• Ads by Google:
     




    Get email alerts Celiac.com E-Newsletter

    Ads by Google:



       Get email alertsCeliac.com E-Newsletter

  • Announcements

    • admin

      Frequently Asked Questions About Celiac Disease   09/30/2015

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to FREE Celiac.com email alerts What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease? - list blood tests, endo with biopsy, genetic test and enterolab (not diagnostic) Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet Free recipes: Gluten-Free Recipes Where can I buy gluten-free stuff? Support this site by shopping at The Celiac.com Store.

DH Photo Bank
2 2

134 posts in this topic

Oh my goodness! I had the 'flesh eating' lesions on my lower belly. I really think it was several lesions side by side that just grew into each other. They have healed and now are the dark purple color.

I know you have been so strict on being gluten-free, I want to cry for you! Do you think your doctor will order light therapy for you?

Wish you could take Dapsone or maybe the topical? I think I'll have my niece take photos of my healed skin after being on Dapsone since 10/20/12. So sorry for you. . . . :(

Thanks dear. I doubt a GI has any clue about light therapy. And yes, sometimes you get the flesh eaters where you get 2 or 3 next to each other & then they all grow together to make one huge lesion.

Maybe the topical Dapsone..... I don't know. Just have to talk to him & see.

My other worry is that if I go the Tetracycline route that I am deathly allergic to Penicillin & what if I develop an intolerance to tetracycline? If I get really sick & need it then I won't have any options left to me.

There are time that .38 is looking better & better.

0

Share this post


Link to post
Share on other sites
Ads by Google:
Ads by Google:


There are time that .38 is looking better & better.

Hope we're talking about a bigger bra here :D

0

Share this post


Link to post
Share on other sites

There are time that .38 is looking better & better.

Oh Squirmingitch ... put those thoughts way out of your mind! The topical Dapsone is ACZONE® and you may want to research to see if your doctor will prescribe it for you.

When I asked for Dapsone, I mentioned the topical to my PCP and she didn't seem to recognize the name. Since she agreed to order Dapsone, I didn't press her further about the topical med.

Your GI may not be familiar with light therapy but I know the Derms do. Hang in there! Prayers and ((hugs)) to you.

0

Share this post


Link to post
Share on other sites

Continuing the progression of the lesions. These photos were taken today. They were much angrier looking a few days ago --- lobster red, but I could not bear to take photos of them at that point. They have been terribly painful & remain so. I have found the best thing at this point is Vaseline. And ice packs. But one can not spend all day laying on ones back with ice packs on. Life goes on & food needs to be prepared, groceries need to be gotten etc.....

I would add that these photos disprove those texts which say the lesions last a couple/few days. WRONG. Sometimes they do --- maybe in the beginning or very mild flares but an individual lesion can last for a full month or more. Also those texts that state that dh has to be blisters. WRONG. Some of what you see began as blisters, some did not --- those were the "bite" kind --- but undoubtedly ALL dh.

This first one is what the flesh eater has turned into.

8434301996_77bc217692.jpg

This is what my front looks like now.

8433219679_38c3911b4f.jpg

This is the underside of my breast.

8434308572_53555972e5.jpg

0

Share this post


Link to post
Share on other sites

Oh man!! I look at these pictures and can't begin to imagine what that feels like :unsure: I will never complain about my psoriasis again, I promise.

0

Share this post


Link to post
Share on other sites
Ads by Google:


Squirmy . . . I can tell they are healing. Pray it continues to heal and quickly! I understand about the allergy to penicillin and needing a fall back drug, for an emergency. My Gpa, Dad, siblings and now my nephew is allergic to penicillin. My Gpa was given it, in error while admitted to hospital for pneumonia and died in 1963. :(

Hang in there!

0

Share this post


Link to post
Share on other sites

Wow, finally I find someone who has it as bad as I do/did. I am/was covered from head to toe. So bad I kept myself covered unless I was at home and even then my daughter couldn't stand to see it and avoided me a lot of the time. It is now going away. I had a dermatologist who was very helpful with the itching part by putting me on Gabbapentin which lowered the nerves reaction to wanting to itch. It worked for me at least.

0

Share this post


Link to post
Share on other sites

I have a patch of my finger that looks pretty much exactly like yours dani, except even smaller. It came acouple weeks ago, got super itchy, then went away and is coming back again. I am not diagnosed with dh, but I haven't had it checked out either. It's not bothering me much.

My sister, whose bloodwork is negative for celiac disease, has had eczema as long as I can remember, and I think my finger looks very much like her rashes. Of course this isn't definitive, I still think my sister's a celiac.

I also get noticeable blisters (hardly noticeable on my fingers but they're definitely there) on my forearms. That's been around for a couple of years, and they itch pretty bad, but I've never had them clump.

Now I do have dandruff that itches pretty badly and it has gotten worse after getting a bit better. I've had that for decades though, never really went to someone to talk about it or look into it. And I did get a rash on the back of my neck after eating nuts that I'm guessing had cc. (I also had an immediate burning reaction in my mouth and then nerve pain in my teeth/gums for prolly a week after.) But the rash on my neck honestly wasn't that itchy even though it was by far the largest patch of affected skin I've had. It did make its way to the back of my ears and they itched, and moved up a bit into my scalp which also itched for a couple weeks, but when that happened the skin just looked dry, no blisters anymore.

"Skin was very prickly and burned, did not like having anything touch it"

This is familiar to me. I randomly get patches of skin that will get very sensitive when anything touches it, and the skin's response to being touched just didn't feel normal aside from the burny, uncomfortableness. Of course I've never had my entire body feel like that, and no rash has ever happened afterwards. But since my finger has decided to break out again, when I touch the skin it feels like there's a coating on it, something that makes the sensation of touch on it muffled. But I never had the sensitivity that I've gotten before. I figured since I have peripheral neuropathy that my patches of skin were a nerve issue of celiac disease or just something else entirely, not a skin issue. Perhaps there is some overlap here that doctors are missing, skin has neuronal receptors.

I would not be very happy with a diagnosis of the eczema of unknown cause. Like getting diagnosed with IBS. It's only useful if they figure out what causes it or gets rid of it.

I feel so bad for all of you who have such bad rashes!

0

Share this post


Link to post
Share on other sites

I thought that a thread containing a collection of the different shapes and forms of DH could be helpful to people looking for something to compare their own rashes with. So go ahead and post your rashes here to help others find a point of reference. Please add associated symptoms and a short history.

I am however doubtful of this idea being a good one because some people might add photos that are not related and confuse people who are new to all this. I hope it will be ok and if it's not then it's ok to delete this thread and I apologize in advance ;-)

Since I haven't seen a rash that is milder than mine I think that it's actually a proper coincidence that mine is the first one :-)

These images were taken when the rash was in it's mildest form. It has sadly developed since these photos were taking, and gets pink swollen bumpy areas under the blisters. It is also starting to spread to the next finger and on the webbing between my fingers.

The rash used wake me up at night with a blistery, throbbing, itching, and burning finger when I used to consume gluten. Now it mostly burns whenever it shows up with very mild itching. The water in the blisters is clear.

http://rainytown.se/images/external/20120524_065253.jpg

http://rainytown.se/images/external/20120524_065311.jpg

http://rainytown.se/images/external/20120524_065505.jpg

Important: Please note that I'm self-diagnosed, meaning this rash is based on my own speculations based on my symptoms all put together.

That is NOT DH.

0

Share this post


Link to post
Share on other sites

That is NOT DH.

And that is NOT HELPFUL. Would you be so kind as to explain your reasoning.

0

Share this post


Link to post
Share on other sites

That is NOT DH.

 

It looks quite mild, but it certainly could be DH.  I get blisters and red spots on my fingers all the time.  The blisters are sometimes very small, just pore sized.  Stingy, burny, itchy and blisters sounds a whole lot like DH to me.

0

Share this post


Link to post
Share on other sites

My finger looks almost identical to the OP Carybear. The rash on my finger has since improved and gotten worse a few times, and the blisters have gotten bigger, and the blisters look like this when a tad larger.

http://dermatlas.med.jhmi.edu/image/Dermatitis_Herpetiformis_4_030330

 

The dry, peeling skin is what comes afterwards, and yes, that's what's most prominent in the photos daninero posted, and I agree, that doesn't look like DH to me either.

0

Share this post


Link to post
Share on other sites

Hi

I have what I call 'classic DH' with lesions like Sqitch (sorry about that abbreviation :D) on scalp and just occasional on shoulder blades and buttocks. (Used to have it very badly on all three of those places) and have scarring to this day on back and buttocks. Astonishingly symmetrical! Lesions on scalp vary in severity but never gone and worse for iodine and thyroid meds. 

Anyway - dani nero's finger pics got me wondering because I get that and have had it on underside of forearms. Extremely itchy and I have always assumed it was Contact Eczema that arrived out of the blue at intervals. Now I'm wondering if it's a variation of DH!!

0

Share this post


Link to post
Share on other sites

I'm a newbie, I love this site! I can relate to everyone, most post are from last year. Are y'all still post here?

I use Clobetasol Propionate cream it really helps.

0

Share this post


Link to post
Share on other sites

That is NOT DH.

 

Oh my . . . Carybear, you do not have DH?  I would like to know how you diagnosed by the picture too.  Just curious.   :rolleyes:

 

I have been diagnosed with DH with 2 doctors in agreement and the rash on my hands looked exactly like 'Dani' presentation.  The blisters on my hands were extremely small, fluid came out after scratching and they eventually had the peeling dry skin.  The sting, itch and burning was intense!  I don't have a photo of my hands but wish I did so I could post.  BTW, I don't think any of us can diagnose anyone. . . just able to offer ideas and such.

 

To anyone interested. . . my skin was almost healed after being on Dapsone and I was so happy.  I decided to try to stop the Dapsone to see if I could just depend on the gluten-free diet.  After 2 weeks . . . I found out just how much the medication helps.  I am now  back on it but suffering with a renewed breakout on my stomach, lower back and buttocks.  Actually the breakout is in the same places that had been healing.   :(

0

Share this post


Link to post
Share on other sites

Hi

The only time mine vanished (to my surprise) was when I had a course of strong antibiotics and steroids to treat a bad chest infection. It came straight back afterwards (this was over 20 years ago). 

It was somewhat helped by a long course of oxytetracycline antibiotics (sp?) prescribed for it by doc who said it was infected skin (?????????). Came straight back after and a second course had negligible effect. (Again, this is years ago)!

0

Share this post


Link to post
Share on other sites

that's what mine looks like. I had one on my bottom and that's what was biopsied last week. results aren't back yet but I've been gluten free since July so it could be negative. My derm said visually it does look like DH. I also had a cluster on my thigh and now I'm left with the marks, taking forever to heal.

0

Share this post


Link to post
Share on other sites

Ok, I'll add mine:

This first one is February 2013, right after my first biopsy:

P1130004_zpsc2d1f767.jpg

This is late March 2013:

Photoon3-28-13at1102AM_zpsa1ba4d32.jpg

And this is what it turned into by Summer 2013:

Photoon8-20-13at122PM_zps88304470.jpg

It's alarmingly symmetrical, with the right side being somewhat more impacted:

Photoon8-20-13at121PM_zps7511c9f2.jpg

0

Share this post


Link to post
Share on other sites

oh gosh abby that looks painful. mine is only a few spots here and there.

0

Share this post


Link to post
Share on other sites

oh gosh abby that looks painful. mine is only a few spots here and there.

It's pure misery. :(

For three years, my rash was just a few spots (like in the first picture). Then it just exploded this year and is taking it's sweet time calming down.

0

Share this post


Link to post
Share on other sites

It's pure misery. :(

For three years, my rash was just a few spots (like in the first picture). Then it just exploded this year and is taking it's sweet time calming down.

Oooo ItchyAbby it really does look very red and angry, no wonder you say its pure misery it must drive you absolutely nuts,

at the moment mine are on the back of my legs and over my derrière too so I can't really photo those, but they are at that sore stage now,

The Gastro Doctor wanted to have a look at my rash,

but when I told him It was covering the back of my legs by my buttocks he chuckled and swiftly changed his mind

I guess some Doctors are still embarrassed about stuff like that , I would have shown it to a medical audience if they would have done the biopsy for me :P

but It just seems so difficult to get biopsied in the UK

0

Share this post


Link to post
Share on other sites

that's what mine looks like. I had one on my bottom and that's what was biopsied last week. results aren't back yet but I've been gluten free since July so it could be negative. My derm said visually it does look like DH. I also had a cluster on my thigh and now I'm left with the marks, taking forever to heal.

What a great dermatologist you have, no one has even suggested a biopsy for me at all ,

I think I may have to pay a private dermatologist to get a biopsy, but I wouldn't know where to start ,

Good luck with your biopsy, hope you get some answers,

Please let us know how you get on

0

Share this post


Link to post
Share on other sites

Abbster,

 

Just know that we are all here to help you get thru this !!!  I hope you are able to see some improvement as quickly as possible.  I see more baths and foot rubs in your future :D

 

All my best,

 

Colleen

0

Share this post


Link to post
Share on other sites

Hey Abbs,

 

I was researching DH this morning and I came across a guy named Jean-Paul Marat.  He lived in the late 1790's.  Anyway, It was the opinion, after his death, that he was suffering with a horrid case of DH.  He was a Doctor himself. Of course little was known about Celiac/DH so diet change was never a concern.  I was reading that he spent most of his life in bathtub with soothing herbs and a wrap around his head.  I tried for the life of me to find the herb mixture he used but no luck there but he used a cloth soaked in vinegar around his head to control itching there.  So I was thinking that maybe you might want to trial using a cloth and laying it on one of your areas of DH for itch control.  I don't know how practical that would be for you but I wanted to mention it anyway.

 

Colleen

0

Share this post


Link to post
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!


Register a new account

Sign in

Already have an account? Sign in here.


Sign In Now
2 2

  • Forum Statistics

    • Total Topics
      106,795
    • Total Posts
      932,489
  • Member Statistics

    • Total Members
      64,281
    • Most Online
      3,093

    Newest Member
    Michaeldp
    Joined
  • Popular Now

  • Topics

  • Posts

    • Sounds like gluten ataxia, or the form of celiac I have where it also attacks my nervous system and brain. I would get a celiac test if I was you, you have to be eating at least half a slice of bread or a few crackers for 12 weeks before hand and go to your doctor and ask for a full celiac panel. From there you need to be eating it for still and get a endoscope with biopsies to check for intestinal damage. Now to help with the mental issues I will tell your right now a good b-vitamin supplement will help you with the fog and depression a bit. I suggest Liquid Health Stress & Energy and the Neurological support one. Take 1 tbsp each 3 times a day. You will notice a huge difference in it. Being liquid it is easier absorbed by your body, if you have celaic then your intestines will also be damaged making where getting these nutrients is more difficult for you body. NOW as to the cheesy bread I hear you on that. I love eating Juilans bakery toasted read with dayia cheese on it.... I was using hte provolone for awhile but am now using the almond bread with daiya dairy free swiss. Love a good cheesy toast and egg white open sandwich with some avocado myself. I also posted a recipe in the baking section where you melt the daiya dairy free cheese shreds and mix them in with the flour blend I use that is gluten-free and make cheesy bread rolls out of them. I have a garlic and cheddar one.....you name just inspired the idea of using a bit of turkey bacon in the cheddar biscuit version.....would be epic
    • I have used Voltaren before, and I experienced that little rush afterward. I never had any reaction to it, and I can't even use makeup that has wheat germ oil in it. I have also had some fairly violent reactions to other medications. That little rush faded after a while, but after an increase in the strength of the gel I did feel it again for a day or two. So from my perspective, it should be ok.
    • I know some people who have tried straw bale gardening, especially for strawberries. I don't know anyone that has had much success with it. All of them thought it was more trouble than it was worth.
    • Hello everyone! This site is awesome! I've been experiencing anxiety, depression and an over all since of non well being. Although I have been going through some rough times but this has lasted for 6 long months. My I've had many blood tests done and this one was concerning me. My CBC iron panel thyroid panel and all others have come out just fine. Does anyone have insight on the following results. Please help and thank you! I also tested positive for some Corrine food allergies. IgE Food w/Component Reflex II Immunoglobulin A, Qn, Serum 435 HIGH   Ref Range: 90-386 mg/dL t-Transglutaminase (tTG) IgA <2 Ref Range: 0-3 Negative 0 - 3 Weak Positive 4 - 10 Positive >10 . Tissue Transglutaminase (tTG) has been identified as the endomysial antigen. Studies have demonstr- ated that endomysial IgA antibodies have over 99% specificity for gluten sensitive enteropathy. Endomysial Antibody IgA   Negative     Ref Range: Negative 
    • Hi,   my history is the following: I used to eat a lot of foods with gluten & cheese together. They would make me seriously happy and and I was extremely content just eating a pizza and bread with cheese and things like this... Now obviously I'd have cycles... where I eat tons of gluten/cheese foods in combination... feel super content and thats it... Then the effects would wear off and I had to start a diet.. where I'd do modified versions of fasting or so for a few weeks... During that phase I'd get very depressed... but after a few weeks of no-gluten... I'd eat bread with cheese again and I felt like I was in heaven. I'd get extremely high from this stuff... like seriously I'd feel amazing... (I guess it's the morphine like effects of this foods)  but after some when I hit age 22 or so I started to get serious trouble... ....   I started getting serious neurological issues from it... like I could't put my words together... I'd have paranoia & feel like everything is unreal... I've been diagnosed with numerus psychiatric issues since then... My main problem right now is that my brain isn't functioning... I can't comprehend what people are saying and when I want to say something my words don't come easily... Like if I am in a conversation for a longer time this issues is barely noticable at all... But if I wake up... and I try to talk... there's no way.. if I haven't talked for a while it's like you could ask me and I couldn't comprehend what you say and couldn't put my words together in the way I'd like to... I feel kinda stupid sometimes... because I know I'm rather smart but when I have a conversation my speech seems very unsophisticated... --- I tried to change my diet.. with varying success... like I would feel great in the morning and feel completely depressed in the evening for no apparent reason whatsoever... at all! And I feel I can attribute this to traces of gluten which feels like this:   ---- When I have traces of gluten inadvertently... I suddenly feel like everything is kind of unreal around me... I feel depressed in a "opiate withdrawal" kind of way... I don't know how to explain it... it's just painful in the sense that I can't just enjoy having a conversation... like I have a conversation but I don't feel "the thrill"... everything is totally bland and I just feel depressed in the background... like I don't want to do anything and no matter what I do.. it feels completely pointless because I can't comprehend why I suddenly feel this way...    And it's not like I feel this way 24/7... that's the thing... it comes and goes and comes and goes... sometimes I feel completely fine in the morning or even for 2 days or so.... and then I feel completely like s$#& and devoid off all satisfaction for 3 days where I feel I'm going completely crazy & I can't talk.. can't comprehend... feel super weird when talking to people... and then the next days I just feel suddenly "normal"... like this relaxed and easy-going feeling in your body and wanting to be social and to communicate and just have fun... but then... when I eat some food and I feel it has gluten.. it hits me in a subtle way... where I suddenly loose all joy in life for days... and then it just dissapears... I've been struggling with this for years now and I can't seem to comprehend or get on top of this issue... Do some of you guys have similar experiences?        
  • Upcoming Events