Someone asked if I would post my regimen. I think I did somewhere else before, but here's an update.

-Low fat diet
-Mild exercise (stationary bike and stretching mainly)
-Eat nuts every day (for vitamin E, etc.)
-Green tea
-Multi-vitamin (for "mature" people, loaded with extra Bs, etc., and also has lycopene and lutein and bilberry, on and on)
-L-Carnitine (250 mg once in the morning and once at night)
-Grapeseed (50 mg tablet - ...

Ok.....this is a spin-off from the "Nerve Regeneration" thread I just started. I mentioned the commonality of PPARs in it.

I see now, that a researcher has found the same thing I was about to post (several abstracts), so I'll save time and just post his synopsis, which I retrieved from the NMSS website. He has been given a pretty large grant to proceed with his research. This sounds promising:

Hi, folks!

Just when I thought I had "read it all"! Here's something I ran across that I found interesting. Don't ask me who this gentleman is exactly , but s/he's from the Brain Research Institute at the University of Zurich (that's Switzerland, right? :wink: )

Anyway, it's pretty easy reading. For some reason, I found "something" in it interesting, and maybe with ...

Something I have seen mentioned on other forums:

Some MSers have trouble reading postings that have alot of sentences run together. Separating paragraphs like this is apparently a help.

I know I am especially guilty of running sentences and paragraphs together in some of my long posts.

Are there other suggestions you folks can give to make it easier to read posts? Perhaps some pointers on making posts more easy to follow.

Bigger fonts? There ...

Dr. Scott is no longer doing phone consultations for LDN scripts, so if you are using him, you need to make other arrangements to get your LDN for now. I wish I knew more to tell you, but I don't.

If you would like to write a letter to him stating how much difficulty you had in finding someone to prescribe LDN and how it helped you, that might be of some benefit to help ...

had to recently switch insurances, and my neuro just called and said they dont accept my insurance i need to find a new doc, :evil: i am planning on calling NMSS for a refferal but was wondering if anyone on here happened to know of anyone .

thanks a lot

Here's a subject that probably hasn't been discussed for while, if ever, here. Relationships with people with MS.

As we all know, it was eventually determined that I do NOT have MS. Yippee! BUT..........of course after all of this time and my intense involvement with MS, I have made several friends with MS.

I just had a doctor appointment with my PCP a couple of days ago, and we got into an interesting discussion regarding ...

I have been under the impression that Vitamin C is generally not recommended for people with MS because it may stimulate the immune system. I started to read more about it and came across this news release. Discovery Shows New Vitamin C Health Benefits

Has anyone heard that fish oil is good for MSers?