Jacquie802 Posted May 31, 2012 Report Share Posted May 31, 2012 Has anyone noticed or had a severe urgency to urinate after tachycardia episodes? I've been experiencing this and the ER doctors looked at me like I was crazy... Quote Link to comment Share on other sites More sharing options...
ophelialit Posted May 31, 2012 Report Share Posted May 31, 2012 I think they must teach that particular look in med school ("Frown slightly at the patient while tilting your head slightly to the left. Now raise your right eyebrow. Good! Now you look like you doubt everything they say!") Anywho, yes, I have this exact same symptom quite frequently, and it seems to pop up whenever I have an adrenaline surge for ANY reason (near-miss traffic accident, a shirtless-Brad-Pitt-movie-scene, presenting to a large group of people, etc.). I think it's actually pretty common, but docs always want to test for diabetes and the other go-to diagnoses. Just another joyful symptom of our wacky condition! Quote Link to comment Share on other sites More sharing options...
Katybug Posted June 1, 2012 Report Share Posted June 1, 2012 Yes, it's a POTS thing. Your autonomic system helps to regulate, or in our case dys-regulate, urination. I definitely could graph my POTSy symptoms and the frequency of my urination and make a perfect correlation. Quote Link to comment Share on other sites More sharing options...
sue1234 Posted June 1, 2012 Report Share Posted June 1, 2012 I have to say that I have been a frequent urinator(?is that a word --- do I get frequent urinator miles?) for a few years. In April I had to do the mixed meal test, where I definitely took in more sugar at that one meal than I would normally eat in 5 days. I noticed I had to keep getting up to go urinate, way more than I do at home. I guess the higher glucose levels caused it, even though it was not up in the diabetic level, but high for my normal anyway. Now that I've given up all outright sugar, I urinate less often. Quote Link to comment Share on other sites More sharing options...
jpjd59 Posted June 1, 2012 Report Share Posted June 1, 2012 Yes, it is one of the many annoying POTS symptoms. Quote Link to comment Share on other sites More sharing options...
picaresque Posted June 1, 2012 Report Share Posted June 1, 2012 Yes, I'm with you there. And Midodrine has just made it worse for me. Quote Link to comment Share on other sites More sharing options...
puppylove Posted June 1, 2012 Report Share Posted June 1, 2012 Yes, so annoying. And drinking soooooo much definitely doesn't help. Quote Link to comment Share on other sites More sharing options...
McBlonde Posted June 3, 2012 Report Share Posted June 3, 2012 Yep.... the more I drink, the more I urinate. Also, every time I have an "episode" it includes increased urination. Just can't hold it even with Florinef. Quote Link to comment Share on other sites More sharing options...
Lemons2lemonade Posted June 3, 2012 Report Share Posted June 3, 2012 yes, i think of it as my body's way of disposing of the adrenaline byproducts from the episode...however, urinating all the time doesn't help the tachy much Whenever this happens, i take it easy on my feet and have more salt and water. Like mcblonde, i use florinef as well, and it still happens--just not as bad. Quote Link to comment Share on other sites More sharing options...
ramakentesh Posted June 5, 2012 Report Share Posted June 5, 2012 Sure. Occurs in many POTS patients. And is the topic of investigation. Quote Link to comment Share on other sites More sharing options...
jenglynn Posted June 6, 2012 Report Share Posted June 6, 2012 So odd.... I have so many symptoms where I may fit right in- Orthostatic Intolerance, tachycardia (50+ sitting and 80+ Hr standing but I haven't stood in forever), daily syncope, headaches, visual disturbances (double vision, floaters), no appetite, dizziness, shortness of breath, many more that may not relate so won't mention - but my bladder problem is now and has always been extreme retention. I drink as much as I'm supposed to, eat all that salt, but I'm lucky to go once every 2-3 days. I almost have that urge but it is there - forever, sometimes in the middle of the night if I'm tired, I may doze and wake a few times and then get back to bed after an hour or two. Received a TERRIbLE concussion that way but my family did not know who I was for 2 weeks I was so angry and aggressive and I don't think I've been the same since (early Feb). Finally agreed to what I swore I'd never agree to and that's a bedside commode I take Midodrine too- 15 mg 3x a day which seems typical. There just seem to b a few key areas where I just don't fit in...JenSo odd.... I have so many symptoms where I may fit right in- Orthostatic Intolerance, tachycardia (50+ sitting and 80+ Hr standing but I haven't stood in forever), daily syncope, headaches, visual disturbances (double vision, floaters), no appetite, dizziness, shortness of breath, many more that may not relate so won't mention - but my bladder problem is now and has always been extreme retention. I drink as much as I'm supposed to, eat all that salt, but I'm lucky to go once every 2-3 days. I almost have that urge butisut there - forever, sometimes in the middle of the night if I'm tired, I may doze and wake a few times and then get back to bed after an hour or two. Received a TERRIbLE concussion that way but my family did not know who I was for 2 weeks I was so angry and aggressive and I don't think I've been the same since (early Feb). Finally agreed to what I swore I'd never agree to and that's a bedside commode I take Midodrine too- 15 mg 3x a day which seems typical. There just seem to b a few key areas where I just don't fit in...Jen Quote Link to comment Share on other sites More sharing options...
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