Paresh is the President and spokesperson for Down Syndrome Association of Peel. Paresh, along with his wife Anju, were among the founding members of the original DSAP group that started over six years ago. When Paresh is not working in the fast-paced world of staffing and recruitment, he is usually at home with his family, or out at a DSAP event. His goal is to ensure that the voices of all parents with Down syndrome children, as well as adults with Down syndrome, are heard loud and clear, and to affect change in our community for the betterment of families and individuals touched by Down syndrome.
Carlo DiCarlo is honoured to serve as the Vice-President of DSAP. Carlo believes that everyone has a purpose in life and unique gifts to share. A couple of years ago, Carlo was blessed with his daughter Laurel who was born with Down syndrome. Laurel has opened Carlo’s eyes and empowered his family so deeply that he feels compelled to do more.
It is no secret that in various parts of the globe children from the Down syndrome community are seen as a burden to their society. Carlo believes that it is everyone’s fundamental responsibility to advocate for the Down syndrome community and to rebel against such preposterous notions.
Carlo DiCarlo is committed, deep in his core, to helping others understand the intrinsic value that our children bring to the world. As a teacher, Carlo watches children grow and evolve each and every day. It is Carlo’s hope that as a society we can embrace all children with exceptionalities and make them feel loved and accepted.
Ellie De Souza
Ellie De Souza is the mother of a 32 year-old boy with Down syndrome and a 35 year-old girl. Ellie is a grandmother of two beautiful girls. Ellie is a grandmother, a partner, a marathon runner, and has completed two Ironman competitions. She is proud to be a co-founder of the Peel Caring Network for Challenged Kids before it merged with the Down Syndrome Awareness of Peel.
Anju Misty is a mother of three beautiful girls with the youngest having Down syndrome. As one of the co-founders of the Down Syndrome Association of Peel, Anju is passionate in advocating for the rights for individuals with Down syndrome. Anju believes these individuals deserve to be contributing members of society. As a professional in Human Resources supporting organizations in health care, Anju is also actively involved in school parent councils. In her spare time, she enjoys travelling, reading, dancing, and creating everlasting memories with her family and friends.
Mellissa is the co-founder of Down Syndrome Association of Peel. She is also a proud mother of two beautiful girls. Mellissa likes to travel and explore new cities and places. Her children and husband inspire her every day to be a better person and they fill her heart. Mellissa loves to help people and to lead them in a positive direction.
Subcommittee Chair: Education
Lisa recently retired as a teacher from the Halton District School Board and is a mother of three sons. Her son, Luke, is 26 years-old. Lisa has been involved with the Caring Network for Challenged Kids and the former Peel DS parents, support group for approximately 20 years. She is on the provincial Executive Board of DSAO (Down Syndrome Association of Ontario), representing our Peel group. Lisa is pleased to be supporting families of DSAP with children 21 years of age and older.
Subcommittee Chair: Social Events
Kamila Moran is a mother of two beautiful daughters. She was inspired by her daughter, Sara, along with others, to form a not-for-profit organization to better the lives of individuals with Down syndrome, to advocate and make a change. In her spare time Kamila enjoys traveling, camping, hiking, movies, design, photography, and spending time with her family and friends.