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

Has This Happend To You

cat3883

Recommended Posts

cat3883 Explorer
cat3883
Posted

I am 6 days gluten free. I must say my brain fog is better but I am having trouble sleeping. I go to sleep rather easy but I am waking up around 4 or 5 am the last few mornings a cant go back to sleep. I must say one of my main symptoms of celiac disease was fatigue as I could and would sleep about 12 to 14 hours a day. Please tell me this gets better!! But on a good note I have been told by a few people that I have more coloring in my face.

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

Celiac.com Sponsor (A8-M):


ShayFL Enthusiast
ShayFL
Posted

Yes it does get better. In the early days I was waking up that early because I was "starving". I ate like crazy for the first 6 weeks. My body was playing catch up. I sleep great now!

lisa25 Rookie
lisa25
Posted
Yes it does get better. In the early days I was waking up that early because I was "starving". I ate like crazy for the first 6 weeks. My body was playing catch up. I sleep great now!

Shay,

Kind of off track from the original post, but I saw that you recently became corn free, grain free...etc. What made you decide to do this? Did you get tested? I have been tested through enterolab and came back positive for gluten, dairy, and soy. I am wondering if there are more things since the test only included gluten, dairy, soy, egg, and yeast. I have been feeling better, but not all the way better. I still take excedrine several times a week, still get really tired, still feel nauseas some of the time.

ShayFL Enthusiast
ShayFL
Posted

Over time you just realize what bothers you and you cut them out. I have been corn free for years. It always bothered me. I recently tried adding some back in. It still affects my blood sugar but no other symptoms. I am trying to keep my BS stable, so I wont eat it often...hardly ever...if at all. I dont need it in my diet. I cut out the grains because in general I do not tolerate starchy carbs very well. It really messes with my BS and I get digestive symptoms. The SCD diet is what I eventually adopted because it is what I am basically eating/not eating anyway.

ravenwoodglass Mentor
ravenwoodglass
Posted
I am 6 days gluten free. I must say my brain fog is better but I am having trouble sleeping. I go to sleep rather easy but I am waking up around 4 or 5 am the last few mornings a cant go back to sleep. I must say one of my main symptoms of celiac disease was fatigue as I could and would sleep about 12 to 14 hours a day. Please tell me this gets better!! But on a good note I have been told by a few people that I have more coloring in my face.

It should resolve soon. One thing that may be going on is that gluten was a neurotoxin for you. Your brain got used to having it's own gluten supplied drug stash, so to speak, and now it has to learn how to sleep without the soporific effect of the gluten. For most this should resolve within a couple of weeks at the most. As long as you don't regluten.

Puddy Explorer
Puddy
Posted

Yes, the same thing happened to me. The first 6-8 weeks I was gluten-free I woke up at 4AM every day! It was driving me crazy, but it gradually stopped happening and now I get a full night's sleep.

Mtndog Collaborator
Mtndog
Posted

it happened to me as well and eventually got better. Hang in there- up from here!!!!

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

Celiac.com Sponsor (A8-M):


MNBeth Explorer
MNBeth
Posted

Yup; me too. Now I'm back to sleeping like the dead.

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      126,814
    • Most Online (within 30 mins)
      7,748
    judy regina
    Newest Member
    judy regina
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.7k
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • trents
      Asking for Help Understanding Endoscopy/Biopsy Lab Results

      By trents · Posted

      Well, the only thing I would conclude with would be, if you choose not to trial the gluten free diet, is to encourage you to get periodically tested, either antibody blood tests or the biopsy or both. I think it something that needs to be monitored.
    • Sking
      Asking for Help Understanding Endoscopy/Biopsy Lab Results

      By Sking · Posted

      So the strange thing is I don't have any symptoms at all, except the soft stools (comes and goes) which they told me was from the Lymphocytic colitis. I had some mild positives on my antibody test and one gene was positive which is what made my doctor go ahead with the endoscopy. The reason they started any of this was finding the lymphocytic colitis this past summer after I had C Diff and she said, Well....it may be from something like Celiac.... Definitely a lot to learn through all of this and I appreciate people like you taking the time to help out a stranger like me!
    • trents
      Asking for Help Understanding Endoscopy/Biopsy Lab Results

      By trents · Posted

      Well, I wouldn't rule either out. And you might consider trialing a gluten free diet for a few months to see if symptoms improve. That would tell you a lot. By the way, the incidence of other bowel diseases is higher in the celiac population than it is in the general population. And even if you don't have celiac disease, you could have NCGS. Gluten is just problematic for a lot of folks for various reasons.
    • Sking
      Asking for Help Understanding Endoscopy/Biopsy Lab Results

      By Sking · Posted

      Thanks for taking a look. I also just did some research and saw that increased numbers of intraepithelial lymphocytes and villous distortion can possibly be from lymphocytic colitis (which I was diagnosed with this past summer)....so fingers crossed this is what she will say it is.  
    • trents
      Asking for Help Understanding Endoscopy/Biopsy Lab Results

      By trents · Posted

      IMO, Part 3 has some abnormalties that could indicate the early stages of celiac disease but the doctor is tentatively thinking not, at least at this point.
×
×
  • Create New...