By Vicky Passingham But in her teens, ME - also known as chronic fatigue syndrome - took its toll on her body to such an extent it had all but given up ...
I decided to put this blog together in the hope it would help, people who had ME, in our local area to find us on the net. As you will see from reading the blog, we are working closely with the Primary Care Trust, to bring improved facilities for people like ourselves to this area. We are very much hoping this will come into being, as promised by April 2008. We keep close links with our local media, and they are informed of any changes, we have also been known to do media interviews outside of our area, with the support and help of http://www.afme.org.uk/,
and http://www.meassociation.org.uk/
If you wish to contact the group, you can post a comment to us, together with your email address, and we will get back to you as soon as we can, thanks.
For general media interviews about ME, please feel free to contact Action for ME at
http://www.afme.org.uk/, and/or
http://www.meassociation.org.uk/(please copy and paste link into browser, thank you).
