Our Annual Patient Information Days are large, friendly gatherings of around 100 patients affected by all the rare endocrine conditions that AMEND covers. A variety of talks are given by a range of medical experts, including specialised sessions for each disease. A creche and activities for children are usually provided.
Our event changes annually between venues in central London and elsewhere in the UK.
“….it was good to chat with [the medical speakers]. You assembled an excellent panel of speakers who are open and approachable as well as knowledgeable. We also met some interesting people among the other delegates. The venue was good too, and the dinner was excellent.” (patient)
“Brilliant day and so well organised. Thrilled to have been able to attend. Topics so relevant and make you feel in control of your condition. Thank you.” (patient)
“Having attended the event I feel support in meeting others with MEN” (patient)
Next Annual Information Day (2019)
We are currently working on the programme for our 2019 Information Day. It will be held in Sheffield, South Yorkshire on Saturday 11th May. You can already reserve your place(s) via our Eventbrite account.
2018 Annual Information Day
Videos include: Dealing with Diagnosis and Uncertainty; Communicating with your GP; Working with your MDT; Getting Involved in Research and Preparing for Surgery.
2017 Annual Information Day
Videos include: Sharing Difficult News with Friends and Family; Understanding Research; Overview of MEN1, MEN2, MEN3 and SDHx; Introduction to and Update on ACC; Using Social Media for Support.
2016 Annual Information Day
Videos include: Basic Overview of MEN syndromes; MEN1 PNETs; Steroids Made Easy; Starting a Family; Care of the Pregnant MEN Patient.
Earlier Annual Information Days
Visit our YouTube channel for more videos on a variety of topics.