You may ask how. What comes next?

The answer is simple. It is you.

Your voices, your networks, your willingness to open doors, share resources, and guide us towards a more scientific and preventive approach. It is doctors and pathologists who believe in early testing. Families and caregivers who speak up. Institutions that stand with us. And a system that is pushed, persistently and purposefully, to make testing mandatory. Through films, medical education, partnerships with pharma, corporates, and anyone willing to help move the needle. Whatever it takes.

It may sound difficult. But it is far from impossible. The seed has already been sown. All it needs now is consistent care and collective effort to grow into something lasting.

What lies ahead is the strengthening of community, capacity, and shared purpose across the entire Thalassemia ecosystem. Every step forward is about bringing people closer, not as separate voices, but as one growing movement.

We are building connections across the country, reaching out to organisations, warriors, caregivers, and communities who want change as deeply as we do. This spirit of collaboration will continue to shape everything we do next.

Our vision goes far beyond any single initiative.

• We imagine a powerful, global wave of Thalassemia awareness driven by storytelling and social media that informs, educates, and moves people to act.
• We want to uplift Thalassemia warriors by giving them a platform where their opinions matter, where their voices are seen and heard, and where the narrative shifts to one that is truly warrior centric.
• We aim to connect with every Thalassemia society in the country, not as individual organisations, but as one team working towards one shared goal.
• We want to build a nationwide network of committed volunteers who can support these missions on ground, wherever they are needed.

These are the thoughts that wake us up every day.This is the energy that keeps us moving.

And this is only the beginning of something much bigger.