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Too Many Going Gluten-Free? - Food Safety News


Scott Adams

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Food Safety News

Unlike Celiac Disease - a known condition in which damage to the stomach lining by gluten prevents patients from absorbing food's nutrients - gluten intolerance does not have one common medical explanation. When eating less gluten alleviates a person's ...

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"We must prevent a possible health problem from becoming a social health problem," says the report. "Self-prescription of gluten withdrawal by a growing number of patients inevitable leads to a series of problems: subsequent inability to diagnose or exclude celiac disease, deleterious health effects from the probably suboptimal adherence to a gluten-free diet in the case of patients with undiscovered celiac disease, and the high economic burden related to an unjustified gluten-free diet," the authors note, according to Open Original Shared Link.

Good heavens, yes, we most certainly most stop these patients from thinking for themselves because we all know that without the wisdom of a DOCTOR advisisng them they are totally incapable of following a strict gluten-free diet, and they just enjoy spending money in an unjustified manner (and depriving doctors from their rightful income) :P

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When eating less gluten alleviates a person's gastrointestinal problems, he or she is diagnosed with gluten intolerance. A sensitivity to gluten, notes the commentary, is likely the sign of another underlying disorder - such as Celiac Disease or Irritable Bowel Syndrome - rather than a disease in and of itself.

Eliminating gluten could even be detrimental to pinpointing the root cause of a patient's digestive issues, say the authors, as it could mask the symptoms of Celiac disease, leading to a misdiagnosis.

If some of these people were to wait to get a "proper" diagnosis of celiac, they may be so sick or worse, by the time tests pick it up. Then again there are some people who will never test positive.

My 11 year old son has never tested positive on yearly testing since he was 7 years old and had a negative biopsy also. I finaly gave in and decided to trial him gluten free without any "positive" testing. It has made a big difference in him and he decided for himself to stay gluten free!

And lets not forget about IBS. We wouldn't want to miss out on that diagnosis...(little hint of sarcasm <_< )

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      I read that as well but I saw the Certified Gluten free symbol that is the reason I ourchased it.
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      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
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      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
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