Pain in people with multiple system atrophy (MSA) – a web-based survey

Are you a person living with MSA or are you caring for a person with MSA?

People with MSA frequently experience pain, but its frequency, core features and risk factors are still poorly understood.

We, a team of researchers from the Medical University of Innsbruck in Austria, launched a web-based survey to learn more about your pain or the pain of the person with MSA you care for. The completion of the questionnaire will require approximately 30 minutes. If you (or the person you care for) do not have pain, you are still welcome to answer some useful questions.

Click on the link below to read the informed consent and start the survey:

For more information, contact us:

Thank you for helping us develop better treatments for people living with MSA.


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