Major Sleep Disorders And Celiac REM Sleep Disturbance, Restless Legs Syndrome, Nightmares, Night Sweat
#1
Posted 31 May 2008 - 10:19 PM
I feel like they are ready to give up on me since we did the whole 24 hour sleep/nap study in January and weren't getting anywhere. I haven't talked to the doctor there yet about Celiac, but I will on Monday. I have been doing other things related to health, like telling my other doctors, nutritionist, therapist... I never knew why I wasn't absorbing medications and had to be on superhigh doses to even get a small affect. I'm sure that Celiac is why. As I heal, possibly I might be able to change some of the dosages of my drugs.
Right now though I am reading this section and seeing that a lot of Celiacs have problems with sleep. I didn't know I was Celiac, so could not have known there was a connection. It makes sense though.
Anyone have really SEVERE sleep problems who has noticed a huge change in their ability to sleep? I would love to hear some view points. Thanks!
#2
Posted 31 May 2008 - 10:35 PM
Good luck!
citykatmm, on May 31 2008, 09:19 PM, said:
I feel like they are ready to give up on me since we did the whole 24 hour sleep/nap study in January and weren't getting anywhere. I haven't talked to the doctor there yet about Celiac, but I will on Monday. I have been doing other things related to health, like telling my other doctors, nutritionist, therapist... I never knew why I wasn't absorbing medications and had to be on superhigh doses to even get a small affect. I'm sure that Celiac is why. As I heal, possibly I might be able to change some of the dosages of my drugs.
Right now though I am reading this section and seeing that a lot of Celiacs have problems with sleep. I didn't know I was Celiac, so could not have known there was a connection. It makes sense though.
Anyone have really SEVERE sleep problems who has noticed a huge change in their ability to sleep? I would love to hear some view points. Thanks!
If we try to serve both sides, we cannot stand our own ground.
Japanese proverb
Celiac.com - Celiac Disease Board Moderator
#3
Posted 01 June 2008 - 05:17 AM
kenlove, on Jun 1 2008, 02:35 AM, said:
Good luck!
I have found that gluten-free diet is not enough to lessen my sleep problems and have found no sugar diet to help a great deal but then I was just diagnosed with Lyme also and the continued sleep problems after going gluten-free may be related to Lyme.
hth
Gluten free since July 2007
Clinical dx celiac disease November 2007
Self-dx Lyme disease May 2008
Lyme confirmed positive Western Blot May 2008
#4
Posted 01 June 2008 - 08:56 AM
I'll still get night sweats if I have cheese or ice cream after 4pm or so.
ken
susieg_1, on Jun 1 2008, 04:17 AM, said:
hth
If we try to serve both sides, we cannot stand our own ground.
Japanese proverb
Celiac.com - Celiac Disease Board Moderator
#5
Posted 01 June 2008 - 07:59 PM
kenlove, on Jun 1 2008, 02:35 AM, said:
My daughter has RLS and the medicine they put her on...(the name escapes me at the moment)....was originally intended for Parkinson's. It has since then also been approved for the treatment of RLS.
"The greater the obstacle, the more glory in overcoming it."--Moliere
"I may not have gone where I intended to go, but I think I have ended up where I needed to be."--Douglas Adams
Friends may come and go but Sillies are Forever!!!!!!!--Amanda
_________________
gluten-free since 1/08
#6
Posted 01 June 2008 - 09:11 PM
#7
Posted 02 June 2008 - 03:39 AM
HTH
#8
Posted 06 June 2008 - 07:06 AM
RiceGuy, on Jun 2 2008, 03:39 AM, said:
HTH
I am also a very light sleeper, anything will wake me up. But I also found that gluten free doesn't quite get rid of my sleeping problems. I think sugar aggravates everything-i get muscle twitches and shakiness and some nerve tingling when I eat it too late at night, when I sleep. It's profoundly annoying. I'm still trying to figure out what's making me clench/grind my teeth. My doctor wants me to do a neuro-adrenal test, to find out if any of my hormones are low and causing my sleeping problems. A word of wisdom with sugar--even fruit teas seem to do it for me. I use the natural loose teas, so theirs no actually sugar in it, but the fructose from the fruit itself gives me sleeping problems. Good luck!
Diagnosed with TMJ/07
Diagnosed with blood test to gluten, wheat and brewer's yeast delayed food allergy 01/08.
Gluten free since 01/08.
Diagnosed with Vitamin D insufficiency 01/08
Diagnosis of Carpal Tunnel/Thoracic Outlet Syndrome repealed and attributed to gluten allergy 1/08
Diagnosed with Candida 03/25/08
#9
Posted 06 June 2008 - 08:55 AM
hope you feel better soon.
Graves disease June 2008
Candida overgrowth / started treatment November 2008
#10
Posted 24 June 2008 - 05:21 AM
MELINE, on Jun 6 2008, 12:55 PM, said:
hope you feel better soon.
For me, sleep disorders were some of the first issues I started to have. Then again, most of my symptoms were neurologic rather than g/i. I have excessive daytime sleepiness and a REM sleep disorder, and the treatment that has worked best for me involves higher doses of stimulant medications during the day. If I take them, I tend to sleep a little better at night. If I don't, I don't sleep - and I'm exhausted during the day. I have theories medically as to why, but ... given that I also had short-term memory and concentration issues, this worked well for me.
If a sleep doc isn't amenable to working with you, find another. Being sleepy all the time is lousy.
#11
Posted 11 July 2008 - 01:06 PM
The sleep paralysis remains though. In fact, before we got our dog Ninja, I had rare episodes lasting for hours (I could see the clock, THAT SUCKED), and I had shorter episodes EVERY NIGHT. Amazingly enough, once we got Ninja, he started waking me up at night (which I found irritating at the time) until one day I could feel myself sinking into it when out of nowhere he tackled me, barking and jumping on my chest (he's a 45 lb dog, ugh!). When we went on vacation (and couldn't take him) the episodes came back and suddenly I realized I hadn't had one in MONTHS!!! He still pushes me awake once or twice a night, but I haven't had any problems since!
I also didn't have many digestive issues, but I had TONS of neuro stuff happening. Not one of the 12 doctors I saw during that time saw anything, but it took 10 min of me "googling" my symptoms to find you guys! Thank goodness!!
Sorry if that was rambling and pointless!
#12
Posted 11 July 2008 - 07:55 PM
Inconclusive Blood Tests, Positive Dietary Results, No Endoscopy
G.F. - September 2003; C.F. - July 2004
Hiker, Yoga Teacher, Engineer, Painter, Be-er of Me
Bellevue, WA
#13
Posted 09 August 2008 - 12:07 PM
hope this helps
Tazzie
citykatmm, on Jun 1 2008, 12:19 AM, said:
I feel like they are ready to give up on me since we did the whole 24 hour sleep/nap study in January and weren't getting anywhere. I haven't talked to the doctor there yet about Celiac, but I will on Monday. I have been doing other things related to health, like telling my other doctors, nutritionist, therapist... I never knew why I wasn't absorbing medications and had to be on superhigh doses to even get a small affect. I'm sure that Celiac is why. As I heal, possibly I might be able to change some of the dosages of my drugs.
Right now though I am reading this section and seeing that a lot of Celiacs have problems with sleep. I didn't know I was Celiac, so could not have known there was a connection. It makes sense though.
Anyone have really SEVERE sleep problems who has noticed a huge change in their ability to sleep? I would love to hear some view points. Thanks!
#14
Posted 10 August 2008 - 03:20 AM
I had a neurologist for a year, who was telling me my headaches were being caused by pain in my neck, he said I was not getting the proper sleep because my neck was preventing it, and he put me on Topamax, starting at 50 mg, building up to 125 mgs. At times, I did seem to sleep better, or was just very sleepy. My headaches did not change much, then they became worse again. HE NEVER ONCE SUGGESTED SLEEP APNEA.
I finally did get an appt with the neurologist that I intially wanted, and as he was asking me these questions, I kept thinking, what does this have to do with neuropathy. He asked about my headaches, when do I not have one, which I told him, I ALWAYS have a headache, sometimes worse than others, but ALWAYS. He asked about my memory, to which I said, "My what?" He laughed and said, "Yup, just what I thought!" Then I told him memory wise, there are so many times my thoughts can not connect, I can't spell simple words, I can't write a word correctly while someone spells it to me, etc. Then of course, he ask me to open my mouth wide, to which he said, "Yeah, your mouth is too small, your air passages too small too, you have sleep apnea, you need a sleep study done!" Of course, me being the smarta@#, I asked for that in writing!!!
He prescribed a sleep study, and some physical therapy on my neck. He told me to try 10 sessions and see if my headaches have improved. Well, after 10 sessions, the difference is, my neck pain is worse and has increased two-fold...at 5 seesions, my left side was worse than my right, and the left side had not been hurting (my neck pain radiates down into my shoulder on the right side, now the left is worse), plus, my headaches have not changed. But, I did give PT a try, and that's what counts.
My appt will be soon to do my night with a CPAP machine, so they can see how well I do with it. I too, take B12, a sublingual methycobalamin 3000mcg. I have been taking B12 for over 3 yrs now.
Last week, in another forum, the administrator bumped an old thread up for another person. I was reading the thread, and the initial question was: How do you think things have improved for you since going gluten-free. I posted twice in that thread, in 2004, four yrs ago, and four yrs into my gluten free life. I posted that many things had improved, but not my sleep. That I was still having issues with sleep--I do not remember ever thinking I had sleep issues. Someone told me that my memory has just erased those thoughts and memories. They say sleep apnea does that to a person. WOW huh?
Long Island, NY
Double DQ1, subtype 6
We urge all doctors to take time to listen to your patients.. don't "isolate" symptoms but look at the whole spectrum. If a patient tells you s/he feels as if s/he's falling apart and "nothing seems to be working properly", chances are s/he's right!
"The calm river of your life approaches the rocky chute of the rapids - flow on through. You are the same water. The rocks cannot hurt you. Remember, now and then, that you are the water and not the boat. Flow on!
#15
Posted 08 December 2008 - 12:14 AM
Glad to hear about your dog. I had a dog like that years ago. If anything was wrong with me she'd lie on top of me to "protect" me. It was sweet.

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