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Mrs. Burschman

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Posts posted by Mrs. Burschman

  1. Maisie I hate the flavor of bananas and always have! As well as their mushiness.

    haha, Mrs. Burschman. Actually, I really shouldn't be low on potassium bc I choke a banana down everyday plus two glasses of milk

    I don't like them, either. I only eat them if they're green, because then they have less flavor. Ugh.

  2. Also, sometimes antidepressants HELP POTS SYMPTOMS. A lot of us take them, even if we haven't had problems with stress/anxiety, because they calm down the sympathetic nervous system, which tends to be out of whack in a lot of us. I get PHYSICALLY sick as a dog when I don't take my Paxil.

    You're right about not getting off of them, however. I don't see that happening for me anytime soon, unless I find some miracle cure elsewhere.

    Amy

  3. I think I'm the opposite. I had an ovarian cyst rupture, and I thought I was going to die. I think the emergency room literally thought I might die. It took four times to find a pulse, and my hands and feet were starting to go numb. I was fully conscious, though. I don't think they quite knew what to make of me. :lol:

    Amy

  4. I have a full-time job as an RN in a children's hospital. I just finished nursing school in May, and have been working up until the end of September, when POTS kicked me hard and I couldn't get out of bed. I've been on medical leave since then, but have to go back to work in mid-December or I will lose my job. I don't know how people do it! I'm not sure what's going to happen to me. My health is so unpredictable day-to-day... and you can't do 12.5 hour shifts like that, so I'm trying to figure out if there's something I can do as an RN where there is more flexibility and I don't have to spend so many hours on my feet in stressful conditions...

    I seriously don't know what to do, and I'm self-supporting...

    If ANYONE has any suggestions for me, I would LOVE YOU FOREVER!!!!!

    Stacy

    A lot of hospitals offer "Ask a Nurse" hotlines that are staffed by nurses. Would that be an option? Or doctor offices. At least the hours would likely be shorter. It sounds miserable!

    Amy

  5. The doctor also went through my meds list and told me to stop taking :paroxetine, antihistamines, H2 blockers, montelukast, asthma inhalers, epi-pen, paracetamol and codeine as they would make my POTS worse. The SSRI was actually prescribed for POTS, and without the allergy stuff my POTS is so bad I can hardly get out of bed. I can probably learn to live without the painkillers but I get so many blackout-EDS related injuries that I do take intermittent painkillers.

    That doctor sounds like a moron. Seriously.

    Amy

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