I am new here.. New to the world of pots.
I was diagnosed just a couple of days ago.
While researching it I came across a very moving post (below) from a rugby player "troot12". His post was from 2 years ago.
Does anyone know what happened to him and if he is ok?
Hello! Nice to meet you!
Thank you so much for replying
In the many hours I have spent combing forums to learn about pots I see that a lot of posts are a few years old. It's be great if role came back and posted now to say how they are and how their treatment worked over the last few years.
I also want to add that I'm so glad I found this site.. It seems so much more positive than other places I stumbled across..
I hope that for at least some, they dropped off because they were able to find ways to cope with the disability successfully and just didn't feel the need to come back. It is kind of sad when some who used to be regulars here disappear, but perhaps they will come back.
I am 28 and wondering if I have this.. I want to get tested...I have had so many issues since 2008. I pass out when I stand sometimes, my feet turn purple when I stand for long period. Mornings when I get out of bed are rough, my heart feels like its going to explode. Always exhausted. My muscles hurt so bad. Does this sound like any of you all? thanks, Kristin
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