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Celiacs And Anxiety


dantefishell

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dantefishell Newbie

Hi I have a 7yr. old who was diagonsed with Celiacs Disease 5yrs. ago. She has sever Seperation Anxiety and I was wondering if anybody else suffers from anxiety? I was wondering, I know they don't obsorbe certain nutrients due to the Gluten free diet. Does anybody else have a problem like this?

Thank you


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OptimisticMom42 Apprentice

Hi I have a 7yr. old who was diagonsed with Celiacs Disease 5yrs. ago. She has sever Seperation Anxiety and I was wondering if anybody else suffers from anxiety? I was wondering, I know they don't obsorbe certain nutrients due to the Gluten free diet. Does anybody else have a problem like this?

Thank you

The gluten free diet doesn't impede absorption. Before going gluten free, gluten causes damage to the intestines. The damage impedes absorption. Within the first year of being completely gluten free the damage should heal and allow normal absorption. A lot of moms use a gluten free children's multi-vitamin to make sure the kids are getting everything they need.

A lot of us have anxiety when we get glutened. Could your daughter be ingesting something that is not safe? Also, think hard about your own behavior. Is your child mirroring the concern she has seen you display? I would have seperation anxiety if I was asked to leave my gluten-free child at a day care. Hope this helps RA

CeliacKate29 Newbie

Hi! My name is Katie and I'm 21 years old. I was diagnosed with Celiac Disease exactly one year ago. Ever since I was young I had anxiety and panic attacks regularly. I was diagnosed with panic disorder when I was 12 and have been seeing a therapist ever since. My anxiety got worse when I left for college and I was put on the anti-anxiety medication Lexapro. Even though the medication and therapy helped immensely, once I found out I had Celiac Disease and switched to a gluten-free diet my anxiety and panic attacks have completely gone away. After about 2-3 months of being gluten-free I noticed a huge difference in myself and truly believe that I was having panic attacks and severe anxiety because I was lacking in nutrients. I hope that helps!

judyg Newbie

I was diagnosed in September 2009 with Celiac and have had anxiety my whole life. I definitely feel better, but I am also on medication since it took so long to get diagnosed.

I had my 9 year old tested for Celiac in September and it was negative. His anxiety got really bad and my new doc tested him with more detailed test for Celiac and he is positive and also lactose intolerant. It has been hard but eliminating Gluten and Dairy has helped his anxiety already and it has only been 2 weeks.

You are lucky to catch your daughters Celiac young, just as I am my sons, because they can avoid many of the health issues that people who get diagnosed later in life have, by following the Gluten Free diet.

conniebky Collaborator

I've had a problem with panic attacks for about 10 years, and boy, I'll tell ya what, those are horrible and come from absolutely NOWHERE!

I've also become extremely antisocial and want to stay in the house and avoid other people at all costs. I haven't so much as talked to a guy on the phone since 911 happened. That's been like 10 years almost, since I've had a date or anything.

I haven't had a store bought haircut for years and years.

This has all gotten SOME better since my 3 weeks of gluten-free. I'm not as angry anymore, either.

This is gonna sound all sappy and pollyanna-ish, but I've noticed just in the last week, that I enjoy the smell when I go outside after it rained. Kentucky is SO beautiful. I noticed how green/blue the grass is in a field by work. The wildflowers, they're beautiful popping out yellow purple and red, they are just beautiful.

I've put my car radio back to the rock station instead of talk radio. I've been actually looking at myself in the mirror, I haven't done that in forever. I use this tiny little compact mirror on my sofa in the mornings to put on my mascara, but these last couple of days, I've looked at myself and brushed my hair in the mirror. oK, that sounds just stupid....guess ya had to be there ....

I just got sick and tired and felt old in the joints and panicked all the time. I couldn't tell you when I stopped enjoying life, but somewhere along the line, I did.

I guess what I mean is that it's like...I'm waking UP, I'm starting to be me again or trying to even think to remember who me was or is.

knittingmonkey Newbie

Hi I have a 7yr. old who was diagonsed with Celiacs Disease 5yrs. ago. She has sever Seperation Anxiety and I was wondering if anybody else suffers from anxiety? I was wondering, I know they don't obsorbe certain nutrients due to the Gluten free diet. Does anybody else have a problem like this?

Thank you

I suppose I've been suffering with separation anxiety for about 5 years. Started having trouble at work with concentration, dreading the 20 mile commute, ultimately I lost my job, so now I'm home alone most of the day. I just haven't wanted to make any social overtures. Now since I've been diagnosed celiac last month I'm wondering just how much celiac has affected my social life. And now I have additional anxieties about food, especially shared-food situations, like parties and chili cook-offs. Heck, Honey gave me a kiss yesterday; a big cookie-crumb laden moustache kind of kiss! My lips slammed shut so fast my neck muscles started cramping. It looks like anxiety's here to stay...

One thing's for certain; I absorb more nutrients now on the Gluten-Free diet than I did on a wheaty diet. I'm looking forward to the healing my small intestine will experience without gluten in my food. I've been assured; there really isn't any real reason to eat wheat, it's nutrients are easliy gotten from other foods.

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    • xxnonamexx
      I read that as well but I saw the Certified Gluten free symbol that is the reason I ourchased it.
    • cristiana
      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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    • trents
      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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