These health literate tools can help you get patients up to speed on MM.
- Help patients spread the word about MM in their communities
- Build strong relationships with patients and care partners
- Keep people engaged in the care process
That’s My Word® is an educational campaign sponsored by Johnson & Johnson to improve health equity for communities of color affected by multiple myeloma (MM). When people like you choose to take action and close health gaps in diverse communities, we can create a major impact on the lives of people fighting MM. You are making real change possible, one visit at a time.
Studies have shown that when Black MM patients receive equal access to care, they can have better treatment results.
“I’ve learned the value of being vocal…My (HCPs) were proactive in asking me what resources I needed and connecting me with other patients.”
— Thomas Goode, multiple myeloma patient and patient advocate
In consideration of the time spent participating in this activity, Thomas Goode was paid an honorarium by Johnson & Johnson.
“...You're gonna have a much more successful visit when there's a two-way conversation going.”
— Amy Pierre, RN, MSN, ANP-BC, Nurse Practitioner, Memorial Sloan Kettering Cancer Center
In consideration of the time spent participating in this activity, Amy Pierre was paid an honorarium by Johnson & Johnson.
These leaders are setting the example for what it means to give your word to Black communities impacted by multiple myeloma.
Amy Pierre, RN, MSN, ANP-BC, Nurse Practitioner, Memorial Sloan Kettering Cancer Care
Cesar Rodriguez, MD, Associate Professor of Medicine, Icahn School of Medicine at Mount Sinai
Ellen Dillard, RN, Nurse Practitioner
Every patient with multiple myeloma that you care for has a different story. You may hear from your Black patients that it has taken a while for them to receive a diagnosis, or they might have been misdiagnosed, or received a delayed treatment. In your visits with Black patients, you have the opportunity to not only help address issues of health equity, but you can also begin to heal relations between Black communities and the healthcare system.
Ways to connect with MM patients and care partners
Make time to talk with the patient and their family. Build trust by understanding their concerns and preferences. Get to know them as a person first.
Ask patients about previous experiences they’ve had with doctors—positive and negative. Find out how they like to learn, and present information to them in ways that make it easier for them to take it in.
Talk about each patient’s treatment expectations and fears. Use shared decision-making to give patients a plan they had a hand in making.
Because MM is a chronic condition that needs long-term management, the family will also feel the impact. Build trust with a patient’s care partner as well so MM patients have strong support over time.
Why it matters
41.2% of Black Americans have little trust or no trust at all in doctors.
82.4% of Black Americans believe that race plays a great role or somewhat of a role in the care they receive.
Only 24% of Black Americans think their complaints are heard without bias.
As treatment progresses, the care partner may take on a larger role and get more involved.
Taking time to see that each patient feels seen and heard is an excellent way to establish respect and trust—laying the foundation for good collaboration throughout treatment.
Every patient with multiple myeloma that you care for has a different story. You may hear from your Black patients that it has taken a while for them to receive a diagnosis, or they might have been misdiagnosed, experienced a delayed diagnosis, or received a delayed treatment. In your visits with Black patients, you have the opportunity to not only help address issues of health equity, but you can also begin to heal relations between Black communities and the healthcare system.
Ways to connect with MM patients and care partners
Make time to talk with the patient and their family. Build trust by understanding their concerns and preferences. Get to know them as a person first.
Why it matters
41.2% of Black Americans have little trust or no trust at all in doctors.
Ask patients about previous experiences they’ve had with doctors—positive and negative. Find out how they like to learn, and present information to them in ways that make it easier for them to take it in.
Why it matters
82.4% of Black Americans believe that race plays a great role or somewhat of a role in the care they receive.
Talk about each patient’s treatment expectations and fears. Use shared decision-making to give patients a plan they had a hand in making.
Why it matters
Only 24% of Black Americans think their complaints are heard without bias.
Because MM is a chronic condition that needs long-term management, the family will also feel the impact. Build trust with a patient’s care partner as well so MM patients have strong support over time.
Why it matters
As treatment progresses, the care partner may take on a larger role and get more involved.
Taking time to see that each patient feels seen and heard is an excellent way to establish respect and trust—laying the foundation for good collaboration throughout treatment.
“We still need to educate all healthcare providers on how we need to treat everybody in a unique way, it’s not just one recipe...Empowering patients to be accountable for their own health, and at the same time, make them comfortable to ask the questions they need to ask…”
— Cesar Rodriguez, MD, Associate Professor of Medicine, Icahn School of Medicine at Mount Sinai
In consideration of the time spent participating in this activity, Dr. Rodriguez was paid an honorarium by Johnson & Johnson.
Although treatments for MM have improved over time, the road ahead can still be tough for some people living with multiple myeloma, especially those facing health disparities. As a medical professional, your care means so much to the people being treated for MM. When you learn about their specific challenges and roadblocks, you show them how invested you are in their individual experiences and personal treatment success. Give your MM patients your word that you will be a champion for change to help close multiple myeloma health disparities.
These health literate tools can help you get patients up to speed on MM.
Introduce your patients to multiple myeloma and help them stay on top of their health by knowing what to look out for.
This checklist can help people seeking care for MM with information on signs and symptoms, blood tests, and stages of MM progression.
Tell patients about the C.R.A.B. criteria, asking for a specialist, and empowered self-advocacy so they can better own their health and get the best multiple myeloma care available.
Bring patients information to help them identify individuals for their support team and locate support groups for Black people with MM.
Introduce your patients to multiple myeloma and help them stay on top of their health by knowing what to look out for.
Tell patients about the C.R.A.B. criteria, asking for a specialist, and empowered self-advocacy so they can better own their health and get the best multiple myeloma care available.
This checklist can help people seeking care for MM with information on signs and symptoms, blood tests, and stages of MM progression.
Bring patients information to help them identify individuals for their support team and locate support groups for Black people with MM.
“That’s My Word® has definitely helped and is helping to bring people in the fold who did not necessarily have the skills and the tools to manage their care with their provider and be a part of that team.”
— Tiffany Hawkins-Williams, multiple myeloma patient and patient advocate
In consideration of the time spent participating in this activity, Tiffany was paid an honorarium by Johnson & Johnson.