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

Graduate School Reasearch In Education


hwaters34

Recommended Posts

hwaters34 Newbie

Hi All-

New to the site. I'm a Silly Yak (yahoo member). I'm 36, a celiac (dx 0ct 03) and have 4 kids, two with celiac disease.

I'm a teacher who is in grad school and am gathering my own research on celiac disease and school.

Q: How does the gluten free diet effect children's feelings about school? (But from the kids perspective--not the parents!!)

I'll be posting questions, and looking for kids to keep a "feeling" log during school in the near future--but I'm looking to see if people will be willing to help. I'll take all ages, including college.

Has anyone seen research focused on school from the kids perspective? I've been searching and have yet to find a close link. e-celiacs.org has an art on celiac disease in kids--but not hard facts stuff.

Thanks in advance for anyone willing to help. When the time comes, a letter from my school advisory board will be included--just saying that I'm for real. :)

Heather


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

That is really interesting to think about. How did you come up with this topic? Is it from your own chidren since 2 have Celiacs and two don't?

I would think the answers would really vary depending on when the child was diagnosed. I was diagnosed my senior year of High School (and am now a sophmore in college) and am sure that the feelings I feel about school and Celiacs are very different from those of someone diagnosed when they were a baby or very young. When younger kids get diagnosed I am so happy because they won't remember how life was when they ate gluten (taste and pain -wise) as much as adults do.

I am sure you will find people willing to help you. Good luck!

Kristina

hwaters34 Newbie

Thanks for your response!

The topic is close to home--obviously. I want to share celiac disease with teachers in the field, and this will do it (my class will know more!). Also, as a parent who is celiac disease and who has celiac disease I go through different problem solving techniques when thinking out being out of the house for long periods (like when a meal will be eaten). To take care of myslef, I don't stress so much. I know I can always eat a baked potato or dry salad (yum, I know--but I won't pass out). With the kids, (mine are young, 4 and 6 w/celiac disease) it consumes my thoughts because they depend on me to take care of it while we are out. And, they are not going to eat a salad or bp!!

I also feel, as a parent, one of my main responsibilties is to feed my kids (you know, the basics: food, clothing shelter). Simple! I think about gluten free all the time when they are out of the house. I want to now how much are they really thinking about it.

I've been thinking about homeschooling my kids too. I want them to love learning and I want to see if celiac disease is taking fun out of learning because school and gluten-free are not always easy.

Thanks for your time,

Heather

celiac3270 Collaborator

I agree--the opinions are going to vary. For myself, though: I've always liked school, always tried extremely hard and been the top of my class...basically no problems or aversion to education here :lol: . I don't think the celiac necessarily affects a person's perspective on school, but you might feel a little left out.....(w/ food and all)

KaitiUSA Enthusiast

I've always liked school too. I loved high school and now I love college. Not even the gluten-free diet changed it. :D I'm sure answers will very though

Good luck with research :D

hwaters34 Newbie

I think they will vary--but I think it will be interesting/helpful to see the factors that contribute. I might find something that can help parents and kids who are having a difficult time! :)

Heather

Merika Contributor

Hi Heather,

There is a book, available on this site and amazon I think, called "personal stories on celiac disease" or something. It is 3 page stories by all sorts of people on how they got diagnosed and their reactions and whatnot. There is a chapter written by people diagnosed as kids, and another chapter written by people diagnosed as teenagers. Very different stories in the two chapters. You may want to check it out.

Merika


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



Celiac.com Sponsor (A8-M):



FaithInScienceToo Contributor

I believe the book the previous poster is refering to is entitled, "A Personal Touch On... Celiac Disease (The #1 Misdiagnosed Intestinal Disorder),"

by Berlin, Stone.

Best wishes with your research,

Gina

angel-jd1 Community Regular

Several of us that post on this board are in that book (just a side note).

-Jessica :rolleyes:

hwaters34 Newbie

Ahh--yes-I know the book. I wanted to write my "story" but was slow moving to do so. :(

Thanks!

Great advice!!!!

Heather

hwaters34 Newbie

Hi All--I meet (again) with my professor after class and he says it is a no-going with my cliac research. He thinks there is not enough there to "learn" from the project. He thinks I could write it without research. Hmm--maybe some of it...

Thank you to all who said they'd help!

Heather

dreamhouses Newbie

Hi Heather, I was so excited about your research project till I got to the last post about your professor not supporting it!! I'm wondering if you are in the psych dept. or med school or what. I guess that would change how appropriate the research would be. Despite his/her response I think its really cool that you are channeling your energy and thoughts on celiac into what you may be able to study. Maybe you could just re-package it a bit for the professor. Could widening the topic a bit to include other health issues be to your advantage? Like maybe comparing the effects of several different health issues which change specific ways that kids are able to function in the school situation. Maybe a hypothesis that deals asks how health issues affect a childs self concept, and assesses how much support or lack of support they need to compensate for that. A lot of that seems to be uncharted territory in the research area. From what I can tell there really isn't much of a format for educators to rely on in helping students cope with these types of health issues. Lots of strategies and laws now cover various learning disabiliites, but the health issues can also impair kids learning situations because of the additional pressure it puts on them. I can tell by your enthusiasm on is that you really have something to offer with this type of work even if this doesn't turn out to be the place. Good luck, and keep up your creative thinking. Dreamhouses

  • 2 weeks later...
Holly04 Rookie

Gluten-Free + School = No Fun

I'm Holly [Age 13] and I don't really like being gluten-free at school. I get frustrated when they see other people eating gluten. I'm not saying I would cheat. But every single day I think, 'What if I just took one little bite of that pizza' or 'Maybe just a taste of that breaded chicken'. But I know I can't and I know the result. Not good. But you know- there are some people who try to hide their food so it doesn't make me feel bad; some who don't care what I think; some who don't know I have Celiac; and some who rub it in your face. None of the above are good. Sometimes I wish I never I had Celiac.

One of the science teachers in my school does have Celiac. I've talked to him but its not really any help because he says he cheats all the time. And thats obviously not good. He is the only other person I have talked to face to face who has it and he said he was diagnosed when he was about 40. No help.

In my opinion- I hate being gluten-free around other people. (Except my family)

And I am getting pretty tired of answering "Celiac Disease? Whats that?" or "Eww you have a disease. Get away"

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,726
    • Most Online (within 30 mins)
      7,748

    Holly B
    Newest Member
    Holly B
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.4k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Marie70
      Wow!! Scott, Trent and Christiana thank you so much for your fast replies!! The information you have shared with me has helped me tremendously.   Thank you for all the articles.  I appreciate you all so much!! I’ll keep you posted in this post.  I will encourage her to get tested.  I feel a little better!
    • DayaInTheSun
      It was gradual, just not being able to catch my breathe like I always had to take a deep breathe even taking a few steps I would be winded.
    • cristiana
      Hi Marie Welcome to the forum. I am so sorry your daughter is pointing the finger at you like this.   I am afraid children of any age can be very cruel to their parents - I certainly look back at some of the things I said to my mother and father in the past, and wish I could unsay them.  Sometimes people just need a safe place to vent, and unfortunately having a go at one's parents is the all too easy option.  If she is anything like me, she will regret what she says one day.  (Oh... if only I had the chance rewind the clock!) I just wanted to add one more thing to Trent's and Scott's excellent posts and that is regarding diet:  I have to say, not one person  (my nutritionist, my gastroenterologist or GP) has EVER suggested that a poor diet was the cause of my coeliac disease.    In all the various clinics I have attended these past nearly 12 years no-one has ever asked if I was brought up on processed food, or questioned if I eat 5 fruit and veg a day.  Sure, unfortunately I am only too well aware that I could do a lot better with my diet and it's a constant challenge for me not to give into what I like (unfortunately I've always had a sweet tooth).   But I know some super healthy 10 fruit and veg a day types who still got coeliac disease, and equally, a lot of people who eat all the wrong stuff and they still have cast iron stomachs. Do encourage her to get checked though - it may be that she hasn't got coeliac disease at all. Come back to us if you need any more support through the process. Cristiana
    • trents
      Welcome to the forum, @Marie70! The first thing to know is that celiac disease has a genetic base. The two main genes that have been identified as providing the potential to develop celiac disease are HLA-DQ2 and HLA-DQ8. About 40% of  the general population carries one or both of these genes. However, only about 1% of the general population ever develops celiac disease. So, we know that in addition to possessing the genetic potential to develop celiac disease, there has to be some triggering environmental or medical "stress" factor (or factors) that switches the gene or genes on such that they are awakened from their latent condition and become active. What may be the triggering factor (or factors) is the subject of much debate. Here is an article that discusses this subject: Second, what will your daughter have to say if her testing for celiac disease is negative? She may have to add crow to her diet. Third, and this is what I really want to focus on because my wife and I are dealing with something similar in our relationship with our own adult daughter: the real problem is not whatever shortcomings you, as the family cook, may have had when providing meals, the real problem is with your daughter's heart/soul/attitude. If it turns out to be true that she has celiac disease, it is likely she would have developed the condition sooner or later even if her diet had been healthier while growing up. She is angry about the prospect of having to deal with the dietary and social limitations that having celiac disease would impose upon her. She doesn't want to face up to the fact that this may be a new reality that will dramatically changer her life and she is looking for someone or something to blame. And she has conveniently turned her wrath on you rather than saying to herself, "Okay, this is what it is. Now what can I do to make adjustments in order to with it the best way I can?"  When faced with a life-changing reality, people will either accept it for what it is, make adjustments and move on or they will become angry and look for something or someone to blame and get stuck. For now, at least, your daughter has chosen the latter option. Don't let her problem destroy both of you.
    • Scott Adams
      It sounds like you’re carrying a lot of guilt, but please know that you didn’t cause your daughter’s potential celiac disease or your son’s Crohn’s. These conditions have strong genetic components, and while diet can influence symptoms, it does not cause autoimmune diseases. You did the best you could with the knowledge you had at the time, and no parent is perfect. Your daughter’s frustration is understandable, but it’s likely coming from a place of fear and uncertainty rather than true blame. Let her get tested, and if she does have celiac disease, you can support her moving forward. Instead of focusing on guilt, try shifting the conversation toward healing and learning together. You’re not alone, and you don’t deserve to carry this weight on your own. This article might be helpful. She needs to be screened for celiac disease before she can be sure that she has it. Another approach not discussed in the article is a genetic test for celiac disease, which she could do without eating gluten.      
×
×
  • Create New...