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

Gluten Allergy? Looking For Help/advice!


Benn

Recommended Posts

Benn Newbie

Hello everyone, I hope its ok to post this here, and I apologise in advance for the length of this, I hope someone takes the time to read it all and help me or give me some advice!

My name is Ben, and I have just turned 22, for the past year and a half I have had a constant pain in my stomach/belly, it never goes away or eases up, it stays there all day, all night, not a minute of relief.

I went to the doctors and had urine/blood tests done, I'm not diabetic, I then spent 8 months on medication for stomach ulcers, they did nothing so I had the test where a camera is inserted down your throat, I am all clear of ulcers.

my doctor then sent me on my way with the words "There is nothing left it could be"

I later returned and was told it could be IBS, however I don't have any of the symptoms apart from stomach pain, however the doctor said with IBS the pain is only present for a short amount of time, but mine never goes.

They don't seem to understand that my life has come to a stand still, I have done nothing for the last year as I am just in pain all the time, and it makes you feel very fatigued.

I Recently switched to a gluten free diet in hopes that this could be the cause, I felt no difference, 2 weeks on the diet go by and I eat some bread that is not gluten free, and I suddenly notice the pain has increased, so I think the pain is slowly going, but its so slow i don't notice until i eat something that sets it off.

I have been gluten free for 5 weeks now, however I have had the odd gluten meal when I have been stuck out etc...

I still have discomfort in my belly while on the gluten free diet, but its no longer a huge pain, but its not 100% gone..

So basically i wanted to know if anyone has had a similer expericance to this?, am I on the right track? how long did it take for your pain to clear after starting a gluten free diet?

what steps can I take to solving this?

I hope someone can help me, im sorry if this is posted in the wrong place <3


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Welcome to the board. Benn.  :)

 

It sounds like gluten could be an issue for you - I think you are on the right track.  However, you might want to consider being tested for celiac disease before you go gluten-free.  Eating gluten-free will eventually cause all celiac tests to show a negative result once the autoimmune reaction finally stops.  To get a positive test, you must be eating gluten (equivalent of 1-2 slices of bread per day) in the 8-12 weeks prior to blood testing.

 

The blood tests you want are:

 

tTG IgA and tTG IgG

DGP IgA and DGP IgG

EMA IgA

total serum IgA (a control test)

AGA IgA and AGA IgG (older and less reliable tests)

 

You can also have an endoscopic biopsy done to look for the intestinal villi damage caused by celiac disease.  It only requires a 2-4 week gluten challenge.

 

If you are not going to test for celiac disease, and you still want to determine if gluten is a problem for you, then you will have to tighten up your diet to 100% gluten-free.  Right now it sounds like you are eating "gluten-lite"; in order to reap the benefits of the gluten-free diet (if gluten is a problem for you) you will need to be totally gluten-free.  No cheats, check all labels, recheck your spices, sauces and cooking supplies, get rid of contaminated foods (like sugar that had a flour coated measuring cup dipped into it), and check your kitchen tools for cracked and scrathed items that could have gluten in it.... The toaster has to go too.

 

Once gluten-free, keeping a symptoms and food journal will help you keep track of changing symptoms.  Some of my symptoms were very slow to change so being able to look back and compare really helped me.

 

I had some symptoms that improved in the first week. A few more got better in the first month, and most were gone within the first 9 months.  I still have some symptoms that I'm hoping will disappear after 2 years gluten-free.  LOL  Generally, I advise people to give the diet close to 6 months before you judge it's effectiveness.  Prior to that, a bit of backsliding is common so waiting longer to judge is a good idea.

 

Also, about half of all celiacs are lactose intolerant before starting the gluten-free diet. Eventually many celiacs regain the ability to tolerate milk, once the villi which make lactase heal, but in the mean time, lactose intolerance can cause quite a bad pain.  Perhaps it is something else to consider.

 

L-glutamine can help with faster healing too.... That's my only trick.  

 

Good luck with whatever you decide to do.  Let us know how it goes!

NatureChick Rookie

My abdominal pain was actually a B12 deficiency. It wasn't constant, but the pain could be bad for months at a time. The nerves in your digestive system are the first to act up if you're low on B12. And if you get tested, definitely get a copy of the results. The U.S. range for normal goes much lower than some other countries and symptoms can occur at levels that still fall within the normal range. U.S. low = 200. Japan's low = 500. My lab results came back with a notice that symptoms can appear at levels below 400.

But that is the only idea I have for what could be causing the pain because that is what caused my pain. There are a ton of things that can go wrong in the digestive system so I'd keep looking answers. I personally abhor the term IBS because it basically means the doctor gave up trying to figure things out. 

Vitamin and mineral deficiencies are easy to test for, just a blood draw and aren't that expensive so I'd start there.

But if you do turn up being deficient in something - then you have to start asking why, and gluten intolerance is on that list. When they run the tests, if you have multiple deficiencies, it can also lead you in one direction or another as to possible causes because some combinations are more common for some health issues. I'd also note that just going gluten-free is not enough to correct vitamin deficiencies. You need to do more than wait to heal and eat well to correct many of them. I'm not a fan of supplements, but they can be a necessary evil.

Also, if you check back, describing the pain a little might help people come up with other ideas. For instance, cramping could mean a different problem than bloating. And where the pain is, left/right, top/bottom can mean different things as well.

Gluten intolerance generally means bloating and either constipation or diarrhea or both, though lots of people add on a few additional symptoms as well. Fructose intolerance is known for cramping and diarrhea. All-over pain and feeling as if you have hard knots in your intestines and sometimes shooting pain the spleen would be how I would describe my B12 symptoms.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
×
×
  • 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.