Katybug Posted September 23, 2011 Report Share Posted September 23, 2011 Hi all! Does anyone know if there are any non-profits out there that do fundraising for Dysautonomia/POTS research? I ask because my doc says that since we POTSies are not really money-making for the hospital he works at, he does not receive a lot of funding. I just wonder if any of us have started to try to raise funds to support our cause. Any information is appreciated. Quote Link to comment Share on other sites More sharing options...
sue1234 Posted September 23, 2011 Report Share Posted September 23, 2011 I assume Vanderbilt, who has a dedicated research facility for dysautonomia, is doing all the research needed for POTS. Even though I haven't seem them make any progress in causes or treatment for the 5 years I've been paying attention, they are a dedicated dys. research facility. I just feel they need to widen their research views. Quote Link to comment Share on other sites More sharing options...
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