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Lessons from ME/CFS: Finding Meaning in the Suffering
If you're aware of my previous articles here at Phoenix Rising then it's pretty clear that I don't generally spend my time musing upon the philosophy of the disease. I find it better to spend my time reading research and trying my best to break it down to its core elements and write...
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POTS studies recruiting participants

Discussion in 'Problems Standing: Orthostatic Intolerance; POTS' started by taniaaust1, May 8, 2011.

  1. taniaaust1

    taniaaust1 Senior Member

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    Sth Australia
    I hope no one minds I posted this twice as it belonged in the "active clinical studies" forum part but I want to make sure that those with POTS see this so wanted to put it here too as it could be of great help to someone..

    Seeing all these POTS studies they are trying to recuit POTS patients for.. blew me away. http://www.clinicaltrials.gov/search/term=Postural Tachycardia Syndrome Wow finally attention seems to be being put into POTS.

    Ive found joining studies often useful to find out more about my health issues..
    or in some of these cases could be very useful if someone wants to try out new treatments for their POTS (thou of cause you never know if you are in the control group or getting a trial drug).
  2. TinyT

    TinyT Senior Member

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    Australia
    They sound really interesting Tania, Wish I was was in the US & could get involved!
  3. Esther12

    Esther12 Senior Member

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    I've heard that interest has picked up in autonomic things recently.

    I wouldn't be surprised if this research was more helpful for CFS patients than any of the 'CFS research' going on.

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