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  • Réjean Perron
    Réjean Perron

    Psychiatric Symptoms and Gluten

    Reviewed and edited by a celiac disease expert.

    Journal of Gluten Sensitivity Winter 2007 Issue. NOTE: This article is from a back issue of our popular subscription-only paper newsletter. Some content may be outdated.

    Psychiatric Symptoms and Gluten - Image: CC BY 2.0-- jared422_80
    Caption: Image: CC BY 2.0-- jared422_80

    Celiac.com 10/08/2021 - I live near Montréal, in Québec country and I’m webmaster of a new French web site called SOSGLUTEN.CA devoted to gluten sensitivity.  The first time I saw the word “gluten” was in year 2000.  At that moment my wife, Danielle, was very sick and while she was waiting for a diagnosis from her doctor, I discovered an ailment called “celiac disease” on the Web.  That was my first meeting with the word “gluten”.  When she went to the doctor to finally receive what is, effectively, a diagnosis of celiac disease, she had already been on a gluten-free diet for three weeks, based on my own findings.  After that, I continued to read, read, and read again, anything on the web concerning celiac disease and gluten sensitivity.  

    In 2002 when my youngest daughter, Manon, received a diagnosis of anxiety and depression, I requested a blood screening for celiac disease.  As you may have expected, the doctor initially refused.  It was only after my insistence that he finally ran these tests.  From this, Manon received a diagnosis of celiac disease and she stopped having to take Paxil after six gluten-free months.

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    In 2003, I helped a sister of my wife, Suzanne, to understand that gluten might be behind her skin disease and other health problems.  She finally received a diagnosis of dermatitis herpetiformis and celiac disease after seeking a second medical opinion.  In 2004, I also helped another sister of my wife, Noelline, to understand that gluten might also be behind her bone pain, joint pain and many other health problems.  Despite two negative blood tests and two negative biopsies, she started a gluten-free diet and it turned out to be the best decision of her life.

    Moore recently, in 2005, I requested, for me and my son Eric, the opinion of Dr. Kenneth Fine via Enterolab.  My son, a young engineer of 25 years old had joint finger pain and he was always a little bit depressive.  I frequently had esophageal reflux, indigestion with chest pain, and insomnia since I was three or four years old  (I’m  now 53 years old). The diagnosis from Dr. Fine was a diagnosis of gluten sensitivity for my son Eric with a copy of HLA DQ2 gene (from his mother) and for me a diagnosis of gluten sensitivity with only gluten sensitive genes.

    Today, we are all on a gluten-free diet and have been since Christmas 2005, and all symptoms have disappeared for Eric and me.

    As you can understand, avoiding gluten is in the center of our lives, and that is the reason I have decided to create a French web site devoted to celiac disease and gluten intolerance.  I now have personal proof that gluten intolerance is not limited to celiac disease.  

    To conclude, the main goal of this article is to share my family’s experiences with you, and to ask you to visit my web site at: https://www.sosgluten.ca.  



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    CBird

    I had been on Zoloft 1yr and Effexor 12yr before discovering I was Non Celiac Gluten Sensitive (NCGS) at 62 years of age, 2010. I'd suffered from depression, clinical anxiety/panic attacks since 21yr old. I discovered this on my own. In & out of therapy for decades. I had to be tapered off Effexor as I was addicted (yes it can happen). I was a graphic artist in between jobs, no health insurance at the time; the test was unreliable anyway at that time. My childhood was filled with abusive trauma, so I needed the help & guidance in therapy. The anxiety/panic, however, kept me in therapy far longer than necessary, needlessly expensive too.

    My sister nearly died at 6mo old in 1948. She was starving to death when a new doctor finally diagnosed her with Celiac. Food went through whole. Her problem, right?! NOT! Who knew; certainly not my doctors! Painful bouts of IBS also cleared up going gluten free, along with foggy brain, inappropriate bouts of rage, and frequent irritability. My emotions were extremely overwhelming to me. My low self esteem was compounded by the anxiety/panic and rage/irritability. I discovered foggy brain when being able to finish reading a scientific technical paper three years into being gluten-free. Realized that I could have gone to college if I'd been able to focus.

    My daughter is now diagnosed with NCGS in her mid forties. No food problems perviously. She's was in and out of the hospital for a year with unexplained painful bouts of indigestion not being able to keep water in. Hospital tests didn't determing anything. Functional medicine doctors did, through DNA testing and elimination dieting. Her symptoms are very different than mine. She's a software engineer, something my lack of focus would never have allowed. Her diet is stricter as well. So this can apparently run in families!

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    trents
    11 minutes ago, CBird said:

    I had been on Zoloft 1yr and Effexor 12yr before discovering I was Non Celiac Gluten Sensitive (NCGS) at 62 years of age, 2010. I'd suffered from depression, clinical anxiety/panic attacks since 21yr old. I discovered this on my own. In & out of therapy for decades. I had to be tapered off Effexor as I was addicted (yes it can happen). I was a graphic artist in between jobs, no health insurance at the time; the test was unreliable anyway at that time. My childhood was filled with abusive trauma, so I needed the help & guidance in therapy. The anxiety/panic, however, kept me in therapy far longer than necessary, needlessly expensive too.

    My sister nearly died at 6mo old in 1948. She was starving to death when a new doctor finally diagnosed her with Celiac. Food went through whole. Her problem, right?! NOT! Who knew; certainly not my doctors! Painful bouts of IBS also cleared up going gluten free, along with foggy brain, inappropriate bouts of rage, and frequent irritability. My emotions were extremely overwhelming to me. My low self esteem was compounded by the anxiety/panic and rage/irritability. I discovered foggy brain when being able to finish reading a scientific technical paper three years into being gluten-free. Realized that I could have gone to college if I'd been able to focus.

    My daughter is now diagnosed with NCGS in her mid forties. No food problems perviously. She's was in and out of the hospital for a year with unexplained painful bouts of indigestion not being able to keep water in. Hospital tests didn't determing anything. Functional medicine doctors did, through DNA testing and elimination dieting. Her symptoms are very different than mine. She's a software engineer, something my lack of focus would never have allowed. Her diet is stricter as well. So this can apparently run in families!

    One recent large study done by the Mayo Clinic determined that 44% of the first degree relatives of those with celiac disease also have celiac disease themselves. Other studies have placed the incidence at closer to 10%. And we also know that NCGS is approximately 10x more prevalent in he population than is celiac disease. Yes, certainly these things do run in families.

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  • About Me

    Réjean Perron

    A lot of my free times since summer 2000 were devoted to reading hundreds and hundreds of studies on celiac disease and gluten sensitivity. The main reason for this is that my wife received a diagnostic of celiac disease in 2000, followed by the youngest of our daughters two years after. My son and I are also gluten sensitive but not celiac. In 2006, I created a French website called SOSGluten.ca to help all French-speaking people of planet, to better understand the negative impact of gluten on human health.


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