Happy new year, and let's FIGHT FOR OUR RIGHTS IN 2004 TOGETHER

[Guest guest]

Look what Jane, UK has to say

(Her son 13 year old, suffers from ME-CFIDS)

I wish:

That we could coalesce as an International ME/CFS/CFIDS/PVFS et al

Community worldwide. That we would recognise that the SHEER WEIGHT

of our numbers is our strength. That through the use of our numbers,

we would force proactive change.

That we could agree on just *one* issue to start with. One at a

time. With no arguments and no dissent. That we would help each

other to build the One Click engine to achieve our objectives.

That we would build our One Click engine with peace, with harmony,

with cohesion and with style in the most utterly legal fashion. That

we would focus our engine on specific and agreed problems in each

country, turn by turn.

That ALL would join us in this endeavour. Thousands upon thousands

upon thousands of us. Millions. That we would feel sufficiently

confident in our endeavour that other Communities would join us.

Those from Well World and Ill World alike. Those who understand our

plight, who sympathise and would help us.

That this would be the first time that a community of the

disenfranchised and so sick has achieved such an historic

objective. From our sick beds. The internet has made such a

difference to us and our ability to communicate.

LET US USE THE INTERNET PROACTIVELY!

That our plea for research on this physiological illness would be

listened to. That massive amounts of money would be poured into

studying the aetiology and the epidemiology of our illness. That the

diagnostic bio markers that we so badly need found at last. It is

this that will make the medical industry, the insurance industry, the

pharmaceutical industry and government take note. This above all.

I wish that through the coalescing of our ME/CFS Community, we would

make a huge and substantial difference for all sufferers worldwide.

I wish for all sufferers to be treated with understanding and

compassion. That efficacious treatments backed by sound research be

made available to our ME/CFS alphabet soup diagnoses Community.

I wish for Ben to get better.

I wish for all ME/CFS/CFIDS/PVFS et al sufferers to get better.

I wish you all a very Happy New Year.

And lastly, I wish to thank those people who have helped me and Ben

personally. And those people who have helped me so much with One

Click. Who have used a proportion of their valuable Up Time to give

me sound advice and counsel. You know who you all are. Thanks from

the heart.

Jane

London UK

*********

Join us right NOW:

THEONECLICKPROTEST

or see here what its all about:

www.feel.ch/cfs.htm

thanks and lot of strength

fox

Switzerland