Invitation
Transcription
Invitation
The Silent Angels Gala Please join us for Our Honored Guests Dinner, Dancing, The NJRSA and The Silent Angels Gala The Silent Angels Gala is our largest fund-raiser to benefit Rett syndrome. This year, at the 24th annual NJ Silent Angels Gala, we are excited to have you join Silent Auction, Raffles and Fun at the NEW JERSEY RETT SYNDROME ASSOCIATION us as we honor two grandparents, Linda Albanese and Joan Lauria. Your commitment helps support the families in New Jersey living with Rett syndrome. Last year we presented our second Rett Syndrome Seminar at the Make-A-Wish Castle which was attended by parents, teachers and therapists from the tri state area. The Natural History Study we hosted here in NJ for 8 years is helping direct the current research. There are now several human drug trials enrolling children around the world that are providing promising results. With your help, in just 7 years, NJRSA has been able to give over $500,000 to the research funds at the International Rett Syndrome (RettSyndrome.org), Rett Syndrome Research Trust (ReverseRett.org) and the Rett Syndrome Center 24th Annual Silent Angels Gala at Montefiore Children’s Hospital. Things are looking incredibly promising, and our dream of a “Miracle Cure” gets closer every year. Your contribution helps us continue to support our families as we work toward that cure. We thank you for helping us move closer to our goal. Your help is our hope! Learn more at www.rettsyndrome.org or www.njrsa.org. to Benefit Rett Syndrome . Saturday, March 5, 2016 . 6:00 pm Westmount Country Club 728 Rifle Camp Road Woodland park, New Jersey 2016_gala_invite_sketch.indd 1 Linda Albanese Grandmother of Michelle, age 13 Michelle was diagnosed with Rett in April of 2007 at the age of 4 ½, and so began a new life for Linda and her husband Don of Bloomfield, NJ. They have 2 sons, Michael and Mark. Michael and his wife Cordelia are Michelle’s parents. They live in Las Vegas. From day one, Linda has been devoted to RTT research. For 7 years she accompanied Michelle and her mom to Oakland CA for the Natural History Study. She is always raising funds for research, with the help her son Mark and daughter in law Kim, through her Christmas card list, art sales, garage sales, Girls’ softball events as well as events held by the West Essex HS Tennis team where Don taught and still coaches. She has donation jars in local shops and restaurants and the “famous” Hot Bagels Abroad shop that got TV attention for RTT when the jar was stolen. Linda also teaches about Rett in schools in NJ and NYC, speaks to Women’s Key clubs and to anyone who will listen. She and Don are determined to make a difference for our “Silent Angels”. Joan Theresa Lauria Grandmother of Carly, age 18 Joan has worked tirelessly for Rett ever since Carly was first diagnosed at the age of 2. Joan was married to Dr. John V. Lauria for 59½ years. She worked for Johnson and Johnson and in her husband’s office for many years. Joan has five children, eight grandchildren and one great grandchild and is tennis player extraordinaire. Joan’s daughter and son in law Joan & Carl Raso are Carly’s parents. Joan continues to raise funds and awareness throughout the year, but at Gala time, she writes a personal letter to all of her many friends which always generates a great amount of donations. She is always talking about Carly and Rett syndrome and anxious to share her hope for a cure for Carly and all of our “Silent Angels”. 12/29/15 10:33 AM About Rett Syndrome What is Rett Syndrome? Rett Syndrome (RTT), a genetic neurological disorder affecting development in childhood, has been identified almost exclusively in females. RTT results in severe movement and communication problems following apparently normal development for the first six months of life. The characteristic features include loss of speech and purposeful hand use, occurrence of repetitive hand movements, abnormal walking, abnormal breathing, and slowing in the rate of head growth. No cure for Rett syndrome is known...yet. The New Jersey Rett Syndrome Association Gala Committee Leslie Greenfield, Chair Theresa Bartolotta Carla BenEtatos Robin Diamond Catherine Gavallas Mike Greenfield Bill Jones Karen & Bill Keegan Lanie & Ben Laskowitz Joan Lauria Kim Poulos Lieberz Susan Long Karen & Steven Medlin Carol Nightingale Eleni Passalaris Wendy & Nick Petruzzelli Joan Raso Maryanne & Ben Riegelman Judy & Gerard Saydah Gladys Thomson Edie Zarillo The New Jersey Rett Syndrome Association (NJRSA) is a registered 501(c)3 organization dedicated to serving the families affected by Rett syndrome. The mission of the New Jersey Rett Syndrome Association is to support local families as we raise awareness and funds for ongoing research that will improve the quality of life for girls and women affected by Rett syndrome. to early intervention, treatment, support and research. 2016_gala_invite_sketch.indd 2 Silent Angels Gala New Jersey Rett Syndrome Association We believe that by raising the awareness of Rett syndrome we can increase recognition and foster public attitudes conducive 24th Annual WWW.NJRSA.ORG Saturday, March 5, 2016 at 6:00 PM Westmount Country Club, WOODLAND PARK, NJ 12/29/15 10:33 AM
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