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 us.
EURO-NMD is a European Reference Network for the thematic grouping of rare neuromuscular diseases (NMDs). NMDs collectively affect an estimated 500,000 EU citizens and result in significant costs...
France
The EPNS is an international and independent non-profit making Society for physicians, health professionals, scientists, and students with research and/or clinical interest in Paediatric Neurology....
France
The French Health Care Network for rare neuromuscular diseases aims to coordinate, facilitate and promote professional interactions between the various players in neuromuscular diseases.
France
The French Society of Myology (SFM) was founded in 2002. Its aim is to promote myology in all its aspects (research, academia, university, public), to give it a national visibility, to disseminate ...
France
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