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chefgirlrd

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  1. I just found this journal article about a study done using a website that helps with balance retraining and reducing dizziness. The patients in the trial did not have POTS, but it might be worth trying to see if it helps anyway. The website with the exercise program appears to be free. Here is the link to the article that includes a link to the website: http://www.annfammed.org/content/15/3/209
  2. I just recently started getting IV Lacted Ringer's infusions and I cannot tell any difference in the way I feel. I am only getting 500 ml and am going to talk to my doctor about increasing to 1L to see if that makes any difference. Beta blockers made me feel worse, too. I think I have learned that what in theory should help does not always help in real life.
  3. I forgot to mention that I first tried the pill form of the licorice root and I did not see any benefits but then I tried the liquid extract form and it did help me.
  4. I take both Florinef and licorice root and have not had any problems with high blood pressure. However, everybody is different so that is something to keep in mind and monitor.
  5. Well, it hasn't gone away, but I am able to reduce it. Treating my POTS has helped. Also, taking Licorice Root extract and Ashwagandha (for adrenal support), Glutathione (for detox), and Eleuthero Extract (siberian ginseng) helps improve my energy. I can really tell if forget to take those.
  6. Hello everyone! I have been lurking for a few months, but this is my first time posting. This forum has already been very helpful. I was diagnosed with POTS about a year ago and have since had to find a new Primary doctor. I have an appointment with one soon who came recommended by a family member. However, I am not sure if she is familiar with POTS and I am wondering if anyone has any suggestions for seeing a new doctor? From what I have heard, she is very nice and is willing to learn. Is there any information I can bring with me about POTS? Journal articles? I need a Primary with visiting privileges to my local hospital and who is already familiar with my medical issues in case I ever need to be admitted there. Otherwise, I will just end up with the doctor on call that day and there is no guarantee they will know anything about POTS. Any help would be greatly appreciated.
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