Well, it certainly isn't a celebration. But after what I have gone through with doctors. When I asked my first GP for a referral to a neuro, she told me I was fixated on a diagnosis of MS and I was going to waste my money paying for a neurologist. Then the first neurologist Literally laughed me out of his office- he was a Parkinson's specialist- after my first MRI came back "normal", yet I was unable to walk, spasming throat muscles, vision problems, stuttering and slurring my speech, numbness, tingling, heat sensitivity, incontinence, cognitive problems.... and the second Neuro said "come back in a year, we'll do another MRI" while I sat in her office in a wheelchair, when only 3 months previously I had been snowboarding twice a week. My sister has this disease, I know what it is. And now I finally feel some validation for my insistence on good health care. Its still scary to think i have a damaged spinal cord, and who knows how much else that's still "invisible" to the MRI. I guess when I had my first attack last year, I just knew, so I have had a lot of time to process it. Though I still kinda feel like I got hit by a truck...
:) Meagan
Well, I'm glad to know that your symptoms are validated, although it's always a bittersweet thing to celebrate the finding of a lesion!