Re: went to see my neuro this week

[Guest guest]

--- Joanne

I to am SPMS and have been on LDN for 5 months. I had a lot of

stiffness in the beginning but now every day I feel better and better!

Stick to the LDN, You won't be disapointed!

Steve

In low dose naltrexone , " Johanne F " <johannef@s...>

wrote:

> Hi,

> I seen my neuro this week. His name Dr Jack Antel. he does MS

> research for MS at the McGill university in Montreal, quebec.

>

> I asked him if he'd do a study on LDN. He said no.

>

> why ?:

>

> -Because you need at least about 500 ms patients

>

> -Because once you're progressive, lesions don't happen anymore

>

> -Because it would cost about 500,000$ canadian for 2 MRI per

patient

>

> -Because it is very difficult to construct a study that will give

> them correct data. He says that it is difficult to measusre how,

> what exactly the endorphins did. (or something to that effect)

>

> Also I brought him a few articles which were posted here that are

> supportive of naltrexone in some fashion or other. Well he knows

> most of these scientists and about their work.

>

> this week he has a meeting with scientists who research MS. He's

> suppose to find some info about the goat serum.

>

> He knows I used beestings for 3½ years and he said something like

> he was a bit disappointed with me because I'd switch to LDN. I

think

> he thinks the histamine in beesting is more in-tune with the

> current theory about MS.

>

> So I left a bit discouraged but I'm sticking with LDN anyway.

>

> It took 87 days for me to get ride of stiffness from LDN and I do

> sleep much better. But that's all I've notice so far. I have

> secondary progresssion MS.

[Guest guest]

Right now I find 3mg works best for me

> Tazz, what mg of LDN are you on?

>

> valerie