I became a trustee for Pseudomyxoma Survivor this year. I really wanted to do something positive after being diagnosed with a recurrence in 2020.
Meet trustee Clare
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Trustees articles
Meet Alison, one of our trustees
It’s Trustees’ Week from 1st-5th November 2021 and we’re hoping to give you an idea what it’s like to be a trustee with Pseudomyxoma Survivor. Alison shares her experiences of becoming a trustee with Pseudomyxoma Survivor
Georgina
It is with a heavy heart that we announce that our friend and colleague, Georgina Morgan has died. We have been honoured to have Georgina as a Trustee here at Pseudomyxoma Survivor for over two years.
Trustees Week 12th November
Here at Pseudomyxoma Survivor, we’re supporting Trustees Week, running from 12th-19th November, showcasing the work trustees do and highlighting opportunities for you to get involved and make a difference. We’ll be looking at different aspects of being a trustee and we’ve asked our trustees to share their thoughts on being a trustee.
Where did we come from?
Launched by Dawn Green in 2011, Pseudomyxoma Survivor works to improve the lives of the living with PMP, as a patient or as a caregiver. Struggling to find support herself, Dawn was keenly aware that there was a lack of emotional support for anyone with the disease. She dedicated the website to the memory of a fellow PMP patient, Julie Stanton.
Just who are we?
You’ve liked our Facebook page, followed us on Twitter, added us to your circles on Google+, subscribed to the blog and read the website (you haven’t? … well, that’s ok [sort of] — but hey, now is a good time to do so, right?).
But just what is Pseudomyxoma Survivor and who are the faces behind the name?