Parliamentary Advocates for Rare Diseases
At a Policy Event organised at the European Parliament in Brussels last month, EURORDIS re-launched the Network of Parliamentary Advocates for... Read More
Not-for-profit patient-driven organization. Provide support and information for patients with Alpha-1 and their families. Promote education and awareness of the disease. Advocate for Alpha-1 patients and community.
Subscribe to our mailing list and stay informed and connected!
Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information.