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

How Long Do Waves Of Fatigue Continue?


hopefulinmybody

Recommended Posts

hopefulinmybody Apprentice

Hi Everyone,

I'm starting to feel concerned and thought I would reach out to this great community for a perspective.

I got my biopsy dx of moderate to severe damage (celiac sprue) 12 weeks ago and have been gluten-free since.

I also went gluten-free for two months after testing positive on my blood tests, and that time I felt pretty good after three weeks and my energy was consistent.

This time (after the five-week gluten challenge and biopsy) I am still not able to exercise and every week or ten days I have about three days where I am exhausted and even typing (like now) feels tiring. I feel so tired I just want to stay on the couch. My muscles ache. I thought this was normal celiac recovery and then I went to a tango lesson today (couldn't cancel at late notice) and explained I was low energy. After hearing me describe my fatigue the teacher asked if I had been tested for lupus--then I freaked out thinking, I don't want to have something else on top of celiac. Flares of fatigue seem to be a chief symptom of lupus.

So my question is, Is this normal during the healing process of celiac to have these "flares of fatigue"? I would say that generally I feel at about 70% of my normal, pre-celiac energy then I have these flare days that are two-three days in a row when I am at 30%. I can still do the basics of daily living but don't want to do much else.

I am going to do a blood test tomorrow to check my IGG/IGA antibodies to determine whether I am still eating gluten and have an appt. set up with my primary care doctor Monday to ask about testing for other things. Is this common (or not uncommon) to feel so tired 2-3 days in a row during recovery?


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



Celiac.com Sponsor (A8-M):



domesticactivist Collaborator

I wonder if you are still getting cross-contaminated? You mention waves of fatigue which makes me think maybe you are periodically getting glutened. I made a post on how to really go gluten-free. Maybe it'll be helpful in getting you thinking of potential sources of cross-contamination.

cahill Collaborator

Have you had your thyroid tested??

When I had ANA testing done I came back moderately positive but negotiate for lupus. My hashimoto antibodys were thur the roof.(998.75 with a range of <10.10 being normal )

hopefulinmybody Apprentice

Hi! Thanks for these ideas.

As far as cross-contamination goes, it's possible and I hope that I will find out as as a result of the blood test this morning. I am *so* careful already. I can only wonder, is it the cheaper possibly gluten-containing Whole Foods conditioner I bought so I didn't spend $10 on a gluten-free version? Beans and rice from a 99% gluten-free raw foods restaurant? It's hard to imagine. I moved into my own place a month ago so the kitchen was bare but maybe I didn't clean it thoroughly enough? I will take everything out to clean it again.

The Hashimoto idea I will mention to my doctor when I see him Monday. Any other ideas appreciated, I will present him with a list of things to test drawing on the wisdom of the celiac crowd. :)

Skylark Collaborator

Have you had your thyroid tested??

When I had ANA testing done I came back moderately positive but negotiate for lupus. My hashimoto antibodys were thur the roof.(998.75 with a range of <10.10 being normal )

This. You sound hypothyroid, hopeful. It is extremely common in celiacs. Hypothyroid can cause abnormal response to exercise and fatigue. Are you cold, skin dry, hair dry or even falling out, mind foggy or forgetful? Those are other symptoms.

...and before you posted I thought my 432 Hashi's antibodies was through the roof. Turns out I'm only halfway up the elevator! :lol:

Kim69 Apprentice

I am really tired too. And have ruled out thyroid problems. I too am thinking of lupus and want to get ANA test done I got it done 1 yr ago which was 1:80 speckled. It wasnt followed up and apparently with lupus it can fluctuate. Will let you know how I go over the next few weeks - I am getting tested for SIBO and candida (for gas and diarrhea). My Coeliac blood tests are normal and so are hormones, iron, zinc but vit d is a tiny bit low but I suspect that it wouldn't cause problems. Am trying to cover many bases!

maximoo Enthusiast

have your iron and vit D levels chkd if you already haven't.


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



Celiac.com Sponsor (A8-M):



hopefulinmybody Apprentice

have your iron and vit D levels chkd if you already haven't.

Thanks for these additional ideas. I am still not sure what is going on . . . Since I posted I have seen my doctor and had some good days and then bad days again for the last four days.

I got my gluten antibody results. My IGG is 1.04 with a standard range being less than .9 and my IGA is 2.04 with a standard range being less than .9. Initially (when I first tested positive before going gluten-free) my IGA antibodies were 6x the normal range. And now they are 2x. And the IGG was initially 2x and is now almost normal. My gastroenterologist said this is an excellent result and that most celiacs do not return to the normal antibody range for whatever reason. I hadn't heard that before. Has anyone else heard this? When I saw the results I thought they indicated I was still getting gluten, but according to him I am doing well.

My primary care doctor said I don't have lupus. Or fibromyalgia or CFS. He says my thyroid is normal but I am looking and seeing that he only tested for TSH in November, and not T3 and T4. I am wondering if drilling down is necessary to understand if I am hypothyroid, as someone suggested. I get the sense that he is annoyed with me and he acts like I am wasting his time. Somehow the ideas is that once Western medicine provided an answer for why I was feeling so bad (celiac) but that doesn't mean it always will. His recommendation was to wait a month and then see how I feel (it has been three months gluten-free now) and then check in. No one really has an explanation for why I feel so tired half the time and my only bottomline steps now are the following:

--reduce the amount I am doing and rest more

--throw out the old mesh wire colander and get a new one (I realized this may be a source of CC)

--get gluten-free conditioner (I lapsed on that one and bought a cheaper kind, but hey, I'll try anything now)

--get a new doctor (I moved and am thinking to get a new one is closer who seems more open to talking this through and figuring out what is going on. . . )

--write down asbolutely everything I consume now in a phone-based journal along with my symptoms

I am hopeful and also quite tired by this--it is hard to be so vigilant and keep working on all of this when the condition is making you tired to begin with. I really want to just feel great. When I went for two months gluten-free in Argentina I actually did feel good consistently and I just want to feel that way again!!!

MUCH MUCH THANKS! This community is quite stellar.

--

hopefulinmybody Apprentice

I decided after writing this post to try once more with my current doctor by writing him an email listing the things I would like to be tested for. I'm going to research this but also thought I would ask if anyone else has any other ideas. I know for starters that although my TSH is good years ago either T3 or T4 was way low, so I will mention this for one. Thanks!

dilettantesteph Collaborator

It's possible that you are a super sensitive celiac. You could try cutting out the processed foods for a couple of weeks to see if that makes a difference. Eat just produce and meat. Skip anything processed, even oil and spices, don't eat in restaurants, and see what happens. If it works, then add things back one per week and see what is causing your reactions.

Lori2 Contributor

I am hopeful and also quite tired by this--it is hard to be so vigilant and keep working on all of this when the condition is making you tired to begin with. I really want to just feel great. When I went for two months gluten-free in Argentina I actually did feel good consistently and I just want to feel that way again!!!

It seems like I have been working on this for months and the progress is slow. However, I have had a few GOOD days--really good--enough to know what it feels like. I WANT MORE and I won't quit until I get it.

bartfull Rising Star

"Waves of fatigue" is exactly how I described it to a friend the other day. She suggested I load up on protein early in the day, and don't eat anything sweet (including fruit and carrots) until after supper. I tried it and it works! It seems every time I would eat something sweet, my sugar would spike, then fall rapidly, leaving me so tired I needed to go lie down. Since she told me that though, I have much more energy. And on top of that, about twenty minutes after I eat something sweet, I can go to bed and get a good night's sleep - no small feat for someone who has suffered from insomnia for years!

hopefulinmybody Apprentice

Interesting. I will look into elimination diets and doing just meet and veggies (or almost only, whatever I can manage). I did feel better when I was eating more broccoli. I also have the intuition that I need red meat and chicken. I relate so much to the others who are dealing with the ups and downs of energy. I asked God today in the kitchen to jut let me feel well again. It's so hard to feel like a broken record in your head thinking about all this. I told God I will take advantage of every opportunity to enjoy life and help others if I can feel consistent normal energy again!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,948
    • Most Online (within 30 mins)
      7,748

    Stephanie94
    Newest Member
    Stephanie94
    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

    • 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
    • DebJ14
×
×
  • 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.