Life 4 Liam Short
A short, captioned cut of Liam — park, hat, the boy the work is for.
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 Families. Follow along on X @Life4Liam and Instagram @rarekido and YouTube @Life4LiamAndFriends.
A short, captioned cut of Liam — park, hat, the boy the work is for.
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 articleThe second annual fundraiser recap. About $50,000 raised to keep the gene-therapy path moving.
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.
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 articleJordan and Jen share video from the first Rare Disease Day fundraiser.
Watch on XThe first Rare Disease Day gathering. About $25,000 for Iowa research, and NPC family stories in the room.
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.
FOX5’s Behind the Badge segment with Kelly McMahill on the Mitchells, LVMPD, and Behind the Blue.
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.
Send a YouTube, news, or podcast link to jordan@life4liam.com and we will add it here. Stories from other NPC families are collected on Families.