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David Cox

Check out David's blog on the homepage - he really needs our support right now.
I met him at the Manchester CML meeting & thought he was a really nice person.
As a marine, I thought that he'd sail through his transplant - it just goes to show that CML doesn't obey by the rules,
Barbara

I am really sorry to hear that David is suffering with such serious complications caused by GVHD. I will send a message of support to him... thanks for letting us know here.

I hope you are well. Did your doctor manage to set up a patient group?

best....,
Sandy

Hi sandy,
Dr N is helping organise a national CML day here in France for November 14th - there will be simultaneous meetings in several big cities. He's asked if I'd be interested in taking part in patient discussion groups.
Have just received a mail from someone called Frédéric from Novartis, he wants to phone me tomorrow about the Lisbon meeting.
I've told him to contact leucémies-chroniques@medicaliste.org
& Leucémie Espoir here in France,
best wishes
Barbara