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About the4richards

  • Birthday 03/09/1962

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    ann arbor, mi

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  1. I've been away for awhile. Feeling pretty good. Just popped in and saw this topic. This was one of my first symptoms and one of the worst. Docs couldn't explain it and said it was just part of my autonomic system that was going haywire. I would gasp for air during the day and wake up gasping at night. Also had the rubber band lightly twinging feeling. I realized I was shallow breathing a lot. So I started doing deep breathing / holding / forcing both in and out with closed, pursed lips. If you try it, it should make noise. There's a post somewhere on the technique. I can't say this was what made the gasping go away, but I strongly feel it helped.
  2. I had no problems with swings. Loved roller coasters. But sick with driving and flying. I once went to a gym that had an elevator. Once we were up (one floor) I grabbed at the wall and asked how they could stand working out there when the floor swayed. Ha...the floor was fine. I haven't been on an elevator since that I don't experience phantom floor movement.
  3. CarrieJessica, Mine weren't like yours, but I had them after my TTT and during my worst flares. Docs said it was normal for dysautonomia. They put ice on the back of my neck...said it calmed the nervous system somehow. It worked, but the whole thing was scarey.
  4. I also had very frequent low grade fevers with no apparent infections. Docs kept wanting to give me antibiotics even though they couldn't find anything but fevers persisted. All stopped when I got POTS a little more under control. More frequent, smaller meals and cut out sugar and "white food".
  5. I am totally off all meds. I still have POTS symptoms. Lately I've been about 70 bpm supine and 125 upright. I can normally deal with it but the heat has been doing a number on me. We've been putting in fence posts the last month and yesterday I couldn't even rake in grass seed without panting and sweating like crazy. My bp and hr went too low on the meds and I prefer being off them and sitting when I have to.
  6. Somehow I missed this topic. This was one of the first symptoms I had prior to POTS diagnosis. I told my doc that I would periodically realize that I needed to take a breath, like my body had forgotten to do it automatically. They kept trying to tie it to sleep apnea but it was during the DAY. I did not have sleep apnea, but I would also wake up needing to breath...similar I guess, but I did not have obstructed breathing...just stopped. Very scarey. Finally with POTS diagnosis, one doc said it probably was POTS related as breathing is part of the automatic nervous system and just about everything it does was wacky in me at the time. This finally went away about the same time as my increased blood pressure symptom (a couple of months from diagnosis, about 4 months in total) For me, lots of good things happened when I started eating more frequent/smaller meals, and cut out sugar and flour(moderately low carb diet).
  7. I had migraines prior and during my first flare. Beta blockers helped everything for me. I finally was able to get off the beta blockers and now I get an occassional migraine, though not as bad as they used to be.
  8. OK...I'm probably not supposed to do this... I'm on a lot of "daily sales" sites and this one popped up today. It seems like a good deal and it's a good thing for us to have... http://1saleaday.com/ It's a wrist heart rate monitor for cheap cheap cheap. It has to be purchased TODAY 4/20 by midnight. Sorry if I violated any rules...feel free to delete...
  9. I noticed about a year before my first flare that any exposed areas to the cold and I get hives. Even in 50+ temps if there is a wind. I've even gotten them when I prepare cut up chicken for dinner, my fingers will be little itchy sausages for a while. I can't even have ice in my drinks. Lovely when you live in Michigan!
  10. Mine was sudden onset with mostly good days. Rama said " Strangely I now realise I had mild Livedo reticulitis on my palms since i was a kid." I didn't know what this was so I googled it. I've had this on my legs since I was a kid and didn't think anything of it, I just avoided shorts a lot! I also had migraines prior to and during my first big attack.
  11. Thanks for all the tips everyone. Kimbellgirl - I guess I was dehydrated...all the excitement and I forgot to drink all my fluids. That definitely helped the tachycardia. The headache is hanging around. Dizzy- I tried a round of rotating tylenol and ibuprofin and the headache laughed at me. So I'm sending the kids off to bed early and trying the "hang your head off the bed" followed by a glass of wine and lights out. On a good note, my son is doing great and doesn't even need pain meds even though he has 3 pins set in his arm!
  12. My son fell and broke his arm Saturday afternoon which worked it's way into emergency surgery at 4am(yeah, that's Easter morning). I stayed awake the ENTIRE night and through the next day. So I was awake from 8am Sat morning till Sunday evening at 9pm. NO SLEEP at all. I tried several times to sleep but I was so worried I just couldn't shut off my brain. I did sleep really well last night for 10 hours, but I have a terrible headache(since yesterday afternoon) that ibuprofin doesn't help and my heart rate is much higher than normal. I can live with the racing heart (as we're all kinda used to that), but this headache is a killer. Any advice? I've tried ibupofin, mild meditation, caffine...I'm hoping if I fix the headache maybe the heart will get back to my normal.
  13. This book excerpt tells a about the anaerobic threshold concept and what happens during the different "phases". http://books.google.com/books?id=BC9SiAsUPqsC&pg=PA258&lpg=PA258&dq=exercise+test+%22metabolic+phase%22&source=bl&ots=8VZKX_iqZp&sig=4wljz4aTtH5FQhUBPWykjXURZIo&hl=en&sa=X&ei=j851T-vkPOOU2wXo8sixDQ&ved=0CHYQ6AEwCQ#v=onepage&q=exercise%20test%20%22metabolic%20phase%22&f=false Textbook of work physiology: physiological bases of exercise, By Per-Olof ├ůstrand
  14. I had posted about this also. ======= Posted 15 July 2010 - 09:22 AM I've been experiencing some dramatic hair loss lately. I've noticed it for a couple of weeks now. I did some research and have found that this can occur for some of the following reasons: a) 3-4 months following a major illness (my POTS came on suddenly and severely, putting me in the hospital 3 times in March of this year) b.) beta blockers have been responsible (I'm on a low dose atenolol. I started out on 150 a day and am down to 25) c) over doing some vitamins (like A). I haven't been taking any new vitamins. So...I have pretty thick hair and am still fine, but have definitely lost about 1/4-1/3 so far. A couple of people have actually commented (without prompting from me). (a) above usually stops without complete loss. (b.) stops when you stop the drug. =========== I don't know if my loss was from drugs or being sick but I was lucky and was able to stop Atenolol. It has completely grown back. Good luck...
  15. After a lot of research, I insisted on an endo and the glucose tollerance test. I am pre-diabetic. This article http://care.diabetesjournals.org/content/26/5/1553.full#sec-54 explains a lot. Some people cannot handle even pre-diabetic levels of glucose. They get POTS symptoms. I have been lower carbing for 2 years now. It has GREATLY improved my POTS. I still get flares but they're many months inbetween and not very bad, and they only last a day or two. I still have HR swings, but they do not bother me. I also had the OGTT (3 hour sugar test) a couple of times when I was pre-teen. I was normal, but I was having POTS symtoms even then. I keep my carbs to 50-120 ish a day. I do NOT go over 40 per meal. I have cut out all sugar, potatoes, rice and flour. This is a great site if you're interested in lowering carbs and the damage that can occur with higher readings. http://bloodsugar101.com/ I'm not saying this is everyone's problem, and I don't know if it is my problem, but if not, it sure is exacerbating my POTS symptoms.
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