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Stomach And Intestinal Spasms


kwylee

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kwylee Apprentice

I've been at this now for about 15 months - gluten-free/DF/SF, non celiac (by blood and biopsy) but gluten intolerant (Enterolab). In the past 6 weeks I've noticed that my system has changed. I was feeling GREAT for over a year and then I started with nausea at times, always after I eat no matter what I eat, even though sometimes I eat very little and still hungry. If I go a day eating very little, it seems to get better, then the process starts up slowly again with the first meal I have. This nausea sometimes then turns into a feeling like my stomach and intestines are in spasm. It's not painful (yet) but certainly uncomfortable and scary. Nothing really helps this, not even pepto. Usually it's worse after lunch and dinner and if it's still bad by bedtime, resolves by the time I wake up. Oddly enough, when I'm not nauseous, my appetite is still intact.

GI's done some testing (blood work, hpylori, endoscopy, colonoscopy, abdominal ultrasound, even a stress test) and all looks good except a bit of scarring in my stomach - not sure from what, no idea how old it is, plus he noticed a slight acid reflux, which was a surprise too. I've never really had intestinal trouble in my life - my symptoms pre gluten-free were neuro, dizziness, which I don't seem to be having now unless my stomach is really upset. I thought I had the answer a couple weeks ago when I realized that the Burt's Bees lip gloss I wear has soybean oil in it. I stopped using it but no decrease in symptoms (and my lips are chapped!!!!)

Does anyone else have experience with intestinal spasms? Is this what others call bloating? It literally feels like someone is twisting my insides, starting with my stomach, then the sensation usually moves into my intestines.

Also, does anyone know if "scarring" found in my stomach could spontaneously be causing the onset of any of this? I can see it causing nausea perhaps, but intestinal spasms? Could it be interfering with my digestive process further down the line? Could slight acid reflux cause this?

GI prescribed Prilosec for acid reflux but it really didn't do anything to help and I have to go back in a couple weeks. After all these tests, I can't help thinking it's something simple. Perhaps a new food intolerance?

Any ideas or similar experience is appreciated.

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tlmcneal Newbie

I've been at this now for about 15 months - gluten-free/DF/SF, non celiac (by blood and biopsy) but gluten intolerant (Enterolab). In the past 6 weeks I've noticed that my system has changed. I was feeling GREAT for over a year and then I started with nausea at times, always after I eat no matter what I eat, even though sometimes I eat very little and still hungry. If I go a day eating very little, it seems to get better, then the process starts up slowly again with the first meal I have. This nausea sometimes then turns into a feeling like my stomach and intestines are in spasm. It's not painful (yet) but certainly uncomfortable and scary. Nothing really helps this, not even pepto. Usually it's worse after lunch and dinner and if it's still bad by bedtime, resolves by the time I wake up. Oddly enough, when I'm not nauseous, my appetite is still intact.

GI's done some testing (blood work, hpylori, endoscopy, colonoscopy, abdominal ultrasound, even a stress test) and all looks good except a bit of scarring in my stomach - not sure from what, no idea how old it is, plus he noticed a slight acid reflux, which was a surprise too. I've never really had intestinal trouble in my life - my symptoms pre gluten-free were neuro, dizziness, which I don't seem to be having now unless my stomach is really upset. I thought I had the answer a couple weeks ago when I realized that the Burt's Bees lip gloss I wear has soybean oil in it. I stopped using it but no decrease in symptoms (and my lips are chapped!!!!)

Does anyone else have experience with intestinal spasms? Is this what others call bloating? It literally feels like someone is twisting my insides, starting with my stomach, then the sensation usually moves into my intestines.

Also, does anyone know if "scarring" found in my stomach could spontaneously be causing the onset of any of this? I can see it causing nausea perhaps, but intestinal spasms? Could it be interfering with my digestive process further down the line? Could slight acid reflux cause this?

GI prescribed Prilosec for acid reflux but it really didn't do anything to help and I have to go back in a couple weeks. After all these tests, I can't help thinking it's something simple. Perhaps a new food intolerance?

Any ideas or similar experience is appreciated.

Sounds a lot like my daughter, non-celiac gluten intolerant. She had major knife like chronic pain in her stomach which lessened considerably with gluten-free diet, an anti-spasmodic and low dose anti-depressant. What has never disappeared completely is the nausea. Sometimes it lessens during the day as she eats, but it is always present in the morning, and frequently awakens her at night. She takes generic zofran as needed, but it still doesn't stop it. We are trying to figure out if there are other food intolerances besides gluten and dairy. I'll be interested to hear how you make out.

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kwylee Apprentice

I know how miserable she must feel. Not sure how old she is but at any age, nausea can really impact your quality of life. I think the worst part of all this for me is not knowing what's causing it.

The first thing that came to mind when I read yours was soy. 15 months ago, I didn't chuck all my "gluten symptoms" until I totally removed that from my diet too. So that may be something to consider, and just like gluten and dairy, it's hidden in many foods. Last time I checked, I can't tolerate soybean oil or ingredients like soya lecithin. And you may be already familiar with cc from shampoo, lotions, lip gloss, etc.

I actually had an appt with my GI yesterday and she thinks I have an excess of stomach acid (from what I do not know, because I thought your stomach acid declined as you age and I am 56) - Anyway, she also thinks that the scarring found in my stomach may be the culprit - supposedly from some past trauma, surgery or infection and that has me more than a little perplexed. Anyway - she prescribed a strong acid reducer and something to rebuild my mucosal stomach lining which she suspects is deteriorated. For the spasms she prescribed generic Bentyl. I have to say that I've taken all of it for 24 hours and do not feel any better just yet but I am hopeful. I'm sitting here starving but do not want to eat because I know I will get nauseous. Errrrr.

I hope you can figure out what is going on for your daughter. If all this works for me, or if it doesn't, I will let you know. I'm fairly tenacious and do not give up easily so I intend on getting the answer, fixing this and moving on.

Thanks for writing.

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frieze Community Regular

Sounds a lot like my daughter, non-celiac gluten intolerant. She had major knife like chronic pain in her stomach which lessened considerably with gluten-free diet, an anti-spasmodic and low dose anti-depressant. What has never disappeared completely is the nausea. Sometimes it lessens during the day as she eats, but it is always present in the morning, and frequently awakens her at night. She takes generic zofran as needed, but it still doesn't stop it. We are trying to figure out if there are other food intolerances besides gluten and dairy. I'll be interested to hear how you make out.

I would be thinking hypo glycemia

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  • 3 weeks later...
kwylee Apprentice

Just an update on all this. I'm feeling much better now, back to my old post-gluten self. I've read about alot of people taking a step back in their symptoms and I can only say I seem to have experienced that first hand. In my case, I think it was the synergy of a few things that started the ball rolling, giving me mystery nausea and weird stomach spasms beginning a few months ago.

As recently as a week ago, doctors tried hard to sell me on what was causing my trouble, after testing me for everything short of CHOLERA - even urging me to have stomach surgery to remove a bit of scarring I've lived with for many years with no problem. But all along I suspected it was something very simple. And after the last couple weeks of progressively feeling better (even SANS all the medication Drs. originally put me on - yes - I am hard-headed and hate to take pills until I'm convinced it is 100% necessary) I think I have it figured out. Simple cross contamination. This has been a good lesson - sometimes when you think you know something for sure, look again with fresh eyes.

Burt's Bees lip gloss - gluten free but contains soybean oil. Loved it for years - but in the trash!

Mercola probiotics - touted as gluten free but a specific quizzing of the company revealed that they are NOT manufactured in a gluten free factory.

Dr. Ohirra's probiotics. I had taken them before seemingly with no problems so thought they were OK. A simple reading of the label prominently showed (duh) "contains soybeans" - although they assured me it should not affect me, perhaps with a weird stomach acid rev the pills were breaking down in my system before they reached the proper destination.

The only thing I know for sure is that I'm feeling great again - no nausea, no bizarre stomach spasms. All since I've removed all of those things, retaining the abdominal scar tissue as a souvenir. I have some Custom Probiotics in the mail to me (fingers crossed), but I'm also going to try my hand at making homemade sauerkraut. Made me realize how lucky I was to stumble onto this whole gluten problem over a year ago. If not, I may have wound up with unnecessary surgery, and since it was the only thing doctors didn't test, I admit that it was still possible to have died of cholera. I'm starting to really feel safe in my gluten free world!!!

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maelenebaby Newbie

hi there thats great u found out it was cross contamination. i suffer from really bad intestinal cramps almost like someone is twisting them and the pain can last for hours. one thing that has literally kept me out of the hospital is natures sunshine intestinal soothe and build. please people if u suffer from diarrhea, pain and any other symptoms, try this. i accidently ate gluten one time and was in the hospital they wanted to take out my appendix because of the symptoms they were so similiar. but it was a gluten attack. nothing they gave me worked until i took a few of those pills and surely the next day i was fine.

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    • cristiana
      Thank you for your post, @Nedast, and welcome to the forum. There have been many posts on this subject on the forum, it is interesting to read of your experiences. Although I've not had TMJ, except from time to time have had a bit of mild tension in my jaw, I have had issues with my trigeminal nerve.  I read that sometimes a damaged nerve in coeliacs can heal after adopting a gluten free diet.  I try to keep out of cold winds or wear a scarf over my face when it is cold and windy, those conditions tend to be my 'trigger' but I do think that staying clear of gluten has helped.   Thank you again for your input.
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      I made an account just to reply to this topic. My story resembles yours in so many ways that it is truly amazing. I also suddenly became lactose intolerant, went a little under 10 years attributing all my symtoms to different body parts, never thinking it was something systemic until much later. I had the same mental problems - anxiety, depression, fatigue, etc. In fact, the only real difference in our story is that I was never formally diagnosed. When I discovered that my myriad symtoms, that had been continuous and worsening for years, all rapidly subsided upon cessation of consuming gluten, I immediately took it upon myself to cut gluten out of my diet completely. I live in America, and had lost my health insurance within the year prior to my discovery, so I could not get tested, and I will never willingly or knowingly consume gluten again, which I would have to do in order to get tested now that I have insurance again. But that is not the point of this reply. I also had extreme TMJ pain that began within months of getting my wisdom teeth out at - you guessed it - 17 years old. I was in and out of doctors for my various symptoms for about 5 years before I gave up, but during that time I had also kept getting reffered to different kinds of doctors that had their own, different solutions to my TMJ issue, an issue which I only recently discovered was related to my other symptoms. I began with physical therapy, and the physical therapist eventually broke down at me after many months, raising her voice at me and saying that there was nothing she could do for me. After that saga, I saw a plastic surgeon at the request of my GP, who he knew personally. This palstic surgeon began using botox injections to stop my spasming jaw muscles, and he managed to get it covered by my insurace in 2011, which was harder to do back then. 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