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

Questions About Hemirrhoids


Sweetfudge

Recommended Posts

Sweetfudge Community Regular

how do i know exactly if i have them? i explained my symptoms to my dr, and he said i did, and prescribed me first some hydrocortizone enemas (which i hated!! <_< ), then some cream to use there. the cream helps, but don't feel like it's enough. plus it was a $50 tube, which only works for a couple hrs, and i don't have the money to use it every time i hurt down there. what else works? also, my husband told me about some coworkers who used these enemas or something, i thought he said a salt, that is supposed to suck out of your colon the deposits that cause hemirrhoids-thereby reducing further outbreaks. anyone know about these? i seem to get them alot, and would like whatever i can get to help make them go away!! thanks!


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



Celiac.com Sponsor (A8-M):



DingoGirl Enthusiast

Hi there,

I had hemorrhoids once....I"ll NEVER forget it. :huh:

The only way I can describe it is - - it felt like someone had a pair of needle-nosed pliers on my anus and was twisting it ferociously. Dear gawd! Creams did nothing. Eventually, they went away on their own - - but had they/it? stayed, I would have had it lanced...that is one treatment option that works.

I'm not sure why an enema would work - - a hemorrhoid is a blood vessel with too much pressure on it and it nearly bursts, but not quite - it bulges - hence the pain. Straining to defecate really contributes. If they get too big or too painful, I would look into having them lanced.

Ouch.......... :huh:

Sweetfudge Community Regular

i don't know if mine are constant, or if they come and go, but i seem to notice them most when i'm having other intestinal issues (after ingesting gluten, or something else i'm sensitive to). i feel them a couple times a month. they suck so bad!!! the enema my dr gave me was a form of hydrocortizone, but all it did was make me feel like i was on my period, except in the wrong area <_< .

the one my husband mentioned was supposedly some natural preventative that i guess reduced the chances of getting one. he says his coworkers swore by them, that they'd been hemorrhoid free for years. i'd love that!!! i'd consider the lancing, if i had $$ or insurance :(

Ridgewalker Contributor

One alternative to try for temporary relief-- Witch Hazel pads. They can be found in any drugstore and are pretty cheap. Keep them by the toilet (or in your purse, they come in a small tub) and dab the area every time you go in the bathroom. The relief is gentle and temporary, but they are helpful.

I found them very soothing to use on that whole area after the births of both my children. I also use them when I'm hurting from particularly bad bouts of diarrhea.

They might be worth a try!

Worriedwife Apprentice

Another thing to try is a sitz bath, which you can pick up at a drug store. It's a basin that sit in the toilet, with a pouch that you fill up with warm water. There is tubing that goes from the pouch to the basin, and then it sprays up into the anal area to help soothe and reduce the hemerrhoids. Its like sitting in a warm bath, except you don't have to fill up the tub. It always works for me.

Guest j_mommy

I 2nd the sitz bath!!! They are most helpful for outer or close to teh surface hemmriods though. Another option is if they get very bothersome.....you can have them removed. They surgically take them off!!!!

Phyllis28 Apprentice

In addtion to the other suggestions, you can purchase at the pharmancy a special pillow for sitting on. The pillow has a hole in the middle to help relieve the stress when sitting.


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

You can also get the witch hazel pads in the form of wipes (Preparation H makes them). If you use them after every bowel movement instead of toilet paper, it will help to prevent them.

My husband's proctologist suggested this to hubby and said tp is one of the worst things for causing hemmorhiods.

Acersma Rookie

I have suffered from Hemmoroids since I was 16...over 15 years now:( I use preparation H cream, enema to help the bowel movement, the Tucks wipes instead of toilet paper. Try not to strain...easier said than done when some days you may be constipated then a few hours later have diarrehea. Sitz bath will help. Don't lift or carry anything more than 15 pounds. and if all of the above doesn't work get them cut out. When I had my daughter they were HUGE and I couldn't wipe so I used a squirt bottle from the hospital which I am sure you could get one from the drug store and I put some anti bactereial soap and water and washed that area w/ that. Good luck. I am sorry that you are dealing w/ this...they hurt!

Jody

Sweetfudge Community Regular

thanks all for your ideas. feeling better today, thankfully! though i may just have to invest in those witch hazel wipes.

My husband's proctologist suggested this to hubby and said tp is one of the worst things for causing hemmorhiods.

interesting...

ravenwoodglass Mentor
i don't know if mine are constant, or if they come and go, but i seem to notice them most when i'm having other intestinal issues (after ingesting gluten, or something else i'm sensitive to). i feel them a couple times a month. they suck so bad!!! the enema my dr gave me was a form of hydrocortizone, but all it did was make me feel like i was on my period, except in the wrong area <_< .

This statement is really very telling IMHO. Do you have DH by any chance? I had problems with 'hemmies' for most of my life. For me they are caused directly by the effect of gluten leaving my body. Once I realized this, which wasn't until after diagnosis and a few good glutenings, they became much less of a concern for me. Painful yes, and I second the sitz bath for relief. The cortizone will help with the inflammation until the reaction subsides. The cortizone would also help with any internal 'blistering' or DH type reaction, ie. the awful itch when a reaction occurs but I wouldn't do anything about them as a preventative other than being gluten-free. Also with the reaction you mention from cream you should make absolutely positive that it is gluten free, gluten can be absorbed by the mucous membranes and if the cream is making you swell it may not be safe.

hathor Contributor

The suggestions about temporary relief of symptoms are all good. Believe me, I've been there frequently enough.

I think it a good idea to eat a diet high in fiber, too, and drink lots of liquids. Take magnesium supplements if necessary. Do what is necessary to have bowels that function regularly and stools that are soft. My flareups come when I'm constipated or my stools are particularly hard. This seems to be due to my food intolerances.

If people still have problem when gluten free and having fiber and liquids (regular exercise, too), they should try going off dairy. That commonly binds people up. I remember that my problems got better, albeit not cured, when I eliminated dairy a number of years ago. Every time I try to have cow's milk, the interior of my large intestine turns to concrete.

On that lovely note, I'll leave you :rolleyes:

saaa-wheat<3 Apprentice
This statement is really very telling IMHO. Do you have DH by any chance? I had problems with 'hemmies' for most of my life. For me they are caused directly by the effect of gluten leaving my body. Once I realized this, which wasn't until after diagnosis and a few good glutenings, they became much less of a concern for me. Painful yes, and I second the sitz bath for relief. The cortizone will help with the inflammation until the reaction subsides. The cortizone would also help with any internal 'blistering' or DH type reaction, ie. the awful itch when a reaction occurs but I wouldn't do anything about them as a preventative other than being gluten-free. Also with the reaction you mention from cream you should make absolutely positive that it is gluten free, gluten can be absorbed by the mucous membranes and if the cream is making you swell it may not be safe.

I have DH and even my GI doc looked at me funny when I told him that I get 'rhoids when I am glutened, so I'm glad to read that I'm not such a freak after all (I love this place).

I use generic Prep H Cooling Gel (has more medicine in it than the witch hazel wipes), sometimes a calendula ointment and always take a magnesium/cal/vitD supplement.

ravenwoodglass Mentor
I have DH and even my GI doc looked at me funny when I told him that I get 'rhoids when I am glutened, so I'm glad to read that I'm not such a freak after all (I love this place).

I use generic Prep H Cooling Gel (has more medicine in it than the witch hazel wipes), sometimes a calendula ointment and always take a magnesium/cal/vitD supplement.

Actually you are not a freak at all. In more medically advanced countries they use a gluten suppository and then biopsy the rectal tissue to rule out celiac. They also are working on an oral test that works the same way. Even those without DH will have a reaction. A much more civilized method IMHO, as it means they don't poison someone for months to still risk a false negative.

Sweetfudge Community Regular
This statement is really very telling IMHO. Do you have DH by any chance? I had problems with 'hemmies' for most of my life. For me they are caused directly by the effect of gluten leaving my body. Once I realized this, which wasn't until after diagnosis and a few good glutenings, they became much less of a concern for me. Painful yes, and I second the sitz bath for relief. The cortizone will help with the inflammation until the reaction subsides. The cortizone would also help with any internal 'blistering' or DH type reaction, ie. the awful itch when a reaction occurs but I wouldn't do anything about them as a preventative other than being gluten-free. Also with the reaction you mention from cream you should make absolutely positive that it is gluten free, gluten can be absorbed by the mucous membranes and if the cream is making you swell it may not be safe.

i don't know if i have DH. it's not obvious if i do. the only places my skin acts funny are on my scalp (big white ugly flakes and itching constantly), and the hemmi's which i have noticed do correlate with my body reacting to a food flare up (beginning to think i might be dairy intolerant as well as celiac).

Actually you are not a freak at all. In more medically advanced countries they use a gluten suppository and then biopsy the rectal tissue to rule out celiac. They also are working on an oral test that works the same way. Even those without DH will have a reaction. A much more civilized method IMHO, as it means they don't poison someone for months to still risk a false negative.

wouldn't that be excellent?!

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to annamarie6655's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Airborne Gluten?

    2. - Kirita posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Recovery from gluten challenge

    3. - annamarie6655 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Airborne Gluten?

    4. - trents replied to Mell2's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Rectal pain


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,240
    • Most Online (within 30 mins)
      7,748

    TwinJan
    Newest Member
    TwinJan
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Hello, @annamarie6655, Yes, there's many of us who react to airborne gluten!   Yes, animal feed, whether for chickens or cats or dogs, can release airborne gluten.  I can get glutened from the bakery section at the grocery store.   The nose and mouth drain into the digestive system and can trigger systemic reactions.   I find the histamine release in response to airborne gluten will stuff up my sinuses and bother my eyes.  High histamine levels do cause anxiety and migraines.  The muscle spasms can be caused by high histamine, too.  The digestive system may not manifest symptoms without a higher level of gluten exposure.   Our bodies make an enzyme, DAO (diamine oxidase), to break down histamine.   Pyridoxine B 6, Cobalamine B12, Vitamin C, copper, zinc, and iron are needed to make DAO.  DAO supplements are available over the counter.  Taking a B Complex supplement and additional Thiamine in the form Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) helps reduce the amount of histamine being released.  Mast cells without sufficient Thiamine have an itchy trigger finger and release histamine at the slightest provocation.  Thiamine helps mast cells refrain from releasing their histamine.    I find taking additional TTFD thiamine helps immensely with neurological symptoms as TTFD can easily cross the blood brain barrier without a carrier.  High histamine in the brain can cause the muscle spasms, anxiety and migraines.  Vitamin C really helps with clearing histamine, too.   The Digiorno pizza mystery reaction could have been caused by a reaction to the cheese.  Some people develop lactose intolerance.  Others react to Casein, the protein in dairy, the same as if to gluten because Casein resembles the molecular structure of gluten.  An enzyme used in some dairy products, microbial transglutaminase, causes a gluten reaction because it is the same as the tissue transglutaminase our bodies make except microbes make it.  Those tTg IgA blood tests to diagnose celiac disease measure tissue transglutaminase our bodies release as part of the autoimmune response to gluten.   You're doing great!  A Sherlock Holmes award to you for figuring out the connection between airborne gluten and animal feed!!!  
    • Scott Adams
      This article may be helpful:  
    • Kirita
      I’m wondering if anyone has had any experience with the gluten challenge. My teenager completed a gluten challenge over the summer, it ended up being 10 weeks although she stopped being consistent eating gluten after 6. Her previous endoscopy was negative but this past August it was positive after the gluten challenge. If you have done the gluten challenge, how long did it take you to feel back to normal? It took about two months before she got “glutened” again but now she’s having difficult coming back from that and has a lot of fatigue. I’m hoping someone has some advice! 
    • annamarie6655
      Hello everyone, I was on here a few months ago trying to figure out if I was reacting to something other than gluten, to which a very helpful response was that it could be xanthin or guar gum.    Since then, I have eaten items with both of those ingredients in it and I have not reacted to it, so my mystery reaction to the Digiorno pizza remains.    HOWEVER, I realized something recently- the last time I got glutened and the most recent time I got glutened, I truly never ate anything with gluten in it. But i did breathe it in.    The first time was a feed barrel for my uncle’s chickens- all of the dust came right up, and most of what was in there was wheat/grains. The second time was after opening a pet food bag and accidentally getting a huge whiff of it.    When this happens, I tend to have more neurological symptoms- specifically involuntary muscle spasms/jerks everywhere. It also seems to cause migraines and anxiety as well. Sometimes, with more airborne exposure, I get GI symptoms, but not every time.    My doctor says he’s never heard of it being an airborne problem, but also said he isn’t well versed in celiac specifics. I don’t have the money for a personal dietician, so I’m doing the best I can.    is there anyone else who has experienced this, or gets similar neurological symptoms? 
    • trents
      I was suffering from PF just previous to being dx with celiac disease about 25 yr. ago but have not been troubled with it since. Not sure what the connection between the two is of if there is one. But I do know it is a very painful condition that takes your breath away when it strikes.
×
×
  • 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.