Dear HU members, I know most of your are in the UK, but we've been piloting something called "Patient Cafe" with US patients where people chat online on video live about important "living with" CLL issues. I think you will find the accent different but the issues the same. Here's a link to the latest one in a series of 4 so far: patientpower.info/video/how...
Our hope is to do this with folks from the UK and many other countries and I would love your thoughts.
The discussions are led by carol Preston a 17p Cller.
Best Wishes, Andrew Schorr, living with CLL since 1996.
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