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

Newly Diagnosed And Depressed About It All


aroche84

Recommended Posts

aroche84 Rookie

For the last several years I have delt with stomach pain, nausea, vomiting, and increased fatigue. I spent most of the time being told I was "fine", "stressed", or "trying to do to much without rest" by doctors. Recently I received a call on a Saturday from my doctor who re-evaluated my upper endoscopy and colonoscopy (spelling) results. When he did he noticed that part of my small intestine had errosions in it and that I was displaying all symptoms of Celiac Disease. He told me that he felt confident enough to say that he was 99% sure that I did have celiac disease but that a blood test would need to be done in order to 100% diagnose the celiac disease.

Immediately I looked up Celiac and found that I had all the symptoms minus seizures that were associate with celiac disease, including a itchy rash composed of small bumps all over my arms, legs, back, and stomach. My doctor initially thought that these were grass mite bites prescribed a steroid and prescription strength benedryl and sent me on my way. I have become overwelmed with what I can eat/can't eat, why am I so fatigued, pain in my stomach, the pain of the bumps, and the depression of what did I do to cause this. I have always considered myself a semi healthy eater. Other than brussell sprouts there is not a vegetable I don't eat, likewise with fruit. I prefered a salad over a cheeseburger and while I could probably exercise a little more I was never unactive by any means.

I guess what I am wanting to know is does this get easier? Will there be a time when I go to the grocery store and I am not constantly looking up every food on my phone and crying because it seems like nothing I used to buy is gluten free. I have eaten quite a bit of cottage cheese and fruit because I know that those items are safe. It just seems so overwhelming and I don't know what to do. Any help or words of wisdom would be greatly appreciated!


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



Celiac.com Sponsor (A8-M):



eatmeat4good Enthusiast

Thank God your Dr. finally figured it out! And now you will get better!

Think fresh meat, chicken, fish, vegetables, nuts, seeds, and forget the packaged goods for best results. I did use dairy in the beginning and ignored the advice not to eat dairy. Later I regretted that decision...several months later I realized dairy was not OK for me. Most newly diagnosed cannot tolerate dairy because the tips of the villi produce the enzyme for digesting dairy and they have been eroded by Celiac often. You may be ok for a while with it...but later you may start reacting. For now...choose one salty treat and one sweet treat...gluten free of course...and otherwise stay only in the meat and produce sections...

Reading labels becomes a lifestyle.

Healing takes time.

Fresh meat and vegetables and fruit are best.

Packaged goods are not only expensive but they offer very little nutrition.

Having said that...I couldn't have lived without Snickers and Cheetos in the beginning. This was my salty and my sweet snack. The rest of the time I cooked whole foods.

So happy you found out! And I hope you heal really fast!

Oh, and Udi's bread is the only one I will eat...and only occasionally.

Take a deep breath! Lot's of recipes and helpful people here. Welcome to feeling better.

Marilyn R Community Regular

Hi Ashley, and welcome to the forum!

Yes, omg the diet gets easier! Shopping gets easier.

Do use the seaarch engine on the forum (upper left) to learn about cross contamination (cc) if you haven't already.

As for grocery shopping, it will be difficult at first, but then you learn to go to just the aisles that have the stuff you need (whole foods, like meat and fish and vegetables).

Kettle brand salt and pepper potato chips are great if you feel like cruising down the snack section. If you can tolerate corn, most corn chips are gluten-free (including Fritos, last time I checked, but that's been awhile.)

Try to focus on what you can have vs. what you can't, and that you have a disease but it's a disease you can control with what you eat, which is pretty cool, vs. what most people have to contend with who have autoimmune diseases.

It takes awhile to feel better, but I think you'll be happy in the long run that it is "only" celiac disease.

When you're ready, it also pays to check out health and beauty products.

Good luck!

challengeaccepted Newbie

Hi Ashley, and welcome to the forum!

Yes, omg the diet gets easier! Shopping gets easier.

Do use the seaarch engine on the forum (upper left) to learn about cross contamination (cc) if you haven't already.

As for grocery shopping, it will be difficult at first, but then you learn to go to just the aisles that have the stuff you need (whole foods, like meat and fish and vegetables).

Kettle brand salt and pepper potato chips are great if you feel like cruising down the snack section. If you can tolerate corn, most corn chips are gluten-free (including Fritos, last time I checked, but that's been awhile.)

Try to focus on what you can have vs. what you can't, and that you have a disease but it's a disease you can control with what you eat, which is pretty cool, vs. what most people have to contend with who have autoimmune diseases.

It takes awhile to feel better, but I think you'll be happy in the long run that it is "only" celiac disease.

When you're ready, it also pays to check out health and beauty products.

Good luck!

I agree. I was diagnosed 1yr, 2 months ago. I had a huge pity party for myself, but then realized that being handed the answer to a lifetime of pain and discomfort, was something to celebrate.

Instead of getting down on what you think you can't eat, get excited at what you can! Still all the fresh veggies and fruits, tasty unprocessed meats, eggs. You will get to discover new grains! Like Quinoa. You can still eat rice, potato, rice noodles/wraps. Anything fresh and wholesome is now your ticket for relief and fullness.

Try a tasty stirfry, with fresh garlic, ginger and some hot chile's. You don't need a sauce, and when you aren't feeling so overwhelmed, then go do some more grocery sleuthing.

Baby steps. Like grilled broccoli, with olive oil and sea salt as a side dish for a beautiful bbq'd steak and mashed potato's.

You can do this, focus on the small things, the staples, and everything else will come in time.

Also, depending on where you live, some natural food stores offer tours(free) and will highlight sections in the stores that will have what you need. Nature's Emporium is huge for that up here in Canada. Gluten free signs clearly marked in every aisle.

Keep it whole and fresh!

Good luck and know you are not alone. All of us were where you are right now.

Bubba's Mom Enthusiast

Congratulations on getting a diagnosis! Now you have some answers, and on a strict gluten free diet your health will improve.

I'm newly diagnosed too, and the grocery store really brings on feelings of overwhelm and great sadness. I'm sure with time we'll know what to get and can breeze through?

Stay to the outer parameter(other than the bakery) for healthy fruits and veggies, meats, and dairy(once you're allowed to have it).

Do take vitamin suppliments, fish oil, D3 that are gluten free.

I have been reading everything I can find on the topic, and if you have damage to the intestine, raw veggies are harder to digest at first. Eat them cooked or steamed until you heal. Dairy is diogested from an enzyme in the small intestine, so if you have damage you won't digest it. Hold off on it for now.

Try to focus on what you CAN have, rather than what you can't.

T.H. Community Regular

So sorry it's been so hard! *hugs*

And yeah, it's hard in the beginning, because there is so much information that you don't know and it's something that you HAVE to deal with every day now. But really, it's like anything else new: starting a new job, having a baby, moving to a new city. You'll be bombarded with new information constantly, and it'll feel like you'll never figure it out. And then you'll remember some things, and then more, and figure out even more, and eventually, you'll have it all down pat, knowing what you can eat and can't, knowing what brands are good and what aren't, skimming through labels like it's nothing. It really does get easier, but ...yeah, it sucks for the first couple of weeks to months, usually.

BUT...there's one thing you get right now that you wouldn't get with everything else new: you'll be feeling BETTER at the same time. It is amazing how much easier all this new stuff is when suddenly, you're not nauseated and miserable and exhausted all the time.

I found out I had lots of other foods I couldn't eat, too (dairy, soy, potatoes, eggs...sugarcane and coffee. :huh: ) I dropped SO much food from my diet. If you'd told me it was going to happen ahead of time, I would have been crying like a baby. And instead, when I was eating crappier food (still trying to figure out how to cook without all those other ingredients at the time), and had less choices, and SHOULD have been depressed as all heck. That was the time I was feeling energized and upbeat and so awake and aware of the world for the first time in YEARS that even with all the foods I was missing, I was still feeling SO much better.

It's weird, but it works out like that for a lot of us. Hard to feel too bad about the diet when you start feeling so much BETTER. But you have to GET to that better part before it really hits.

I would second the idea of looking up how to avoid gluten cross contamination. I know of one gal recently who went gluten free but wasn't avoiding cross contamination, and she still couldn't get better until she did. Might as well start off strong, even if it's hard, and get better faster, yeah? :-)

Good luck! Hope that your recovery is smooth and fast!

Marilyn R Community Regular

One other thing I wanted to add is that what you're going through is perfectly normal. I started crying the first couple of times I went to the grocery store. And probably the first times I went shopping, I left with less than 10 items because I felt so overwhelmed from reading labels and worrying.


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



Celiac.com Sponsor (A8-M):



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. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

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

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.