This introductory webinar shares an overview of the planning necessary for special needs parents to ensure that their children are as comfortable and secure as they (and you!) age.<\/p>\n\n\n\n
Please keep in mind that it will take time to do all of this and be kind to yourself. You\u2019re watching this so you\u2019ve already made some progress!<\/p>\n\n\n\n
Despre acest webinar<\/strong><\/p>\n\n\n\n Planning for all the future possibilities for our children with severe epilepsy and developmental challenges is scary, we know (and are feeling the pressure to get started too).<\/p>\n\n\n\n This is hard stuff to think about but with the leadership of the Angelman Syndrome Foundation\u2019s Adult Transition Taskforce<\/a> (they have developed a thorough checklist to help guide us through the process) and the guidance of a Certified Financial Planner who started Protected Tomorrows<\/a> to help us do just this, we hope this webinar helps you move forward with this important future planning.<\/p>\n\n\n\n Paneli\u015ftii no\u015ftri au fost:<\/strong><\/p>\n\n\n\n Mary Anne Ehlert, CFP had a successful career in the financial industry when she decided to act on her lifelong desire to specialize in serving the families like hers and founded Protect Tomorrows<\/a>. The source of her inspiration was her younger sister, Marcia who had cerebral palsy<\/p>\n\n\n\n Robin R. Wilkerson, PhD, RN chairs the Adult Taskforce<\/a> at the Angelman Syndrome Foundation<\/a>. She is a retired Professor of Nursing whose research focus is families of individuals with developmental disabilities. Her youngest, Paige, is 27 years old and has Angelman syndrome.<\/p>\n\n\n\n Amanda Moore is the CEO of the Angelman Syndrome Foundation<\/a> and mother to twin boys, Jackson and Baden. Jackson was diagnosed with Angelman syndrome in January of 2017<\/p>\n\n\n\n