#DARE TO THINK RARE
Our Mission
We are driving an attitude change towards rare diseases amongst medical students and doctors in training.
With over 7000 rare diseases, it’s impossible to know about all of them. However it is possible for doctors to:
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Appreciate that rare diseases are collectively common
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Recognise the exceptional challenges faced by patients with rare diseases
M4RD provides education in the Rare Disease field for medical students and doctors in training. Our ultimate aim is to improve the patient-doctor relationship and speed up the journey to diagnosis.
1 in 17 people will be affected by a rare disease at some point in their lives Source: Rare Disease UK
The Unusual Suspects: Rare Diseases in Everyday Medicine
Videos from this year’s symposium at The Royal Society of Medicine will be released weekly. Starting with Dr Richard Scott, Clinical Lead for Rare Disease at Genomics England and a Consultant in Clinical Genetics at Great Ormond Street Hospital.
Subscribe to M4RD to be updated on the next video release
Looking for a Rare Disease Resource? Browse, search and contribute to our growing database. Visit the Resources menu above.
Wolfram Syndrome UK (WSUK)
PopularPosted 7 months ago by Tracy Lynch
We are the only charity and support group in the UK for individuals and families...
Patient Groups / UK / 230 views
Posted 6 months ago by Jo McPherson
Neurofibromatosis type 1 (NF1) is a neurogenetic condition that approximately 1 in every 2,700 people...
Learning Resources / 204 views
TRAPPED – an insight into two sisters’ struggle to access treatment for a rare genetic disease
PopularPosted 5 months ago by Lucy McKay
Abstract: Medical student training is largely focused on acquiring knowledge of diseases and their management,...
Journals and Articles / 163 views
The Gauchers Association
PopularPosted 7 months ago by Sarah Allard
The Gauchers Association provides support and advice to patients and their families, supports research, and...
Patient Groups / UK / 203 views
Posted 6 months ago by Jo McPherson
This toolkit sets out the latest thinking in EDS, including the new approaches to diagnosis...
Rare Disease Guidelines / 193 views
Posted 3 months ago by Daniel Lewi
The CATS Foundation was established in June 2011 by Daniel and Patricia Lewi after their...
Patient Groups / UK / 90 views
