Register now for the CanFASD newest webinar presentation on Friday July 10, 2020 at 1:00pm EST. Dr. Dorothy Badry, CanFASD’s Child Welfare Research Lead, will be discussing loss, grief, and resilience in relation to FASD along with members from the CanFASD Family Advisory Committee and the FASD community.
Loss and grief seem to go hand in hand in relation to FASD and this experience deeply impacts the lives of children, youth, adults, families and support networks. Many children become involved in the child protection system early in their lives, which can result in involvement with the justice system in adolescence and adulthood. Mothers experience their own loss and grief regarding their child’s disability. Some mothers frequently lose the opportunity to parent their children, often due to active substance use.
Beyond diagnosis, FASD is a complex psychosocial/emotional experience that requires ongoing supports to navigate life on a daily basis. Individuals with FASD often experience mental health challenges, poverty and homelessness. Other losses for individuals living with FASD include being misunderstood, facing challenges in relationships, ever-present stigma and social exclusion.
FASD often goes unrecognized by many professionals and this contributes to ineffective support, unrealistic expectations, frustration, loss and grief, all of which contribute to higher levels of vulnerability. Individuals and families have cumulative experiences of loss, grief and hurt, particularly when they feel professionals do not understand their experience and the impact of FASD in daily life. Training on FASD and practicing FASD informed care is essential to minimize further marginalization and oppression of individuals and families. The COVID-19 Pandemic has resulted in a loss of supports for individuals living with FASD. This loss creates new and unexpected challenges that we will talk about from a personal, professional and parent perspective.
At CanFASD we are constantly aware of the challenges faced by individuals with FASD, their families and their support networks and we continue to be amazed at the capacity for resilience and hope. In this webinar we will use contemporary theory to explore loss and grief as it relates to FASD, and will hear from the voice of an advocate and public speaker living with FASD, and the voices of parents from the CanFASD Family Advisory Committee. Register now!
This presentation is part of CanFASD’s Webinar Series, one of their responses to the COVID-19 pandemic. These webinars are designed to bring evidence-informed research on FASD to Canadians from the comfort of their own homes. Watch their last webinar with CanFASD Senior Research Lead, Dr. Jacqueline Pei.