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Transforming lives through access to genomic
knowledge

100% of your money to connect people in need to lifesaving information.
Join our monthly giving community and transform lives for families around the world. Every single penny will help to save lives by connecting people in need.

Half of the world’s population has no ACCESS to healthcare. We’re on a mission to change that. Here’s how.

REAL IMPACT

We invest in building long-lasting solutions together with local governments, NGO’s and
industry.

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LOCAL PARTNERS

We partner with local organisations around the world who are working empowering people in local communities.

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WE PROVE OUR IMPACT

We monitore and analyze the social impact of projects you fund to ensure your money is spent on saving lives.

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WITH YOUR HELP

We are fundraising to setup our first community project. SEE HOW YOU CAN HELP

But we’re not done yet. We need your help. Here’s how you can get involved

WHY CONNECTIVITY?

According to the WHO and the World bank, half the world population has NO access to essential health services.
Learn how access to healthcare can improve health,
save lives, boost local economies, empower families, and give kids more time in school.

GET INFORMED

Do something crazy to raise
money to contribute building a
better world

FUNDRAISE

Give €30 and you can
help to connect a person
in need.

DONATE NOW

Experience how connectivity
is changing lives around
the world.

WATCH OUR VIDEOS

Ask for donations instead of
gifts and your birthday will
change lives.

PLEDGE BIRTHDAY

HGF:
Saving Lives

Help us solve the global
ACCESS to healthcare
problem.

GIVE MONTHLY

Sponsor an entire connectivity project.

For €10,000 or more you can fully fund
a patient recruitment campaign to connect
people with a certain medical condition.
100% funds connectivity projects.

Pre-order: Saving billions of lives by connecting people to lifesaving information. A story of hope, faith and a mission to build a future with access to lifesaving information for all.

Buy the book, an inspiring personal story from Human Genome Foundation founder Susanne Baars.

Connecting the Dots.

“Diagnosed with the rarest type of Usher in the world, access to genomic knowledge could possibly bridge the gap for my daughter between loss of both vision and hearing  and finding a cure, by connecting a lot of dots in a complex healthcare ecosystem!
– Jeroen de Punder

Let us tell you more.

We will email you to start the conversation.

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