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

Teenager Just Diagnosed


jackie4

Recommended Posts

jackie4 Apprentice

Hi! I am feeling a little overwhelmed. My daughter's doctor said that her biopsy came back positive for celiac. She then said that she wanted to talk to the pathologist and run one more sllide test. Has anyone ever heard of this before. I usually ask a lot of questions but I wasn't prepared for that diagnosis. I know very little about celiac disease although I have already spent hours on-line. My daughter, who is 14, is having a hard time. She lives on peanut butter and white bread and bagels. Any recommendations for a good gluten-free bread. Thanks . Jackie


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



Celiac.com Sponsor (A8-M):



Guest nini

my five year old loves Kinnickinick Tapioca Italian Rice Bread... and just about all the other Kinnickinick products... very very good and you can order them offf their website if you can't find them locally.

It's all about attitude. Focus on what your daughter CAN have, not what she can't. I've got a lot of great info if you'd like me to e-mail it to you...

nisla@comcast.net e-mail me if you want the info and that way I can attach the files for you.

Open Original Shared Link

Rachel--24 Collaborator

I like the tapioca bread nini mentioned. Also, if you have a Whole Foods in your area they have a really good sandwhich bread from the WholeFoods GlutenFree BakeHouse. There are also some great recipes for making your own bread.

TCA Contributor

I made the Bob's Red Mill Homemade Wonderful Bread Mix and it was really good, plus I can get it at Kroger. My son is really pickyy, but we have found lots of things that are ok for him to eat. We're also noticing that he's trying more foods now that he's been gluten free for a while.

mommida Enthusiast

I agree with the Kinninick tapiocca rice bread suggestion, but what ever bread you try, TOAST it. Glutino makes very good bagels, and Foods by George has a good english muffin (It is about three times the size of the english muffins I was used to). The recipe in Bette Hagman's Gluten Free Gourmet for French bread is awesome right out of the oven, but it has a shelf life of about 15 minutes in my opinion.

Laura

chrissy Collaborator

hey nini---can i get those files and info from you too? it has gotten alot easier already, but i sure could use some more ideas! jackie, my twins that are just recently diagnosed are 14 years old also------maybe your daughter would like to chat on line with them or e-mail them?

christine

skinnyminny Enthusiast

Hey

I also use the Bobs Red Mill Mix I have never baked it in the oven but we purchased a Kusinart bread maker at Williams Sonomma ( about $100 dollars) but it is well worth it all you do is add the mix and wet ingridents and you have the best bread I really felt as if I was eating real white bread, I also LOVE peanut butter if you daughter does also I buy Vans frozen waffles at either Kroger or Wild Oats, the Apple Cinniman are my favorite, they also have Orginal, Blue Berry and Flax that are alll gluten and dairy free. I toast them in the toaster and top with peanut butter and or apple butter! good luck! and I know how your daughter feels I was diganosed at her age too but hang in there it will get easier.


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



Celiac.com Sponsor (A8-M):



fisharefriendsnotfood Apprentice

My name's Jackie and I'm 14. :) Basically, if you toast your bread it'll taste a lot better. Also, peanut butter of whatever takes away the taste of the bread anyway so it doesn't matter to me.

If your daughter wants to talk sometime, I'm here.

-Jackie :)

Guest nini

the files I have are in a zip file and I can easily e-mail them to anyone IF you e-mail me first! That way I can attach the file... I don't know how to do it through a pm or e-mail through this site... (don't think it can be done.) So just send me an e-mail request at nisla@comcast.net for my newbiesurvivalkit zip file... I'll be more than happy to send it.

Guest Robbin

Hi again everyone, I hope I am not being a pain since I have been reading almost every post and category and commenting on alot, but I am so glad to see others with teenagers on here with ideas. My youngest (almost 13) is allergic to soy, all nuts, most raw vegetables (cooking changes the chemistry my dr. said which is why raw makes him break out in hives, but cooked doesn't) lactose intolerant, and the only fruits he can eat are cherries, pineapple, pears and apples. He is also allergic to goat's milk. I nursed him for 2 1/2 years too, so the breast-feeding protection didn't work so well on this kid. He is showing such classic celiac symptoms and I am convinced he is and his brother and I are as well. He is so thin and gaunt looking it breaks my heart, but he has been eating a little better lately since I have cut the gluten out at home. I mentioned before on another thread that he refuses to pack his lunch and eats only a few items on the menu at school. He says he isn't hungry anyway. Teens can be SO frustrating. He loves Italian ice and I noticed a pattern that when he goes for a long time without eating much, if I give him one of the little cups (Luigis) without making a big deal of it, a little while later he will eat a little better at dinner, so maybe something to "tweak" your childs' appetite sometimes is needed. Maybe low blood sugars or something. I don't know, but thank God for vitamins (gluten-free), gatorade, chips and ices, because sometimes that is all this kid eats. I think it is the fear of diarrhea and stomach aches, I can't blame him there. I will try the breads mentioned. Thanks for the great info! Robbin

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      125,929
    • Most Online (within 30 mins)
      7,748

    quilterjoyce
    Newest Member
    quilterjoyce
    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...