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:
    Support Celiac.com!
    eNewsletter
    Donate

Can I Ignore My Celiac?


mayray

Recommended Posts

missy'smom Collaborator
I'm even afraid to use my Kitchen Aid mixer that I used before

BF

If yours is a stand mixer you can give it a good thorough regular washing and be good to go. Don't be afraid to use it. I'm using mine. I put the whisk through the dishwasher. An all-purpose spray will cut through any greasy build up on the main part. The Kitchen Aids are made well with virtually no crevices for stuff to get into. I gave away my cheap hand mixer because I could see flour in the vents and it wouldn't come out. It would be a shame to get a new one(KA) and they make our work easier.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Fiddle-Faddle Community Regular
. In terms of making non-gluten bread, what kind of flours do y'all recommend?

The easiest to start with is Roben Ryberg's buttermilk bread (can you have milk products??), which is in her book, The GLuten-Free Kitchen. If you don't have it, PM me, and I'll PM it to you (can't post the recipe here without violating copyright, as I don't haver her permission).

You will need something called Xanthan Gum. It is expensive (usually around $12 for a tiny bag), but absolutely necessary. Without it, your batter will turn to glue. It also lasts forever, as you only use 1-2 teaspoons at a time. You'll also need potato starch and cornstarch, baking powder, baking soda, yeast (but NOT quick-rise, and NOT bread machine yeast, just plain simple yeast), buttermilk or buttermilk powder, and salt. I modify the recipe by greasing the breadpan and then "flouring" it with corn meal, which makes a great crust. The recipe doesn't call for an egg, but you can add 1 or two--the protein helps hold the structure of the bread together.

gluten-free breads rise best in glass baking pans. I don't know why. They work better in the oven than in breadmakers, at least in my experience.

Link to comment
Share on other sites
anemic Rookie

Is the diet a bugger? YES! Are you worth it? ABSOLUTELY! We all miss beer and delivery pizza and eating whatever, whenever. It gets easier with time but will never be perfect- just keep on trucking along!

Link to comment
Share on other sites
Shamrocks Newbie

I felt SO horrible prior to going Gluten-Free - THAT IS WHAT MAKES ME STAY ON MY GLUTEN-FREE DIET!

Link to comment
Share on other sites
lovegrov Collaborator

While untreated celiac does increase your chance of certain types of cancer, it's not inevitable or even a huge chance. The main threats come from other complications, such as nerve or heart damage, malnutrition, anemia, osteo, brain problems, and developing other autoimmune conditions, just to name a few. Some of these complications can also kill you; others make your life miserable.

richard

Link to comment
Share on other sites
gfp Enthusiast
While untreated celiac does increase your chance of certain types of cancer, it's not inevitable or even a huge chance. The main threats come from other complications, such as nerve or heart damage, malnutrition, anemia, osteo, brain problems, and developing other autoimmune conditions, just to name a few. Some of these complications can also kill you; others make your life miserable.

richard

I think people do tend to obscess over cancer.... when many of the other complications kill you just as surely and others take away most of the pleasure of life..

On the other hand I think a bit of whatever works for you is OK so long as people don't just look at the big C and dismiss it and not realise they are far more likely to have other complications...

Link to comment
Share on other sites
Jestgar Rising Star
While untreated celiac does increase your chance of certain types of cancer, it's not inevitable or even a huge chance.

I felt this way too, until I was talking to a guy from Ireland about Celiac disease and lymphoma. I mentioned that even though the risks for lymphoma were quite a bit higher in Celiacs, they were so low to start with that it probably wasn't relevant. His response was simply, that may be true, but I personally know of two who have developed lymphoma.

Soooo, now I'm thinking that maybe the risk is even higher than we think.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



mamabear Explorer
While untreated celiac does increase your chance of certain types of cancer, it's not inevitable or even a huge chance. The main threats come from other complications, such as nerve or heart damage, malnutrition, anemia, osteo, brain problems, and developing other autoimmune conditions, just to name a few. Some of these complications can also kill you; others make your life miserable.

richard

Open Original Shared Link

This is a new(March 2007) article that pretty well states the longer it takes to diagnose celiac( or the longer a celiac eats gluten....same difference)..the higher the risk of cancers...GI being the most likely. BTW,it is very hard to find GI lymphoma . The only good noninvasive clue is suspicion of "haziness" on a CT of the abdomen and the gold standard again being endoscopy.

Link to comment
Share on other sites
mamabear Explorer

Open Original Shared Link

Here is a less scary article and even gives a possible plus side to breast cancer. However, my mother died of breast cancer and she was my apparent link to celiac . There are other articles that support a lesser fear of malignancy but none are as current as my first post in this thread.

Having already had a major malignancy and autoimmune disorder diagnosed alongside the celiac diagnosis makes me very careful about the gluten free diet.

Link to comment
Share on other sites
lfij Newbie

ignoring celiac is sort of like commiting to swallowing a tablespoon of drano a day, really not a good plan.

Link to comment
Share on other sites
Guest Happynwgal2

To mayray:

I am 54, and have been sick my whole life and was only diagnosed last December - after I asked for a gluten test. My doctors told me it was nothing to worry about, that it was IBS (Irritable Bowl Syndrome), but I could never accept that. I went from doctor to doctor, and finally figured it out myself, after years of depression, anxiety, stomach aches, diarreah, bloating and severe cramping. I felt I could eat nothing. It was emberassing to go to dinner at restaurants, or at friend's houses because I would almost always get so sick that I sometimes had to spend time in the nearest bathroom only 15 to 30 minutes after eating. I cannot tell you how sick I felt. It was awful; the older I got, the worse it got.

I did not listen to my doctors, just could not believe it was "all in my head", and went on a discovery tour, so to speak, that took me the better part of 10 years before I finally cut out gluten - and felt better within just a few days.

The result of my eating gluten for 54 years: I have hypothyroidism, my adrenal glands have stopped functioning, and I have secondary food intolleraces like cheese, yoghurt, eggs and yeast. I am still hestitant about adding new foods to my diet like beans and some fruits that used to make me sick. My intestines were/are so messed up that it will take months, if not a couple of years to heal.

I am fortunate that I have not developed other more serious illnesses - the list is long. My nephew who is 30 is slightly autistic - he is a high functioning autistic who can even drive a car - his autism may have been caused by celiac - we don't know for sure, but it could well be. He is religious about his diet and NEVER eats gluten, cheese or other things he cannot tollerate. Because he is so careful I believe his autism is not as bad as it otherwise could have been, and he is a very pleasant young man to be around, very funny and very intelligent.

Celiac runs in my family from my mom's side. My brother, the father of my nephew, is probably also gluten intollerant, although he does not get sick very often. I have encouraged him to get tested, but at 52, is just too stubborn... sigh... A cousin is also allergic to wheat and eggs - I assume it is gluten, but don't know for sure because I have lost contact with him. He is the son of my mom's brother, so again, it is all on my mom's side of the family. It runs in families and is hereditary. I am more and more concerned that my 4 year old granddaughter has celiac - my daughter will soon have her tested. Some of her symptoms are very much like my health problems when I was a child.

In my 20's, or even early 30's I was not as sick as I was at 54 - year after year of taking poison into my body finally took it's toll.

Going on a non-gluten diet has been frustrating because of the additional foods I cannot eat. But my health is better than it has ever been, and I am no longer depressed and anxiety ridden. I am starting to understand what it feels like to be "normal".

I know it is difficult to go gluten free. But the alternatives are so scary and so painful, that I would encourage you to do the best you can. I also LOVE bread, pizza, cookies, Little Debbie snack cakes (the Boston creams - yum), but I will NOT eat them any more. I never had beer or other alcoholic drinks, so those are not a great loss for me.

Good luck to you. Keep reading the postings here - you will find lots of encouragment that may help you more than any other help you could get in regard to this. I sometimes laugh at some of the postings because humor certainly helps many - and myself - to deal with this frustrating illness.

You will be in my thoughts and prayers...

:)

Link to comment
Share on other sites
Kyalesyin Apprentice

All this just makes me glad that my wife was diagnosed in her 20's. I haven't told her about all of the risks yet, I don't want her to worry, but its definitley giving me good reasons to read the labels carefully.

Link to comment
Share on other sites
Fiddle-Faddle Community Regular
I felt this way too, until I was talking to a guy from Ireland about Celiac disease and lymphoma. I mentioned that even though the risks for lymphoma were quite a bit higher in Celiacs, they were so low to start with that it probably wasn't relevant. His response was simply, that may be true, but I personally know of two who have developed lymphoma.

Soooo, now I'm thinking that maybe the risk is even higher than we think.

And I just lost a friend in February to lymphoma. He was tested for WHEAT ALLERGY (which was negative) instead of for celiac....

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
      121,224
    • Most Online (within 30 mins)
      7,748

    Suzi374
    Newest Member
    Suzi374
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Suzi374
      Hi, I attended a neurologist appt last Tuesday, which I nearly cancelled, due to ongoing numbness and tingling in toes to mid foot. One of the first things he asked was ‘are you celiac’. I’m not. He thought all reflexes were ok but at the last minute decided on nerve conduction tests which were low normal. He was a little confused as he felt they should be better and tried a new set of probs, all the time, giving me multiple shocks which were not enjoyable lol. Anyway, he’s now ordered tests for myeloma, and all the vitaminy things that so many of you mention on here, also tests looking for autoimmune responses. I already have Hashimotos. Interestingly, to me, but maybe someone out there can relate or knows more than i do, although I was a nurse, but ED not ‘weird symptoms’  nurse. Anyway back to the interesting thing, I took duramine in 2013 to lose weight which caused a massive panic attack when I stopped taking it and half my hair fell out. I only took it for a week but it was horrible and I regret it. It triggered ongoing panic attacks which are horrendous. So I feel like I’m a bit crazy. Then in 2020 I had this sudden onset of horrible pain when trying to eat a cinnamon roll. It continued and I lost around 20 kgs. I had two gastroscopes and a colonoscopy and they were all normal. I scored a barium swallow and CT angiogram. All normal. The pain subsided a little but I was left with reflux and an awful feeling that I couldn’t get air when I ate some foods. This was not anxiety.  The anxiety was separate and I still maintain this. This was something to do with eating. It was like the air was thick but I wasn’t short of breath. I just had the sensation I was, then it triggered anxiety. Anyway, I had other weird things- couldn’t bend knees to shave legs in shower lol. Knees felt stiff and swollen but they weren’t. Knee WOUld swell up randomly but mri showed minimal issues. A bit of a meniscus degeneration but insignificant. Then the buzzing sensations in my head, the feeling like someone was stabbing me with something sharp. So now, I pre empted his tests, although I don’t think I’m celiac because it should have come up on gastroscopy, I’ve gone off gluten. Since Tuesday last week so 9 days. Since then I don’t appear to be as constipated, I realised I got through today without a nap and I’m not tired, maybe it’s just today and not related but I get very tired normally and sleep straight after work often, I can bend my knees and shave my legs lol, the buzzing vibrating has gone from my head, I had to call and ambulance as my heart decided we were off on a run, but we weren’t running and I’ve been a bit twitchy at bed time when trying to sleep, reflux is improving, I did get the weird suffocating feeling a bit when eating today but not as bad normall. Tingling and numbness still present and I felt like it moved up my legs a bit today but I’m a bit jittery. So I don’t know if it’s celiac disease or a gluten intolerance but I think, and it may be wishful thinking because my symptoms do make life a bit challenging, but maybe I’m feeling better. I don’t feel as cloudy. My thinking feels crisper. Like there’s no buzzing and I’m not fighting to break through the cloudiness now. I hope so much that this may help me feel a bit better moving forward. It would be a miracle as I really have struggled to work and parent and keep the house clean and I’m always anxious and exhausted.  If you get this far, please tell me if you you can relate to any of the above. Oh and tonsils out 5 years ago but before that antibiotics multiple times a year, sometimes intramuscular because they were so bad.  Op was meant to take 30 mins, it took 1.5 hours due to size of them. 
    • Peace lily
      Im still not gaining weight I’m on a gluten free diet . And still having issues with constapation started priobiocs figured it would help been over two weeks . I guess it’s going to be a long road for me .
    • Smith-Ronald
      Enlarged lymph nodes in neck and groin with celiac are not uncommon. They can take time to reduce even after going gluten-free. Monitoring is key.
    • Bayb
      Hi Scott, yes I have had symptoms for years and this is the second GI I have seen and he could not believe I have never been tested. He called later today and I am scheduled for an endoscopy. Is there a way to tell how severe my potential celiac is from the results above? What are the chances I will have the biopsy and come back negative and we have to keep searching for a cause? 
    • Aussienae
      I agree christina, there is definitely many contributing factors! I have the pain today, my pelvis, hips and thighs ache! No idea why. But i have been sitting at work for 3 days so im thinking its my back. This disease is very mysterious (and frustrating) but not always to blame for every pain. 
×
×
  • Create New...