alex3619
Senior Member
- Messages
- 13,810
- Location
- Logan, Queensland, Australia
Thank you Cort
Hi everyone,
I'ld like to second everything on this thread and add something extra.
There are lots of things lacking in the lives of ME and CFS patients. One that is rarely addressed is a place in the community. Phoenix Rising is like a second home for many of us. The people at PR are almost family, we have a sense that we have a place in the world and there is still meaning to our lives.
Without Phoenix Rising this would not be possible.
Without Cort, Phoenix Rising wouldn't exist.
Only a small minority of ME and CFS patients have had a positive global impact. I consider you to be one of them Cort.
Thank you,
Alex
Hi everyone,
I'ld like to second everything on this thread and add something extra.
There are lots of things lacking in the lives of ME and CFS patients. One that is rarely addressed is a place in the community. Phoenix Rising is like a second home for many of us. The people at PR are almost family, we have a sense that we have a place in the world and there is still meaning to our lives.
Without Phoenix Rising this would not be possible.
Without Cort, Phoenix Rising wouldn't exist.
Only a small minority of ME and CFS patients have had a positive global impact. I consider you to be one of them Cort.
Thank you,
Alex