Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

Dealing with Celiac


AmandaWiggin

Recommended Posts

AmandaWiggin Newbie

This year has been a very trying year for me. In October 2015 a blood lab was done that had shown me as Celiac positive.... due to having no gastrointestinal issues at the time it was told maybe it was a false positive to go about my life, unless symptoms showed.

then the weekend before Easter 2016 I went to NYC for a show and after a 3 hour drive home... my stomach was in agony.... I tried the first thought to mind was to go to the restroom... at this point I realized I could not go.... within 3 days I went from not being able to pass a bowel movement to not being able to urinate. Scared I went to my doctors who became very concerned and sent me to the hospital.... I was catheterized where they drained 900L of urine. I went through everything under the sun... enemas, magnesium, miralax, suppository and finally a manual disimpaction.    I was tired and embarrassed,but I made it through and they sent me home thinking it wa fixed.  The following day I realized that I still could not go to the restroom, I had no appetite or thirst.... I went back to the hospital on April 1st where they catheterized me once more and pulled another 1,000 L.    They decided to hospitalize me and during the 1-3rd I went through a sigmoidoscopy.... released I had no appetite, but was better and on meds to help my bowels work.   I had to stop them for just a weekend for a test, one day off and I had issues... and once again on April 15th was hospitalized through the 19th where I went through a colonoscopy and endoscopy.    It was found that I had full Celiac, Esophogitis, and chronic gastroenteritis.

 

my Celiac was found to be so bad that I couldn't even handle trace amounts of gluten. Eating out was no more, for just because it said gluten-free didn't mean it was... why? Because it was cooked on a glutened surface and became traced gluten.

 

this has been a very rough time... learning what is and is not gluten and watching my family eat out while I watched. Changing your eating habits after 30 years is not exactly easy.  And due to my Celuac and other chronic health issues it's made blood labs helter skelter, I've lost tons of weight... at current my celiac is in flare. Ow and I've lost 18lbs in 3 weeks not having a real appetite.

 

im sure others can relate and I found this forum thanks to twitter... I hope others can share their stories.  This is a long and not so easy road.

----------------------------------------------

but here's a great little dinner...

gluten free pasta (prefer barilla spaghetti. )

     -cook the pasta, and drain it-

use gluten free teriyaki sauce and pour a little bit in the pasta and mix cook a little (about 2 minutes to let the sauce simmer and mix well)

 

then cook kabasi (spelling?). When it's done cooking, add a little teriyaki to this as well and cook in. 

 

Take me kabasi and pasta and mix!  ?

 

Its tastes fabulous and then cook cook a veggie on the side if you prefer one.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Welcome Amanda!  

Gosh, I can not believe that your doctor did not catch you celiac disease diagnosis!  (Sadly this happens all too often.) Actually, anemia is the most common symptom of celiac disease.    I too, did not have GI issues when I was diagnosed and I had Marsh Stage IIIB villi damage.  

I hope your recovery from your recent glutening is quick!  

 

Link to comment
Share on other sites
GFinDC Veteran

Welcome to the forum Amanda! :)  Boy, that sounds like a pretty rough time you've had.  I hope your doctors referred you to a dietician for info on how to eat gluten-free.  But if they didn't, no biggie, we have lots of experienced people on the forum who can help.  There is a beginners' thread  called Newbie 101 stickied at the top of the 'Coping With" forum.  It might help some.

Your doctor should also test you for vitamin deficiencies, as the can happen due to gut damage.  Some of the vitamins we tend to be low on at first are Vitamin D and the B vitamins.

I suggest that you switch to a simple, un-processed food diet for a few months.  Whole foods and very little processed foods.  Making all your food at home is good way to be sure you know what is in the food you eat.  Meats, veggies, nuts and fruits should be your main foods IMHO.  Most gluten-free processed foods are low in vitamins and high in carbs.  So they aren't a big help when try to rebuild your body.

You might also benefits from pro-biotics.

Pepto Bismol, and Milk of Magnesia are helpful at times, plus some plain old aspirin.  Peppermint tea can  help to get gas out of the stomach.

Try to avoid eating out at restaraunts for a while, and even eating food other people (like family members ) make.  You picked an interesting time to get diagnosed, right before the Thanksgiving holiday!  But there are threads on Thanksgiving ideas in the forum that might help.  You can search for Thanksgiving and find some.  Most meats are gluten-free but do check the label.  The most likely ones to have gluten are pre-spiced meats.  Turkeys sometimes say they have wheat or barley ingredients but often enough it is in a separate gravy packet you can toss out, no problem.

Your symptoms should begin to improve after going gluten-free, but it may take months or years to fully recover,  Our bodies need a lot of protein to heal the damaged tissues, so give it what it needs.

Betaine HCL and digestive enzymes may help also.

Link to comment
Share on other sites
Ennis-TX Grand Master

Yeah the constipation threw my doctors off at first too, used to spend 5-10days then have to drink 2-4times the dose of a laxative to have a normal bowl. On the bright side after years of gluten-free gluten has the opposite effect at first then the constipation which clears in a day. Now days I still maintain a 50-80g of fiber (nut, seeds, veggies) a day and regular magnesium supplementation.

I have shared many a horror stories here from my experiences, it helps to come out. I have shared my mental traumas, my family issues and interactions, and issues with people who seem to make a joke out of it and try to poison me (literally we got this guy on camera). And those regrettable issues where you run into a common food that they change the ingredients or prep on. I even started posting on a blog about some random issues I run into and how I deal with my life now days.

We are all different in how our body reacts to gluten and the issues that develop, I am sure you can find someone to give you plenty of pointers with similar issues here, But you should always check with a dietician about developing a diet around your issues. Welcome to the forum and we are here to help.

Link to comment
Share on other sites
AmandaWiggin Newbie

I was lucky and had a good GI doctor who referred me to nutrition and I now also use an app on my phone called the gluten free scanner.   

 

Life is certainly not easy, I don't eat out and most times we have to prepare two meals in my house... sadly I don't know where in my fam the celuac came from.... my grandmother has no want in being tested, and my father was adopted.... mom passed away.   So it's a mystery I will never know.  Until I became sick I had no warning signs or issues.... the celiac was found because my RA doctor decided to randomly check by blood.   Since April I have become much more knowledgeable.... but I still go through ups and downs where I start loosing significant amounts of weight but I test negative for anemia.    My Vit D is always low no matter how long I take the 50,000 unit pills I get it up, then doc has me do over the counter 2,000mg a day and within a month it drops to below severe.

Link to comment
Share on other sites
Ennis-TX Grand Master

Yeah I was adopted and to this day we can not get my birth mother to release medical records, we found out when I was in my 20s and thought I was literally dying, even running a bucket list. Went from over 200lbs to under 130lbs in a 6 months at 5' 11", I have posted my diet and talked about it pretty much eat like a body builder, whole bunch of fats and protein. Supplements arranged around my needs and eat a balanced meal based around what my body needs, of whole foods. Dealing with some complications with the disease now and seeing doctors but aside from the anemia (Intestinal Bleeding) I am doing pretty good. Started off using a food scanner on my phone with a app, but I am now a master at reading labels and knowing my brands.

Link to comment
Share on other sites

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Suzi374 replied to Suzi374's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Lots of tests

    2. - Suzi374 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Lots of tests

    3. - Peace lily posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Would like to gain weight

    4. - Smith-Ronald replied to Soleihey's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Lymph nodes

    5. - Bayb replied to Bayb's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Trying to read my lab results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,224
    • Most Online (within 30 mins)
      7,748

    Suzi374
    Newest Member
    Suzi374
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Suzi374
      And I’m anaemic, however I’m also female and vegetarian. I had an iron trans a couple of years ago however it’s starting to dwindle and taking supplements doesn’t seem to work. I can’t seem to absorb it. 
    • Suzi374
      Hi, I attended a neurologist appt last Tuesday, which I nearly cancelled, due to ongoing numbness and tingling in toes to mid foot. One of the first things he asked was ‘are you celiac’. I’m not. He thought all reflexes were ok but at the last minute decided on nerve conduction tests which were low normal. He was a little confused as he felt they should be better and tried a new set of probs, all the time, giving me multiple shocks which were not enjoyable lol. Anyway, he’s now ordered tests for myeloma, and all the vitaminy things that so many of you mention on here, also tests looking for autoimmune responses. I already have Hashimotos. Interestingly, to me, but maybe someone out there can relate or knows more than i do, although I was a nurse, but ED not ‘weird symptoms’  nurse. Anyway back to the interesting thing, I took duramine in 2013 to lose weight which caused a massive panic attack when I stopped taking it and half my hair fell out. I only took it for a week but it was horrible and I regret it. It triggered ongoing panic attacks which are horrendous. So I feel like I’m a bit crazy. Then in 2020 I had this sudden onset of horrible pain when trying to eat a cinnamon roll. It continued and I lost around 20 kgs. I had two gastroscopes and a colonoscopy and they were all normal. I scored a barium swallow and CT angiogram. All normal. The pain subsided a little but I was left with reflux and an awful feeling that I couldn’t get air when I ate some foods. This was not anxiety.  The anxiety was separate and I still maintain this. This was something to do with eating. It was like the air was thick but I wasn’t short of breath. I just had the sensation I was, then it triggered anxiety. Anyway, I had other weird things- couldn’t bend knees to shave legs in shower lol. Knees felt stiff and swollen but they weren’t. Knee WOUld swell up randomly but mri showed minimal issues. A bit of a meniscus degeneration but insignificant. Then the buzzing sensations in my head, the feeling like someone was stabbing me with something sharp. So now, I pre empted his tests, although I don’t think I’m celiac because it should have come up on gastroscopy, I’ve gone off gluten. Since Tuesday last week so 9 days. Since then I don’t appear to be as constipated, I realised I got through today without a nap and I’m not tired, maybe it’s just today and not related but I get very tired normally and sleep straight after work often, I can bend my knees and shave my legs lol, the buzzing vibrating has gone from my head, I had to call and ambulance as my heart decided we were off on a run, but we weren’t running and I’ve been a bit twitchy at bed time when trying to sleep, reflux is improving, I did get the weird suffocating feeling a bit when eating today but not as bad normall. Tingling and numbness still present and I felt like it moved up my legs a bit today but I’m a bit jittery. So I don’t know if it’s celiac disease or a gluten intolerance but I think, and it may be wishful thinking because my symptoms do make life a bit challenging, but maybe I’m feeling better. I don’t feel as cloudy. My thinking feels crisper. Like there’s no buzzing and I’m not fighting to break through the cloudiness now. I hope so much that this may help me feel a bit better moving forward. It would be a miracle as I really have struggled to work and parent and keep the house clean and I’m always anxious and exhausted.  If you get this far, please tell me if you you can relate to any of the above. Oh and tonsils out 5 years ago but before that antibiotics multiple times a year, sometimes intramuscular because they were so bad.  Op was meant to take 30 mins, it took 1.5 hours due to size of them. 
    • Peace lily
      Im still not gaining weight I’m on a gluten free diet . And still having issues with constapation started priobiocs figured it would help been over two weeks . I guess it’s going to be a long road for me .
    • Smith-Ronald
      Enlarged lymph nodes in neck and groin with celiac are not uncommon. They can take time to reduce even after going gluten-free. Monitoring is key.
    • Bayb
      Hi Scott, yes I have had symptoms for years and this is the second GI I have seen and he could not believe I have never been tested. He called later today and I am scheduled for an endoscopy. Is there a way to tell how severe my potential celiac is from the results above? What are the chances I will have the biopsy and come back negative and we have to keep searching for a cause? 
×
×
  • Create New...