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

Really Ticked Off At Doctors Right Now


xjrosie

Recommended Posts

xjrosie Apprentice

A little background on me: now 34 years old, with two of three of my kids diagnosed with celiac. Those two kids also (separately) have hypothyroidism and diabetes type 1. Before their diagnosis, I had no clue what Celiac Disease was. Now that I've experienced it, I'm kind of ticked off. I think I might have it, and I think I've been suffering with it my whole life.

When I was younger, my parents didn't really feed me, so I was very underweight and didn't have any actual symptoms that I could think of. But when I finally moved out at 16 and was introduced to food, I started having problems. I couldn't keep weight off (and I was not a big eater, I just ate regular meals). I began an unending stint of anemia so severe that when I tried to donate blood they told me to see a doctor immediately. I haven't been able to donate blood since I was 18, even though I take iron supplements. I had to quit sports because I couldn't breathe well and was getting depressed. I never felt good after eating, never.

As soon as I had my first daughter, I kind of went off the deep end and tried to get in shape after some nasty comments from my ex about my figure. I pretty much ate cucumbers and grapes, drank water, and took vitamins. So that didn't help. But when I met my husband, I started taking care of myself. Eating balanced meals regularly, exercising properly and such. I started gaining weight again. I thought this was my only problem. Between 2000 and 2003, I went from 145 pounds to 275. I paid so much money to different programs to lose weight. I tried every type of diet under the sun. Finally I had gastric bypass surgery. I did great, I lost the weight. Shortly after, I divorced and started dating someone who I can see from hindsight was pressuring me to "stay pretty" so I went back to barely eating to keep the weight off.

Now that I am single, I have been eating regularly again (without so much exercise, but I'm working on it) and I have gained weight back. I'm up to 210 after being down to 135 after my surgery. Needless to say, it doesn't make me feel good. But my daughters were diagnosed with Celiac, and the doctor said they must have got it from me (my oldest doesn't have the same dad as my younger two) since I have hypoglycemia already there are no indications from the dads' sides of the family of any autoimmune problems. I started thinking about my history.

My brother and my best friend both told me that I have complained about not feeling good as long as they can remember. I do remember laying down on my friend's couch lots of times because I felt like crap. It was always after eating, and we usually ate pizza when we hung out.

I even called my ex-husband and asked him. He said he can't remember a time where we had a meal and I didn't complain.

Even my co-workers (when I had some) used to make comments about how I was always "not feeling good."

I have ugly, white bumpy patches of skin all over my arms. I have headaches all the time (and always have, that I can remember). Bowel movements are irregular and urgent - and I usually only have about two a week (not fun). It's been that way since high school, except after the surgery. It's hard to tell whether my depression could be a symptom, because I've been bipolar for so long and they thought it was caused by my upbringing.

I was even treated in high school for "excessive gases" that were working away at my intestine.

Anyway, now I'm thinking that I could have had Celiac Disease this whole time, and I altered my body when all I probably needed to do was lay off the gluten! It totally makes sense to the people in our lives who have chosen to become educated about Celiac, because they've seen me in the past, and hear about the symptoms when I tell them what it can do.

As soon as I get insurance again, I'm going to get tested, but for now, it's just my theory. But it just makes me upset that I have been dealing with this for almost 20 years. Eighteen years of feeling like crap, feeling like I look like crap, hiding myself, wanting to not be around because I'm so depressed, and all I needed to do was change my diet. I feel like I've been robbed, because I have such an uphill battle now to fight to get back to healthy. Grrr!!!!!


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



Celiac.com Sponsor (A8-M):



rosetapper23 Explorer

Be thankful that you found out now--and not 20 years from now. Many of us on this forum did not discover the link to celiac until we were in our 40's, 50's, and 60's. We also had led tortured childhoods and adulthoods because no answers were forthcoming from the numerous doctors we saw about our unending list of symptoms.

That said, I hope that you're planning to follow a gluten-free diet from now on. You mentioned being tested when you get insurance, but if you follow the diet, you'll test negative for celiac. Since your symptoms fit closely with a diagnosis of celiac and you have two children with it, I don't see why you would bother with testing. Others on this forum might disagree with me, but it sounds as though you desperately need to go gluten free immediately. Believe me, it won't be the uphill battle you're expecting--it'll be downhill now that you know (or suspect) what has been causing you to be so ill. Very shortly, you're going to feel great!

I am SO very glad that you have finally figured out what is wrong.

ciamarie Rookie

All I wanted to add is that I agree with rosetapper23. Don't wait until you get insurance to start eating gluten-free, and after you're eating gluten-free any test (except genetic) would come out negative. And many of us (including me) can look back and wish we'd have known sooner...but we're on our road to health now. That's what is important.

Skylark Collaborator

Yeah, a lot of us have similar missed diagnosis stories. It sucks. I was bipolar too before I got off gluten.

Before you go gluten-free you do have some testing options. You could get a home test kit. Open Original Shared Link Some cities have university celiac centers that offer free testing.

If you can afford it, you can probably get a celiac panel though Open Original Shared Link This would be a full celiac panel.

Open Original Shared Link

This less expensive test is less thorough but it is a new and very sensitive celiac test.

Open Original Shared Link

Once you've done either or both, go gluten-free and don't look back! There is a chance of false negatives, but it is good to have an idea of whether you might be celiac rather than gluten intolerant.

xjrosie Apprentice

I've slowly started to go gluten free. My kids already are, but with all the food I have that is not, I can't afford to waste any. I am attempting to sell my excess food that we can no longer eat to a friend of mine, which will in turn buy more gluten-free.

I am thankful that I found out now, but if I had known beforehand, maybe I wouldn't have had gastric bypass. Because of that surgery, there are so many more foods now that I cannot eat simply because they don't digest, not because I'm allergic.

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

      Going for upper endoscopy today

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

      Going for upper endoscopy today

    3. - marlene333 replied to Grace Good's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Bee balm lipbalm not gluten free

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      4

      Related issues


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,267
    • Most Online (within 30 mins)
      7,748

    Kristine Ryder
    Newest Member
    Kristine Ryder
    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

    • Wheatwacked
      Hello @Midwesteaglesfan and welcome. A result greater than 10 U/mL is considered positive. Some labs use 15 as the cutoff, but 34 is in the positive.  The endoscopy and biopsy is looking for damage to your small intestine.  I don't don't think 5 days is enough to repair the damage. This comment is effectly your answer, regardless of your biopsy results.  The endoscopy has been the Gold Standard diagnostic, and most healthcare providers won't diagnose celiac disease until your intestinal lining Marsh Score reaches stage 3. You don't really want to wait for the damage to get worse, especially since only five days mostly gluten free gave you relief.  Yes, migranes is one of the 200 symptoms that may be caused by Celiac Disease. Malabsorption Syndrome is often comorbid with celiac disease.  The western diet is deficient in many vitamins and minerals.  That's why gluten processed foods are fortified.  Gluten free processed foods are not; Vitamin D deficiency is a virtual given.  40 to 60% of the industrial population is deficient in vitamin D, Damage to the intestinal lining from celiac disease can decrease the number of vitamin D receptors.  So now you get no vitamin D from the sun (skin cancer scare) the major source of vitamin D, plus absorbtion from food is poor because of intestinal damage.   Low iodine intake is getting more of a concern because the major source of iodine used to be bread (dough conditioner with iodine was stopped in the US in the 1970s), dairy (lactose intolerance from eating quick pickles with vinegar instead of fermented pickles which supply lactase excreting lactobacillus to improve Lactose intolerance. Commercial Dairies have wheat, barley and rye added to the cow feed. Some say they are sensitive to milk protein, but it is the gluten added to supplement the cow feed to increase milk production that becomes part of the milk protein causing the problem.  And people use less iodized salt.  In the US intake of iodine dropped 50% from 1970 to 1984. Switch to Grass fed only milk and consider supplementing Liquid Iodine drops to your diet.  The omega 6 to omega 3 ratio of commercial milk is 5:1; Organic milk is 3:1 and grass fed milk is 1:1. The typical western diet is around 14:1, optimum for humans is 1:1.  Wheat flour is 22:1 omega 6:3.  Choose vegetables lower in omega 6, it is inflammatory. Eat fermented foods and switch to Grass fed only milk.  Some say they are sensitive to milk protein, but it is the gluten added to supplement the cow feed to increase milk production that becomes part of the milk protein.   
    • Midwesteaglesfan
      At 41 years old I have been fighting fatigue and joint pain for a couple months.  My family doctor kept saying nothing was wrong but I was insistent that I just didn’t feel right.  Finally after running several blood labs, one came back showing inflammation in my body and I was referred to a rheumatologist.  He was extremely thorough and sat with me and my family for a good hour asking questions and listening. He ordered X-rays of all my joints and more bloodwork.  He suspected some sort of reactive inflammatory arthritis.  My TTG (Tissue Transglutaminase) came back at 34. he told me to try going gluten free and out me on Salfasalzin to help the join inflammation.  Over the next couple days going gluten free and doing a lot of research and talking to people with celiacs,  we found that I should have an upper endoscopy for insurance purposes in the future.  I reached back out to my rheumatologist and expressed this concern and he got back to me stating I was correct and resume regular gluten diet and stop the medication until after that scope.     They were able to schedule me in for 2 days later.  I had been gluten free, or as close to it as I could be for about 5 days.  I know I ate some brats with it but wanted to use them up.  My symptoms had gotten slightly better in those 5 days.  I felt less fatigue and joint pain was slightly better(it had gotten really bad) so for these last 2 days I’ve gone crazy with wheat bread, pasta and such.  I’m hoping those 5 days didn’t screw this endoscopy up.  I can’t imagine after a life of gluten, my intestines healed in 5 days and after eating gluten again for these couple days,  my stomach hurts, joint pain is coming back up so I know the inflammation is there.   Hinesight after this diagnosis, I have had chronic migraines since my late teens.  Has that been a lingering symptom of celiacs all these years?  I’ve never really had the stomach issues, for me it came in heavy these last couple months as the fatigue, just always feeling tired and exhausted.  And the joint pain.     So getting in the car for the 2 hour drive to the hospital for this scope now.     Wish me luck!
    • marlene333
      To play it safe, use Vasoline Lip Therapy. No questions as to it containing gluten.
    • Mari
      jmartes, Thank you for sharing  more information with us. Most of us Celiacs whose problems do not clear up with in a few years have to decide what to do next. We can keep seeing DR.s and hope that we will get some  medication or advice that will improve our health. Or we can go looking for other ways to improve our health. Usually Celiac Disease is not a killer disease, it is a disabling disease as  you have found out. You have time to find some ways to help you recover. Stay on your gluten-free diet and be more careful in avoiding cross contamination . KnittyKitty  and others here can give you advice about avoiding some foods that can give you the gluten auto immune reaction and advice about vitamins and supplement that help celiacs. You may need to take higher doses of Vit. B12  and D3.  About 20 years before a Dr. suggested I might have Celiac disease I had health problems that all other Dr said they could not identify or treat. I was very opposed to alternative providers and treatments. So many people were getting help from a local healer I decided to try that out. It was a little helpful but then, because I had a good education in medical laboraties she gave me a book  to read and what did I think. With great skeptism I started reading and before I was half way through it I began using the methods outlined in the book. Using those herbs and supplements I went from hardly able to work to being able to work almost fulltime. I still use that program. But because I had undiagnosed celiac disease by 10 years later some  of my problems returned and I started to loose weight.    So how does a person find a program that will benefit them? Among the programs you can find online there are many that are snake oil scams and some that will be beneficial. by asking around, as I did. Is there an ND in your area? Do they reccomend that person? If you would like to read about the program I use go to www.drclark.net   
    • Scott Adams
      It's unfortunate that they won't work with you on this, but in the end sometimes we have to take charge of our own health--which is exactly what happened to me. I did finally get the tests done, but only after years of going down various rabbit holes and suffering. Just quitting gluten may be the best path for you at this point.
×
×
  • 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.