Welcome to LASID!
Latin American Society for Immunodeficiencies. Uniting Latin America in the pursuit of excellence in immunodeficiency research and care.
Learn more about our mission here.
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LASID President’s Vision
Dear Members of the Latin American Society for Immunodeficiencies (LASID),
I am deeply honored to serve as the new President of LASID and am excited for the journey ahead in immunodeficiencies research and care in Latin America.
Key Initiatives and Invitations:
- Summer School 2024: I am thrilled to announce the upcoming Summer School in 2024, a prime opportunity for learning, sharing, and networking. I encourage participation from everyone as attendees, speakers, or mentors.
- LASID Meeting 2025 in Argentina: We are excited to host the next LASID Meeting in Argentina. This event promises to showcase our latest research and clinical advancements, as well as Argentina’s rich culture and hospitality.
- Committee Collaboration: Our committees are crucial to LASID’s success. I invite you to join and contribute your skills and perspectives, shaping the direction and impact of our society.
- IEI Registry Participation: Contributions to the Immunodeficiency Diseases registry are essential. Your input helps in understanding immunodeficiencies in Latin America comprehensively.
- Academic Webinars: We will continue our series of webinars to keep our members updated with the latest in immunodeficiency research and treatment, also serving as a platform to share your work.
- Active LASID Membership: I urge you to engage actively with LASID in research, clinical care, or education. Your involvement is vital to our community and mission.
Closing Thoughts:
As we begin this new chapter, let’s harness our unity and commitment to improve lives affected by immunodeficiencies. I am eager to collaborate with you all and see the impact we will make in this field.
Warm regards,
Dr. Lorena Regairaz President, Latin American Society for Immunodeficiencies (LASID)
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Patients and health policy organizations
Iniciativa ALAS
ALAS is an alliance of associations across countries dedicated to ensuring the right to health for individuals with primary immunodeficiencies. By fostering collaboration and advocacy, ALAS plays a pivotal role in shaping health policy, aiming to improve access to care and support for those affected by these conditions. Through its efforts, the initiative seeks to create a unified voice that influences health policy, ensuring that the needs of individuals with primary immunodeficiencies are recognized and addressed at both national and international levels.
IPOPI
IPOPI is a non-profit international organisation and the leading advocate for primary immunodeficiency (PID) patients worldwide working in collaboration with patients, doctors, politicians, regulators, pharmaceutical industry and other relevant stakeholders. para garantizar el derecho a la salud a personas con inmunodeficiencias primarias
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