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

When Will Food Taste Good Again?


cdford

Recommended Posts

cdford Contributor

When will food smell and taste good again? I accidentally got into some gluten in August and still have no desire to eat. I can handle homemade hot chocolate or chocolate milk, but nothing else seems good. My system is back working again, but I just don't want any food. What happened to those good old days when I craved broccoli or greens???


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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator

It takes awhile...I didn't like food for the first few months. First, I hadn't found many good gluten-free foods to begin with. Second, I had a sort of aversion to food (not anorexia or anything--just that i wasn't hungry) because I knew that when I ate and my stomach didn't digest, I'd eventually get stomach pains, vomiting, etc.

I'd been this way for a long time. I still feel rather I-don't-care-ish about what food I eat. Maybe it's due to symptoms that come when I eat a lot...I think a lot of it is that with all the temporary restrictions I'm enforcing: no acid (tomato sauce, ketchup, oranges, grapefruit, etc.), not a lot of fat (since the doc. said it's hard to diget), which is tough since I want to eat fat and i should gain weight anyway....etc.

My situation probably isn't the same as yours because I want certain things. I have constant and nearly uncontrollable cravings for sweets, in particular chocolate and also, but less intensely, for softdrinks. I think it's easy to get dejected, though, when there's so much you want to eat, but can't (even if only temporarily). I think after awhile it's to the point where you don't care really what you eat at all. I went many months eating kinda on autopilot....I also noticed that I wasn't very hungry ever--appetite increasing lately. Don't know if this is any help--I just saw something in common between your story and me a couple months ago.

cdford Contributor

I have always eaten pretty healthy, so craving chocolate milk and fried potatoes is a new one for me. Those two things are the only things that look good or smell right. At least I am not gaining back any weight!

Guest PastorDave

I am really curious where this notion that gluten free tastes bad? I can understand when you feel sick and don't want to eat, but I have heard people say that gluten-free is a bland diet. I am careful what spices I use, I have the advantage of being near an Amish bulk food store where they grow the spices so I know they are gluten-free, but I use the spices to make a normally "bland" meal (such as rice and pork chops) terrific! Experiment with what you liked before as well. I loved donughts, and my wife has made some gluten-free ones for me. What a treat to have them, even though it won't be every day (way too much work) I enjoy the treat. It makes me appreciate it more.

I don't know if this helps, but I do know that living gluten-free is 90% attitude. If you don't let it get you down, even when you have a really bad reaction, then you can get back on your feet faster. :P

MySuicidalTurtle Enthusiast

I started to find the gluten-free food good after about a month or 2. . .when I did swimming we used to form good swimming habits by doing them everyday and after like 21 days of doing it it would be natural. . .I applied the same thing to the food. . .eating the new stuff (honeymustard, bread, sauce, and such) that I knew I'd be eating most of regularly and soon enough I started to like it and crave it rather than the old gluten food.

I didn't want food at first either but you just have to do it and eat it. . .then it all comes together. . .

kactuskandee Apprentice

cdford,

I'm going to take a wild guess here that your body may be craving certain nutrients you're not getting...like more calcium and Vit D (in the milk) and the magnesium in the chocolate, or even the gut-tolerable form of Vit C in potatoes. Then too the added amino acids in the milk you may need especially if you're under any stress. Unfortunately chocolate can create migraines in Fibro folks..Maybe you can try beefing up your vitamin/mineral intakes and see what happens. You may just find yourself wanting the greens and broccoli again.

Just my 2 cents worth....Oh and BTW, if you check any thyroid boards you're not suppose to eat the broccoli anyway....infact not any cruciferous veggies unless over cooked.

Kandee

celiac3270 Collaborator

That's definitely true. I got a chart from Jessica's Yahoo Support Group that says which nutrients you're lacking if you have certain cravings...really helpful...I think I posted it up here awhile ago, but I don't remember where--


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



Celiac.com Sponsor (A8-M):



cdford Contributor

I had not thought about the vitamin issue with the odd cravings. That may be why the orange juice jug keeps getting empty as well. I'll start back onto my injections of b vitamins and magnesium. Man, those mag sulfate shots are no fun.

It is not that I find the gluten-free foods untasty. I have been an excellent cook for much of my life and have transitioned to the gluten-free diet by adjusting spice usage, etc. My family enjoys the foods I cook (I am not one to cook multiple meals...it is tough enough to finish one from a wheelchair or walker). I just don't want anything. Even when I think I am hungry I look at the pantry or in the fridge and nothing strikes my interest. Most of us have experienced that but it is usually when we really don't need to eat anyway.

I must admit that I miss those days of begging my best friend next door for that last bag of broccoli when I had gone through all of mine. It used to be the family joke when I would be steaming veggies at 2 a.m. At least I was a good role model for dietary habits!

Anybody have any suggestions for a reasonably priced vitamin regimen? I used Shaklee for years but they are not gluten-free and most contain soy. My budget is really tight on a disability income.

jknnej Collaborator

I don't know if this is the type of vitamins you're looking for, but TwinLab is sold at Safeway and they have a B complex and a multi daily vitamin. They're about $15 for 60 day supply.

cdford Contributor

Thanks for the info. I am on B complex, B-12, folic acid, and magnesium sulfate in injection form. While I hate having to give myself shots, they really work. I understand from someone in my church that caltrate 600 is gluten-free, but I have not tried them. I will check on the brand you suggested for a multi-vitamin. I think Perrigo labs' vitamins are gluten-free also but I have not verified with them. I know they have a gluten-free lab for their otc meds (sold in Kroger, Target, and Walmart). We look for the little rounded rectangle with a comma thing hanging off the right side that is their logo since we know there cannot be gluten in them.

tom Contributor

I was gluten-free 10 mos b4 going casein-free also. It was only then that i began to enjoy eating again. Previously, no matter how good the food was - even a fav food - eating was just a chore and 2 bites in i was ready to be done.

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 Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Newly diagnosed mam to coeliac 11 year old

    2. - trents replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Newly diagnosed mam to coeliac 11 year old

    3. - Dizzyma posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Newly diagnosed mam to coeliac 11 year old

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

    • Total Members
      132,923
    • Most Online (within 30 mins)
      7,748

    cmckurtz
    Newest Member
    cmckurtz
    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
      Hi @Dizzyma I note what @trents has commented about you possibly posting from the UK.  Just to let you know that am a coeliac based in the UK, so if that is the case, do let me know if can help you with any questions on the NHS provision for coeliacs.    If you are indeed based in the UK, and coeliac disease is confirmed, I would thoroughly recommend you join Coeliac UK, as they provide a printed food and drink guide and also a phone app which you can take shopping with you so you can find out if a product is gluten free or not. But one thing I would like to say to you, no matter where you live, is you mention that your daughter is anxious.  I was always a bit of a nervous, anxious child but before my diagnosis in mid-life my anxiety levels were through the roof.   My anxiety got steadily better when I followed the gluten-free diet and vitamin and mineral deficiencies were addressed.  Anxiety is very common at diagnosis, you may well find that her anxiety will improve once your daughter follows a strict gluten-free diet. Cristiana 
    • trents
      Welcome to the celic.com community @Dizzyma! I'm assuming you are in the U.K. since you speak of your daughter's celiac disease blood tests as "her bloods".  Has her physician officially diagnosed her has having celiac disease on the results of her blood tests alone? Normally, if the ttg-iga blood test results are positive, a follow-up endoscopy with biopsy of the small bowel lining to check for damage would be ordered to confirm the results of "the bloods". However if the ttg-iga test score is 10x normal or greater, some physicians, particularly in the U.K., will dispense with the endoscopy/biopsy. If there is to be an endoscopy/biopsy, your daughter should not yet begin the gluten free diet as doing so would allow healing of the small bowel lining to commence which may result in a biopsy finding having results that conflict with the blood work. Do you know if an endoscopy/biopsy is planned? Celiac disease can have onset at any stage of life, from infancy to old age. It has a genetic base but the genes remain dormant until and unless triggered by some stress event. The stress event can be many things but it is often a viral infection. About 40% of the general population have the genetic potential to develop celiac disease but only about 1% actually develop celiac disease. So, for most, the genes remain dormant.  Celiac disease is by nature an autoimmune disorder. That is to say, gluten ingestion triggers an immune response that causes the body to attack its own tissues. In this case, the attack happens in he lining of the small bowel, at least classically, though we now know there are other body systems that can sometimes be affected. So, for a person with celiac disease, when they ingest gluten, the body sends attacking cells to battle the gluten which causes inflammation as the gluten is being absorbed into the cells that make up the lining of the small bowel. This causes damage to the cells and over time, wears them down. This lining is composed of billions of tiny finger-like projections and which creates a tremendous surface area for absorbing nutrients from the food we eat. This area of the intestinal track is where all of our nutrition is absorbed. As these finger-like projections get worn down by the constant inflammation from continued gluten consumption before diagnosis (or after diagnosis in the case of those who are noncompliant) the efficiency of nutrient absorption from what we eat can be drastically reduced. This is why iron deficiency anemia and other nutrient deficiency related medical problems are so common in the celiac population. So, to answer your question about the wisdom of allowing your daughter to consume gluten on a limited basis to retain some tolerance to it, that would not be a sound approach because it would prevent healing of the lining of her small bowel. It would keep the fires of inflammation smoldering. The only wise course is strict adherence to a gluten free diet, once all tests to confirm celiac disease are complete.
    • Dizzyma
      Hi all, I have so many questions and feel like google is giving me very different information. Hoping I may get some more definite answers here. ok, my daughter has been diagnosed as a coeliac as her bloods show anti TTG antibodies are over 128. We have started her  on a full gluten free diet. my concerns are that she wasn’t actually physically sick on her regular diet, she had tummy issues and skin sores. My fear is that she will build up a complete intolerance to gluten and become physically sick if she has gluten. Is there anything to be said for keeping a small bit of gluten in the diet to stop her from developing a total intolerance?  also, she would be an anxious type of person, is it possible that stress is the reason she has become coeliac? I read that diagnosis later in childhood could be following a sickness or stress. How can she have been fine for the first 10 years and then become coeliac? sorry, I’m just very confused and really want to do right by her. I know a coeliac and she has a terrible time after she gets gluttened so just want to make sure going down a total gluten free road is the right choice. thank you for any help or advise xx 
    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
×
×
  • 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.