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Ttg Improved But Symptoms Not


adevers

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adevers Newbie

Hi. This is my first post, but I


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Jai Rookie

Wow. Sorry about your struggles. I have no answers really, just sympathy. I went gluten free in June, and initially improved, but have had abdominal pain resurface and am in the process of trying to figure out what's going on. There doesn't have to be only one thing wrong! What about other food intolerances? Soy? Corn? Eggs? What is she eating, when she eats? I can sympathize with the fear of eating! Been there, actually I'm still there. Let me just say that I love rice! Nothing bad ever happens when I eat rice ;)

I wish you and your family strength and luck!

BabsV Enthusiast

Wow, I'm so sorry for your daughter. I am so not an expert but I can share my story. One of my main symptoms of Celiac Disease was intense abdominal pain -- prior to my Celiac diagnosis I had two doctors agree it was a 'functional' pain issue and they put me on anti-anxiety medicines (one made me horribly ill as it interacted with another medicine I was on and one relaxed me but did nothing for the pain!) They wanted to put me on tri-cyclic antidepressants but I have a problem with serious side effects to a lot of medicines and the doctors were really worried that TCAs would cause all sorts of problems for me. During this process I did a lot of research and using TCAs is one way to work with functional pain issues...along with Cognitive Behavior Therapy. So it is a valid approach for functional pain issues with certain health conditions (e.g. GERD)...BUT...it did nothing for my Celiac pain. Not sure if Zoloft is a TCA (they are an older class of antidepressents); I was told TCAs are supposed to work better with pain than some of the newer classes of antidepressants, e.g. SSRIs.

At this point I'm not even 3 months into the gluten-free diet and while my pain issues have decreased a bit I still have pain every day, usually after eating. I started keeping a food diary and have eliminated some items that seemed to be making the pain worse (raw fruits & veg, beans, corn, fruit juices, etc.) I'm sticking to a very plain diet of chicken/turkey/fish, rice and potatoes, cooked fruits & veg. No dairy, no sugar, no gluten-free replacement foods. I'm just trying to add some nuts as of today. This approach seems to be helping somewhat...I figure I just have to continue healing and give it more time. I've ordered some gluten-free probiotics and will start those as soon as they come in.

She just might need more time for the pain issues to resolve.

pricklypear1971 Community Regular

First, I'm sorry to hear your daughter is going through this.

Second, are you sure she isn't getting glutened? I know you're being careful but it sounds like she is very sensitive, so extra precautions may be needed. Read on the supersensitive forums for ideas.

Have you checked with Pfizer to ensure Zoloft is still gluten free? It looks like it is from web searches but formations change. Are there any other meds that might contain gluten?

I would try elimination diets based on the major allergen groups: milk, soy, egg, nuts. I'm sure I'm forgetting something...

And finally, yes it can take a long time to heal.

Have you considered acupuncture for the pain? I know she's little but perhaps this would work. I've seen many posts about how acupuncture works well for Celiac nerve issues.

Good luck!

adevers Newbie

Thanks so much for your reply. She's actually on an NG feeding tube right now. However, the elemental formula being fed to her does contain soy. We're looking to potentially change the formula to remove soy as well. Thanks again for your input. I wish you the best in solving your struggles as well. It's great to have a community that can relate!

adevers Newbie

Thanks a lot for your reply. I think your situation sounds very similar to my daughter's. I'm encouraged that you're seeing some improvement after 3 months of eating gluten-free despite the 'functional pain' diagnosis. Happy to hear that for you. My gut feel tells me the same thing you you suggested....that she just needs more time. She's actually on an NG tube exclusively right now, so other than soy (which is in her elemental formula), her food intake should be ok. I wish you the very best in your recovery. Thanks again for your input!

adevers Newbie

Thanks a lot for your reply. Good question about her meds. We have looked into many of her meds, but we do need to do a thorough check to ensure she's not getting gluten that way. Will also look further into acupuncture. Interesting idea. Thanks again for your thoughts. I really appreciate it!


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Bubba's Mom Enthusiast

I'd be suspicious of the soy. Once I went gluten-free I found I was reacting to even very small amounts like soy lethicin. If I ingest it I get bad pain in my belly, GERD, too.

I've cut that from my diet and the pain went away.

Your Dr.s DX might be correct, but in a lot of cases they don't have answers as to why something happens. They seem to prefer to prescribe a med to counteract the symptom rather than searching for the true cause?

Good luck to you both!

adevers Newbie

We've seriously considered removing the soy. I guess between our doctor suggesting that it wasn't an issue and the fact that her diet is already so restricted, we'd decided not to remove soy to this point. However, my gut tells me that it's worth a try. Anyone know how long is a fair trial for soy elimination? Thanks so much for your input. I really appreciate it.

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    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
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      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
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