Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Migraines - Giving Gluten Free A Try


Zook

Recommended Posts

Zook Newbie

Hi all. I'm hoping you'll share your insights with me. I don't have concerns that I have celiacs, but I was thinking about giving a gluten free diet a try. My main complaint is migraines and chronic daily headaches. I know that going gluten free will be a challenge, but I've tried everything else and am desperate. I do have abdominal pain, fatigue, and a consistent blah feeling, but generally not any other symptoms of celiac.

One of the reasons I'm targeting gluten is that I can't take vitamins without getting a severe migraine, and I know that gluten is in most vitamins. I'm also zeroing in on certain breads/pizza as possible triggers.

Think it's worth a shot?

Also, I have a stupid question(s) (I know, no stupid questions, only stupid people ;0). Are whole cut oats considered gluten free? And I see that whey protein is in yogurt. That's bad, right? Oy this is hard and I haven't really started yet. What other ingredients might include gluten?

What do you all eat if you can't have bread, dairy, and soy? I don't think dairy and soy are a problem for me, but I'll have to test that out too. I found a website where I can order gluten free food and vitamins, so that should help.

Thanks!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



jerseyangel Proficient
Hi all. I'm hoping you'll share your insights with me. I don't have concerns that I have celiacs, but I was thinking about giving a gluten free diet a try. My main complaint is migraines and chronic daily headaches. I know that going gluten free will be a challenge, but I've tried everything else and am desperate. I do have abdominal pain, fatigue, and a consistent blah feeling, but generally not any other symptoms of celiac.

One of the reasons I'm targeting gluten is that I can't take vitamins without getting a severe migraine, and I know that gluten is in most vitamins. I'm also zeroing in on certain breads/pizza as possible triggers.

Think it's worth a shot?

Also, I have a stupid question(s) (I know, no stupid questions, only stupid people ;0). Are whole cut oats considered gluten free? And I see that whey protein is in yogurt. That's bad, right? Oy this is hard and I haven't really started yet. What other ingredients might include gluten?

What do you all eat if you can't have bread, dairy, and soy? I don't think dairy and soy are a problem for me, but I'll have to test that out too. I found a website where I can order gluten free food and vitamins, so that should help.

Thanks!

Hi and welcome, Zook,

You may very well find that a gluten-free diet helps out with your migraines. Migraines are a symptom for some people with Celiac. Your abdominal pain, fatigue and "blahs" are also things that may improve. I think it's definately worth a shot. The diet is healthy and won't hurt you.

When you go gluten-free, go all the way and try to be as close to 100% as possible to see if this is an issue for you. (You didn't mention this, but if you think you ever want to be tested for Celiac, don't begin the diet untill after the test--doing so will skew the results. Just an FYI.)

The problem with oats is that most that you find in the regular grocery stores are cross contaminated during harvesting, storing, and/or shipping. There are specialty brands that you could use. Many here on the board have had success with them and can steer you to the best ones. Some people who are intolerant to gluten will also be intolerant to the protein in oats. Not everyone, though.

Whey protein is from dairy--it's not a gluten issue.

Some of us buy or make breads made with rice or other "safe" grains. Most Celiacs can still enjoy dairy and soy if they choose--it's an individual thing. I, for instance, developed additional food intolerances after going gluten-free, so I have to avoid soy, dairy, and a few others.

On this site, there are lists of safe and forbidden foods.

There's no such thing as a stupid question here! Ask away--we're more than happy to help :)

Zook Newbie

Thanks for the response, it was very encouraging. I've been looking at other posts and I see some references to migraine relief with this diet. I'm totally psyched! Someone mentioned a hung-over feeling after eating wheat... and I've had that feeling but never associated the two. The gluten-free diet will be hard, but if I start feeling better, it'll be worth it.

Jestgar Rising Star

Hi Zook

My friend got rid of 90% of her migraines by stopping gluten and she's currently working on which other foods are triggers.

It's totally worth a shot.

Zook Newbie

Wuhoo!!!!!!! That's really great to hear. :D:D:D

It's beyond me why not one of the zillion doctors I've seen have ever mentioned this.

Ursa Major Collaborator

While gluten may well be your problem, I just want to mention that all of your symptoms could also be caused by nightshade vegetables (potatoes, tomatoes, peppers, eggplant). With me, potatoes will cause gastrointestinal distress, and tomatoes cause the migraines. Plus, of course, gluten is a huge problem as well.

tarnalberry Community Regular

Many people here found their migraines eased a little, a lot, or went away entirely when gluten free.

Some of us did not, however. I'm on daily preventatives (topamax), and found that seeing a chiropractor to correct a significant forward head posture and loss of curvature in the cervical spine almost entirely got rid of the non-migraine frequent headaches. Being dairy free is also important for me to maintain in order to stay as free of headaches as possible; it's a more potent trigger for me than gluten, in that regard.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Idiote Savante Goddess Rookie

Has anyone else been Rx'd Elavil for migraines? I can't take Topamax bc of family hx of kidney stones -- but the Elavil is making me extremely emotional. I got a ticking off at work yesterday for being short tempered AND reading the Heifer International brochure I got in the mail made me cry. My daughter thinks it's made me very unstable and that I should quit taking it.

I do see the neuro on Monday -- will ask him to order the gene test --- and I think after that (the appointment, not the gene test), I'm just going to break down and go gluten-free rather than just wheat-free (FYI, wheat allergy, rice allergy, negative blood test - but haven't eaten much wheat in over a year) and see if my brain fog (Hey, I've coined a new disorder -- Adult Onset ADD) improves.

Zook Newbie

I've tried a lot of meds for the migraines, but not Elavil. I found that I can't tolerate the side effects of them so I stopped. I will say, however, that had they been effective, I likely would have stuck with it. Is it working for you and have you been on it long enough to adjust to the side effects? Maybe there is a similar drug that might not affect you as badly. I've gotten to the point where most of the time I just suffer. I can't take most abortives because of a heart condition, and the one I can take is addictive and will cause wicked rebounds. I usually save that for when I just can't take it anymore. I hope you find an answer soon. I'm trying not to get my hopes up too much about a gluten free diet, because after this, I don't know what to try.

Aligray Apprentice

Zook! Welcome!

I used to have DAILY headaches before going gluten free. Some were dull and others I could not open my eyes. But now, the headaches are completely gone. They only come back if i have been cc'd or glutened accidentally.

Good luck to u!

If u do the diet, u need to go at it 100%. I think it would probably be great for u. It takes patience and time but u can do it!

-Ali :)

oldsalt19 Newbie
Hi all. I'm hoping you'll share your insights with me. I don't have concerns that I have celiacs, but I was thinking about giving a gluten free diet a try. My main complaint is migraines and chronic daily headaches. I know that going gluten free will be a challenge, but I've tried everything else and am desperate. I do have abdominal pain, fatigue, and a consistent blah feeling, but generally not any other symptoms of celiac.

One of the reasons I'm targeting gluten is that I can't take vitamins without getting a severe migraine, and I know that gluten is in most vitamins. I'm also zeroing in on certain breads/pizza as possible triggers.

Think it's worth a shot?

Also, I have a stupid question(s) (I know, no stupid questions, only stupid people ;0). Are whole cut oats considered gluten free? And I see that whey protein is in yogurt. That's bad, right? Oy this is hard and I haven't really started yet. What other ingredients might include gluten?

What do you all eat if you can't have bread, dairy, and soy? I don't think dairy and soy are a problem for me, but I'll have to test that out too. I found a website where I can order gluten free food and vitamins, so that should help.

Thanks!

I went gluten free just yesterday and I'm already feeling better.

As my (probable) gluten intolerance has become worse over the years, so have my headaches. Some were helped by migraine meds and some were not. We'll see.

CMCM Rising Star

I spent over 12 years suffering mightily from recurrent migraines that could last for days. When Imitrex first came out it helped, but I lived in mortal fear of running out of them.

After going gluten free and ALSO cutting back on dairy and all sugar in a major way, my migraines miraculously disappeared. I haven't had one in a year and a half, not one. So I can say that for me, gluten and perhaps the other things I mentioned (in larger amounts) were all responsible for my migraines. I suspect that it was mainly if not entirely gluten, since I now have small amounts of dairy and occasional sugar without problems. :rolleyes:

Zook Newbie

Thanks so much for the feedback. It's encouraging to see such positive results. I'm definitely on board with going 100%, but when I saw there was gluten in ice cream I about had a fit :blink: . Sounds like it's worth it to limit dairy and sugar as well. Thanks again!

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to Leslie Clark's topic in Gluten-Free Foods, Products, Shopping & Medications
      14

      Hidden Gluten in distilled vinegar

    2. - Manaan2 replied to Leslie Clark's topic in Gluten-Free Foods, Products, Shopping & Medications
      14

      Hidden Gluten in distilled vinegar

    3. - BIg Nodge replied to BIg Nodge's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Opinions on my test results/symptoms

    4. - Dawn Meyers replied to Dawn Meyers's topic in Related Issues & Disorders
      16

      Vaccines

    5. - Scott Adams replied to Dawn Meyers's topic in Related Issues & Disorders
      16

      Vaccines


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,856
    • Most Online (within 30 mins)
      7,748

    Dawn McDonald
    Newest Member
    Dawn McDonald
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.4k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      @Manaan2, I was on Miralax for several months after I crushed three vertebrae and fractured my hip.  The compression fractures of my vertebrae affected the Vagus nerve that stimulates digestion and intestinal movement, peristalsis. Miralax just didn't relieve the constipation I was experiencing at all.  Nothing budged.  I tried Milk of Magnesia (magnesium oxide) which pulls water into the digestive tract, and found that rather harsh and dehydrating.   Bad idea. I was already taking thiamine in various forms, Benfotiamine, TTFD (tetrahydrofurfuryl  disulfude), Lipothiamine and Allithiamine.  Click on my name, then Activities in the pull down menu to get to my blog to learn more about my journey with thiamine.   Since we need more thiamine when we are physically ill and emotionally stressed, I decided to focus on TTFD,  Benfotiamine, and magnesium l-threonate.  Within a week of increasing my doses a bit, my constipation was gone.  It took several more months to heal the compressed nerve damage.  For pain, I take a combination of TTFD, Pyridoxine B 6, and  Cobalamine B12 which together have an analgesic effect.  I can't function with pharmaceutical pain killers, besides they cause constipation.   Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Yes, I did just stop the Miralax, but I wasn't on it as long as your daughter.  Yes, there's a difference between adults and children.  Yes, my circumstances were different than your daughter's, but thiamine deficiency does affect the nerves and the brain.  A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function (which activates the Vagus nerve and controls digestion).   I recommend you visit Dr. Chandler Marrs' website, hormonesmatter.com.  Dr. Marrs worked with Dr. Derrick Longsdale, a pioneer in thiamine research, specifically with children and autism spectrum disorders.  She has been very helpful to me when I reached out to her.  She would be better able to guide you about your daughter's care. https://hormonesmatter.com/sibo-ibs-constipation-thiamine-deficiency/#google_vignette Do stay in touch, please.  You can start another thread or personal message me any time.  My heart goes out to you, your husband, and especially your daughter.   Namaste
    • Manaan2
      @knitty kitty  The information you've provided is invaluable!  I have a lot more homework to do before we make the official switch but you have significantly increased my hope that we can get her off Miralax (she started at 3 years old and is almost 8!).  This weekend my husband and I plan to solidify all the details for a start point, then adjust as we go along.  I realize that everyone's body is different, then there's also the fact that she's a child but just out of curiosity if you don't mind sharing and if you'd rather not, no problem at all-how long did you take Miralax before switching and when you switched, did you just completely stop the Miralax or was there a period where you did Miralax and the supplements?  I plan to research that piece this weekend but just curious what you did.  
    • BIg Nodge
      Scott, thanks so much for the thoughtful replies. My doctor did actually just re-order thyroid labs to see what is going on with my TPOs. I agree that will be interesting information.  I think I know the answer to this, but as far as the biopsy . . .. that would be quite conclusive as far as celiac goes, but a negative result would not rule out NCGS, correct? Does NCGS also cause damage to the lower intestine/leaky gut?  I appreciate the thought that I should be open-minded to other causes. I did not have dysautonomia on my radar, so I will look into that. From a quick scan at the potential symptoms it seems like almost anyone could convince themselves they have it, very broad! I can see why that is a tricky one to diagnose. I did also show low vitamin D, I'm in New England so that is somewhat common. I have a memory of low iron on some lab result as well but I can't find it, so I'll look into that. My cholesterol is high too, so working on that.  While the initial adjustment was tough, I have actually adapted fairly well to going gluten-free at home. The tough part for me is I love eating out and traveling, so that has been a challenge. I suppose if the answer ends up being NCGS then I could maintain a mostly gluten-free diet but also experiment with the occasional splurges. Snowboarding just doesn't feel right without a beer in the lodge . . ... cider is just not the same!  Thanks again.  
    • Dawn Meyers
      I did some research and found out that vaccines put preservatives, sugar alcohols and metals in them. Which I have a intolerance too.  I was supposed to do testing to find out metal's I was allergic to because I can't  wear jewelry of any kind. Mayo felt I had other allergies also.
    • Scott Adams
      For individuals who have experienced negative reactions to the flu vaccine, there are alternative formulations that may reduce the risk of allergic responses. Traditional flu vaccines are typically produced using egg-based methods, which can pose issues for those with egg allergies. However, there are now several egg-free options available, such as cell-based and recombinant flu vaccines. Recombinant Vaccines (e.g., Flublok Quadrivalent): These are produced without the use of eggs and are grown in insect cells, making them a suitable option for individuals with egg allergies. Cell-Based Vaccines (e.g., Flucelvax Quadrivalent): These vaccines are also egg-free and are produced using mammalian cell cultures, which can be a safer alternative for those with egg allergies. Other Considerations: If you have had a reaction to a specific component of the flu vaccine (e.g., gelatin, preservatives, or antibiotics), discussing your medical history with a healthcare provider is crucial. They can help identify vaccines that exclude these ingredients. It's important to consult with an allergist or healthcare provider to determine the safest option based on your specific allergies and medical history. They can also provide guidance on pre-vaccination testing or desensitization protocols if necessary. Also, at @trents mentioned, could you be getting hidden gluten in your diet? Do you eat in restaurants? If so, this could be why you still have high gluten antibodies.
×
×
  • Create New...