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Justin30

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  1. Hi, I have been experiencing a significant amount of pain lately. My Dr peescibed me Tramadol. I have POTS but the exact type has been undermined though I had a tolt table test to confirm. I know Venafalxine is similar to Tramadol in structure and did very poorly on venefalaxin. My question is have people here with POTS benefited or experienced no issues while using Tramadol? Or positive experiences? It would be greatly appreciated to get some feedback. Thank you in advance
  2. Hello, I was wondering if any of you have had chest pain from POTS? I have been diagnosed and the Dr said it was normal but it has been getting worse the last while. It is now almost a daily occurence. I am on Florinef and salt/potassium mix. Feedback would be much appreciated. Thanks, Justin
  3. Hi, Dr Oaklander at Harvard and one of her colleagues has been doing a lot on SFN and its role in FM, Dyautonomia, GWI. She has a couole of videos online but it her colleague (cant remember the name) thats shows dymylination of the small fibers that constrict around the blood vessels to push blood along.... I am to wiped out to search for the names and that stuff ATM...searching Oaklander should bring up stuff. Like others have mentioned they meaning Dr Oaklander is using IVIG with success in SFN. I hope you get everything sorted out and get some treatment.
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