Jump to content
  • 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 And Gluten Free Diet


danzn16

Recommended Posts

danzn16 Rookie

Have any of you experienced a decrease in the number of migraines you get by going on a gluten free diet? I've had migraines since I was 3 years old and nothing I've done has helped. My chiropractor thinks I have a gluten sensitivity and thinks I should stop eating gluten and that it would help my migraines. Any one have any experience?

Thanks!


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



Celiac.com Sponsor (A8-M):



psawyer Proficient

Welcome to the forum.

I had migraines for years, but they stopped completely on the gluten-free diet.

coffeetime Explorer

Ditto the last post, actually the only way I know that I've been glutened is when I develop a migraine a couple of hours after.

danzn16 Rookie

my doc said it takes 3 weeks to get gluten out of your system. i've been on a gluten free diet for almost 2 weeks. i've had 4 migraines since then. so i'm hoping it's just because gluten is still in my system, or even from withdrawal. i hope it helps!

eatmeat4good Enthusiast

I had migraines that got increasingly worse until they almost never stopped for 7 years. Within 3 weeks of going gluten free, I knew it was the answer and I would get better being gluten free. Hang in there. I still get a menstrual migraine but it is nothing compared to the gluten migraines. Be very careful of trace gluten and cross contamination because even particles will cause a gluten headache for me (and maybe you too). I hope your Dr. is right and your headaches go away completely.

ravenwoodglass Mentor

Mine also stopped once I went gluten free. It took me a while to get strict with the diet and become aware of Cc risk so I had a couple the first month or so but now I only get them with a glutening.

danzn16 Rookie

Mine also stopped once I went gluten free. It took me a while to get strict with the diet and become aware of Cc risk so I had a couple the first month or so but now I only get them with a glutening.

How do you get strict with the CC? I am strict at home but not so much when I go out to eat. What do you say to your server to decrease risk of CC?


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

How do you get strict with the CC? I am strict at home but not so much when I go out to eat. What do you say to your server to decrease risk of CC?

I very rarely go out to eat and when I do I only go to someplace that has a gluten free menu. If you don't know what places near you have a gluten-free menu then go online put in your city and the words gluten free restaurant and you will find your options. We can never assume from the menu that something is gluten free. Some places even mix pancake batter in with their eggs to make them fluffy. Fries need to be asked about and if the anything is cooked in the same fryer as gluten foods then it will not be safe. Plain steak or chicken cooked in a clean pan and seasoned at the table with salt and pepper should be okay as should a baked potato and veggies with no seasoning. Some of us will bring our own salad dressing and ask for a plain salad with no dressing. There are some folks who are sensitive enough to cross contamination that they will eat before they go and simply enjoy others company.

sreese68 Enthusiast

How do you get strict with the CC? I am strict at home but not so much when I go out to eat. What do you say to your server to decrease risk of CC?

I bought several of these dining cards and love them! Open Original Shared Link The color coding is very nice, and they're laminated. I keep one in my wallet. I also like her grocery guide. It fits into my large purse.

psawyer Proficient

The link in the prior post gets a 404 error, but I think this is the correct one: Open Original Shared Link

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.