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

It Hit Me Last Night


veryami1

Recommended Posts

veryami1 Apprentice

So it finally hit me last night.  My husband got home from work and was asking about dinner. I didn't feel like eating. He reheated chicken and I just watched him eat. 

 

Then the tears came. I've only cried happy tears over my diagnosis (being happy that I finally had a solution), but this was the first time it really hit me. I have Celiac disease. This isn't something I have to deal with for a few months. This is a lifestyle change that I have to continue, forever.  I was upset last night because I was tired of eating the same things (I know I need to experiment with cooking). I went to lunch with a friend and I was frustrated that somehow a non-gluten friendly item ended up on my plate. I'm tired of explaining to restaurants how careful they need to be. I'm tired of going places and having to constantly worry about what I can/can't eat. I fear that when I have kids, we'll have to go places that I won't be able to eat.  I worry that the next time a friend invites me over, I'll offend them by asking what they are cooking (happened already).  I worry that I will eat something wrong accidentally, but by the time I find out, I just have to deal with the symptoms. I'm am pretty much in constant worry. What if?

 

I know that in the long term, I will feel better. I feel better already. But on a daily basis, this is an internal struggle that I am learning to fight.

 

How do you cope? How do you deal?

 

 


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



Celiac.com Sponsor (A8-M):



surviormom Rookie

Its the doctors that frustrate me now, not the food.  I love real food.  So do my kids and husband.  Shop the perimeter and cook real food.  It is delicious.  i still have my pains, now and then, so I still have a problem and the doctors frustrate me, that will not go away soon unless you have a great doctor.  But the food we can fix that.

moosemalibu Collaborator

Accept the grieving process. Get sad, get mad, then get over it. But don't just push it aside, brush it away like it isn't worth mourning. Because it is HUGE to change your lifestyle. So go through the process and once you feel better you'll just wonder when it happened; when did I feel good again? And come here and vent your frustrations. I get tired of the same food all the time, too. Get a few cook books and start experimenting. TRy out old favorites with substitutions... it will get better. ((Hugs))

BlessedMommy Rising Star

I agree, there is a mourning process. I have been gluten free for over 4 years and I think that I'm still dealing with a bit of sadness that I will have to continue to eat this way forever. And it's not because gluten free food tastes bad, but I'm more mourning the loss of spontaneity, if that makes sense. The loss of being able to order something off a restaurant menu without stressing or eat food that a friend has made, without playing the 20 questions game.

 

So, you're not alone!

w8in4dave Community Regular

I know I was kinda the same way. I didn't cry tho. But I was upset about eating the same foods. And saying something to the waitresses and stuff. It becomes second nature. I ask for Gluten free menu but have to scrutinize it for corn products. My friends just accept it now. The way I got over the same foods is I use seasonings. Now my husband walks in the door and says that smells amazing! I kinda like it on his Pizza night I get a steak :) There is always a yeng to the yang you just have to find it. I agree the perimeter of the store is good! Eat whole foods fresh fruits and veggies with good gluten-free. Spices and you'll be healthier than ever! :) 

Gemini Experienced

I never had any problems going gluten free because I was so very sick at diagnosis....it was super easy for me.  HOWEVER......one day, the Greek festival returned to my city after a devastating fire in the church stopped the celebration for about 4 years.  I was so excited because my husband and I enjoyed going and eating all that fantastic Greek food, made with love by all the little old Greek ladies in the church.  As I excitedly told my husband about the banner I saw and how we could go and......and...... :o ....I did this and broke down in tears as it hit me that I would never, ever be able to eat at the Greek festival again.  That was the one bad moment I had so I understand your feelings, even if mine was over one issue with being gluten free.  But, I can assure you, this too shall pass and you will become very OK with this.  I learned how to make gluten-free Greek food.....expect the Spanakopita.  I am waiting for the day when I see gluten-free phyllo dough in the freezer section of the food store!  :)

KCG91 Enthusiast

Yeah I get you :( It still surprises me how emotive food can be - particularly when you're denied it (whatever gluteny thing that may be) and when you have to be on your guard or defensive if you trust someone else (a friend or a chef) to arrange your food. Like moosemalibu said it is a grieving process because you suddenly have to say goodbye to something. I'm six months in and I'm expecting it to catch me out again before my 'anniversary' - seasonal food = emotive food haha! Next up is the city's beer festival and BBQ season :( 

With friends and family I try to keep it fairly light - if they are interested and supportive I'm happy to chat about it but otherwise it's my diet, my health and none of their business. For myself, if I feel frustrated by what I am/am not eating I try to focus on how much better I'm feeling and how proud I am of myself for adapting to a new diet (and then tuck into my favourite gluten-free snack and/or ... and ... a glass of wine :D) It gets better. 


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



Celiac.com Sponsor (A8-M):



Adalaide Mentor

I had my moment a few weeks after my diagnosis. We live with my in-laws and they brought home KFC and left it on the kitchen counter. I went to the kitchen for a snack or drink or something, I don't remember, and smelled it and just completely lost it. I was a train wreck, and I thought I was completely crazy for feeling that way about freaking CHICKEN! But everyone here helped me realize I wasn't crazy, and it wasn't just about chicken, it was about everything that was happening. It's okay to mourn what you've lost, because it isn't just food. It's freedom and memories and so much more. So rant, rave and get it out so you can move on without the baggage. And we're here for you. (((hugs)))

sarahdea Rookie

Oh yeah. I totally had a few moments of anger and tears and denial and defiance (yeah. don't do defiance. I got sick a couple times when I just said "screw it") 

 

What finally gave me peace was redoing my kitchen. I bought a good paleo diet cookbook (I can't eat dairy either)  I spent an entire day cleaning out a bunch of old stuff, installing a couple of shelves...and I splurged on a bunch of the alternative food stuffs from the health food store. I spent about $150 bucks total, but MAN it was SO good for me psychologically to take control. 

 

Now I just think ahead and keep stuff on hand like PB and celery, carrots and hummus, canned tuna and chicken to make salads...I made a really good "paleo bread" recipe. I am discovering what gluten-free beers taste good.  I have control of it and it really helps. 

 

My bf and I used to eat out a lot so that is still a PITA but we tend to frequent the same places, and the wait staff / cooks are really awesome and helpful. 

 

((((((hugs))))  Best of luck, I hope this post is helpful! 

livinthelife Apprentice

HUGE GREAT BIG HUGS!!! I completely understand too. Just when I think I know all the stuff I can't have, I find something else. Last week it was those robin eggs for Easter. Technically, I think I *knew* I couldn't have them but it wasn't until my hand was going to them for my yearly gorge that I truly KNEW I couldn't have them. I'll neither confirm nor deny tearing up at Walmart. 

 

So I came home and baked bread, brownies, and cornbread. And made a huge pot of beans and ham. And drank wine. And ate dark chocolate. 

 

It's up and down. More ups lately!!

 

Also, I agree about how much more in control I felt after I cleared out my entire kitchen and started over. That was probably the single most comforting thing that I did. 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.