Eurordis General Assembly 2018 by Pseudomyxoma Survivor | May 9, 2018 | All Countries, Patient Advocacy, Raising Awareness | 0 comments Susan’s representing Pseudomyxoma Survivor at the EURORDIS – European Rare Diseases Organisation General Assembly this week. Related Posts Helping Children Cope with a Parent’s PMP Di... Why you should see a PMP specialist I can’t say it enough… are you dealing with a PMP specialist? If not, I would say you must. They are the ones that have seen this stuff and the wei... Alice’s diagnosis story Supporting the Peritoneal Malignancy Institute in ... We got the day off to a great start at the Patients Wellbeing Day in Basingstoke by making a donation to the Peritoneal Malignancy Institute. This don... Submit a Comment Cancel reply Your e-mail address will not be published. Required fields are marked *Comment Name * Email * Website Sign me up for the newsletter! Notify me of follow-up comments by email. Notify me of new posts by email. This site uses Akismet to reduce spam. Learn how your comment data is processed.