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

Normalizing Sleep Patterns?


BlessedMommy

Recommended Posts

BlessedMommy Rising Star

I've often had trouble wanting to go to sleep at the correct time. I have noticed though lately that I'm consistently feeling tired at the appropriate time and am having a much easier time going to bed--I don't have to force myself so much to get to bed.

It makes me wonder if this is symptom resolution or if it's just a side effect of me getting older and more tired. LOL! At any rate, I'm sleeping better and also have an easier time being up and alert at the appropriate time.

Can gluten issues cause problems with sleep and circadian rhythm?


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

.....wait until perimenopause hits....then all bets are off!

Seriously, I started sleeping poorly due to hormonal shifts. Waking up to night sweats. I still wake up with a flash, but now it is a feeling of impending doom -- no not doom, but that something is coming and instantly I am roasting. No sweating though. Used to have to change my nightgown and I slept on beach towels. Things are improving!

I am on the menopause side now, but still getting flashes. I work with older ladies and they report still getting them in their 80's!

There are so many issues with celiac disease, that I do not doubt that it impacts sleep patterns.

bartfull Rising Star

My sleep has improved tremendously on the gluten-free diet! I had terrible insomnia before and although it did get worse during menopause I had it long before that. Now I sleep like a baby. I'm usually in bed by eight o'clock and up at four. (Yeah, I know that sounds crazy but if I want to get anything done it has to be in the morning before I go in and open the shop.)

sweetsailing Apprentice

I have never, like never, been a morning person by any stretch of the imagination.  Now I have never had trouble sleeping, in fact, one could argue that I sleep too much!  Since being gluten free for over a year now, I am suddenly becoming a morning person.  I wake up spontaneously with the sun (no alarm clock) and I am refreshed and ready for the day.  Literally all my life, I never understood people who woke up before 11 am. LOL :D   Symptom resolution?....perhaps

julissa Explorer

I'm past menopause, and my issues are that I go to sleep with no problem at an appropriate time, but I get up somewhere around 3 AM and can't get back to sleep for hours, sometimes not until I am almost due to wake up. this really affects my days. I was always a great sleeper in my younger days, but now, it's a problem. things are no different than when I ate gluten. 

Serielda Enthusiast

I can agree with the  hormonal issues  very much so post  hysterectomy in 2011, I thought i was doomed to be an insomniac for the rest of my life. But that over time  tonned down, now I have issues if I eat a lot of  photoestorgenic foods. Now when I first started my  journey of gluten free, I had some wicked sleep issues, and once in a while I still do.  Most of my issues  was stressors e.g. people bungee jumping on my one last little nerve.  Now something I have noticed after some  experimentation of me wanting to debunk the study, is  that watching T.V before bed or using a tablet and cellphone before bed causing you  sleep cycles to be  a bit screwy. I stopped putting my phone by the bed and moved it across the room, and don't use my laptop or  watch tv before bed and noted I feel like I am getting better rest, but it is way to early for me to tell. Plus the data samples in  the  sleep study done on   tablets and electronics before bed was seriously under what a standard sample should be. The laws of  standard normal and the centeral limit therom state anything lower than 30 (Open Original Shared Link There may be a bit of truth to the blue light emission from  those devices causing problelms. 

I do know the few times since  diagnosis that I was glutened by  freak accidents my sleep was  craptastic , so unless an unknown ingestion of gluten, it might and i mean a minute  chance  it could be   electronics  causing it. However I would  look to see if there was subliminal  stressors going on.

Glutenbola Newbie

I was recently diagnosed with Celiac disease and I haven't quite started the diet yet. I'm going to start this weekend by slowly going into it. Recently I've been noticing that I've been going to bed later and I've been waking up earlier when I used to not do that. I am extremely tired throughout the day. But, I cannot go to sleep at night. I will be up until 4 o'clock in the morning sometimes just laying there. I'm in high school still so I don't really take medicine for it. I'm not sure if this is related to my diagnosis, since I haven't really started my diet yet, but if it is can someone please let me know so I can talk to my doctor about it? I just found this website today and I'm loving it I feel so informed now and, I feel that there are so many more people out there with this disease that, I didn't even know of. It shows me that I'm not the only one in that this disease can be common and that there are other people out there going through what I'm going through. The diagnosis was hard on me because I'm still in high school so, I have a lot of free time and, that free time I used to spend with my friends and at school I eat the school lunches which now I won't be able to do that. So this transition is going to be hard on me but with this forums help I feel like I can get through it. Thank you everyone.


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

I was recently diagnosed with Celiac disease and I haven't quite started the diet yet. I'm going to start this weekend by slowly going into it. Recently I've been noticing that I've been going to bed later and I've been waking up earlier when I used to not do that. I am extremely tired throughout the day. But, I cannot go to sleep at night. I will be up until 4 o'clock in the morning sometimes just laying there. I'm in high school still so I don't really take medicine for it. I'm not sure if this is related to my diagnosis, since I haven't really started my diet yet, but if it is can someone please let me know so I can talk to my doctor about it? I just found this website today and I'm loving it I feel so informed now and, I feel that there are so many more people out there with this disease that, I didn't even know of. It shows me that I'm not the only one in that this disease can be common and that there are other people out there going through what I'm going through. The diagnosis was hard on me because I'm still in high school so, I have a lot of free time and, that free time I used to spend with my friends and at school I eat the school lunches which now I won't be able to do that. So this transition is going to be hard on me but with this forums help I feel like I can get through it. Thank you everyone.

Welcome to the board.  :)

Give yourself a lot of time for symptoms to normalize.  It can take many months to recover.

 

My sleep problem was sleepiness. I had a tough time staying awake past 9:00. If I was working out, I was in bed shortly after 8:00!  LOL  Now I can actually stay awake until 11:00 or so if there is a show I want to see.  I can actually stay awake for a New Year countdown.  It took over a year to get to that point though.

Glutenbola Newbie

That's awesome !! I'm so glad you're finally happy with that. ☺️ Thanks for the help!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,945
    • Most Online (within 30 mins)
      7,748

    Miyasato
    Newest Member
    Miyasato
    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.