The WMS has been providing advice for people with neuromuscular disorders, and their healthcare providers since the start of the COVID-19 pandemic. Two documents were created to help patients, carers, and medical providers. One is about COVID-19 and neuromuscular disorders, and the other is about the vaccines. The WMS will keep updating the advice as things change. The documents have been translated into many languages by WMS members from around the world which demonstrates the true value of sharing this information as well as the international reach the neuromuscular community has.
The World Health Organisation asked the WMS to help spread information about COVID-19 and other important communications to national neuromuscular organisations. The WMS has made a network for these organisations and wants to make a list of all the organisations involved. If your organisation wants to be listed, you can fill out a form. If you're not a WMS member, you need to make a free account first. This Directory is for information purposes only, the WMS doesn't take responsibility for the content of other organisations' websites.
If you have any queries, please contact Bhavnita Patel admin@worldmusclesociety.org.
ASGCT is the primary professional membership organization for gene and cell therapy. The mission of ASGCT is to advance knowledge, awareness, and e...
Read more
The AOMC was established: to promote, establish, undertake, carry out, develop, maintain, operate, run, manage train, help or administer soci...
Read more
The object of the Society is to act as a multidisciplinary professional body of experts to promote the clinical practice, education and advancement...
Read more
CMT-NET is an interdisciplinary German network with the intention of bringing together experts from different areas of research to collaborate on t...
Read more
DMD Aileleri Derneği (can be translated in English as DMD Families Association) is a young and rapidly growing association which was established in...
Read more
EAMDA is a nonprofit umbrella organization that connects together neuromuscular disorders associations across the European Union. EAMDA supports NM...
Read more
EURO-NMD is a European Reference Network for the thematic grouping of rare neuromuscular diseases (NMDs). NMDs collectively affect an estimated 5...
Read more
ENMC background The European Neuromuscular Centre (ENMC) was founded in 1992 by a group of European patient associations that dedicated itself to ...
Read more
The French Health Care Network for rare neuromuscular diseases aims to coordinate, facilitate and promote professional interactions between the var...
Read more
MD-NET (Muscular Dystrophy Network) is a Germany-wide consortium funded by the BMBF to improve medical care for people with neuromuscular diseases ...
Read more
Myo-Care National Foundation is an Egyptian non-profit NGO dedicated to optimizing medical care, research, and access to therapy for muscular dystr...
Read more
The Peripheral Nerve Society is an international non-profit organization of scientists, physicians, and other healthcare providers working together...
Read more
The French Society of Myology (SFM) was founded in 2002. Its aim is to promote myology in all its aspects (research, academia, university, public),...
Read more SOLANE se ha impuesto como misión promover el conocimiento, el avance, la difusión y la investigación en el campo de las enfer...
Read more
The purpose of the Foundation is to promote scientific research in the field of neuromuscular diseases in Switzerland. This is done primarily by an...
Read more
TREAT-NMD is a network for the neuromuscular field that provides an infrastructure to ensure that the most promising new therapies reach patients a...
Read more
Our association exists because we, as affected people, know exactly what it means to live with a rare disease from the group of the centronuclear m...
Read more
