Bookbot

dataMSA Surveys for Multiple System Atrophy

Patient Data Report

Autor*innen

Speichern

Parameter

  • 223 Seiten
  • 8 Lesestunden

Mehr zum Buch

(2019 Edition) When I couldn't find patient-driven information about MSA, and when my doctors didn't have a lot of information about patient experiences, I set out to create a way patients could share their experiences. In this 2019 edition, dataMSA collected information from more than 1000 persons worldwide who have been affected by MSA (patients, caregivers, loved ones to those lost). This text is an invaluable resource for health care providers, support staff members and others who seek information about multiple system atrophy. Sections of the data were presented at the 2018 International Congress of Parkinson's Disease and Movement Disorders in Hong Kong. No revenue is collected from the surveys and patients remain confidential. 100% of the profits from this book will be donated to support research for a cure. Bill Sydnor, MSA patient/ dataMSA creator /<a target="_blank" rel="noopener nofollow" href="http://www.dataMSA.com">www.dataMSA.com</a>

Buchkauf

dataMSA Surveys for Multiple System Atrophy, Bill Sydnor

Sprache
Erscheinungsdatum
2015
Einband
(Paperback)
Wir benachrichtigen dich per E-Mail.

Lieferung

  • Gratis Versand ab 14,99 € in ganz Deutschland! Mehr Infos.

Zahlungsmethoden

Keiner hat bisher bewertet.Abgeben

Titel
dataMSA Surveys for Multiple System Atrophy
Untertitel
Patient Data Report
Sprache
Englisch
Autor*innen
Bill Sydnor
Einband
Paperback
Seitenzahl
223
ISBN10
1519729103
ISBN13
9781519729101
Reihe
Schlagwörter
Medizin
Beschreibung
(2019 Edition) When I couldn't find patient-driven information about MSA, and when my doctors didn't have a lot of information about patient experiences, I set out to create a way patients could share their experiences. In this 2019 edition, dataMSA collected information from more than 1000 persons worldwide who have been affected by MSA (patients, caregivers, loved ones to those lost). This text is an invaluable resource for health care providers, support staff members and others who seek information about multiple system atrophy. Sections of the data were presented at the 2018 International Congress of Parkinson's Disease and Movement Disorders in Hong Kong. No revenue is collected from the surveys and patients remain confidential. 100% of the profits from this book will be donated to support research for a cure. Bill Sydnor, MSA patient/ dataMSA creator /<a target="_blank" rel="noopener nofollow" href="http://www.dataMSA.com">www.dataMSA.com</a>