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

Biopsy


averyevansmom

Recommended Posts

averyevansmom Apprentice

My son had his biopsy done today and although the results won't be in until next week, the doctor did mention some issues with the small intestine. There was inflammation and three white spots or patches. Has anyone had any mention of this? There were no other noticeable problems seen. I asked what those things could mean and she said it could be from allergy then I asked about celiac and she said yes, it could be that. My son was seen by an allergist last Friday and tested negative for everything tested for (dairy, soy, all nuts, wheat, fish, corn, citrus, and eggs) the usual stuff. We ran the RAST today for these and others as well per the allergist and the GI is running all the celiac tests again. Has anyone heard of this? My little guy is still sleeping off the anesthesia from this a.m. He was awake this afternoon and ate and now he's sound asleep. Poor guy. Just glad it's over. I'm planning to start the gluten-free diet as soon as I'm able to go food shopping and have my lists ready. Any sound advise? My kids are big on snacks. They love goldfish, pretzels, cheeze nips, they eat lots of pasta and bread. Whole foods here does not carry the Kinnikinnk(sp?) and the bread I tried is nasty. It's called Glutino and it's hard as a rock. I wouldn't feed it to my dogs. Yuck. My son loves his bread. How about a butter or spread without dairy or soy? So many questions, so little time.

Thanks.

Becky


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



Celiac.com Sponsor (A8-M):



averyevansmom Apprentice

Anyone?

bluelotus Contributor

Enjoy life makes great bagels (even cinnamon raisin), cookies, and breakfast bars.....I don't have kids myself, so I am not sure how their little taste buds would react, but I think the products are tasty. They make bread too, but I haven't tried it. Enjoy life is free of all common allergens, even dairy and soy. Another brand to try is Ener-G, the bread is pretty bad, but they make good pretzels, though I am not sure if they are soy free. Both these brands have websites if your Whole Foods doesn't carry them (my Whole Foods does, but they don't carry the bagels :( ).

I also know that Cranraisins (not the trail mix) are gluten-free and so are Sunmaid raisins. I can't eat these b/c the extra fiber bothers me. I am not sure if your son is too young for these tiny foods, but maybe these will help.

Hmmm.....trying to think of more ideas. EnviroKids gluten-free cereal is good (by Nature's Path). Some (like Gorilla Munch and Panda Puffs) are likely large enough for your son to eat as finger food.

Nana's makes good gluten-free cookie bars. I like the banana kind. If you son likes banana bread, he should like those. They have a website too.

I am sure that others here can help you out with the more mainstream brands. I was having problems with some, so I try to avoid them and stick with the predominantly gluten-free brands. One mainstream product that I have had great luck with is Smucker's Natural Peanut Butter. Very yummy.....great kids snack with celery and raisins.

Hope these ideas help!

katerinvon Rookie
My son had his biopsy done today and although the results won't be in until next week, the doctor did mention some issues with the small intestine. There was inflammation and three white spots or patches. Has anyone had any mention of this? There were no other noticeable problems seen. I asked what those things could mean and she said it could be from allergy then I asked about celiac and she said yes, it could be that. My son was seen by an allergist last Friday and tested negative for everything tested for (dairy, soy, all nuts, wheat, fish, corn, citrus, and eggs) the usual stuff. We ran the RAST today for these and others as well per the allergist and the GI is running all the celiac tests again. Has anyone heard of this? My little guy is still sleeping off the anesthesia from this a.m. He was awake this afternoon and ate and now he's sound asleep. Poor guy. Just glad it's over. I'm planning to start the gluten-free diet as soon as I'm able to go food shopping and have my lists ready. Any sound advise? My kids are big on snacks. They love goldfish, pretzels, cheeze nips, they eat lots of pasta and bread. Whole foods here does not carry the Kinnikinnk(sp?) and the bread I tried is nasty. It's called Glutino and it's hard as a rock. I wouldn't feed it to my dogs. Yuck. My son loves his bread. How about a butter or spread without dairy or soy? So many questions, so little time.

Thanks.

Becky

I think pancakes are everyone's first effort at gluten free bread substitute. The can be made easily without gluten or dairy, and make great finger food sandwiches. Rice crispy treats can be gluten free. My daughter (age 2 today!) really likes rasins, papaya spears, crasins, rice crackers, rice based graham crackers, frozen peas, popcorn, bananas, chocolate, corn tortillas, french fries. All the peanut butters I have checked are gluten free, and jelly should be. There are rice noodles available. Cornstarch based sauses and gravies are OK. Plain meats, potatoes, rice, and vegies are already gluten free and can be prepared without making a lot of changes in routine. Watch out for processed prepackaged foods, many of them have gluten based fillers or sauses.

Hope this helps. Good luck.

Karen S

taweavmo3 Enthusiast

Regarding the inflammation, my daughter had that as well. So, I would definately say that could be a sign of celiac.

Now, in terms of the diet.......I have a few ideas for ya! If you don't have a big selection at your Whole Foods, you may have to do some buying online. I've been extremely lucky in that I have a great selection at stores around me, so we've been able to try lots of different things. The only brand of bread my kids will touch is Kinnikinnick. Another one you may try is Gluten Free Pantry white sandwich bread mix. I haven't tried this yet, but I have loved everything else from them so far.

For Pancakes, our favorite BY FAR has been Gluten Free Pantry Muffin and Scone mix (can't remember if it's dairy free or not, but I know you mix it with OJ instead of milk, and it's delicious). A close second is the Kinnikinnick pancake mix. We don't like Pamela's all that much, but I know others do. It just wasn't sweet enough for us. Can you tell I don't make anything from scratch??? Lol, there are just so many good mixes available, and I know they will turn out!

Snacks I would say are the biggest challenge for us too. My kids used to eat goldfish and all that stuff by the truckload, so it was an adjustment for them in the beginning. But, there is still plenty to choose from. For snacks, Emmie loves the whole line of Envirokidz foods....they make cereal, snack bars (kind of like rice crispie treats) and animal crackers. She also eats fruit w/peanut butter, rice cakes, marshmallows, Craisins (yummy), chips, Midel cookies, and carrots with ranch dip or hummus.

That's all I can think of at the moment, but I know others will have ideas for ya. I try to stick to mainstream products to cut down on cost, but when I splurge I usually stick with Kinnikinnick or Gluten Free Pantry, since those are two brands I can trust that their products will taste pretty good! Nothing sucks more than spending nearly $10 on something that no one will touch. Have fun shopping, and we're here if you need any help!

Guest nini

I would highly reccommend trying to order the Kinnickinick sandwich bread, as most of the others out there are just nasty. I keep the extra loaves in the freezer and the loaf I am using in the fridge... for sandwiches I nuke the slices for about 30 seconds or toast them... My daughter won't eat any other kind of gluten-free bread.

EnerG has good pretzels and crackers as well as Glutino Brand... Enjoy Life Foods has lots of snacks that are yummy, MiDel Gluten free cookies are also good kid snacks, Fruit snacks (check w/ mfr.) are a good option, fresh fruit, fresh veggies and a dip (like a yummy salad dressing he likes)... I gotta go get ready for work, I'll try to post more ideas later.

debbiewil Rookie

For snacks, you can use some regular ones that they might already be used to. Lays Stax chips are gluten free (not the regular Lays - some of the regular ones may be cross contaminated, and some of the regual flavored chips may contain gluten). Some of the corn chips and rice cakes are gluten free. My little neice loves to dip food. We get gluten-free ranch dressing, peanut butter, salsa, etc. and put it on a plate with some fresh veggies, fruit, and gluten-free chips and she's happy.

Debbie


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



Celiac.com Sponsor (A8-M):



key Contributor

My son loves crunchy cheetos(we use these in place of crackers). They are messy though. We also like Envirokids gluten-free vanilla animal cookies. We keep brown rice cooked and spaghetti noodles from Tinkyada. It helps to have stuff cooked on hand. I also like the personal pizza's made by Kinnikinnick. HE likes these alot. Also cheese sticks if he can have those.

My son also eats quite a bit of yogurt.

Good luck.

Monica

averyevansmom Apprentice

bluelotus,katerinvon,taweavmo3,nini,debbiwil and key

Thanks so much for the information. My son is 3 and can eat pretty much anything at this point. He doesn't like much meat though. I expect most kids his age don't. I've been trying to find as much info as possible on the regular foods that I can for him. We are all going gluten free even before the results come in. I just want to see if there is any change in him. I assume it will take a little time to see the change. He's such a good little guy. He is such a spaz today, really goofy and giggly. Not the norm for him at all, he's usually quite mellow and laid back except when he's in pain or having some sort of reaction to something. I don't mean to repeat myself but has anyone heard of seeing the white patches in the small bowel as well as the inflammation? I'm wondering if they go hand in hand with celiac. I just received Dangerous Grains from the library and started to read it last night. I was exhausted so didn't get through much.

Again, thanks to everyone.

Going to Trader Joes tonight to see if they have a better selection than Whole Foods. The only problem is TJ's is about 45-50 min as opposed to WF's which is 15-20 min. Oh, well, when it comes to the kiddies, parents will go to the ends of the earth.

Becky

chrissy Collaborator

becky, before we were even suspecting celiac in our kids, one of my twins had an endo with biopsies because she also has reflux. her intestines were fine (no damage, no inflamation) but her esophagus was covered with white patches. the ped gi told me it was either food allergies or a fungal infection. it turned out she had esophageal thrush.

christine

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,860
    • Most Online (within 30 mins)
      7,748

    Rena Celiac
    Newest Member
    Rena Celiac
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • 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    
×
×
  • 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.