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

Positive Test....skin Symptoms Not Typical


brizzo

Recommended Posts

brizzo Contributor

I guess this is more of a venting on my part....but I was diagnosed by enterolab this month. Here's my gripe. I have no intestinal symptoms. I only have DH "like" symptoms on my scalp; NO WHERE ELSE!. Only my scalp. I have been on a gluten-free diet for two months with pretty damn good results. I still have the occasional "blister" here or there. But it has been due to CC at wendys , ignorance about certain alcohol products, and other foods. (still new at this =) I will not take meds. I DO NOT trust 1/2 the meds out there, and refuse to poison my body by taking them.

I guess my question is ....has anyone else heard of someone having DH on the scalp only, or am I just a freak? :ph34r: Just curious. And yes, I tested positive at enterolab. My results are below.


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

I used to have a rash on my scalp that I never had tested for being DH. I asked my doc about the rash (she also practices holistic medicine along with conventional). She said it was from the constant inflammation in my system ... my adrenals were fatigued and unable to come up with the hormones necessary to heal the rash. Now that I'm addressing my adrenal fatigue, the rash is clearing up.

frenchiemama Collaborator

I know that it is fairly common to get DH on the scalp. Only on the scalp? Not sure, but everyone is different. DH is always supposed to be symmetric, but I have one spot that isn't (I got it on both hands, both knees, both ankles, but only one elbow). Not typical, but not impossible either.

  • 2 weeks later...
almostnrn Explorer

I had spots on my scalp until I gave up my beloved Aveda shampoo which was pretty much like liquid gluten, lol. I have not heard of anyone just getting it in one area but then again if I had a nickel for every time a dermatologist told me "you can't get DH there" I'd be a millionaire. Be happy the diet is working and don't press your luck...I have found mine got worse after time.

mouse Enthusiast

One of my doctors was telling me that a friend of his in medical school got diagnosed with Celaic Disease and the only thing he had was DH on the scalp and only the scalp. He had no symptoms at all. Just the terrible rash and itching on his scalp.

  • 2 weeks later...
dyankeetoo Newbie

Hi, Brizzo: I'm pretty much a lurker here, but I have to tell you...I've had the scalp problem my entire life, and I'm 59 years old. Only recently developed the blisters all over, and I haven't had the biopsy yet. I'm betting on a positive, though, as I've been gluten free for three months, and I've begun to see a positive difference in my energy level and...HOORAY the constant nausea and stomach aches, running like a crazy person to the jon are gone (except for one instance when I made meatloaf with corn chips and paid dearly). Apparently I'm one of those who can't tolerate corn either.

Do the scalp itchies clear up when you take antibiotics? Mine do, but come right back as soon as I've finished the course. Thank goodness I have thick hair.

Best,

Laurie

  • 3 weeks later...
bwizzle Newbie

Hey brizzo and anyone else experiencing problems here. I want explain my situation. I am a 22 year old male and have been experiencing scalp "pustules" going on 5 years now. I have been to numerous doctors and had every test done (blood and biopsies) and yet to find a solution. Antibiotics work and when i go off of them, my condition returns. I am seeing an allergist and he bleieves its a food allergy. After doing some research I believe it is DH. I have just started my gluten free diet along with a detox system. I do no really have any other symptoms besides these itchy bumps on my scalp. Also my skin gets really itchy and I was wondering if anyone else experiences this. And the symmetric thing, yes it forms symmetrically only my scalp. I am sick of seeing new doctors and putting antibiotics in my body. I went through college with this plague and i know how hard it is to deal with. I am going to give this diet a shot because i am at the end of the road.

Brad


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



Celiac.com Sponsor (A8-M):



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. - Flash1970 replied to Ginger38's topic in Related Issues & Disorders
      25

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - Adeling commented on Scott Adams's article in Product Labeling Regulations
      2

      Global Experts Recommend Gluten Reference Dose: What It Means for Celiac Safety (+Video)

    3. - Sue7171 replied to Ginger38's topic in Related Issues & Disorders
      25

      Shingles - Could It Be Related to Gluten/ Celiac

    4. - sc'Que? commented on Scott Adams's article in Product Labeling Regulations
      2

      Global Experts Recommend Gluten Reference Dose: What It Means for Celiac Safety (+Video)

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

      What's your daily meals? Protein bars?

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

    • Total Members
      133,177
    • Most Online (within 30 mins)
      7,748

    Charlene Kearley
    Newest Member
    Charlene Kearley
    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

    • Flash1970
      Try heallix solution. It's at heallix.com It's a silver and fulvic acid solution.  I just put it on a cotton ball and wiped the shingles area. I also took a little internally once a day. I can't remember how many times a day I applied to the area. Probably  3-4 times a day. It was the only thing that stopped the nerve pain. I don't know if the vaseline is good.  The shingles need to dry out and heal.  Wash everything that comes in contact  with them in hot water. Don't use or wear anything twice. 
    • Sue7171
      My husband just had shingles going on 7 weeks now. We had been putting Vaseline on the blisters and lidocaine cream and he was prescribed an antiviral.  Also he still has the nerve pain it was bad and is getting better it is his upper left torso. His dr prescribed gabapentin 300mg 3x a day and he's also taking naproxen 500ng 2x a day and tylenol 1000mg every 6 hrs. Hope this helps  The lidocaine cream is by tylenol and is available in a large tube on Amazon or at Walmart 
    • xxnonamexx
      What are your daily meals? Guilty pleasure snacks? Protein bars? I feel when looking for gluten free foods they are filled with sugar cholesterol. Looking for healthy gluten-free protein bars. Something to fill since sometimes I feel like not to eat anything. Especially if on vacation and unsure of cross contamination I figure go with a salad and protein bar to fill and play it safe.
    • trents
      Unfortunately, there is presently no test for NCGS. Celiac disease must first be ruled out. NCGS is thought to be much more common than celiac disease. We know that celiac disease is an autoimmune disorder but the mechanism of NCGS is less clear. Both call for an elimination of gluten from the diet.
    • Seabeemee
      Thanks for your reply Trents…most appreciated.  I am unfamiliar with celiac labs terminology so I wanted to know if the presence of HLA variants (DA:101, DA:105, DQB1:0301 and DQB1:0501) that the labs detected had any merit in predisposing one to be more sensitive to gluten/carbs than the general population?  Also,  I found what you said about NCGS very interesting and I appreciate you mentioning that.  I’ve worked hard to research and advocate for myself with my Hematologist and now with a new GI, since my bowel surgery and to maintain my Vitamin B12 health concurrent with keeping my levels of Iron in the optimal range. I’ve been tested for SIBO (do not have it), biopsy showed negative for HPylori, and have had Fecal studies done (nothing showed up) and I understand how a loss of a large amount of bowel could be highly impacting re: SIBO, malabsorption and motility issues. So I’ve managed pretty well diet and elimination-wise until just recently. That said, this new problem with extreme bloating, distention and upper girth, NAFLD just occured over the last 4 months so it is new for me and I thought celiac might be a possible issue. I’ll probably just continue on in this less gluten/carbs seem to be better for me and see how reintroducing certain foods go.  Thanks again.    
×
×
  • 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.