TREAT-NMD can advise if a registry is available for a particular neuromuscular condition (contact email) and a list of registries by disease can be found here. The data in registries can be entered by patients themselves, by their doctor or by a combination of the two.
Registries can:
Identify participants for clinical trials
Help develop care standards, to help improve the care people receive
Support specific research questions
Provide information for doctors and scientists to learn more about neuromuscular diseases
Represent a link between patients and the research community, providing the opportunity for people to receive information directly relevant to their condition (for example, through newsletters)

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