IMPULSAT is the official spanish non-profit association representing people having Congenital Merosin-deficient Muscular Dystrophy (LAMA2-CMD1A). We are a non-profit association of relatives, doctors, scientists and friends of people affected with this disease.
We collaborate with the scientific community, both at national and international level, with the aim of promoting and financing new research lines which contribute to the development of treatments and a cure for this disease. We also collaborate with federations who promote care work in order to improve life conditions of children and adults affected with LAMA2-CMD1A.
To know more on this disease please click here.
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…
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…
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,…