Severe tingling, burning + pain in both legs
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Hi everyone,
I've been having severe tingling and pain in both my legs (toes, feet, calves and knees) for about seven months now. On running a few tests, I found six months ago that I was deficient in vitamins B12 and D, which was set right. The neurologist said my symptoms were due to the deficiency, however, the condition has steadily worsened in spite of the deficiency being rectified.
Here are the tests I've done:
Vitamin B12 and D: Levels stable for the last 4 months
Thyroid: Normal
Sodium, calcium, potassium: Normal
Iron: Normal
Bloodwork, ANA, dsDNA all normal.
Rheumatoid factor negative.
The pain is worse at night and while lying down. The docs have told me I've got Restless Leg Syndrome. I took Pregabalin for about a month and Ropinirole for ten days but both didn't help with the tingling - in fact the side effects were terrible.
I'm not on any medication as of now and the pain + tingling has worsened, now almost constant, like there's electricity shooting up my legs all the time. I'm unable to do anything physically exerting like climbing stairs. Walking makes my feet hurt terribly (which I believe is not the case in RLS?).
Does anyone have suggestions to confirm the diagnosis? Is there something I'm missing? I'm due for an LS MRI, but the docs have said it is most likely to come clear.
Thanks a ton!
17 likes, 568 replies
katie159 moimystique
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Jimjamcolly moimystique
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Hi ..just wondering how you are getting on I have the same symptoms as you .they are giving me 250000 vitamin d a week as it's low so they think this might be the reason . It can take 3 months I'm in so much pain .thank u
jane75220 Jimjamcolly
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Jimjamcolly jane75220
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jane75220 Jimjamcolly
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Vitamin B12 deficiency or pernicius anaemia can be the reason why one has peripheral neuropathy. If you are unable to absorb Vit B12 then drs ca prescribe injections. If you see the pernicious anaemia society you will see lots of info on burning legs etc.
jane75220 moimystique
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allen49243 moimystique
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jane75220 allen49243
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allen49243 jane75220
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jane75220 allen49243
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allen49243 jane75220
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christy463 moimystique
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I finally have a diagnosis. I've only been dealing with all of this since November 2016 and thankfully I work for/with a wonderful medical practice that went above and beyond to figure out what was going on with me. I've had every blood test imaginable, MRIs, Neuro vision testing and have seen a neurologist and now a rheumatologist. All my labs have been normal for the most part until this past week when my rheumatologist ordered 16 additional labs one of which was the Smith Antibody that came back positive which confirmed I do have Lupus. My PCP suspected it from the start, but with my ANA and RA being normal he wanted to see what the specialist thought. My PCP has started me on meds and I'm praying they work. I really hope and pray you all find answers about the cause of your symptoms.
susan75999 moimystique
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allen49243 susan75999
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mercedes3 moimystique
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Google Statins and side effects
mercedes3
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