A pesquisa realizada pela Parkinson & Movement Disorder Alliance pode ser visualizada através do link: https://t.co/dEbuhPQXBj
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In the same @PMDAlliance survey discussed yesterday, around 50% of respondents (people with PD and their care partners) reported that they had not received education on non-motor symptoms. What is your experience? (Professionally or personally) #MDTeaClub
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In an online survey by @PMDAlliance, care partners were more likely than people with Parkinson's to report that NMS were more challenging than motor symptoms. Any thoughts, from personal experience, on why this may be? #MDTeaClub https://t.co/eaO8TvfgHg ht
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Impact of non-motor symptoms in Parkinson's disease: a PMDAlliance survey | NDT @DovePress https://t.co/yPgBEHafg4 #PD