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Join Date: Jul 2010
Posts: 458
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Member
Join Date: Jul 2010
Posts: 458
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I'm not sure about too many blood vessels, but I did have a dopplar done when the pooling started, and they said it came out as normal. Would that problem show up on there?
I don't see pooling anywhere else, but I suppose it could be possible.
So you think I have something more severe than POTS? I wonder how I would find out if that is true... not that it really matters, but I'm trying to get disability right now since I'm bedridden, and every diagnosis is crutial right now... I need to know exactly how bad it is so I can tell them.. they are still asking for more information and deciding on my case.
The problem is, it was at Mayo that I was diagnosed. I can't get back to Mayo to be retested, and I don't think they do those tests around here.
I'm just so frustrated that Mayo didn't bother to tell me about this--and a lot of this could have been prevented/treated early on.
No, I have no done the compression stockings. I cannot because of the PN... I can barely handle regular socks and cannot have anything touching my feet--and they said I would have to put those on over my feet and that it would be extremely painful.
One doctor gave me a cream form of whatever it is that people take when they think they are having a heart attack... nitro something or other... to open up the blood vessels and allow the blood to flow... but it didn't do anything.
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♥ "Hope is more than a word; it's a state of being. It's a firm belief God will come through. Life brings rain... hope turns every drop into the power to bloom like never before." -Holley Gerth ♥
My name is Sarah and I am 25 years old. I have a lot of chronic health problems. Peripheral neuropathy and POTS (postural orthostatic tachycardia syndrome) keep me bedridden the majority of the time. I also struggle with degenerative disc disease, disc desiccation, spondylolisthesis, arthritis, polycystic ovarian syndrome (PCOS) with insulin resistance, allergies, sound sensitivities, and other health problems.
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