Beyond Scleroderma began as a multi-media capstone project by a talented group of students from De La Salle-College of Saint Benilde in Manila, Philippines. The website and docu-series were produced to raise awareness and educate others on Scleroderma, a rare autoimmune disease with no cure as of 2025.
Through the website and online media, we hope to:
Show that you can still have a fruitful and meaningful life even after diagnosis.
Empower patients, caregivers, and anyone who knows and loves someone with this disease.
Raise enough awareness and eventually find a cure to improve the quality of living for generations to come.
With that being said, the Beyond Scleroderma team is open to projects and collaborations. Email us your proposal to scleroderma.awareness.phils@gmail.com
Beyond Scleroderma began as a multi-media capstone project by a talented group of students from De La Salle-College of Saint Benilde in Manila, Philippines. The website and docu-series were produced to raise awareness and educate others on Scleroderma, a rare autoimmune disease with no cure as of 2025.
Through the website and online media, we hope to:
Show that you can still have a fruitful and meaningful life even after diagnosis.
Empower patients, caregivers, and anyone who knows and loves someone with this disease.
Raise enough awareness and eventually find a cure to improve the quality of living for generations to come.
With that being said, the Beyond Scleroderma team is open to projects and collaborations. Email us your proposal to scleroderma.awareness.phils@gmail.com