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

What Can I Expect...


supermaltese

Recommended Posts

supermaltese Newbie

Oh how I craved wheat. Gluten-free wheat, bread, pasta, rolls, pizza, tortilla IS DISGUSTING. I quit eating gluten December 5, 2014, but it wasn't until maybe 2 weeks ago that I stopped craving it.

 

I have diagnosed myself with Celiac's Disease. The process by which I arrived at my conclusion took 30 years. When I was very young, around 3 I began to get rashes behind my knees, inside my elbows, and on the back of my neck. At first, they seemed to only bother me when I was hot, or outside in the sun. I would scratch util I drew blood, and never get to the itch. It was like my bones itched and my skin was half-numb.

 

In my late teens I began having more itching all the way up and down my arms, on my chest about 1 or 2 inches below my neckline, all around my neck, on my face and forehead, my ears, and all over my head. Around 21 years old, these symptoms increased again and went from mild to severe, to mostly just severe. Around age 26, these symptoms increased again to periodic episodes of extreme bouts or fits. Like drowning, or being consumed in a fire, nothing else exists when one of these episodes comes on me. It's like a panic attack. I don't have enough hands to scratch every inch of my body :( Not that that would really help. Bathing irritates my skin, but so does not bathing. Every lotion (whether from the doctor, over the counter, hypoallergenic, organic, etc) brings on either a full blow episode or extreme itching in the area where I applied the lotion.

 

Without exception, every doctor I've ever been to (and there's been a lot) has never done or said anything helpful. The most common "reason" they give me for my skin "rash" is Atopic Dermatitis. They tell me, that sometimes the body develops an immune response and that I'm actually allergic to my skin and there's nothing they can do for me. They've given me Benadryl and other antihistamines, and water-based ointments with triamcinolone as the active ingredient (a steroid). The steroid helped a lot when I first started using it (age 21-25) but I couldn't use it for more than a day or two or it would have a negative effect. At various times throughout my life I've attempted to cut certain things from my diet, to see if my symptoms cleared up. Late last year I finally figured out that gluten was the problem and I've been gluten free since December 5, 2014. Since then my worst episode has only been mild to severe. I have not had another hell/drowning/ I'm-wish-I-were-dead episode.

 

Late last year I was able to determine that I would eat bread and then have an episode a few days later, or a few hours later. This was not always so. In the past, I've cut wheat from my diet for 30 days and still had hell episodes. As I've gotten older, the time between eating gluten and the time that I break down into having an anxiety attack + scratching episode has been decreasing. Now? If I eat a sandwich now, I'll be itching by the end of it, or not more than 1 or 2 hours later.

 

As the OP began with brain damage, my cognitive ability has declined a lot since high school (I'm 33 now). In high school I found it difficult to recall information I had read. Now, I find it difficult to recall something you told me 30 seconds ago. 20 years ago, I could type 65 words a minute with a 90% accuracy. Now, I can type 25 words a minute with a 70% accuracy. (Last year) My wife can be talking to me and I lose track of what she's saying halfway through the sentence. She'll tell me that she has a doctor appointment on a certain day and time, and an hour later I won't remember that she has a doctor appointment, or that she mentioned the doctor at all. (ALL SYMPTOMS HAVE IMPROVED A LITTLE SINCE DECEMBER 2014)

 

For the last 3 years, I've had another problem. I'd get up out of bed and fall down, or fall into the wall so I could hold myself up. I would take a few seconds to figure out where I was. I might be doing research on the internet (trying to) get up to go to the kitchen for a glass of water and wander around the house for 10 minutes because after a few steps I forgot what I was doing or where I was going. These VERY SCARY episodes have decrease in frequency.

 

Since I'm not eating gluten, I cannot be tested for Celiac's Disease, but that's okay because it's clear that I have it and not just a non-celiac's gluten intolerance. I'm not going to eat some gluten just so I can go to the doctor. Having done a lot of reading on the topic, I know there's really nothing any doctor can do for me. My best bet is to study nutrition and eat the best I can and try to heal.

 

I shake a lot, and it's not connected to my blood sugar levels. I've been tested for hypoglycemia and am borderline with lower than normal blood sugar levels. My hand-eye coordination is horrible. I'm having trouble spelling words and was nicknamed Mr. Webster in high school because I have always been able to spell even some of the most complex words.

 

:::MY QUESTION FOR THIS COMMUNITY::::

 

Have you gone for as long as I have with this disease but without a proper diagnosis? What can I expect as far as healing? Will my symptoms continue to improve, or is this the best I can hope for? Is there more I should change in my diet aside from just cutting out gluten? (I've also stopped eating other grains such as corn and all corn byproducts such as corn syrup and high fructose corn syrup)

 

Please discuss what I can expect? I've read that Celiac's Disease can kill, but I cannot find more than just generalized information about life expectancy? Do you know anyone who's died from, or because of complications due to celiac's disease?


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



Celiac.com Sponsor (A8-M):



GF Lover Rising Star

The OP referred to in the above post is from this thread: https://www.celiac.com/forums/topic/111581-brain-damage/

 

Colleen

cyclinglady Grand Master

Most of us have gone for years or decades without a proper diagnosis or even a clue that gluten was making us ill. There are over 300 symptoms of celiac disease and each present differently. I suggest you research the University of Chicago's celiac website. They are a leading researcher in the US.

Healing differs for everyone. It can depend on how well you adhere to the diet or what damage has been done. For example, I will never get my vertabrae fractures reversed and I will never regain that 1" in height! Nerve damge is the most difficult to heal or reverse. Just ask a diabetic!

Eliminating diary for a while can be helpful as well as indentiying any intolerances you may have.

I wish you well!

knitty kitty Grand Master

Open Original Shared Link

I found this article very interesting. I have symptoms similar to what you describe.

Fifty-one years undiagnosed. Fifty-two years old...still trying to sort it all out.

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. - Rogol72 replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    2. - Scott Adams replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    3. - Scott Adams replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results

    4. - deanna1ynne replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,441
    • Most Online (within 30 mins)
      7,748

    Linda Boxdorfer
    Newest Member
    Linda Boxdorfer
    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

    • Rogol72
      @HAUS, I was at an event in the UK a few years back. I remember ringing the restaurant ahead to inquire about the gluten free options. All I wanted was a few gluten free sandwiches, which they provided and they were delicious. The gluten-free bread they used was Warbutons white bread and I remember mentioning it on this site before. No harm in trying it once. It's fortified with Calcium and Iron. https://www.warburtonsglutenfree.com/warbs_products/white-loaf/ The only other gluten-free bread that I've come across that is fortified is Schar with Iodized salt, nothing else.
    • Scott Adams
      In the U.S., most regular wheat breads are required to be enriched with certain B-vitamins and iron, but gluten-free breads are not required to be. Since many gluten-free products are not enriched, we usually encourage people with celiac disease to consider a multivitamin.  In the early 1900s, refined white flour replaced whole grains, and people began developing serious vitamin-deficiency diseases: Beriberi → caused by a lack of thiamin (vitamin B1) Pellagra → caused by a lack of niacin (vitamin B3) Anemia → linked to low iron and lack of folate By the 1930s–40s, these problems were common in the U.S., especially in poorer regions. Public-health officials responded by requiring wheat flour and the breads made from it to be “enriched” with thiamin, riboflavin, niacin, and iron. Folic acid was added later (1998) to prevent neural-tube birth defects. Why gluten-free bread isn’t required to be enriched? The U.S. enrichment standards were written specifically for wheat flour. Gluten-free breads use rice, tapioca, corn, sorghum, etc.—so they fall outside that rule—but they probably should be for the same reason wheat products are.
    • Scott Adams
      Keep in mind that there are drawbacks to a formal diagnosis, for example more expensive life and private health insurance, as well as possibly needing to disclose it on job applications. Normally I am in favor of the formal diagnosis process, but if you've already figured out that you can't tolerate gluten and will likely stay gluten-free anyway, I wanted to at least mention the possible negative sides of having a formal diagnosis. While I understand wanting a formal diagnosis, it sounds like she will likely remain gluten-free either way, even if she should test negative for celiac disease (Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If her symptoms go away on a gluten-free diet, it would likely signal NCGS).        
    • JoJo0611
    • deanna1ynne
      Thank you all so much for your advice and thoughts. We ended up having another scope and more bloodwork last week. All serological markers continue to increase, and the doc who did the scope said there villous atrophy visible on the scope — but we just got the biopsy pathology report back, and all it says is, “Duodenal mucosa with patchy increased intraepithelial lymphocytes, preserved villous architecture, and patchy foveolar metaplasia,” which we are told is still inconclusive…  We will have her go gluten free again anyway, but how soon would you all test again, if at all? How valuable is an official dx in a situation like this?
×
×
  • 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.