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Seborrheic Dermatitis
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Hi everyone! So I have had scalp/skin seborrhea for the past 3 years. My dermatologist has prescribed me numerous ointments and medications, all of which i stopped applying after I googled the ingredients. About 7 months ago I was speaking to a family friend who is currently in med school, he advised me to try cutting out gluten as dermatitis was an inflammatory disease which can be triggered by the protein in gluten. I immediately stopped eating gluten and within weeks all signs of my SD were gone. Even if I cheated a little bit, I would immediately get red and itchy. I don't completely understand the correlation between gluten and seborrhea but I have read that gluten causes autoimmune reactions in the body. Psoriasis runs in my family as well as asthma, arthritis, reflux and IBS. I have had acid reflux since I was born as well. I am thinking about being tested for Celiac's but I have had an endoscopy before and all they diagnosed me with was reflux. If anyone has any thoughts on this or has experienced the same thing please share. i do not completely understand the idea of gluten intolerance quite yet! Thanks :) 

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The University of Chicago's Celiac website is a great place to start!  Here's a link regarding the actual blood tests that your doctor can order.  You must be eating gluten though (for a couple of months) in order to get a valid result.  

 

http://www.cureceliacdisease.org/wp-content/uploads/2011/09/CDCFactSheets3_Antibody.pdf

 

If positive, you may need an endoscopy where the doctor should take up to six or seven tissue samples (biopsy).  It sounds like your doctor just did a visual on your last endoscopy.  

 

Welcome to the forum and search the forum for topics that might apply to you (e.g. your SD)!  There's a wealth of information about celiac disease and gluten intolerance.

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    • Oh, Trish at the GlutenFreeWatchDog tested Planter's honey roasted peanuts three years ago.  The can did not state gluten-free, but showed no gluten ingrediants (per Kraft policy).  Test result: less than 5 part per million which is pretty much gluten-free.  
    • What if it were something else that glutened you?  Maybe you ate too much of a good thing?  I once (three months post dx) ate too much gluten-free fried chicken, vomited, passed out and fractured my back (osteoporosis) in the process.  Paramedics, ER doc and Cardio all thought I was having a heart attack.   No.  It was sheer gluttony and bad bones.  Not good to overload with a damaged gut.    Maybe you did get some contaminated nuts.  Afterall, anything processed is suspect.  What might be well tolerated by some, might be too much for others.  We all have our various levels of gluten intolerance.   The old 20 parts per million is just a guideline, but science does not really know (lack of funding......doe anyone really care enough to find out?)  My hubby has been gluten-free for 15 years.  When I was first diagnosed, I tried to eat the gluten-free foods that I normally gave him.   Problem was he was healed and I was not.  Things like Xanthan Gum in commercial processed gluten-free breads make me feel like I have been glutened, but it is just (and still is) an intolerance.  So no bread for me unless I make it myself using a different gum.   Too lazy, so I do without.   so, ask your doctor if you really want to know or lay off the cashews and test them again in a month using a certified gluten-free nut.  I wish this was easier!    
    • I have intolerances to a few foods now, so I was wondering about that.. I love cashews though, and a month or two ago I was eating them all the time with no problems at all. I mean, could I really have developed an intolerance to them since then? I don't know if they're made on shared lines (it didn't say on the package so I assumed they weren't), but I'll give them a call. I'm really, really sensitive to cross contamination. Even if something is just made in the same facility (but not on shared lines) it will make me sick. If that's not it, then I'm not really sure
    • Research with KP and find a celiac-savvy GI in your area ( read the biographies). and ask your PCP/GP for a referral to that specific GI (not his buddy).  Ask the GI for the rest  of the celiac panel or proceed with an endoscopy/biopsies -- 4 to six.  Keep eating gluten daily until all testing is complete.  Document and request in writing.  Do not worry about symptoms.  There are over 300 of them and some celiacs have none!   Research all that you can about celiac disease.  The University of Chicago has a great celiac website that has testing Information etc.   Poet me know how it works out.  Hope you feel better soon!  
    • I react to both wheat and barley.  I've opted to just go completely gluten free, for the sake of simplicity and my sanity.  I don't have a diagnosis of celiac disease, but I strongly suspect it.  Unfortunately, I'm not willing to endure the misery of staying on gluten long enough to pursue further testing.  I just know I need to avoid the gluten grains, so I do.  
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