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Post by Anna Roan on May 3, 2014 21:49:50 GMT
Get to meet some other people here and introduce yourself to the POTS community! My name is Anna Roan the admin of this little forum here, I've had POTS for about 4 years now and know how hard it can be to find reliable information on the internet and that I was frustrated there wasn't a real place where we could get together and meet on the internet that I had found. If you have any questions, suggestions or just want to chat I'm always willing to lend an ear just message me and I'll be happy to reply
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Post by MessJess on May 6, 2014 22:17:33 GMT
Hey My name is Jess and I've had POTS for about 7 years. It took a long time for doctors to take me seriously, we're talking years. I got blown off, given misinformation, and even told that it was in my head so it's great that now I have more information then ever before but it would still be nice to talk to some people who actually understand what this is like, also I don't want anyone to have to go through what I did so I want to spread awareness as much as possible. Anna I think this is a wonderful idea
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Post by ixregardo on May 11, 2014 16:51:50 GMT
Hi all, I'm Diane! I was just diagnosed with POTS, though I get the feeling that's not the full reason behind my illness. We shall see
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Post by gcolilli on May 26, 2015 10:02:41 GMT
It's taken my doctors 10 years to finally find that I have POTS. I was tested for everything there could possibly be. I've been sent to so many doctors and put on so many different medications finally having an answer is awesome but there not being a cure really stinks :/
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