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

Psoriasis And Dh


krisb

Recommended Posts

krisb Contributor

For a few years now I was told I had psoriasis. Is it possible for a DR. to not recognize DH and think it's psoriasis? I have it on my elbows, some on my fingers and toes. It's so itchy it makes me nuts. It's the bumps like the pics I see. It's just not horribly bad looking all the time.


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



Celiac.com Sponsor (A8-M):



frenchiemama Collaborator

Well, my DH was "diagnosed" as:

- foliculitis

- staph infection

- eczema

- "some kind of dermatitis" (at least that one was close)

and of course my personal favorite:

- a physical reaction to mental distress (ie, I'm crazy and it's all in my head)

I could imagine that DH could be misdiagnosed as psoriasis. However I believe that psoriasis is an autoimmune condition too, I guess it's possible to have both, or to have celiac disease and psoriasis. I actually do have eczema on my fingers as well as DH. You should get a biopsy to be sure.

bluelotus Contributor

I have psoriasis on my knees, elbows, and toe nails.....when it gets on the nails, its gross, kind of looks like fungus, but I had a clipping sent off to a lab 2x to be sure. The itchness will flare up once in a while, but most of the time it just looks like paler, slightly bumpy spots on my elbows and knees. Almost forgot, I get it on my scalp too, and it feels bumpy and itchy, though doesn't flake much. I have never seen DH, so I hope my description of my experience helps some......

lovegrov Collaborator

I've had both and they looked nothing alike on me.

richard

gf4life Enthusiast

I have both too. I agree with Richard, mine looked totally different. My psoriasis is getting worse since going gluten-free, which is frustrating for me. I was hoping it would get a bit better, but no. :(

My psoriasis is like white flaky skin all piled up, layer upon layer. When I soak it and brush it off the skin underneath is red and smooth, and very tender. It will bleed if I am too vigorous with the cleaninf off the dead skin. It does itch, but not as bad as the DH. I have it on my knee, ankle, above one toe, scalp and elbow and sometimes get the pain in the elbow joint that is compared to arthritis. It is a pain in the you know what. On my scalp is the most frustrating. It is hard to scrub off. If I wash my head daily with shampoo it dries out, itches more, and looks like I have dandruff really bad. If I go more than 2 days without shampooing, then my head is so greasy it is disgusting. What is the worst is when I have both the psoriasis and the DH going at the same time on my scalp!

My DH looks like red bumps and they blister and itch. Then I scratch them and they take forever to heal, since they keep itching and I keep scratching them open... Sometimes I only have a few, sometimes a cluster. Not very often anymore. Only if I get glutened by accident!

God bless,

Mariann

krisb Contributor

My DH looks like red bumps and they blister and itch. Then I scratch them and they take forever to heal, since they keep itching and I keep scratching them open... Sometimes I only have a few, sometimes a cluster. Not very often anymore. Only if I get glutened by accident!

quote]

It looks sort of like dead skin with red bumps on it. They look like hard blisters. The bumps itch so much and I scratch them open also. I will wake up at night scracthing so much. I've tried different steroids, light therapy, and moisturizer and it never helps. Actually, it looks so much better since I started the gluten-free diet a week ago. I'm assuming it has to be active to get a biopsy right? When I get them on my fingers and toes it's just the bumps. The skin isn't dry around it. It's just a few very itchy bumps. Enough to drive me nuts.

Does sporiasis get bumps also?

gf4life Enthusiast
Does psoriasis get bumps also?

Mine doesn't.

The DH I had when I was still on gluten was losts of small red bumps and blisters on my hands and it itched and was also very painful! I was so glad to get off gluten and it went away. My palms felt like a thoughsand needles were pricking them.

If it were me, I would have a dermatologist (preferably a different one) re-evaluate the psoriasis. You could have both and maybe the DH was popping up through the psoriasis patches? Seems weird, but you never know.

I think your DH has to be active to be biopsied, but I am not sure. I couldn't get to a dermatologist fast enough and you couldn't pay me enough to have stayed on gluten for one more day! I don't know if they have tests for psoriasis. I was diagnosed by the doctor just looking at the patches and occasionally they giove me a different cream for it. None of them seem to work very well. My BIL has psoriasis really bad and he gave me some of his new creams that his doc prescribed. If they work I will ask my doc for some, but so far they only temporarily moisturize the areas and then a few hours later they are dry again and all white and itchy...

Also I have heard others say that their psoriasis got somewhat better when they went off gluten. So I'm crossing my fingers for you! :D

God bless,

Mariann


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



Celiac.com Sponsor (A8-M):



krisb Contributor

Mine doesn't.

If it were me, I would have a dermatologist (preferably a different one) re-evaluate the psoriasis. You could have both and maybe the DH was popping up through the psoriasis patches? Seems weird, but you never know. ]

I had an allergist diagnose it before this celiac diagnoses came about. I never brought it up to a dermatologist. I guess we will see if it completly goes away on gluten free. Then I will have an answer.

jenvan Collaborator

Mariann-

AH! I so relate on the psoraisis...mine has gotten worse since going gluten-free. I can't figure out why. Perhaps my body has more energy to attack my scalp now that it isn't attacking my intestines? I pretty much have it within my hairline...but I worry it will take off in other places. My father has had it terribly all over his body for years. I wish there was a better treatment for it. I am looking into alternatives. I read about some who got rid of their's with the SCD diet...

gf4life Enthusiast

krisb,

You might want to see if you can get to a dermatologist. There are so many different skin conditions out there, it could be that you have something completely different that either DH or Psoriasis.

jenvan,

If you decide to try the SCD diet and it works for you, then let me know. I did wonder if because I am eating more starchy grains now if that might be making it worse...or maybe it is like you said, my body had more energy to attack its skin instead of the intestines! :blink: I might look into the SCD diet, but I am just not in the dieting mood. It is so much work providing 4 out of 5 in the family with gluten-free meals, and making my husband his separate meals, not to mention the rest of my life getting in the way! I am lucky if I have time to eat anything, but to try to eat gluten-free AND follow a diet just seems overwhelming to me right now...

God bless,

Mariann

jenvan Collaborator

I'll keep you posted Mariann....

krisb Contributor

What is the SCD diet?

If you decide to try the SCD diet and it works for you, then let me know. 
jenvan Collaborator

Kris-

Go here to read a great summary of the diet: Open Original Shared Link Basically, it is a more restrictive diet for those with crohn's ibd, unresponsive celiac...some parents put their children on it as a treatment for autism as well. It is a more restrictive diet than going just gluten-free, but has helped many people apparently, as well as quite a few on this board. You can also view the book on amazon .com and read all the success people have had on it.

Go here to read an ongoing discussion here for those on the SCD: Open Original Shared Link

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. - Churley replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      10

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    3. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    4. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      20

      Insomnia help

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

    • Total Members
      133,348
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Churley
      Have you tried Pure Encapsulations supplements? This is a brand my doctor recommends for me. I have no issues with this brand.
    • asaT
      plant sources of calcium, such as spinach, have calcium bound to oxalates, which is not good. best source of calcium is unfortunately dairy, do you tolerate dairy? fermented dairy like kefir is good and or a little hard cheese. i do eat dairy, i can only take so much dietary restriction and gluten is hard enough! but i guess some people do have bad reactions to it, so different for everyone.  
    • asaT
      i take b12, folate, b2, b6, glycine, Nac, zinc, vk2 mk4, magnesium, coq10, pqq, tmg, creatine, omega 3, molybdnem (sp) and just started vit d. quite a list i know.  I have high homocysteine (last checked it was 19, but is always high and i finally decided to do something about it) and very low vitamin d, 10. have been opposed to this supp in the past, but going to try it at 5k units a day. having a pth test on friday, which is suspect will be high. my homocysteine has come down to around 9 with 3 weeks of these supplements and expect it to go down further. i also started on estrogen/progesterone. I have osteoporosis too, so that is why the hormones.  anyway, i think all celiacs should have homocysteine checked and treated if needed (easy enough with b vit, tmg). homocysteine very bad thing to be high for a whole host of reasons. all the bad ones, heart attack , stroke, alzi, cancer..... one of the most annoying things about celiacs (and there are so many!) is the weight gain. i guess i stayed thin all those years being undiagnosed because i was under absorbing everything including calories. going gluten-free and the weight gain has been terrible, 30#, but i'm sure a lot more went into that (hip replacement - and years of hip pain leading to inactivity when i was previously very active, probably all related to celiacs, menopause) yada yada. i seemed to lose appetite control, like there was low glp, or leptin or whatever all those hormones are that tell you that you are full and to stop eating. my appetite is immense and i'm never full. i guess decades or more ( i think i have had celiacs since at least my teens - was hospitalized for abdominal pain and diarrhea for which spastic colon was eventually diagnosed and had many episodes of diarrhea/abdominal pain through my 20's. but that symptom seemed to go away and i related it to dairy much more so than gluten. Also my growth was stunted, i'm the only shorty in my family. anyway, decades of malabsorption and maldigestion led to constant hunger, at least thats my theory. then when i started absorbing normally, wham!! FAT!!!    
    • nanny marley
      Great advise there I agree with the aniexty part, and the aura migraine has I suffer both, I've also read some great books that have helped I'm going too look the one you mentioned up too thankyou for that, I find a camomile tea just a small one and a gentle wind down before bed has helped me too, I suffer from restless leg syndrome and nerve pain hence I don't always sleep well at the best of times , racing mind catches up I have decorated my whole house in one night in my mind before 🤣 diet changes mindset really help , although I have to say it never just disappears, I find once I came to terms with who I am I managed a lot better  , a misconception is for many to change , that means to heal but that's not always the case , understanding and finding your coping mechanisms are vital tools , it's more productive to find that because there is no failure then no pressure to become something else , it's ok to be sad it's ok to not sleep , it's ok to worry , just try to see it has a journey not a task 🤗
    • nanny marley
      I agree there I've tryed this myself to prove I can't eat gluten or lactose and it sets me back for about a month till I have to go back to being very strict to settle 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.