Our first event to make the MUCO Association familiar with our project was a success. Last Wednesday we organized a conference where we invited Stefan Joris, the head of the association, and students from the different years at the RMA.
I thought Cystic Fibrosis was only a lung disease. I am shocked to see how big the impact is on the life of a patient.Officer-Student 158 SSMW
This conference was not only useful for the Association but also for the team of Project SSMW. Being able to understand how people with Cystic Fibroses live, makes it possible to organize some activities together when possible. We are looking forward to support this Association now we’ve seen what amazing things they do.