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 Our Content
    eNewsletter
    Donate

What Are Some Ways I Can Stay Focused And On Track?


wilem008

Recommended Posts

wilem008 Contributor

I cheat on my diet all the time and I suffer for it!

Its stupid I know but when I went gluten free I had to cut out all the foods I love - especially bread!

I make myself gluten-free bread and I have gluten-free pasta but I eat at restaurants (a few times a week) a lot too and thats where the problems occur!

I guess I just feel left out. Everyone orders garlic bread and I have to sit there and pretend I dont want any....I sneak myself a little piece when I know full well that I shouldnt!

How can I control my cravings - How can I stay focused?


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



Celiac.com Sponsor (A8-M):



smiles Rookie

Wilem,

changing your diet is not easy, but as you know any little amount of gluten can hurt you if you have celiac/gluten intolerance. i know what you mean about the whole going out to dinner thing. before i decided to go gluten free, i was eating everything and going out everywhere to eat 5 or 6 days a week.

what has helped me stay on it was avoiding going out to eat as much and trying to limit the places i go to to to gluten friendly only. luckily i have been able to find 2 restaurants. one is a privately owned restaurant. the other is bonefish grill. if there are any by you, check them out. the food is good.

as for the bread thing, i know it is not easy. what helps me is to eat something light beforehand. that way i won't be salavating for the evil bread and can focus on my drink or the conversation. it really does help. i also try to keep snacks with me all the time and try and eat a lot throughout the day so that i never feel starved. starving will make you want to cheat. some snacks i keep with me are vegetables such as carrots or rice crackers. i also keep a beverage with me at all times. sometimes i think i am hungry when i am really just thirsty. you can also make things ahead of time such as breads, muffins, whatever and freeze them.

lastly, i focus on the foods i can have rather than on the foods i can not have. when i am in the supermarket i do not even look at the foods i can't have. it takes a lot of commitment and time. i also found that once i was able to completely cut out the gluten the cravings for it started to go away. i now look at gluten like it is poison.

do not beat yourself up if at first you are having trouble. this is normal. it may take several months before you are able to completely cut it out. the important thing is you are on the right path. i hope this has helped. :)

home-based-mom Contributor
I cheat on my diet all the time and I suffer for it!

Its stupid I know but when I went gluten free I had to cut out all the foods I love - especially bread!

I make myself gluten-free bread and I have gluten-free pasta but I eat at restaurants (a few times a week) a lot too and thats where the problems occur!

I guess I just feel left out. Everyone orders garlic bread and I have to sit there and pretend I dont want any....I sneak myself a little piece when I know full well that I shouldnt!

How can I control my cravings - How can I stay focused?

Suggestions:

1) Remember how sick you get and focus on that.

2) Take gluten-free garlic bread with you. Eat yours when they eat theirs.

3) Don't pretend you don't want any. Pretend it's dog poop and is contaminating everything it touches and everyone who is touching it.

4) This is tough but read posts and signatures on this forum about members parents, aunts, and uncles. Pay attention to the debilitating health issues. These people spent a lifetime eating gluten but shouldn't have and suffered immensely with cancers, pain and emotional issues among others. Ditch the victim mentality (poor me I can't eat garlic bread) and Praise The Lord that you have information that has enabled you to take a very simple step to take charge of your own health and keep from ending up that way.

5) Remember you can't change that you have celiac or gluten intolerance. You CAN change your attitude. It's like that cheesy saying goes: Success comes in CANS. :P

Salem Rookie

I used to go to a restaurant starving hungry. When the bread came, I would dive in. The next day I would be laying on the couch wanting to die. So stupid! Now I eat a bit before I go out so I won't be tempted to eat the bread.

For me, bread was like crack. I craved it, but it was killing me. I needed to stop eating bread to stop the cravings. Now I can look at (glutenous) bread and it doesn't look good to me. I think of the bloating, the pain, the brain-fog. I'm not interested anymore. No bread is worth that pain.

samcarter Contributor

Every week my family and I go to a wonderful restaurant that serves piping hot, delicious sourdough bread at the table. I used to dive into that basket like I was starving. (I usually was--we walk to the restaurant and it's about 1/2 mile or more).

I manage to not eat any while buttering some for my kids, by remembering how awful I feel when I eat gluten. How depressed I get, lethargic and the gas and bloating. Sometimes I bring a couple of homemade gluten free pancakes, to spread with butter, but I'd rather just go without than use a substitute. I get a soda, which I love and don't have the rest of the week, and enjoy that. I make sure to eat something before we head out so I'm not that hungry.

You might want to order a gluten-free appetizer when you sit down, so you have something to nibble on while they're eating the garlic bread. Call ahead or check the menu online to see what you can eat. Usually what we're missing when we eat with others is just the feeling of sharing the same food, of all doing the same thing. It's hard to be the only one not eating.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,392
    • Most Online (within 30 mins)
      7,748

    laurenM
    Newest Member
    laurenM
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.9k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • NavyMom
      Hi CathiJean, Wipe those tears my friend.  Finding out that you have celiac just gave you the cheat code on how to start feeling better!  It may feel like a loss right now, but honestly within 6 months you will start feeling better.  Within a year you will look back and wonder how in the world did I survive feeling like that for what feels like a lifetime?  You mentioned 15 years, that's about how long I have been really ill as well.  I had told every doctor I saw that I kept getting sick, infections, hair loss, joint pain, etc. and nobody would listen to me until I turned 45.  I went in for a colonoscopy and the doc says how often do you have bowel movements and I said usually between 10-15 times a day.  Suddenly I had someone actually listen to me and the testing began.  What I can tell you is use this forum, talk to peers, read everything you can about how to gluten-free your kitchen, encourage your family to participate in your journey (trust me they love you enough to make the effort), how to order food in restaurants, and how to avoid cross contamination.  Accept that you will make mistakes and allow yourself grace as you implement your new normal and have a clear understanding that going gluten free will begin healing your body in ways that you will not even begin to understand until you actually do it.  So, have faith that the nutrient deficiencies that you are probably experiencing right now can be corrected and you are on a bright path to feeling SO much better.  Think about how incredible your mom journey is about to become as you begin to feel better!!  Your kids are going to be amazed at your energy levels, ability to play and go do stuff...you are leveling up knowing that you have Celiac.  Knowing gives you power my friend, harness it and have gratitude that it was discovered...even if the docs missed it - you know now and keep moving forward.  You got this!! 
    • trents
      If you have been eating the gluten equivalent of 4-6 slices of wheat bread daily for say, 4 weeks, I think a repeat blood test would be valid.
    • englishbunny
      it did include Total Immunoglobin A which was 135, and said to be in normal range. when i did the blood test in January I would say I was on a "light' gluten diet, but def not gluten free.  I didn't have any clue about the celiac thing then.  Since then I have been eating a tonne of gluten for the purpose of the endoscopy....so I'm debating just getting my blood test redone right away to see if it has changed so I'm not waiting another month...
    • trents
      Welcome to the forum, @englishbunny! Did your celiac panel include a test for "Total IGA"? That is a test for IGA deficiency. If you are IGA deficient, other IGA test resultls will likely be falsely low. Were you by any chance already practicing a reduced gluten free diet when the blood draw was done?
    • englishbunny
      I'm upset & confused and really need help finding a new gastro who specializes in celiac in California.  Also will welcome any insights on my results. I tested with an isolated positive for deamidated IGA a few months ago (it was 124.3, all other values on celiac panel <1.0), I also have low ferritin and Hashimotos. Mild gastro symptoms which don't seem to get significantly worse with gluten but I can't really tell... my main issues being extreme fatigue and joint pain. The celiac panel was done by my endocrinologist to try and get to the bottom of my fatigue and I was shocked to have a positive result. Just got negative biposy result from endoscopy. Doctor only took two biopsies from small intestine (from an area that appeared red), and both are normal. Problem is his Physician's Assistant can't give me an answer whether I have celiac or not, or what possible reason I might have for having positive antibodies if I don't have it. She wants me to retest bloods in a month and says in the meantime to either "eat gluten or not, it's up to you, but your bloodwork won't be accurate if you don't" I asked if it could be I have early stage celiac so the damage is patchy and missed by only having two samples taken, and she said doctor would've seen damaged areas when performing endoscopy (?) and that it's a good sign if my whole intestine isn't damaged all over, so even if there is spotty damage I am fine.  This doesn't exactly seem satisfactory, and seems to be contrary to so much of the reading and research I have done. I haven't seen the doctor except at my endoscopy, and he was pretty arrogant and didn't take much time to talk. I can't see him or even talk to him for another month. I'm really confused about what I should do. I don't want to just "wait and see" if I have celiac and do real damage in the meantime. Because I know celiac is more that just 'not eating bread' and if I am going to make such a huge lifestyle adjustment I need an actual diagnosis. So in summary I want to find another doctor in CA, preferably Los Angeles but I don't care at this stage if they can do telehealth! I just need some real answers from someone who doesn't talk in riddles. So recommendations would be highly welcomed. I have Blue Shield CA insurance, loads of gastros in LA don’t take insurance at all 😣
×
×
  • Create New...