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

Tiny Red Bumps


Mother of Jibril

Recommended Posts

Mother of Jibril Enthusiast

I tried looking through old posts for something like this... but I can't seem to find anything that matches just right.

I have some tiny, red, itchy bumps on my hands that showed up in the last few days. They're about 1mm in diameter... not on my palms, and I only have about half a dozen. No bumps on the rest of my body. It's too cold for most bug bites (we just had our first snowfall yesterday). Plus, if were something like scabies, wouldn't they have chosen a warmer part of my body? :huh:

I called to make sure our turkey was gluten and corn free... a "halal" brand (the Muslim version of Kosher)... and the guy said it was fine. Now I wonder. :( I've also been constipated and having some mild abdominal pain the last couple of days. Can you get DH on your hands?

I already had a dermatologist appointment scheduled for Friday... I'm just curious to hear any ideas on what this might be.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

I usually have at least one of these intensely itchy little bumps on the backs of my hands and fingers, often several, although none right now. I have no idea what causes them. But then again I am vey much a skin problem kind of person!!

Mother of Jibril Enthusiast
I am vey much a skin problem kind of person!!

Me too! I went straight from teenage acne to adult acne :( I also have halo nevi (places where my skin is reabsorbing a mole) and rosacea. Thankfully, on the gluten-free diet the long-time rash on my buttocks has gone away! :lol: My rosacea is looking better too.

mushroom Proficient

I finally no longer have the rash on my upper arms that my mother used to tell me was caused by not eating my vegetables :P

luciddream928 Explorer

I get those tiny red bumps too. Exactly how you described. I am convinced they have to do with gluten intolerance because when I am accidentally glutened and all my typical symptoms reappear, the rash is soon to follow. I can't even really call it a rash, the bumps cluster together but not all over my hands, just the joints of my fingers and the top of my right foot.

Incidentally, my mother gets these bumps in the exact same places as me, and we have similar digestive problems. Mine are more severe though. Not sure if it's DH per se, but related to gluten, IMHO.

Mother of Jibril Enthusiast
I finally no longer have the rash on my upper arms that my mother used to tell me was caused by not eating my vegetables :P

:lol::lol::lol:

My parents told me the rash on my buttocks was "sweat pimples."

I get those tiny red bumps too. Exactly how you described. I am convinced they have to do with gluten intolerance because when I am accidentally glutened and all my typical symptoms reappear, the rash is soon to follow. I can't even really call it a rash, the bumps cluster together but not all over my hands, just the joints of my fingers and the top of my right foot.

Incidentally, my mother gets these bumps in the exact same places as me, and we have similar digestive problems. Mine are more severe though. Not sure if it's DH per se, but related to gluten, IMHO.

Right! The bumps are around the joints on my hands... not really enough to call it a "rash." When I see my parents next month I'll have to check their hands ;)

Incidentally, I see we share the DQ7 gene. I'm pretty sure I got that one from my dad.

ksymonds84 Enthusiast

I get those too. The last time was an hour after having Mcdonald's frenchfries (went through drive up and didn't pay attention if they were using a dedicated fryer...my bad). They are usually up and down my fingers with a few on the front of my hands. Mine go away pretty quickly though which is why I think its glutened related but not DH. I also have rosacea, keep waiting for it to go away, glad yours is getting better, it gives me hope!


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



Celiac.com Sponsor (A8-M):



Mother of Jibril Enthusiast
I also have rosacea, keep waiting for it to go away, glad yours is getting better, it gives me hope!

What really helped with that was taking Betaine HCl with protein meals. I don't know exactly how it reduces inflammation, all I know is that it improves my digestion. Hypochlorhydria (low stomach acid) is one cause of rosacea. For the first time in years I don't look like I have a sunburn on my face! :) I still flush very easily, but it goes away in a few hours.

mushroom Proficient
I also have rosacea, keep waiting for it to go away, glad yours is getting better, it gives me hope!

My rosacea has gone away too. Now it only comes back with a glass of wine.

ksymonds84 Enthusiast
What really helped with that was taking Betaine HCl with protein meals. I don't know exactly how it reduces inflammation, all I know is that it improves my digestion. Hypochlorhydria (low stomach acid) is one cause of rosacea. For the first time in years I don't look like I have a sunburn on my face! :) I still flush very easily, but it goes away in a few hours.

Good info, I will check into it!

ksymonds84 Enthusiast
My rosacea has gone away too. Now it only comes back with a glass of wine.

I'm fine with a little white wine but if I drink red, I look like rudolph! :lol:

zeta-lilly Apprentice
I finally no longer have the rash on my upper arms that my mother used to tell me was caused by not eating my vegetables :P

I've always had little red bumps on my upper arms. So does my dad and a friend of mine (who has pretty severe colitis). They're not itchy or anything. Is that what you're talking about or it is that Dermatitis herpetiformis? I never thought about it being related, but I haven't been gluten free long.

mushroom Proficient
I've always had little red bumps on my upper arms. So does my dad and a friend of mine (who has pretty severe colitis). They're not itchy or anything. Is that what you're talking about or it is that Dermatitis herpetiformis? I never thought about it being related, but I haven't been gluten free long.

Yeah, those were what I had on my upper arms. Different from the itchy ones on my hands, and definitely not DH.

julirama723 Contributor

Aren't those little red bumps (on the arms) Keratosis Pilaris? I have those. They went away for a while (when I was grain-free) but now they're back.

Ugh, also had the butt bumps. Those are THE WORST!

Mother of Jibril--I think you'd posted in a different topic that there might be a relation between KP and celiac? I've read quite a few Celiac/Gluten-Intolerant people also have KP! Do you think the bumps on your hands are KP?

julirama723 Contributor

Oh, threadjack--question about the rosacea--how do you know if it's rosacea and not just rosy cheeks?

My doctor tested me for lupus because my face was so red. I have one sip of wine and I look like Rudolph, too.

Mother of Jibril Enthusiast
Ugh, also had the butt bumps. Those are THE WORST!

Mother of Jibril--I think you'd posted in a different topic that there might be a relation between KP and celiac? I've read quite a few Celiac/Gluten-Intolerant people also have KP! Do you think the bumps on your hands are KP?

I did see that post about keratosis pilaris... very interesting! It sounds exactly like the "arm rash" that other people on this thread have described. I don't think that's what my bumps are though, since I don't have hair follicules around the joints on my hands.

The "butt bumps" ARE annoying! The worst for me was taking a bath... it hurt to sit on the hard surface, and then the bumps would get inflamed from the heat and stick to the tub. :angry: I'm planning to ask the dermatologist about those too.

Oh, threadjack--question about the rosacea--how do you know if it's rosacea and not just rosy cheeks? My doctor tested me for lupus because my face was so red.

Good question! This diagnosis came from my dermatologist. I went to her because I thought I might have vitiligo. In addition to the white spots on my hands (halo nevi), I also pointed out that the skin around my eyes was really pale compared to the rest of my face :ph34r: (Not just rosy cheeks from sunburn or being outside... I looked like that all the time). She checked me with a Wood's lamp and said it's not vitiligo... she suggested rosacea and gave me a Rx for Finacea. I really hate trying new products on my face because my skin is SO sensitive, but it actually helped. Now that I'm corn and gluten-free and taking Betaine HCl with protein meals, I don't even need to use the Finacea!

You're absolutely right that the redness of lupus and rosacea can look similar. I wonder if there's any connection. My ANA was 33, not high enough to be positive for lupus, but definitely showing some autoimmune activity. One of my aunts has lupus... it's associated with the DQ7 gene.

  • 2 weeks later...
Mother of Jibril Enthusiast

OK... so the tiny red bumps on my hands started drying up about a week after I got glutened (on Thanksgiving <_< ).

I got glutened again on Monday (darn holidays!!) and the bumps are back... only this time, I'm also using some new shampoos that my dermatologist prescribed for yeast overgrowth on my scalp. My scalp is fine (I don't think the shampoos have gluten), but the daily showers are killing my skin! The bumps have spread up my arms and are SO itchy. Grrrr.

I'm going to call the dermatologist's office tomorrow and ask what they recommend. There's no way I'm going to last for the next six weeks on this regimen. :angry:

I can hardly wait until the holidays are over so I can go on the SCD. For now I'm just eating as little processed food as possible.

fedora Enthusiast

this was one of my worst symptoms. My little fluid filled blisters were on my palms and fingers. they got so bad that they ate my hand. It was terrible. I got staph and strep in them and could only use my thumb and forefinger. talk about scary. I took antibiotics and used steriods. The rash got better. But when I went off wheat it completely went away. when I would eat wheat, it would come back.

Now I only get them when my digestion gets messed up, but only a few at a time. I don't think it is always gluten related. I know people who get them from corn and I think it could be leaky gut related.

My grandmother(dad's mom) also got them and my mother, but my mom's were from soap.

I also would get itchy buttocks that would get bumpy. In fact, I itched everywhere.

my rash was called Dyshidrotic Eczema. there are photos and info on several websites. my dr says it is allergy related. It is connected to nickel allergy too.

I washed my hands as little as possible, showered with gloves and used gloves to wash dishes. fun days those were.

Mother of Jibril Enthusiast

Ahhhh.... yes. I looked at some websites and DE fits my symptoms better than anything I've seen before. Thank you for that suggestion!!

My first outbreak was not too bad. Just a few blisters on my hands. This time it's also on my palms and my feet <_< I took a couple of CC risks and now it looks like I'm paying the price. I'm trying not to scratch... how scary to get a staph infection!

I'm still going to call the dermatologist tomorrow. There's no way I can keep taking showers every day when it's making the itching worse. Maybe she'll have some other suggestion.

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. - hjayne19 replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      11

      Insomnia help

    2. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      43

      My journey is it gluten or fiber?

    3. - knitty kitty replied to Charlie1946's topic in Related Issues & Disorders
      45

      Severe severe mouth pain

    4. - Lkg5 replied to Charlie1946's topic in Related Issues & Disorders
      45

      Severe severe mouth pain

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,098
    • Most Online (within 30 mins)
      7,748

    BothySmithy
    Newest Member
    BothySmithy
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • hjayne19
      Hi @knitty kitty  Just revisiting this to get some help. I found after understanding the extent of my anxiety, my sleep got a little better. Flash forward to a few weeks later I have had a few bad sleeps in a row and I feel desperate for a good nights sleep. I understand worrying about it won’t help but one thing I had tied things too was dairy. Initially when I went gluten free I felt great for the first few weeks then started having some stomach pain. So thought maybe I was lactose intolerant. I started eating lactose free Greek yogurt and that did help take the cramping away I guess. Over the last few months I haven’t eaten it every single day and I went a few weeks without it. The last few nights I did have a small amount with breakfast and noticed that was the only new thing I’ve really added to my diet. I had seen a few other posts about this. Is it possible to still react to lactose free? Would this potentially be a dairy allergy? Or something else. 
    • xxnonamexx
      I have taken the vitamins for a week. Haven't noticed any major changes but I will give it more time to see.
    • knitty kitty
      @Charlie1946,  Sorry I sidetracked your thread a bit.  Apologies. Proton pump inhibitors, like Omeprazole, change the pH in our gastrointestinal systems which allows opportunistic microbes to move in and take over.  Have you been checked for SIBO?  There's a significant link between length of Omeprazole use and SIBO.  I had SIBO, thrush (Candida) and lichen planus and other problems while I was on Omeprazole.  I had to stop taking it.  It was a horrible time, so I understand how painful and frustrating it is.   You change your microbiome (the bacteria and microbes living inside you) by changing what you eat.  They eat what you eat.  Change the menu and you get different customers.   I changed my diet.  I cut out dairy because I was reacting to the casein and lactose.  I cut out all processed foods and most carbohydrates. I ate meat and veggies mostly, some fruit like apples and mandarin oranges.  By cutting out all the excess carbohydrates, lactose, and empty carbs in processed gluten-free foods, the opportunistic microbes get starved out.  SIBO bacteria send chemical messages to our brains demanding more carbs, so be prepared for carb cravings, but don't let the microbiome control you!   The skin and digestive system is continuous.  The health of our outside skin reflects the health of our gastrointestinal system.  Essential B vitamins, like Thiamine B 1 and especially Niacin B 3, are needed to repair intestinal damage and keep bad bacteria in check.  Niacin helps improve not only the intestinal tract, but also the skin.  Sebaceous Hyperplasia is linked to being low in Niacin B 3.  Lichen Planus is treated with Niacinamide, a form of Niacin B 3.   Vitamins are chemical compounds that our bodies cannot make.  We must get them from our food.  If our food isn't digested well (low stomach acid from Omeprazole causes poor digestion), then vitamins aren't released well.  Plus there's a layer of SIBO bacteria absorbing our vitamins first between the food we've eaten and our inflamed and damaged villi that may have difficulty absorbing the vitamins.  So, taking vitamin supplements is a way to boost absorption of essential nutrients that will allow the body to fight off the microbes, repair and heal.   Doctors are taught in medical learning institutions funded by pharmaceutical companies.  The importance of nutrition is downplayed and called old fashioned.  Doctors are taught we have plenty to eat, so no one gets nutritional deficiency diseases anymore.  But we do, as people with Celiac disease, with impaired absorption.  Nutritional needs need to be addressed first with us.  Vitamins cannot be patented because they are natural substances.  But pharmaceutical drugs can be.  There's more money to be made selling pharmaceutical drugs than vitamins.   Makes me wonder how much illness could be prevented if people were screened for Celiac disease much earlier in life, instead of after they've been ill and medicated for years.   Talk to your doctor and dietician about supplementing essential vitamins and minerals.   Interesting Reading: The Duration of Proton Pump Inhibitor Therapy and the Risk of Small Intestinal Bacterial Overgrowth: A Systematic Review and Meta-Analysis https://pmc.ncbi.nlm.nih.gov/articles/PMC12250812/#:~:text=The long-term use of,overgrowth dynamics is less clear. Lichenoid drug eruption with proton pump inhibitors https://pmc.ncbi.nlm.nih.gov/articles/PMC27275/ Nicotinamide: A Multifaceted Molecule in Skin Health and Beyond https://pmc.ncbi.nlm.nih.gov/articles/PMC11857428/
    • Lkg5
      My sebaceous hyperplasia and thrush disappeared when I stopped all dairy.
    • Charlie1946
      @knitty kitty Thank you so much for all that information! I will be sure to check it out and ask my doctor.  I am just at a loss, I am on my 2nd round of miracle mouthwash and I brush and scrape my tongue and (sorry this is gross) it's still coated in the middle 
×
×
  • 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.