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9 Comments

  1. Tired Scholar
    11 January 2011 @ 10:39 am

    I am wondering if there is a connection between gluten and glutamate- seeing as glutamate is a key player in many people’s migraines (see http://www.reuters.com/article/idUSTRE67S1PN20100829) and if gluten-free diets reduce glutamate levels that might explain the effect.

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  2. Emily
    11 January 2011 @ 5:15 pm

    As always very interesting, especially the non-celiac people who have been helped.

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  3. Vikki
    12 January 2011 @ 7:50 am

    Only been recently diagnosed with silent migraines ( not always presented with headpain or sometimes headpain when it’s too late to do much than just shut down and sleep ). Over the years have been tested for gluten intolerance/coeliac and have tried gluten free diets & wheat reduced diets. On reflection and going off what I have been doing the last 6 months – I’m not sure that gluten is an issue that is connected for me and the migraines however I do know that certain wheat based products trigger a stomach migraine or the beginning of a migraine in the form of stomach cramps/wind/bloating/toilet running to etc that was always put down to gastro bugs or IBS. Too much white bread, pizza & pasta set me right over the edge so I either try to avoid them or if I don’t I make sure I don’t eat any more of them within 36-48 hours. I have noticed though that being on migraine prevention meds ( Topamax ) has increased my tolerance for these items though as I went for about 3 days straight recently where they were all pretty much on the menu breakfast, lunch and dinner ( I had no other options ) and I only had a migraine when the weather changed about a week later.

    Bodies are both a miracle and weird 🙂

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  4. B
    12 January 2011 @ 7:58 am

    I went gluten-free over a year ago and find that if I accidentally ingest gluten, within hours I get one of the worst migraines on my pain scale. I had to do it based on B12 and iron deficiencies, but it is definitely worth looking at gluten and other common allergens as a trigger.

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  5. Christine
    16 January 2011 @ 2:16 pm

    Does anyone have any tips on eating gluten free at restaurants?

    Also I’ve been tested and know I don’t have celiac, but I have also read that some people might have gluten sensitivities and intolerances and not the full blown celiacs.

    *Someone mentioned soy, this is a HUGE trigger for me, so I stay away from soy. And beware, most peanut butter contains soy! Stick with the natural peanut butter if you find that soy bothers you.

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  6. Aurora
    25 January 2011 @ 8:39 pm

    I do come back and read posts and comments. When I had all of those migraine days, this site was the company of my misery.

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  7. gg
    27 January 2011 @ 10:09 pm

    I totally agree with the comments above. I have been suffering from migraines for the last 20 years +. I have discovered that I am intolerant to wheat but i am not celiac ( I did a test). My migraines have gone worse since I moved to Canada 10 years ago and since the birth of my child.

    Apparently the gluten content is higher here in North America than in Europe. When i was growing up I ate french baguette and cheese everyday. If I follow the same diet here my migraine are worse than ever. You can call it placebo effect or not as soon as I go back to France I have less migraine. I have tried everything. Ostheopathy, homeopathy and naturopathy and preventive treatment with amytriptilline. If i reduce my wheat intake i feel better and less migraine. Nevertheless I still have the migraine as the beginning of my cycle. But as most readers above I tolerate my migraine even more and I am able to function and do the minimum at home. I truly believe the correlation between migraine and gluten but my doctor laughed at me when I suggested it few years ago….I read carefully each label and I try not to eat processed food even pizza…

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  8. Gail
    21 November 2013 @ 11:55 am

    I have been trying gluten free for a couple months now since my doctor informed me her debilitating migraines disappeared with this diet. My headaches were CHRONIC, leaving me bedridden in agony for at least 2 weeks out of the month. (I am post menopausal and my headaches began around age 20).
    I was discouraged at first with no improvement until I discovered the brand of yogurt I was eating daily was not gluten free. Since then I have studied up on how to read labels, and when in doubt to contact the manufacturer (including vitamins/supplements) to verify it is truly gluten free.
    Since being more discriminating and allowing time on this diet, here’s what I’ve noticed so far:

    1. If I feel a headache beginning, it usually ends up NOT manifesting into a migraine and disappears, not having taken any meds!

    2. If I DO get a headache it is mild and responsive to meds.

    3. The headaches are so infrequent now they have almost disappeared!

    4. It is raining out now–a switch from yesterday’s weather ( a usual trigger for me). Yet NO HEADACHE!

    I truly believe you have to be both diligent in making sure your foods are truly gluten free as well as giving it a good few months at least as a trial.

    HOPE THIS HELPS SOMEONE OUT THERE!

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  9. Catherine
    31 March 2021 @ 2:33 pm

    Hey there,
    I know I’m late to the GF comments given how long ago you published this post, but it is nice to see I am not the only one who cut out gluten and saw a big difference in migraines. A doctor-friend of mine suggested I take gluten out of my diet and see if that would stop the 3 solid weeks of migraines (back in 2015). It worked for a little while, then they came back, so I took dairy out as well. That worked for a little while, then they came back, so I took exercise out after that. Oh, and no alcohol at all, that was a terrible trigger. So, 2016 was a miserable year. But after a year, I started to re-introduce everything and I can exercise, eat dairy, and drink a little bit, but still no gluten – UNLESS I’m in France, in which case, I can eat my heart out on baguettes and croissants without any migraine consequences. Go figure. One other thing that triggers them are any natural supplements that are vasodilators. Unfortunately, I always find out the hard way. 🙁 Thanks for starting this website!

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