Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Trying To Figure Out My Sleep Problem


covsooze

Recommended Posts

covsooze Enthusiast

I'm going to the GP on Friday to discuss my tiredness and sleep problem. I know there's probably more than one thing going on here (eg anemia/ hypothyroid may well be contributing to the tiredness), but I want to get to the bottom of my sleep problem.

I've never slept particularly brilliantly, usually waking up once or twice a night, but in the past couple of years, its become much worse. This has happened with the general onset of my coeliac symptoms, although hasn't imporved since going gluten-free 6 mths ago. I don't think it's gluten keeping me awake.

I generally don't have probs going to sleep, I just wake up and/or surface lots of times in the night, resulting in me feeling exhausted. It doesn't help that if I wake up I then feel like I need a pee. I can often pee quite a bit at night, but I don't think it's that that disturbs my sleep.

Sometimes I have difficulties falling to sleep as my legs are restless. I've never been formally diagnosed with RLS. When I wake up in the night, i'm rarely aware of my legs, so don't know if it could be that :unsure:

I've got a bad back which has plagued me on and off, but it doesn't explain why I wake up so many times each night.

I've been on anti depressants for the last year, but my psych doesn't think my sleep probs are emotional/ mental and I agree.

So I'm wondering, could it be RLS? Other food intolerances????

Any thoughts would be really appreciated as I can't imagine my GP getting very far with this :rolleyes:

Susie x


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



Celiac.com Sponsor (A8-M):



BRUMI1968 Collaborator

A few things come to mind:

1. what are the meds? Often they have side effects of insomnia, and even your GP can't keep track of all the side effects of all the meds s/he prescribes.

2. are you drinking liquids past 7pm? are any of them caffeinated? do you drink caffeine at all? do you eat late?

3. in "eastern" medicine, WHEN you cant' sleep is as important in determining WHY you can't sleep. In other words, folks who wake up between 1 and 3 might have liver troubles, whereas someone who can't fall asleep well may have spleen troubles. It might be worth looking into.

4. weird noises. weird light.

5. can you breath well through your nose - or do you get stuff in the night.

covsooze Enthusiast

Hi Bully4you :)

The meds are cipralex (your brand in the US is lexapro). I've just read Lisa's thread about her side effects of coming off lexapro and CDFamily posted on there about the effects lexapro can have on sleep. I never knew that - maybe that's a big contributing factor.

I generally only drink water. If I do have caffeine it will be max one cup a day of tea and no later than 3pm. i do drink water after 7pm as I get so very thirsty all the time. It makes me feel thirsty just thinking about it (it's 9.30pm here).

As for the times I wake up, it probably is mostly the early hours :unsure:

Weird noises and light....well there are the martians next door come to think of it :P

I often have a stuffed up nose, day or night coz of my allergies. A few weeks ago I bought a new allergy friendly pillow and pillow protector and it does help with the sneezles somewhat....I don't think it's that that's always waking me up though.

Will research lexapro more

Guest cassidy

It very well could be RLS. Most people with RLS go to the doctor for sleep problems. 10% of the population has RLS but it is often undiagnosed. Hopefully, your doctor knows about it and can help you.

Lymetoo Contributor

I used to wake up all the time and then I would have to pee. Well, I later began having trouble with frequency during the day and was finally dxd with IC, Interstitial Cystitis.

What I'm saying is that it COULD be the bladder waking you up.

RLS is another possibility, that's for sure. I hope your dr can help!!

sspitzer5 Apprentice

Hi Susie,

The same thing happens to me with sleep. I wake up so many times and I don't have to pee, so I don't think that's it for me. It's usually happens between 2 am and 6 am. Drives me nuts. Would love to have an answer for this. One doc said it was my adrenals being stressed and weak.

S

  • 2 weeks later...
cottonwoodian Newbie
I'm going to the GP on Friday to discuss my tiredness and sleep problem. I know there's probably more than one thing going on here (eg anemia/ hypothyroid may well be contributing to the tiredness), but I want to get to the bottom of my sleep problem.

I've never slept particularly brilliantly, usually waking up once or twice a night, but in the past couple of years, its become much worse. This has happened with the general onset of my coeliac symptoms, although hasn't imporved since going gluten-free 6 mths ago. I don't think it's gluten keeping me awake.

I generally don't have probs going to sleep, I just wake up and/or surface lots of times in the night, resulting in me feeling exhausted. It doesn't help that if I wake up I then feel like I need a pee. I can often pee quite a bit at night, but I don't think it's that that disturbs my sleep.

Sometimes I have difficulties falling to sleep as my legs are restless. I've never been formally diagnosed with RLS. When I wake up in the night, i'm rarely aware of my legs, so don't know if it could be that :unsure:

I've got a bad back which has plagued me on and off, but it doesn't explain why I wake up so many times each night.

I've been on anti depressants for the last year, but my psych doesn't think my sleep probs are emotional/ mental and I agree.

So I'm wondering, could it be RLS? Other food intolerances????

Any thoughts would be really appreciated as I can't imagine my GP getting very far with this :rolleyes:

Susie x

I was diagnosed after my primary care doctor sent me to a sleep specialists. That was eight years ago. I am now under his care with a cpac mahine for assisted breathing at night. The sleep test is an overnight stay at a local hospital or lab. They are becoming more commen even in small communities.

They check not only for sleep apnea, but for any conditions which may disturbing your good nights sleep.

Best wishes for your improvement. :D


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



Celiac.com Sponsor (A8-M):



wozzy Apprentice

Do a sleep study.

I did one...they said I have sleep apnea, which I would have never expected because I'm not fat and I don't snore. During my sleep test, I fell asleep in 7 minutes and I didn't go into REM sleep, which makes them think I have narcolepsy. I also had over 8 arousals per hour, which is a lot. Now I'm fighting my insurance company to cover the narcolepsy test.

They gave me a CPAP, but I pull it off in my sleep every night, so it's not helping.

I had mono last fall but the blood test says it's gone. I'm getting an ultrasound of my gallbladder next week because I get throbbing pains there sometimes. I'm also seeing an ENT to see if he can help with my congestion/sleep issue. And I'm trying to take the narcolepsy test...there are milder forms of it.

  • 4 months later...
kiwifruta Newbie

Hi. I had exactly the same problem, always waking up during the night and therefore not being alert during the day. I cured it by taking vitamin B supplements and making sure I got regular exercise.

Those with coeliac disease have an extra demand for the B vitamins (1). Whether we just don't utilise them well or just use a lot I don't know. If we don't get enough B vitamins we can get a bit anxious (well I do anyway). I have found that B complexes with B12 seem to more beneficial.

I recommend taking a vitamin B complex, consuming 100mg of vitamin B6 a day to start off with and then adjust as necessary.

all the best

Dwayne

(1) this is according to Adelle Davis, google her or search amazon for more information.

TestyTommy Rookie

I agree that B vitamins (esp B6) are important, but consider thay you might be dehydrated. I had exactly the same problem: wake up after a few hours sleep, feeling like I had to urinate, but not thinking that was the problem. I even tried not drinking for a few hours before bed, but that just made me wake up earlier.

What 'worked' to some extent was getting up as soon as I woke up, going to the bathroom, and then drinking a glass or two of water. I was usually able to fall back asleep quickly. It was sleep in 2-3 hour increments, but it was better than not sleeping.

A lot of celiacs experience an increased need for water (check some of the other threads; there are quite a few about drinking water). Going gluten-free had helped, but I'm still drinking way more than healthy people.

It's worth a try --- drinking water is easy and doesn't cost anything!

plantime Contributor

Dwayne is right about the B vitamins. I use a liquid SuperB Complex in my cran-grape juice 1/2 hour before bedtime. That is also when I take my Lexapro. When you take the Lexapro is important, even though the pharmacist might say it is not. I start falling asleep about 1/2 hour after taking it, so I take it at bedtime.

When I had my sleep test done, the doctor explained that in sleeping, the first few hours are the deepest, then sleep starts to get lighter, which allows for easier interruption. This lighter sleep is when most people rouse out completely, having wake cycles. Once I learned that this is normal, I stopped fretting over how many times I wake up each night. Once I stopped fretting, I stopped feeling tired all day. I was amazed at how much better I felt when I stopped worrying about how many times I woke up during the night.

kiwifruta Newbie

TestyTommy Thanks for the information about the extra demand for water that coeliacs need. I didn't know about that, a new thing for me to google.

How are you guys with tree nuts and whole corn pieces?

Tree nuts bloat me up.

Ground corn is fine but if I have whole pieces of corn the next day my upper back is sore.

chau

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. - RMJ replied to Rhenriksen's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      8

      Just diagnosed with Celiac! Scared and feel alone.

    2. - trents replied to Iris Kraft's topic in Gluten-Free Foods, Products, Shopping & Medications
      15

      Inhaler problem

    3. - Ann13 replied to Iris Kraft's topic in Gluten-Free Foods, Products, Shopping & Medications
      15

      Inhaler problem

    4. - trents replied to Iris Kraft's topic in Gluten-Free Foods, Products, Shopping & Medications
      15

      Inhaler problem

    5. - Ann13 replied to Iris Kraft's topic in Gluten-Free Foods, Products, Shopping & Medications
      15

      Inhaler problem


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,826
    • Most Online (within 30 mins)
      7,748

    Krista Q.
    Newest Member
    Krista Q.
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      71.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • RMJ
      If your celiac antibody tests are still positive that may explain the ongoing symptoms.  You might examine your diet and try to get those tests in the normal range before doing something like an MRI or CT scan.  It took me almost six years to get all of my antibody tests in the normal range.  At first I thought I was eating gluten free by avoiding wheat, rye and barley in the ingredient list.  Then I made sure foods were labeled gluten free, one antibody was still positive.  Now if I eat processed foods I buy certified gluten free or foods labeled gluten free from companies with good reputations in the celiac community. 
    • trents
      @Ann13, thanks for the clarification. I think I understand your point now. Yes, I realize gluten can produce non Gi Reactions. Let us know if you find out that there is gluten in these inhalers. I have my doubts but gluten does show up in strange places. It could also be manufacturer dependent of these inhaler products are generic.
    • Ann13
      Not everyone will be allergic to whatever they're using in food. There is another forum re people who are posting they have vocal cord & throat issues after they eat breads & pastas which stopped after they removed those foods from their diets. Same as me...gluten doesn't react as gastrointestinal it reacts orally. Which is why I'm saying ensure all your food isn't what you're having a reaction to.  ...& I used Cornflakes as an example because some gluten free people would assume it's gluten free but if they're allergic to barley they will have a reaction...nothing to do with their inhaler.  You're missing my points a lot & frustrating so I'm done commenting. You really need to ensure your food isn't what's causing the issue. I am checking with symbicort manufacturer to check their ingredients.  Good bye... I'm done with this. 
    • trents
      I certainly agree with all that. However, you also mentioned cornflakes with barley malt but that would obviously not be gluten free since barley is a gluten-containing grain. And the chemicals they spray on grains would affect everyone, not just those with gluten disorders. I'm just trying to figure out what this thread has to do with the main subject this online community is focused on. Is the point of this thread that having a gluten disorder makes someone more susceptible to reacting adversely to inhalers? That could be but it may have nothing to do with the inhaler having gluten. It could have to do with, say, having higher systemic yeast counts because the celiac community generally suffers from gut dysbiosis. So it would be easier for celiacs using inhalers to develop thrush.
    • Ann13
      Re food,  I said the gluten free thing isn't necessarily about gluten itself, but chemical sprays they use on GRAINS which cause allergic throat & vocal cord issues regardless of the inhaler you're using.  Your issue may not be the inhaler but eating gluten free food that still will bother you because they have been sprayed with certain chemicals. Barley & oats cause vocal and throat issues with me as well as gluten free flours. We didn't have gluten issues in the world yrs ago...the food changed somehow or they're using sprays that cause reactions in some people.  Re inhaler: Symbicort is registered as gluten free but companies can change their ingredients at any time so you may want to check with the company who makes it and get an ingredient list.  I don't believe I'm reacting to the inhaler...I believe it's a gluten free pasta I've been eating so I'm taking it out of my diet. I've used the inhaler for over 1 year and no problems up until now so I suspect it's the pasta. 
×
×
  • Create New...