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

Newly Diagnosed And Curious


Npealer

Recommended Posts

Npealer Rookie

Hi everyone,

I am newly diagnosed with Celiac's (as in the last week) and I am curious how many other's have stories like mine.

I have never been someone who had a lot of allergies, stomach issues or anything else of the sort. I really thought that I was going to be diagnosed with RA or Fibromyaglia. For the last couple months I had more of the brain fog, fatigue, insomnia, bone and joint pain as well as neuropathy in my hand and arm. My doc ran a blood panel on me that just about tested for everything under the sun, I even had an MRI done hours before my official diagnosis came in. After reading some of your stories how you had years without any real help or correct diagnosis I feel lucky that I was diagnosed rather quickly. Of course it is not what I thought it would be and as soon as I learned what was wrong I went home and started reading labels. I meet with a nutritionist tomorrow and I am taking my husband with me so he can understand exactly what my diet restrictions are.

So I was just wondering how many of you had more of the symptoms I had VS the stomach issues more commonly associated with celiac disease? I have been very strict with my diet this last week and I already am starting to feel much better. I finally got rid of the headache that had been plaguing me and I already feel like my sleep is starting to return to normal. My next challenge will be to navigate my diet thru a weekend in Vegas.


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



Celiac.com Sponsor (A8-M):



adab8ca Enthusiast

First, welcome! You are now finally on the road to health.

I am one of you in that I thought I was going to get diagnosed with MS or ALS or some neurological problem or cancer. I had bad neuropathy in my feet and hands. Terrible headaches. Weeks and weeks of headaches. Anxiety attacks that were unbearable and horrible depression. Insomnia where I did not sleep for days. I did lose weight (quite a bit) and had NO appetite but it wasn't an upset stomach at all, just not hungry. It was a shock to everyone that I had celiac (especially myself). I am very tall, pretty robust (although not fat, you would never call me skinny). My vit D was low, my iron was marginal as was my B12 but my bloodwork didn't seem to scream HOUSTON WE HAVE A PROBLEM WITH ABSORPTION.

I am 6 months gluten-free today and have more good days than bad. Depression and anxiety are gone, I sleep. I still have some neuropathy pain but 6 months ago, I was SURE I was going to end up in a wheelchair. My nerves were so painful I had to sleep with pillows under my knees so my heels wouldn't touch the bed.

But enough about me! I am glad you are already starting to feel better and if you have any questions, ask away

Ada

Npealer Rookie

Thanks Ada! I feel like I have learned a ton in this last week but have miles to go. I am sure I will be asking a lot more questions in the weeks to come :)

Korwyn Explorer

I didn't start developing GI issues until about 6 years before I was diagnosed. I had a lot of other wierd 'random' issues though, and also developed neuro and psych (depression, panic attacks, severe insomnia). I was very 'asymptomatic' - whatever that means these days. :) I mean when the Red Book lists over 300 known symptoms, conditions, and linked/related disorders, how can you possibly define symptomatic/asymptomatic?

MrsVJW Newbie

Don't fear Vegas if you're gluten free! We made our first trip there last November, and were even able to hit some of our faves (Pinks hot dogs - no bun or chili for me, Fatburger - no bun, the chili there is OK) and there are tons of options and the servers and staff there seem to know the basics and just ask. Most of the higher-end restaraunts will be able to make accomidations from gluten-free if you can't find something thay already works on the menu. I think the La Salsa Cantina at the Forum Shops has a menu that is a little different than their other locations - I think their tortilla chips are okay (if they are fried in-house, I don't think the use shared cooking oil with any flour tortilla things). The only really bad thing about a Vegas trip is the sad airport offerings to and from, lol.

Brigit Apprentice

Your story sounds like mine.

For the past year, I've had that brain fog (where you can't seem to string a sensible sentence together), tiredness (even though I'd sleep 8 hours) and bone and joint pain. My fingers would hurt the most and I'd just 'feel bruised'.

I also had very sore eyes and my hair was falling out.

The doctors just kept checking my iron levels and telling me to take tablets, even though my levels kept dropping, they didn't do much, except finally move me onto iron drips this past year.

I hope your husband understands and is wonderfully supportive and that you soon start feeling the results of eating gluten free.

And ask lots of questions on this forum, everybody is super helpful and it'll make the transition in your lifestyle smoother and quicker!

All the best!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,551
    • Most Online (within 30 mins)
      7,748

    Newest Member

    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

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • 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.
×
×
  • 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.