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Magnesiumgirl

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Posts posted by Magnesiumgirl

  1. Hi guys.

    My veins close up so fast! They did have me bend over with my hand down once. She got more than she would have otherwise, but still not the whole order. Most of the blood-drawers (sorry, can't figure out how to spell their proper title!) refuse to touch me. The one is always really sweet, but even she qets flusstered. Oh well, at least I have somewhere that they are nice to us.

    I've never had them use a plain syringe before. I wonder if that would work, mine are so small they have to use the butterfly.

    I drink a Ton (about 10 glasses) of water before going in too... Oh well, it is what it is, right?

  2. I've been at the doctor's office and they've gotten it in the low 70's high 60's, so nothing compared to the other peole on here! I can hit 75 and feel fine, but other times it will give me trouble at 90/something... *sigh* Just another thing I don't understand about us dysautonomics...

    Sorry, I don't know why I said waaay lower. That was silly of me.

  3. Do you have trouble with getting your blood drawn?

    They can never find a vein on me. It can take them 3-9 sticks.

    It only gets worse after they finally get the blood:

    I was just there today, they only took four vials of blood, and I am so POTSie! I have not been this POTSie in a long time. :(

    I was wondering if this was a POTS or Dysautonomia thing. If anyone else has trouble with blood draws, I would love to hear about it.

  4. Hi Brye!

    Yes, I have finally stopped passing out as frequently as I used too. I am at the point now where I can shower and be out in public by myself :D!!!!

    It just struck me as odd that there are so many of us POTSies when there are so many different types of Dysautonomia. However, what you said about the POTS being a sort of sign that there is something going on with the autonomic system does make sense.

  5. Let me start off by saying that I have POTS. My three most debilating symptoms are: insomnia, fainting, and shortness of breath.

    I was just wondering why there seem to be so many POTSies in relation to other forms of Dysautonomia. Just in what I have read it seems like ALMOST everyone has POTS. Even those with other dx as well, have POTS. Am I just not looking hard enough, or are there a lot of POTSies?

  6. Welcome!

    I am so happy you found this place! There is so much to be learned from the post on here.

    I hope you and your doctors find the meds that work well for you soon!

    Or at least the right combination of things that give you some good days.

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