Rosanne provides round-the-clock care and supervision to her mother who is in the final stages of dementia--all with no pay.
We explore the ways gender identity and sexuality affect caregiving relationships and outcomes.
A member of the Well Spouse Association offers insight on the spousal caregiving experience.
It is never too early to talk with a parent about their future care wishes, but it can be too late. Here's how to start the conversation.
Sarah talks about her father's ALS diagnosis and self-identifying as a caregiver.
Jay shares the ways her attitude toward caregiving changed after she became her father's primary caregiver.
A death doula shares eight questions that can bring joy, clarity, and healing to an end-of-life experience.
Women have been the face of caregiving for generations. Learn more about the unique experiences they share in providing care.
Whether you’re new to caregiving or interested in what to expect, these four tips can reduce your anxiety and prepare you for future challenges.
Though it may seem ill-fitting, bringing humor into the end-of-life experience can offer relief and help families and friends create new, cherished memories.
The five love languages can be applied to the loving care and support we give to those living with dementia.
Use these 20 questions to spark meaningful conversation with a loved one about their life and memories.
Male, spousal caregivers discover personal ways to find meaning and purpose in their caregiving and, in the process, challenge the stereotypes often attributed to this cohort of caregivers.