wow, victoria, that is awesome!
i had to laugh when i read the first bit of your post, because exactly what you were afraid of, is exactly what happened to me, yesterday!
i was told anxiety, but nonetheless, she ordered an mri for my back/brain as she was concerned about one thing, the band of tightness i've been having.
good for you, i'm sure you presented yourself well and how fabulous to find a doc. who is together in this with you!!!
yayyyyy!!!
Oh, Goodness me!!! You found a doctor that LISTENED to you carefully, LOOKED at you carefully, and THOUGHT about what he was learning. You found a jewel. Also one that knows how imperfect the tools of diagnosis are in MS.
Hearing my diagnosis was indeed a woohoo! moment for me. I knew I had it and had been shabbily treated previously. A month later I was less enthralled, but the validation and the name of my enemy were huge for me.
Please keep us informed and ask any questions you need to.
Quix
I have been struggling with this stuff for nearly 10 years. It started when I was in middle school, but my dad wasn't to keen with us going to the doctor and spending lots of money on tests when he thought we just had a headache or girly problems.
Finally after high school, well when I finally got a job that would give me insurance, when I was 20. I was able to go to the doctor for things like; numbness, pain in my limbs, blurred vision, double vision, spasms, headaches, bowel problems, balance issues and a feeling like I put my cell phone in my head and it was stuck on vibrate.
Recently, in the past 4 months I've had pain/numbness/tingling in my left side of the body. Feeling like I was walking on stones and it hurt like heck to walk around. Cloudy mind and a buzzing in my head. Weakness and fatigue.
I am not hoping it is MS, I am hoping that it is something simple. My CBC, B12 and other blood tests all came back normal. I have been fighting to get some answers for a very long time. So I'm at the point now where I just want a diagnosis, I don't care what it is, I just want to find out what it is so we can start treating it.
Thank you all for your support, answers and suggestions!!
Victoria
I'm glad that your first visit with this neurologist went well. I have no idea how long you've experienced your symptoms or what they are, but compared to most of the stories on this forum, it seems like you're a lot better off than most. If there were ever a fairy tale story of being diagnoses with a neurological condition, it seems like this is it.
The fact that your doctor outright said you have three worrisome symptoms (all classically MS at that) is a bit strange to me because most doctors, regardless of specialty, don't disclose too much of their initial thoughts until they have done test like the MRI, EMG and lots of blood tests. Then again, like I said, I don't know your diagnosis journey or how long you've been in limbo.
This all being said, however, I have to agree with Lulu and push the point that while it -is- excited to be heard, feel taken care and maybe even finally get a diagnosis, having MS isn't really a "woohoo" moment for most people. If you get diagnosed, that's merely the beginning of a long journey and a struggle for some. This doesn't mean to say that it's a "doomed" diagnosis because leaps and bounds are being made every day, but just try not to get ahead of yourself. We're here to catch you if you stumble, though, but it's probably best to not stand with your eyes closed if you fall over. ;)
-treebranches
I am pleasantly surprised by this doctor. He seems like a one of a kind so far. He listened to each and every one of my symptoms. He asked questions and listened to my answers.
He then went through the whole neurological exam. Testing my reflexes, motor skills, eyes and watched me walk. He said that there are 3 worrisome symptoms. That when he rolls that sharp object on the bottom of my foot my toes flex upwards each time. He did that like 6 times on each foot. Then when I held my arms out in front of me and stood with my feet together and closed my eyes I fell over, twice. And the fact that it hurts when I put my neck down, causes a lightning strike down my back and to my legs.
He is sending me for a MRI of my brain and cervical spine. They said hopefully I can get in today, but if not it will probably be Thursday.
He also said "sounds like MS", he said it may not be though. He also said that even if the MRI's come back normal we can do a LP and even if that comes back normal "it doesn't mean you don't have it". He seems to rely a lot of my symptoms and not so focused on the tests. Although he did say "sounds like MS". Woot!!
I'm really hoping it will be today!!! OH, I'm so relieved that he believed everything I said and didn't discount anything.
Victoria
Good Luck,
Stand your ground, explain everything that is going on. Like Lulu said don't mention that you think it might be MS because then they will more than likely blow it off.
Be persistant in what you want. That is what you have to do with most neoros.
I wasn't persistant at first and i am now into my 2nd year of seeing him and still undiagnosed. But I have learned to be persistant.
The last thing I want is to be diagnosed with MS but at least I would have a diagnosis. The not knowing is the part that bothers me the most.
Good luck and keep us informed
Paula