Ben Wilson's fatherly intuition led to his son's ultra-rare diagnosis. After a year of being told nothing was wrong, whole exome sequencing gave the Wilsons an answer—and a way to get ahead of what comes next.
After Yojana's experience with her daughter, Kaya, who battled sphingosine phosphate lyase insufficiency syndrome (SPLIS), Yojana founded Kaya Girl Legacy and dedicated herself to advocating for universal access to genetic screening. In this compelling piece, she wonders how genetics could be part of everyday life and a part of how we understand ourselves.
After her daughter Lyla was diagnosed with retinoblastoma at 18 months, Meg turned to genetic testing for answers—and found a different kind of peace.
The day our son was diagnosed with Wolfram syndrome, our world changed in an instant. Here's what we learned about early diagnosis, rare disease, and why knowing — even when it's hard — is always better than not knowing.
A story about the power of early intervention—and the family who refused to wait. Meet Forrest, whose journey helped inspire the creation of GeneSprout.
