Does anyone else have sensory overload to the point where they have difficulty even being near a family member at home? Is this just my ME/CFS getting worse? My daughter's has been getting worse too. Or is there something else going on as well, neurologically?
I'm homebound, mostly bedbound...
Several years ago, I became aware of the book "The Highly Sensitive Person" by Elaine Aron, and other similar works. I definitely fit the model described, but there is, admittedly, a significant overlap between being a highly sensitive person (HSP) and many possible ME/CFS or fibromyalgia...
(If this is in the wrong place, I hope someone lets me know how to post it where it should be!)
I'd like some thoughts, experiences, ideas on finding an alternative to Klonopin for sensory overload. I am very isolated socially, can rarely even see my own family. I learned from experience that...
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