Rare As One Network

Bringing legal support to patient-led organizations working to improve the lives of people affected by rare disease.

Help pave the way for transformative advancements in the field of rare diseases.

Rare disease is anything but rare. As many as 7,000 rare diseases affect 300 million people globally. Yet worldwide, patients are meeting these challenges head-on. Rare disease research often involves navigating complex regulatory landscapes. Lawyers are needed to ensure compliance with all relevant regulations and laws governing research, clinical trials, and the eventual dissemination of treatments.

Our Partners

WTA lawyers are working closely with patient-led organizations in the Rare As One Network. Partners include:


There are 22 projects looking for volunteers to assist in Rare As One Network work.

Stay up-to-date when new Rare As One Network projects are posted.