Livie’s Legacy – A little girl with a big heart

The John Ritter Foundation and Olivia Petrera-Cohen’s family invite you to join the “Love for Livie Legacy Benefit” on November 3rd, 2017 at Lavo in NYC. All proceeds from this benefit will be used to fund research on the disease that took Olivia from her family a month before her second birthday.

Olivia had a rare disease called Multisystemic Smooth Muscle Dysfunction Syndrome (MSMDS), a disease described a few years ago by Dr. Milewicz and her research group at the UTHealth John Ritter Research Program. It is our hope that sweet, brave, beautiful Livie’s spirit and legacy will live on in this effort to help other children with this disease.

For more information on MSMDS, or to support Livie’s legacy by attending the benefit or making a donation go to loveforlivie.org



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