MNsue Posted July 27, 2006 Report Share Posted July 27, 2006 My Dr. could not answer these questions for me, but I thought it would be interesting to find out how others with POTS have faired with their neurological issues. Thanks for your updates.Rhonda Quote Link to comment Share on other sites More sharing options...
Dizzy Dame Posted July 28, 2006 Report Share Posted July 28, 2006 I have raynauds in my hands and feet, as well as documented peripherial neuropathy. The numbness/tingling has slowly gotten worse, but my POTS hasn't. I also have difficulty swallowing and occasional difficulty chewing. So far I'm not being treated for any of the neuro stuff, but that should change pretty soon. Quote Link to comment Share on other sites More sharing options...
dano2718 Posted July 30, 2006 Report Share Posted July 30, 2006 Rhonda - Still investigating my fatigue condition, but my POTS was first discovered on a TTT, not by excessive orthostatic symptoms. I think mainly now, I have an inherited neuro (muscular ?) issue I got from my dad - who said he passed the TTT just fine. I suspect I should be getting more muscle weakness and wasting if I progress as he has. Quote Link to comment Share on other sites More sharing options...
jdqm Posted July 31, 2006 Report Share Posted July 31, 2006 i see the neuro for the first time on wednesday, so we will see. Quote Link to comment Share on other sites More sharing options...
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