Published Date: 05 June 2009
The willingness of teenage myalgic encephalomyelitis sufferer Hayley Keen to share her experiences and her generosity in raising funds (Eastbourne Herald, May 29) for the Association of Young People with ME makes a valuable contribution to our understanding of this baffling, complex, neurological illness, which we need because sufferers do not all start or progress in the same way.
Eastbourne Herald
The administrators of the ‘Living With ME’ website do not advocate the use of any particular type of medication, treatment or healthcare! YOU should ALWAYS seek advice from a DOCTOR / GP / CONSULTANT before undertaking or ceasing any treatment!
This entry was posted
on Monday, June 29th, 2009 at 10:00 am and is filed under ME News & Views.
You can follow any responses to this entry through the RSS 2.0 feed.
Both comments and pings are currently closed.