This May has been the first of the Solidarity Network of Physiotherapists, which we started with the idea of ​​creating a shared solidarity that raises awareness about minority diseases and muscular dystrophy in the world of physiotherapy. Public resources are not dedicated to rare diseases but there is a lot of energy we are receiving […]

Organizations, companies, bet on a Corporate Social Responsibility (CSR) that gives impulse to research in rare diseases. The 2020 has been a tough year for people living with a disease, but we do not give up! From the ImpulsaT Association we have chose to continue raising awareness and involving society in the research of congenital […]

2020 has been a tough year for people living with an illness, but let’s not give up! From the ImpulsaT Association we are committed to continuing to raise awareness and involve society in the research for congenital muscular dystrophy due to merosin deficiency. THANKS partners, donors, organizations, entities, families Download the spanish version of the […]