news! I hope the meeting goes well. I would suggest

sharing some of the stories too.

My husband had a wonderful e-mail today from one of his classmates from High

School that he saw at a class reunion. had shared that he had MS last

year. The classmate's sister has MS also. He e-mailed today to share

that his sister is having an amazing recovery and getting out of the wheel

chair with this new drug called LDN. It was so cool for to e-mail that

he is also on this drug and doing fantastic.

Bless your heart Leatha for working hard to help others hear about LDN.

My best

Aletha

[low dose naltrexone] MS Society program

>I have been reading posts on this forum for some time, and am very happy

> to have a place to go for information. I have ordered Revia from Mexico,

> and will start as soon as it arrives. (I was unable to find a doc who

> would prescribe.)

>

> I have recently joined the board of the local MS Society (Omaha,

> Nebraska), and am on a committee organizing a symposium to combine with

> the annual meeting in October. I have been told that the new national

> president is much more open to consideration of " alternative "

> treatments than was her predecessor, and we hope that she will attend. I

> would very much like to have someone come and speak about ldn. Who would

> you recommend, and how do I get in touch with them? We expect about 200

> people to attend the meeting, and while that's not a lot of people, it

> would be a way to spread the word to at least that many more folks.

>

> Thanks in advance for your suggestions.

>

> Leatha

> leathaj@...

>

>

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