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 Our Content
    eNewsletter
    Donate

Worse Before It Gets Better?


JBird

Recommended Posts

JBird Newbie

Hi :) I'm new to the forum. I was diagnosed in the fall last year, and have really been having a hard time. I'm not having a hard time making the diet change...I cook and am not picky about what I eat so switching to the gluten-free diet has been easy. Can't say it's been easy on my body as much as my taste buds though!

Since January I've been very strict about my diet. I have had maaaybe 5 meals with something gluten in it. Recently, I decided I needed to eat more vegetables and protiens, and cut my diary intake to 1/3 of what it was. I'm sensitive to lactose and have definitely noticed a difference in using lactaid milk, lactose free sour cream, and using lactaid tablets when eating cheese.

In the past month though I became constipated,(sorry gonna get kinda gross here) used Miralax a few times, and now it's soft but I'm still having a hard time just going at all or feeling like I've gotten it all out. Plus! I get enormously bloated and even have a hard time farting or it's like a stink-bomb when I do. And I'll stay that way for hoooours!

Like I said, this has been going on for a month and I don't know what to do! Is this a result of the veggie increase or just the time it takes for your body to become adjused to the gluten-free diet? I heard it can get worse before it gets better.

Thanks for reading!! So desparate for answers :(


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



Celiac.com Sponsor (A8-M):



mamaw Community Regular

You are still new to the gluten-free diet.. It can take some up to a year or even longer to completely heal, some even in five years they have trouble...Research on this was done. Some see healing almost immediately. It is what your body chooses to do.

As for theBig C. Many of us suffer from that... Miralax is not habit forming like many other products so it is okay to use it when needed. dairy can also cause the Big C...

now for eating gluten foods maybe five times since Jan2012 ************ way toooo much. You should be eating zero gluten.....everyday ...there is a difference in not knowing a food contained gluten & knowing & still partaking of that food...I'm not sure which you fall under! But that alone could cause the Big C

Do some research to learn about hidden gluten so as to not make yourself ill.....

Drink plenty of water. The rule is take your body weight & divide in half ie: 100# equals 50 ounces in water each day. not all at once like five sips every half hour or so. until your body gets used to processing that much water. Most never consume enough pure water..

Glad your taste buds are enjoying the gluten-free foods..Great choices are available... .

blessings

mamaw

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. - trents replied to barb simkin's topic in Related Issues & Disorders
      8

      celiac, chocolate and alcohol

    2. - barb simkin replied to barb simkin's topic in Related Issues & Disorders
      8

      celiac, chocolate and alcohol

    3. - trents replied to barb simkin's topic in Related Issues & Disorders
      8

      celiac, chocolate and alcohol

    4. - barb simkin replied to barb simkin's topic in Related Issues & Disorders
      8

      celiac, chocolate and alcohol


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,332
    • Most Online (within 30 mins)
      7,748

    Roxy79
    Newest Member
    Roxy79
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      So, you had both and endoscopy with biopsy and a colonoscopy. That helps me understand what you were trying to communicate. No, no! It never occurred to me that you were trying to mislead me. It's just that we get a lot of posters on the forum who are misinformed about what celiac disease is and how it is diagnosed so I need some clarification from you which you were so gracious to give.
    • barb simkin
      I had both the genetic genes for celiac.  My gastroenologist advised he also took a biopsy during one of my colonoscopies and endoscopy and advised I had celiac disease, along with stomach ulcers from my esophagus stomach down to my small bowel. I was shown the ulcers on the catscan and endoscopy report.  I also had polyps in 3 places throughout my large bowel. I was on a strict diet for months following.  I am sorry if I didnt define how I was diagnosed with celiac disease.  I am sorry if you think I was misleading you. I also had to pay $150.00 for the genetic testing.
    • trents
      So, I'm a little confused here. I understand you to say that you have not been officially diagnosed with celiac disease. Is this correct?  You have had genetic testing done to check for the potential for developing celiac disease and that was positive. Is this correct? I think you meant to type "gluten sensitivity" but you typed "gluten insensitivity". Just so we are clear about the terminology, there is celiac disease and there is NCGS (Non Celiac Gluten Sensitivity). They are not the same but they have overlapping symptoms. Celiac disease causes damage to the small bowel lining but NCGS does not. NCGS is often referred to in short form as gluten sensitivity. However, people often use the terms celiac disease and gluten sensitivity interchangeably so it can be unclear which disease they are referring to. Genetic testing cannot be used to diagnose celiac disease but it can be used to establish the potential to develop active celiac disease. About 40% of the general population has one or both of  the genes that have been most strongly connected with the potential to develop active celiac disease but only about 1% of the population actually develops active celiac disease. This makes the genetic test useful for ruling out celiac disease but not for diagnosing it. A colonoscopy cannot be used to diagnose celiac disease because it doesn't permit the scope to go up into the small bowel where celiac disease does the damage. They use an endoscopy ("upper GI) for checking the small bowel lining for celiac damage.
    • barb simkin
      I did nor read the chocolate pkg as it was of fered to me and I ate 2 pcs. I do know that only very dark chocolate and and a very few others are gluten free. Most alcohols contain gluten. I have several yrs of not knowing my celiac condition as docs would not do the test. After looking on the internet about my sufferings I insisted on the gene trsting which showed positive for gluten insensitivity and a biopsy on my next colonoscopy that also showed positive which could not help the damage done to my small bowel. So I very rarely have a glass of wine
    • trents
      @barb simkin, are you sure the chocolate products are gluten-free and not "manufactured on equipment that also handles wheat products and tree nuts", i.e., cross-contamination? And what kind of alcoholic beverages are we talking about? Most beers are made from gluten-containing grains. Just checking.
×
×
  • Create New...