I won't bother boring you with all the facts and figures there are much better sites than mine with all the info - the only thing I really know is that there are far too many of us, people don't understand and too many doctors don't care. So as well as sharing a little of my life with you, I will also be trying to raise awareness and pass on the latest information and campaigns.
Coming shortly - other pages of interest, and constant picture updates, so I hope you will come back and visit soon.
|I would just like to send mucho love to hubby, Mike
and kids Sam and Steve – without their love
I would not have made it this far!
Also huge, huge (((((((((hugs)))))))) to
Allyoops, Betty, Jane, John, Gill and
all the rest of the gang for all their support!
Humour is certainly the best medicine!
|Welcome to Foggy Corner|
|Special huge (((((((((((hugs)))))))))) to my grandson Thomas.......... trouble with a capital T !!!! guaranteed to always make you smile!|
|Like the butterfly,
I have the strength and the hope to believe
I will emerge from my cocoon...
Kirsti A. Dyer, MD, MS
Hi I'm another CFS/ME sufferer! I was diagnosed with it in March 2000.
|For further information contact -|
|Action for M.E.,UK
M.E. Association., UK