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

Nsaids And Dh


Lola B

Recommended Posts

Lola B Rookie

Can anyone shed some light on the connection between NSAIDs and DH? My teenage daughter has DH and she also suffers from chronic migraine headaches. She had been taking Aleve, and her DH is flaring back up again. The dapsone doesn't seem to be helping control these new flareups. Thanks!


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



Celiac.com Sponsor (A8-M):



Dan300 Newbie

Hi Lola, Dr Tom O'Bryan ( a Chicago area Dr ) travels around the country giving lectures to doctors and the public about Gluten intolerance, in part of it he talks about migraines where a study was done with 10 severe cases that tried thr GFD. 7 had full recovery , 2 no change , 1 refused the diet. www.theDr.com hope this helps Dan

gaingus Rookie

I remember going through the same issues myself. There was a very small thread asking about Microcristaline Cellulose some time back (it is in the inactive ingreditents list on Aleve).

https://www.celiac.com/gluten-free/index.php?showtopic=17030

As for me, I quit using it and have gone to plain tylenol for headaches and the migraines are few and far between. The only DH flare-ups I get now is from accidental glutening.

I've done some other google searches on it and found that the FDA says it is safe as long as proper manufacturing processes are used.

Lola B Rookie
I remember going through the same issues myself. There was a very small thread asking about Microcristaline Cellulose some time back (it is in the inactive ingreditents list on Aleve).

https://www.celiac.com/gluten-free/index.php?showtopic=17030

As for me, I quit using it and have gone to plain tylenol for headaches and the migraines are few and far between. The only DH flare-ups I get now is from accidental glutening.

I've done some other google searches on it and found that the FDA says it is safe as long as proper manufacturing processes are used.

Lola B Rookie

Thanks for the info! One more ingredient to be on the look out for.

ChemistMama Contributor

Lola=

From what I've read, yes there is a link between NSAIDS and flares.

Open Original Shared Link

BEfore I was gluten-free, the two things that would make my DH worse were iodine and advil. Make sure she takes a vitamin that is low in iodine (less than 150 mg), I use iodine free vitamins. I'm not brave enough to take advil yet. I've heard that once the gluten is 'out of your skin', maybe after a year, you can bring iodine and NSAIDs back into your diet.

I also found an article where they studied the effect of ibuproven on dapsone levels but there isn't abn abstract, so I'll keep hunting.

Open Original Shared Link

I would suggest to her to try tylenol for migraines and see if this helps.

flourgirl Apprentice

Hi Lola. I hear ya. When I was a teen I had chronic migraines. Bad enough they used to put me down for days. Even as an adult I would get occaisional migraines. I'm convinced that they were Celiac related. I also used to get terrible rashes and blamed them on poison ivy. Anyway, after I was seriously ill and finally got a diagnosis (also had DH almost everywhere at the time) I went gluten-free. No more migraines! After about 1 1/2 years no more DH. I stopped all salts, anything with iodine and realized I could take nothing except tylenol for pain while I had DH. Good luck to your daughter in getting rid of both!

Oh, yeah....I did not try dapsone, but there are bath soaks, and a clear Calamine that may help alleviate the burn.


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



Celiac.com Sponsor (A8-M):



GottaSki Mentor

I recently discovered that Advil Gel Caps caused my first ever rash.

I have always used Advil or Generic tablets, not gels for pain. This past December I bought Gel Caps and had my first ever itchy rash...lasted for 7-8 weeks.

During this time I was being tested for many different illnesses and was in the docs office often. As I became more frustrated with lack of diagnosis my blood pressure was rising at each doctor visit (I have reg very low BP). Anyway...doctor suggested I switch to tylenol for pain as advil can raise BP. The rash disappered. It was not until just last week that I discovered it was the gel caps.

Last week I went back on advil for pain because tylenol doesn't work for my arthritis type symptoms. I felt like I'd been glutened...could not find the gluten in the gel cap ingredients or online, but went back to reg advil tablets and have had no reaction.

While I can not prove the gel caps caused the rash...the timing is dead on.

Lola B Rookie

Very interesting about the gelcaps. My daughter had been taking Aleve gelcaps for the migraines and new DH breakouts kept erupting. They seem to be clearing up now that she's off of the Aleve. We'll switch to Tylenol for the migraines - although it doesn't seem to help as much with the headache pain, but it's better than having both the headache and the intense itching of the DH.

  • 2 weeks later...
BigDogz Explorer

I used to take Advil or Aleve years ago for menstrual cramps and did well with them. I stopped taking them 6 or 7 years ago because I was finding I was getting horrible stomach pains whenever I took them. Thinking back, they may very well have been gel-caps as I do remember buying that version for some time, although I can't definitively say it was during the stomach pain issues. Anyways, Doc suggested I switch to Tylenol. It didn't work as well, but at least the stomach pain went away.

In the past 6 months I was plagued with headaches (prior to going gluten-free) and was finding that I was taking Tylenol nearly every day, sometimes several doses per day, to control them. It seemed to help the headaches but, all of the sudden, the stomach pain was back and it seemed to correlate with the ingestion of the Tylenol doses. It didn't seem to matter if I was using namebrand or some generic knock-off, either.

I've gone back to using the Aleve and, so far, I've not had any problems. Then again, since going gluten-free I've not had nearly the occasion to take anything since the headaches are now (YAY!) few and far between. I can't say that I've noticed any corresponding flare-ups in my rashes from re-starting the Aleve but I was taking a short course of Prednisone for a case of poison ivy (I was able to confirm my exposure) and THAT medicine seemed to set the DH rash into high gear!

Has anyone else had stomach issues with taking Tylenol or am I just some utterly unique freak of nature?

  • 3 weeks later...
hollyfolly Newbie
I remember going through the same issues myself. There was a very small thread asking about Microcristaline Cellulose some time back (it is in the inactive ingreditents list on Aleve).

https://www.celiac.com/gluten-free/index.php?showtopic=17030

As for me, I quit using it and have gone to plain tylenol for headaches and the migraines are few and far between. The only DH flare-ups I get now is from accidental glutening.

I've done some other google searches on it and found that the FDA says it is safe as long as proper manufacturing processes are used.

What is a DH flare-up? I'm new and seeing all these posts that are really scary! Trying to gather info, thanks.

lovegrov Collaborator
What is a DH flare-up? I'm new and seeing all these posts that are really scary! Trying to gather info, thanks.

If you don't already know what DH is, you probably don't have to worry. DH is dermatitis herpeteformis, essentially the skin version of celiac. Most people with celiac don't have it.

richard

  • 2 months later...
Razzy Newbie

"We'll switch to Tylenol for the migraines - although it doesn't seem to help as much with the headache pain, but it's better than having both the headache and the intense itching of the DH."

I am a nurse, and have DH. I have had severe migraines since I was 12, but much less often since I went gluten-free, and I only use Tylenol to treat them.

Migraines occur because, in response to "triggers", the blood vessels inside the brain dilate (swell/get bigger) and irritate the trigeminal nerve that supplies feeling to your face and head.

Ibuprofen (Advil/Motrin) and other true NSAIDS (Non-Steroidal Anti-Inflammatory Drugs) like Naproxen (Aleve) and Aspirin relieve pain through the reduction of this inflammation and swelling.

Tylenol is not the same class of medication and does not reduce inflammation: it really ONLY takes care of the pain by a different mechanism. Because it doesn't directly reduce the swelling, it typically takes more doses of Tylenol to get comfortable, and the pain relief can feel less complete than with NSAIDS.

However, you can help Tylenol to work better for you: drink a strong cup of tea or coffee just after taking it, prepared any way you like it. The caffeine in these beverages will constrict the blood vessels, achieving a similar reduction in the swelling from inflammation to that which NSAIDS provide. Other gluten-free caffeinated beverages will do just as well.

Another helpful thing to do that assists with reducing the swelling and numbing the pain is to apply a cold pack to your head for 20 minutes at a time(frozen peas or corn wrapped in a dishtowel will do nicely) directly over the area that hurts the worst. For me, that's always my right eye and forehead.

Wearing sunglasses (even inside), darkening the room, and being in a quiet room (or one with "white noise" like a fan) can all help to make the headache go away more quickly by reducing environmental "triggering".

Hope this helps....remember that free advice can sometimes be worth what you pay for it. :D

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,032
    • Most Online (within 30 mins)
      7,748

    CE1963
    Newest Member
    CE1963
    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

    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • 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.