Multiple Myeloma Research Foundation®, Inc. (MMRF®), Bristol Myers Squibb (BMS) &
Diverse Research Now (DRN): CARE Initiative
You don’t have to navigate multiple myeloma alone.
Goals and Implementation
The CARE Initiative is designed to activate and empower informal support ecosystems—including patients, caregivers, family members, and close friends—to improve health outcomes for patients with multiple myeloma in underserved U.S. communities.
What Does DRN Do in This Project?
UPCOMING FREE DRN CARE EVENTS
✨ Chow & Chat
Join us in person for culturally relevant gatherings that bring people together over a shared meal. These events feature caregiver-focused education, health talks, and meaningful conversation in a warm, community-centered setting.
*In-person multiple myeloma events are currently held only in San Diego, CA and Houston, TX.
💻 Chit & Chat
Prefer to join virtually? Our online sessions offer expert presentations, live Q&A discussions, and opportunities to connect with other caregivers from anywhere.
Whether you attend in person or online, these events are designed to be safe, empowering spaces where you can meet others who understand your journey, share experiences, and gain practical tools to strengthen your caregiving and advocacy.
Did you attend one of our events? 🔗 Please provide your feedback here!
ADVOCACY SUPPORT HUB
At Diverse Research Now (DRN), our programs are designed to support you every step of the way—especially if you’re navigating multiple myeloma or considering clinical research.
🤝 Study Buddy Program
You don’t have to go to medical appointments alone. Through our Study Buddy Program, trained advocates—often from similar cultural and language backgrounds—can accompany you to your medical visits. They help make sure your questions are asked, your concerns are heard, and your care needs are clearly understood. Our goal is to help you feel confident, supported, and empowered in every healthcare conversation.
*Study Buddy Program is currently available in San Diego, CA & Houston, TX only.
💬 Safe Space Program
If you need someone to talk to, we offer confidential 1:1 support calls. These Safe Space conversations are designed to help you think through clinical trial decisions, understand your options, and support your emotional well-being. We are expanding bilingual support—especially Spanish-speaking advocates—to better serve diverse communities.
*Available nationwide in the United States.
Helpful Resources & Educational Materials
Check the links:
🟦 🔗 Multiple Myeloma: What You Need to Know
🟩 🔗 Bone Health and Multiple Myeloma: What You Need to Know
🟪 🔗 Multiple Myeloma Patients Getting On The Right Track
Download as PDFs below:
📄 Multiple Myeloma: What You Need to Know
📄 Bone Health and Multiple Myeloma: What You Need to Know
📄 Multiple Myeloma Patients Getting On The Right Track
MMRF website has many resources on their Education Resource Hub page at Multiple Myeloma Patient Education Resource Hub | The MMRF
Interview with
Multiple Myeloma patient
Check out our podcast episode
Voices of Inclusive Research (VIR)
with a Multiple Myeloma patient that we supported
Ready to Be Part of Research — Beyond Multiple Myeloma?
If you’re open to learning about research opportunities beyond multiple myeloma and would like to receive information about other studies that may be a good fit, we invite you to fill out the form.
There’s no pressure and no commitment — just trusted education and information to help you explore your options. If something aligns with your interests, we’ll share the details and let you decide what feels right for you.
Our goal is simple: to provide clear, supportive information so you can make informed choices at your own pace.
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