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

Headaches


Kenster61

Recommended Posts

Kenster61 Enthusiast

Hi,

I get these headaches almost every day. Even when I'm relatively gluten-free. I never made the corelation but I'm wondering if this is a part of the condition. If we are losing nutrients this might be a symptom of that. If you have them what do you take for them.

Ken


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



Celiac.com Sponsor (A8-M):



Nashville Contributor

I've had headaches on a regular basis for the past four years. Nothing too bad, but just enough to bother me. I have been gluten free since Nov. 1 and the headaches have not subsided much, if any. I am being patient, realizing that it can take a long time (maybe a year or two) for my intenstines to fully heal and help my body get all the nutrients it needs. In addition to these headaches, I suffer from fatigue, as well. Nothing that keeps me from work or living a relatively normal life, but I don't feel up to excercising, or anything like that.

Janine Newbie
Hi,

I get these headaches almost every day. Even when I'm relatively gluten-free. I never made the corelation but I'm wondering if this is a part of the condition. If we are losing nutrients this might be a symptom of that. If you have them what do you take for them.

Ken

Hi Ken- I get headaches nearly every day (including several bad migraines a month) and went off gluten for 7 months without any improvement in them. I am off gluten again because I relate so strongly with all the symptoms I read here. I know my intestinal track improves off gluten. Maybe the headaches and migraines will eventually go away if we heal? I know a lot of celiacs get migraines. I also have sleep apnea, but have had no headache relief after a few months on the breathing machine. Sigh... I have been fighting migraines for 25 years... I hope gluten free living will help you.

Janine

Guest cassidy

I used to have headaches all the time. Very intense ones where light bothered me and I would want to curl up in a ball and cover my head.

I went to a chiropractor and she said most headaches are caused by your liver. I didn't really believe that. Then she pressed near where my liver was and pressed on other pressure points and my abdomen started gurling and she said my liver was dumping. 15 minutes later the headache was gone. I kept going to her and the headaches stayed under control, and she could stop one if they started, but then I moved.

Since going gluten-free, my headaches are gone. If I get glutened then come back and last for 1-3 days after I eat something bad. I was wondering if the headaches being related to gluten makes sense with the liver thing. If your liver processes toxins in your body, and gluten is toxic to us, maybe the liver doesn't like it when you eat gluten?

You said you are "relatively gluten free," I'm not sure that makes sense. Either you are, or you aren't gluten-free. Even a tiny bit can bring on symptoms and isn't good for your body. If you become completely gluten-free, maybe your headaches will go away. Maybe not, but it is probably worth a try.

Turtle Enthusiast

I too have had this headache issue. I talked to my DR about it and his concern was CROSS CONTAMINATION.....My dr has encouraged me to not eat out at all & really watch my own kitchen to assure everything is gluten-free for the next 3 months to see if there is any improvement so he can determine whether this is a CC issue or something else. He also recommended for me to continue w/ massage therapy to assist w/ any stress in the neck and back. If you can't afford massage therapy like myself, look into a massage school in your area. I go to the one near me and it's only $30 for an hour. So far i've only had headaches once or twice....It's been my understanding from my DR and from many people on this board that Cross Contamination can be the culprit in a lot of cases....hope this is helpful and hope you feel better soon!

Turtle

sparkles Contributor

I suffered from migraines for about 40 years....very intense migraines that could be triggered by many foods, stress, light, etc... When I found out that I had celiac disease and became gluten free, the migraines disappeared. Even foods (like chocolate) that once triggered severe migraines no longer triggered them. I know that my migraines were related to celiac disease. I have not had a migraine since becoming gluten free and I was even free of headaches in general. Unfortunately, headaches have started again....not migraines, thankfully, just plain old uncomfortable headaches. I haven't figured out what is causing them as they seemed to have started last fall and I usually wake up with a headache. I do not think that I am as gluten-free as I would like to be as I have started eating out more and have started trusting labels when they say gluten-free so my diet has expanded some. I really think from experience....only 4 years as a celiac....but our diets really create havoc to our systems. Even the smallest amount of gluten seems to affect me....so now I am even trying to stay away from products that say they are gluten-free but are produced in a plant where wheat is used. Companies like McD need to be upfront with the customer. If wheat is used and then "processed out" (as McD is claiming), that needs information that is available to us and then we, as consumers, can decide if it is worth the risk. Unfortunately, I think sometimes gluten can be consumed and there are no symptoms immediately so we think that some foods are safe. But it seems to be a vicious cycle....I guess, for me, I should just go back to a hamburger with a lettuce salad and lemon for dressing. That was my diet for about 5 months after finding out I had celiac disease. I did feel better but ended up being very isolated. Anyway, I seemed to drift off the subject....Migraines are a symptom of celiac disease.... You might want to make sure that you are really gluten-free. Eliminate any and all processed foods (including things like rice that have been processed), even those that are gluten-free and go back to just basic meat (unprocessed), fresh veggies and fruit. I bet you will feel better.

jerseyangel Proficient

For about the last 2 years that I was eating gluten, I would often wake up with headaches that would seem to come from the base of my skull. It would hurt from the back of my neck on up. I quickly noticed that those headaches came at the same time as my stomach acting up worse than usual. The strange thing was that the headache felt better when I got up--it was much more painful to lay down when I had it. I also have hip pain and through reading here, I understand that those are 2 locations that are affected by Fibromyalgia--although I was never Dx with it. Since being gluten-free, those headaches are much improved, as is the hip pain--but neither is completely gone.


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



Celiac.com Sponsor (A8-M):



Kenster61 Enthusiast

Guest cassidy
I meant that I try very hard to eat gluten free but because of cross contamination or eating at a place that doesn't understand or care I get glutened. I try not to but it happens.

I completely understand that because it happens to me as well. I thought you meant that you cheat on the diet or you didn't feel that small amounts would hurt you. My company is going to PF Chang's for a dinner and I was happy to see they had a gluten-free menu, now I'm a bit concerned.

  • 2 weeks later...
Guest adamssa

Hi~

How long after becoming Gluten free did it take for your migraines and headaches to go away?

I am just becomng gluten free now (1 day so far), after about 6 months of having hardcore symptoms that the docs didn't know what they were. The headaches are the worst part of it for me, and I am anxious for them to go away. I am eating absolutely no gluten at all...

Sara

Jen H Contributor

I used to get massive migraines before my diagnosis. I think my migraines were related to food. After about 3-4 months on the diet they finally went away.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,898
    • Most Online (within 30 mins)
      7,748

    MLucia
    Newest Member
    MLucia
    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

    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
×
×
  • 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.