WELCOME TO YOUR
GLOBAL PATIENT
COMMUNITY
WELCOME TO YOUR
GLOBAL PATIENT
COMMUNITY
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Find people with a similar gene mutation to save
your life
Globally there are 800M+ patients with rare genetic diseases and cancers, lacking access to treatments. SocialGenomics is here to help you connect.
Find patients with gene mutation
SocialGenomics network helps you to easily find and connect with other patients in the world with similar rare gene mutations. Help each other and create meaningful friendships.
Genomics Research
We use the world’s most advanced algorithms and deep-learning network to get online, fast accessible and affordable access to personalized treatments.
TRANSFORMING LIVES BY CONNECTING PATIENTS TO LIFESAVING INFORMATION AND
TREATMENTS
Thinking different
Apply today
We are saving lives by connecting people, patients, loved ones and passionate scientists to discovery treatments and accelerate medical breakthroughs. Using a freely accessible, easy to use, multilingual artificial intelligence platform. Using one global platform people from all around the world can contribute saving lives.
Solving diseases through genomics
Globally there are more than 400M+ patients with a rare disease and another 400M+ patients with a rare form of cancer – caused by a unique pattern of genetic mutations – searching for other people with the same disease cause and experts who are working on finding a cure. By improving our understanding of genetics, demographics and disease outcomes scientists can discover new medicines & reach out to patients faster.
Bringing the world together
Imagine we could connect a sweet little dutch girl suffering from rare brain cancer with a little boy in Japan with exactly the same rare brain cancer – who is carrying the key to save her life… with the speed of light!
SocialGenomics is building technology to empower people, doctors and scientists from around the world to share & connect unique knowledge to save many lives, speed up medical breakthroughs, improve access to medicines and lower costs.
This will cut billions of dollars in national healthcare costs, and break the cycle of poverty for families in every state. This will help patients to:
- Discover treatments faster
- Bring medicines to market faster
- Save lives of next generations
Easily find other patients who can help
you
One platform for everyone
This platform empowers patients with all kinds of ethnicities, nationalities, genders, and ages on one single inclusive platform.
Simple application process
Within minutes you can apply & receive information about how it works, how you can share your story to help yourself, other people like you and all next generations.
Cutting-edge AI technology
Using advanced algorithms we help you connect with others with a similar genetic mutations to share & connect life changing experiences.
Discover how to
accelerate drug discovery
& development
Find research easily
Connecting people with all kinds of medical conditions, ethnicities, nationalities, genders and ages on one single inclusive platform.
Improve access to newly discovered treatments
Take action by filling in a simple questionnaire, share your experiences to help yourself, other people like you and all future generations.
Improve access to medicines.
Get real-time insights into statistics of people with the same condition, gene mutation, where they live and how they deal with the situation.
SAVING MY DAUGHTER’S LIFE
“In 2011 our daughter was diagnosed with a terminal disease, the doctors couldn’t help her any futher. By connecting to other patients with the same genetic mutation and initiating research, we saved my daughter’s life. SocialGenomics is using technology to digitize this process! Using the power of AI and patient communities to easily share, connect and multiply lifesaving information. And honestly, that is all what matters in such a situation. As every day counts.”
– Christian Kromme
SAVING MY DAUGHTER’S LIFE
“In 2011 our daughter was diagnosed with a terminal disease, the doctors couldn’t help her any futher. By connecting to other patients with the same genetic mutation and initiating research, we saved my daughter’s life. SocialGenomics is using technology to digitize this process! Using the power of AI and patient communities to easily share, connect and multiply lifesaving information. And honestly, that is all what matters in such a situation. As every day counts.”
– Christian Kromme
Making treatments available, accessible and affordable for everone
Patient Empowering
Find people, passionate scientists and research using multi-dimensional matchmaking based on specific gene-mutation that is causing the disease
Global Connectivity
Leveraging the internet to connect patients from all over the world. To get online, fast accessible and affordable access to lifesaving information and treatments.
Genomics-driven innovation
Using the world’s most advanced algorithms to find & connect patients with similar characteristics, gene mutations and pathologies.
Saving lives together
Global platform for patients to help themselves, others like them and all next generations to come.
One small step can save a life
The Human Genome Project was one of the great feats of exploration in history. A collective action by scientists – looking to sequence and map all of the genes of a single human being – from all over the world. To solve individual diseases we now need the collective action from patients.
What if you could contribute to save a life?
Listen to our heros I
Collective action
“Scientists from around the world collectively worked on unraveling the mystery of the first human genome and made history. This enabled us to transform traditional medicine into prevision medicine in just 15 years. Using disruptive technology it’s now time to make this life saving knowledge accessible for all humans on our globe and beyond!”
– Susanne Baars,
Founder SocialGenomics, Neuroscientist
A global community with patients who truly understand you
Using knowledge from current generations to help save next generations. Help scientists and inspire millions of other people to do the same.
