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Rose11

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Posts posted by Rose11

  1. Of course, everyone reacts differently to any kind of medication, but I have heard many people can have trouble with Topomax with cognitive impairment. Since you mentioned you are going on an interview, you may want to try it over a weekend OR  after the upcoming interview.    Can you see another doctor about your health issues to see what they say?  Good Luck on your upcoming interview and overall in general...

     

     

  2. Call whichever doctor prescribed your beta blocker in the past and see if they could call it in for you tomorrow. 

    I would leave a message for your PCP and just tell them it is personal and ask that doctor for the beta blocker if you feel that is the best doctor to prescribe it for you.

    How frustrating that you have been going for 20 years to this office to be treated this way.  You definitely should share with your PCP about your experience. 

    Good Luck

  3. I thought I saw some examples of exercises on Dysautonomia international website under patient tab then under exercise.  They were YouTube videos.   I wonder if you do a search directly on YouTube for Dysautonomia or POTs yoga, you might find something.   It's good to start very slowly with any exercise, including yoga?

  4. I read on someone's post that they use cell salt for POTs. I can't seem to find that post again to see who it is to ask about it. What is cell salt? Which brand is best? What does it do? I would appreciate any input on this subject. Thank you.

  5. I bet it was frustrating and upsetting. It was good that you did go for a little while. There may be other gatherings where they just play video games or hang out and talk that you can participate in.

    Unfortunately, many people don't understand and it is hard, but people on this site, do understand the limitations and frustrations.

    My saying is tomorrow is a new day and there's a chance it can be better.

  6. Sorry you are having so many problems right now. Never feel guilty when needing extra rest, just do it. That will give you the energy to do other things you enjoy. I'm sure your parents are frustrated, since they probably did not get training on Dysautonomia when they were in medical school. Perhaps they would be willing to take a little time to find research on the subject through medical journals. Many parents who are not physicians do research to better understand what their children are going through. They don't need to have all the answers. Maybe they can help you come up with questions for your upcoming doctor appointments. Good Luck and keep sharing on here. Hope you have a wonderful weekend!

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