This Is MS Multiple Sclerosis Community: Knowledge & Support

Hi!

It was a French gut back in 1800 and something after autopsy on an ms patient discovered lesions on the brain.

This theory as I see it has never ever been challenged. Big mistake.

If original theory incorrect all that follows is flawed.

They chose to run with this theory and not Palmers a Chiropractor that had 5 cases of patients going into full remission, that proof they ignored.

There are many many others, this includes young adults in.. limboland.. they exhibit all of the physical ms symptoms but produce clear MRIs and LPs This indicates to me that they have gone with the wrong theory.

There are other reasons, but as people have been told over and over again that any dispute or question means that they are in denial.

Well hello!! to the medical world .. I stand up (meterphorically that is)

And DENY IT. I know that I do not stand alone, others have their doubt to

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I do my own research, and find my own answers Its good to talk

feeoo1, i totally totally agree. have been trying for yrs to have dr.'s look deeper and differently into my case. but, i think as long as we were more or less kept in the dark there was control and they figured it was kind of like the pied piper leading. but we are not in the dark since the internet especially and we are no longer walking in the dark. and a lot of this will be up to us to demand this. just as ccsvi has gotten known and people getting help and the research being done. when we finally get this all put together things are just bound to get better and better.

all that said, i still get pissed off big time learning that all these connections were available and known in the medical world and were conveniently or otherwise shoved in the closet.

but times are changeing. we just have to make it change. the old way of thinking and treating will not go down without a fight----but now we can fight back

i dont know which to try more?

get more patients to try it or
try to get Dr's to understand it?

sorry wrong place

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I do my own research, and find my own answers Its good to talk

It's out of our hands now. Which is a very good thing. The doctors are at work on this. We did good getting it to the doctors.

what doctors are at work on this? how?

i never saw any studies or trails

i've been under the understanding that there are trials and papers published on ms up the whazoo for yrs.. . the results---still no valid answers or treatments that do much all fda approved etc. but for sure eventually they will screw the good body parts up. now there are real people you can reach out and touch that are getting relief of some symptoms without harming the rest of their body. now, it might not suit main stream med. but, the proof is in the pudding.
and i hope someday when someone ask me my name-i can say just call me "puddin"

You made me smile, Blossom. I hope and pray for that for you and everyone else, too.

Hugs!

Trish

Just a small note if you happen to know people showing symptoms who have clear brain MRIs, make sure the spine gets checked too, my neurologist was on the fence for awhile about whether or not to diagnose me with MS (which now I'm kind of pissed he waited, but that's another issue entirely) and the second he say my spinal MRI he got off the fence.