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Update on Jessie's status and some words of wisdom from her article, 6 Ways to Help When Someone Has Cancer, originally published in an October 2008 issue of Parade magazine.
Jessie has written about her perspective as the patient in an extremely stressful situation. I can add a different one: that of the husband of my seriously ill wife.
It could happen tomorrow. The doctor says, "I'm sorry, I have bad news," and suddenly your life is turned upside-down, leaving you reeling from the shock of a potentially life-threatening diagnosis. Here is some advice on getting through that initial period.
I had breakfast this morning with my friend, Dave Garcia. Dave is a pit boss on the graveyard shift at the Belagio Hotel in Las Vegas. He is also a 52-year-old chronic lymphocytic leukemia survivor. Today he was to see his oncologist and get his latest blood test results. Would his white blood count be in the normal range? As you can imagine, Dave was on pins and needles.
A TIME article this week reveals new research that 'doctors who are more empathetic actually have healthier patients.' More on empathy and its role in health outcomes.....
For more than three weeks I have been hanging around the ICU. Lara, my friend and colleague, is poised between life and death, having rejected her five-year-old transplanted lungs. She awaits the gift of a chance for life from another donor. Lara wants so much to live. During her last conversation with me before being placed on a ventilator, she talked about her fear. Now breathing and most everything else is done for her. Drugs keep her oblivious to the suspense.
In The New York Times This Life column, 'You Look Great and Other Lies', Bruce Feiler shares what he learned after his diagnosis and treatment for bone cancer. Bruce describes the gestures and words that are helpful and offers cautions about what not to say/do when someone you care about is ill.
The experiences and emotions brought on by having an illness or disability can be complex and sometimes unexpected. In this blog roundup, three patients share theirs.
Medical student Katherine Ellington grapples with reconciling her two roles as daughter and doctor-in-training as her mother recovers from a heart procedure.
This interview with Connie Davis is the second in a series of brief chats between CFAH president and founder, Jessie Gruman and experts - our CFAH William Ziff Fellows - who have devoted their careers to understanding and encouraging people's engagement in their health and health care.
In this round-up, patient bloggers describe a mix of difficulties they experience in everyday conversations due to their illnesses.
Erica Kosal's husband, Jim Young, has battled complications of chronic Lyme disease since his diagnosis in 2008. In 2010, Jim's hospitalization for respiratory problems took a turn for the worse, resulting in a 3-week ICU stay.
I was first diagnosed while on vacation in 1994. A doctor entered the room and, without warning, said that I had 'a terminal and incurable form of leukemia' and 'less than five years to live.' Just like that. Turns out he was wrong'
People who are dying have much living to do, whether it is measured out in days, weeks or months, and the demarcation lines between the living and the dying might as well be drawn in pencil. But the truth is that it's important to talk about dying and what it means to each of us.
During Thanksgiving week, many patient bloggers shared what they were thankful for. Though there were many ' here are what four of them had to say.
The essays collected here reflect on what it felt like as a patient with a serious illness, to cobble together a plan with my clinicians that works and to slog through the treatments in the hope that my cancer will be contained or cured and that I will be able to resume the interesting life I love.
Recent health behavior research news stories: Friendships Are Good for Our Health | Obesity Lowers Quality of Life in Boys | Health Centers Have High Satisfaction Rates | Diabetes + Depression Increases Risk of Death
How many friends/family members/social workers does it take to change the mind of a frail person? Even if the frail person was/is one of the leading geriatric social workers in the country?
This week in health news: When dieting encouragement goes wrong | What works for more walking at work | Vaccines: Not just for babies | Health insurance matters for cancer survivors
I was naive when I decided to enter medicine. My impressions then were that doctors always “did” stuff—for patients, and to patients. We would do stuff to you (examinations, blood tests, scans, surgeries) in order to help you.
When I signed up for palliative care in 2011, I thought I’d made my last medical decisions. In the future I’d take the least-invasive, lowest-cost approach to medical care and forego dramatic, expensive treatments. If only life with advanced cancer were so simple!
Coast-to-coast, stress is the norm for most Americans: 55 percent of people feel stressed in everyday life, and far more women feel the stress than men do. It will take a village to help manage stress, including but not limited to our doctors.
I don't know if it's growing older, or New England winters, or the meds I take, or watching Homeland and Downton Abbey in the same week – but my memory isn't as crisp as it used to be. My partner, Richard, has become part of my cerebral cortex...
As a very stubborn and advice-resisting ill partner myself, I can't say if this issue is gender-specific. But I do know it's an issue most couples dealing with illness face, more than once. Here are my two suggestions for what to do when your partner resists your advice...
We've watched it many times on television or in a movie: The patient lies in the intensive care unit, gravely ill, with the family at the bedside. The doctor walks into the room and asks, "What do you want us to do?" and opens up a huge can of worms that is, in fact, ethically incorrect. The first priority that a physician has is to their patient...
"All your Prepared Patient essays do is complain about your health care and your doctors. That's why I don't read them." Yowzah! Do I really complain? Not to be defensive, but I don't think so. Every week I work to vividly describe insights that might shine a little light on this project that patients, caregivers, clinicians and policymakers – well, the list goes on – share of trying to make health care more effective and fair...
Should you bring someone with you to your next doctor's appointment? If you're asking, the answer is yes. If you're asked, how do you be the best companion? Prep in advance, listen, record and ask questions. Know why you're going. That means two things...
I was reluctant to attend. I didn't have leukemia and am not a "touchy-feely" person, which was my perception of a support group. However, I dragged my IV pole of medications and went to this meeting where I met my first fellow myeloma patient named Jim – finally, someone who had the same disease as me. So to this day, whenever I meet with one or a group of myeloma patients, I make the following plea...
I was once someone who never felt that I'd be normal again. But recovery is made up of small steps that lead us to a successful life – these steps toward wellness matter, because being active versus passive about your recovery greatly increases the likelihood of a positive outcome...