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

2 Weeks Gluten Free And Feeling Great!


Pegleg84

Recommended Posts

Pegleg84 Collaborator

Hello everyone,

A couple weeks ago, after several consecutive days of feeling absolutely rotten after eating, I decided to take some action and go gluten free. I haven't been diagnosed with Celiac, but have been having numerous increasing symptoms for at least a year. My mother, sister, and several family members have the disease. I have gotten IgA/IgG (whatever) testing done twice now and have been told it was negative (though I havn't actually seen the results for myself, which I will ask my doctor for the next time I see him)

anyway, I thought if I try the GFD and feel better, then I might be on to something. I feel so much better! The first few days were still touchy, but I havn't had any significant stomach problems for at least a week, except for when I broke down and had a cookie the other day. I learned my lesson! Other than that and a couple sips of beer (and only a sip!), i've been as strict as possible. Of course, working in a pizza place probably doesn't help.

It hasn't been long enough to tell if other symptoms, such as depression/anxiety, liver counts, constipation, etc, are getting significantly better yet, but definitely haven't gotten worse. My anxiety has been up, particularly the day after I had the cookie, but that could be due to some significant stress/changes in my life right now.

In any case, even if I don't actually have celiac, I definitely have gluten issues or I wouldn't feel so much better.

I am moving cities in a month to go to school in Toronto. Until then , I will stick more or less to the GFD, though will probably indulge in a few things (like the beer my BF and I just made)once I'm finished working, basically go on one last gluten binge, spend a week recovering, and then go strict on the diet from the moment I get on the plane.

So, what do you think? Should I simply stick to the diet as a self-diagnosis, or should I go back on gluten and get an endoscopy done in the near future?

Anyway, just wanted to get any opinions or advice

thanks again

Peggy


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



Celiac.com Sponsor (A8-M):



Rebecca's mom Rookie

How "strong" are you? By which I mean when you are up in Toronto, do you think that you will be able to resist the urge to eat gluten if you don't know that you have a positive celiac disease diagnosis? If you are one of those people who has excellent self-control, then you probably can decide if you want to be tested or not. If, like most of us, you may find yourself tempted to say, "Well, just this once.....", you may need to have the test done, just to keep you on the straight and narrow if you feel tempted to "cheat"!

Just a thought - it sounds like you are leaning in the "right" direction, though -

Teresa Koch

CeliBelli Newbie

Peggy,

I highly recommend you get tested again, this time with the newer antibody and genetics tests from a leading lab such as Prometheus or Kimball Labs, or their Canadian counterparts. There is an excellent set of essays by Dr. Scot Lewey elsewhere on this website that discusses genetics testing, which with your family history sounds like a must. You can find those essays here:

https://www.celiac.com/authors/45/Dr.-Scot-Lewey

As Rebecca's Mom said, you will stick to the gluten-free diet better if you have the certainty of a diagnosis. You may also need an official medical diagnosis in hand when dealing with doctors and hospitals in the future, since they don't give much credence to self-diagnosis.

And if you already know you have other family members with it, you will want to know whether you carry the gene(s) before you have children, if that is what you choose to do.

Good luck!

Rebecca's mom Rookie

Peggy,

One more thing that you may want to keep in mind is that I believe in Canada if someone has a positive medical diagnosis of Celiac Disease, they get some sort of tax break or assistance to "shoulder" the additional cost of a medically necessary diet. Also, if you have a celiac disease diagnosis, you will be able to go to the food services folks at the university you will be attending, and they will work with you to ensure that you are getting "safe" foods .

I would talk with your doctor and see if there is any way that you can get a test without having to do a gluten challenge. A good GI doctor who is knowledgeable about celiac disease should be able to look at your symptoms and your response to a gluten-free diet and tell you where to go from there.

You may want to contact your local Gluten Intolerance Group (GIG) chapter and find out which doctors they recommend in your area. Just go to the national GIG website, and they should have a link to your state/area's nearest chapter.

Best of luck!

Teresa Koch

Fort Worth, Texas

Pegleg84 Collaborator

Thanks for the replies

I would love to have a diagnosis, finally, but I may have to wait a little longer. Unfortunately, scheduling a biopsy before I leave probably isn't possible. I'm basically going to act as though I do have the disease, which will be tricky at times, but I'm pretty confident. I guess I just have to get used to asking virtually anywhere I eat what's in the food. I'm already used to scouring labels. And I was pleasantly surprised that brown rice pasta is pretty good. Trust me, I'll have little trouble feeding myself.

If all goes well this summer, I'll go back on gluten and try to get a biopsy done in the fall. Yes, I know about the tax-break on gluten-free food (which my mom is now taking advantage of). But as long as I can find a source of cheap rice, I'll be fine. Also, there are allegedly quite a few gluten-free restaurants in the city, which I will have to track down on weekends.

So, I will keep you posted.

thanks again for your support

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    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

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.