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

Sensitive To Gluten And Milk, With Mostly Psychiatric Symptoms


gliadin-raider

Recommended Posts

gliadin-raider Newbie

Hello.

About 6 weeks ago, I decided to try a gluten and milk/casein free diet to see if it would benefit me. I have a pretty sad mix of symptoms, starting with problems with sleep since I was approximately 6 weeks old, ADHD-like symptoms for my whole life, and a chronic depression for seven years that among other things has left me extremely emotionally numb as well as with no appetite or thirst, and constantly sluggish and confused. I have responded poorly to terribly to every medication I have tried, almost 15 of them, so I am pretty motivated to try out other treatments. My stomach has never really been much of a problem for me, except when I am sick or under heavy stress, which is why I have never suspected a food allergy/intolerance or anything like it.

After 2 weeks without milk and with a reduced amount of gluten (I had accidently been eating some without knowing) I seemed to have improved a little bit, so I tried to eat gluten on purpouse again to see how I would react. In about 10 minutes I started to feel confused, spacy and weird, and it got gradually worse during the day until I was depressive and unstable during the evening. So ok, that kinda confirmed my intolerance to gluten for me. The next day I felt good again, so I decided to try the milk too. I had a glass and didn't seem to react to it, so I took another half an hour later. Still nothing. I seemed fine until 2 hours later around 4 PM when I felt a little tired. I went to bed to take a little nap...and woke up 4 hours later. I hadn't been tired before the test and hadn't slept worse than usual, and I have never slept that much spontaneously before, so that was a bit odd. The next days I felt worse and worse and I suspected I was reacting to the milk in a more delayed way. Took about a week to recover to where I was before the test...

I will get a stomach biopsy this week, and will get my antibodies tested again after that. I had them tested once before for celiac but that didn't show anything, but maybe something will show up now, who knows. I am clearly intolerant to gluten and milk anyway, regardless of what the tests say.

Does anyone else here have had problems such as these, with no stomach problems and no obvious reaction to food until after having excluded them for some time and then tested? How long did it take for you to experience significant improvements in your symptoms?

Also, I have had several stomach problem since I started the diet. I was constipated for 4 days shortly after starting the diet, and have had daily minor pains in my stomach. And without going into any messy details, I have also had some problems with my feces which have _always_ been fine before. In fact, this is kinda weird as my stomach has mostly been fine through my whole life. I don't understand why it would get worse now. Some kind of withdrawal reaction?

Thankful for any replies.

  • 2 weeks later...

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



Celiac.com Sponsor (A8-M):



Kamma Explorer

Hi Gliadin raider...

I present mostly with neurological symptoms like ataxia, vertigo and balance problems.

I was going to ask if you are still consuming gluten? You said you were going to be tested soon and you need to be consuming gluten for quite a few weeks prior to that test or you might have skewed/negative results.

Welcome to the board!

pricklypear1971 Community Regular

Regarding your stomach issues:

You could be going through withdrawal. You could not be eating a balanced diet with enough fiber - its hard to change your eating habits quickly, but you'll get there. You could be uncovering other food issues now that you've eliminated two biggies - it happens all the time. It can just be a part of healing - most of us have wild rides the first 6 months.

Kamma is right - for the best test results you do need to continue to eat gluten. Since you've been tested before, and it was negative, you may not think its worthwhile to eat gluten again. Many people choose that option.

Probably more importantly, you need to get your vitamin levels checked. Iron (complete panel), d, b's, k. Celiacs and I think ncgi's are frequently low and it will help to raise them.

Best of luck to you. Congrats on figuring out your gluten and milk issues!

Skylark Collaborator

You are not alone. I had bipolar illness from gluten. I had all the GI trouble as well and it took me a while to heal. It sounds like you were going pretty fast! :)

As other folks have said it would be good stay on gluten for a bit longer to get celiac testing. It's possible to have "silent" celiac with no GI symptoms.

gliadin-raider Newbie

@Kamma

I am not consuming milk or gluten anymore. The testing I did was an endoscopy plus a biopsy, and I thought any damage as revealed by these tests would be too extensive to heal in just a few weeks to heal, unless I am mistaken? I have not tested for antibodies or anything like that yet. They didn't see anything on the endoscopy, but results on the biopsy will be back in 2 weeks (not sure what exactly they are testing it for though).

And thanks for the welcome.=)

@pricklypear1971

Whatever I have experienced the last weeks seems some kind of withdrawal. Most of the new issues seem to have calmed down by now though, but I still don't feel as good as I did for the first week.

6 months, gee... I have been mostly clean for about 1 month now, almost clean for 1 and a half. Seems like I still have some way to go then...

I don't think fiber was the issue really, I started to consume soy and pure oats (guaranteed gluten free by Sweden's food agency) early in the diet switch, so if anything I think I am getting more

fibers now than I did before. Anyway, whatever made my stomach upset, it seems gone now.

I have tested my vitamin and mineral levels several times before without anything low showing up, including several D vitamin tests.

What is a "complete panel" though? Does it differ from a normal test (which I suppose is what I did)?

@Skylark

Yeah, whatever I have seems to be "silent" in regards of GI symptoms. Stomach/GI has never been much of a problem for me, until I began the diet... The issues I had are gone to 90% now, with only some minor pains once or twice a day at most, no pains at all at best. How long did it take for you to improve in your bipolar-ish symptoms?

Considering how I now seem to react even stronger than before to gluten and milk/casein, I am not that eager to eat it again for any longer period. Perhaps a week at most of one or the other.. Is it that important to eat it for a prolonged period for the antibody tests (assuming the endoscopy/biopsy doesn't require this too, see above)? I will discuss this with my doctor and a specialist in this if we can find one, but I hope I won't need to eat either again for several weeks to get positive tests... I believe a diagnosis doesn't strictly require a positive test because they are not yet 100% as of today (for non-celiac sensitivity, anyway) -- does anyone have an idea? From what I have read a response to food challenge would be enough, even if no antibodies are found.

pricklypear1971 Community Regular

All you need to eat for a Celiac panel is gluten. You could leave the milk out.

Different Celiac tests measure different things, but the iga antibodies drop quickly. More than two weeks without gluten, IMO, is too long without gluten for accurate testing.

You can still be NCGI without a positive endoscopy or blood work. The only way to accurately dx it currently is with a gluten-free trial.

And soy is a big problem for some people. Most say their symptoms from soy are as bad or worse than from gluten. Many of them neurological. If you don't feel improvement i'd experiment with dropping it.

And a complete panel for iron is one that measures iron stores, circulating levels, etc. Many doctors just order ferritin.

gliadin-raider Newbie

Ah, yes, probably wouldn't have to eat both at a time.

How long would I have to eat gluten again for antibody levels to rise?

I think Iga was what we tested a year ago with negative result though.

I have considered dropping soy too, but I don't seem to have a problem with it. At least it doesn't seem to be interfering with the improvements I get

from my current diet. I may consider dropping it once the improvement from gluten and milk subsides, but those seem to have been the major ones for me.

Ok, I think I have just done a ferritin test then. Will consider a more extensive test after discussing with my doctor, thanks.


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



Celiac.com Sponsor (A8-M):



pricklypear1971 Community Regular

They say to eat gluten for 3 months prior to testing. There's no good information about how long to add it back if you just dropped it. Sorry.

Were you iga deficient when they tested? Were your levels below normal? That could be one reason your tests are negative. Also, I think many tests are dependent on iga - so it wouldn't just invalidate one test. You'll want to research the tests and see.

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.