Multiple Sclerosis: New MRI Contrast Medium Enables Early Diagnosis In Animal Model (
 

In particular at the early stage of the disease, drug treatment is effective. Up to now, how-ever, an early diagnosis is frequently not established with certainty, especially if no inflammatory lesions are ...



More...

(From Topix Neurology)

This is great newd for those folks who are in limbo!

I wonder how long it will take before it's approved for use?

And what's the chemical compound of this new Gadofluorine M? If it contains Iodine many people won't be able to tolerate it due to allergic reactions to Iodine.

But it is good news for advances in MRI Technology!

made me wonder...hmmmmm things that make you gooo hmmmmmm

so much for neurologists around here, that say your MRI is clear..YOU CANT HAVE MS..huh.....hmmmmmm

still wondering here what the heck I have, hugsss,sarah

spoken like a true limbolander at heart....hey Nancy, I know the feelings..hugsssss,sarah

Nancy since 1999, sxs...and mine have been since...let me think....wow wait....it was 1999 shortly after having a baby...so October 99...hmmmmm maybe we have a 99 disease...where you from again.??? hugssss, and if you need to chat or vent with me about sxs..or life with limbo...pm me..hugsssss,sarah

You've heard of the forty-niners? Well, Sarah, you and I are the ninety-niners. :)

That was a very weird year... everyone was worried about being "Year 2000 compliant." I lost my left-side hearing, had an operation on my ear on December 21 which didn't help, and in the end I was NOT "Ear 2000 compliant!"

Between my hearing loss and all the other weird symptoms that happened that year (AND my father-in-law getting diagnosed with cancer, AND I can't remember what else...) I thought the Millennium had come early. :)

Yep, true limbolanders like you and me Sarah, we have earned the privilege of being incorrigibly pessimistic about the possibility of getting diagnosed--or of any doctor even giving a **** about following up.

All those implied promises, by new doctors, new tests, etc.... it all counts for nothing. You are lucky if you find something that helps your symptoms. (I did.)

Nancy T.

Well, they do have a blood test for NeuroMyelitis Optica, and when I had that test (it was negative!) the Nurse Practitioner had told me it was a new test that helped them distinguish MS from the NMO. I was glad my test came back negative, since they were thinking about diagnosing me with NMO instead of MS because I had spinal lesions and ON and no real obvious brain lesions.

Hi Erin--that's good if they have a blood test that's good for something! I don't think that was the one I was thinking of, but anyway, I'm glad they were able to rule it out for you.

Nancy T.