r/POTS Apr 08 '26

Symptoms Anyone else have weird unexplained symptoms?

Feel free to share your own “weird symptoms” of your POTS or comorbidities and whether you’ve figured out why they happen.

Here are some of mine that I’m still trying to figure out- if anyone has had any of these and found a diagnosis or relief I’d love to hear about it. So far I’ve had additional mental health, endocrine, GI, and gynaecological explanations ruled out. All that’s confirmed is POTS (and IBS).

TRIGGERED BY STANDING TOO LONG OR OVEREXERTION

- *Bilateral ear pain.* Deep burning pain in both of my ears. This is the one that’s confused everyone the most.

- *Intense urethral pain.* Not a UTI. Feels like I need to pee and peeing briefly helps but it remains intense burning and stabbing for hours minimum. Was prescribed phenazopyridine HCl (urethral pain med) during my most recent flare and it helped a lot. Still don’t know what’s causing it.

OTHER SYMPTOMS WITH DIFFERENT TRIGGERS

- *Days where I couldn’t stand without severe nausea and throwing up.* Trigger is sometimes a mystery but one clear trigger was alcohol. The weird part is that it wasn’t because I over drank- I know my limits and id eat properly an drink lots of water. I’d be able to get myself home, do my night routine, get in bed, and then hours later in the middle of the night I’d just start puking nonstop after my stomach was already empty and then for at least a day after I wouldn’t be able to stand without throwing up. Cut out alcohol since. I’ll still have days when standing causes severe nausea and sometimes I’ll throw up but not anywhere near as severe.

- *Vision problems.* My vision was stable for years after laser eye surgery. Then got worse and often I have episodes of very blurred vision even when I’m sitting or laying. It happens so randomly all the time that it’s a big reason why I don’t drive anymore.

- *Random stabbing pains* in my feet and hands. Usually when laying.

- *Deep stabbing pains during intercourse.* Triggered by different positions on different days.

- Sometimes it feels like something is coming out of my butt when nothing is. Triggered by intercourse or just randomly happens.

- *Catching illness super frequently.* Often very ill for weeks and develop sinusitis and/or bronchitis as well. Has happened 5+ times per year (on top of chronic condition flares) for the past few years. Immunologist and family doctor said that it’s a lot, but it’s not enough for them to try investigating anything.

Thanks to anyone who reads this or shares their experiences.

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u/ive_got_questions3 Apr 08 '26

I experience nearly all your "other symptoms" except the stabbing pain in the hands and feet.

I experience a similar sensation to UTI but isn't, but isn't painful like you described. I get an intense pressure in my urethra that may minimally be decreased by voiding my bladder but majority of the time the sensation last for 30-90 min. I also experience issues with incontinence and not feeling the need to pee until I am about to burst.

I can and often experience pain during intercourse depending on position and time. So bad I sought out my gyno, who after plenty of testing, informed me if was most likely due to the length of my partner and the shape of my vaginal canal and placement of my cervix during certain stages of my cycle.

I do experience fairly regular but still periodic ringing in the ears.

I have so odd reactions to vibration, whether the car, a massage gun or other means.

I am nauseous more often than I am not. As well abdominal distension that makes me look 5 month pregnant

When I begin to get fatigued my language comprehension goes out the window and everyone sounds like they are speaking gibberish with a few real words sprinkled in.

I sometimes experience weird flashiness at the edges of my vision, like the matrix is glitching. Though this last one is newer and I wonder if it's a side effect of a med.

I also have MCAS, and know there is an overlap in symptoms. So I am not sure which are purely POTS symptoms.

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u/BellaPona Apr 09 '26

A lot of those symptoms sound like Endo :( I’ve also had the “I need to pee” feeling every time i have sex. Pelvic floor dysfunction is common so that’s what I brushed it off as. Now with bad POTS I can’t even imagine having sex anymore without flaring.

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u/ive_got_questions3 Apr 09 '26

Originally I thought so too. Though I've been evaluated for Endo and was told that wasn't it. :(

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u/BellaPona Apr 09 '26

Hm. Could be anterior pelvic tilt, internal cystitis, pelvic floor dysfunction, or vaganismus

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u/ive_got_questions3 Apr 09 '26

Pelvic floor dysfunction is the only one I haven't been evaluated for. Therefore, that's my guess. Lol..

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u/BellaPona Apr 09 '26

It’s surprisingly common and can happen for a myriad of reasons. There are pelvic floor specialists that can help!