This site uses cookies to improve your experience. To help us insure we adhere to various privacy regulations, please select your country/region of residence. If you do not select a country, we will assume you are from the United States. Select your Cookie Settings or view our Privacy Policy and Terms of Use.
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Used for the proper function of the website
Used for monitoring website traffic and interactions
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Strictly Necessary: Used for the proper function of the website
Performance/Analytics: Used for monitoring website traffic and interactions
Grant is also a nurse practitioner and palliative care consult service provider at the University of Maryland Medical Center. Since then, community-based palliative care growth has been slow but steady in the MA landscape, according to Grant. Freeland specializes in geriatrics, advance care planning and home-based primary care.
Brody is also a registered nurse in end-of-life care. Our mission is to build expert teams who can then provide expert care and an extra layer of support to persons living with dementia and their care partners,” researcher Ab Brody, associate director and founder of the Hartford Institute for GeriatricNursing at Aliviado Health. “Our
We covered some of our questions on the podcast, others you can ponder on your own or in your journal clubs, including: Maries tele/video palliative care intervention was tailored/refined with the help of a community advisory board. So their caregivers did focus groups. And they had to have a family caregiver. Our consultation.
There is a lot of literature suggesting that standard transplant care doesn’t really meet the needs of these patients and their caregivers. Then we looked also a little bit long-term at three and six months, and we also looked at caregiver outcomes. Eric: Well, let’s talk about caregivers. Eric: Okay. Tom: Yeah.
We organize all of the trending information in your field so you don't have to. Join 5,000+ users and stay up to date on the latest articles your peers are reading.
You know about us, now we want to get to know you!
Let's personalize your content
Let's get even more personalized
We recognize your account from another site in our network, please click 'Send Email' below to continue with verifying your account and setting a password.
Let's personalize your content