Diverse Research Now

Diverse Research Now Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Diverse Research Now, Nonprofit Organization, San Diego, CA.

Diverse Research Now (DRN)
is a nonprofit organization dedicated to increasing diversity in clinical research through education, community conversations, and supportive programs that help people make informed health decisions.

Up to $1,500 in financial assistance may be available for multiple myeloma patients β€” and that's just the start. πŸ’™Join u...
06/12/2026

Up to $1,500 in financial assistance may be available for multiple myeloma patients β€” and that's just the start. πŸ’™
Join us for a free, supportive event featuring Dr. Craig Cole, M.D. for an expert presentation and live Q&A β€” bring your questions, big or small. You'll also learn about free support services , patient resources from the Patient Navigation Center, and a chance to win Visa gift card raffles just for attending.
πŸ“… Tuesday, June 16, 2026
πŸ•“ 4:00 – 6:00 PM PT
πŸ’» Live on Zoom Webinar
πŸ”— Register here:
https://us06web.zoom.us/webinar/register/WN_9PSE30PuTNOel_SnaJ9YBw
Know someone who could benefit? Please share the link. We'd love to see you there. πŸ’™

 πŸ”¬ Take Action to Protect Independent Science at the NIHA proposed rule change could shift authority over NIH grant revi...
06/09/2026

πŸ”¬ Take Action to Protect Independent Science at the NIH

A proposed rule change could shift authority over NIH grant review and funding decisions away from career scientists, researchers, and program officers and place greater control in the hands of senior political appointees.

Independent, expert-led scientific review is a cornerstone of evidence-based research. Decisions about research funding have long relied on scientific expertise, peer review, and merit-based evaluation.

πŸ“’ The public comment period is now open, and your voice matters.

We encourage researchers, healthcare professionals, advocates, patients, and community members to share how this proposal could affect their work, their field, or the future of scientific research.

πŸ—“οΈ Submit your public comment by July 13, 2026

πŸ”— Submit a comment: bit.ly/NIHpubliccomment

πŸ“š Learn more about the proposed rule: bit.ly/NIHmoreinfo

Every comment counts. Help support a transparent, independent, and expert-led scientific review process.

with Renarda Jones

Living With  ?  You Are Not Alone. Ask a Narcolepsy Medical Expert any question   at our Free Virtual Event! Join us for...
06/09/2026

Living With ? You Are Not Alone.
Ask a Narcolepsy Medical Expert any question at our Free Virtual Event!
Join us for a FREE Virtual Narcolepsy event TOMORROW on June 10th from 12:00–1:00 PM PST and connect with a Narcolepsy medical specialist who will be answering YOUR questions in real time.
Register now to save your spot: πŸ”— https://us06web.zoom.us/.../reg.../WN_MoLpmnYkT96O9o85LKWaqw
This is a safe, supportive, and welcoming space designed for people living with Narcolepsy, caregivers, and anyone looking for trusted information and community support.
What You’ll Learn:
Latest treatment developments and what’s coming next
Information about clinical research opportunities you may qualify for
Answers to your questions directly from a medical specialist Resources and support from a community that understands - Plus, attendees will have a chance to win Visa cards during our live ! (Must be present to win.)
No pressure. No obligations. Just real information, support, and honest conversations.
Event Details - Date: June 10th Time: 12:00–1:00 PM PST - Location: Virtual Zoom Event - Cost: Free Register now to save your spot:
Time & Location: Jun 10, 2026, 12:00 PM – 1:00 PM PDT
Zoom Webinar
with Renarda Jones

06/05/2026

Trust starts with education, grows through community, and leads to meaningful participation.

When diverse voices are included, research works better for everyone.

Stay curious. Stay hopeful. And keep showing up for the work that moves us forward.

06/05/2026

We are not just participants in research anymore. We are shaping it.

When communities are included, science becomes stronger, more accurate, and more human. This is about showing up, building trust, and creating space for the next generation to lead.

We are not waiting for change. We are creating it.

06/04/2026

πŸ’œ Living with Multiple Myeloma? You're not alone.

Join us on **June 16** for a FREE online event designed to help you get answers, discover resources, and connect with a supportive community.

🎀 Hear from Dr. Craig Cole, M.D., a Multiple Myeloma expert from Karmanos Cancer Institute.

πŸ’¬ Ask your questions live during an interactive Q&A session.

πŸ“Œ Learn about free support services, financial assistance resources, Safe Space Calls, Study Buddy services, and other programs that may help you navigate your journey.

🎁 Plus, attendees will have a chance to win gift card prizes!

πŸ—“οΈ June 16, 2026
πŸ•“ 4:00 PM PT | 5:00 PM MT | 6:00 PM CT | 7:00 PM ET
πŸ’» Live on Zoom

πŸ‘‰ Register here:
https://us06web.zoom.us/webinar/register/WN_9PSE30PuTNOel_SnaJ9YBw

Know someone affected by Multiple Myeloma? Tag them or share this post. Everyone is welcome. πŸ’œ

06/04/2026

Do you have questions about Narcolepsy that you’ve never had the chance to ask a medical expert directly? CLICK HERE TO SAVE YOUR SPOT NOW: https://us06web.zoom.us/webinar/register/WN_MoLpmnYkT96O9o85LKWaqw
πŸ’™ Join us LIVE on June 10th (12–1 PM PST) for a FREE virtual Narcolepsy event where a Narcolepsy medical specialist will answer YOUR questions in real time.
No complicated medical jargon. No pressure. Just honest answers, support, and valuable information that could help you or someone you love.
πŸ”₯ During this FREE 1-hour online event, you’ll get:
βœ… Live Q&A with a Narcolepsy medical expert
βœ… Updates on new potential treatments & what’s coming next
βœ… Information about clinical research opportunities you may qualify for
βœ… A supportive community that truly understands

🎁 PLUS: Visa gift card raffles for attendees (must be present to win!) Whether you’re newly diagnosed, struggling with symptoms, supporting a loved one, or simply looking for answers β€” this event is for you.
⚠️ Spots are limited and registration is required.

This episode is a powerful reminder that inclusion in research is about people, voices, and real impact.When communities...
06/03/2026

This episode is a powerful reminder that inclusion in research is about people, voices, and real impact.

When communities are seen, heard, and included, we create better science and better outcomes for all.

🎧 Tune in to hear how representation, trust, and community are shaping the future of clinical research.

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San Diego, CA

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