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

I Don't Want Celiacs Anymore


justjess22

Recommended Posts

justjess22 Newbie

I am very new to this site. I usually lurk for longer to get a feel for the place before I post, but I'm too upset right now to do that. I just need help and support, I guess, and I don't know what else to do.

 

I was diagnosed with celiacs (blood test only) when I was 16. My brother was an infant and very sick. He was diagnosed with a blood test as well, and transformed into a healthy baby. It was actually his pediatrician who suggested I be tested as well. I had gone to the doctor's appointment for him and I just looked so sick that the pediatrician strongly suggested I be checked. Later, my younger sister was also diagnosed with a blood test.

 

I went cold turkey gluten-free-- immediately. I followed it religiously for years and felt much better. Then, I studied abroad in college. I actually lived on a ship for four months, as in on the ocean, away from land for days or weeks at a time. When the ship did make port, it was in a foreign country from Ghana to Mauritius to Viet Nam. Food supply on the ship was limited and I don't have to tell you that gluten-free wasn't exactly easy to come by in some places I went. Long story short: I dropped the gluten-free diet.

 

I have never fully returned to it. For three years I have been half-assing it. I tell myself different things. "I'm not that sensitive. I was never fully diagnosed. I don't feel that bad. Avoiding it sometimes is enough."

 

I began seeing a new doctor recently and asked to be re-tested. Again, just a blood test confirms high levels of antibodies. My doctor handed me the diagnosis and sent me away within three minutes. Nothing was mentioned of an endoscopy.

 

But right now, I am so angry. My pity-party is in full swing (I am sobbing as I write this). I don't want this. I don't want to live worrying about every single thing that ever comes near my mouth. I don't want to never taste my favorite foods again (yeah of course there are gluten-free options, easier to find every day. But they aren't even close to being the same). I'm a broke college kid and can't afford much food to begin with (gluten-free replacements are expensive, and so is plain meat, and fresh produce).

 

I don't think I can do this.... I really don't. I can't handle this now on top of everything else. I don't know what to do.


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



Celiac.com Sponsor (A8-M):



CajunChic Explorer

I hear ya! I'm almost a year and a half gluten-free and am completely SICK of thinking about it, talking about it, and paying for it. However, when I think of the diseases I can get if I'm not diligent, it puts me in my "grateful to have an answer" mood. We're talking diabetes, thyroid disease, arthritis, CANCER to name a few! Imagine celiac and other diseases to deal with, as many celiacs do deal with others.

I'd certainly rather deal with a diet before activating more diseases. Maybe ask your parents for help with making meals to take with you since you have celiac siblings. Look for a support group in your area. My favorite coping method: prayer! I believe God gives us all different issues to deal with to make us better people. I know it's my Christian view, but it's what gets me through.

You can do this. Think of your health 5, 10, 20 years down the road. It gets better.

Waitingindreams Enthusiast

Hi there, and welcome to the forum. You definitely came to the right place - there are tons of people on here that are willing to help you ease into this transition. It does get easier with time. Check out the Newbie 101 forum. :)

 

We all know how you feel. Although I feel so much better since going gluten free, in my case - going gluten free wasn't enough. Now I have to avoid all grains and other foods that I am sensitive to, like soy. Before being diagnosed, I was getting progressively worse. I didn't look or feel like myself. I developed embarrassing skin issues (rosacea, seb. dermatitis) I gained about 60 pounds in 2 months,(and went up about 4 pant sizes) and suddenly I couldn't stay awake. On top of that, I was having dizzy spells and I never really felt fully *there*. 

 

Now, I am doing and feeling much better. My skin is clearing up, my energy levels are improving. My hair looks and feels healthier. I've learned so much about food and how to take care of my body that I don't even miss eating the way I used to. The only thing that was so great about it was the ease and convenience. 

 

I never used to cook, but now I am getting creative and trying out a bunch of recipes. It is completely overwhelming and I am still overwhelmed, but then I remember how far I've come and how sick I used to be. I am happy I actually pay attention to what is going in my mouth - we absolutely should! They put a lot of unnecessary crap in our food. 

 

As for eating gluten free being expensive, it's really not! I buy bagged lettuce (a lot of times S&S does a buy 1 get 1 deal) you can grab some cucumbers or other vegetables you like. They have tons of gluten free salad dressings, or you can just use olive and vinegar. I add a can of black beans for protein (throw them in a bowl and microwave them - good with salad, or on rice) You can find gluten free chips (a lot of tostitos chips are gluten free - Fritos are, for example. And as far as junk food goes, Fritos aren't terrible - they only have 3 ingredients) and salsa for quick snacks. Grab peanut butter and some gluten free crackers (or apples)

 

Produce really isn't expensive. Of course it depends on the store, but I can usually grab 3 cucumbers for under a dollar. You can definitely do this. You have to do this - we have to do this. We are all in the same boat. 

 

I miss feeling more 'normal' (being able to eat whatever I want, etc) but at the same time - I didn't even feel normal then becasue I always had "stomach issues" that eventually developed into more. I'd rather be healthy eating my zucchini pasta than sick eating pizza. Btw though, some gluten free pizzas really are fantastic. Same with gluten free mozzarella sticks..and I've tried a gluten free calzone that is amazing.

 

Another quick gluten-free meal (I make these for my bf and he's not gluten-free - he loves them) is to make "grilled cheese pizza" using gluten free bread. gluten-free bread is a little pricier, but if you freeze it you can make it last for a long time and it's definitely worth the cost. Just mix gluten free sauce (Barilla and Prego both have gluten-free sauce) with shredded cheese, and butter the bread as normal. I couldn't eat it because I am currently on the world's strictest diet, but I can't wait to try it. 

 

^And I agree with the post above me. It definitely does get better. I have come so far this past year. Looking forward to making more progress. :)

mamaw Community Regular

hello & welcome

celiac   is  a  hard  disease  to swallow for many. but  it is  what  it is  so  at  some  point  you  will have to bite  the bullet  &  go back to being  gluten-free 100% of the  time  24/7   for  life...   celiac  is  not  just  a  diet  it  truly is a lifestyle change.. ANd  NO ONE  Wants  to  have  it...You did  it  before  & you  can  do it  again.....it  is  much  easier  now  to live  a  healthy happy gluten-free  life with  many  restaurants, & gluten-free  food  available....you  actually did it  when it  was  much harder  to  find  gluten-free  so  you  must  train your  brain to do it  again... the  brain  plays  tricks on  our  thinking  so  get  out  of your  head......

Waitingdreams  is  a perfect  example  of  how  one  can  make  changes  in  their  life...she  came  in  at  the  bottom of the  pit (so to  speak) &  has  listened  & learned by trial & error  until  she got  it. Her  rewards of  hard work & challenges have  paid  off  & now  she to  sees  light  at the  end  of a LONG road....she   is  willing  to give it all she  got  & then some....

It is  natural to feel  sad ,& blue   but  once  you  get  rid  of that  baggage  &  get a game plan in place  you to  will be  able  to defeat  a  big dragon in your  life.. You  will get  great satisfaction  in knowing  how  strong  you really are  & how  happy & healthy  you will  be....

Don't  fight  it  until  another  autoimmune  creeps  in on you  or  even  worse  a  cancer......

This is  one  of the  easiest  diseases  to  control without  chemo,  deadly drugs, or  being  connected to some  machine  for  hours/days....we  just  need  to  be special & eat  special food... can't  get  much  easier...you make the  choice  which  disease  you would  choose!

You CAN  do  this  &   you now  have a  team  of  celiac who  are  onboard  with you to  give  you any help  you  need.. Just  ask

 

hugs

SMRI Collaborator

Well, you can choose to not go gluten-free and just feel cruddy for the rest of your life?  Yes, I miss things, donuts, I really want a good donuts, but I don't want to spend 2 days in the bathroom just to have that donuts either.  There is a adjustment period and you just have to go through a second one.  Eating gluten-free at home is not difficult, there are plenty of options that are just regular, every day foods.  Eating out, yes, that is an issue and even at places that are good for Celiac's, you take a risk.  I am just getting over a bad glutening from a restaurant I've been to several time that was always good in the past, now I won't go there again.  I guess if I had to pick, I'd rather have Celiac than Diabetes.

nvsmom Community Regular

(hugs)

Yeah. :( It is not fair.  We just have to go with the hand we are dealt and make the best of it because it isn't going to change. Try to remind yourself that it could be worse - much worse. Celiac isn't great but it is doable. 

 

Stock up on some cheap gluten-free treats (chips, cookies, whatever) and when you cook, make extras and freeze it so you have food on hand.  Same goes for baking.  Make it easier on yourself by planning ahead as much as possible.  It is a pain, but health is worth it.

 

Go gluten-free. Now. Give away the gluten.  Treat yourself right.  (hugs)

C-Girl Contributor

Justjess22: you lived on a boat and sailed the world! You're adventurous! Embrace this as another challenge. You can do it, you've already proven it. Just think about how your little brother was transformed from sickly to healthy, and keep that image in your mind. It's very important that you heal now and stay gluten free, because the older you get, the longer it will take you to heal.

You are strong enough to do this. You can do this.


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



Celiac.com Sponsor (A8-M):



beth01 Enthusiast

I'm in my late thirties and wish I could go back to my early twenties and find out I had Celiac. Yes it's hard, but so is being sick too often. I would give anything to have the time back I've missed with my kids the last year due to feeling like total s$#&, and this is gluten free after years of not. Yes it sucks, but it is better than the alternative. Have your pity party but then throw on the big person panties and get your diet in check. You'll thank yourself later, trust me.

Azenka Newbie

The worst glutening symptom for me is depression. It's a b%$@# because of course, when it happens, I want to not care about my diet too. And it takes a while for me to feel better afterwards too. And because mood is so subjective anyways, I don't even know necessarily if I've been glutened or I just feel like crap for other things. It's hard because it sabotages me into eating things that I know I will react in some way shape or form to (even if it's all supposedly gluten free), which of course just makes it all worse...these cycles.

 

Don't fool yourself by thinking you don't have it just because you haven't had an endoscopy; ultimately it's an auto-immune disease, and intestinal damage is just 1 facet of it. Skin issues, nerve issues, intestinal issues...The very fact that you have antibodies in your bloodstream should be raising alarm bells in your head. Auto-immune antibodies-your body is damaging itself.

 

It's not a struggle if it just IS. I can only follow this diet because it just IS. That's why things like dairy, and chocolate, and processed meats, mango, and all these other foods I know I shouldn't have, I fail and sometimes indulge in. Because to me those're foods where 'Well, this is the reaction I get to it, is it worth it?' 

But not if it's gluten. I can easily avoid things that have gluten because I know that whatever damage happens to me, I'm damaging myself in serious ways that, to me, are subversive.

 

It's a mindset, being gluten free. If I had to struggle everyday and overcome urges to eat gluten everyday, I could not do it. But I don't think of it that way. For instance, when I moved in with my current partner, me telling him our kitchen MUST be gluten free, he, in the throes of newfound love, did it no questions. He also wanted to be 100% gluten free himself so we wouldn't have to worry about hands and kisses etc, which meant being as gluten free and as careful as I am. He'd come home and tell me about times when he considered getting something to eat on the way home that had gluten, and then he'd be proud of himself for resisting the urge. Which is great and all, but I bluntly told him that if I had that attitude towards it, I would fail sometimes. It cannot be a struggle for me. It must be an acceptance. I do not pass by restaurants and consider eating at them. I do not imagine it. I do not allow myself to float the idea of eating foods I should not have. This, I firmly believe, is the difference between me successfully living versus being disabled. 

 

If you do not go all or nothing, you are floating the idea of it, allowing yourself to listen to cravings, and if, as it is with me, gluten affects you mentally, you are completely sabotaging your will by occasionally indulging. It's not an indulgence, you're poisoning yourself.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,547
    • Most Online (within 30 mins)
      7,748

    gizmo1jazz2
    Newest Member
    gizmo1jazz2
    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.