California Black Health Network’s New Campaign Zooms in on Patient Rights, Empowerment

0
California Black Media

By Edward Henderson, California Black Media

California Black Health Network (CBHN) recently launched its “Health 4 Life: Healthy Black People Campaign.”

The campaign aims to empower and educate all Black Californians with “How do I…” (HDI) information and resources needed to effectively navigate the health care system. It also provides tips for advocating for friends, family, and themselves when undergoing medical treatment.

In addition, the campaign advises Black patients on how to respond when faced with discrimination.

“We are working to ignite a Black Health Movement here in California and create a more empowered community of individuals and patients to become proactive about their overall health and well-being, focus more on prevention, and take ownership of their health and healthcare,” said Smith. “We need to know that there is such a thing as a patient bill of rights, and we need to know how we can exercise our rights as a patient to get the healthcare we deserve and to make the healthcare system work better for us and be responsive to our needs.”

On July 18, CBHN launched a 5-part webinar series titled “Making the Healthcare System Work Better for You,” to help the African American communities in the Golden State understand how to make more informed healthcare decisions and how to make the healthcare system work better for them.

The series featured speaker is Dr. Glenda F. Newell-Harris, M.D., a physician, author, speaker, and patient advocate.

Newell-Harris has been at the forefront of addressing health disparities and championing equal access to high-quality healthcare for all. Her passion, she says, even prompted her to write a book on the subject along with a colleague, Dr. Brenda Springs.

“It’s very important that you need to understand you have rights as a patient. You may feel when you are in a medical situation that you’re at the mercy of everybody that is there. But even in that process, you do have rights,” Newell-Harris added. “Patients of color are often the ones who are disenfranchised.”

An example of some ‘How do I’ questions the campaign answers are; How do I take action to protect my health? How do I find the right healthcare provider for me? How do I know what my plan covers? How do I prepare for my visits? How do I speak up for my and my family’s health?

Through the HDI Campaign, CBHN is working to create a more empowered community of individuals who are proactive about their overall health and well-being, focus more on prevention, and take ownership of their health and healthcare. To accomplish this, one part of the HDI Campaign is focused on health education.

The first webinar focused on patient rights – “Part 1: Know Your Patient Rights. Newell-Harris delivered a presentation that highlighted patient rights surrounding information, disclosure, insurance coverage, choice of providers, emergency services, treatment decisions, respect and non-discrimination, and patient responsibilities.

“From a standpoint of goals and objectives, patient rights were created to build trust and confidence within the healthcare system, to strengthen the bond between you and your healthcare provider, and also to empower you to take charge of your health,” said Newell-Harris.

While patient rights are not legally enforceable, they present a guideline as individuals travel along their medical journeys, so people feel empowered as to when and where to ask the right questions. For example, Newell-Harris stressed the importance of the patient’s right to ask about how many times a doctor has performed a certain procedure, the health record of a hospital, and the right to report concerns or issues with the care you received.

In terms of respect and discrimination, Newell-Haris emphasized the importance of cultivating a relationship with your primary care doctor that is rooted in respect.

“We must demand respect in our visits. If you’re in a medical encounter and you don’t feel like you’re being respected, you don’t hear what the doctor says to you, you don’t listen, and you defiantly will have questions if you are going to follow his or her instructions. If you don’t feel like you’re respected, there are a lot of things you can do with your primary care relationship.”

Lastly, Newell-Harris spoke about the responsibility that individual patients have in the healthcare relationship. She stressed the importance of understanding your insurance plan and deductibles, the health needs of your family, keeping appointments, and being honest with your doctor about taking medications.

“Keep in mind that this is a partnership. There are some things your doctor needs to do, and there are some things that you need to do as well,” she said. “Will you have hiccups along the way? For sure. But hopefully they will happen with you being wide open to the knowledge, you’ve had clear communications, you have been part of the decision making and you feel like you are in this as a partnership with your doctor.”

The remaining webinar schedule is as follows:

  • August 8 – Part 2: How to Communicate with Your Healthcare Provider
  • September 19 – Part 3: How to Navigate Through the Healthcare System
  • October 24 – Part 4: How to Advocate for Yourself and Your Loved Ones
  • November 21 – Part 5: How to Participate in the Decision-Making for Your Care

For more information and to register, visit cablackhealthnetwork.org/events.