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smitten_hussy in dysautonomiaaa


Hello! Welcome to the official dysautonomia community! My name is Paige and I'm your mod. I noticed there wasn't a dysautonomia community and I had to make one! I hope others like me find this place so we can all come together and have somewhere to talk and meet others and form a support group.

You can post about anything concerning your illness and how it's changed your life.

I started having problems in October of 2006. I didn't get diagnosed until January 2007. I was hospitalized for over a month and every three months I'm usually back in the hospital for IV therapy. I've gone through a lot and I know I always will. I went through a long depressing period and I finally got through it and I would really like to try to help others who are struggling with depression on top of all of the other problems. It is very hard and it's even harder when you feel alone and don't really have anyone to talk to about it.

I always feel like when I complain about my dysautonomia and mitral valve prolapse that people think I'm wanting attention or throwing myself a pity party! I'm sure you know what I mean. It's hard NOT to talk about it! It's a huge part of your life. So, this is going to be a safe place where you can bitch and complain as many times as you want to! :)

I made my own website (check user info) about dysautonomia and mvp. I tell about my story, who I am aside from the illness, symptoms, and many other things. So, that will save me from rambling on about ME. If there's anything you'd like to know just ask!

So, let's start telling our stories and sharing our every day experiences!


I know this post was several months ago, but I am here to help you, too.

My name is Jessica Sami Pennington. I have MSA and my primary problem is POTS, I also have every movement disorder (it seems) known to the medical community. I have slowed down considerably. I just want you to know that I am here, too.
All my love, Samibebe

August 2007

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