G-RAY
GENETIC RESOLUTIONS
Intelligence in Medical Science
based on genetics and molecular biochemistry to help misunderstood people and their symptoms
After years of studying existing scientific literature on PubMed related to specific polymorphisms and rare genetic mutations in affected individuals, and by comparing whole genome sequencings (WGS NGS) within support groups, I have developed a comprehensive understanding of the genetic similarities and differences among patients presenting with comparable symptoms and separating them into single or combined genetic inheritances (mostly non-rare within 10-20% of the population).
Motivated by a desire to assist others and foster global awareness of frequently misunderstood symptoms—which often result in predominantly negative psychosocial outcomes due to physicians assigning psychiatric or common psychological diagnoses based solely on symptoms rather than investigating underlying causes—I committed to deepening my scientific inquiry.
This involved extensive interviews with chronically ill individuals to explore their backgrounds, genetic profiles, and personal circumstances in greater detail.
Through my undergraduate studies in ethics, psychology, physics, genetics, molecular biochemistry, law, and economics, combined with years of hands-on experience using clinical and scientific tools, I have developed a solid foundation and profound confidence in conducting research, analyzing relevant data, and validating hypotheses in collaboration with expert physicians and academic researchers.
As someone who is subclinically neurodivergent and exceptionally skilled, I bring creativity, out-of-the-box thinking, advanced neuro-communication abilities, and strong social skills. These qualities enable me to deeply understand individuals and their symptoms, aligning these insights with their unique genetic profiles.
Through my work in recent years, I have had the opportunity to connect with several exceptionally skilled experts in the field of unresolved diseases — either through research collaborations or by using their tools.
Among them are the Director of the Department of Research and Science at the University of Utah and Frameshift Genomics (USA).
Supported by Harvard University’s edX online courses, I have studied extensively to achieve a full understanding while receiving top grades. I have also worked with tools from AG Seelow, Charité – Universitätsmedizin Berlin (GER), and engaged in valuable discussions with Heike Sachtleben (Expert Advisory Board, Long COVID, GER).
Special thanks go to Eliane Reichardt, expert psychologist for highly and exceptionally gifted individuals (GER), and Dr. Henn, specialist in biological internal medicine (GER).
About Me
Medical Background
Suffering from MCS (several enzyme defects accounting for detoxification problems), ME CFS (immune deficiency of the immune cells in tissue) and chronic stress disorder (high stress hormones from chronic immune reactions) as well as chronic pain (hypersensitive Nerve Receptors through a gene polymorphism)
Supporting Chronically Affected People
What helped me, could also help others, everyone is a bit different in terms of genetics, but understanding your personal genetic and environmental situation helps greatly in dealing with it all.
The Project
Apart from my full disability, i try to research more, when my symptoms allow me to.
Therefore i am not working a full time job, but voluntarily and on a non-profit basis.
This approach enables me to remain independent in my free thinking and being able to get the best ideas in the end apart from global consistent convictions and consensus.
I'm always happy to find new contacts that give me inspiration and widen the base of good, open and social people to work on this world-wide project together.
Connecting and sharing realities and knowledge is a basic pillar of a positive existence today.
Happy to socialice
Getting to know contacts from all over the world helped me find my way, new friends, a pleasant atmosphere of work and life and the ability to help others better than before.
It's a great way to achieve more international understanding and motivate other professionals and affected individuals again with new insights to address and treat affected individuals and their symptoms properly.