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 ?
Stem Cell Transplant 
Stem Cell Transplant update
Energy costs and inflation going through the roof and now the NHS finally gone to pot!!
