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Cognitive Impairment, Safety, and Parkinson's 

Davis Phinney Foundation for Parkinson's
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4 окт 2024

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Комментарии : 14   
@christinewinterton7111
@christinewinterton7111 Месяц назад
Thank you guys, this was marvellous. Connie looking forward to the Caregiver Session in the Parkinson Conference in Auckland New Zealand. Once again thank you all for the knowledge shared. Christine
@IOSALive
@IOSALive 4 месяца назад
Davis Phinney Foundation for Parkinson's, I really enjoyed this video, so I hit the like button!
@davisphinneyfdn
@davisphinneyfdn 4 месяца назад
Thanks!
@johnbutters3312
@johnbutters3312 4 месяца назад
hello from Auckland New Zealand. Thank you. The discussion is 'Dignity Therapy' for me as a care partner.
@alisonmyers8968
@alisonmyers8968 27 дней назад
As a PWP face-to-face conversations are vital. Its often difficult to write. Its often impossible to write digitally.
@davisphinneyfdn
@davisphinneyfdn 18 дней назад
Thank you for sharing your experience. Nothing can take the place of face-to-face interactions.
@splashesin8
@splashesin8 4 месяца назад
Thank you for elaborating on what makes a neurologist specialist in movement disorders & Parkinsons. This also helps me to know what I'm up against trying to find a way to get to one. ❤
@davisphinneyfdn
@davisphinneyfdn 4 месяца назад
Glad you found this valuable! It's also worth considering that it is possible for an experienced general neurologist to be as knowledgeable as a movement disorder specialist (MDS) about treating Parkinson's. For some people, a general neurologist may be as helpful or even more helpful than an MDS, especially if appointments with a general neurologist who is very familiar with Parkinson's are easier to access.
@mieliav
@mieliav 4 месяца назад
thank you. I'm grateful for all your ideas and advice.
@davisphinneyfdn
@davisphinneyfdn 4 месяца назад
You're welcome! We are grateful for Jori; our other Care Partner Meetup guests; and, of course, our panelists, too!
@jimrkelly
@jimrkelly 4 месяца назад
I was not the primary care partner for my mother when she had Parkinson's nor was I the primary care partner for my brother when he had Parkinson's but I am the primary care partner for my wife who was recently diagnosed with Parkinson's. That being said I wish I had a resource like this years ago but am grateful I have it now. Thanks for all you do! Great program!
@davisphinneyfdn
@davisphinneyfdn 4 месяца назад
Thanks for your comment. You've had a lot of Parkinson's in your life, and we're glad you've found us. Reach out to us at carepartners@dpf.org if we can help. Note that we do not publish videos of every session of our Care Partner Meetup, but you can sign up to attend our future meetups live here: davisphinneyfoundation.org/event/parkinsons-care-partner-meetup/ And your wife may be interested in our Living with Parkinson's Meetup. We post recordings on this channel, but she can sign up to attend live here: davisphinneyfoundation.org/event/webinar-series-living-with-parkinsons-meetup/
@alisonmyers8968
@alisonmyers8968 27 дней назад
can you show that web address in the chat?
@davisphinneyfdn
@davisphinneyfdn 25 дней назад
Do you mean the address for the persevere study? Here is the screening site: redcap.rush.edu/redcap/surveys/?s=FDN3MJNCYAHTPHWM
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