Anyone also have MS?

[jesimae]

 I’ve been gluten free now for eight years. I have had two separate biopsies confirming celiac disease. I’ve had scopes since diagnosis that showed regrowth of microvilli. The diet has worked and I gained back all the weight that I lost before diagnosis.

 Lately, I’ve had some alarming symptoms. I’m having trouble making certain expressions with my face, I have a very hard time finding words or pronouncing words. I’ve had loss of feeling in my hands And numbness in tingling. I also get strangled very easily when I’m drinking or eating. I’m experiencing a trimmer in my right hand particularly although I’ve never had a very steady hand.

The doctor checked all my vitamins etc. and put me on vitamin D months ago, but other than that everything has been fine as far as blood work.

I have not changed anything. Just wondering if any of you have experience this and if you found out what caused it. 

[scholoring]

I don't have MS but I have a similar disease. I know it's really frightening to suddenly have these sort of symptoms but the good thing is is that with MS if you find you have it or something similar, there are a lot more options and research available than what once was. So even if you have it, it dosn't mean that you have to live a life not worth living. There are options! Especially if you are willing to change up your lifestyle habits.

that being said, have you gone over your test results yourself? Perhaps  you are having a sneakier form of vitamin deficiency. Specifically with B12. I hope you are able to find a good resolution for this!