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

Thoughts On These?


Jdorrferball

Recommended Posts

Jdorrferball Rookie

I posted several months back about myself and concern over possible celiac. I still don't have any definitive answers from a doctor but I DO know for certain that gluten is my enemy :)

Now I have some concerns about a rash that my daughter has. It is different than the rash I have but it's widespread and terribly itchy for her. Wondering if y'all could give me your thoughts on some pics :)

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

This rash in the pics is her back and just above her rear end. She also has this rash on her stomach, around the underarms on the back side, and on her forearms and elbows. She has an appointment with a dermatologist in 10 days but thought I would ask you real experts first! I don't want to mention the possibility of DH if the doc is gonna think I'm nuts. I just have this gut feeling about her. She is one of my children who threw about after going back on gluten after a gluten free trial. Thanks for any help y'all can offer :)


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



Celiac.com Sponsor (A8-M):



squirmingitch Veteran

First, I am no expert. I can share with you what I have learned. 

I do not understand what you mean when you say "she is 1 of my children who threw about after going back on gluten after a gluten free trial". What is threw about? 

As to the photos...... could dh look like that? Yes. Can many other skin conditions look like that? Yes.

You haven't given us much info. to go on. You've posted the photos & told us it's terribly itchy for her & where it appears on her. 

Is she gluten free? Has she been on any antihistamines to determine if it's an allergy or otherwise resolves with antihistamines?

I'm sorry, but I don't remember your story, your history at all.

Finally, she is your daughter & you call the shots in the docs office. The doctor works for you. You can tell him that YOU want him to do a dh biopsy on her. Do you really care if he thinks you are nuts? This is your daughter we're talking about & as long as your insurance will cover the cost of the biopsy & lab for it or you are willing to pay for it yourself if insurance will not cover it then what reason can the derm have for refusing to do a dh biopsy? You can tell him/her that if they refuse then you will go elsewhere.

Jdorrferball Rookie

Sorry...it should say she was one of my children who threw up, not threw about. Her primary care doc put her on oral steroids to see if they would help. At the time she only had the rash on her stomach. The steroids helped a tiny bit. When the ten days on the steroids were up, the rash came back worse and in places she didn't have it before...life her forearms and elbows. She is not gluten free at this time.  You are right I do call the shots and it is my child. I'm also the mother of a special needs child who was made to feel like an idiot over and over again for a long time. No one would believe me when I knew in my gut there was something terribly wrong from birth. Turns out I was right. Guess I'm still a little sore after being treated like a fool for so long. Thanks for your help :)

squirmingitch Veteran

I'm so sorry you had to go through that with your special needs child! (((HUGS))) That has to be a horrible thing for a parent to have to endure when you know you're right.

And not being in your position, it's easy for me to say this, but I would tend to think that experience, as awful as it was, would make you more determined to not let them treat you that way again or to allow them schluff off what you as a mother feel in your gut. Believe me, I'm not honking on you! And I greatly sympathize with the position you're in but maybe you can be a bit more assertive?

 

Okay, on to your daughter. Next question --- how long has it been since she went back to eating gluten? When she went back on gluten, how long did the vomiting last? 1 day, 2 etc...? Did she have any other symptoms besides vomiting when she went back to gluten? Also, how long had she been off gluten?

 

I don't understand why the doc put her on oral steroids. To stop her vomiting? Or did it have to do with the rash? How long has she been off the oral steroids? The fact that the rash flared like it did when she went off the steroids is very telling. Have you tried antihistamines to see if they make the rash go away or if they help with the itch?

 

It's good that she is eating gluten now. For a dh biopsy, she will have to have been eating gluten for 2 months prior but the glitch is that she also needs to have been off the steroids for at least 2 months & that would include topical steroids. And don't let any doc tell you otherwise! You don't want to walk away with a false negative.

 

Is anyone in your family dx'd celiac? If they are, that will help when you talk to the doc.

 

I certainly would get her rash biopsied for dh! How old is she? And before she went gluten free for that trial, did she have rash or any celiac GI symptoms?

 

Do you know how the biopsy for the dh rash is properly done?

Jdorrferball Rookie

Okay let's see... She is 9 1/2 with no real digestive complaints. She has been eating gluten for several months (August I think) and was only gluten free for about two weeks before my husband gave her and the other children gluten "without thinking about it". She only threw up once and had a headache for a couple of days. She has always had some problems with what we thought was eczema off and on since she was around 3. For as long as I can remember she has had rough feeling skin on her stomach.

A few months back the "eczema" started looking different and was on her stomach which was new. Made her an appointment right after Christmas and she was given the oral steroids because it was too widespread for topical. The steroids helped a little but by no means got rid of the rash. A matter of days after she finished them the rash popped up in new places and was worse looking than in the pics I posted. Those new areas on her forearms and elbows are actually cleaning up right now.

We don't have any diagnosed celiacs in my family. The short version of my history is: diarrhea for four years starting right after giving birth on 2009, lifetime of migraines, tired with a general vague unwell feeling as far back as I can remember, perforated colon while pregnant in 2013, told I have Crohn's disease following surgery for the perforation, weird rash started a few months after surgery that comes on when I eat gluten and goes away when I don't.

I think I know how the biopsy has to be done: next to the effected area, must be eating gluten, and at least a couple months after finishing the steroids. Is that right? Thank you so much!

squirmingitch Veteran

OK! Looks like she's going to be just shy of 2 months off the steroids when she has the appointment. I'd say it's a good chance that she actually does have dh. I hope you can get a proper dx. Yes, you have the right of it for how the biopsy is taken. She very well could have had eczema as skin conditions are common with celiacs but you see her everyday & know your child & if it took on a different look then I believe you. Do you have photos of what the rash looked like when it flared right after she got off the steroids? If so, they would be great to print out & take to the derm with you. And take these photos too. You need something for the derm to see. And that brings up a potential problem..... if she doesn't have any places -- fresh, new, active places, then the derm won't have anything to biopsy. You'll have to wait until she has something to biopsy which is going to be a PITA but you gotta do what you gotta do right? 

 

Now that you reminded me of your history I am remembering. You were likely triggered by the pregnancy in 2009. Ahhh yes, the stupid rash that makes getting a dx so very, very difficult. :ph34r:  :ph34r:

 

Hopefully, you can get to the bottom of it with your daughter. Let us know please how things go. 

squirmingitch Veteran

BTW, how are you doing? Are you managing okay not getting cc'd with gluten eaters in the house? And how are you feeling these days? Things getting better?


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



Celiac.com Sponsor (A8-M):



Jdorrferball Rookie

I'm doing pretty well. Thank you for asking! I have had some back and forth periods of eating gluten. Had a heart attack in September that took us completely off guard. Turns out it was caused by a tear in one of my arteries. Nothing at all to so with cholesterol and such. In fact my cholesterol is only 80!!

Being gluten free does bring me a lot of improvement...no headaches, no bloating, more energy etc. However the diarrhea is not resolved, at least not entirely.

squirmingitch Veteran

I'm so sorry to hear about the heart attack. Must have scared the living daylights out of all of you! 

 

Stay the course with the gluten-free; it takes a long time for some to heal. You also may have some other issue but stick with the gluten-free & see how it goes & then you can start running down the cause if things don't improve.

 

Wishing you all the best & I mean it when I say let us know what happens with your daughter.

Jdorrferball Rookie

I will DEFINITELY let you know. Thanks so much for all of your help and kind words!!

squirmingitch Veteran

YVW. I'm happy to do it. :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,979
    • Most Online (within 30 mins)
      7,748

    volivier
    Newest Member
    volivier
    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

    • trents
      @Riley, on this forum we sometimes get reports from people with similar experiences as you. That is, their celiac disease seems to go into remission. Typically, that doesn't last. At age 18 you are at your physical-biological peek in life where your body is stronger than it will ever be and it is able to fight well against many threats and abuses. As Wheatwacked pointed out, absence of symptoms is not always a reliable indicator that no damage is being done to the body. I was one of those "silent" celiacs with no symptoms, or at least very minor symptoms, whose body was being slowly damaged for many years before the damage became pronounced enough to warrant investigation, leading to a diagnosis. By that time I had suffered significant bone demineralization and now I suffer with back and neck problems. Please, if you choose to continue consuming gluten, which I do not recommend, at least get tested regularly so that you won't get caught in the silent celiac trap down the road like I did. You really do not outgrow celiac disease. It is baked into the genes. Once the genes get triggered, as far as we know, they are turned on for good. Social rejection is something most celiacs struggle with. Being compliant with the gluten free diet places restrictions on what we can eat and where we can eat. Our friends usually try to work with us at first but then it gets to be a drag and we begin to get left out. We often lose some friends in the process but we also find out who really are our true friends. I think the hardest hits come at those times when friends spontaneously say, "Hey, let's go get some burgers and fries" and you know you can't safely do that. One way to cope in these situations is to have some ready made gluten-free meals packed in the fridge that you can take with you on the spot and still join them but eat safely. Most "real" friends will get used to this and so will you. Perhaps this little video will be helpful to you.  
    • Wheatwacked
      @Riley., Welcome to the forum.   It was once believed that Celiac Disease was only a childhood disease and it can be outgrown.  That was before 1951, before gluten was discovered to be cause of Celiac Disease, also called Infantilism.  Back then Cileac Disease was thought to be only a gastro intestinal disease, once you  "outgrew" the colicky phase, you were cured. You were so lucky to be diagnosed at 5 years old so your developing years were normal.  Gluten can affect multiple systems.  The nervous system, your intellegence. The muscules, skeleton. It can cause neurological issues like brain fog, anxiety, and peripheral neuropathy.  It can cause joint pain, muscle weakness, and skin rashes. Epilepsy is 1.8 times more prevalent in patients with celiac disease, compared to the general population. Because through malabsorption and food avoidances, it causes vitamin D and numerouus other essential nutrient deficiencies, it allows allergies, infections, poor growth, stuffy sinuses and eustacian tubes. There is even a catagory of celiac disease called "Silent Celiac".  Any symptoms are explained away as this, that or the other thing. Gluten is one of the most addictive substances we consume.  Activating the Opiod receptors in our cells, it can numb us to the damage that it, and other foods are causing.  It has become socially acceptable to eat foods that make us feel sick.  "There's a pill for that".   It is generally accepted that n fact you are weird if you don't. The hardest part is that if you don't eat gluten you will feel great and think why not.  But slowly it will effect you, you'll be diagnosed with real diseases that you don't have. You'll be more susseptable to other autoimmune diseases.  As you read through the posts here, notice how many are finally dianosed, after years of suffering at older ages.  Is it worth it? I think not. Perhaps this book will help:  Here is a list of possible symptoms:   
    • Riley.
      Hi! Im Riley, 18 years old and have been diagnosed for 13 years.. the testing started bc I stopped growing and didn’t gain any weight and was really small and thin for my age.  I got diagnosed when I was 5 and have been living gluten free since, in elementary and middle school it was hard for me and I kept contaminating myself bc I wanted to fit in with my friends so so badly. I ate gluten secretly at school and mostly regretted it 30 minutes later.  I’ve had symptoms like diarrhea, nausea, headaches, stomachaches, threw up a lot and was really emotional.  In 2022 I really started working on myself and tried to stay gluten free and if I did eat gluten I wouldn’t tell anyone and suffer in silence.  Last year in July I begged my mom to let me „cheat“ one day bc I just wanted to fit in… I ate a lot of different stuff, all the stuff I missed out on in my childhood like nuggets, pizza and all that.. I didn’t have symptoms that day and was doing really fine My mom and I wanted to test how far we can go and said we would test it for 12 weeks to get my blood taken after to see if I’m doing good or if symptoms start showing  As a now 18 year old girl who finally gained a normal weight and doesn’t get symptoms I’m to scared to get tested/my blood taken cuz I finally found comfort in food and it got so much easier for me and my family.  A year and 4 months later i still didn’t get any symptoms and have been eating gluten daily.  I’m scared to get tested/my blood taken cuz what if I’m actually not fine and have to go back to eating gluten free. Any tips to get over that fear and „suck it up“ cuz I know I could seriously damage my body… sorry if I seem like a idiot here… just don’t really know what to do :,)
    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
×
×
  • 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.