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Old 04-07-2009, 06:24 PM #11
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freeinhou freeinhou is offline
In Remembrance
 
Join Date: Oct 2007
Location: Fairfield Glade, TN
Posts: 847
15 yr Member
freeinhou freeinhou is offline
In Remembrance
freeinhou's Avatar
 
Join Date: Oct 2007
Location: Fairfield Glade, TN
Posts: 847
15 yr Member
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Quote:
Originally Posted by craterhead View Post
I had 2 mri's within 11 mos. the second showed 7 lesions mostly in the white matter. I used this forum actually to find information for placement. Thank you for that. Finally got to the "specialist". He claimed what the radologist saw what just an interpertation. As if we were discussing art. And what he saw was not there. I was corrected there are no such things as "lesions" they are merely shadows. People with ms I am told don't get headaches. Don't have tremors. Or petite mal seizures. I initially was told I have ms by another dr and then this Dr says you may, you may not. Even if you did I wouldn't treat it. What? So he ordered an mri of the spine. He remarked of my physical strength. Well I KEEP strong. This is frustrating to say the least. It took weeks to get an appt with this guy. He asked no medical history. Perhaps I should get a second opinion. I don't know. Does anyone have anything they can share as far as their own symptoms or side affects? Thanks so much. Stephanie
Steph -

First off, welcome to the board!

I was told I have MS in early 1988. Symptoms at time, among other things - severe back of neck pain. This finally went away in 2004.

First grand mal seizure - 2/93. Last seizure - 9/94.

First MRI - 3 lesions, 4/89 (there was a long waiting list back then for an MRI).

Last MRI - ~ 30 lesions in 2003. I don't need to know any more at this point.

Your doctor does not appear to understand MRI lesion distribution or presentation in MS patients. I would suggest a second opinion.

Side note - lesions do come and go. Your body is capable of healing itself. I got 15 years of MRI films... In my case - outright symptoms seem to come and go.

Lesion count (gray and not active or white (with contrast) active) really isn't an indication of where you might be with the disease. Location is probably a bigger player. As I understand it, 85% of people with MS aren't outwardly affected by the disease. I'm in this group, even after 21 years.

MS treatments - beer. bar-b-q, and coffee seem to work. I don't know about them crab's... Never been on one of them (ok - copaxone for a couple of months in 2003).

Tom
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