For parents of children with invisible disabilities, including autism, ADHD, anxiety and a range of conditions, it is often a challenge to convince those in authority that one’s child requires services beyond what a family can typically access. This situation is further complicated when neurodiverse children exhibit behavioral difficulties, which are sometimes falsely attributed to poor parenting by those with limited training in invisible disabilities.
The purpose of this workshop is to introduce parents to basic advocacy strategies. Examples will be specific to the Ministry of Children and Family Development (MCFD), including the need to:
Educate social and mental health workers about your child’s diagnoses and requirement for services.
Develop your communication skills in advocating for services.
Create a paper trail - document your interactions with MCFD employees when requesting services.
Understand how to appeal a decision made by an MCFD employee, when necessary, including MCFD’s internal complaints policy, the role of the Office of the Representative of Children and Youth and the Ombudsperson.
We will also review the various service areas within MCFD to better understand what services it is responsible for providing, including:
Children and Youth with Special Needs
Children and Youth with Mental Health
Family Services including Child Protection Services
At the end of this workshop, participants will be able to:
Define their role as an advocate for their child.
Identify basic advocacy skills.
Identify key resources that can provide support for children with an invisible disability.
Describe key steps in developing an advocacy strategy.
About the Presenter
Deborah Pugh is Executive Director of ACT – Autism Community Training, a registered not-for-profit society. She has been an advocate for children, youth and adults with autism, and their families, for the past 25 years, both provincially and federally. In her work with ACT, Deborah focuses on the important role that providing evidence-based training has in improving the lives of those with diverse neurological conditions, which are usually invisible, increasing the challenges of finding appropriate levels of care. She also has a keen interest in supporting parents of all children advocate effectively for their children.
Prior to returning to Canada, Deborah was a journalist in the UK and the Middle East, working for The Guardian and the BBC. In 2016, Deborah was awarded the BC Association of Speech-Language Pathologists’ Distinguished Service Award and UBC’s Health & Wellbeing in Children, Youth and Adults with Developmental Disabilities – Outstanding Contribution Award.
Morning Break; Refreshments Served
Lunch; Bring or Buy Your Own
Afternoon Break; Refreshments Served
Get 20% off by registering three or more attendees at once (not valid with other discounts).
Special rates for 3 or more people watching via web streaming on the same screen. Contact ACT for details.
Parents, Para-Pros & Students
Early Bird Rate ends
April 16th, 2020
Regular Rate ends
May 14th, 2020
Late Rate begins
May 15th, 2020
ACT fundraises to provide bursaries for low-income participants and/or those travelling from outside their home regions to an event. ACT only provides bursaries prior to registration. You are welcome to call or email ACT's office (email@example.com) for more information. ACT provided over $11,000 in bursaries in 2019 and gratefully accepts donations to our bursary fund to allow us to provide a greater level of support. Donate to our bursary fund.
Learn more about how to register using the ACT event bursary program.
Parents who receive Autism Funding may use 20% of the
total for equipment, books, training and travel costs.
ACT's live events are considered eligible expenses by
the Autism Funding Branch. Please pay when you register; the Autism Funding Branch will reimburse parents after the event.
More Autism Funding Information >
This event is available through live web streaming as part of our response to COVID-19. Visit our web streaming page for more details.