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

Other Foods Causing Problems....


BeckyW

Recommended Posts

BeckyW Contributor

My daughter recently tested positive for Celiacs on bloodwork, neg biopsy and has 2 genes for Celiacs. She has been gluten-free for over 2 weeks and has made some progress some days and then some days she seems worse. I believe there are other foods causing problems as I have read many people have problems with. She has been dairy free now for about 1 and 1/2 weeks. I believe fruit may also be a trigger. My problem is what is left for her to eat? I am not sure what to feed her any more. She has no energy and is very thin. Can anyone please give me ideas and suggestions on what foods are "safe" for her to eat?

I am not getting much help from the doctors. The gastro said it is IBS and all the foods he wants her to eat and the ones causing the problem. I have learned more from people on this board from any doctor we have been too! Thank you for sharing your stories and your encouragement.

Becky


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

Well, as you may know already, there can be hidden sources of gluten in foods, skin/hair care products, and contamination from foods being served to others or while stored in the fridge.

Other possible problematic foods can be soy, dairy, tree nuts, peanuts, corn, yeast, sugars...the list is practically endless. It depends on the individual, but those are very commonly found to cause reactions.

What sort of symptoms is she experiencing now? Is it the same as while on gluten?

BeckyW Contributor

She is experiencing basically the same symptoms she had when she was eating gluten but not as bad. She had abdominal pain, gas, bloating, C and feels nauseous. I don't think she is getting glutened, we have read every ingredient, called companies before using products and are very careful with food preparation. I think there is some other food triggering the symptoms and not sure how to go about finding this out.

She doesn't want to eat or drink and is having problems with the dehydration. I have many food intolerances and I am pretty sure she also does.

If anyone has suggestions on how to figure this out I would sure appreciate them!

RiceGuy Collaborator

Many recommend keeping a food journal. Mark down everything she eats, the time, etc. Then when symtoms arise, you'll have a better picture of things, and will hopefully see a pattern.

If she has had any of those items recently that commonly cause reactions, I'd start there. Go for the top allergy suspects first (unless she hasn't eaten any of it). Oh, and don't overlook nightshades, like tomatoes, potatoes, etc. Seems those can also be a problem.

Ursa Major Collaborator

Hi Becky, and welcome to this board. I recommend you follow the link in my signature on lectins, it sounds to me as if they could be the problem. Rice and eggs cause me to have almost the same symptoms as if being glutened, and so does soy. Potatoes cause similar problems as well.

Anyway, you would do well to read what it says, and try eliminating lectins to see if it helps.

I hope you figure it out!

AndreaB Contributor

Soy and dairy are probably the two biggest aside from gluten. Corn is also a problem for many. If you have the funds I would suggest enterolab (Open Original Shared Link) to see if she has an intolerance to dairy, soy, eggs or yeast. That is all the test for aside from gluten issues and genes. If it proves to be too much of a challenge right now to do an elimination diet you could get allergy testing to try and nail down foods she may be reacting to also. I had allergy testing done which led me to get the family tested by enterolab. Anything I put in the signature area is active sensitivity from enterolab testing (aside from my allergy results).

Welcom, the people on this board are great! :P

wozzy Apprentice

Has she gotten any other allergy tests? Scratch tests, blood tests, ect.

Also, sometimes it can take awhile to start feeling better because of the damage gluten does. 2 weeks may not be enough time to be completely better. Also, depending on how familiar you are with gluten, you could be unknowlingly feeding her stuff with gluten in it, either from the product itself or from cross contamination.


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



Celiac.com Sponsor (A8-M):



BeckyW Contributor

Thanks for all your responses. We are currently doing a food journal but I cannot connect any foods to the symptoms. She is always worse at night after dinner, before bed. I think she needs more healing time. She has been allergy scratched tested a few months ago but no foods were positive. My food allergies/intolerances that I react digestively do not always show up on the scratch test either. We just went to a new allergist/ENT who sent her blood out to a lab in Maine. This is the only lab he trusts for the RAST testing - I think it is Allutest or something similar. We are waiting on the results. They take about 3 weeks.

The ENT also gave her a cavemans diet to try. Fresh meat, fruits and veggies and no processed food. I think we will cautiously try this but watch the fruits as they seem to be a trigger. I did buy some babyfood for her to eat too. Hopefully that will give her some nutrition.

Thank you again for your help and please let me know any other suggestions!

Archived

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

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,918
    • Most Online (within 30 mins)
      7,748

    Dizzyma
    Newest Member
    Dizzyma
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Dizzyma
      Hi all, I have so many questions and feel like google is giving me very different information. Hoping I may get some more definite answers here. ok, my daughter has been diagnosed as a coeliac as her bloods show anti TTG antibodies are over 128. We have started her  on a full gluten free diet. my concerns are that she wasn’t actually physically sick on her regular diet, she had tummy issues and skin sores. My fear is that she will build up a complete intolerance to gluten and become physically sick if she has gluten. Is there anything to be said for keeping a small bit of gluten in the diet to stop her from developing a total intolerance?  also, she would be an anxious type of person, is it possible that stress is the reason she has become coeliac? I read that diagnosis later in childhood could be following a sickness or stress. How can she have been fine for the first 10 years and then become coeliac? sorry, I’m just very confused and really want to do right by her. I know a coeliac and she has a terrible time after she gets gluttened so just want to make sure going down a total gluten free road is the right choice. thank you for any help or advise xx 
    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
×
×
  • 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.