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

Is Celiac My Magic Bullet?


AerinA

Recommended Posts

AerinA Rookie

Hi everyone.

Sorry in advance for a long post...

Basically, I'm one of those people with a really, really, really complicated medical history. I was born with a kidney deformity, got that taken care of. I've had problems with ADHD my whole life, had migraines since 4th grade, I don't remember ever NOT feeling sleepy (not quite narcoleptic but close), most recently had thyroid cancer. Every time they come up wtih some new diagnosis for me I think "hey, maybe THIS will fix my brain fog!" or, "maybe I'll start to be less sleepy now!" My immune system has always been terrible too, and I have a bad habit of nearly bleeding out on the surgical table. I'm so tired of feeling like a dysfunctional human being, like my body is falling apart--I probably couldn't list all my symptoms if I tried, since I don't know what's causing what, I don't even think I could make a comprehensive list.

Most recently, I changed endocrinologists due to my synthroid not absorbing at all, and my previous doc not really paying attention (my TSH was 27 even taking my meds every day ?!?!) She immediately found that I had undetectable levels of D2 as well, though I had small amounts of D3. She says she strongly suspects celiacs, but doesn't want to put me through a biopsy. I haven't yet gotten to scrutinize the results of the blood work they did, whatever it was.

Based on my lifelong symptoms, I'd say that a lot of things would be explained by celiacs, but I'm overweight (used to be under but... with the thyroid issues it's hard to know the real cause of that), tend to have IBS problems but NOT the classic multiple bathroom trips (tends to be the opposite), and I have had so many other conditions (and surgeries, and treatments, and everything else) that I have no idea if I'm barking up the wrong tree. A biopsy doesn't sound like the end of the world, but what if it's negative? I've been at a loss for a really long time, it would be SO nice if going gluten-free fixed stuff, but I hardly dare to hope for it. Anybody have input or experience similar things? Any advice at all would be much appreciated.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

I think you need to get a copy of your blood test results to find out what tests they did and what the results were. If they did not run the celiac panel they should do so. If they did you need to know what the results were, especially iif she strongly suspects celiac disease.. One doesn't normally have a biopsy just for low vitamin D.

ravenwoodglass Mentor

Do get a copy of the test results. If they are positive it sounds like your doctor will consider you diagnosed. Since there is a chance of a false negative with the biopsy anyway some doctors are diagnosing without one. After you are done with all the testing you choose to do give the diet a good strict try no matter what the results of testing.

T.H. Community Regular

...and if the tests and biopsy are both negative? There is absolutely nothing stopping you from trying the diet yourself, either. A number of people here have tested negative for celiac disease, both blood and biopsy, but had symptom improvement (or complete reversal) on a gluten free diet.

Re: the symptoms? I don't have the big D, either. I never thought I had gut issues, but now I notice I get the opposite when I get gluten, too.

eatmeat4good Enthusiast

I've been overweight too and that is also a symptom of Celiac, not just the weight loss. It has to do with swelling and inflammation. Your thyroid medication not being absorbed is another indicator. I just read the book by Peter Green, Celiac A Hidden Epidemic. In this book he discusses exactly what happened to you in the case of your Thyroid med not being absorbed and he describes two cases where women were diagnosed with Celiac because their astute doctors recognized the medication was not being absorbed.

Ask for a full Celiac Panel and if you want the biopsy ask for it. After everything else you have been through, it seems ridiculous that your Dr. "doesn't want to put you through that" particularly if it will give you a diagnosis. However, like they said above, if your Dr. is willing to diagnose you without the biopsy based on your bloodwork, then you will be able to get on with eliminating gluten from your life and start feeling better.

What you are describing as brain fog began to lift for me withing the first two weeks of being gluten free.

You just may have your answer now.

Do dare to hope.

AerinA Rookie

Thanks for the input, everyone.

I've been on the diet for a month now, I still haven't seen my doctor again post-blood work so I haven't gotten to analyze it, but I'm feeling much more awake and "with it" now, so I'm staying on the diet regardless of what it says. It can only get better from here.

eatmeat4good Enthusiast

That is wonderful!

Thanks for posting, I was wondering how you were doing.

I hope everything continues to get better.

It is really amazing how incredibly ill one can be from gluten.

At 4 months into this diet, I continue to get better everyday.

Take care.


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



Celiac.com Sponsor (A8-M):



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. - Florence Lillian replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      13

      gluten free cookie recipes

    2. - Russ H replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    3. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

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

    • Total Members
      132,916
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.