By Jenn Brown — 2019
Frank Ostaseski, an internationally respected Buddhist teacher and pioneer in end-of-life care, has accompanied over 1,000 people through their dying process.
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CLEAR ALL
Both providers and patients do have power to shape their experience together, especially if they take the time to have a few crucial conversations. In the spirit of palliation, here are a few things, as a physician, I wish I could share more often with patients and their caregivers.
Becoming a cancer caregiver will change your life in many ways, and your loss could be profound. Learning how to cope with the grieving process will help.
It is extremely difficult for anyone, especially young people in their 20s and 30s, to be told that their treatment(s) haven’t worked. If the cancer you have continues to progress despite treatment, it may be called end-stage cancer.
A cancer diagnosis brings a wealth of psychological challenges. In fact, adults living with cancer have a six-time higher risk for psychological disability than those not living with cancer.
The time between diagnosis and death presents an opportunity for “extraordinary growth.”
This is written for the person with advanced cancer, but it can be helpful to the people who care for, love, and support this person, too.
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When I got sick, I warned my friends: Don’t try to make me stop thinking about death.
Families of terminally ill cancer patients may be more satisfied with the end-of-life treatment their loved ones receive when it involves hospice care, a recent study suggests.
A month ago, I felt that I was in good health, even robust health. At 81, I still swim a mile a day. But my luck has run out—a few weeks ago I learned that I have multiple metastases in the liver.
They’re changing how we approach end-of-life care.