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We joined the haemophilia community to raise awareness about haemophilia A, a rare inherited blood disorder.
We are pleased to share that we have facilitated interactive sessions bringing together patients, experts, and key healthcare stakeholders to comprehensively map patient needs. Additionally, we have developed patient testimonials to share their stories and provide insight into how they manage their daily lives.
Our mission is to integrate the entire health ecosystem to improve the quality of life for individuals living with haemophilia A. We call on all stakeholders to commit to transforming the healthcare landscape, ensuring patient needs are met, and driving meaningful progress through collaboration.
Discover more insights and hear directly from patients by downloading our summary or white paper, The Haemophilia A Care Pathway: Needs and Aspirations to Build a Better Future.
This initiative has been realized with support from S.A. Novo Nordisk Pharma N.V. and AHVH, the Belgian patient association.
Download the one-pager summary
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Curious to hear Noémie's haemophilia story?
Curious to hear Tibor's haemophilia story?
Download the full white paper
The haemophilia A care pathway: Needs and aspirations to build a better future
Download the full white paper
The haemophilia A care pathway: Needs and aspirations to build a better future
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