Rare Disease Action Plan 2022 – focus on priority 2, action 7
In my last post I introduced some of M4RD’s initial thoughts on the Rare Diseases Action Plan 2022 Action 6. Now I’d like to continue exploring Priority 2; ‘increasing awareness […]
Emma Huskinson
About Emma Huskinson
Posts by Emma Huskinson:
Westminster, Rare Collaboration and Rare Diseases Action Plan 2022
Last Monday I attended a reception at the House of Commons to celebrate the 40th anniversary of the Society for Mucopolysaccharide Disease, or MPS. MPS is a member of the […]
M4RD: Quarter 1 and Rare Disease Day 2022
Spring is in the air and the team at M4RD have been reflecting on what has been a HUGE first quarter for us. Most notably, we have grown. Melissa, our […]
Syndromes without a name (SWAN)
It’s my first blog post for M4RD and I have been thinking back to when I was first introduced to the field of rare diseases, whilst in Med School. At […]