Your contribution helps provide the education, information, and research needed to accelerate patient awareness and access to transformative therapies.
New therapeutics, when developed properly, have unlimited potential to benefit millions of patients suffering from diseases and disorders, many currently without adequate treatment options.
Unfortunately, patient access to these therapies often does not happen, or does not happen quickly enough. Until cell and gene medicine is better understood and gains widespread acceptance as a safe and viable therapeutic option, patients will not be able to benefit.
This is where we fit in.
The ARM Foundation for Cell & Gene Medicine has initiated multi-year programs designed to:
promote public and patient awareness and understanding of the science, benefits, challenges and opportunities of ethical cell and gene medicines, including gene therapies;
increase discussion, transparency and emphasis around the safe and responsible application of breakthrough gene editing techniques;
help stakeholders understand the differences between cell therapies, gene therapies and gene editing; and
increase awareness, understanding and acceptance of these technologies to aid in clinical trial recruitment and, ultimately, widespread clinical therapeutic use.
Together, we can create strong strategic communications and engagement programs, including news and social media outreach, online education, and public service announcements. We can ensure transparency in research and development information, contribute science writers’ guides, host science briefings, and more.
