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

Newbie


Maryw88

Recommended Posts

Maryw88 Apprentice

Hello all,

I have been going it alone for about a year and a half and am hopeful this board will open me up to some support.

I have been suffering with migranes, numbness and tingling for years. A few years ago I started having stomach troubles; mainly severe gas and cramping after eating. I went to the doctor to be told it was IBS. His advice was to stop eating fruits and veggies :)

I wasn't convinced so I went to an allergist. I tested positive from a skin prick test for wheat. When I started avoiding wheat I began to feel better and became more aware of my symptoms and the reactions I was having to food. I also started to notice severe gastro reactions to barley and oats. Additionally I have found that I am lactose intolerant and soy intolerant. Soy actually causes worse gastro symptoms than gluten. I also get pretty severe acid reflux.

I then decided I would cut out gluten all together and noticed a dramatic improvement of almost all my symptoms. Gastro symptoms and nuerological symptoms are almost gone. My Vitamin b12 and Vitamin D levels are almost non existant. Sublingual tablets have helped here but I am still very run down. My doctor does not see how this could be related but I think it could be lack of absorbtion.

My biggest frustration at this point is a lack of respect or compassion from my doctors concerning my intolerances. I was actually tested recently by my physician after finally complaining enough. The results were negative which I now realize was because I have been gluten-free for over a year. I am in the process of waiting to go to the University of Chicago Celiac center to see if they can tell me I am not crazy for suspecting celiac.

Bascially I am just hoping to find out if anyone else has a similar story. Have any of you had similar symptoms? Am I crazy for feeling that Celiac is the right diagnosis here? My physicians seem to think I'm nuts but it just feels so much better to be gluten-free/soy free/ dairy free. Any advice from the board would be appreciated. Reading all your posts has really helped.


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



Celiac.com Sponsor (A8-M):



ukdan Rookie

No, you're not crazy- either that or we both are! Apart from anxiety and dizziness I haven't had many neuro symptoms like yours (although those are related to celiac) but I've had all the stomach problems.

I have been similarly lumped into the 'ibs' category (pending upcoming biopsy results) but found I have been much better off gluten, dairy and soya. You may also want to look into sugars as well as fructose malabsorption may be an issue seeing as you appear to be quite sensitive at the moment.

If you feel better without it don't worry what the doctors do or don't label you with, you're not alone!

Bubba's Mom Enthusiast

Hello all,

I have been going it alone for about a year and a half and am hopeful this board will open me up to some support.

I have been suffering with migranes, numbness and tingling for years. A few years ago I started having stomach troubles; mainly severe gas and cramping after eating. I went to the doctor to be told it was IBS. His advice was to stop eating fruits and veggies :)

I wasn't convinced so I went to an allergist. I tested positive from a skin prick test for wheat. When I started avoiding wheat I began to feel better and became more aware of my symptoms and the reactions I was having to food. I also started to notice severe gastro reactions to barley and oats. Additionally I have found that I am lactose intolerant and soy intolerant. Soy actually causes worse gastro symptoms than gluten. I also get pretty severe acid reflux.

I then decided I would cut out gluten all together and noticed a dramatic improvement of almost all my symptoms. Gastro symptoms and nuerological symptoms are almost gone. My Vitamin b12 and Vitamin D levels are almost non existant. Sublingual tablets have helped here but I am still very run down. My doctor does not see how this could be related but I think it could be lack of absorbtion.

My biggest frustration at this point is a lack of respect or compassion from my doctors concerning my intolerances. I was actually tested recently by my physician after finally complaining enough. The results were negative which I now realize was because I have been gluten-free for over a year. I am in the process of waiting to go to the University of Chicago Celiac center to see if they can tell me I am not crazy for suspecting celiac.

Bascially I am just hoping to find out if anyone else has a similar story. Have any of you had similar symptoms? Am I crazy for feeling that Celiac is the right diagnosis here? My physicians seem to think I'm nuts but it just feels so much better to be gluten-free/soy free/ dairy free. Any advice from the board would be appreciated. Reading all your posts has really helped.

Hello..and welcome!

It's very common to go unDXed or mis-DXed. They say the average prson takes around 11 years to get a correct Dx.

Like you, many Celiacs find out on their own that they're reacting to gluten. Many of us have additional intolerances.

Once you go gluten-free the tests will not detect it. The only test they can do is the genetic one, which doesn't always paint a clear picture either.

Most Dr.s think of Celiac disease as a rare thing. That's what they're taught in medical school. Add to the mix that 20-30% of us test negative in our blood work.

It's insulting to have Dr.s dismiss your symptoms or Dx. I've run across this myself. Even after getting a positive Dx for the long list of symptoms I had, my Primary care Dr. said he didn't agree with my Dx and wasn't willing to do the follow up blood tests to determine any vitamin/mineral deficiencies. I had the GI run the tests and got a new PCP. You are correct that vitamin levels get low due to malabsorption.

Stay 100% gluten-free, and stay away from your other intolerances too. You know your body better than any Dr.!

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    2. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    3. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    4. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    5. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,158
    • Most Online (within 30 mins)
      7,748

    MollyK
    Newest Member
    MollyK
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      This article does not address migraines at all.  Yes, red wine and sulfites are often mentioned in connection with migraine triggers. With me, any kind of alcoholic beverage in very modest amounts will reliably produce a migraine. Nitrous oxide generators, which are vaso dialators, also will give me migraines reliably. So, I think most of my migraines are tied to fluctuations vascular tension and blood flow to the brain. That's why the sumatriptan works so well. It is a vaso constrictor. 
    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
×
×
  • 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.