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Articles by Susan

Susan Oliver was diagnosed with pseudomyxoma peritonei (PMP), and she underwent surgery to remove the disease. Years after her surgery, Susan became an advocate for PMP awareness and the Chair of Pseudomyxoma Survivor. Grateful thanks to Susan for her continued support, her write ups of conferences and meetings and her crafty ideas as well as the support she shows to patients.

New Year, New Trustee

We’re starting off 2023 with a new trustee. Please join us in welcoming Tim to our board of trustees. He brings a wealth of knowledge and experience that will add value and strength to the team.

A day for remembering

Audrey Hepburn believed that ‘As you grow older, you will discover that you have two hands, one for helping yourself, the other for helping others’ and this is the ethos of 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.

We’re looking for trustees!

We are now looking for able and motivated individuals to join our Board of Trustees, to help lead and guide our important work. Mainly, we are looking for people who are excited by the work Pseudomyxoma Survivor does, share our values and will play an active part in the work of our Board. Is this you?

The Gifting Season is Underway…

The Gifting Season is Underway…

Our first box of Christmas goodies is going out tomorrow – our way of saying “thank you” to the amazing hospital consultants and staff that have helped look after pseudomyxoma survivors on the wards.

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Multi-disciplinary Diagnostic Centres

Multi-disciplinary Diagnostic Centres

Through Cancer 52, Pseudomyxoma Survivor has received a special invitation to view a multi-disciplinary diagnostic centre (MDC) in action. MDCs are being trialled here in the UK and they are set up so that patients who present with non-specific symptoms can go to a one-stop shop and have all of the tests they require to help with a diagnosis.

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PSOGI 2018

PSOGI 2018

Pseudomyxoma Survivor representatives once again attended the bi-annual Peritoneal Surface Oncology Group International (PSOGI) conference, this time it was in Paris. The PSOGI aims to “improve the treatment and survival of peritoneal cancer patients by educating patients, by training physicians, by organizing meetings and by performing basic and clinical scientific research into peritoneal cancer and the different treatment modalities”.

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Gearing up for PSOGI 2018

Gearing up for PSOGI 2018

The PERITONEAL SURFACE ONCOLOGY GROUP INTERNATIONAL conference, now in its 11th year, is almost upon us. I can't quite believe it's been two years since we attended the one in Washington DC! PSOGI is a non-profit organisation which aims to promote research, education,...

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Update from our Chair

Update from our Chair

Following on from the two successful patient days held at Basingstoke Hospital and The Christie, I have been busy attending meetings with Cancer52, Eurordis, National Voices and I secured a bursary place at the Public Health England Conference in Manchester in June....

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Peritoneal Tumour Patient Day at The Christie 2018

Huge thanks to everyone who came to speak to us at our table at the Peritoneal Tumour Patient Day at The Christie yesterday. It was lovely to see some old friends and to make lots of new ones. We were overwhelmed by the donations the charity received and so busy that...

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