Because I am very involved in the congenital heart disease family because of my son I know a lot of people that took part and my friend said the Anthony Nolan Trust was represented so ........... I was wondering if any of the MPN people who've had SCT 'S could represent MPNs to raise awareness . It is in Liverpool next year and I for one would go along to support .
What do you think ?
Written by
Helen1952
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