With all the expertise on this forum I am hoping one of you knows alittle on this topic. I am one of those unfortunate folks floating out here with crazy life altering symptoms and no solid diagnosis. A few years back I was told possible MS, then they changed it to aspartame toxicity, now Im a luni-tune with very low vitamin D.
I believed them when they told me I didnt have MS a few years ago. That my defeicits were from aspartame. Since the beginning of October my life has changed, I am half the person I was. I am officially on my third neurologist. I finally went to an MS center last week. They ordered some labs that previously were not done. My TSH is on the lower side of normal 0.32 and my vitamin D is 13.
I have an increase in abnormal areas on my brain from 4 years ago, negative spinal tap, negative c & t spine. For 2.5 months I had parathesias that were almost unbearable during the night, muscle spasms mostly left sided but eventually I had them in my right arm as well. Head pressure beyond belief and fatigue like I have never known possible.
I have been given tegretol, buspar, ativan, wellbutrin, pristique, baclofen, flexeril, vicodin, and a whole host of other meds. They keep saying I am depressed and anxious...well wouldnt anyone if their life changed this significantly?
I am a nurse by trade, I am not ignorant to health issues and my symptoms are more than real. I rarely feel the parathesias the last two weeks. Mild spasms in my left foot and calf only now. Fatigue is still unbelievable. I am not taking any of those meds anymore as most make me feel completely out of it.
My questions are this...can low vitamin D cause parathesias? I know it can cause cramps. I also read an article yesterday that said MS can cause low vitamin D and low vitamin D has been thought to kick off MS. IS there any truth to that?
I would welcome any cause for my issues at this point instead of depression and anxiety. I would be thankful if it was a nutrition/vitamin issue in place of MS. I just have a strong gut feeling they are overlooking MS and I will end up going another few years without treatment.
The MS center NP was terrific and spent over an hour with me, for which I am most thankful. She said they didnt send the brain discs and she wanted to rule out some other things in the meantime. I am due to follow up in January. Funny thing, I called yesterday when I saw my lab results ( I have access to them on hospital site) and they didnt have the results (anither hospital) so I faxed them to her. I still havent received a call back so I am assuming my value of 13 isnt that crazy terrible?
Thanks for all your input when folks have questions...yoi guys are great!