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How Can I Get the Best Multiple Myeloma Care No Matter Where I Live?
“[Myeloma] patients who are African-American and Hispanic typically get to the right treatment much later. In a lot of cases they may not get to the right treatment at all. We also know that the burden of cost of care is much higher for minority patients.” - Dr. Sikander Ailawadhi

There is a critical need to raise awareness of the treatment gaps among minority populations living with multiple myeloma. How can myeloma patients get the best care no matter where they live when factors like age, geography, socioeconomic status, ethnicity, gender, and insurance type heavily influence the path to empowerment?

On July 29th @ 11AM PT/2PM ET, register to join our panel of distinguished myeloma experts and patient advocates who will tackle how we achieve health equity for multiple myeloma patients no matter geography. Register now, and submit your questions to question@powerfulpatients.org

Register and join us to learn:

● How myeloma patients can get the best care no matter where they live
● Where to access actionable and meaningful myeloma educational resources
● How to avoid roadblocks to care; for example, the cost of treatment
● Important questions for your support team, and how to ask them
● Empowerment tools for informed and shared decision-making with your care team

Jul 29, 2020 11:00 AM in Pacific Time (US and Canada)

Webinar is over, you cannot register now. If you have any questions, please contact Webinar host: Diverse Partners in Your Myeloma Care.