Looking Ahead to Change: Little by Little
I don't make New Year's Resolutions. I don't think I ever really did, but the last decade or two would have been enough to stifle that impulse. I've just been too aware that I don't have that much control over what happens in my life.
Discuss the article on the Forums.

POTS studies recruiting participants

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

  1. taniaaust1

    taniaaust1

    Messages:
    10,189
    Likes:
    8,678
    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

    Messages:
    149
    Likes:
    1
    Australia
    They sound really interesting Tania, Wish I was was in the US & could get involved!
     
  3. Esther12

    Esther12 Senior Member

    Messages:
    6,856
    Likes:
    15,847
    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.
     

See more popular forum discussions.

Share This Page