Americans pay more for most medications than most countries. The power of the pharmaceutical lobbies is a topic for another day. But the consequences are real for every American, whether using private insurance, Medicare, Medicaid, other insurance or paying out-of-pocket. A friend of mine was recently diagnosed with a type of adult-onset asthma. After three…
The Patient Navigator Blog
Four things you must know when serious illness strikes: Get Smart Fast. Get Organized. Stand Your Ground, Nicely. Always Follow Up. Read this article for detailed helpful hints.
Being diagnosed with a serious illness is a frightening experience. It is important that you research and educate yourself about your disease and learn to communicate with your medical team. An informed patient gets better results.
The holiday season – beginning with Thanksgiving and through the New Year – can be unbearably hard if you are grieving the loss of a loved one. Here are my tips to survive.
Patient advocacy, or patient navigation, is gaining attention as an emerging profession, both in the media and in the popular lexicon, because it fills so many gaps in the current American health care system. This is especially true today as we continue implementation of the Patient Protection and Affordable Care Act, which is changing the landscape for consumers in how health care is delivered and paid for in this country.
Easter Seals Project ACTION and the American Medical Association have a new pocket guide for patient transportation options before or after a medical procedure.
Patient navigation and patient advocacy are dynamic and growing professions. This article explores the background and current landscape of patient navigation and advocacy.
The bewildering sensation of too much information, yet not enough knowledge to use it, is the reality for many people faced with a serious illness or condition. How do you decide what to do?
Every person has the right to fully participate in decisions regarding his or her own health care. This legal doctrine is called the right to informed consent. As a patient or caregiver, you have the right and responsibility to obtain as much information as you need to be able to commit to a course of treatment or testing process.
People who are multiracial are one of the fastest growing demographic groups in the United States. However, despite donor drives and new efforts to utilize social networking to increase the number of donors, they are also the most under-represented in the marrow registry.
When her son’s pediatrician said she had never heard of the National Cancer Institute (www.cancer.gov), this young mom was blown away. Should she worry about entrusting her son’s care to a doctor who has never heard of this world-famous institution? Comments invited.
The March 4, 2010 New York Times included the following article which discussed the emerging profession of health navigators and patient advocates. Take a look. http://tinyurl.com/healthnavigatorNYT
The words “clinical trials” can conjure up images of desperate medical experiments with little hope of success. In reality, medical advances and breakthroughs can and have resulted from clinical trials. Without them, we wouldn’t have many of the treatments we have today.
Many of you reading this blog have experienced some type of difficult health situation, for yourselves, a friend or family member. It’s also what makes so many of us passionate about helping others through their illness. It’s why Patient Navigator exists. Since it’s the New Year, most people take some type of inventory of their…
Patient Navigator LLC highlighted in National Comprehensive Cancer Center article on cancer navigation.