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Supporting tests and lack of other apparent symptoms rules out obvious suggestions / ideas...
Along with a variety of meds, I am on Synthroid (0.1 MG) and and TopamaxTopamax Topamax sprinkle (300MG). Before I see another specialist, I'm looking around on my own.
I spoke to my neuro's office yesterday after they reviewed the results of my blood test. As a refresher, the test was ordered by my GP, not my neuro. GP recommended that I see a rheumatologist, etc...
Neuro was as confused, as I was, in regards to [all the concern] and assured me that this type of result (see post above) is VERY OFTEN seen in patients like me, with MS (just as I suspected) ...
I have an appointment with him next week but see no reason I should be "re-diagnosed" for MS which, I believe, is where all this was heading! D'oh!!
Looks like this time it really IS one for the MS bucket.
[Duplicate post on another forum to close out discussion.]
Wow...I'm having EXACTLY the same experience. My general practitioner wants me to go back to the rheumotologist because of a high ANA titer. I started here and then they decided it was ms after 2 years of testing. Its like I'm back to square one. Is it possible to have lupus and ms at the same time?
I started with gp in Jan of 09 with the symtoms of pain in body and the blood test were on. after many blood test with a ANA of 1:1280 Speckled. Sent to rheumotologist and no ansewers from him. Finally sent to nurologist after talking my GP into sending me and had a EMG and a small nerveNerve biopsy Nerve conduction velocity biopsy, have found no ans to the high ANA ( if any body else has an reason for the high ANA that would be helpful, with all other blood test neg). Just thought that with the symptoms of fatigue and the ANA you might check out the EMG to start ruling out small fiber nuropothy.
I spoke to my neuro's office yesterday after they reviewed the results of my blood test. As a refresher, the test was ordered by my GP, not my neuro. GP recommended that I see a rheumatologist, etc...
Neuro was as confused, as I was, in regards to [all the concern] and assured me that this type of result (see post above) is VERY OFTEN seen in patients like me, with MS (just as I suspected) ...
I have an appointment with him next week but see no reason I should be "re-diagnosed" for MS which, I believe, is where all this was heading! D'oh!!
Looks like this time it really IS one for the MS bucket.
[Duplicate post on another forum to close out discussion.]