Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Extremely Confused


averyevansmom

Recommended Posts

averyevansmom Apprentice

I heard from Children's yesterday via voice mail. They reviewed my sons biopsy slides and had the same findings of inflammation of the duodenum (small intenstine) as Hasbro. However, when I do speak to the Dr. I will mention that when the doctor performing the biopsy at Hasbro came out of the operating room, she told my husband and I that she saw 3 white lesions (spots) and a LOT of inflammation. Anyway, he mentioned on my voice mail doing more testing. I have no idea what that means since every possible blood test that I know of has been performed. (I think). I hope he's not suggesting another endoscopy. He has responded so well to the diet that I shudder to think of putting him back on gluten. It would kill me. He never complains of belly aches anymore and the only time he has a bad poop is when he accidently gets gluten or has dairy or yogurt (is yogurt considered dairy) the dietician says it should be okay. I'm so scared I'm having anxity attacks. I feel like I'm starting at square one. I don't want him to suffer. I feel bad enough when he has a pasty sticky poop because he cries and screams when I have to wipe him. He fights so hard. Maybe I should be looking at something else. The doctors have no answers, he has no food allergies, so I have no idea what direction I should be going. I'm really scared for him. My well being is taking a real hard hit. I suffer from clinical depression and this only makes it worse, not to mention the fact that my family feels my anxiety and frustration. And my son shouldn't have to suffer for doctors mistakes. Boston Children's is very knowledgable in Celiac and has a Clinic so I really don't understand. Am I a one of THOSE kinds of mothers. God I hope not. Please help.


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



Celiac.com Sponsor (A8-M):



mmaccartney Explorer

My heart and prayers go out to you. Having a sick child is a very hard, trying thing to deal with.

Yogurt is absolutely Dairy, (BUT my GI told me I could have that and cheese what a riot!). Avoid it. If your son cannot have dairy, avoid anything with milk, casien, lactos, whey, and there are more. Though you indicate no food allergy, here is some good information on the hidden sources of milk: Open Original Shared Link

My sons (4 and 3) have severe food allergies, the oldest is anaphylatically allergic to peanuts and tree nuts, allergic to milk, eggs, wheat, dogs, and fish. I also believe he has Celiac disease (from me). He's also a vegetarian by his own choice, not relevant but I'm proud of him for finding his values so early on and sticking with him. The youngest is allergic to milk and eggs.

We are still dealing with the "my tummy hurts" all the time. Currently we have begun an elimination diet to identify what is left in his diet that is causing him problems. I pray that it is NOT Corn of Soy, they are the staples of his diet, his primary protein source, and his favorite food items!!!

It makes me sad and depressed to be sick myself when I get glutened or ingest dairy, but to see my little ones sick is 100 times worse.

my opinion, if you know in your heart and mind that gluten is a major problem for your son, forget the doctors and the test. I would not ingest gluten for the sake of a positive test at this point, my original testing got messed up since I went gluten free before being fully tested and diagnosed...but SO WHAT! I was dying, slowly, and painfully. When I changed my diet, I began to get better within days. A few days after going gluten free and feeling better I ate a Wheat Waffle just to see, and back came the arthritis, the abdominal pain, my diarrhea, vomiting, etc. DONE! I made my own diagnosis....

besides, my Rheumotologist's mother had celiac disease so she is quite knowledgeable about it, told me one time "Why do you want further testing, you know that you had a positive response to the diet, and even had some bloodwork come back funny. You know how to get better, what would more testing really tell you?" Now, she isn't a Celiac specialist, but she deals with digestive issues all the time, and her own mother had Celiac, and she is an medical doctor.

So, my opionion....avoid milk at all costs, and don't go further with testing if it requires posioning your son. If the response to the diet is positive and he is getting better, thank your God (or Higher Power) and move on towards a healthy life for him.

IF your son, later in life, feelds the need to go on a "gluten challenge" and have further testing, let him make that choice...and you'll never feel guilty about that!

Also another option, have genetic testing done, this requires no gluten ingestion!

Good luck, and keep us all posted...

Guest nini

my daughter did not have a biopsy, and her bloodwork was inconclusive... I knew in my heart that gluten was her problem and when I took gluten out of her diet, her health improved miraculously.

You do not need to put him through any more testing. You already have your answer. Gluten is a serious problem for him. It does not matter one whit if it is Celiac or just Gluten Intolerance, the treatment is exactly the same. Keep him gluten free and get him healthy and stop worrying about it. My daughter has been gluten free for almost 3 years now and she knows when she gets exposed to gluten, it makes her tummy hurt and she get's D, and sometimes even breaks out in hives. Her pediatrician finally acknoweledged that she is Celiac by POSITIVE DIETARY RESPONSE and the fact that I have it.

chrissy Collaborator

our ped gi said that inflamation is something you would see with celiac.

christine

averyevansmom Apprentice

Thank you Michael and Nisla

Just spoke to the doctor and reiterated what the Hasbro doc told me after the biopsy and he thought it was interesting, especially the white lesions. I also asked if everything was non-positive, why was Evan responding so well to the diet. He was surprised to hear that. He said that was pretty much a confirmation. He was also considering inflammatory bowel disease but it requires a different diet. He said to get the numbers of the tTG and the other blood test that was done so he can see just how negative they were and the gene test should be done within the next week or so. We see him for a follow-up on 3/16. He said while Evan was young to just assume and treat him as though he has Celiac's and when he gets older, if we want to do more testing, we can. So the yogurt's a no no? He does want to do some follow up bloodwork. I just hope they will give him a diagnosis if all else but the diet is negative.

Thanks again to everyone for your encouraging words and thoughtfulness.

Becky

averyevansmom Apprentice

Chrissy

Funny, you must have been replying the same time I was. I thought inflammation was thought to be found with celiac. Thanks. Wanted to make sure it was something I didn't just make up. Evan (Bubba) had a nice BM tonight.Yeah. This a.m not so much, could've be residual yogurt in his system though. Do any of you or your kids have "normal" bm's every time?

mmaccartney Explorer
So the yogurt's a no no?

Becky

If dairy is a problem (casien or lactose) then yogurt is out. There are soy yogurts available if he can tolerate soy. Check into it, I like to eat a kind I get at Trader Joes, as well as a kind produced by Silk Open Original Shared Link

If ice cream is something he'll miss, there are many soy ice creams out there. I like the kind from Turtle Mountain the best as they actually test their batches for contamination!!!

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



lbsteenwyk Explorer

This is regarding the yogurt question -

Many people with newly diagnosed celiac disease are lactose intolerant, simply due to malabsorption caused by the celiac disease. When the intestine heals, the lactose intolerance may resolve too. So, I would take your son off dairy for 3-6 months and then reintroduce dairy slowly. Start with lower lactose products like cheese or yogurt and see what his response is. He may not need to be on a dairy free diet permanently.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      125,930
    • Most Online (within 30 mins)
      7,748

    Robert Osborne
    Newest Member
    Robert Osborne
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      I've been using a Brita water filter for well over a decade without any issues. I seriously doubt that these water filter companies would use glues that would end up in your water, as that would be counter to what they are trying to do, which is to purify tap water. Please provide some specific evidence to back this claim up, as such speculation can cause undo fear, as well as reputational damage to these companies. Don't get me wrong here, I am not saying that this isn't possible, but is very unlikely.
    • trents
      Welcome to the forum, @aperlo34! You said you had a colonoscopy "ordered" in July? Has that procedure happened yet? A colonoscopy cannot be used to diagnose celiac disease so I assume the order for the colonoscopy is to check for something else. The procedure used to diagnose celiac disease is the endoscopy. So, I assume you have had blood antibody testing done and it was positive and then you had an endoscopy/biopsy done to confirm those results? That is the normal process for diagnosing celiac disease. Have your constipation/irregularity problems improved since going gluten free? Some of the continuing symptoms you describe would seem to fall into the category of neurological effects (muscle twitching, shakiness, weakness and headaches) and others such as dry eyes, fatigue, stiffness and joint aches sound like they could be autoimmune effects. Are you taking any high potency to vitamin and mineral supplements? Celiac disease often/typically results in vitamin and mineral deficiencies due to malabsorption from the damage to the small bowel lining it causes. I note that your vitamin D levels are barely within normal range and the only B vitamin testes is B12. The B vitamins and D3 are very important to neurological health. And the several B vitamins all work together synergistically. So, they all need to be up to snuff, not just B12. I would suggest starting on D3 supplementation in the amount of about 5000 IU daily and also a high potency B-complex. Costco's Nature Made and Kirkland brand products are good quality and priced well and usually gluten free (and will state so on the packaging). Realize also that gluten free flours and facsimile foods are not fortified as are their FDA mandated gluten equivalents. So, when you cut out gluten, you cut out a significant source of vitamins. One thing to be aware of is that Celiac disease is an autoimmune disorder and autoimmune disorders tend to cluster. That is, when you have one you there is a good chance you will develop others in time. I don't wish to alarm you because I know you have said you already struggle with heath anxiety but many of your symptoms make me think you have some other autoimmune condition going on in addition to celiac disease. Have you been checked for Sjogren's or lupus for instance?  Finally, I am including an article that is helpful to newly diagnosed celiacs in getting a head start on the learning curve of eating gluten free:   
    • Scott Adams
      This article may also be helpful as it offers various ways to relieve the itch:  
    • Scott Adams
      The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.      
    • cristiana
      Hi @aperlo34 Welcome to the forum. I am so sorry to read that you have been going through all of this.    Firstly, I should say that your experience of anxiety is very common, and also, the worsening of symptoms is also something we see reported quite a lot on this forum.  Achy joints, twitching as you describe and other symptoms were things I had and they all seemed to worsen for a while before they got better.  I am a coeliac based in the UK and here, unless we are extremely fortunate or pay for private treatment, we are tested for very few deficiencies - my iron was low, my B12 borderline normal and vitamin D borderline normal, but I have absolutely no doubt in my mind that had I had the full spectrum of vitamins and minerals tested, it would have shown deficiencies.  Your test reveals normal levels but it could well be you are lacking in something not on that list. My nutritionist at the time put me onto a broad spectrum supplement of every vitamin and mineral under the sun for a few months, until my GP said she thought there was too much Vitamin A in the pill so told me to stop taking it!  But one thing you could do is to take something similar which will address any deficiencies you are unaware of.   I would say one Vitamin which you could should supplement is Vitamin D.   Your lab reports show you are borderline normal, I'd say there is quite a lot of room for improvement there.   Symptoms of deficiency/low levels include:  Muscle pain, Bone pain, Increased sensitivity to pain, A tingly, “pins-and-needles” sensation in the hands or feet, Muscle weakness in body parts near the trunk of the body, such as the upper arms or thighs, Muscle twitches or tremors, Muscle spasms (source: https://www.yalemedicine.org/conditions/vitamin-d-deficiency) When I first joined this forum ten years ago or so, I found myself in the company of a lot of people complaining of twitches and spasms, and others who shared that it took a few months to clear (disappointing, but realistic!) which gave me hope that what I was encountering was temporary.  And indeed it was ...  it took a while but things did get better. As I mentioned earlier, anxiety is problem for many newly diagnosed coeliacs and when adrenaline is running through you it can exacerbate or even cause twitching and spasms.  This happened to me, my eyes twitched, my calves twitched etc.  Trying to understand the anxiety and what to do about it, I bought these two publications.  They helped me no end, and they may help you. https://www.amazon.co.uk/Depression-Cure-Six-Step-Programme-Without/dp/0091929814 (Yes, it says depression, but this book helps with anxiety, too, through physical exercise,  omega-3 fatty acids,  natural sunlight exposure,  restorative sleep, social connectedness and meaningful, engaging activity) https://anxietynomore.co.uk/product/at-last-a-life/ (Note, there is a lot of help on the anxietynomore website). So aside from the anxiety, the other thing you need to do is to keep away from gluten.  This will help you. I apologise for all the reading you have to do, but hopefully something will help. Lastly, did they test you for any thyroid issues, to which some coeliacs can be prone? Do come back to us if we can help further, and remember, there is a good chance that what you are experiencing is temporary.😊 Cristiana
×
×
  • Create New...