Connect with others who understand.

  • Learn from expert-reviewed resources
  • Real advice from people who’ve been there
  • People who understand what you’re going through
Sign up Log in
Powered By
Real members of MyFibroTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Sleep - Amount Per Day

A MyFibroTeam Member asked a question 💭
Sydney, AU

Hi all,

I know everyone is different but can you tell me how much sleep you are able to get a night? And if you're able to sleep during the day?

I'm averaging 4-5 hours broken sleep (in bed for 8 hours) and so tired and aching throughout the day but too sore to sleep, and if I do doze off for 40 minutes or so I wake up more jarred & sore.

I used to sleep (and need 8-9) hours a night & at least wake up refreshed.

Any feedback would be great guys.

Thanks

Kimberly x

February 17, 2016
 â€¢ 
Be the first to react

Answer Summary

Members connected over the struggle of getting quality sleep with fibromyalgia, with most reporting only 4-5 hours of broken sleep per night... Read more

Members connected over the struggle of getting quality sleep with fibromyalgia, with most reporting only 4-5 hours of broken sleep per night despite spending 8-12 hours in bed, and many never reaching deep REM sleep due to constant pain signals keeping the mind active. Several members shared strategies that sometimes help, including hot baths before bed, melatonin (though it can worsen restless leg syndrome for some), sleep masks with soft music or binaural beats, limiting daytime naps to protect nighttime sleep, and short walks in sunlight or cold air to fight daytime exhaustion. A recurring theme was accepting the unpredictability of fibromyalgia sleep patterns, with members describing wildly varying cycles from sleeping 12-14 hours some nights to being awake for days, and finding peace in no longer making firm plans while being grateful for understanding loved ones.

A MyFibroTeam Member

When I was first diagnosed I was given the explanation that even when our bodies are at rest our minds are so busy fighting the pain that it can't find a cause for that deep REM sleep is impossible. It's also the explanation I've been given for the fog, overwhelming brain activity that just temporarily stops our cognitive thought process. I have to be careful what kind of stores I go into because if they're very noisy or crowded with stuff or people I will get overwhelmed. It's an explanation if not a solution. Peace.

February 19, 2016
A MyFibroTeam Member

On a good night i get5 hours. I have started to take melatonin it seems to help a bit.....I too use to sleep at least 8 hours a night

April 16, 2016
A MyFibroTeam Member

@A MyFibroTeam Member Louisiana is in the South, on the gulf of Mexico.

February 19, 2016
A MyFibroTeam Member

@A MyFibroTeam Member... Louisiana, USA

February 19, 2016
A MyFibroTeam Member

@A MyFibroTeam Member I get the Charlie Brown wah wah wah's a lot too. One person, one thing, one day at a time. It's the best we can do. Hugs from the bayou!

February 19, 2016

Related content

View All

Dose Any One Have Butrans Patches What Dose An How Do You Find Them

A MyFibroTeam Member asked a question 💭
Ellesmere Port, UK

Have You Tried Magnesium Citrate For Sleep? I'm Taking 400mg Per Day.

A MyFibroTeam Member asked a question 💭
Vancouver, BC

Fatigue

A MyFibroTeam Member asked a question 💭
Fresno, CA

Continue with Facebook
Continue with Google
By joining, you accept our Terms of Use, and acknowledge our collection, sharing, and use of your data in accordance with our Health Data and Privacy policies.
Already a Member? Log in