From 2014-2019, dataMSA collected data and information from more than 1100 individuals from across the globe who were living with Multiple System Atrophy (MSA), and from caregivers and loved ones of those lost to MSA.

The data is made available at no cost to groups, agencies and medical personnel providing treatment, education and research for MSA.  

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Current dataMSA Objectives:

-Encourage  individuals affected by MSA and/or thier caregivers/loved-ones  to access and utilize the information found in the dataMSA Surveys for Multiple System Atrophy.

 - Encourage the sharing and distribution of data and information found in the dataMSA Surveys for Multiple System Atrophy to health care providers, health educators and neurological research centers worldwide.
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1. Please contact dataMSA@yahoo.com 
2. for more information.
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dataMSA Survey Reports in Print... 

dataMSA Surveys for Multiple System Atrophy- Patient Data Report: 2014-20219



 An excellent resource for doctors, medical providers and support members-

Includes  survey results from more than 1000 individuals affected by MSA worldwide.

All proceeds donated to MSA research.

Order yours by clicking below-

dataMSA Patient Data Report

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