Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Celiac.com!
    eNewsletter
    Donate

Frequent Urination


tamika

Recommended Posts

tamika Rookie

Is it just me or does it seem like when you eat something you shouldn't....you have to urinate more frequently? Maybe it's just me but I was wondering if this happens to anyone else.

Link to comment
Share on other sites

Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



GFreeMO Proficient

Is it just me or does it seem like when you eat something you shouldn't....you have to urinate more frequently? Maybe it's just me but I was wondering if this happens to anyone else.

Yep happens to me every time I get glutened by CC. I also get bladder spasms with it. Drives me nuts.

Link to comment
Share on other sites
tamika Rookie

It is so aggravating....thanks for responding:-)

Link to comment
Share on other sites
RiceGuy Collaborator

One thing which may help, is to make sure you replenish your electrolytes. Coconut water (not the milk) is supposed to be very good for this, as it is an excellent source of potassium and other minerals. Or you can try a potassium supplement, or even a sports drink. Sodium is also an important electrolyte.

Link to comment
Share on other sites
captaincrab55 Enthusiast

One thing which may help, is to make sure you replenish your electrolytes. Coconut water (not the milk) is supposed to be very good for this, as it is an excellent source of potassium and other minerals. Or you can try a potassium supplement, or even a sports drink. Sodium is also an important electrolyte.

Most of those Sports Drinks set off my Gout...

Link to comment
Share on other sites
Robert16 Newbie

Yes happens to me also thought i was just crazy i glad to see this is part of beeing glutened

Link to comment
Share on other sites
Loey Rising Star

Is it just me or does it seem like when you eat something you shouldn't....you have to urinate more frequently? Maybe it's just me but I was wondering if this happens to anyone else.

I am constantly needing to urinate and even get up once or twice a night to go. Yet another pleasant side effect of this illness. Thanks to those who wrote suggestions above this. I LOVE coconut water but didn't realize it was good for us!

Loey

Link to comment
Share on other sites

Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



curiousgirl Contributor

I am constantly needing to urinate and even get up once or twice a night to go. Yet another pleasant side effect of this illness. Thanks to those who wrote suggestions above this. I LOVE coconut water but didn't realize it was good for us!

Loey

any possibility of diabtes??

Link to comment
Share on other sites
Loey Rising Star

any possibility of diabtes??

No, I had that checked. But thanks for asking. I might ask my new GP to recheck me. Can it show up if you've already tested negative for it? I just moved to a new town/state so I have only seen a GI so far. Have the name of the GP and will make an appointment.

Link to comment
Share on other sites
glutenfreesavvy Rookie

I have the same problem - although it varies in intensity...kinda weird. It's a pain, though, isn't it? One thing that helps me a lot is using homeopathic remedies. A good place to find out which one you might try is:

Open Original Shared Link

I have no personal/financial interest in the site, by the way...I'm just a happy homeopath. :-)

Faydra

Link to comment
Share on other sites
GuyC Newbie

Being of the male persuasion, I was having a bit of prostate trouble for the last 2 years. I would have to get up 3 or 4 times a night. The doc checked everything out and said I was healthy. Due to my celiac diagnosis on 10/27/10 and being gluten-free since, I've just noticed I no longer have any prostate issues! I never would have connected the two. I'm still not feeling well overall, but this is one positive sign on the road ahead!

Link to comment
Share on other sites
dilettantesteph Collaborator

I have that problem when glutened.

Link to comment
Share on other sites
kenlove Rising Star

It does take time and there are a number of other factors including sugar levels. I used to get up every hour on the hour and they told me it was normal. I didnt want more drugs. Cutting back on the carbs made all the difference.

good luck

Ken

Being of the male persuasion, I was having a bit of prostate trouble for the last 2 years. I would have to get up 3 or 4 times a night. The doc checked everything out and said I was healthy. Due to my celiac diagnosis on 10/27/10 and being gluten-free since, I've just noticed I no longer have any prostate issues! I never would have connected the two. I'm still not feeling well overall, but this is one positive sign on the road ahead!

Link to comment
Share on other sites
missy'smom Collaborator

No, I had that checked. But thanks for asking. I might ask my new GP to recheck me. Can it show up if you've already tested negative for it? I just moved to a new town/state so I have only seen a GI so far. Have the name of the GP and will make an appointment.

Diabetes test results are not a simple matter of positive or negative. Blood sugars and imbalances fall along a wide spectrum. Know your numbers-ask for them and know what they mean and where you fall on that spectrum. A one-time blood sugar number or a fasting blood sugar number is not an accurate indication. An A1C would be better.

Blood sugar problems can crop up at any time so can and should be re-evaluted at any given time if there seems to be a concern.

It is possible to have blood sugars that are elevated enough to cause frequent urination but not be oficially diabetes. As Ken mentioned, dietary changes can address that. It's still important to know your numbers.

Link to comment
Share on other sites
Looking for answers Contributor

When my Rhemy was screening me for Lupus he said that frequent urination is a symptom of Autoimmune Disorders. I don't have more insight to share other than that, but it also happens to me when I eat something I shouldn't have.

Link to comment
Share on other sites

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - plumbago replied to Suzi374's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Lots of tests

    2. - trents replied to Suzi374's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Lots of tests

    3. - Suzi374 replied to Suzi374's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Lots of tests

    4. - Suzi374 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Lots of tests

    5. - Peace lily posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Would like to gain weight


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,224
    • Most Online (within 30 mins)
      7,748

    Suzi374
    Newest Member
    Suzi374
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • plumbago
      I'm also a nurse, but one who has worked in chronic care, and to some extent, it is more satisfying to see patients through to a diagnosis (as opposed to working in the ED), but an accurate diagnosis does not occur not as often as it should! Your posting presents a lot of information. But a couple of things I can respond to. One, celiac disease is diagnosed by endoscopy and biopsy of the duodenum. So, pathology will need to weigh in. It's not diagnosed on gastroscopy. (At least, not as far as I know). Two, did you get blood tests for celiac disease? You will need to be eating gluten in order for those to be accurate. Three, where was the CT angiogram (of what)? I could go on and on, but thought I'd start there.
    • trents
      Was a biopsy done when you had your gastroscopy? Concerning your anemia, are you B12 deficient? It's nearly impossible to get sufficient B12 if you are a vegetarian unless you take supplements.
    • Suzi374
      And I’m anaemic, however I’m also female and vegetarian. I had an iron trans a couple of years ago however it’s starting to dwindle and taking supplements doesn’t seem to work. I can’t seem to absorb it. 
    • Suzi374
      Hi, I attended a neurologist appt last Tuesday, which I nearly cancelled, due to ongoing numbness and tingling in toes to mid foot. One of the first things he asked was ‘are you celiac’. I’m not. He thought all reflexes were ok but at the last minute decided on nerve conduction tests which were low normal. He was a little confused as he felt they should be better and tried a new set of probs, all the time, giving me multiple shocks which were not enjoyable lol. Anyway, he’s now ordered tests for myeloma, and all the vitaminy things that so many of you mention on here, also tests looking for autoimmune responses. I already have Hashimotos. Interestingly, to me, but maybe someone out there can relate or knows more than i do, although I was a nurse, but ED not ‘weird symptoms’  nurse. Anyway back to the interesting thing, I took duramine in 2013 to lose weight which caused a massive panic attack when I stopped taking it and half my hair fell out. I only took it for a week but it was horrible and I regret it. It triggered ongoing panic attacks which are horrendous. So I feel like I’m a bit crazy. Then in 2020 I had this sudden onset of horrible pain when trying to eat a cinnamon roll. It continued and I lost around 20 kgs. I had two gastroscopes and a colonoscopy and they were all normal. I scored a barium swallow and CT angiogram. All normal. The pain subsided a little but I was left with reflux and an awful feeling that I couldn’t get air when I ate some foods. This was not anxiety.  The anxiety was separate and I still maintain this. This was something to do with eating. It was like the air was thick but I wasn’t short of breath. I just had the sensation I was, then it triggered anxiety. Anyway, I had other weird things- couldn’t bend knees to shave legs in shower lol. Knees felt stiff and swollen but they weren’t. Knee WOUld swell up randomly but mri showed minimal issues. A bit of a meniscus degeneration but insignificant. Then the buzzing sensations in my head, the feeling like someone was stabbing me with something sharp. So now, I pre empted his tests, although I don’t think I’m celiac because it should have come up on gastroscopy, I’ve gone off gluten. Since Tuesday last week so 9 days. Since then I don’t appear to be as constipated, I realised I got through today without a nap and I’m not tired, maybe it’s just today and not related but I get very tired normally and sleep straight after work often, I can bend my knees and shave my legs lol, the buzzing vibrating has gone from my head, I had to call and ambulance as my heart decided we were off on a run, but we weren’t running and I’ve been a bit twitchy at bed time when trying to sleep, reflux is improving, I did get the weird suffocating feeling a bit when eating today but not as bad normall. Tingling and numbness still present and I felt like it moved up my legs a bit today but I’m a bit jittery. So I don’t know if it’s celiac disease or a gluten intolerance but I think, and it may be wishful thinking because my symptoms do make life a bit challenging, but maybe I’m feeling better. I don’t feel as cloudy. My thinking feels crisper. Like there’s no buzzing and I’m not fighting to break through the cloudiness now. I hope so much that this may help me feel a bit better moving forward. It would be a miracle as I really have struggled to work and parent and keep the house clean and I’m always anxious and exhausted.  If you get this far, please tell me if you you can relate to any of the above. Oh and tonsils out 5 years ago but before that antibiotics multiple times a year, sometimes intramuscular because they were so bad.  Op was meant to take 30 mins, it took 1.5 hours due to size of them. 
    • Peace lily
      Im still not gaining weight I’m on a gluten free diet . And still having issues with constapation started priobiocs figured it would help been over two weeks . I guess it’s going to be a long road for me .
×
×
  • Create New...