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pots

Recent contents Top users
  1. B

    Neuropathic POTS

    Is this TMS? Anyone have experience ?
  2. T

    Bulging veins on feet and legs?

    Hi group. I have overcome so much I’m sure this is tms as well but my fearful brain is on and I can’t find any success stories that really help me. I had a diagnosis of pots and histamine intolerance with the usual physical symptoms. I rarely get them any more (the dizziness, sneezing...
  3. samuelp180

    Symptom imperative new symptom

    Hi I am diagnosed with cfs and pots and have been doing fairly well the past few years with the tms approach. However, the past week my arms have get sore like I just worked out even tho I have not worked out at all recently. Not trying to search for reassurance but has anyone else experienced...
  4. C

    Intro- CFS, Long Covid, Feeling lost

    Hi everyone. This is my first post here and I'm so glad I found a place like this. Looking forward to hearing from all of you and sharing my full recovery story one day. Until then, I'll just cut right to it. In early February of 2020 I got hit with Covid and then West Nile a month later. After...
  5. A

    Is POTS and CFS/ME be helped by this program?

    Hi, I am just looking into TMS and figuring out if it can help me. I’m 29 years old and this is a little of my story... I am hoping I can be directed to a program or practitioner that uses the Sarno approach, but for Postural Orthostatic Tachycardia Syndrome and CFS/ME. I was also diagnosed by...
  6. fern

    POTS (dysautonomia)

    A friend of mine was recently diagnosed with a condition that I had never heard of - POTS (postural orthostatic tachycardia syndrome, a form of dysautonomia). Since a lot of the functional issues she deals with are similar to mine, I looked it up and was surprised to see that my constellation...
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