. @blakegriffin23@TeamLou23@OldenPolynice1@HARPER04_5@Matt_Barnes22 My nephew is a HUGE Clippers fan battling Hunter Syndrome (MPS II),a rare disease with no cure.We’re hosting a charity event July 19th 9am–12pm at Rancho Sports Facility.Your presence would mean the world💜
Project Alive and @BuiYahHoops are hosting a charity basketball event on July 19, 2026 to raise funds toward improving the lives of families living with Hunter Syndrome. This is for Skyler, Ollie, and all of the MPS kiddos around the world. Event Info, registration, spectator tix, sponsorship, and donation options can be found in the link below. Please participate, donate, and share. Thank you.
https://t.co/NzjeybF25G
As rare genetic disorder causes her son to regress, Carrboro mom teams up with UNC doctor studying new treatment https://t.co/HBxLwak6rb #MPSII#huntersyndrome
Coming out of school, I turned down an agate job at the L.A. Times. Needed to write, see? Figured I’d get there soon enough.
Twenty-six years later…
I’m writing sports columns for the L.A. Times. Surreal.
I love L.A. and I love sports. Let’s rock:
🔗https://t.co/YXSj3s3a2U