Partner with CMDN
Together, we can ensure no myeloma patient in China fights alone.
Who We Are
CMDN (China Myeloma Digital Network) is a nonprofit, patient-founded organization supporting 2,000+ multiple myeloma patients and families across China. We independently curate evidence-based resources and provide free, unbiased navigation for international patients seeking approved CAR-T therapies in China.
Our Impact at a Glance
2,000+
Patients & Caregivers Supported
Active members in our patient community
50+
Evidence-Based Guidelines
Curated from NCCN, IMWG, CSCO & more
71+
Clinical Trials Connected
Including CAR-T and bispecific antibodies
2
Languages Supported
Full bilingual platform (中文 / English)
Community Profile
Our community represents a diverse cross-section of the myeloma patient population in China, offering authentic, first-hand perspectives on the Chinese treatment landscape.
Coverage
30+ provinces across mainland China
Composition
Patients, caregivers, and family members
Disease Stages
Newly diagnosed through relapsed/refractory
Engagement
Daily peer support and knowledge sharing
Content Focus
Evidence-based guidance, CAR-T navigation, and research records
Platform
WeChat groups + chinamyeloma.org (bilingual)
Why Partner with Us
Largest Grassroots Myeloma Community in China
Direct connection to 2,000+ actively engaged patients and caregivers, providing authentic patient voices and real-world insights from the Chinese myeloma landscape.
Evidence-Based Bilingual Knowledge Platform
50+ authoritative clinical guidelines translated and localized for Chinese patients, sourced from NCCN, IMWG, CSCO, and other leading institutions.
Bilingual Evidence and Navigation Infrastructure
Editorial workflows supporting evidence-based guidance, verified hospital records, transparent disclosures and bilingual clinical trial summaries.
Local Execution, Global Standards
Proven ability to translate global advocacy initiatives into locally impactful programs that resonate with Chinese patients and families.
Partnership Models
Content & Knowledge Sharing
Co-develop or translate patient education materials, clinical guidelines, and awareness resources for the Chinese myeloma community.
Joint Awareness Campaigns
Collaborate on global initiatives such as Myeloma Action Month, World Cancer Day, and regional awareness events with localized Chinese execution.
Research & Data Collaboration
Share patient insights, real-world data, and community feedback to support global research and improve treatment outcomes.
Capacity Building & Training
Exchange advocacy best practices, organizational development strategies, and patient support program methodologies.
Resources for Partners
Download our materials to learn more about CMDN and explore collaboration opportunities.
CMDN Overview Deck
A comprehensive introduction to our mission, community, and partnership opportunities.
Community Impact Summary
Key metrics and milestones from our patient support operations.
Brand & Media Kit
Official logos, brand guidelines, and approved imagery for co-marketing.
Our Knowledge Sources
Our evidence-based content is built upon guidelines published by these leading global authorities. We independently curate and translate their publicly available clinical guidelines for Chinese patients:
Let's Connect
We welcome conversations with international myeloma organizations, research institutions, and advocacy groups. Reach out to explore how we can work together to improve outcomes for myeloma patients.
Start a Conversationglobal@chinamyeloma.org