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

Desperate For Answers Feeling Worse Almost One Month Later


rene83

Recommended Posts

rene83 Rookie

Good evening everyone I'm coming to you hoping for some shredded insight as to what I'm experiencing. I was diagnosed with celiac disease almost one month ago I quit gluten cold turkey and have progressively started feeling worse and worse and worse to the point that I cannot function. I was a silent celiac with none of the typical symptoms it was a fluke that we found out after I went into my physician complaining of weight gain and chronic fatigue. Since I went gluten-free I've been going through the worst withdrawals. I have been exhausted to the point I cannot function I am now having diarrhea I've been having constant headaches have been completely unable to sleep and have been so weak that I can hardly stand long enough to take a shower.

My physician has me on a plethora of supplements including multivitamins digestive enzymes and amino acids to try to bolster my already depleted system but nothing is helping.

I'm so upset that I'm almost one month in and feeling physically and mentally worse than I have ever felt in my life. I honestly want to just go eat a big old loaf of bread and hope that I will at least go back to feeling normal. I felt crummy to begin with but I feel absolutely horrific now. From everything that I've been told and have read I should be starting to feel better now does anyone else have experience with this?

I'm sorry that I'm unloading I just reached a breaking point mentally between how crummy I feel and how little I can function. I also apologize if there are any typos or weirdness in my words is I've been using my voice recognition from my phone and I may not have caught the errors when I proofread.


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

You are not alone!  Those with more experience can probably contribute more, but here's my two cents.  Just had Hashimoto's and anemia when I went for a routine colonoscopy.  Blood test positive.  Ate gluten for the next six weeks like a mad person (e.g. loaf of sourdough per day).  Ended up with abdominal symptoms.  Went gluten-free the day of my endoscopy.  Felt bad for about six to seven  weeks.   Not just abdominal symptoms but anxiety too.   Worried that I'd continue to get worse.  But suddenly I was much better!  Abdominal symptoms only appear when I have been glutened.  Found that I can not tolerate quinoa or gluten-free oats.  Working on the anemia and my whacked out thyroid.  Mentally, I'm pretty calm now.  Of course there's that menopausal thing going on but I can handle it.  Reduced my work load but just saying "no".  

 

Road my bike today for 45 miles and came back tired but not exhausted!  It just takes time!  Hang in there!

rene83 Rookie

Thanks. I am an absolute mess I've been very careful to make sure I did not get glutened. I don't understand why I am so much worse when I should be getting better

shadowicewolf Proficient

Withdrawl. That is probably part of what is making you feel so bad. Gluten is addicting.

 

Its only been a month. Give it some time.

rene83 Rookie

Is withdrawal normally this bad?! I literally cannot function between the brain fog the horrible weakness in the dizziness I feel like death

Dugudugu Rookie

Yes, the withdrawel can be this bad.

Hang in there pal! Everything is going to be alright.

rene83 Rookie

Holy hell. How much longer should I expect this to last? I seriously asked my physician to put me in a medically induced coma until all of this passed LOL


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

(hugs) You definitely got the short end of the stick when it comes to withdrawal.... a month is a long time.

 

My withdrawal lasted over 2 weeks. I think at 3 weeks it was starting to lighten up a bit. The migraine lasted 10 days, non stop... I still remember that one - it was a doozey.  The fatigue goes with it all. I remember feeling like my get up and go had just gone. I wasn't extra sleepy but I didn't want to move, just sit... alone.

 

Withdrawal will pass. I've heard it can take some up to a couple of months for their body to adjust.  I have also heard that once gluten is gone, other problems can rear their heads - it's almost like it sees it's chance to make you miserable and goes for it. If it lasts a lot longer (past 2 months), you might want to look into other causes like thyroid issues and nutritional deficiencies.

 

I hope the worst is almost over for you!

1desperateladysaved Proficient

My withdrawal lasted at least 3 months.  I think it kept extending when I continuously removed other foods that were causing problems. I also had cross contamination and silly mistakes.   I did have some better days during those few months, but did feel like death was coming, or like I needed to start all over again, on the bad days.

 

I discovered, during that time, that my lowest lows were often followed by the highest highs.  When I felt like I was dying I simply decided to hang on for the next day.  I made it each time.  Many times the next day was better, but sometimes it took another day.

 

I consider taking away gluten a natural way of dealing with celiac.  It is not drugs or surgery.  In many years of trying to heal naturally I learned that for me, "Any reaction is a good reaction."  A reaction means your body is still fighting.  It realizes a change.  Hang on and ride it.  Take some down time when you can.  It is a strain for the body to recover, but it is doing it.

 

I hope you will feel clear headed and stronger soon.

Diana

rene83 Rookie

I wish I had good days. So far I've felt worse each and every day that passes.

Jash Newbie

Hi Rene,

 

I’ve also had some unexpected symptoms going off gluten. Not much happened initially. But after a few days I thought I might be getting a little more energy and mental clarity. Oddly, a 15min bike ride caused me to have stiff-muscle pain, as if I’d worked out like hell. I bike everyday and that doesn’t normally happen. The same happened for other body parts doing other routine exercises. However now, rather than taking 4-5 days to recover as it did prior to going gluten-free, it took only a day. I do FEEL stronger, but, when I actually tested that, it turned out that I was weaker (couldn’t lift as much). It may be noteworthy that for my size I’ve been quite strong my entire life and massage therapists more than once have remarked how my muscles seemed to be in a constant state of exertion. I’ve had intense cravings at times as well, but not for gluten foods per se. Finally at about the 2-month mark I had my first ‘normal’ bowel movement in about 20 years and I feel pretty good but I’m even more exhausted in the morning than normal. Two other peculiar things have happened. I suddenly developed an allergy to hazelnuts and have had all the blood vessels in one of my knuckles break when I was holding something heavy for a few minutes.

 

So this is my take. I think the feeling of being stronger may be due to reduced inflammation and being better able to feel the difference between relaxed/contracted muscles. If the primary response to gluten is an immune/inflammatory response than likely my whole system has been activated and inflamed forever. I wonder if it’s possible that the inflamed state was actually helping maintain a certain level of muscle tone which has now been removed, leading to more normal recovery times but to less demanding workouts. If the immune system was never able to disengage that may explain why it couldn’t respond to hazelnuts before. Or, it’s still in overactive mode but doesn’t have gluten to attack.

 

In any illness symptoms likely build upon each other. As one system becomes incapacitated it causes stress on another system, etc. So when the problem is removed there could be numerous things that need to be rebalanced to reach ‘normality’ again. The friend who told me about the test I took said she felt a bit better in 3 weeks but it wasn’t until 6-8 months that she really felt it. She says she’s never felt that good in her entire life. Hang in there Rene, the fatigue could actually be a positive sign, of recovery. And mood is extremely sensitive to energy levels. Drink A LOT to help speed the recovery and be sure to check that you’re not deficient in something else now, as a result of not eating all the things you used to eat. 

taynichaf Contributor

Good evening everyone I'm coming to you hoping for some shredded insight as to what I'm experiencing. I was diagnosed with celiac disease almost one month ago I quit gluten cold turkey and have progressively started feeling worse and worse and worse to the point that I cannot function. I was a silent celiac with none of the typical symptoms it was a fluke that we found out after I went into my physician complaining of weight gain and chronic fatigue. Since I went gluten-free I've been going through the worst withdrawals. I have been exhausted to the point I cannot function I am now having diarrhea I've been having constant headaches have been completely unable to sleep and have been so weak that I can hardly stand long enough to take a shower.

My physician has me on a plethora of supplements including multivitamins digestive enzymes and amino acids to try to bolster my already depleted system but nothing is helping.

I'm so upset that I'm almost one month in and feeling physically and mentally worse than I have ever felt in my life. I honestly want to just go eat a big old loaf of bread and hope that I will at least go back to feeling normal. I felt crummy to begin with but I feel absolutely horrific now. From everything that I've been told and have read I should be starting to feel better now does anyone else have experience with this?

I'm sorry that I'm unloading I just reached a breaking point mentally between how crummy I feel and how little I can function. I also apologize if there are any typos or weirdness in my words is I've been using my voice recognition from my phone and I may not have caught the errors when I proofread.

This scares me... I am the same way when I stop eating gluten... I'm tired and a mess when I'm eating it, and then once I stop i'm exhausted, but I can usually sleep very well, but I also need to take constant naps to get through the day.. Plus go to bed at around 7ish. I ve only been gluten free for about 2 weeks though, so i'm afraid that one month gluten free will make me feel as crappy as you :(

 

One thing, maybe you have another food intolerance? Some celiac members suggested that I get my thyroid tested and something about hypoglycemia.. Maybe you should do the same?

 

 

 

So sorry that your going through this!

pricklypear1971 Community Regular

Are you eating enough? I know in the beginning I didn't - because it was hard to identify safe foods....

And your body is healing, despite how crappy you feel...and that takes energy. Or, I should say, it's changing.

Good luck. I know it's difficult and scary.

rene83 Rookie

I haven't been eating enough. Can't stand long enough to cook anything and the diarrhea makes me not want to eat.

On a positive note it looks like some of my symptoms are bad reactions of one or more of the dozen supplements my dr prescribed. So I'm feeling a little better now that I dc'ed those and am figuring out what's making me sick

nvsmom Community Regular

:) Good! perhaps this is that corner which will make all the difference.

Fire Fairy Enthusiast

My two cents. You could be having other food issues due to silent damage done to your digestive tract. If it doesn't get better soon you might try an elimination diet. For me Dairy, Egg and Soy had to eliminated. I was lucky in that I was able to add them back after two years. Dairy and egg went straight through my colon and took everything with them for days afterward. Soy made my flight or fight response go into overdrive. There are several other foods that could be issues so you really might want to try an elimination diet.  

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.