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

New Here And Totally Overwhelmed


Rhonda-R

Recommended Posts

Rhonda-R Newbie

For the past 6 years my family's life has been consumed with learning about Crohn's disease. My son was diagnosed at age 11 and he's had a terrible time with it. I was diagnosed with Ulcerative Colitis 2 years after his diagnosis, but I ignored my problems to deal with his. I really didn't have the energy to give to my own issues and so, I simply pushed myself through.

In November my son was in the hospital for 3 weeks. During that time we met a physician that we bonded with right away. He told us that he wished he could follow us at his integrative medicine practice, but he has a 2 year waiting list. After seeing my son and chatting with us many times during my son's stay we found we meshed well and were sad we wouldn't be able to continue to see him. The day prior to my son's release the doc talked to the other physicians on his staff and convinced them to fit both of us in right away.

My doctor ordered so many tests I thought I'd be anemic from the blood work. One of the tests she ordered was a Celiac Disease Panel. I'd never considered that I may have Celiac Disease. I'd been on the SCD diet for over 6 months when I had the test done. I didn't eat any grains prior to the test and I still had 20 U/mL of Gliadin AB IGA in my blood. My IGA Serum fell within normal limits and the Tissue Transglutaminase AB IGA fell in the negative range, but my doctor still told me to stay away from gluten. She said that the antibodies have a crazy half life and take a long time to work out of our system. Does anyone know if the other levels were low because I hadn't ingested gluten in over 6 months?

My B12 levels were very low, as were my vit. D so I'm taking injections every other day for the B12 and supplements for the vit. D. My thyroid isn't working, my adrenals aren't working... lol, I'm a mess.

My son's blood work will be back any day now, and I'm worried that he will also have the burden of Celiac disease on top of his Crohn's disease. His food allergy tests came back and he's already allergic to many nuts, soy, corn, etc.. the list is long. I'd like to find foods away from the SCD that he can eat so he can gain a few pounds. At 6 foot tall, 130 pounds is mighty skinny.

After spending 6 years with Crohn's I feel like I know sooo much about that disease and here I am, starting at square one with something new. It's just so overwhelming I'm frightened that I'll fail and get worse. I'm tired as tired gets, sick of being sick and just barely able to hope. Any help, direction, etc would be appreciated. I did order the Dummies book.

Thanks

Rhonda


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

It is overwhelming at first. The good news is that with a diagnosis of UC you may find that the gluten free diet helps you bring that undercontrol or even into remission. It may also help with your son's Chrons. No matter what his test results do give the diet a good try for you both. You have come to a good place for support and info. Read as much as you can here and ask any questions that you need to. I am really glad for you that you seem to have found a good celiac savvy doctor. It may make a big difference in your health and quality of like.

Jestgar Rising Star

It will get easier. Just start as best you can with reading labels, and realize that before too long it will no longer be so awkward and time consuming.

It really will be fine.

Wolicki Enthusiast

It does get easier. Take a deep breath, and read lots of labels and threads on this site. If you have questions, someone here has an answer, almost always. Try to stick with whole, unprocessed foods- proteins, fruits and veggies. It is hard to digest many things while your intestines are healing. You should definitely give up dairy for a while. it is also common to have reactions to potatoes, tomatoes, eggplant and peppers, corn, soy, nuts and eggs. It's best to stay away from these until you have healed. Simple meals with few ingredients is the way to go.

It may also help to take daily probiotics and enzymes with meals until your gut is healed. Be sure to check the labels on your prescription meds, toothpastes, anything that will go into your mouth. Try to eat foods that you have prepared, because the risk of cross contamination is great at restaurants, or meals prepared by well meaning loved ones.

There's definitely a learning curve, so read, read read! When in doubt, don't take a chance, call the company.

Rhonda-R Newbie

Thanks for your replies. After 6 months eating SCD I've become accustomed to eating a pretty simple diet. We're taking good probiotics and L-glutamine. It was interesting reading Ravenwoodglass's tag lines. I've been diagnosed with so many things, or should I say misdiagnosed. Although I have had dermatitis herpetiformis covering my arms and legs, it was a doctor that saw me after they had disappeared who finally did a Celiac Panel on me. I'm just surprised that so many of my health issues may have started from Celiac Disease and I hope that learning to eat gluten free will help turn some of it around. I'm not sure I want the early menopause to reverse itself.. I really don't want to go through that again. I'll have to read through the board's forums to see how many people have stories like I do. I'll not be surprised to be one of many.

At the moment I'm trying to figure out how stringent I need to be about cross contamination, gluten in my shampoos/lotions, etc...

Thanks again for the replies,

Rhonda

ravenwoodglass Mentor

Thanks for your replies. After 6 months eating SCD I've become accustomed to eating a pretty simple diet. We're taking good probiotics and L-glutamine. It was interesting reading Ravenwoodglass's tag lines. I've been diagnosed with so many things, or should I say misdiagnosed. Although I have had dermatitis herpetiformis covering my arms and legs, it was a doctor that saw me after they had disappeared who finally did a Celiac Panel on me. I'm just surprised that so many of my health issues may have started from Celiac Disease and I hope that learning to eat gluten free will help turn some of it around. I'm not sure I want the early menopause to reverse itself.. I really don't want to go through that again. I'll have to read through the board's forums to see how many people have stories like I do. I'll not be surprised to be one of many.

At the moment I'm trying to figure out how stringent I need to be about cross contamination, gluten in my shampoos/lotions, etc...

Thanks again for the replies,

Rhonda

I would be as strict as you can at first. Many of us have issues with shampoos and lotions that have gluten ingredients and CC from the manufactoring process or from crumbs and such in our homes and restaurants. Celiac is an autoimmune reaction. Our bodies create antibodies and those antibodies are reactivated with a surprisingly small amount of gluten.

My OB/GYN told me my periods might start again, celiac had driven me into a very early menopause, and I felt the same way you do. Now however I wish it had started again. Even though it would have been a pain to deal with again.

mommida Enthusiast

If you weren't eating gluten before your testing it will throw off the results.

It sounds like the doctor just wants you to get better as quickly as possible. The gluten free diet can help with the Chrons.

The diet gets easier with time. Every one here has experience to help you through. Keep a food journal to keep track of hidden gluten or other food intolerances.


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



Celiac.com Sponsor (A8-M):



LDJofDenver Apprentice

It can be a little overwhelming at first. We

Rhonda-R Newbie

Thanks for the links, I'm looking them over and doing quite a bit of reading. I'm still overwhelmed, but I'm tackling it. LOL, it's not like I can give up or stop eating!

I'm lucky to have a Gluten-Free store an hour from our home... everything in the store is gluten-free and my son and I giggle and race from item to item checking for soy and corn (his allergies.) I've been chatting up my local grocery and they have a 7 page list of Gluten-free products they carry now. They're in the process of listing the items by isle, personally I'd love them in their own area!

My son's tests came up negative for Celiac, but he's been following the SCD diet for 6 months, so we really don't know. What I do know is that when we removed the grains from his diet all of his stomach pain, diarrhea, etc. disappeared and his once totally ulcerated colon started healing. To me, that's really enough evidence. I don't want to start feeding him wheat and have him suffer just to get a formal diagnosis.

Are there blood tests available for Celiac Disease that don't require gluten consumption? I remember reading about a DNA test. I guess I can google that next. All of this research is keeping me from my housework... darn it! *grin*

~Rhonda

GFinDC Veteran

You can get a genetic test done but it doesn't prove that you have celiac. Many people have the celiac genes but don't have the disease (autoimmune reaction) The reaction to the diet seems pretty clear though.

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
      132,156
    • Most Online (within 30 mins)
      7,748

    Shrub
    Newest Member
    Shrub
    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.