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:
    Where Your Contribution Counts!
    eNewsletter
    Support Us!

"the G-free Diet"


Miss Emily

Recommended Posts

Miss Emily Apprentice

I went to Barnes and Noble today and read through Elizabeth Hasselbeck's new publication, "The gluten-free Diet." First of all, I have to say that I do think that the book is great news by the way of awareness for Celiac Disease. However, it had inaccuracies throughout the publication that I found extremely frustrating and I would have liked to see her work with the Celiac Disease Foundation. The most alarming for me was her constant mention of the fact that she "cheats" on her diet. Especially in her chapter, "How not to be a Party Pooper" where she mentions more than once that she will sacrifice herself and risk it and eat a potentially glutenous food to be polite. She even goes as far as to say that at a White House Dinner she ate a gluten filled meal but said

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



mushroom Proficient

I am in total agreement with you, Miss Emily. Any statement that trivializes the response to gluten is very damaging to our cause. I believe the people most likely to cheat (my sister is one of them) are those who do not experience the full GI response and are therefore not aware of the harm they are doing themselves.

Link to comment
Share on other sites
curiousgeorge Rookie

My son's ped told me I couldn't possibly be compliant with the diet and must cheat. I was furious.

Link to comment
Share on other sites
MySuicidalTurtle Enthusiast

I put this on hold at the library. Can't believe she'd cheat like that- especially at a White House event! There, if anywhere, could they cater to dietary restrictions, I am sure. It is way better not to eat than to cheat. Anyways, I'll read the book when it comes in and see how I like it.

Link to comment
Share on other sites
jerseyangel Proficient
Can't believe she'd cheat like that- especially at a White House event! There, if anywhere, could they cater to dietary restrictions, I am sure. It is way better not to eat than to cheat.

My thoughts exactly.....I guess what she eats is her own business, but I think it's irresponsible to put it in a book that is supposed to help people with the gluten-free diet.

Kinda like the diet is all well and good, except for special occasions. Gee...if only <_<

Link to comment
Share on other sites
DingoGirl Enthusiast

Wow, this seems to somehow defeat our cause. :(

My thoughts about Elisabeth have always been that she was diagnosed at a very young age, and really didn't suffer all of the terrible, lingering effects of undiagnosed celiac, and that it pretty much just hit her intestinally and nowhere else.

I sort of think that what we need is a REALLY famous person to become very deathly ill, by degrees and over a prolonged time, from celiac......then recover and tell his or her story. (would not wish that on anyone but, that's what I think).

My dream is that we get a group of long-suffering celiacs who have recovered on Oprah.

not bloody likely. <_<

Link to comment
Share on other sites
Tim-n-VA Contributor

I know more about Elizabeth than I'd like to but...

She was not diagnosed early. She had no choice on what to eat while on Survivor and had GI symptoms improve on the restricted diet during the show. The problems came back after her return leading to eventual discovery of the problem with gluten.

I'd read somewhere that the book was co-written by Dr. Peter Green but I checked Amazon and it only lists him as providing the forward.

It doesn't take long on this board to see that the responses to gluten vary in type and in intensity. Except in the most general sense, what one of us can get by with has very little exportability to others.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Miss Emily Apprentice
It doesn't take long on this board to see that the responses to gluten vary in type and in intensity. Except in the most general sense, what one of us can get by with has very little exportability to others.

Unfortunently, that is not true. It may SEEM like the reaction time and intensity of Celiac patients varies. However, whether an individual is actually experiencing symptoms or not from ingesting gluten, the small intestine is being compromised regardless. In fact, many sufferers never have GI upset or common reaction symptoms. This is part of the reason Celiac is so misunderstood and so widely misdiagnosed. Therefore, no matter the differences in diagnosis etc. every Celiac will only be able to "get away with" the same 10 to 20ppm of gluten exposure before compromising their health and safety (this is true whether they experience symptoms at 3ppm, 20ppm or an entire slice of bread).

Link to comment
Share on other sites
Miss Emily Apprentice
My thoughts exactly.....I guess what she eats is her own business, but I think it's irresponsible to put it in a book that is supposed to help people with the gluten-free diet.

Exactly! Thank you. Yes, this book is marketed as a "Survival GUIDE" for the gluten free diet. In fact, I found this publication in both the Self Help and Diet section of my local bookstore. Therefore, if she is dispensing advice to "guide", then some of her opinions could be detrimental to an unaware/newly diagnosed Celiac. She made her personal choices everyone's business by putting them in her book and labeling it as a guide.

Link to comment
Share on other sites
mimommy Contributor
First of all, I have to say that I do think that the book is great news by the way of awareness for Celiac Disease.

The most alarming for me was her constant mention of the fact that she "cheats" on her diet.

Are you kidding me? My issue with statements like this is that it leads the public to beleive that people with Celiac can tolerate gluten now and then or in small amounts.

That being said, Miss Hasselbeck is an advocate for Celiac Disease and must remember that her words impact the general public in a huge way.

I am in total agreement with you, Miss Emily. Any statement that trivializes the response to gluten is very damaging to our cause. I believe the people most likely to cheat (my sister is one of them) are those who do not experience the full GI response and are therefore not aware of the harm they are doing themselves.

My son's ped told me I couldn't possibly be compliant with the diet and must cheat. I was furious.

I have not read her book, but I do agree that Miss Hasselbeck has helped create a new awareness of Celiac disease. I find that if I mention to people that my daughter has celiac, they actually know what I'm talking about. 6 months ago, that was just not the case.

However, I also agree that there is a huge misconception about celiac on an almost global level. Few, if any, who do not have it realize that it truly is a disease, not an allergy. I reinforce to my child constantly that if she didn't know for sure that he had celiac disease, she may be tempted to "cheat" on the diet. I explain to her that although she may not be having any GI pain from it, she is still causing damage to her body that will sooner rather than later create even more pain and problems. The general public is clearly not aware of that fact.

My daughter's ped's partner gave me the same kind of advice, Curious. When he presribed an over the counter pain reliever for her sore throat, I said I wasn't sure if it was gluten free. He responded, "Well, that is exactly why it is impossible to be on a completely gluten free diet!" I was stunned, although not really surprised. Did he think that we were following some sort of new age diet craze? He had her positive biopsy results IN HIS HANDS!!! I think that maybe it would be better to educate himself on the disease to better treat the patient. Or lobby and advocate a little to drug makers and the FDA to clearly mark drug labels, rather than judge a parent/patient. But, hey, that's just mho.

It really is up to each of us to create awareness, so kudos to EH and her book. Each individual must be their own best advocate, double for parents. So keep on learning, keep on trying, keep on helping.

Link to comment
Share on other sites
Miss Emily Apprentice

I agree with your statements. We must all be adocates for Celiac Disease if we want to educate the public with correct information. Also, I do recognize that Miss Hasselbeck's book is spreading awareness, which is wonderful. I just can't help wishing that she would have worked more closely with the CDF and NFCA. I think this would have prevented any confusion or errors in her book. Because, after all, we want the correct information being marketed, right? So, hopefully if enough people voice their opinions she may amend some of the information in some way or another. The sections regarding "cheating," using the "gluten-free" diet as a weight loss solution or "fad" diet, avoiding talking about Celiac and hiding it at social functions, etc. just create more misconceptions about Celiac Disease. At the very least, I would hesitate reccomending her book to the newly diagnosed and suggest more medically sound and informative publications (such as those written by physicians and the medical community in collaboration with the CDF). Hopefully, her book will cause a positive chain reaction in publications!

PS. I printed this letter from the CDF and slipped it is a copy of her book before I loaned it, just as a precaution :)

An Open Letter from the Executive Director of the Celiac Disease Foundation

Wednesday May 6, 2009

Elaine Monarch, Founder and Executive Director of the Celiac Disease Foundation, tonight sent the following open letter to the celiac community:

Celiac Colleagues:

I am writing to call your attention to the current publicity surrounding the new book, The gluten-free Diet, A Gluten-Free Survival Guide, by Elisabeth Hassselbeck, co-host of The View. While it is important to call attention to celiac disease, the information must be accurate

Link to comment
Share on other sites
DingoGirl Enthusiast
I know more about Elizabeth than I'd like to but...

She was not diagnosed early. She had no choice on what to eat while on Survivor and had GI symptoms improve on the restricted diet during the show. The problems came back after her return leading to eventual discovery of the problem with gluten.

Yup, she DID find improvement on Survivor, and I think she was about 20-ish years old? I guess I consider that early as I wasn't diagnosed until I was 44. I had NO intestinal troubles for my entire life and was extremely physically strong and healthy at age 20, with a stomach of steel and perfectly normal bowel issues until about four years before dx....but had mental/neurological celiac all of my life. :(

so - all I meant was that......she was relatively young at time of dx and didn't have to go through two or more decades more, become increasingly sicker.....

hey, she referenced this forum in her book......

wonder if she's reading this thread?

:lol:

Link to comment
Share on other sites
Miss Emily Apprentice
hey, she referenced this forum in her book......

wonder if she's reading this thread?

:lol:

Hopefully she is! It's an amazing forum! :)

Link to comment
Share on other sites
sbj Rookie

I think part of the problem (cheating) might be in the marketing of the book. The book itself is titled "The gluten-free Diet, A Gluten-Free Survival Guide." Notice that it is NOT called A Gluten-Free Survival Guide for Celiacs. I may be mistaken, but from what I have read and seen, she is at least partially trying to sell this diet to everyone, not only to celiacs. In that sense it is quite true that there are many gluten intolerants who can cheat on this diet. Dr. Fasano himself has stated that there are some who are gluten intolerant but who have a level of symptoms such that they can tolerate a slice of pizza every once in a while. (Of course this is dangerous for celiacs.)

I also wonder if someone who has read the book can fill me in? It is my understanding that she basically self-diagnosed after the show and going gluten-free. She later had a genetic test and with the positive response and genetic test she is a "diagnosed" celiac. I have not heard if she has conducted a challenge to test positive via blood panel and I have not heard that she tested positive via endoscopic biopsy. If true (that she diagnosed based on symptoms, diet change, and genetics alone), then it is quite possible that she is gluten intolerant and does not have celiac disease.

I don' think it serves the celiac community well to have so many people out there pushing the gluten-free diet as a healthy lifestyle choice. We all know people who see this as a diet and everyone cheats on diets. These authors have to make very clear the difference between a diagnosed celiac and those who want to try a diet because they feel that gluten, in general, is not healthy for anyone.

Link to comment
Share on other sites
FMcGee Explorer

Right - one healthy eye roll from waitstaff is all I needed to get annoyed with the people who have made gluten-free a fad. I would not eat like this if eating gluten had no effect on me. I really love the heck out of gluten-full foods (pardon me, I'm not even three weeks in yet and still get really sad when my boyfriend orders tiramisu), so I don't get why people would do this to themselves if they tolerate gluten just fine. So, there's probably a combination - I'm annoyed with the people for making it a fad that waiters can ignore, and I'm perplexed at their bizarre decision that treats going gluten-free like it's no big deal and anyone can do it if they want. Petty? Probably. :)

Link to comment
Share on other sites
LDJofDenver Apprentice
I am in total agreement with you, Miss Emily. Any statement that trivializes the response to gluten is very damaging to our cause. I believe the people most likely to cheat (my sister is one of them) are those who do not experience the full GI response and are therefore not aware of the harm they are doing themselves.

People need to understand that this is a medically prescribed diet. Not something we can cast aside every time there's a birthday cake or pizza at the office. While, like the American Diabetic Association Diet (intended for Diabetics), it may be true that anyone (non-celiacs) adhering to this "diet" may experience benefits, the public needs to understand that for us, it is not simply an option.

From the University of Chicago Celiac Disease Center: "The only treatment for Celiac Disease at this time is a strict gluten free diet. It can be an overwhelming lifestyle adjustment, but it is a medical requirement to contain the disease.

It is important to remember that for someone with celiac disease, following the gluten free diet is not a trend or an option, rather it is a medically required prescription."

Maybe we can forward that information to Elisabeth H?

Link to comment
Share on other sites
Amyleigh0007 Enthusiast

I bought and finished the book today. I too was concerned with some parts. She says McDonalds fries contain gluten. She says the gluten free diet is good for people who want to lose a few pounds before swimsuit season. Several times she referred to Celiac as an allergy. My $20 would have been better spent on those yummy new Betty Crocker mixes.

Link to comment
Share on other sites
heatherjane Contributor
She says McDonalds fries contain gluten.

Actually... McDonald's website DOES say that they are made with hydrolyzed wheat protein.

Open Original Shared Link

Link to comment
Share on other sites
Amyleigh0007 Enthusiast
Actually... McDonald's website DOES say that they are made with hydrolyzed wheat protein.

Open Original Shared Link

But the end product does not contain detectable amounts of gluten. Search this forum for more info. I don't know the specifics but McDonalds fries are safe to eat.

Link to comment
Share on other sites
FMcGee Explorer

I don't get her claim about the gluten-free diet being good for weight loss at all. Avoiding processed foods is good for weight loss, gluten or not. But it seems like if you want to subsist entirely on gluten-free processed junk food, the world is your oyster.

Link to comment
Share on other sites
psawyer Proficient
But the end product does not contain detectable amounts of gluten. Search this forum for more info. I don't know the specifics but McDonalds fries are safe to eat.

I don't think there is a single subject that has generated more discussion here than the McDonalds fries question.

As Amy says, search this forum for lots and lots of posts since the question first came up in February of 2006. Then make your own personal decision about whether to eat them. For me, the possible undetectable amount of gluten from the flavor pales in comparison to my worry about in-restaurant cross-contamination. For the record, I eat the fries occasionally without problems.

Link to comment
Share on other sites
mommida Enthusiast

One small McD french fry made me sick. What ever you choose to believe cross-contamination is very serious and seems to be higher risk in a fast food environment.

We all have free will decisions to make. Elizabeth is sharing her personal decisions about her diet, maybe because pictures may show her with gluten suspect foods.

A diet restricting higher calorie, gluten food can be used to lose weight. Everytime someone/anyone requests gluten-free food it gets the word out there ~We need gluten free food choices!

Let's hope the pros outweigh the cons of this book. :D

Link to comment
Share on other sites
psawyer Proficient
One small McD french fry made me sick. What ever you choose to believe cross-contamination is very serious and seems to be higher risk in a fast food environment.

I do not discount the risk of CC. What I did say was that the risk of CC is a much larger concern to me than the wheat-in-the-flavor-in-the-oil controversy. My view, FWIW, is that if you are concerned about the level of gluten from the wheat derived ingredient in the flavor in the oil, then you probably should not even consider eating in any fast food establishment.

That's my opinion. Yours may vary.

Link to comment
Share on other sites
mommida Enthusiast

It goes back to the question, How much gluten causes a reaction? One answer I found was ONE MICRON.

So if your stuffing anything over one micron in your mouth, it's your judgement call. ;)

Link to comment
Share on other sites
Amyleigh0007 Enthusiast

I did not mean to stir up a McDonalds fries issue. I have belonged to this forum for a year now and I should know better :rolleyes: Anyway, my point was Ms. Hasselbeck's book contained concerning material (IMHO).

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      120,508
    • Most Online (within 30 mins)
      7,748

    Penny Lowery
    Newest Member
    Penny Lowery
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.2k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • McNish
      If you're ever in the Peoria IL area - Queen of Squash is 100% gluten-free.   Pekin (just outside Peoria) Whiskey Taco is 90% gluten-free.  The owner's mom is Celiac so they get it!   Just let your server know.   https://thequeenofsquash.com/ https://whiskey-taco.com/
    • trents
      Do you have online access to your celiac panel test results such that you could post them? tTG-IGG is kind of a secondary test. A weak positive in that one could indicate celiac disease but since it isn't as specific a marker as the tTG-IGA it is not real convincing. You could also have NCGS (Non Celiac Gluten Sensitivity) for which there is no test. Celiac disease must first be ruled out. It is 10x more common than celiac disease and shares many of the same symptoms. Some experts believe it can be a precursor to celiac disease. The antidote for both is the same: total avoidance of gluten.
    • powerofpositivethinking
      I haven't been on this forum for a long time, but it was absolutely wonderful during the diagnostic process!  My path for celiac disease diagnosis was the following: -Had normal IgA level, and my only serology positive test was the DGP IgG -Deficiencies in both Vitamins D and K that did not increase at first despite massive supplementation -Diagnosis of fat malabsorption both total and neutral -Diagnosis of severe exocrine pancreatic insufficiency (EPI) -Testing was completed to rule out causes of EPI, and the only one not ruled out was celiac. -Both traditional endoscopy and pill capsule endoscopy yielded negative results for biopsy confirmation, but my GI doctor said that both procedures simply could have missed the damaged spots. -EPI and fat malabsorption resolved after taking Creon for 6 months since my EPI was caused by celiac -23 and Me said I don't have either of the two prominent genes for celiac disease   Remember that you might not have 'textbook' symptoms, but you still may have celiac disease.   Also, I am SO incredibly grateful for this site for all the learning it has allowed me to do. I have a senior dog, and these last few weeks with her were very scary! After two hospital stays, she finally received an IBD diagnosis after having gastroenteritis and pancreatitis. I know that celiac disease is not IBD, however, through reading this site, I learned more about it. I was relieved when I found out she had IBD and not cancer this past Wednesday. I know IBD can be managed thanks to what I've learned here!  So celiac.com, not only did you help me, but you helped my pup too! Thank you ❤️  
    • SuzanneL
      It was tTG IGG that was flagged high. I'm not sure about the other stuff. I'm still eating my normal stuff. 
    • cristiana
      Thank you for your post, @Nedast, and welcome to the forum. It is interesting to read of your experiences. Although I've not had TMJ, from time to time I have had a bit of mild pain in my jaw, sharp stabbing pains and tingling in my face which appears to have been caused by issues with my trigeminal nerve.  I read that sometimes a damaged trigeminal nerve in coeliacs can heal after adopting a gluten free diet.  I try to keep out of cold winds or wear a scarf over my face when it is cold and windy, those conditions tend to be my 'trigger' but I do think that staying clear of gluten has helped.  Also, sleeping with a rolled up towel under my neck is a tip I picked up online, again, that seems to bring benefits. Thank you again for your input - living with this sort of pain can be very hard, so it is good to be able to share advice.
×
×
  • Create New...