Contacts
Jennifer Strobel is an avid supporter of families affected by autism in southern Nevada. Jennifer was a FEAT board member for over five years and is currently the Executive Director for FEAT. Jennifer resides with her husband Mike and has three children Taylor 15, Peyton 13 and the newest addition to the Strobel family is Brenden weighing in at 2lbs 12oz - He is now almost two years old and doing fantastic! Jennifer’s daughter Peyton was diagnosed with autism at age four and began intensive ABA therapy shortly thereafter. Peyton is also actively involved in Girl Scouts, Swimming, Dance, Horse back riding and Art. It is Jennifer’s goal to help educate the Las Vegas Valley on autism and also be a resource for families that need support, encouragement and hope.
Sara Limbaugh is a board member for FEAT of Southern Nevada and also the chair person for FEAT special events. Sara and her husband, Scott moved to Las Vegas 14 years ago . They have 2 amazing children Aaron 12 and Molly 10. Aaron was diagnosed with Autism at age 3. He had an ABA home program through The Lovaas Center and made great gains. Aaron is on a baseball team , skateboards and is a Boy Scout. Sara started with FEAT 8 years ago and has remained active in the organization. She feels volunteering for such an outstanding organization is the best therapy.
Eve Whitehead has lived in Las Vegas for over 29 years. She works part time but her full time job is as a mom to three beautiful children, Chandler, Connor, and Marie. Connor, now age 11, was diagnosed with autism over 9 yrs ago. At the time, Eve and her husband sought the support and help they needed from the members of FEAT. Her son has made great gains and they know the importance of early intervention and the support needed for families beginning this changing chapter in their lives. Eve has served on the board of FEAT for over 6 years and is the chair of parental support and silent auction gala. Sharing her knowledge and giving support to families who share the daily challenges and triumphs of having a child with autism.
Lynnette Medina is married to Jose Medina and a mother of 4 children - Julia 10, Diego 9, Mateo 6, and Aaron 4. Lynnette is a full time student at Nevada State College working on her bachelor's in psychology. Her hope is to achieve her master's in Occupational Therapy at Touro University. She is also a stay at home mom. Her son, Diego was diagnosed with autism at the age of 3 by CCSD, but was noticed to be developmental delayed at the age of 10 months. He went through NEIS for services until he was 3 years old and then transitioned to the school district. Diego has had ABA therapy for over 5 years. Diego did not talk until he was about 4 1/2 years old. He has had speech therapy for over 7 years and occupational therapy for 5 years. He now has limited verbal skills, loves the computer, Disney movies, jumping on the trampoline, pirates, and parties! Lynnette's goal is to educate families and give them strength and support.