Mrs. Burschman
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Posts posted by Mrs. Burschman
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I don't tell anyone unless I have reason to. That's not very often. I'm lucky in that my case isn't really severe enough that it causes me many problems (unless I get dehydrated or have to stand too long.)
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Oh man, poop fruits...that had me cracking up. Never thought of that before!
Not the most appetizing description ...
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Not exercise, but I could see how it could happen. I've gotten them from overstimulation and even being angry.
Amy
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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.
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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
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I'd rather have a Yuengling! That's good beer!
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I think this is actually a pretty common occurence. I've never had it happen, but I've heard of it happening to a lot of people.
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Ouch! I've only had individual muscles -- usually a calf, foot arch or under my chin if I yawn too big.
It sounds awful!
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Maybe you're low on potassium? (Sorry -- banana joke.)
I got this really bad when I tried to stop my Paxil. Hands and feet both tinging. It's an icky feeling.
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I'll come to your pity party! I'll bring pretzels. And punch.
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Welcome! Glad you found us, sorry you had the need. Yada, yada.
Sounds like you fit in with us!
Amy
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I can't give you any of that, but I can give you an ehug!
((((firewatcher))))
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Great! I've sold two houses, and I know how stressful it can be. I'm so happy for you!
Amy
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I CAN'T STAND riding in the car. The lurching and turning, especially in stop-and-go driving, make me feel awful. I'm fine if I'm driving. I think then, I know what's coming, so my body isn't surprised by every little movement.
Amy
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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.
Amy
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I work full time, but it's a total desk job (copywriting and blogging.) I do walk to and from work, however. I'm usually OK upright if I'm moving.
Amy
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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
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I suspect that it was the heat and the distress of the appointment combined that triggered the fainting (can you dehydrate from crying??).
YES. At least I have before.
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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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Hi Lynn! Nice to "meet" you!
I'm glad you found our site (but sorry that it sounds like you fit in.)
Welcome to the family!
Amy
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Very interesting. It would be great if he turned out to be right.
Amy
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I've felt "too drooly" at times. Annoying! Glad to know I'm not the only one!
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I do find if I drink a large amount of very cold water it will help - seems to chill me at the core. But overall I still feel very sick in the summer - I dread summers!
I love to slurp on ice cubes -- for the same reason.
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I'm always worse at PMS time, too. Digestive and bladder discomfort seem particularly worse.
Why, I do not know. I'd guess hormones, but it would just be a guess.
Amy
Uti Treatment, Antibiotic What Has Been Your Experiences
in Chit-Chat Forum
Posted
I WON'T take Cipro, and docs won't prescribe it for me, because I got a clostridium difficile colitis infection that took a year to get rid of the last time (and only time) I ever took it.
I've found that Macrobid works just fine for me.