Life 4 Liam
Meet the NPC Superstars
Played at the Starlight Soirée. A little girl’s voice walks through the NPC Superstars — their names and faces, the hard parts of this disease, and the joy that is still theirs. Kelly Lee, Gracie’s mom, made the film.
Watch
Hear the story in their own voices.
Interviews we have done, and pieces others have made, so visitors can sit with Liam’s family for a few minutes. Other NPC family stories live on Friends. Follow along on X @Life4Liam and Instagram @rarekido and YouTube @Life4LiamAndFriends.
Life 4 Liam Short
A short, captioned cut of Liam — park, hat, the boy the work is for.
Southern Nevada family fights rare childhood Alzheimer’s
Abel Garcia talks with the Mitchell family about Liam, insurance barriers, cross-country drives because Liam cannot fly, and the race for a cure.
Read the Channel 13 article2026 Starlight Soirée recap
The second annual fundraiser recap. $50,000 raised and sent to Dr. Mark Schultz for the research.
Will You Fight With Us?
A 54-second Rare Disease Day short. Liam was diagnosed at two months. The family chose to fight, and asks others to fund the gene-therapy path with them.
Federal funding fight hits home for families afflicted by rare diseases
The Sun sits with Jennifer, Jordan, and Liam at Cure 4 the Kids — diagnosis, daily life, Adrabetadex, and why federal rare-disease funding matters.
Read the articleFirst Rare Disease Day fundraiser recap
Jordan and Jen share video from the first Rare Disease Day fundraiser.
Watch on X2025 Race Against Time fundraiser recap
The first Rare Disease Day gathering. $25,000 raised and sent to Dr. Mark Schultz for the research.
Las Vegas officer and wife search for a cure for their son’s rare disease
Denise Rosch’s Channel 3 package on Liam’s NPC diagnosis, a hard week of walking regression, and the Mitchell family’s race to find a treatment.
Fighting for a Cure: Supporting Liam's Battle with NPC
FOX5’s Behind the Badge segment with Kelly McMahill on the Mitchells, LVMPD, and Behind the Blue.
Jordan Mitchell on raising Liam with NPC
On Global Niemann-Pick Awareness Day, Jordan — then an LVMPD IT manager — opens up about Liam’s diagnosis and what the family is fighting for.
Have another interview?
Send a YouTube, news, or podcast link to jordan@life4liam.com and we will add it here. The children’s stories are on Friends.