Jump to content

  • 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 Our Content
    eNewsletter
    Donate

Uncomfortable (literally) Question

Sweetfudge

By Sweetfudge
in Coping with Celiac Disease

Recommended Posts

Sweetfudge Community Regular
Sweetfudge
Posted

Ok, I've got this problem, and I'm starting to think it might be gluten-related.

I've been living gluten-free for almost 2 months and last week accidentally ingested some. Had my stomach, gas, bloating symptoms, but I've also had another symptom which makes me think this correlates.

I have this horrible irritation around the outside of my colon (sorry, trying not to be gross about this). It's insanely itchy, and when I go to the bathroom it feels like I'm trying to push a cactus out (OW!).

I told my husband and he thinks it's hemmroids. But after reading about hemmroids, I don't think it's that. There's no bumps or blisters that i can feel.

Dr gave me suppositories which are basically hydrocortizone. I tried those a couple of times but it just made my underwear feel sweaty/damp. I'd rather just use the cream if that's the solution.

I thought it just came and went randomly, but maybe it has to do with gluten irritation. Because I can't remember having the irritation since I went gluten-free, until this week.

Wanted to know if anyone else suffers like this....

Thanks :)

Sorry to gross everyone out :P

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

Celiac.com Sponsor (A8-M):


Rikki Tikki Explorer
Rikki Tikki
Posted

Your husband is probably right. They can be inside the colon.

Canadian Karen Community Regular
Canadian Karen
Posted

Don't worry - we talk about this stuff all the time! It's kinda hard to gross us out....

That happens to me quite regularly also, regardless of getting glutened or not. But then again, I have continuing "issues" even though I am gluten free (like going to the bathroom 30 times a day, which makes it quite understandable in my situation......) I didn't think it was hemmroids either, but when I had my last colonoscopy, the doctor said they were up there......

Karen

elonwy Enthusiast
elonwy
Posted

This is gross, but appropriate, just throwing up a warning.

When I get glutened, and before I knew to go gluten-free, I got these fun things called anal fissures. These are tiny little perforations kinda like paper cuts, that occur right around the sphincter. They're really hard to see, they itch like hell, and it hurts like blazes to go to the bathroom. My doc isn't sure why, but this is a definite gluten symptom for me. Sounds alot like the same thing. Basically you just have to wait for them to go away.

Elonwy

BRUMI1968 Collaborator
BRUMI1968
Posted

I got the fissures too, from extremely hard stool, when I first went gluten free (was always on the C side of things). Now I find it itches down there when I've got a yeast problem going on; and if I quit all the sugar and fruit, it gets better.

Good luck.

Canadian Karen Community Regular
Canadian Karen
Posted

Can anyone explain to me why the doctor would see hemmroids in me when I have had nothing but diarrhea for the past decade???? Seems odd to me, I thought hemmroids were from having to push out a hard bowel movement.....

Karen

ravenwoodglass Mentor
ravenwoodglass
Posted

If you lived in Europe they would biopsy a bit of your rectal tissue to confirm the celiac. Gluten effects the mucous membranes. If everyone with hemmies went off gluten they would in most cases be gone. What you are feeling is the mucosal tissues reaction to the gluten passing out of your system. This effect can also be caused by gluten contamination through femine hygine products like perfumed pads or the adhesives in panty liners. This will pass after the gluten is out of your system completely and no longer being excreted in your stool. I know this doesn't help the irritation you are experiencing and I wish I knew something that would. I got CC last week working with a colored cement for stained glass garden stones and am still doing the booty scoot. I avoid using anything other than a cool bath with NO bath products.

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

Celiac.com Sponsor (A8-M):


Sweetfudge Community Regular
Sweetfudge
Posted
  • Author

Thanks for replying everyone :) . So whether they're fissures or hemmroids...what can I do to ease the discomfort? Use cortizone cream? Neosporin? Or do I just have to suffer? lol! I was going crazy last night in bed and finally got up and put a little witch hazel on a cotton ball and applied that. It helped, a bit. Anyway, thx again!

loraleena Contributor
loraleena
Posted

Anal itching can be caused by candida overgrowth down there.

jerseyangel Proficient
jerseyangel
Posted
Can anyone explain to me why the doctor would see hemmroids in me when I have had nothing but diarrhea for the past decade???? Seems odd to me, I thought hemmroids were from having to push out a hard bowel movement.....

Karen

I don't think I've ever been constipated in my life. Seriously. My problem is very much the opposite--imagine my surprise when the gastro found internal hemmorhoids during my colonoscopy last year.

When I get glutened, or eat certain foods that I'm intolerant to, I get the same burning and itching.

I don't use anything for it, I find cool/lukewarm water as good as anything else.

BRUMI1968 Collaborator
BRUMI1968
Posted

Use Cottonnelles instead of TP - that will help. Or any kind of flushable 'baby wipe'

Lymetoo Contributor
Lymetoo
Posted

Check this out ...maybe it will help.

Candida diet and elimination:

Open Original Shared Link

Open Original Shared Link

jenvan Collaborator
jenvan
Posted
Thanks for replying everyone :) . So whether they're fissures or hemmroids...what can I do to ease the discomfort? Use cortizone cream? Neosporin? Or do I just have to suffer? lol! I was going crazy last night in bed and finally got up and put a little witch hazel on a cotton ball and applied that. It helped, a bit. Anyway, thx again!

Vaseline! And Prep H--not the cooling one though--yikes, that hurts! Hopefully as you continue to be gluten-free, the hemmies will be fewer and farther between. If not, you might want to explore dairy. It is a big cause of this for me.

mle-ii Explorer
mle-ii
Posted

Some of your symptoms sound like Proctitis. An inflamation of the rectum and lower colon.

jnifred Explorer
jnifred
Posted

HOLY MOLY....I was just looking into this yeterday for my son......he has very similar issues that youa re describing. He is getting scoped both ends in a little over a week. All his blood tests came back fine, but since I eat gluten free, they eat very little gluten. I was wondering if it was possibly related to gluten. He has had anal fissures and due to that the strep bacteria that lives on everyones skin got inside and he has been fighting peri-anal strep allllllll year. We get rid of it and it comes right back.

Hemmoroids can be internal from all the "stuff" passing through, sort of like overuse.....not necessarily from pushing too hard, just from being used to much.......KWIM???? I've used suppositories and some cream that you shoot up there, both work great for me....but I like the cream better.

and use vaseline when you wipe and soft toilet paper. we have a septic and I've asked several septics guys and they all say I can use the soft stuff. Not had a rpobelm yet, and we've had the tank cleaned out several times since we moved here.

GOOD LUCK!!!

Felidae Enthusiast
Felidae
Posted
This is gross, but appropriate, just throwing up a warning.

When I get glutened, and before I knew to go gluten-free, I got these fun things called anal fissures. These are tiny little perforations kinda like paper cuts, that occur right around the sphincter. They're really hard to see, they itch like hell, and it hurts like blazes to go to the bathroom. My doc isn't sure why, but this is a definite gluten symptom for me. Sounds alot like the same thing. Basically you just have to wait for them to go away.

Elonwy

I used to get those all the time too before going gluten-free.

Can anyone explain to me why the doctor would see hemmroids in me when I have had nothing but diarrhea for the past decade???? Seems odd to me, I thought hemmroids were from having to push out a hard bowel movement.....

Karen

You can get hemmroids from diarrhea too. At least I think I read about it somewhere. I'll try to remember where and post it.

hineini Enthusiast
hineini
Posted

Oh man, I have BEEN THERE! And fortunately am not too embarassed to talk about it ;-P

I thought I had hemmorhoids, due to itching and burning and pain around the anus, pain while going to the bathroom, and also sometimes blood on the toilet paper. However, I got a flexible sigmoidoscopy (with totally clean results) and the doc said what he thinks is that I have "anal fissures"... Small tears inside. I use hemmorhoid pads (they're such a godsend!) for the external discomfort, and the doctor has now given me hydrocortisone suppositories that I use twice a day to bring down the swelling and promote healing, plus hydrocortisone cream for around the external area. It's helping a lot. He also has me doing "sitz baths" (sitting in hot water) daily, which is soothing, and taking lots of fiber supplementation.

Yes, you can get fissures and hemmorhoids from diarrhea, not just from constipation. Diarrhea often burns as much as constipation does when I'm going to the bathroom, due to the fissures.

The other thing I find helpful is baby wipes. I buy unscented baby wipes in BIIIG boxes at Target, and use them instead of toilet paper when I have a #2. It is way less irritating than toilet paper.

TinkerbellSwt Collaborator
TinkerbellSwt
Posted

I also have this same problem. Mine is from C, just as much D. I use the prep-h when it gets bad. That helps me alot. I also use the Cottonelle moist wipes, which help too. The bath with no products in it too, helps. I hope you feel better soon!

ms-sillyak-screwed Enthusiast
ms-sillyak-screwed
Posted

-

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748
    Tara M
    Newest Member
    Tara M
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • cristiana
      Ibuprofen

      By cristiana · Posted

      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      Knowing what to do when feeling unwell.

      By Me,Sue · Posted

      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      The Happy Tart review

      By Francis M · Posted

      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
    • Scott Adams
      The Happy Tart review

      By Scott Adams · Posted

      Is this the same restaurant? https://www.facebook.com/TheHappyTartFallsChurch/ Is it too late to take this up with your credit card company? Normally you have a few months to do a chargeback with them. It seems very odd that they are taking this approach with someone who is likely to be a regular customer--not a good business-minded way of handling things!
    • Scott Adams
      Stomach burning and neuropathy

      By Scott Adams · Posted

      Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.        
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.