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

Am I Having Withdrawal?


KikiB

Recommended Posts

KikiB Explorer

It's been about 3 weeks now that I've been gluten free -- with one medication mishap. I was really looking forward to finishing the testing and going gluten free so that I would feel better. But I don't feel better. I'm not as sick as I was during the gluten challenge, but I'm not better. I still have major fatigue and muscle weakness every single day. And the C is not getting better.

And now I'm depressed too. It's not that I want to cheat, because I have no interest in doing harm to my body. Food is just not that important. But I was sad last night when I went to the bank and for a quick second wanted to go to the bakery and pick up a croissant -- then realized that I could not. I think the reality of it is sinking in. This is permanent -- not a diet. And the reality of how inconvenient this is. I can't stop and pick something up on the way home. I can't eat anything I want. Going out with my friends to restaurants is going to be so much harder. Lunch meetings at work are harder. Today is my first lunch meeting gluten free. Not looking forward to bringing my own food and dealing with the questions. I don't work with a lot of "grown ups" if you know what I mean.

I think my biggest fear is that this isn't the answer to my health problems. What if I don't get better and there is really something else wrong with me? I have fought depression my whole life, but it has not been this bad in a very long time. I'm actually tearing up as I write this. Pathetic.


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



Celiac.com Sponsor (A8-M):



srall Contributor

It's been about 3 weeks now that I've been gluten free -- with one medication mishap. I was really looking forward to finishing the testing and going gluten free so that I would feel better. But I don't feel better. I'm not as sick as I was during the gluten challenge, but I'm not better. I still have major fatigue and muscle weakness every single day. And the C is not getting better.

And now I'm depressed too. It's not that I want to cheat, because I have no interest in doing harm to my body. Food is just not that important. But I was sad last night when I went to the bank and for a quick second wanted to go to the bakery and pick up a croissant -- then realized that I could not. I think the reality of it is sinking in. This is permanent -- not a diet. And the reality of how inconvenient this is. I can't stop and pick something up on the way home. I can't eat anything I want. Going out with my friends to restaurants is going to be so much harder. Lunch meetings at work are harder. Today is my first lunch meeting gluten free. Not looking forward to bringing my own food and dealing with the questions. I don't work with a lot of "grown ups" if you know what I mean.

I think my biggest fear is that this isn't the answer to my health problems. What if I don't get better and there is really something else wrong with me? I have fought depression my whole life, but it has not been this bad in a very long time. I'm actually tearing up as I write this. Pathetic.

This actually sounds pretty normal, esp 3 weeks in. I remember very well trying to come to terms with the fact that I'll never eat a pizza or hamburger again, not another ice cream cone...everything was going to change. I had to learn to COOK for heaven's sake. It's a lot to go through mentally on top of everything that is happening to you physically. I would be willing to bet that if you commit to your diet, and get exercise that the depression will start to lift. It's very very overwhelming, but doable. And the end result (which is feeling good and better health) is so worth it. Remember too that you might need to look for other food intolerances. Good luck!

bartfull Rising Star

The lack of convenience was perhaps the hardest part for me. I was never one for cooking. I'd just pick something up on my way to work most days. Realizing that there wasn't one single place in town where I could just pick something up was tough, and realizing there really wasn't even anything at the grocery store that I could just pick up was even harder. EVERYTHING had to be cooked! I had to start planning ahead! I hated it!

But I learned to plan ahead and cook only one or two days a week. I prepare my meals and freeze them. Then I can just grab one out of the freezer to microwave at work. Yeah, I do have to cook now, but in a way it is more convenient than before because I don't even have to stop at a restaurant or the store. I just open the freezer door.

KikiB Explorer

Thanks srall and bartfull for the encouragement. Unfortunately I cannot exercise because I am too weak right now. When will the fatigue and muscle weakness start improving? I've actually gotten worse the last couple of days.

srall Contributor

Yes the fatigue will go away. But you are only 3 weeks in. Healing might take 6 months to 2 years. And within that space of time you should see marked improvement. Don't let that time frame bum you out either. I think it just helps to be prepared for a little bit of a long haul. I think what most people experience is that you start to have good days along with the bad days. Then you notice that you are having more and more good days and less bad days. But to be honest with you I still have bad days, and bad weeks. I don't think it comes from healing, but from cc because we have to go out into the world.

I've said this many times: Going gluten/dairy/corn/soy free changed my life. I wanted to shout it from rooftops 2 1/2 years ago. Now it's sort of my new normal. But it's a journey. Stay on this board because it's a huge source of support and education.

I still come back and visit when I need the additional boost (got TG cc and am feeling yucky...see it still happens.)

You'll get through it. You are most certainly in withdrawal right now.

Celiac Mindwarp Community Regular

I meltdown down in a store because I couldn't find anything to eat right about 3 weeks. Floods of tears and everything. I think it was reality of lack of convenience hitting.

All sounds pretty normal to me. Hang in there.

Adalaide Mentor

It is totally normal to be emotional at this point. There were times I even cried right in the middle of the grocery store. I didn't get sad and tear up and shed a few tears, I sobbed like a child, right there for everyone to see, making a spectacle of myself. I'm sure it was quite amusing to see a grown woman making an idiot of herself standing in front of the bakery like that.

Much like you (after I initially freaked out) I said to myself, I can do this. I want to be healthy. It's food right? All I have to do is not eat like... bread and stuff. Then over the next few weeks the "stuff" part started to sink in. Stuff meant obvious things like going out to eat, pasta, pizza... and then I couldn't completely random things. Like tomato soup. My immediate reaction there was what the hell is wheat doing in tomato soup?!?!?! Then as soon as I got a handle on things it was time for the Girl Scouts to sell cookies. I got my crap together and suddenly there was an explosion where every business, everywhere was selling red velvet everything, which is like my favorite thing in the whole world. My initial reaction was to want to scream, cry or beat my head of my desk while yelling "why why why why" but I didn't do any of those things. It had been just over half a year and finally I realized and came to accept that this is my life. People around me will eat things I can't every day. I need to suck it up and deal with it like an adult before I end up crazy. It took me six months to get there, and you will too, but give it time. You don't get there overnight. Until then, get mad and cry and whatever as much as you need to.

And as for working with people who aren't exactly grown ups. Let them not be grown ups. You can (hopefully) shut it down with a simple statement about how you were just diagnosed with celiac and can't safely eat out, but you're here for business not to talk about your eating habits. There are also some of us to make it a simple "I have allergies" statement and that's that. End of story, no explanation. Period. No discussion. If pushed you can simply say you'd rather not discuss it. Or, if you are up for educating them you can try. This is sometimes successful and sometimes not, only you can judge your audience.


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



Celiac.com Sponsor (A8-M):



srall Contributor

I have one other word of advice, which may cause some controversy. IF you self diagnosed (I did) I would from the get go just say you have celiac. When I first went gluten free it was out of desperation to feel better but I didn't know what to do besides an elimination diet. Once I'd narrowed down that it was gluten I went to the doctor. She looked at my pictures, heard my symptoms and said, "I believe you have celiac disease, but you'll need to go on gluten for 2 months to test." Forget it, lady. So now I feel like I am constantly questioned/doubted by family members who would not have known the difference had I just said, "yup...a doctor diagnosed me."

I know not everyone here will agree with me, and believe me I believe that celiac is only one part of gluten intolerance but when you tell someone you are intolerant to something they do not get how bad it can be. (5th day on the couch with heating pad...it can get bad)

So FWIW...

bartfull Rising Star

I agree with srall completely! I too am self-diagnosed, and I always say, "Since I was diagnosed with celiac disease, I can't eat that." Or something to that effect. It is not a lie. I WAS diagnosed - by myself. It really IS easier to deal with other people if you say celiac disease rather than intolerance.

Sometimes I just say I have food allergies, depending on the situation, because everyone knows what an allergy is but not everyone knows what celiac is. If I feel like explaining and educating people I say celiac. If I am not in the mood I say allergies and that usually shuts them up.

I have not only sobbed like a baby at the grocery store as Adelaide has, but one time I started yelling! "I HATE THIS! I can't eat ANYTHING!" That was at my lowest point when my other intolerances were at their worst. At that point, it seemed that everything had gluten, soy, or corn in it, and I could eat none of those things. Non-organic foods made me sick back then and I was SO limited. But things have gotten better since. I still can't eat soy or corn meal or whole corn, but I got corn starch back, and I no longer get sick from non-organics.

I have had trouble with salicylates too, but it's been a while since I tried them. I think the thing I miss the most is blueberry pie. I just might get some gluten-free pie crust and make a blueberry pie for Christmas. If it doesn't work for me I can always give it to a gluten-free friend. :)

KikiB Explorer

Thanks everyone. It really helps to know that you have all felt the same way. It's feeling overwhelming when I look at this is for the rest of my life. And I'm discouraged because I had read about people feeling better after a couple of weeks. I guess I'm not one of them. I haven't found much information on withdrawal, but also hoping that would explain a lot of how I'm feeling.

designerstubble Enthusiast

Hi KikiB

Just wanted to let you know I have been gluten-free for 6-7 weeks... I've been through hell. I initially felt a bit better a few days into gluten-free, then suddenly just felt absolutely dreadful. I have had night sweats, joints hurting, muscles hurting, moving odd pains all over my body... Hair falling out, crying at the drop of a hat. Obviously with fatigue... Also insomnia... I'm currently battling with pains in my top right abdomen (gallbladder??) and a moving lump in my throat that comes and goes?? (makes me feel very sick). I still have an MRI and an endoscopy to look forward to. I also thought that I was going to feel better much quicker, and feel depressed about it all. The realisation of our situation just keeps on coming! Also, I just don't understand why?! Did I do this to myself (last 6 yrs of my life very stressful).

It's a lot to take in. I'm a vegetarian with nut allergy, who is now celiac... And I've just cut out caffeine :( chocolate/sugar :( and dairy :(

Just wanted you to know, I'm there... Where you are. Rock n roll, no one else can do this for us. I keep telling myself if the worst of it is just cutting out some food... Then fine, as long as I get healthy again! Fingers crossed for both of us :)

KikiB Explorer

Just wanted you to know, I'm there... Where you are. Rock n roll, no one else can do this for us. I keep telling myself if the worst of it is just cutting out some food... Then fine, as long as I get healthy again! Fingers crossed for both of us :)

Thanks DS. Nice to know I have company.

GottaSki Mentor

Hi Kiki-

You can do this - insert cheerleader icon here ;)

It's a tough dance - you'll take steps forward - you'll take steps backward - but you will learn the dance and then one day you'll suddenly realize the steps aren't as hard as they once were.

Hang in there -- the first months are the hardest -- I promise.

Hugs -- vent as much as you need -- we all have and understand completely.

PS...you too DesignerStubble - Hang in there :)

designerstubble Enthusiast

Thanks GottaSki, it's so great to not feel quite so isolated, to have friends!! Friends that understand. And have knoweledge.

This is such a great support :)

KikiB Explorer

Hi Kiki-

You can do this - insert cheerleader icon here ;)

Yay! I forgot I had cheerleaders!

Thanks GottaSki, it's so great to not feel quite so isolated, to have friends!! Friends that understand. And have knoweledge.

This is such a great support :)

:)

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to tiffanygosci's topic in Coping with Celiac Disease
      14

      New Celiac Mama in My 30s

    2. - SusanJ replied to Jillian83's topic in Coping with Celiac Disease
      5

      Celiac and dermatitis herpetiformis has taken Me from Me

    3. - knitty kitty replied to tiffanygosci's topic in Coping with Celiac Disease
      14

      New Celiac Mama in My 30s

    4. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      14

      New Celiac Mama in My 30s

    5. - RMJ replied to Riley.'s topic in Introduce Yourself / Share Stuff
      4

      Outgrow celiac?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,981
    • Most Online (within 30 mins)
      7,748

    Cathal Brugha
    Newest Member
    Cathal Brugha
    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
      I just want to clarify that what I posted is a category of research summaries we've done over the years, and nearly each one shows that there is definitely a connection to celiac disease and migraine headaches. The latest study said: "the study did indicate some potential causal associations between celiac disease and migraine with or without aura, as well as between migraine without aura and ulcerative colitis...this study did not find evidence of a shared genetic basis..." Anyway, there is definitely a connection, and you can go through more of the articles here if you're interested: https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/migraine-headaches-and-celiac-disease/
    • SusanJ
      Two months ago, I started taking Dupixent for dermatitis herpetiformis and it has completely cleared it up. I can't believe it! I have had a terrible painful, intensely itchy rash for over a year despite going fully gluten-free. See if your doctor will prescribe Dupixent. It can be expensive but I am getting it free. When the dermatitis herpetiformis was bad I could not do anything. I just lay in bed covered in ice packs to ease the pain/itching and using way too Clobetasol. Dapsone is also very good for dermatitis herpetiformis (and it is generic). It helped me and the results were immediate but it gave me severe anemia so the Dupixent is better for me. Not sure if it works for everyone. I cannot help with the cause of your stress but from experience I am sure the severe stress is making the celiac and dermatitis herpetiformis worse. Very difficult for you with having children to care for and you being so sick. Would this man be willing to see a family therapist with you? He may be angry at you or imagine that your illness is a psychosomatic excuse not to take care of him. A therapist might help even if he won't go with you. Also do you have any family that you could move in with (with the kids) for a short time to get away? A break may be good for you both.
    • knitty kitty
      @tiffanygosci, Thiamine deficiency is a thing in pregnancy for "normal" people, so it's exponentially more important for those with celiac disease and malabsorption issues. I studied nutrition before earning a degree in Microbiology because I was curious what the vitamins were doing inside the body.  See my blog.  Click on my name to go to my page, scroll to drop down menu "activities" and select blog.   So glad you're motivated to see the dietician!  We're always happy to help with questions.  Keep us posted on your progress! 
    • tiffanygosci
      Thank you for sharing all of this, Knitty Kitty! I did just want someone to share some commonality with. I did not know This one Deficiency was a thing and that it's common for Celiac Disease. It makes sense since this is a disorder that causes malabsorption. I will have to keep this in mind for my next appointments. You also just spurred me on to make that Dietician appointment. There's a lot of information online but I do need to see a professional. There is too much to juggle on my own with this condition.<3
    • RMJ
      I think your initial idea, eat gluten and be tested, was excellent. Now you have fear of that testing, but isn’t there also a fear each time you eat gluten that you’re injuring your body? Possibly affecting future fertility, bone health and more? Wouldn’t it be better to know for sure one way or the other? If you test negative, then you celebrate and get tested occasionally to make sure the tests don’t turn positive again. If you test positive, of course the recommendation from me and others is to stop gluten entirely.  But if you’re unable to convince yourself to do that, could a positive test at least convince you to minimize your gluten consumption?  Immune reactions are generally what is called dose response, the bigger the dose, the bigger the response (in this case, damage to your intestines and body). So while I am NOT saying you should eat any gluten with a positive test, the less the better.  
×
×
  • 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.