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

Not Feeling Right For Some Time


doree

Recommended Posts

doree Newbie

Hi all,

I think I have reached people who will understand. I have been suffering from severe constipation, gas and poor sleep for quite some time. For relief I had a colonic where I passed out. The colo rectal surgeon put me on meds that worked for a week. When I went back last week I was grossly constipated and forced to endure a humiliating test where I passed out once again. What is worse is he is hinting at cutting out part of my colon which leads to a whole new arena of problems.

Constipation, muscle aches, osteopenia, terrible sleeper, occasional acid reflux and stomach pains. And then the mysterious "cuts" that appear on my torso. Seems like I should bring it up to the doc before I am sent on another humiliating gastro test this week. Yes? 58, and otherwise healthy, no drugs, alcohol, excercise regularly, eat well and drink plenty of water

:rolleyes:

Thank for any insight!


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



Celiac.com Sponsor (A8-M):



ShayFL Enthusiast

Have they tested you for Celiac?

doree Newbie
Have they tested you for Celiac?

no, I feel funy recommending this to the doctor. has not been brought up but my symptoms seem to mimi celiac in my opinion. is it worthwhile to bring up?

ShayFL Enthusiast

Doree, your doctor works for YOU!! You can hire/fire any doctor that is not doing their job. Doctors are just people with specialized training in a particular field (medicine). They are not gods.

Ask for ANYTHING you feel needs to be tested and if they say no or brush you off. Find another doctor.

If you can afford it, you can get your own testing through places like HealthCheckUSA and DirectLabs.

Never let a doctor control your health. YOU owe it to yourself to stand up for yourself. :)

neesee Apprentice

I don't think they would cut out part of your colon because of celiac disease. I have diverticular disease and the are discussing cutting out part of my colon sooner or later. I'll know more next month after the colonoscopy.

Ask your Dr. for the celiac test. It can't hurt.

I have celiac and diverticulitis. The diverticultis if far more painful than the celiac. 20 year ago you couldn't have told me that. the celiac was tearing me up at that point.

I hope you drs come up with some answers and you feel better soon.

neesee

dksart Apprentice

Doree,

I think you were describing many my symptoms before being diagnosed celiac. The gluten-free lifestyle has helped about 90% of my problems. It may seem difficult at first, but three years in it is second nature and I no longer have cravings for any of those nasty gluten filled breads, etc.

Tell your Dr. and no matter what he says, try going Gluten-free.

Good luck.

jerseyangel Proficient

Hi Doree,

Please don't be shy about telling your toctor you would like to be tested for Celiac. Request these tests, which make up the Celiac Panel--

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Total Serum IgA

It's just a blood test--you don't even have to fast for it but be sure to be eating gluten right up until you are tested--not eating it will skew the results.

The treatment for Celiac is a lot less drastic than surgery--the gluten-free diet :)


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



Celiac.com Sponsor (A8-M):



Fiddle-Faddle Community Regular

I just wanted to add that if your doctor is reluctant to order the tests, or laughs at the idea that you may have celiac, or tries to scare you into immediate surgery without a REALLY convincing explanation of the necessity (like, "we have definitively found cancerous growths which need to be removed, NOT "we need to see what is going on"),

#1 FIRE THE DOCTOR

#2 Eliminate gluten and all dairy from your diet

If you start feeling significantly better within a couple of days, you have your answer--no need for further tests.

Be aware that you may find yourself desperately craving gluteny items like bread. Hang in there--those cravings are a sign that you were addicted, and will lessen over several days, and be gone within a couple of weeks. Eat lots of rice, potatoes, meat, chicken, fish (protein is very filling), fresh fruits and veggies, and save Fritos and chocolate chips (dark) for the times when you have the worst cravings.

Avoid the gluten-free breads and cookies you see at the market--they are tough for gluten-damaged tummies to digest, but you can add them in (or better-tasting home-baked ones :) ) after a month or two when your tummy heals (if celiac is the problem for you).

Welcome aboard, ask lots of questions here, and best of luck!

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. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    2. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    3. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

    4. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    5. - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,692
    • Most Online (within 30 mins)
      7,748

    Ali Zaib
    Newest Member
    Ali Zaib
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.