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This is really distressing. Kathleen was one woman who had a major impact from CCSVI treatment. It was so apparent because there was just a massive correlation. She'd feel great right after surgery. Then she'd start feeling awful and sure enough she'd restenosed. Well when that got fixed, she was go...

Ken started it! Bubba, I have a friend that was going through low T and he used Andro gel (probably what you're describing) and it helped in that area a lot. Don't forget dumbass!

Bubs,

I think I remember talking about this, but did you get the Low T test?

One thing is for certain. Just as there are SOME remarkable reports out about having the CCSVI procedure done, there are just as many re; nutrition. Once again, since it seems to be a miracle for some and not others, it just appears that MS is so many things and not just one or MOST would benefit if...

That's what I'm going to do Joan; find a lyme literate doc. That movie does make you go hmmm. Not necessarily about the connection to MS, since there are so many, but the fact that those guys on the IDS appeared to be going "lalalala! I"m not listening to you!" with the data. Some of ...

It is quite possible this has already been posted. Forgive me if this is redundant, but I found this article very interesting. Especially after watching the movie "Under our skin".

http://www.owndoc.com/lyme/multiple-scl ... -cover-up/

You sound just like me BC. Not back to the original, but doing better. Overload of my CNS (too much stress, exertion and heat) and I still feel like ass, but overall, doing lots better than before. As I've said many times, nothing yet can undo damage that has already occured.

I hope she's ok. She's a trip for sure, but you can never question her dedication to all of this. Man I hope she's well.

I just read this entire thread and it kind of cracks me up. I've seen some hair splitting in my time, but this thread takes the cake! But along the way, there were some actual, fact based snippets for the original poster to contemplate/research further. So I hope the original poster got the the help...

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Dr. Siskin uses the flow 'stuff'. He's all about the flow and not just stenosis now.

If you stick with LDN, you will get over the sleep disruptions. Taking it during the day is a decidedly bad idea. I know about circadian rhythms, by there are other rhythms that our bodies go through during the day that are more than just 2x/24 hr. I tried taking it in the morning and felt actually ...

If it's there, it's there in transverse myelitis, which is the 'myelitis' part of NMO. This is what my dx was for years. The japanese don't discriminate. To them, NMO is called Optico Spinal Multiple Sclerosis.

Interesting thread. I don't know how any of us can say what 'gave us' our MS. I mean what about all the people who MS just hit them out of nowhere? I think saying something triggered your MS is an exercise in futility. How do you really know?

I had a 2 year long headache during my dx period and afterwards. I got a prescription for 800mg Ibuprofen and took one every six hours religiously. By the time ai got through with 2 bottles, the headache was only a transient thing. I have no earthly idea if the IB was responsible, but my theory is t...