One rare diagnosis, and a refusal to wait.
My daughter Maia — 22, a university student — was diagnosed in December 2025 with SDH-deficient GIST, an ultra-rare cancer that a routine scan happened to catch. Her story was featured by UC San Diego Health. Reaching a clear diagnosis took three specialist opinions. Reaching a treatment was harder still: the drugs that transformed survival for common GIST do little against this subtype, and almost no research is aimed squarely at it.
I'm Muwaffaq Salti, Maia's father. I spent my career in financial markets making decisions under uncertainty — and I decided not to sit and wait for science to reach a disease this rare on its own.
Mission Pegasus is my response: a focused, personally-funded initiative to compress that timeline — backing the most promising scientific leads, putting them in front of the right laboratories and clinicians, and pushing real treatment options forward as fast as rigour allows. It began with one family's diagnosis; its purpose is bigger — better options for everyone facing this cancer.