CaRAVAN will coordinate research efforts involving all stakeholders including scientists, clinicians, patient advocacy leaders, patients and caregivers.
By providing accessible resources and collaborating under shared and orchestrated research plans, CaRAVAN will help pave the way to transformative therapeutic trials and help unveil scientific breakthroughs that will ultimately bring cures to all vascular anomalies.
We are so much #StrongerTogether.
By 2030, together, identify the biologic mechanisms responsible for all vascular anomalies, bringing therapies that will improve patients’ lives and lead to cures.
Infused with a sense of urgency and driven by the nature of the problem, our passion for improving the lives of those living with vascular anomalies is driven by the CaRAVAN Network’s four core values:
Our team is made up of diverse parents, patients, and family members affected by vascular anomalies, patient advocacy leaders and members, scientists, clinicians, and students who each bring a unique and diverse set of skills, opinions, and perspectives working together to maximize successful research opportunities.
CaRAVAN Network plans to share new research publications, research and educational opportunities for trainees, grant and scholarship opportunities, and just about anything involving research in vascular anomalies so that it gets to you - our amazing vascular anomaly community.