This week is my 28th anniversary of becoming sick (aka "sickaversary") with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome at age 16.
I've spent nearly 22.5 years severely affected.
I'm one of millions around the world.
We need more public and private money to make research progress soon, the quicker the better: my life and the lives of others are passing by.
For anyone interested, here's a list of ME/CFS research funds:
http://phoenixrising.me/resources-2/research-charities
Here's my story as told in the Irish Independent in 2015:
'No one chooses to have ME - everything changed when I became ill'
http://www.independent.ie/life/heal...thing-changed-when-i-became-ill-34153140.html
View attachment 19493
I've spent nearly 22.5 years severely affected.
I'm one of millions around the world.
We need more public and private money to make research progress soon, the quicker the better: my life and the lives of others are passing by.
For anyone interested, here's a list of ME/CFS research funds:
http://phoenixrising.me/resources-2/research-charities
Here's my story as told in the Irish Independent in 2015:
'No one chooses to have ME - everything changed when I became ill'
http://www.independent.ie/life/heal...thing-changed-when-i-became-ill-34153140.html
View attachment 19493