Would like to ask about the treatment one can expect here in North Wales. Though my wife is getting treatment for her Myelofibrosis, we are not sure how good or upto date it is. Probably contact via messaging would be best.
Anybody here being treated in North Wales? - MPN Voice
Anybody here being treated in North Wales?
Written by
jointpain
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Hi. A month or so ago I posted some links on this forum to good practice in Dx and treating MPNs. They might help to provide a standard to assess your wife's treatment against And her locsl haem might find them useful too. All the best
Rachel
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