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

Can't Afford To... Can't Afford Not To


Poppi

New Pots  

16 members have voted

You do not have permission to vote in this poll, or see the poll results. Please sign in or register to vote in this poll.

Recommended Posts

Poppi Enthusiast

So I'm heading out today to buy new pots. I've been gluten free for almost 6 weeks now and I felt amazing for the first 4 weeks but the last 2 I've been slowly sliding backwards with my symptoms. My husband and I think it might just be my system becoming more sensitive so now I'm reacting to the trace contamination from our 10 year old non-stick pots.

So today I go to spend my Mother's Day money on new pots. (I'm pouting because I wanted an iPad or a new summer wardrobe)

Any thoughts on stainless steel vs. new nonstick? I love cooking on nonstick but I'm thinking that stainless steel has the added benefit of not carrying contamination if someone else in the house uses it to heat up some gluteny soup or pasta. I've never cooked on steel so I'm nervous about that but world class chefs use it so obviously it doesn't suck.

This weekend sucks. I'm having a hard time feeling good about life right now. :(


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



Celiac.com Sponsor (A8-M):



cahill Collaborator

So I'm heading out today to buy new pots. I've been gluten free for almost 6 weeks now and I felt amazing for the first 4 weeks but the last 2 I've been slowly sliding backwards with my symptoms. My husband and I think it might just be my system becoming more sensitive so now I'm reacting to the trace contamination from our 10 year old non-stick pots.

So today I go to spend my Mother's Day money on new pots. (I'm pouting because I wanted an iPad or a new summer wardrobe)

Any thoughts on stainless steel vs. new nonstick? I love cooking on nonstick but I'm thinking that stainless steel has the added benefit of not carrying contamination if someone else in the house uses it to heat up some gluteny soup or pasta. I've never cooked on steel so I'm nervous about that but world class chefs use it so obviously it doesn't suck.

This weekend sucks. I'm having a hard time feeling good about life right now. :(

feeling well and being able to enjoy life is SOOOOO much better than a iPad or new summer wardrobe, :D

the new pans will DIFFIDENTLY be worth it, I love my new stainless steel ones but I do have a nonstick frying pan(putting that off limit to gluteney things would be a good idea)

*just a note: shared strainers for reg pasta and gluten free pasta is NOT GOOD,,maybe invest in different styles or colors so there is no chance of a mix up

sreese68 Enthusiast

While I love my iPad, if I were you, I'd buy some pots. Maybe buy a couple at a time? A 4-quart sauce pan and a 12-inch skillet will make a LOT of different things.

I'd prefer to spend $$$ on stainless steel pots since they last forever and $ on non-stick since they get scratched and lose their stick so quickly. I LOVE my All Clad stainless steel, and I buy it from a place that sells irregulars: Open Original Shared Link (They have 20% off sales twice a year, so getting on their mailing list can be worth it.)

This non-stick skillet got the highest ratings at Cooks Illustrated: T-Fal Professional Total Nonstick Fry Pan. Calphalon is good, too.

Stainless cookware is really good for browning meat, and it's great for going from stovetop to oven. It's also good for making pan sauces. Nonstick just doesn't do as good a job for these applications. I use my nonstick (two skillets and one griddle) mostly for eggs, pancakes, and a few recipes that specifically call for it. I use stainless much more than nonstick.

Oh, Bar Keeper's friend does a great job of cleaning stainless when it needs an extra cleaning boost.

Good luck! (I'm not looking forward to replacing some cutting boards, bakeware, toaster, and a few other things I've been able to work around so far, so I feel you on this one! I was fortunate that all my cookware was fine.)

Poppi Enthusiast

I'm home with a nice 12 piece set of stainless steel pots from Costco. Kirkland Brand but they meet all the requirements I had: thick, multi layer bottoms (in this case steel, aluminum and copper), rivetted handles, at least 10 pieces and under $250 ($189.99).

I also got a cast iron pan.

If this makes a difference then I'll add on a few extra pieces that I don't have like a big wok and a bigger stock/stew pot.

mamaw Community Regular

I got all my new kitchen junk for presents!!!! Iknow I would have loved to do something fun with the money I receive for birthdays, holidays & these gifts were all so NOT personal! But my health was way more important .... I got better so my family had their MOM back ( not sick & cranky) & I was able to cook & bake & everyone was happy.. A win win for my family.....

I have always used stainless steel & love it... Coated pans get scratched through time, I even purchased a skillet from Germany once , it costs $300.00 for one skillet it took all my birthday, holiday money& to buy it guarenteed not toscratch.. Man, I loved that pan but after about five years it too became scratched... I contacted the company for a replacement which they said was lifetime, yea right! They were so willing to send a replacementfor$150.00 ...... I reported them but never received a new pan...

Sometimes we want for things we really didn't need in the first place....enjoy your new cookware..........

color-me-confused Explorer

I'm home with a nice 12 piece set of stainless steel pots from Costco. Kirkland Brand but they meet all the requirements I had: thick, multi layer bottoms (in this case steel, aluminum and copper), rivetted handles, at least 10 pieces and under $250 ($189.99).

I also got a cast iron pan.

Cast iron is awesome and we have both a frying pan and a grill pan. Its ability to hold heat is amazing. If you ever find you've got stubborn stuff stuck in it just heat it up scorching hot, throw in 1/3 cup of water and (while wearing a glove) scrape with a spatula. Nothin' survives that steam treatment. As it cools then just scrub out with some kosher salt, lightly oil it, and it's good as new.

If you find you like it then seek out some carbon steel pans for pan frying or cooking sticky stuff like eggs. Once you've gotten used to the (easy!) maintenance of the seasoning you'll never want to use teflon pans again.

Takala Enthusiast

I won't cook on non stick on the stove top. That stuff, when overheated, gives off fumes that can kill pet birds ! :blink: I wish I could more easily find not coated with non- stick cake and bread tins, etc, I've got some cheap - *** ones from China, that the coating CAME OFF ON THE LOAVES OF BREAD when I took them out of the pan - disgusting !

Plus non stick requires wooden or plastic spatulas that are just another potential source of cross contamination if they get into gluten ingredients.

I am a big fan of cast iron pans, and keep several small skillets on the stovetop burner in the back (they're heavy!) and cook on them daily. Keep in mind, tho, you'll have to decontaminate them if they get glutened, also. I use olive oil a lot as I am relatively 'white carbohydrates' intolerant, so any bread- like items like flatbreads tend to be the whole grain, heavier heartier types or things made out of almond meal. If I try to eat low fat it doesn't work for me. Most Americans on a so -called "normal" diet are eating a great deal more of grain servings a day.


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



Celiac.com Sponsor (A8-M):



Racer-J Newbie

I also don't do non-stick stuff. It's just not needed and it doesn't last even if you are cautious. I mean chefs don't use it and people cooked without fine before it came along. It can be really convenient though. Stuff tends to stick to stainless steel if you aren't used to using it. There is a learning curve when it comes to the heat setting on your stove and what you're cooking. Cast iron can be the same way. It just depends on what you're cooking.

I just have a single medium quality stainless steel "saucepan" with a glass lid I got at Target for around $10.00 but, I don't cook often. I got it on the off chance I want to make a stock/soup, need to cook buffalo/bison, cook/steam oysters, toast some sunflower seeds, or do something else I may ever only do ever so often. It's also just me though so, I understand why other people would need multiple sizes and a higher quality item.

Poppi Enthusiast

It's also just me though so, I understand why other people would need multiple sizes and a higher quality item.

Yeah, I cook 3 meals a day for a family of 7 plus I host all the large family gatherings so once a month or so I am cooking for 15-20 people. Good cookware is important.

So far I'm happy with my new pans. Cooking eggs is going to take some practice but maybe I'll just buy a single non stick pancake pan and hide it for eggs and gluten-free pancakes.

Racer-J Newbie

Yeah, I cook 3 meals a day for a family of 7 plus I host all the large family gatherings so once a month or so I am cooking for 15-20 people. Good cookware is important.

So far I'm happy with my new pans. Cooking eggs is going to take some practice but maybe I'll just buy a single non stick pancake pan and hide it for eggs and gluten-free pancakes.

Oh wow lol. Yea, in that situation I would get the highest quality I could find and the largest selection.

I never really got eggs down outside of scrambling or frying them. I could almost get an "omlette" started but then it would just go the scrambled egg route. I rotated them out of my diet before I got to mess around with them to much. It wasn't a big deal though as I always preferred boiled eggs over any other form.

mushroom Proficient

I never really got eggs down outside of scrambling or frying them. I could almost get an "omlette" started but then it would just go the scrambled egg route. I rotated them out of my diet before I got to mess around with them to much. It wasn't a big deal though as I always preferred boiled eggs over any other form.

I find that (if you don't use nonstick) the only reliable way for omelettes is to have a dedicated omelette pan and do not let anybody :ph34r: use it for anything else.

cap6 Enthusiast

I'm not much of a cook and have always had just odds & ends of cookware. Going gluten-free I threw out all of the old stuff and have slowly been adding new everything - pots, pans, glassware, strainer. I even threw away the under the sink bread board. Sort of left a long skinny hole in the cabinet but I feel better. :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    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.