Jump to content
  • 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

How About A New Reality Show?


lonewolf

Recommended Posts

elye Community Regular

...Or sitting in a restaurant, trying to explain what "gluten-free" REALLY means to your eye-rolling waiter, and then watching the platters of pizza, fettuccine alfredo and breaded finger foods drift past to other tables.

....talk about challenges! :lol:


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



Celiac.com Sponsor (A8-M):



Generic Apprentice

My B-F suggested they have to take Immodium also, to get the constipation side of things followed by ex-lax. So they can get the full effect of the block up then blow out. I would like to vote in the women from my daughters school who is completely rude and doesnt care about anyone but herself. I brought paper work in from the DR. and it still wasn't good enough.

angelbender Newbie

"Or - Having 10 minutes to find 7 different public restrooms in the downtown area."

Ooooooooh! This could be whole 'nother new reality show! Feed 'em EX-Lax and see who can find a bathroom the fastest

............IN TIME TO AVOID AN "ACCIDENT"............

How about "How to Get Home With Soiled Garments Without Anyone Noticing?"

amybeth Enthusiast

ROTFLMAO -- "I'd like to buy a bowel" --- OMG!!!!!!!!

One of the challenges must include grocery shopping in a regulary grocery store and reading the labels - winner must be the fastest and have only gluten-free items in cart - 3 meals/day for a whole week.

Want to make it harder ? Give them a budget!

Everyone else will have points taken away for hidden glutens, time spent over 1 hour, and tears shed.

OH - and the starting line has to be in the store's bakery or bread aisle.

he heee.

elye Community Regular

Fantastic...I would watch a show like this. I, too, would also love to buy a bowel. A brand spankin' new, undamaged, pristine lower intestine. Too bad we can't spin the wheel for one of those. :rolleyes:

UR Groovy Explorer

Edited June 2007

I am removing this post. It has no impact on the thread, and I'd rather just forget that particular day. It's personal. :)

stef-the-kicking-cuty Enthusiast

How cruel... I love it :lol:


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



Celiac.com Sponsor (A8-M):



UR Groovy Explorer

I'm removing this one too.

mouth Enthusiast
I keep seeing commercials for new shows that look boring. I think we need a Celiac reality show. How about this:

Contestants are nominated by Celiacs and those with gluten intolerance. The ones chosen are those who have given their Celiac friends the hardest time.

Contestants get one session with a dietician not well-versed in gluten-free eating. They are then given up to two hours a day of internet research for a week before the actual competition

The night before the first full day, each contestant must consume a double dose of Ex-Lax, just to get in the "mood".

Contestants will be monitored by camera constantly - at home, at friends' homes, out to eat, etc. Any time even a speck of gluten is consumed, the contestant will be required to take a double dose of Ex Lax. For blatant cheating, a triple dose of Ex Lax and a bottle of Syrup of Ipecac must be downed immediately.

Contestants will be required to explain Celiac to all friends, relatives and co-workers - probably 10-20 times during the course of the show. They will be required to eat out and make "safe" choices, but if at any time they don't ask for the chef before ordering, the Ex-Lax rule will take effect. Any product they buy at the store without thoroughly reading labels and/or calling the 1-800 number on the package will also give them the Ex-Lax treatment.

Anyone have anything to add?

:lol: THIS IS TOO GOOD!!!!!!!!!!!! I'D LOVE TO SEE IT.. GOOD LUCK AND THANK YOU FOR YOUR HELP.. ANY HELP IS GREAT HELP@!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! KEEP IN TOUCH.. MOUTH

almostnrn Explorer

Oh thanks for the laugh!!! I think its a wonderful idea and it would certainly clear up Celiac disease to anyone who wasn't clear about what it is!

A couple of other ideas...

-Frequent blood tests to check levels of all the important things like thyroid that were destroyed by undiagnosed celiac

-Can't leave out that fun filled scope and biopsy routine!

stef-the-kicking-cuty Enthusiast

Was meant ironical, anyway... <_<

jerseyangel Proficient
Was meant ironical, anyway... <_<

Of course it was! Made me laugh :P

UR Groovy Explorer
Was meant ironical, anyway... <_<

I know

Mtndog Collaborator

OMG- how could I have missed this thread!

You can buy a vowel. I'd like to sell a constipation-I mean consonant. :P

kbtoyssni Contributor

Hilarious! Thank you! Housemates should also periodically speak in foreign languages to simulate brain fog. Contestants must then read technical journal papers in a subject they have never studied and take a test on it.

Jestgar Rising Star

Maybe sometimes at night someone could come in and change all the packaging and newspapers to something that sort of looks like English but isn't really.

And if the house could be on a platform so every once in a while it tips just a bit so you get that off-balance feeling that you aren't really sure about.

marciab Enthusiast

We should tell them that this is only going to last 1 week, afterall most people are accustomed to being sick for a week.

But after the first week, tell them "We are sorry, but you will have to stay here one more week".

Do this repeatedly until they crack ... Then we have to let them go ... :lol::lol:

We can't keep them the standard 11 years it takes to get a diagnosis ...

Marcia

2kids4me Contributor

This thread is too funny! :lol:

I say during week 3 or 4, just when they might be "getting it" ...........put them on a plane, during which no gluten free food is available because they forgot to request a "special meal" when booking / or if they did remember - it wasnt put on the flight (oops sorry).

The flight is a minimum 4 hours long and they arrive after midnight, thus limiting any food selection even more. The next morning, they need to go food shopping and in an unfamiliar environment - find gluten free food other than fruits and veges to eat.

The final week challenge - same as week 2 EXCEPT they are given 6 year old celiac child to a accompany them on the flight, and one non celiac friend who eats in front of them and keeps offering gluten foods. The non celiac is hungry when you land and wants to go to a fast food outlet. The child has to be happy / not hungry on landing, and sit quietly while watching "friend" munch on a cheeseburger fries and a milkshake .

Snappy comebacks required for flight attendents and non-celiac friend as they comment on "fussy eating", "whiny child" and queries as to why the child has to eat"special", or "say one french fry cant hurt".

Sandy

  • 4 months later...
marciab Enthusiast

I'm sorry, but I just had to bump this thread ... This cracks me up ... Marcia :lol::lol:

little d Enthusiast

Im sorry I thought that this was too cute to not say anything

Can we whack them on the head for those of us that get headaches? How about caffeine pills at night so they can't sleep?

and no tylenol in sight

Make all of the contestants live in a house w/ 1 bathroom!

with a closed sign on the door

I think I may pee my pants!!!! Hysterical!

I can just do my pee pee dance

some of them have to be randomly rubbed with fiberglass insulation so they get the DH effect.

Please not the fiberglass how about pioson ivy or maybe both

Yeah, but they can't be voted off to go to a hotel, they have to be voted into the "new intolerance" house where they are assigned a new food intolerance, but not told what it is.

the worst hotel intown so they can get a feel for the anxiety that we sometimes feel

Do you think this could get some people to understand

donna

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.