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

The Happily Divided Kingdom


momxyz

Recommended Posts

momxyz Contributor

ok DD and I are gluten free, for various and sundry reasons. Tho neither of us has a formal diagnosis, both of us are seeing benefits. And, more telling, seeing adverse consequences when we ingest gluten again.

My dear husband, since the kids were little, has been chief cook. It's what worked for us. My involvement in the kitchen (formerly) had been the testing of a new recipe, and, baking at Christmas. Other than that, I have been very happy to allow the Lord of the Kitchen complete reign...

Summer 09, and first my daughter goes gluten free, followed by me 3 weeks later. Houston, do we have a problem?

OUr cooking, especially in the summer, is pretty much whole foods. Fresh fruits, veggies, grilled lean meat, potatoes, brown rice. Since baking is limited to holiday times, wheat flour has not surfaced in the kitchen for many months, and is stored away in airtight containers.

I have read about cross contamination and wondered about how careful we needed to be. Here's what we have done to date.

We have a gluten free shelf in the pantry closet and in the fridge. All items stored in sealed containers.

When my daughter or I cook gluten free stuff, we don't use any of my husband's very nice stick free or cast iron cook wire... we use plain metal stuff that we wash in very hot water immediately prior to use.

We have one baking tray and one pot (again non stick, not cast iron) that is now designated for gluten free cooking. these are not new, we are not in the position right now due to a layoff to make expenditures, but these have been SCRUPULOUSLY cleaned.

We try to coordinate cooking times. So that if my husband wants to eat something "glutenous" we either cook before him, or we cook after him, after a thorough cleaning of kitchen surfaces.

(Happily, my husband is willing to adapt to things like gluten free pizza crust and pasta, so there aren't so many double cooking nights)

Toasting bread: well I haven't found a brand of bread I truly like yet. Any bread I have bought has been converted to bread crumbs for recipes.... and I toasted the bread on the designated tray in the oven, not in the toaster.

Everything seems to have worked so far, but am concerned that we may be hindering even better improvement by not being more scrupulous. We may not be super sensitive, but, would like your feedback...


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



Celiac.com Sponsor (A8-M):



lpellegr Collaborator

If you are vigilant, as you seem to be, then you should be able to avoid contact between your gluten-free food and his regular food. Most cookware cleans up pretty good, although you shouldn't share a colander. I would worry about wheat flour for baking, though, because it's likely to hang in the air and then gradually deposit on cleaned surfaces and get into everything. You might have to find somewhere else for him to bake or switch to all gluten-free.

momxyz Contributor
If you are vigilant, as you seem to be, then you should be able to avoid contact between your gluten-free food and his regular food. Most cookware cleans up pretty good, although you shouldn't share a colander. I would worry about wheat flour for baking, though, because it's likely to hang in the air and then gradually deposit on cleaned surfaces and get into everything. You might have to find somewhere else for him to bake or switch to all gluten-free.

you know, he rarely uses flour... only when he deep fries something, which is not often, and we can work on gluten free alternatives for that pretty easily.

It's really only during the holiday season when the flour comes a flyin'. And in that case I have been the baker...

So this holiday season I am either going to have to adapt my recipes... or bake less, since half the family won't be eating it anyways!

nasalady Contributor
you know, he rarely uses flour... only when he deep fries something, which is not often, and we can work on gluten free alternatives for that pretty easily.

It's really only during the holiday season when the flour comes a flyin'. And in that case I have been the baker...

So this holiday season I am either going to have to adapt my recipes... or bake less, since half the family won't be eating it anyways!

It'll be OK....I went gluten free 3 days before Thanksgiving and I made everything I usually do, but gluten free (stuffing, pies, gravy, etc). I just used recipes I found here or elsewhere on the Internet to help me convert my recipes to be gluten free!

It was all delicious! :)

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    2. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    3. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

    4. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    5. - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,692
    • Most Online (within 30 mins)
      7,748

    Ali Zaib
    Newest Member
    Ali Zaib
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.