Desmitificación de Ensayos Clínicos, Gestión de Voluntarios, Crecimiento de la Comunidad de Defensa e Involucramiento con la HP.
Es un honor formar parte de la Academia GAAPP, un espacio vital para la difusión de información y el fortalecimiento del compromiso en torno a temas clave en la salud.
Reunión MINSAL Mayo 2024.
Ministra Ximena Aguilera, Sub secretaria, Equipo ley: "Ricarte Soto".
Asociación Chilena de Hipertensión Pulmonar en el Congreso ALAT, Asociación Latinoamericana de Tórax.
Simposio Internacional y encuentro Latinoamericano de Líderes de Hipertensión Pulmonar 2024 Colegio Médico Lima (Perú.) Uniendo fuerzas en LATAM y el mundo.
Participación en congreso enfermedades raras, poco frecuentes y huérfanas en Chile 2024 (CERPOCHI.)
Lanzamiento de la Plataforma "Pulmones Vitales", para pacientes con H.P en el Día Latino 2024
Lanzamiento de la Plataforma "Pulmones Vitales", para pacientes con H.P en el Día Latino 2024
Lanzamiento de la Plataforma "Pulmones Vitales", para pacientes con H.P en el Día Latino 2024
Día Latino 2024. Hipertensión Pulmonar Hapchi Instituto Nacional del Tórax. Charlas educativas para pacientes y familiares.
Congreso Hipertensión Pulmonar Indianápolis 2024.
Evento anual “Cambiemos la Historia” en apoyo a pacientes con trasplante de HP.
Participación congreso PVRI asociación chilena de hipertensión pulmonar.
In HAPCHI, Chilean Pulmonary Hypertension Association, we have been working with an unwavering commitment since our foundation in 2013. We are a non-profit civil association, completely independent, with a nationwide scope. Our mission is clear: to improve the quality of life of individuals affected by pulmonary hypertension (PH), a rare but profoundly challenging disease.
HAPCHI was born from the initiative of a group of patients, families, and friends who, aware of the severe challenges associated with PH, decided to join forces to transform the reality of those affected by the disease. These challenges include late diagnosis, lack of information, and limited treatment coverage. Since its inception, the directors and collaborators of our association have selflessly dedicated their time and skills, driven by a deep commitment to the community.
At HAPCHI, we work to: educate, empower, and advocate for the rights of patients with pulmonary hypertension and their families. We recognize the importance of:
Education and Awareness
We organize informational activities, talks, workshops, and campaigns to increase awareness about pulmonary hypertension. Our goal is to provide tools that allow patients and their families to better understand their condition and make informed decisions.
Advocacy
We promote actions to ensure that patients' rights are respected and defended. This includes engaging with health authorities, insurers, and decision-makers to improve public policies and health coverage.
Psychosocial Support
We offer emotional support and guidance to patients and their families, helping them cope with the physical, emotional, and social challenges that the disease brings.
Promotion of Research
We collaborate with researchers, universities, and medical centers to promote studies that advance the diagnosis, treatment, and management of pulmonary hypertension.
Since its foundation, HAPCHI has positively impacted the lives of hundreds of patients and their families across the country. Our work has contributed to a significant change in the visibility of pulmonary hypertension and the quality of care patients receive.
At HAPCHI, we believe that information is power, and that mutual support is the key to transforming lives. Together, we work toward a future where all patients with pulmonary hypertension have access to dignified, timely, and quality care.