PSP Association
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mPower App Users

Documentary film project on medicine and technology seeks Parkinson's patients who have downloaded and are actively using the "mPower" app.

If you are interested in sharing your experience for this piece, we would love to hear from you ASAP and ideally no later than 1/27/16. Please email us at with your answers to the below list of questions regarding your story.


* What motivated you to download and use the mPower app?

* What has your experience using the mPower app been like thus far?

* Has using mPower led to specific insight or a change in your life or condition?

Thank you for your time and we look forward to hearing from you!

Molly Doyle

McBride Casting

Santa Monica, CA

3 Replies

What does this have to do with PSP?


Here is what I found about this app


I have found out that this is a phone app only available in the USA for the time i am informed.


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