21/02/2024                                                                            
                                    
                                                                            
                                            Does anyone know when the which day is the rarest of days in the year? ππ»ββοΈ It's 29th of February, a day that only comes once every four years βΌοΈ This day has also been coined the Rare Disease Day to raise awareness about the > 7, 000 existing rare diseases in the world (according to the National Institute of Health, NIH). π¦ 
In commemoration of this day, BAMEdical is collaborating with M4RD to organise an event on this very topic! πThe speakers invited to deliver this event are Dr. Laura Furness π©Ί, who will be sharing her experience working with patients living with rare diseases, and Mr. Jibreel Arshad π§π½, who will share his story as a patient with lived experience of a rare disease. More information of the speakers are available below.ππΌππΌ
Weβll be talking about why itβs important to be βrare awareβ as a medical students. π§πΎβππ©πΌβπTips on how to approach rare diseases and be prepared for when we qualify, where we may encounter patients living with a rare disease will also be shared through this talk! βπΌπ€©
Come along to learn more about rare diseases! β¨ Pizzas provided! πCertificates provided! π
Event details ποΈ
Title: RARE DISEASE 101 
Date: 28th of February 2024
TIme: 6pm - 7.30pm
Location: The HIVE (UoM Studentβs Union)
β¬οΈSpeaker Information β¬οΈ
Dr. Laura Furness π©Ί
βI am a clinical genetics registrar with a background in paediatrics. I have an interest in rare disease with a passion for family led care. I have a particular interest in translational medicine with experience delivering clinical research in inherited paediatric disorders. β
Mr. Jibreel Arshadπ§π½
βI am a standup comedian living with a rare disease called MPS 4 (Morquio) who will be sharing my story for Rare Disease Day. This is an amazing opportunity to hear firsthand from a patient with lived experience of rare disease.β