Even though National Preparedness Month is coming to an end today, there are easy preparedness steps you can take ALL year to keep your family safe.
Despite the best planning, accidents, injuries, and medical emergencies are unavoidable. Fortunately, thousands of emergency physicians are on duty 24 hours a day, seven days a week, 365 days a year, to take care of you and your family when you need it most.
However, there are some common sense preparedness tools you can use to lower your risk of injury. By planning ahead, you can be prepared, and keep you and your family safe when the unexpected occurs. Continue reading →
For many the initial reaction of hearing “It’s cancer” is shock followed by “I need to get this out.” Michael Sabel, M.D., chief of surgical oncology at the U-M Comprehensive Cancer Center, shares why it’s OK to take a deep breath, and consider all your options before starting treatment.
Take the next step:
Read one patient’s decision on pausing before deciding on her course of treatment
The University of Michigan Comprehensive Cancer Center’s 1,000 doctors, nurses, care givers and researchers are united by one thought: to deliver the highest quality, compassionate care while working to conquer cancer through innovation and collaboration. The center is among the top-ranked national cancer programs, and #1 in Michigan according to U.S. News & World Report. Our multidisciplinary clinics offer one-stop access to teams of specialists for personalized treatment plans, part of the ideal patient care experience. Patients also benefit through access to promising new cancer therapies.
Detecting distress is the first step to helping patients recover.
When going to see a health care provider for an office visit, we expect to be asked about our physical health and have a physical exam that measures our vital signs. Emotional health, sometimes called the sixth vital sign, is harder to figure out. In fact, emotional or psychosocial problems can persist for years without a provider being aware that their patient is in distress.
This has changed for cancer patients, many of whom do experience high levels of distress. The National Comprehensive Cancer Network describes distress as “an unpleasant emotional experience of a psychosocial, social, and/or spiritual nature that may interfere with the ability to cope effectively with cancer, its physical symptoms, and its treatment.” So what is being done to address this? Continue reading →
On Saturday, April 18th the University of Michigan’s Comprehensive Cancer Center Breast Oncology and Community Outreach Programs (with support from the Michigan affiliate of Susan G. Komen, U-M School of Public Health, and QVC presents FFANY Shoes on Sales) will give you the opportunity to learn more breast health, the latest advances in breast cancer and learn about the resources available in the community. The Breast Cancer Summit is held from 10 a.m. to 3 p.m.
I have attended the event in the past and was amazed by the uplifting spirit of everyone there. Breast cancer patients and breast cancer survivors have made up the majority of those who attended. However, there also were healthy, non-cancer patients at the summit who wanted to learn more about general breast health and what type of screening is recommended.
Everyone is at risk for colon cancer, but that risk is not the same for everyone. Colorectal cancer is the third most common cancer affecting men and women and each year, there are about 93,000 new cases of colon cancer and 39,610 new cases of rectal cancer diagnosed in the United States. The average person has a 5 percent chance of developing colon cancer, but some people are at a higher risk.
The most common risk factors for colon cancer are:
What’s in a name? The term palliative care is confusing to many. Oftentimes people associate it with end-of-life care, or hospice care. A poll taken in 2011 revealed that more than 75% of the public lacked knowledge regarding this service.
Although hospice and palliative care overlap in their goals of reducing suffering and providing comfort, the main difference is hospice care is typically for patients who are terminal, or within six months of death, and palliative medicine can be received at any time, whether terminal or not.
Individuals in hospice have chosen to end curative or aggressive treatment, and focus on comfort measures and the dying process. Palliative care patients are often in the midst of active treatment, but need care for distressing side effects from treatment or disease.
Sometimes a referral to palliative care can cause fear in patients and their families because of misconceptions regarding the term. Because of this, some cancer centers have chosen to change Continue reading →
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