Jump to content

forevertired

Members
  • Content Count

    55
  • Joined

  • Last visited

Community Reputation

0 Neutral

About forevertired

  • Rank
    Advanced Member

Profile Information

  • Gender
    Female

Recent Profile Visitors

1,015 profile views
  1. There are motility tests (for example: manometry http://www.biomed.ca...f/51/51_541.pdf) which are used to test whether your bowels have motility issues. My POTS doctor says there are a number of gastrointestinal disorders that can be caused by autonomic nervous system problems. If you think your bowels work too slow or too fast, you can perhaps ask your doctor if he/she would schedule you to have bowel motility testing done. I have not had these as the gastroenterologist said I did not need them as it was obvious my bowels move way too slow. I would still like to have at least the small bowel
  2. Has anyone been diagnosed with this? Have you tried Mestinon for it? I was recently diagnosed with this and was prescribed Mestinon. I would like to hear how other people have dealt with this, what they have experienced, what treatments they have tried, and what helps with the pain.
  3. Your best bet is to be referred to a geneticist. The geneticist would test you for it. If you think you have type 3 some rheumatologists and pain doctors can do the testing for that type, but for the other types I believe the only people that can truly diagnose you with those forms are geneticists.
  4. Glad to hear she has been seen by neurologists. Sorry to hear she is going through so much. I also experience the shivering gone crazy, I find the best way to stop that is to get warmed up, such as being wrapped in many blankets. When I get just the slightest bit cold, even if I shouldn't be, my full body starts shaking like crazy (shivering), and my teeth chatter, and my breath is affected too. Its almost like I am hypothermic (i.e. sympathetic nervous system excitation). I somewhat blame this on my dysautonomia because its like my body can't properly regulate temperature. I figured the shive
  5. Has your daughter seen a neurologist? It might be worthwhile, especially if the spasms are getting worse, if she hasn't, to take her to one (with a videotape of the spasms if they don't occur all the time), just to rule out any neurological causes of the spasms. Did the spasms start before or after she developed POTS? Have you discovered the cause of your daughter's POTS? Does she fall when she has these spasms? Do they cause her pain? Does her head hurt when she has these spasms? Does she experience any cognitive issues, like memory loss when they happen? Do you have a family history of movem
  6. I do admit I am somewhat de-conditioned, especially when it comes to running, weight lifting, and other cardio exercises. I know that if my POTS just magically went away tomorrow, that I would not be able to go back to the amount of exercising I used to do. I do believe that everyone after a period of time (especially if it is years) of not doing something say lifting 50 lbs of weight or running 20 miles will become de-conditioned and will have to work back up to lifting that amount of weight and running that amount of miles, without hurting themselves. My only point is that I don't think my i
  7. I have problems with stairs too. For most of my life I have gone up stairs almost everyday, as I have always lived in a 2 story home, my job is on the 2nd floor, and in school my classes were on different floors. When I developed POTS, I suddenly had a problem where I would be out of breath going up stairs, I would feel palpitations, and I would become quite fatigued, which didn't make sense to me, as I have gone up stairs almost every day of my life for many years. I knew it was not deconditioning, as how could it be deconditioning if I had been doing it almost every day before, and still do
  8. The "losing time" does not seem to be a symptom tied to POTS, at least not from my research on POTS. It sounds like he is having seizures. It could be possible he does have POTS too, although I wouldn't blame his "losing time" on POTS. Is your sister going to have your son do a tilt table test? It has been known for some people who have epilepsy to have a normal EEG simply because they had the EEG when they weren't having a seizure. How did the doctors induce the seizures in your sister? I have episodes of "losing time". It usually only 30 seconds to a minute or so, but it is long enough that
  9. Tachyfor 50years: I am afraid I don't. I also don't know which medical conditions where that would be required. I know that CA is one, as I remember a case where a person was fired because of their health, and it came out that the person was legally required to notify the company of his health condition before being hired. I believe it was related to safety issues. I also know that when I lived in CA, I was told when I took certain meds, that I was supposed to tell my employer, if I had a job that required me to operate heavy machinery, that I was taking those meds. Also, in CA, if you have ep
  10. I ended up telling my boss, even though I was fairly new to the job, because when I first got really sick, it interfered with some of the duties of my job and I was going to several different doctors every week. I still go to the doctor's quite often for someone my age, and unfortunately most of my doctor's only have appointments from 8-5 which requires me taking time off work. I do agree with the others, it all depends on your boss. I had to tell my boss, because my health wouldn't allow me to do some of my duties. I was afraid I would get fired (I live in an at-will state), but there was no
  11. Have you seen a neurologist? If you are concerned about possibly having seizures, it might be beneficial to see a neurologist, to know for sure whether you are or not. The neurologist would possibly also be able to prescribe a medication that could help with your muscle twitches, if those bother you. I am not a doctor, but I have been told that some people with epilepsy have normal EEGs. This is sometimes because they have the EEG when they are not having seizure-like episodes. I see a movement disorder doctor (a type of neurologist) for my muscle twitches, jerks, and tremors. My POTS is tied
  12. My doctor's believe the cause of my POTS is my Parkinson's-like disorder. Carvidopa-Levodopa has helped a lot of my neurological symptoms (like Myoclonus) and helped to lessen some of my POTS symptoms.
  13. If I may ask, ChristyD, POTSGirl, ramakentesh, rachel, and allaboutpeace: How did you get your doctor to prescribe Saline IV as a treatment? What made them suggest it as a treatment (for example they thought it would help with low blood pressure)? Does your insurance cover it?
  14. When I did the poor man's tilt table test it did not show I had postural orthostatic tachycardia. It wasn't until I did the regular tilt table test, that it showed I had postural orthostatic tachycardia. In other words I think it is very possible she has POTS, even though it doesn't seem like it from the poor man's tilt table. It is also possible she has a different form of dysautonomia. Either way it sounds like it would be worthwhile to have her do autonomic testing.
  15. I was diagnosed with CFS 7 years ago. I have never been treated for it. The only comment I got from my doctor, was that he was surprised I graduated from College. I graduated 3 years after being diagnosed with CFS and Fibromyalgia. My symptoms are chronic fatigue, low grade fever, chronic sore throat, muscle weakness, hair loss, eye pain, tinnitus, alcohol intolerance, difficulty swallowing, parasthesias, propioception difficulties, emotional lability, brain fog/ memory problems, chronic muscoskeletal pain, sleep problems, gastrointestinal issues, sensitivities to medications, temperature dys
×
×
  • Create New...