About Me

When Science Becomes Personal: My Experience with Rare Genetics

Hello, I’m Lior. While still working toward my PhD in Biology, my world changed when my own child was diagnosed with a rare genetic condition. In searching for answers, I discovered countless scientific articles and data, yet translating all that technical information into everyday understanding felt incredibly overwhelming.

During that process, I crossed paths with other parents and families in similar situations. I often volunteered to dig up relevant studies and resources for their children’s specific conditions, but it soon became clear that no single, organized service existed to provide this level of detail and clarity. That realization inspired me to establish Geneformation, a consultancy focused on compiling in-depth, research-based insights into user-friendly reports.

I’m not a clinician, so I don’t give medical advice or prescribe treatments. Instead, I build on my background in genetics and my ongoing commitment to staying current with peer-reviewed science. My goal is to give families, caregivers, and adult patients the knowledge needed to ask informed questions and collaborate effectively with healthcare professionals.

Seeking broader impact, I also co-founded a patient advocacy foundation in my country to help push research toward better treatments and outcomes for children like my son. Through Geneformation and my advocacy work, I hope to bridge the gap between complex genetics and real-world needs, offering the kind of guidance I once struggled to find.

Ready to Learn More?

Have questions about a rare diagnosis or want to see how in-depth research could help you?
I’m here to help. Simply click the button to reach out, and I’ll be in touch soon to explore the best way forward.