20/06/2025
I’m sure there’s others here that will understand this and others that will get some insight into the invisible lives of many.
The “Great News” is that since Long-COVID there has been some priority on research and treatment and now guidelines are being updated and new treatments being trialed.
Back when I tackled this for the first time in 2010-13 no research could even explain what was going on so it was very hard to get acknowledged, let alone any clear guidance on what to do about it.
Other than learning how to PACE I really had to find my own way with trial and error and learning how to listen to my body and intuition - which explains why tapping became my go-to tool for awareness and decision-making.
https://www.facebook.com/share/p/1YKYzQBvxu/
A growing body of scientific evidence shows myalgic encephalomyelitis chronic fatigue syndrome – or ME/CFS – is a biological illness, not a psychological one.