Join us as we support the L-CMD Research Foundation’s efforts to raise money for research toward the treatment of L-CMD.

L-CMD is a rare and fatal form of muscular dystrophy. Sadly, children suffering from L-CMD may never achieve walking and statistically have extremely shortened lives.

There are currently no treatments or cures, but there is hope.

Click here for more info and tickets.  Tickets include, beer, wine, food and live music!