Our connection to SMA

Our granddaughter, Lily was diagnosed with SMA type 1 at 10 days old and treated with Zolgensma at 29 days old in 2021. Being from a family of fighters, we dug for information, we learned as much as we could, we found people to connect with and started down the path of becoming advocates for finding a cure. Each year we’ve raised funds to donate to the Cure SMA foundation.

We would love to have you join us for our Dessert and Pottery Night, see below for more information!

Donate directly to our SMA Walk

Shop on September 2nd at 8 am, shop closes at 5 pm on September 6th.