Hi. Does anyone attend / get support from Maggies? I keep thinking about going / finding out about support but just worried they won't know much about PV/blood cancer etc and/or I won't meet thei criteria.
I have the same sort of question re any other help from specialist nurses etc??
I know I've only had one appt at the Christie (next t/c appt next week), and everything is so up in the air/unknown, but I feel so completely alone, really want some support but don't know where to go / how to get it?
Thanks
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MancMermaid
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my gp suggested I go and introduce myself. I was unsure but did. They are fantastic people very friendly and a gentle talk with them put me at ease. I had several open appointments with them for guidance and since fundraised for them. Supportive talking great guidance was what I needed
Hi there, it’s horrible feeling alone with this- I was in exactly the same boat when I was diagnosed and it was frightening. I haven’t heard of Maggies but for all the latest info on MPNs and empathetic listening & support try MPNVoice. Fantastic charity (I worked for them a few years ago!) and they run forums across the UK. The forums are a really good way to meet the doctors, nurses, other patients and get up to date info on everything. They run a buddy system too which can be really helpful.
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