It absolutely amazes me how debilitating the fatigue associated with MS can be day in and day out!
I actually got some good sleep one night and still woke up exhausted and dragging. If I hadn't experienced this for myself over and over I probably wouldn't have believed the stories I have heard from other MS-ers. It never ends. I'm secluding myself more and more. Not wanting to extend my comfort zone past my front door.
Is this really a thing? It's so hard to believe that so many of us can feel this awful every day.
I'd like to hear from you all on this subject... again. Hope you don't mind.
I actually got some good sleep one night and still woke up exhausted and dragging. If I hadn't experienced this for myself over and over I probably wouldn't have believed the stories I have heard from other MS-ers. It never ends. I'm secluding myself more and more. Not wanting to extend my comfort zone past my front door.
Is this really a thing? It's so hard to believe that so many of us can feel this awful every day.
I'd like to hear from you all on this subject... again. Hope you don't mind.
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