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

2009 Thanksgiving Disasters


Ahorsesoul

Recommended Posts

luvs2eat Collaborator

No big disasters this year, as opposed to last year when I made a gluten free pie crust (eggs, xanthan gum, etc) and accidentally used regular flour and spent the rest of the night trying desperately not to barf!!).

I'm giving up in cornbread dressing. It came out better this year than others, but I'm just not a huge fan. I'll continue to try to use my good gluten-free bread and recreate the Pepperidge Farm stuffing I grew up on.

I made a green bean casserole this year using a recipe w/ sour cream and crushed cornflakes (I used corn chex). There is no Progresso Cream of Mushroom soup in any of my stores. It wasn't any good at all and the casserole dish was hardly touched.

The best parts were that I made my pies a week ahead, wrapped them up tightly, and froze them. They were delicious! I also made mashed potatoes ahead and they were good too! I made a few cheese balls that were yummy.

I guess the only real disaster was that we put all the leftover turkey in a big container and put it in the cabinet on the porch. It was cold out there and where we'd put the turkey to brine in a big pot the day before Thanksgiving. Unfortunately... or fortunately, depending on how you look at it... the next day was sunny and 70


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



Celiac.com Sponsor (A8-M):



MindytheOrganist Enthusiast

Every Thanksgiving, we have about 25-30 people at my folk's house. All relatives or guests of relatives. Anyway, we thought we were well prepared to proper feed my hubby (who is gluten-free); well, guess again.

My sister tried to make gluten-free rolls. They never rose, and were horrible-tasting.

I tried to make gluten-free dressing. It also tasted horrible!

Everything else went well. I was able to make a gluten-free pie crust, so he was able to have pumpkin pie. At my Mom's insistence, he was first in line to avoid any possible cross-contamination.

All in all our first gluten-free Thanksgiving was OK. Next time, instead of dressing, I'll probably just make a broccoli-and-rice-and-cheese casserole in place of dressing.

minniejack Contributor

No food disasters, but only at my inlaws long enough to drop off fundraisers--long enough for my sister-in-laws and their adults daughters to have me screaming at my DH for the rest of the weekend and me vowing to not be around them at all over Christmas....

Aargh!!! :angry:

  • 4 weeks later...
Dylan Rookie

Hey Takala, how do yall "designate" times to be in the kitchen? I'm having trouble around the house. When I NEED to eat, the other person happens to be in the kitchen EVERY time. DARNIT! ;p

Takala Enthusiast

Hey Takala, how do yall "designate" times to be in the kitchen? I'm having trouble around the house. When I NEED to eat, the other person happens to be in the kitchen EVERY time. DARNIT! ;p

________________________

Well, it's easy. There's just the 2 of us humans, and assorted pets, and we keep the kitchen here at home gluten free. Several of the pets need to be kept gluten free because they share water dishes, and the 2 dogs which have to be wheat free because of their allergies, were getting sick by drinking out of the other's water dishes.... so I made an edict, no more pet food with gluten in the house to keep the dogs from getting cross contaminated. And don't give the dogs anything that you wouldn't feel safe giving to me. The kitchen is ridiculously small. The biggest dog tends to come in and just sit or lay quietly nearby when somebody is in there, he's the easiest to maneuver around as he is on the floor, but 2 full size humans and a dog... it looks like a game of "Twister".... if we are cooking for each other, whoever wants to be in the kitchen gets to be in the kitchen, and the other one asks if any assistance is needed, otherwise goes and does something else.

When you have been with the same person for over 3 decades, you don't really have to guess what they mean. When we were younger, I cooked dinner a lot, but now if he wants the kitchen, to prepare a specific item, I just get out of the way! In the mornings, because his schedule varies, and he may have to start early, I get in there either before him or let him have it first after grabbing a cup of coffee and going off to read the news. Then he's out pretty quick and I can putter. If I MUST eat something immediately he understands that phrase, but I keep enough things around that are gluten free, like nuts, cheese, or fruit, or peanut butter and rice crackers, that I can just grab and go and retreat into my desk area or to the tray table in the den with it.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,945
    • Most Online (within 30 mins)
      7,748

    Miyasato
    Newest Member
    Miyasato
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • 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
    • DebJ14
×
×
  • 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.