So I was at my primary's for something and asked her if she had gotten the result of the MRI and readier and it was absolutely unremarkable. No previous mention of the other lesions or spots. This is at least comforting as I wonder if I will ever hear from the neuros office ever again. I called again last week and they still didn't have the report. Still doesn't explain the symptoms but for right now I am wondering if the vitamin deficiency still isn't completely cleared up and is going to take time.
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to push for primary to order MRI or leave it to neuro?
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I feel like you are not getting the 'best' that your medical people can do. I don't think vitamin deficiencies 'clear up'! Vitamins are like fuel in your car. They always need to be replaced. If you get to a reasonable value in all of the important elements, then you have to monitor them every few months. Have you had your vitamin D levels checked? You should know that value. Good luck
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Originally posted by JerryD View PostI feel like you are not getting the 'best' that your medical people can do. I don't think vitamin deficiencies 'clear up'! Vitamins are like fuel in your car. They always need to be replaced. If you get to a reasonable value in all of the important elements, then you have to monitor them every few months. Have you had your vitamin D levels checked? You should know that value. Good luck
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I really feel that, since you are located in the 'United States', you should be receiving much better medical treatment from your PCP. If I was you, I would find a new primary. Your doctor recognized that you were deficient in B-12 but didn't test for vitamin D? Come on ! These are blood draw tests ! It's not brain surgery! Good luck
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Update
Originally posted by JerryD View PostI really feel that, since you are located in the 'United States', you should be receiving much better medical treatment from your PCP. If I was you, I would find a new primary. Your doctor recognized that you were deficient in B-12 but didn't test for vitamin D? Come on ! These are blood draw tests ! It's not brain surgery! Good luck
However, I still test positive for Romberg every time, I have nystagmus in my left eye still causing the double vision issue, and I can't tell if my big toe is up or down. The next step is if the medication doesn't fix more of my issues the new neuro suggested an EMG. I had one a little over s year ago that was normal and I'm not sure if I need to push further. I go back in August but this is just frustrating.
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Thanks for the update.~ Faith
MSWorld Volunteer -- Moderator since JUN2012
(now a Mimibug)
Symptoms began in JAN02
- Dx with RRMS in OCT03, following 21 months of limbo, ruling out lots of other dx, and some "probable stroke" and "probable CNS" dx for awhile.
- In 2008, I was back in limbo briefly, then re-dx w/ MS: JUL08.
- Betaseron NOV03-AUG08; Copaxone20 SEPT08-APR15; Copaxone40 APR15-present
- Began receiving SSDI / LTD NOV08. Not employed. I volunteer in my church and community.
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