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

Question About Gluten Challenge


Brittany85

Recommended Posts

Brittany85 Rookie

I've been on a gluten challenge for almost a month in preparation for testing and at first it was unbearable. Almost constant migraines, nausea, fatigue, dizziness, etc. Now, it's eased off quite a bit. Fewer migraines, not a lot of nausea, hardly any evidence of INTENSE glutening like I was experiencing before. I still have fatigue, back to being constipated, super gassy, foggy-headedness, etc., so I'm still feeling the effects of gluten but it feels like my body got a little used to it again...

Is this a common response?


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



Celiac.com Sponsor (A8-M):



ukdan Rookie

I don't know if it is common but I've just finished a challenge (being tested later today) and I can say for me it was the same. I did start to question at times whether I did really have a sensitivity or not when my symptoms lessened occasionally.

All I can suggest from my understanding is that intolerance (whether it is full blown celiac or not) is sensitive to other factors.

Stress for me is one of them and I found my symptoms were worse when I was fighting off these other stressful factors, probably as my immune system was overloaded.

I have also read (I can't remember where now) that reactions to intolerant foods can lessen over a time, not because we become less intolerant but because the immune system becomes so overrun it can't fight back so hard. That's not to say however that the damage is still not being done.

I'd say stick with it if you can as you've lasted this long already but it seems you may already have your answer.

Hope this helps!

jennynic Newbie

I had the exact same experience...I was in bed a lot the first week after reintroducing gluten with migraines and extreme fatigue. My stomach was also really bloated. I wasn't sure I would make it through the entire challenge. Then it was if things leveled out and my energy came back, at least enough so I could go through the daily routine. But I'm still feeling the effects of the gluten and I'm counting the days until my endoscopy (Friday) so I can go gluten free again.

tom Contributor

Wow 3 for 3 - I'm surprised I hadn't heard this before.

I didn't do a challenge so no input here but I do have a question.

Curious about how much gluten you're all consuming for the challenge (& for how long) & whether that's a factor in this. I've seen Drs say 1/2 slice bread/day for a month, or 2 slices/day for 3 months, or eat 'normal' w/out really tracking or go all out pasta/pizza/etc.

So, Brittany, Dan & Jenny, hope you see this & reply.

Thanks :)

Tom

love2travel Mentor

Wow 3 for 3 - I'm surprised I hadn't heard this before.

I didn't do a challenge so no input here but I do have a question.

Curious about how much gluten you're all consuming for the challenge (& for how long) & whether that's a factor in this. I've seen Drs say 1/2 slice bread/day for a month, or 2 slices/day for 3 months, or eat 'normal' w/out really tracking or go all out pasta/pizza/etc.

So, Brittany, Dan & Jenny, hope you see this & reply.

Thanks :)

Tom

I loved my gluten challenge because I got to pig out on gluten. Needless to say I did not get sick before anyway. Now that I have been strictly gluten free for a year I am not about to re-try! :P

Anyway, good doctors recommend the equivalent of 3-4 pieces of bread a day for 3 months. I just ate normally and didn't track it on paper but did mentally, knowing that if I had tons of gluten one day I would have a bit less the next but I tried to be as consistent as I could. I had far more things than bread, though.

ukdan Rookie

I was advised the equivalent of 3-4 slices of bread for 6 weeks, I'll find out soon whether it was enough as I've also heard it should have been longer.

  • 1 month later...
UKGail Rookie

Hi - I've just seen this and am wondering how you all got on with your gluten challenges?

I have just started mine after 6 months gluten free. A new GI, who is a celiac specialist, wants to do an endoscopy and colonoscopy quickly to see what's going on, so I only have to stick it for 2 weeks. Not hopeful of a positive diagnosis after that time, particularly as I am sero-negative. However I am keen to rule out other possible causes of continuing lower abdominal pain and tenderness. I'll be going straight back to being gluten free after the procedure, whatever the result.

Like Brittany, Dan and Jenny, after 6 days on gluten, I am also experiencing a levelling out of symptoms, and they are nowhere near as bad as the rapidly escalating symptoms which led to me going gluten free in the first place. I have essentially gone back to my longstanding level of chronic low/medium abdominal pain with intermittent problems with loose stools/mucus/constipation, plus chronic fatigue, joint and muscle pain, and a sore hip bone. Mild headache, but no migraine. Anxiety, irritablity and brain fog are back after 3 days. That's not good for work. I never associated the non-abdominal problems with gluten until I stopped eating it. I am looking forwarding to rediscovering my engergy and clear brain once the procedures are over.

One weird thing though, I notice the symptoms coming on about an hour or two after eating gluten, and the worst of them wearing off after about 6 hours, provided I don't top up with more gluten in the meantime. A new symptom appeared with yesterday's intake - an inability to walk in a straight line. Thankfully it has worn off and not reappeared today.

For the record, I am eating a large bowl of wheaty cereal for breakfast, and at least 2 slices of bread either at lunch or at dinner. I am still avoiding dairy (which I know I am still intolerant to) and am otherwise still sticking to my strict, low grain, unprocessed wholefoods diet to avoid confusion with any other possible intolerances.


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



Celiac.com Sponsor (A8-M):



tom Contributor

...

A new symptom appeared with yesterday's intake - an inability to walk in a straight line. Thankfully it has worn off and not reappeared today.

...

That's Ataxia, btw. There can be other causes but Gluten Ataxia is the term a Dr would use once convinced the gluten caused it.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    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.