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

I'm Crying Like A Baby


Guest imsohungry

Recommended Posts

Guest imsohungry

I am so upset. I've been crying for the last 30 minutes at work.

You would think I have lost a loved one or something. I feel so ridiculous (b/c I'm normally an upbeat person)....but I'VE HAD IT!

I'm in my late 20's and feel like I'm in my late 80's!

I rarely complain, but I'm tired of having epilepsy, lupus, fibromyalgia, and celiac disease. It seems like my whole life I've been a test subject (possible cancer, possible multiple sclerosis, definitely this or that...).

I just need to vent! I can't handle all of the joint pain, mouth ulcers, migraine headaches, seizures, muscle cramps, restricted eating, fatigue, constipation, hair loss, tremors, acne, dermatitis, drug induced anorexia, loss of vision, esophageal ulcers, esophageal narrowing, and infections!

...But I'll survive. Everytime I end up in the hospital, I tell myself this. I know it's true.

I know others are worse off than me. This isn't a competition though...it's my life. They are entitled to their bad days, and I am entitled to mine.

This is one of them. Thanks for letting me rant for a moment. I've stopped crying. Typing this took my mind off of crying. So without even knowing it, you helped me just by taking the time to read this! ;)

I would love to have some supporting words and input on how you guys "handle it all" (I'm always open for suggestions)! All I ask is that you don't critisize me for needing to vent.

Blessings and many hugs.

-Julie (not usually this down...just having a rough day)


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



Celiac.com Sponsor (A8-M):



dbuhl79 Contributor

Jules,

Vent. Vemt. Vent all you need! These forums are a great place and I am sure you will receive many positive upbeat commentaries. Personally, I have not had health issues to your extent. Although until moving from Michigan to VA I was very healthy, never been hospitalized. Now that I've moved here, I've been through many ordeals, from viral bugs, facial paralysis, a tumor, and a newly found brain abnormality. So I can relate to the test subjet and exhaustive doctor visits.

It does get frustrating and I can tell you I broke down many days just in tears, wanting to know what the heck was wrong with me! Adn even with the explainations, I feel like my life will never resume its normal ways.

However, you will survive! You'll vent, and get through the bad days like today! :) That's what it's all about.

My personal way of coping is through my family and significant other and all of their support. Celiac disease may just be one more thing I add to my list. And they have yet to think I'm crazy. So if you don't have someone in your life that gives that immediate support, I certainly hope this board offers you somewhat of a shoulder to cry on. Just remember you're only human and you have every right to break down! :) Nobody expects us to grin and bear it all the time 24/7. Its insane! :):o

Best Wishes to you and I hope your day has improved or that tomorrow will be 100% better for you! :D

Dana

darlindeb25 Collaborator

awwwwwww :( jules, we all feel for you--believe me, i think all of us have days lke this, i know i do--my man can tell you that i do--he knows days where i cry over nothing, i just feel sad all day and there isnt much that makes me feel better until it is out of my system---dont give up, we are all in this together and we will always listen to your problems and try to help---deb :)

celiac3270 Collaborator

Definitely vent.

Oh, by the way, celiac and my symptoms get me REALLY emotional, as well. By all means, let it out.

I know that there are MANY with far worse than I have. I'm not going to die of celiac. I'm not going to have abdominal pains, vomiting, low weight, nausea, gas, bloating, diarrhea, and the emotions of these symptoms forever. I agree with you on the point that although there are many with worse, it isn't a competition. After all, I look at it as: there are many who have it worse than me, but there are also many who have never faced any problems at all!

Rikki Tikki Explorer

I think that everybody needs to vent and that's ok. We have probably been there at one time or another. All we can really say is that we will feel better and like most people we will have both good days and bad.

I don't think everything revolves around celiac disease but so many people don't know what it is or how it effects us.

Just know in your heart that you will feel better and your usual outlook on life will return. And always know there are people out here that know what you are talking about, understand and will be there for you!

Pegster Apprentice

Poor thing! You have been through a lot. There's a children's story called "It Could Always Be Worse" but I'm sure that at times it seems like it just can't be any worse. The good news is that you don't have cancer and you have a managable disease. The bad news is that it's no fun and there will be bad days and good days. In some ways you are lucky to have a specific diagnosis at a young age, but it must feel that things are rotten all over. Feel free to vent all you need to... Things can only get better!

Guest imsohungry

I've just arrived home, and I was so touched by all of the responses to this post! I've tucked them each into my heart for days when I feel like no one understands me! :)

I'm so happy that I've found this forum. Everyone has been so warm and welcoming. I hope I contribute to people here as much as you all have already done for me.

I had a small seizure earlier tonight (not surprising considering how emotional I've been all day).

But I'm excited because I got to go grocery shopping and buy some more gluten-free brownie mix! (sometimes the small stuff brightens one's day the most).

You guys are the best! Much hugs and blessings to you all! -Jules B)


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



Celiac.com Sponsor (A8-M):



glen4cindy Apprentice

Well, I vented, unloaded, or whatever you want to call it, but, on another forum. I think maybe my post belonged here, but, alas, people here still helped me.

My wife is a great support during this time. Of course, I know that Celiac is a life sentence so to speak. She helps me remain gluten-free, but, at times, messes up. She reads all the labels now, as do I. She misses things sometimes, and any time she tells me I can have something, I always double check! There has been a few times that I notice a label says "contains wheat" when she missed it, so, I never trust her, but, she most often does really well.

Yesterday, she made a mexican dish, minus all sources of gluten until she dumped some taco seasoning into it. My son said "Can Dad have that?" "Oh NO!" she says!

Anyway, my primary coping source is my wife, and this board too. :D

ryebaby0 Enthusiast

(you mentioned mouth ulcers -- folic acid tabs might help that. My son takes them bc his meds tend to do that, and it really helps)

I think no matter what our lot in life, there are times when it is all just too much. Venting and crying are good for you, just like being thankful and all that. (But sometimes you just need to have a pity-party without any of the "but other people have it worse" additions, huh?!) One thing I have been working on is learning to reward/treat myself/celebrate without food! Man is that hard! We're so conditioned that it isn't a birthday without the cake, it isn't dinner out if you don't have a whole meal.... and after we were all tested, it turned up all sorts of weird minor ailments we have to navigate around. I don't have the stamina for re-creating bread, so we just (for the most part) gave it up! And that was such a relief!

Have you ever taken a foreign language? And you know the moment you've really learned it is when you stop translating it back into your first language? Celiac is like that. When you stop comparing every cookie, every bread, every dish and just eat what makes you healthy, it's soooo much easier.

Anyhow --- buy yourself a coveted magazine. New nailpolish. Give yourself 15 minutes of calm on a walk in the middle of lunchhour. Surf the web. Count your blessings with sincerity. Read a stupid bodice-ripper book! Find your best self and be glad to do so. We'll be right here when you need to vent on the bad days, and hope for good ones.....

joanna

mom and wife to celiacs, myself with Hashimoto's and hypoglycemia

Guest gfinnebraska

When I realized that I wasn't being careful enough about cross contamination and that I was eating foods DAILY that had gluten, I went home on my lunch hour and sobbed. I "thought" I was doing SO well! Ugh!! There are times when a good cry is the only answer. THEN you pull yourself up, realize you CAN live through this and go on. I always try and think about all the ways I am healthy, happy and have a wonderful life. I just keep thinking about all the donuts and pizza and cookies I am going to PIG OUT ON in heaven!!!! :D Until then, I am thankful for the life I have ~ family I have ~ friends I have ~ and consider celiac disease a small part of my life.

aaascr Apprentice

Hey Jules in Georgia!

Where in GA are you? I'm in Lilburn - my doc handed me some info on a support group yesterday....if you're close enough, that might help!

At least you were only crying: I simply lost my mind on the soccer field when an opposing player kept on banging (has a bit of impact on my arthritis) into me on purpose when there was no ball play near us. With all the preparation, effort and care I put into my game - she really p'd me off.

So when there was a ball played near us I unleashed - not a very flattering thing to do. So hang in there! We all do "stuff" :lol:

Alicia

mommida Enthusiast

My heart goes out to you.

Take it minute by minute if you. Breathe in, breathe out. (Can you tell I've been through some hard times too?)

Over 15 years ago, someone said to me, (in a not so nice way), you go to sleep, you wake up, and you got over it didn't you? Well it was true, to some degree. I friend of mine who has Lupus with at least 7 uncurable auto-immune diseases told me she deals with some of the pain by imagining what it felt like not to hurt. Sounds confusing but say your hand hurts and you remember what it felt like not to hurt and poof the pain is gone for a little while. If you get good at this and the pain doesn't go away get to the hospital. ( I used it to relieve headache pain for hours when I had meningitis, when I realized the pain was getting that much worse, I needed to be hospitalized.)

By the way search for checker beads. Look at the amazing talent my friends illness brought forth.

Laura

Guest imsohungry

Hey everybody!

I took today off of work! :D I needed to do it for myself...and I'm glad that I did! I have started my antibiotics for this most recent infection that my body is fighting, and I took the day off to "play"...my house is a wreck and I don't even care :rolleyes: Well, I do care, but today is about taking care of myself physically and emotionally ;) (My house will still be here tomorrow...the dirt isn't going anywhere until I clean it...so I'm in no rush)...hee hee. B)

gfinna,

I'm looking forward to that "Lord's supper" too. I'll be the first to eat a yeast roll and toll-house cookie! ;) See ya there one day!

Alicia,

I live out near Conyers and Rockdale County. Kind of in the boonies!

Joanna, Laura, and Glen ((((HUGS))) to you for the encouragement and words written from experience. Those of us that have "been there" often offer more hope and knowledge than any doctor ever could.

Much hugs and blessings to all. B)

-Julie

wclemens Newbie

Hi Jules,

I am so impressed by your positive attitude! I felt better just reading your posts, and knowing that with all the illnesses you have going on, you just keeping getting up and putting one foot in front of the other, following your dreams, even if you have to switch paths to do it. I imagine we have all had some pretty good crying fests, I know I have. I'm going to remember what you said about taking time for yourself, and follow your lead by doing something good for myself today. I'm glad I'm not the only one who let their house go today in order to do something more fulfilling, rewarding, or creative. Yes, it will still be here tomorrow, and I think I'll just wait until then to clean it up. Best wishes and good cheer! Welda

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,397
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
×
×
  • 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.