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Psoriasis?
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I have been suffering from psoriasis for about 8 years now. It started out mild but in the last year or 2 it has become worse. I've also had chronic joint pain in my toes and fingers. Dermatologist basically diagnosed me with psoriatic arthritis but blood tests came back as negative from rheumatologist. My mother has Celiacs and I am being tested this week. I started gluten free yesterday because they now feel that even though I have no stomach issues, the gluten can be causing the psoriasis and joint pain. Anyone else have such issues? I also have terrible fingernails and toenails.

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I hope that you will report back any benefits of your gluten free diet, because there are many people who post on this forum with symptoms that don't sound like classic DH, but could be caused by gluten.

Please note that if you aren't consuming gluten, your test for celiac disease will probably come back negative. You need to be consuming quite a lot of gluten for the test to work.

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I have been suffering from psoriasis for about 8 years now. It started out mild but in the last year or 2 it has become worse. I've also had chronic joint pain in my toes and fingers. Dermatologist basically diagnosed me with psoriatic arthritis but blood tests came back as negative from rheumatologist. My mother has Celiacs and I am being tested this week. I started gluten free yesterday because they now feel that even though I have no stomach issues, the gluten can be causing the psoriasis and joint pain. Anyone else have such issues? I also have terrible fingernails and toenails.

Hi Emily, and welcome to the Board.

What tests did your rheumatologist run for you? Did he do the celiac blood panel or did he just test you for Rheumatoid Factor? If you have psoiratic arthritis, as I do, your RF will most likely be negative. I was never tested for celiac because I figured it out myself and stopped eating gluten - in fact told my doctors that's what my problem was. My new rheumy said, "Well, it's too late to test you now." So, in the event he didn't do the celiac panel you should have it done right away. If you did have the celiac tests it would be useful to see the results posted here with the ranges the lab uses. Sometimes tests that are really borderline are called negative :unsure:

Now, that being said, it is also possible to have problems like psoriatic arthritis caused by gluten and not test positive on anything, even the CRP or ESR, let alone the celiac panel. I did have the GI issues, not the major issues some posters on here have, but other sometimes alarming symptoms and the only one I attributed to food was my reaction to lactose which I realized was an intolerance but did not know of its association with gluten.

So what took me to the rheumatologist was pain in my shoulders wrists, fingers, toes, balls of my feet. Many rheumatologists are ignorant of the relationship between gluten and joint problems and do not think to test you. I did not develop the psoriasis until later, so had had joint symptoms for a couple of years before diagnosis. I see now, going back to your post, that you are being tested for celiac this week. Try to get them to run the full panel, which consists of the following:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Deamidated Gliadin Peptide (DGP) IgA and IgG

Total Serum IgA

Often doctors will run only the tTG and total serum IgA, but the newer DGP seems to be the most specific, reliable test so far developed. I would specifically request that they run that one. And it is best if you stay on the gluten until testing is finished (they may want to do an endo with biopsy) because it is important that you keep the antibodies active because that is what the tests are looking for.

Good luck with your testing and do let us know how things turn out. :) By the way, my fingernails and toenails have gone to hell, and they used to be my star feature :D

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My Mom had psoriasis, and for thirty years she was under a dermatologists's care. Then in 1985 or so, after years of digestive problems, she was diagnosed with Celiac. After she had been gluten free for a while her psoriasis cleared up completely and permanently. And she had it BAD.

So, when I started with psoriasis that kept getting worse, I went gluten free. I saw immediate relief (within two days it started healing.) Unfortunately, I also discovered that corn causes it to flare badly, and I recently discovered that almonds do it to me too. The same may happen to you. There are often other intolerances that are masked by the gluten. I'm still learning and I'm sure over time there will be problems with other foods too.

Start out with plain cooked whole foods - meat, brown rice, and vegetables. But try to stay away from bagged salads and baby carrots - they are washed in a citrus wash derived from corn. I didn't even eat fruit at first because of all the fructose (which can be another thing that causes problems).

You will most likely start to heal and then have ANOTHER problem pop up, just like I have, but try not to get discouraged. You are DEFINITELY on the right track. If you need any more advice on the "psoriasis diet", feel free to PM me.

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    • That's great to hear you are feeling better Nightsky.  I really think when our GI systems are in distress already that it doesn't take much to set off symptoms.  Once I eliminated the other foods that cause me symptoms that helped a lot too.  And added some extra vitamin D to my diet and selenium. Many of us have developed reactions to other foods besides gluten and need to avoid them to keep symptoms at bay.  For me nightshades, carrots, soy, dairy, and celery all cause symptoms.  It took me awhile to figure out all those food culprits, but it made a big difference getting them out of my diet. But we are all individuals, and our bodies react individually.  So you may or may not have additional food intolerances develop. Celiac is one of those life journey things and we learn as we go.  Just keep the bottle of aspirin handy!
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    • You should never have cut out gluten until you had the biopsy done. It's much worse to have to go back on after you've been off gluten for a while. There's no way I could ever do the gluten challenge after being off gluten for even a month because my reactions got so dramatically worse.  Stress definately can trigger celiac- before I was diagnosed - it got the worst after surgery and after a stressful time planning my daughters wedding. 
    • Hi not diagnosed celiac, Welcome to the forum! Your doctor should be sent to remedial celiac disease training.  Since that probably won't happen, I suggest you find a new doctor.  He doesn't know what he's doing when it comes to diagnosing celiac disease. You should not have gone gluten-free before completing all celiac disease testing.  The testing for celiac disease depends on the immune reaction being active.  Removing gluten before testing removes the antigen that causes the immune system to react, and lowers the chances of getting a correct test result dramatically.  The University of Chicago celiac disease center recommends: ******************************************** http://www.cureceliacdisease.org/faq/what-is-a-gluten-challenge/ Prior to blood testing we recommend 12 weeks of eating gluten. Prior to an endoscopic biopsy we recommend 2 weeks of eating gluten. In the case of a severe reaction to gluten, a medical professional may opt to shorten the 12-week challenge and move immediately to an endoscopic biopsy. May, 2013 ******************************************** So you will need to go back to eating gluten before your endoscopy.  That may cause worse symptoms than before when you were eating gluten.  So it would have been better to do all testing before going gluten-free. Can you search for a celiac disease support group in your area?  They exist in many parts of the USA and world.  They can be a good place to get a knowledgeable doctor recommendation.  There is also a doctors subsection of this forum where you can search to see if any doctors in your area were recommended.
    • Hi All, I'm new to this and very confused! I have Lea & Perrins WC sauce, it lists it's first ingredient as Malt Vinegar.  I have the Coeliac Society of Ireland Food List 2015 here, and it says "All Vinegars are Gluten Free including Malt Vinegar." Doesn't that mean that L&P Worcestershire sauce is safe?   Their website states " Lea & Perrins® Worcestershire Sauce is cholesterol free, fat free, preservative free, gluten free and has 80% less sodium than soy sauce. " I'm cooking for my coeliac niece, can't afford to make a mistake!
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