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...
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,...
The Center Origen Salut de Sant Cugat, La Palestra de Llagostera, Noemí Perelló Fisioteràpia Cardiorespiratòria and Redi Espai Salut, from Terrassa, are the first centers to join the Solidarity Network of Physiotherapists in May The Solidarity Network of Physiotherapists, the initiative that invites all pre-professional...
From the ImpulsaT Association we help you to involve your people in collecting resources for the investigation of congenital muscular dystrophy due to merosin deficiency. Tell us your idea and we will help you make it come true. We share some activities already been made: ...
The ImpulsaT Association, which brings together the 26 families in Spain affected by congenital muscular dystrophy due to merosin deficiency, is launching the solidarity action Physiotherapists Network of Solidarity. Children affected by this minority disease need a lot of physiotherapy support to reduce pain and...
On Saturday 30th of January, from 12.30am to 1.30pm we will cook a steak of Iberian strogonoff with pilaf rice and individual carrot cakes for dessert! We will do this with Sesé San Martín, founding partner and director of the TELVA Cooking School, member of...
On December 21st at the Pia de Balaguer school was made a solidarity snack in favor of ImpulsaT. Parents, teachers and children organized this fest to share a moment before the Christmas holidays. The money they raised was donated to the Association to invest in...
On Wednesday, November 11th at 6 p.m, there will be a webinar on congenital muscular dystrophy due to merosin deficiency and the main lines of research in Spain. The webinar will be given by the researchers: Laura Coch. PhD in Biomedicine from the University of...
On Saturday, November 14th at 11 a.m. we will meet on the Jitsi platform to listen to the "Children's stories to fly" from the Anna Roca Theater Company. The solidarity performance will be given by Anna Roca, who has been telling exciting, tender and funny...
On the occasion of the 15N, World Day of Neuromuscular Diseases, families remember that research in rare diseases is negligible. Only collective involvement can help improve the lives of those affected. Most boys and girls with merosin-deficiency congenital muscular dystrophy cannot walk or eat alone,...