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GSRB

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  1. UPDATE

    The gastro called this morning and it has been confirmed Bailey does have coeliac disease. I am so relieved to finally have an answer. He has been gluten free since Friday and we are noticing small changes already. He needs to have follow up blood tests in 6 months the again at 12 months then every 1-2 years after that. As long as there are positive changes with blood results and diet he won't have to undergo another endoscopy.

  2. medical opinion may differ from mine, but i have no love for the doctors who screwed up my 22 month olds diagnosi,, if i followed their direction...he would have died.

    do not make your baby eat gluten if he is suffering. Why torture your little one with food that is,hurting him. Find a doc who will give u a diagnosis based on symptoms/bloodwork.

    What happened with your little ones diagnosis???
  3. Thank you :)

     

    My GP has signed off on the paperwork for us to join the coeliac society and was the one who was more than happy to have the diagnosis as coeliac without the biopsy.

     

    I forgot to mention - my dad has coeliac (diagnosed about 17 years ago). 

     

    Mushroom, i feel as though I am jumping through a lot of hoops and I do wonder how much of this is necessary!!!!  Putting him under a general isn't my favourite option so trying to figure how if it is a good idea to wait or not.

  4. I'm new here and thought I'd say hi!

    I'm in a very confused state at the moment. My 2 year old son had the bloods done about a month ago and his gliadin iga was 5 (negative) but his ttg iga/igg was >300 (very positive!!). My GP was happy to diagnose coeliac on that but my paed wants the biopsy done. The gastro is trying to fit us in before the 9th may.

    Did anyone get diagnosed without the biopsy? Did anyone have the biopsy and it not be coelaic but something else?

  5. Hi all.

    About a month ago we had our 2 year old son allergy tested through NAET testing and he showed a reaction to gluten. We went to our GP and she sent is for a blood test. His results are as follows:

    Gliadin IgA 5 (0-20)

    Ttg Iga/Igg >300 (0-25)

    Based on that, my GP was happy to confirm he had coeliac's disease and not bother with the biopsy. The paediatrician called a week later and said he needs a biopsy done to confirm it. We had taken him off gluten for approx 5 days and had to put him back on it until we get the biopsy. The first three nights after putting him back on gluten saw him screaming all night in pain. He also broke out is a rash. The paed dismissed these and said they aren't related. i disagree.

    We phoned the paed gastro on Monday and first available appointment is end of June!!! The receptionist said to pencil in the procedure for the 9th May and they will try and squeeze us in before then for the consult.

    I honestly don't know if we should even bother with the biopsy. The only thing is what if it is something else? Not sure what that could be but I don't know!

    My daughter tested negative to the disease but positive to the gene.

    I am going to have the blood test today for serology and gene testing.

    Would you go ahead with the biopsy?

    Thanks!

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