Jan
The Independent Newspaper is due to feature the PAL Award initiative in their Rare Disease suppliment on 28th February. My portrait of the Genzyme sponsored group, Students 4 Rare Diseases, will accompany the article.
The founders of Students 4 Rare Diseases, Lucy Lavery, E. Keohane, Hannah Grant, Deborah Fine and Vicki Ward recently held their first meeting with medical students from the other London medical schools at Garrod Building, Taylor Street, London. The purpose of this meeting was to replicate their practice in other medical schools to eventially form a nationwide platform of communication and information about rare diseases.