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Dysautonomia (Autonomic Dysfunction) Community
This patient support community is for discussions relating to Dysautonomia (Autonomic Dysfunction) including: Postural orthostatic tachycardia syndrome (POTS), neurocardiogenic syncope, mitral valve prolapse dysautonomia, pure autonomic failure, autonomic instability and others.
41 - 60 (of 1838) questions
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Avatar universal
Who needs my help to get rid of some of the problems that your being faced with?
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I recently went to the cardiologist and got the diagnosis of vasomotor instability. For the past several years I have had symptoms of POT...
1 answer |
Avatar universal
I have read that there can be an adjustment period, but not sure how long is normal. My lightheadedness and tremors have been worse, and...
7 answers |
Avatar universal
Hi All, I have had to call the paramedics a few times this month due to what my doctor calls autonomic crisis. I had a severe cold and ...
9 answers |
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Hi. I have recently been diagnosed with a 'mild' autonomic dysfunction & have over the last few weeks been experiencing some abnormal car...
2 answers |
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I'm seeing a lot of research being done that links AD and MTHFR methylation errors. Has anyone found that using the bio-available forms ...
886699 tn?1270783344
Does anyone know of a good Dr.that treats dysautonomia (POTS) in South Florida?? I have been to the Cleveland clinic neurology dept with...
37 answers | 3 comments |
Avatar universal
I was wondering if anyone has delt with POTS while pregnant. I am now 21 weeks, the symptoms have started a very long time ago, but I hav...
34 answers | 1 comment |
143746 tn?1301278422
So far my lab work is consistent with hyperparathyroidism. Nevertheless I have had many symptoms of dysautonomia, such as lightheadedness...
2 answers |
Avatar universal
I would appreciate any answers you can give me, When I was younger (2nd grade) I passed out at school, I was standing outside at a flag ...
3 answers | 2 comments |
Avatar universal
Hi everyone, I'm a teenage girl who has been experiencing POTS symptoms for almost 3 years, and was just diagnosed this past October. my...
2 answers |
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Has anyone gone to mayo clinic? What kinds of testing do they do for Dysautonomia there? It is going to be expensive coming from Canada...
2 answers |
Avatar universal
Hi, I just came back from Cleveland Clinic and I tested positive on the tilt table for POTS, but they also told me that it is sec...
36 answers |
Avatar universal
What causes so many auto immune disorders in one person and could it be a sign of blood cancer and how do you get someone to test you for...
5 answers |
Avatar universal
Hello I have ZERO ENERGY all the time! I take midodrine and my BP is usually 100/60. My doctor will not prescribe anything for my excessi...
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I have a few further questions for those who have been diagnosed with Dysautonomia... Has anyone ever received any actual "treatment" and...
1 answer |
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I think this may sound like a crazy question, but has anyone had an issue with hair loss? My hair has always been super thick and it see...
8 answers |
Avatar universal
hi everyone. I'm a teenager who has had POTS symptoms for over 2 years, but was just recently diagnosed this past October. I've fought an...
1 answer |
Avatar universal
Hello from Canada.... Any Canadians experience trying to get a diagnosis in Canadaa? I am 5 years into this battle And just finally getti...
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My daughter-in law has POTS. She and my son have been looking for a doctor in California, preferrably So. Cal. who specializes in POTS (P...
2 answers |
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