I remember when the exhaustion was so pervasive. I had a mental flashback to the lowest days of my ME/CFS years when even holding a glass of water was beyond my strength and the brain fog was so thick that I couldn’t remember my thoughts for more then a moment or two. It used to be long days of running on total empty.
It wasn’t until I understood the role that sleep deprivation was playing in my struggle with ME/CFS that I began to improve. We dissected everything about my nights in order to improve my sleep – Comfort, light, sound, timing and medication. We tweaked and tweaked. When we finally got it right, I was getting about 6 hours of solid, uninterrupted sleep every night.
So yesterday I tweaked a few things in my current sleep environment and I finally slept for 7 hours last night. Even my active brain couldn’t keep my body from finally getting some needed rest. This morning I feel a little more energy and a great deal of gratitude that ME/CFS is a nightmare from my past.
What’s the status of your sleep patterns and environment? What needs tweaking? Please COMMENT on this blog or Send in your thoughts and I’ll post them with your permission. You can use the Contact Form or send an email to Martha at DefeatCFS dot net. And Guest Blogs are most welcome!
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Be Well Again,