Join the revolution
Get your superpowers
It’s time for patients to take control of their health, through their data, to work alongside their doctors and drive research
At Foundation 29 we work with all those who share this
vision creating the necessary tools and initiatives to
Tools that unleash the power of collaboration
The power to drive
Help diagnosis for doctors and patients
Dx29 is a free application that allows patients and doctors to speed up the rare disease diagnosis process.
We apply artificial intelligence to help patients and professionals identify symptoms and predict accurate diagnoses.
The power to share
Sharing medical data for research
HealthData29 makes it easy to share health data sets with researchers for use in medical research in a simple and secure way.
The initiative includes a guide to good practices in the sharing and processing of this data and has been awarded by the Spanish Agency for Data Protection.
The power to reach
PODs technology empowers rare disease patients with their data to be able to activate applications and connections with organizations such as pharmaceutical companies and regulators.
Includes a registry of patient associations with interface for data upload
An NGO of doers, not talkers, fighting hard
for a real change
We are /
Open standard activists, data-driven scientists, patient-empowering advocates, enabling-technology creators and healthcare system changemakers.
We work /
from the patient, with the patient and for the patient
We want /
a new medicine model around patients
Working with their physicians for their health and the health of others in an ecosystem that openly shares its data to advance medical knowledge together.
We are a non-profit foundation. We work for a medicine in which empowered patients take control of their health through their data and work with doctors and institutions to improve their well-being and that of others.
We create technologies that allow a radical change in your capabilities as users and in the entire medical ecosystem.
The activism of patients, their families and associations are at our core. We put special focus on rare diseases. They are in our origin and in our name: February 29, world day of rare diseases.
We want that there are no
patients without diagnosis,
Can you help us to
For F29 the Duchenne Netherlands organisation is a clear revolutionary look on how to lead a rare disease patient organisation
UMA 2021 Summer Courses: The future of healthcare. The patient. How innovation and artificial intelligence can make us more human
This course has been organized with the collaboration of the Department of Healthcare Management and Innovation of the University of Malaga. Has the pandemic changed
Those who share our vision and help us
make it come true
We break barriers
We get awards