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

Should Brother Go gluten-free


whymychildjo

Recommended Posts

whymychildjo Newbie

My 9 year old has been on a gluten-free diet since May 2009. We went through a trip to the ER and several trips to Dr's. We had 2 MRI's and a Sono since we were trying to rule out his appendices. They finally told me he was constipated and make sure he was eating a high fiber diet.

I looked at our diet and we were eating pretty high fiber already. I thought they kenw what they were talking about so I gave him the little fiber wafers. Yes the ones like cookies (Wheat) He was not getting any better but he was going to the bathroom every day.

I had a freind suggest going gluten free. We tried it and he satreted feeling a little better. His pain went from an 8 on a level from 1 - 10 to about a 5. It took about 6 month but now he feels much better. I accidntally glutened him the other day and it was not pretty.

Since he has gone gluten-free I think I probably have issues with gluten as well. Except for bread and pasta we are totally gluten-free at our house. When I have bread or pasta I end up in the bathroom most of the following day.

Now with all the history out of the way. I have a 12yr old son and he has Psoriasis really bad on his head. I have a family history or psoriasis, one of my older sons has it and I have it but it is not bad on myself. Question is does anyone think the psoriasis might be helped with a gluten-free diet?

No one in my family has been tested for Celiac but I would not even think of putting my son back on wheat at this point.


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

[i see you are pretty new to the site here. One of the things that is often reccoememnded is to do a simple whole foods diet. Avoiding processed foods will save you time reading labels and trying to feret out hidden gluten ingredients.

I think it might be good for you to make your whole family gluten free, at least temporarily for about 6 months or so. That would be 6 months time for you to really learn about gluten-free eating and adapt your diet and your kids to gluten-free. By the end of 6 months you all would probably have a good idea if gluten hurts your body. There are blood tests for anitbodies you can get first though. They must be done while your are still eating gluten. Don't stop eating it until after the blood is drawn. The blood tests are not 100% accurate though, so it makes sense to try the diet also.

Another test is an endoscopy with biopsy samples of 4 to 6 sites in the small intestine. The endoscpoy is not nessecarily needed if your blood tests are positive IMHO.

Enterolabs does a stool sample test that may be interesting for you. They can also test for casein and other food intolerance issues. Many celiacs have lactose intolerance, although some get past that after healing a while.

There is also a home test kit or two available. One is Biocard from a Canadian company and another is a mouth swab from a company I don't remember he name of right now.

If you do a google on celiac disease and related condtions or associated conditions you can find lists of other autoimmune diseaes that are more common in celiacs. I am pretty sure I have read about psoriatic arthritits being related although I don't know if that applies to your situation.

There is also a condition called dermatitis herpetiformis which celiacs get that affects the skin.

Anyway, it seems like some testing would be a good idea. Since celiac is hereditary you could have it. Maybe you could check the related conditions lists against your families history of diseases and see if some of them match. There is also gluten intolerance which can cause serious problems for people even if they aren't nessecarily officially celiac diagnosed.

Maybe take a look at the pre-diagnosis forum here also. Lots of info on testing there.

KK555 Newbie

My sons GI doctor was concerned about Celiac because my mom has psoriasis. Celiac disease and psoriasis are cousins in the autoimmune dept. it is very possible your other family members have Celiac too.

minniejack Contributor

Without going into detail about my DS14 and my son's journey, we both started the diet last October. Because I'm not a restaurant, I decided that what I was cooking was good enough for the two of us, was good for everyone.

My DD16 had been eating this same diet for 6 weeks, when she had a Christmas concert. I dropped her off at 7 am and then didn't see her again until 10 pm.

When I was searching for her in the audience, I couldn't even find her. Why not? Well, my former little starch queen, couldn't get to her gluten-free lunch that I had made, so she ate the Wonderbread sandwich that was provided along with the cookies. Then for supper, she went to Quizno's for a sub.

When she appeared to me at the end of the concert, she literally looked like she was 6 months pregnant. Her face was swollen and her eyes were watery--and the following days--watch out what a bit**!

Since she has been on the diet, her acne has cleared up and extreme heavy period problems that she has had since she became a woman has disappeared--one gyne even wanted to put her on the pill at age 11! Menstrual cramping has almost disappeared.

Me?--psoriasis of the scalp has disappeared. Period that hasn't quit for the last 14 years is now normal--and to think--my gyne wanted to do a hysterectomy to see if it would stop--eeks!

We have never been formally diagnosed. I can't see the point after all the good that I've seen on the gluten-free diet. We were like you--many, many tests and scans, and many blood samples given to check for cancer, you name it--including ADHD drugs.

DS's anger issues, lack of concentration, vomiting, diarrhea, night terrors/sweats, acne, and more gone, gone, gone.

My God is An Awesome God.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,653
    • Most Online (within 30 mins)
      7,748

    Janet51
    Newest Member
    Janet51
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      I don't see how cornstarch could alter the test results. Where did you read that?
    • knitty kitty
      For pain relief I take a combination of Thiamine (Benfotiamine), Pyridoxine B 6, and Cobalamine B12.  The combination of these three vitamins has analgesic effects.  I have back pain and this really works.  The B vitamins are water soluble and easily excreted.   Hope this helps!  Keep us posted on your results!
    • knitty kitty
      Welcome to the forum, @Xravith. I experienced similar symptoms before my diagnosis.  Mine were due to the loss of vitamins and minerals, essential nutrients we must get from our food.  With Celiac Disease, the intestinal lining, made up of thousands of villi, gets damaged and cannot absorb essential vitamins and minerals, especially the eight B vitamins.  The loss of Thiamine B 1 can cause muscle loss, inability to gain weight, edema (swelling), fatigue, migraines and palpitations.  Low thiamine can cause Gastrointestinal Beriberi with symptoms of nausea, abdominal pain and bloating.   Thiamine is only stored for a couple of weeks, so if you don't absorb enough from food daily, as the thiamine deficiency worsens physical symptoms gradually worsen.  If you're eating lots of carbs (like gluten containing foods usually do), you need more thiamine to process them (called high calorie malnutrition).  Thiamine works with all the other B vitamins, so if you're low in one, you're probably getting low in the others, too, and minerals like iron, magnesium, zinc, and calcium, as well as Vitamin D..  Talk to your doctor about checking for nutritional deficiencies.  Most doctors rarely recognize vitamin deficiency symptoms, especially in thiamine. Get a DNA test to see if you carry any Celiac genes.  If you do not have genetic markers for Celiac, it's probably IBS.  If you do have genetic markers for Celiac, it's probably Celiac.  I was misdiagnosed with IBS for years before my Celiac diagnosis.   Keep us posted on your progress. P. S. Deficiency in thiamine can cause false negatives on antibody tests, as can diabetes and anemia.  
    • Julie 911
      No she didn't because if I want to ask I have to pay 700$ for 1 hour appointment so I couldn't even ask. I read that fillers like cornstash can alter the result and tylenol contains it so that's why I tried to find someone who can answer. 
    • trents
      Did the GI doc give you any rational for stopping the Tylenol during the gluten challenge? I have never heard of this before and I can't imagine a good reason for it. Ibuprofen, maybe, because it is an anti inflammatory but acetaminophen?  I don't see that it would have any impact on the test results to take Tylenol.
Ă—
Ă—
  • 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.