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

Really Struggling With Diagnosis


Rachel63

Recommended Posts

Rachel63 Newbie

Hi, I have recently been diagnosed with Celiac disease at age 50 and I have to say I am really struggling with this. I know things could be so much worse and in the sheme of things I have been very lucky as there was a few tense days when my doctor and I believed something much more sinister was going on. My problem is everything I enjoy eating is now a forbidden food. I am well aware there are great gluten free options now but I just do not have the time,energy or desire at this point to even try. Is this normal?

 

I run a very busy business with crazy hours and lunch has always been something I grab when i can. I cannot find a single "grab it on the run" option that I actually want to eat! I have never liked salads and would like it even less with no dressing. I usually make quick easy meals at night and now I have to think about every single ingredient and usually end up just making the same sort of meal for my family that I usually would make and not eating myself. I really resent this diagnosis and am so angry that I have lived 50 years without knowing and the effects it has had on me like low iron, fatigue, stomach problems and intolerance to certain foods yet no one ever thought to test why.

 

I know I will cheat. I already have. It was picked up when my doctor ordered a whole heap of tests to find out why I have lost 10kg in the last few months and why I have totally lost my appetite. We thought it could be because i have done so much travelling and maybe picked up a bug. After blood was detected in my bowel and my liver function was all over the place I had a gastroscopy/colonoscopy where celiac was suspected and backed up with a blood test. I also found out I have three bolders in my bile duct and need surgery. I am tired, irritable and resentful of the changes I have to make and grieving all the food I love and the ease of getting food. I want to know if this is normal and how long does it take to adjust and accept; Thanks


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



Celiac.com Sponsor (A8-M):



shadowicewolf Proficient

Hi, I have recently been diagnosed with Celiac disease at age 50 and I have to say I am really struggling with this. I know things could be so much worse and in the sheme of things I have been very lucky as there was a few tense days when my doctor and I believed something much more sinister was going on. My problem is everything I enjoy eating is now a forbidden food. I am well aware there are great gluten free options now but I just do not have the time,energy or desire at this point to even try. Is this normal?

 

I run a very busy business with crazy hours and lunch has always been something I grab when i can. I cannot find a single "grab it on the run" option that I actually want to eat! I have never liked salads and would like it even less with no dressing. I usually make quick easy meals at night and now I have to think about every single ingredient and usually end up just making the same sort of meal for my family that I usually would make and not eating myself. I really resent this diagnosis and am so angry that I have lived 50 years without knowing and the effects it has had on me like low iron, fatigue, stomach problems and intolerance to certain foods yet no one ever thought to test why.

 

I know I will cheat. I already have. It was picked up when my doctor ordered a whole heap of tests to find out why I have lost 10kg in the last few months and why I have totally lost my appetite. We thought it could be because i have done so much travelling and maybe picked up a bug. After blood was detected in my bowel and my liver function was all over the place I had a gastroscopy/colonoscopy where celiac was suspected and backed up with a blood test. I also found out I have three bolders in my bile duct and need surgery. I am tired, irritable and resentful of the changes I have to make and grieving all the food I love and the ease of getting food. I want to know if this is normal and how long does it take to adjust and accept; Thanks

You cannot cheat. That is not an option. If you keep cheating, not only will you not get better, you will also increase your risk of other AI diseases and cancer.

 

Gluten withdrawl is not fun.

 

As for meals, you could make big batches of them on the weekends and freeze them and bring them in. You could use a crock pot and make something that way. Some gluten free bread or corn tortillas, cheese, and lunch meat is quick and easy. Fruit and veggies with a dip is always an option.

nvsmom Community Regular

Wolf has a good point: the first few weeks gluten free often involves a withdrawal that can make you feel exhausted, cranky, headachey and worse than you did before. Not everyone gets it, but it sounds like you're one of the unlucky ones. Hang in there. Once more energy comes back, it will be a bit easier.

 

You should probably make your house as gluten-free as possible. All sauces and condiments should be gluten-free, or else get your own peanut butters and label them clearly as gluten-free.  Get rid of wheat flours, we can't safely bake with those easily... The esiest thing for you to do is to convert your house into a gluten-free home as much as possible. Buy rice noodles and gluten-free bread. Make gluten-free muffins for everyone... Stuff like that. If your faily puts up a fight, and you are the main cook, make meals that are naturally gluten-free like meat and potatoes, rices, chillis, soups, stews (without flour) or burgers (no bun or a gluten-free bun)... I know it's easier said than done - at first all I could see what I couldn't eat but that shifted after some time.

 

Buy some easy snacks to have on hand. Lara bars are handy snacks to tote around. Nuts or trail mix is a good thing to carry too. Make eggs for breakfast and bring extras to work for lunch, or bring last nights's leftovers.... That's one area you can't get around in this disease - you will need to plan your food ahead of time or you'll be eating an apple or a salad while everyone else enjoys their food.  :(

 

And no cheating... It takes weeks for the intestines to heal after consuming gluten, especially early on! After decades of a misdiagnosis (me too) it will take months for your body to be well, you don't want to slow it down. It took me well over a year before my body slowed it's production of autoantibodies; my tests are just now getting back into normal range and if I had been cheating, I'm sure it would still be attacking my intestines. You can't cheat.  Splurge and buy gluten-free goodies and junk food if you are feeling deprived (I sure did in the first few months) but don't cheat.  :(

 

Has your family been tested? It's a partially genetic disease, and doesn't always have symptoms, so your children should be tested as soon as possible as well.

 

Best wishes and welcome to the board.

notme Experienced

((hugs!))  i promise you will feel better if you stick to the diet.  i was in denial for A FEW MONTHS - (who has celiac?  notme!  lolz)  until i got so much worse i couldn't even keep anything down.  i was beyond no appetite - i was starving to death.  it was soo not fun :(  i guess it takes time to wrap your head around the whole thing, but, trust me, it will get easier.  it does sound like you're going through withdrawal - i did, too, but i had the luxury of taking it easy until it was over and i was back on an even keel.  if you have anybody who can cover for you or take vacation (< i know, lolz, i used to have a very busy career) now would be a good time to rest if you can.  what DO you like to eat for lunch or what's your go to snack?  there are plenty of subs/tricks you can get on here and if it's a specific meal or dish, we can help you make it gluten-free.  go on the 'what's for dinner" thread on the baking/cooking section of the forum.  also, if you haven't already, read the "newbie 101" thread in the coping section. 

 

it sounds terrible, but you have a diagnosis, some people just get the runaround and still have no answers.  you seem like a 'take charge' sort of person.  you can do it :) 

 

lolz - ps - i'm 50, too :)  it's for the birds haha but i am not feeling ancient like i was a few years ago!

tommysmommy Newbie

It does such at first but I promise it will get easier. Eating out and convenience are a problem, but you'll figure it out and there is an active celiac community (here, fb, twitter) willing to help. We all get it. It's almost frightening to realize everything you always ate is now bad for you. Guess what, eating so much of that stuff is bad for everyone - once you adapt, you will stop craving it! So the big question is.. what did you eat before? What were your fav foods? I've had to take my entire family of 5 gluten-free & we've found good gluten-free substitutes for everything (except calzones, don't even try on that one). Would be happy to give some recipe/product tips to adapt a meal. Also, I suggest trying to make your family dinner mostly gluten-free & make a little extra to pack for lunch the next day. Or I'll often bake a chicken breast at night to slice up for lunch with some cheese & fruit. It is more work but soon you'll be feeling so much better, it'll be worth it.

NoGlutenCooties Contributor

 I have never liked salads and would like it even less with no dressing. I usually make quick easy meals at night and now I have to think about every single ingredient and usually end up just making the same sort of meal for my family that I usually would make and not eating myself.

 

Salads aren't so bad if you add some nuts, and/or chicken, etc. to spruce them up.  Also, not all dressings have gluten.  I'm partial to Hidden Valley Ranch - certified gluten free.  Newman's Own dressings do not have gluten (not sure if that is true of all varieties/flavors, but I know several of them are safe).  You just have to read the labels carefully.

 

One quick and easy meal idea is stirfry.  There is gluten-free low sodium soy sauce - and it actually tastes exactly the same as the gluten variety.  You can include any combination of vegetables and either chicken or sausage (careful with the sausage though - it can contain fillers too).  I found Aidell's sausage - it is very tasty, minimally processed, no MSG, no Gluten, no preservatives - and it's already cooked so you can just cut it up and pop it in the stirfry and you're good to go.  I have also found that I can hide vegetables in there that I wouldn't ordinarily eat on their own. 

eers03 Explorer

It keeps getting better as you learn how much is still available to you in a gluten free form.  I still eat most of my favorite dishes but with gluten-free substitutes.  I still eat spaghetti, the noodles are derived from rice or corn now...  I still eat cookies.  I buy the gluten-free mix.  

 

As for cheating.  Thats pretty much non-negotiable.  If you think your body is "off" now.  Keep cheating. Upon initial diagnosis, I had no idea how I was going to make it work.  I was miserable.  I think thats a pretty normal reaction.  Trust me, it gets better.  Hang in there!


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Welcome to world of  gluten-free eating!  There are thousands of people here who have gone gluten-free and lived to tell the tale.  I was diagnosed about the same age as you.  Ever hear that song line, I never promised you a rose garden?  Kind of right I suppose.  But  if you stick with the gluten-free diet strictly your body can start absorbing nutrients (vits/mins) again and recover from the damage.  The immune system is very sensitive and isn't going to ignore your occasional cheats.  And the immune reaction goes on for weeks or more.  That's weeks of damage to your body that is preventable.

 

Friday nights used to mean a 6 pack of Sam Adams and turkey pot pies for me.  Being the Halloween season it would have been Blue Moon pumpkin beer instead.  I understand the changes needed seem hard.  But eating gluten-free will make you feel better, be stronger, think clearer, and probably live longer.  All good things.  You can do it! :)   Here are some tips for getting started and threads for info, including surprise!  Stuff to eat!  There is actually a lot of food we can eat, and it is pretty tasty stuff too.  You may end up eating more "real food" instead of processed chemical loaded crap though.  But your body will thank you for not polluting it.

 

Some starting the gluten-free diet tips for the first 6 months:

Get tested before starting the gluten-free diet.
Get your vitamin/mineral levels tested also.
Don't eat in restaurants
Eat only whole foods not processed foods.
Eat only food you cook yourself, think simple foods, not gourmet meals.
Take probiotics.
Take gluten-free vitamins.
Take digestive enzymes.
Avoid dairy.
Avoid sugars and starchy foods.
Avoid alcohol.
Watch out for cross contamination.

Helpful threads:

FAQ Celiac com
https://www.celiac.com/gluten-free/forum-7/announcement-3-frequently-asked-questions-about-celiac-disease/

Newbie Info 101
https://www.celiac.com/forums/topic/91878-newbie-info-101/

What's For Breakfast Today?
https://www.celiac.com/forums/topic/81858-whats-for-breakfast-today/

What Did You Have For Lunch Today?
https://www.celiac.com/forums/topic/87765-what-did-you-have-for-lunch-today/

What's for dinner tonight chat?
https://www.celiac.com/forums/topic/75238-what-are-you-cooking-tonight/

Dessert thread
https://www.celiac.com/forums/topic/93840-whats-for-dessert-tonight/page__pid__802399#entry802399

Easy yummy bread in minutes
https://www.celiac.com/forums/topic/56641-easy-yummy-bread-in-minutes/

 

Super Easy Meal Ideas Anyone?
https://www.celiac.com/forums/topic/97027-super-easy-meal-ideas-anyone/

Good Gluten Free Meals Prepared Using A Microwave?
https://www.celiac.com/forums/topic/102685-good-gluten-free-meals-prepared-using-a-microwave/#entry885634

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,540
    • Most Online (within 30 mins)
      7,748

    Barrie S
    Newest Member
    Barrie S
    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

    • 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.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
    • trents
      Calcium levels as measured in the blood can be quite deceiving as the body will rob calcium from the bones to meet demands for it by other bodily functions. Also, supplementing with calcium can be counterproductive as it tends to raise gut pH and decrease absorption. More often than not, the problem is poor absorption to begin with rather than deficiency of intake amounts in the diet. Calcium needs an acidic environment to be absorbed. This is why so many people on PPIs develop osteoporosis. The PPIs raise gut pH. And some people have high gut PH for other reasons. Low pH equates to a more acidic environment whereas high pH equates to a more basic (less acidic) environment.
    • Celiac50
      Kind thanks for all this valuable information! Since my Folate was/is low and also my Calcium, there IS a chance I am low in B vitamins... My doctor only measured the first two, oh and Zinc as I has twisted her arm and guess what, that was mega low too. So who knows, until I get myself tested properly, what else I am deficient in... I did a hair mineral test recently and it said to avoid All sources of Calcium. But this is confusing for me as my Ca is so low and I have osteoporosis because of this. It is my Adjusted Ca that is on the higher side and shouldn't be. So am not sure why the mineral test showed high Ca (well, it was medium in the test but relative to my lowish Magnesium, also via hair sample, it was high I was told). But anyway, thanks again for the VitB download, I will look into this most certainly!
    • ElisaAllergiesgluten
      Hello good afternoon, I was wondering if anyone has ever brought their anti-allergy pills? I have been wanting to use their Cetirizine HCI 10mg. They are called HealthA2Z and distributed by Allegiant Health.I’m also Asthmatic and these allergies are terrible for me but I also want to be sure they don’t have any sort of gluten compound.    I have tried calling them but to no avail. Has anyone ever used them? If so, did you had any problems or no problems at all?    thank you
×
×
  • 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.