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Avatar universal

Thank you very much

Thank you all for your kindness and taking the time to answer to  my post as cope and deal with MS. You guys are the BEST. I just posted an update on my final diagnosis. I hope it may help someone with my similar situation who thinks or suspect MS. I wish you all well and I thank you again from the bottom of my heart.
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Avatar universal
Just wanted to give you more update on my condition. It been almost two years since I have on this forum. I was here due to suspected MS. For those of you who could related to what was going on with me, you might consider visit to a geneticist.  I had to do  this after I had a genetic adrenal gene mutation and years of being a "medical mystery". I diagnosed with a genetic connective tissue disease called Ehlers Danlos Syndrome. This was the cause of the Autonomic Nervous System Dysfunction which is a great mimic for MS. I do not have MS although my brain lesions resembles MS. My neurologist still plans to monitor this over course of time. Best wishes to all.
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