We have a new website which we will be launching on the afternoon of Friday 4th December.
The new website has been necessitated due to the existing site being run on a platform that will no longer be supported as of February 2021.
We do hope that you find this new site to have a fresher look, be more user friendly and easier to navigate to find the information that you are looking for.
The migration of our website has been carried out in an extremely cost effective way by a friend of the charity at a fraction of the cost that it should have been. Meeting the cost that has been incurred has been made possible because of the very kind and generous donations we receive from our supporters of the charity that include friends, patients and companies. We would of course like to thank everyone for your support and generosity.
We are very excited about our new look website and welcome your feedback/comments once it goes live next week, please send them to info@mpnvoice.org.uk.
Best wishes from MPN Voice
Written by
Mazcd
Partner
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Thank you for all you do in supporting us. MPN Voice has helped me through every step on my diagnosis and ongoing treatment, it’s so reassuring to have the website for information and support. You all do a fantastic job, thank you
Hi Dovme, don't as a rule as questions direct to one person but we both had diagnosis similar time. I have always been interested in your site picture - is that you actually in the boat. Just an intriguing view
No it’s not me! it’s a great picture though paddling through life!
I will add a picture of my ugly mug to my profile as l feel more established now and we have a new MPNvoice layout website. Its good to put faces to names
Thank you Maz. I don't know how I would have coped without this site. Support, guidance, advice and always there even in the middle of the night.I hope I can start giving something back soon.
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