I am planning to go to the CCF in earlyJanuary for second opinion. Symptoms for months and our local Dr's can't seem to do much more. Symptoms include jitters almost all day and upon waking, shake internally, feels like a current or vibration in body at times, numbness in hands, dry mouth and loss of appetite, fatigue and unable to sleep more than a few hours at night. Most routine tests came back normal. On a previous post it was suggested it could be a connective tissue disease. I may have fibromyalgia As well.
BRAIN MRI RESULTS:
I had an MRI and report said "Two Tiny cortical White matter Lesions in the left centrum semiovale which are non specific and my be related to early demyelinations versus gliosis secondary to small vessel disease. Correlation is recommended clinically. No intercranail Masses. Minimal right mastoiditis."
I do not have any major stress in my life other than this mysterous disease.
My Dr. Suggested trying Paxil CR 12.5mg in case its anxiety. I have not started it yet.
Besides the MRI Results above, my question is if I start paxil can it interfere when I go to you guys for furter testing? For example could I develop a side effect from it and no now if its paxil or me? I will want to see a neurologist as well as a rheumatologist depending on what internal medicine eval says .
What do you suggest? currently taking vitamins only. Had high BP before I lost all the weigh, seems stable now. I get occasional premature beats.
Can the MRI results be MS, local Neuro said was probably not but I don't know
Should I wait?