An Invitation From The Finch Family
As some of you know, our 8 year old daughter, Samantha (she’s quite “something”), has a rare autoimmune disorder called Autoimmune Poly-glandular Syndrome Type 1. This genetic disorder affects only 1 in every 2-3 million people. That’s only about 150 people in the United States. There is no cure and treatments are passable at best. Because this condition is so rare, funds for necessary medical research are scarce. With your help, we’re hoping to raise enough in 2016 to fund a single research grant. In our hearts, we know that there will be a cure in Samantha’s lifetime, but we need your help to make that happen. Proceeds benefit The APS Type 1 Foundation, a 501(c)(3) charitable organization.
Here are the Details
When: April 23, 2016, 1 – 4 pm
Where: Agoura High School Gym
Who: Friends & family, kids of all ages
Why: Care about Rare