MPV Voice in Newcastle

[wendycu]

Hi, is anyone on going to the MPV Voice forum in Newcastle on Wednesday. It’s at The Station Hotel.

Do you know what time it starts,I've lost my email with the invite on.

Thank you

[Janis12]

Hi, yes I am going and it starts at 1pm and ends at 5pm, see you there.

[Hidden in reply to Janis12]

I am really disappointed, I had to cancel this couple of days ago due to a liver scan booked same day aahhh Hoping to get some feedback, re interferon shortage, raised liver enzymes if you can help with that Janis, Wendy ? And MPN Specialists accessable for us all, even remotely ?

[wendycu in reply to Janis12]

Thank you. See you there.

[Ipadlin]

Can I ask how you found out about the forum? I only seem to hear about them incidentally when people comment, as you have.

[Mazcd Partner MPNVoice in reply to Ipadlin]

Hi, when we advertise a forum, either an in-person or a virtual one, we send out a mailshot to everyone registered on our mailing list; we put it on our website; and posts on our social media pages; and a post on this forum. If you would like to be registered on our mailing list please email me at [e-mail] and then you will receive our news and updates. Best wishes, Maz

mpnvoice.org.uk/category/ge...

[Ipadlin in reply to Mazcd]

Thanks Maz, I thought I had registered but will do so now!

[JaynieQ]

Hi, I’ll be at Newcastle. It’s my first forum and I’m looking forward to meeting others with our rare condition. It’ll be good to feel less alone… 😊

[2009_JSR]

The Station Hotel is joined to Central Station. Do not do what I did and look for it across the road. Hope you find the forums as supporting as we have.

[Janis12]

Hi again Wendy, there is a buffet lunch before the speakers so get there a bit earlier if you would like to eat. Janis

[wendycu in reply to Janis12]

Thank you, I will be coming straight from work. A little snack will be nice.