Hi, my Husband has been living with Stage 4 Cholangiocarinoma since 2018 when Lung mets were discovered a year on from a Liver resection. He is currently waiting to start 8th line treatment of FOLFOX. Trials for targeted treatment as well as good old Cis/Gem (no immune that wasn't around when he had first line) have got him 7 years down the road and we hope with rebellious rope that Folfox will knock the lung tumours back to get us that bit further along.
Keen to hear if anyone has experience or been permitted to do the FOLFOX pump disconnection and flush at home as AMMF guidance suggests may be possible?
