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

Feeling Really Down


seeking-wholeness

Recommended Posts

seeking-wholeness Explorer

Newbie,

I'm sorry to hear that you are still struggling so much emotionally, but I totally understand your feelings. Back when I was wheat-free but not gluten-free, I felt this way a good portion of the time. I usually feel pretty content with life these days, but when I don't, I CAN'T just tell myself that it will get better soon! I try, but it never works. I feel physically exhausted and mentally foggy, and I remember all the other times I have felt the same way, and I get ANGRY that it is happening again in spite of my best efforts! Fortunately, these episodes are getting less frequent (now they usually just follow eating out). The only thing that works somewhat for me is reminding myself that setbacks happen in EVERY endeavor and that each one teaches me more about what it takes to be gluten-free, so it is at the very least slightly useful.

About communion, I seem to remember reading that gluten-free wafers are available somewhere or other, although the Catholic church may not officially sanction them. (Here is where I bite my tongue--HARD!--on my opinion of any establishment supposedly founded on unconditional love for ALL humankind that would turn around and demand that some of its members unquestioningly sacrifice their well-being and possibly even their very LIVES to uphold the dogmatic assertion that wheat is the "staff of life" and the ONLY vehicle through which transsubstantiation can occur! Is there any way to PROVE this claim? And come on, people--I thought suicide was a mortal sin!) I hate to be the bearer of bad tidings, but I have little doubt that you will have serious problems with depression as long as you continue to consume even a crumb of gluten-based communion host! If it were me, I would try to find a gluten-free host, and if I couldn't, I would work on accepting myself as a worthy individual even without the validation of Communion. NOTHING is worth sacrificing my physical, mental, or emotional health, and actually it is ONLY while I am strictly gluten-free that I can even perceive my value as a person! I hope my input helps you clarify your own thoughts on this matter, but only you can make the final decision as to what is best for you in this situation.

Remember that you are still learning all the intricacies of the gluten-free diet, and give yourself permission to make HONEST mistakes. Beating yourself up over them just adds to your stress level and makes healing that much harder! You will eventually reach the point where eating gluten-free really is second nature, although occasional periods of mourning for your old lifestyle are normal and inevitable occurrences. You CAN do this, and I wish you strength and peace as you journey toward true health! Good luck!


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



Celiac.com Sponsor (A8-M):



GFdoc Apprentice

Being diagnosed with a chronic disease that requires a major lifestyle change is very difficult. I think we all have our ups and downs. I think it is helpful to hold on to your faith...it can get you through alot.

In Judaism, we are taught that you can break a law (ie Kosher rules, etc. ) if it is for medical reasons....A life is held as the most important, over all rules (well, almost all rules). Will your clergy allow you to bend the rules at all? Can you bring your own gluten-free communion wafers? If not, can you find another clergy who will allow you ? (sorry, I'm not that informed about the rules of the church)

I was in a deli yesterday, buying fresh bagels for my mother, and I was close to tears...the smell of the bagels made me want them so badly...but then I remembered another teaching in my faith...that we should stop before eating and pause to thank God... and I try to think of my celiac disease diagnosis as a permanant reminder that I have to pause before eating (to check ingredient labels!) instead of just mindlessly gobbling down my food.

Take each day , one at a time, and you will get through it ...and we will all support each other as best we can.

Sara

LindaB Rookie

Newbie,

I am Lutheran and I explained to our pastor that I cannot have the bread and she completely understood and knew that some churches do have gluten-free communion wafers, however, we do not. So when I go up for communion, the pastor does not offer me bread, but I do take the juice. You are not less of a person because you cannot have the bread, it is just important that you are there.

I have been gluten-free for a bit over a year and am just now feeling pretty good each day. It took a long time for me to heal after 57 years of eating the wrong things and being diagnosed with everything but what I actually had.

Why hasn't your doctor put you on Fosamax which you take once a week if you have osteoporosis. I take this pill and it is supposed to strengthen your bones after the loss of calcium.

Linda

corbintlg Newbie

Newbie:

hang in there. it is tough. I'm 28, diagnosed when I was 2. didn't eat anything I wasn't supposed to until I became a teenager and rebelled. I started eating everything. And continued to do so until about a month ago - when I realized that all of the problems and symptoms I am having are related to my celiac. I think I had convinced myself that I had "outgrown" it - which can NEVER happen. I'm back on the strict diet for 4 days now. wow! what a difference in how i feel. still not feeling "normal", if there is such a thing, but much better. Hard to stick to the diet? you bet. but you know that. I have two wonderful little boys (3 and 4 yrs old) and a husband and I finally came to admitting the truth that my life and health is more important than eating the foods that are ruining/killing me. I went shopping at a health food store this weekend and got so frustrated that I cried all the way back home. But again, I know I have to do this and get back on the gluten free diet and stay on it - for the rest of my life. I have felt depressed alot lately, feeling sorry for myself, etc., but it could be worse. We could all have been diagnosed with a terminal disease. Diet isn't easy, but you know, life isn't easy. Hang in there. So glad to have found this website and message board. Support is the best medicine. and even so much more that people who do not have Celiac Disease, just don't understand it or what we are going through. Good luck.

Guest Libbyk

newbie (or anyone who knows)-

wanted to ask you more about the joine pain thing. did you have it before? I ws diagnosed 6 weeks ago, and in the last 2 weeks, my joints have started to hurt. My knee pain is stopping me from being the athletic person I like to be, and now my wrists and shoulder and elbow hurt. Lame.

I went in for a bone scan today, but won't find anything out for a couple weeks. I am a (other than this whole celiace thing!) robust, healthy 23 year old. So I don't really understand the joint pain thing. Why would it come out now?

peace

Libby

tammy Community Regular

I do hope that you will find the peace you need. This group is a wonderful opportunity for you and all gluten sensitive and gluten intolerant people!

I was diagnosed in December of 2002 and I have Osteopinea.

Your focus will become one of your most important traits. This is a new life, and the mourning of the old life is an ever evolving process. I still struggle with this, although I also have other health issues. Each day is a learning process, and the closer you come to a truly gluten-free diet the better it will be for you. Try not to jump ahead of yourself, don't push your body. Yur body's organs and immune system must be really struggling right now to function. I take 2,000 mg of calcium daily to meet my body's daily intake and when that level falters, I feel it! Everybody's body is different yet all of us need a gluten-free diet for life.

I'm sending you xxxxxxxx hugs because they are the best I can do for you.

Newbie Rookie

Mariann, I love this site too. It always helps me out when I'm feeling down or when I have a kazillion questions! You know, I was actually surprised when you mentioned the joint pain and the potatoes/tomatoes... I haven't really had a lot of tomatoes, but potatoes a fair bit! I would have never in my life guessed that potatoes could be causing the pain... boy celiac is a tricky thing isn't it? See, I've been wondering about this joint pain but I never knew what brought it on. I just told myself "must be the osteoporosis... :P " I used to watch the osteoporosis commercials on tv and think to myself "I don't have to worry about that for a LONG time." I guess the joke was on me. Oh well. I read on the net that osteoporosis can't be cured... but my doctor also told me that he believes because I'm still young (20), I could replenish the bone loss (does that mean that I can be cured of osteoporosis?)

Well, I'll try to minimize my potato intake for a week and see how that goes. I find the reason I eat more is that I crave carbs so much now that I'm g.f. I also find that its one of the few things that are filling... That and rice. My rice intake has probably quadrupled since being gluten free.

Um, about being first in line for Communion to avoid the contamination... One more complication... The priest takes from the Blood before anyone else does... he has to be the first person to take it... and so the Body has to be in it. I wish it were simpler. But thank you very much for the suggestion...

It really touches me to see that people take the time to respond when someone is feeling down... I know for sure there will be more down days in the future... but knowing that this board is here is a big relief.

THANK YOU ALL


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



Celiac.com Sponsor (A8-M):



zippyten Newbie

Hi Newbie and everyone,

I am also a newbie, having been just diagnosed with gluten-sensitive enteropathy & have been on a gluten-free diet one day (help!), which my doctor said could be a 3-month "trial run" with a re-check of bloodwork at the end, but it seems unlikely this'll just be a temporary thing. I'm just starting to do research and learn about celiac disease and have found many of these postings to be tremendously helpful and also a big, big relief.

Right now I'm in the stage of going into the grocery or even health food store and literally having my eyes fill up with tears at the sight of all the food I'm not allowed to have. I hope that doesn't sound too silly. I keep trying to remind myself that there are people a lot worse off, who have cancer for example, and would give anything to just be on a diet that could control their symptoms. But I guess I just need a little time to adjust -- I'm in my 40s and have been eating healthily (I thought) compared to most people, for years now...but I also don't have much experience with depriving myself of certain foods and a big part of my life are foods like bread, bagels, and beer! Well, not necessarily all at the same meal.

I have two children and a husband who are being sympathetic and supportive, which is good, but they're not at the stage (yet) where they're even considering a gluten-free diet for themselves, so I have to do a lot of food prep that involves looking at, smelling, and touching things I can't eat. A real test of will power.

OK, I don't want this to be too long...but regarding the Communion problem. I'm a Roman Catholic, and I spoke to my church about the wafer issue. They've suggested that if I bring in my own supply of gluten-free hosts, the priest would be able to give me communion in the sacristy directly after the mass, or possibly during the mass when everyone else is done, and he would just bless the gluten-free hosts as he does the other ones.

I understand in your church that it's bread rather than hosts being used, but really, the priest has the power to bless whatever bread is being used and I don't think the type should really matter to your clergy if it's not affecting the supply for the entire congregation, but just for one person. I would think it's possible to work out him blessing separately whatever you need to take to avoid getting sick. You need to do a little more research about your own church's particular rules on this (maybe higher up than your own clergy) & present them with a couple of viable options.

And of course, while religious decisions are entirely personal things, if this church is not willing to accommodate you on something like this, if it were me, I'd seriously consider another church that is not so focused on small details that obscure the real purpose of receiving communion to begin with -- which is to receive Christ. Doesn't your church have a way of bringing Communion to elderly or sick people who cannot come to Mass? This is a very similar situation -- you need to receive communion in a particular way based on your health. The bottom line is, what's their final answer to you? Is it "Too bad, I guess you'll never get to receive communion ever again?" Or "We'll help you work this out?"

Anyway, I found a place that sells gluten-free hosts. Here's their info:

Ener-G Foods Inc., PO Box 84487, Seattle WA 98124-5787; 800-331-5222; 206-767-6660; fax: 206-764-3398; www.ener-g.com.

Good luck, & let us know what happens. Thanks everyone.

Ellen

Newbie Rookie

Hi Ellen!

Well, the first thing I want to say is that you shouldn't feel silly about getting sad when you're shopping. That has happened to me a lot, and to many people on this board. There are times when I'll walk into the store and hold myself back from tears. It's a big adjustment. We've all gone through it... and sometimes we go shopping and we're ok with the whole situation, but another week we'll go and we'll feel so terrible over all the things we can't have that are jam packing the aisles and shelves. And I, just like you, have told myself that it could be worse, it could be cancer and of course what a person in that situation wouldn't give to be in our shoes. And sometimes that makes me feel better... and sometimes, even that doesn't cut it and I just feel bad. But what I'm getting at is that this diet and disease is a very big test of patience (And I'm not a patient person...), so don't feel guilty when you're in a bad mood. You have the right to be. We all do. We just have to keep at this I guess. As you can tell from the title of this post, when I wrote it, I was in a really down mood. And the last thing I wanted to hear was " it could be worse ".... because I already tell myself that a million times, and there are days when I just don't care if it could be worse. So don't feel guilty or silly when you get upset. We've all been through it and continue to go through it.

About Communion... To be fair, I haven't really asked them if I could replace the bread with my own. I'll consider doing that and hope it works out. Of course when someone is ill and can't partake of Communion, the priest brings it to him at his house or the hospital or whatever.

Take care and thanks for the reply.

  • 3 weeks later...
LindaB Rookie

Newbie,

I am post menopausal so that must be why I was put on the Fosomax. I am 58 years old and was just diagnosed with Celiac last in December of 2002. My doctor said after being ont he medication for a year he would send me for another bone scan to see if it is working--I sure hope so.

Linda B.

Newbie Rookie

Thanks for all the replies everyone. I hope you're all doing well, and Linda, I hope the medicine is working for you.

Take care.

poeticjul25 Newbie

Hi, my name is Julie and I am a 23-year-old with suspected celiac disease. More about my experience in Boston, Ma. with the gastroenterologist can be found in the doctor's section of this board. Wow, I can really relate to the post about feeling down and disappointed. <_< Going out to eat at restaurants are not exactly exciting--I can only eat salads most of the time, and even then, I have to be careful of the wheat stabilizers in the dressings, and then, I usually am so hungry that as soon as I come home, I pig out on my stash of gluten-free foods. It's annoying, because everything that I see in the supermarket that appears safe has wheat fillers, protein, stabilizers, or starches, but then I tell myself that those types of things are poison to my system anyway, and why would I want to ingest poison? It's a psychological game I play with myself, but still, I do very much crave gluten a lot of the time, although it has significantly faded since going on the gluten-free diet in August of 2003. Sometimes, I do get upset and break down crying, and yes, my joints do hurt at times--specifically my knees and my wrists (and as a writer, I do not really want to develop pain there), and my hip bones sometimes jut out and hurt whenever I am sleeping on my side. This message board has really helped solidify the fact that I am not alone, and that there are other people out there that care and are living with this disease as well. As corny as it sounds, I derive much of my strength from you all, and I wish you all luck in your quests for good health. :)

--Julie from Ma.

plantime Contributor

Julie,

I, too, felt alone until I found this board. It is wonderful, knowing that we are not going through this alone. I don't think of it as "misery loves company", but "someone truly understands." B)

poeticjul25 Newbie

Dessa,

I 100% agree with you--whenever I am feeling a little down about things and how I am feeling, I go on this site and read some of the posts. I know that celiac disease, while it is a huge life hassle, isn't exactly a death sentence, and the people on here really help to drum that into my head, which I so appreciate. I hope that you are feeling well, and continue to feel well for a very long time! :D

--Julie

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,547
    • Most Online (within 30 mins)
      7,748

    gizmo1jazz2
    Newest Member
    gizmo1jazz2
    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

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • 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.
×
×
  • 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.