We will be hosting a new webinar with Dr. Brianne Redquest, our 2021 Dr. Sterling Clarren FASD Research Award winner, on March 19, 2021 at 1:00 pm Eastern Time.
Announcing the 2021 Sterling Clarren Award recipient!
We are excited to announce that this year’s recipient for the Dr. Sterling Clarren FASD Research Award is Dr. Brianne Redquest for her research on understanding and reducing stress in caregivers of individuals with FASD.
Stress Management Strategies for Caregivers
I recently attended an online Parent/Caregiver Masterclass in Stress Management. I learned a lot and wanted to share some of the excellent strategies and resources to help us support our loved ones.
Fetal Alcohol Spectrum Disorder and Stress
Stress is a normal part of our daily lives and certain amounts of stress are important to help us function. Small doses of stress help us meet deadlines, get to places on time, and prepare for important events. However, long-term stress can be harmful and can lead to mental and physical health problems, like depression, substance use issues, and stroke.
What FASD is: a caregiver’s perspective
When asked to write this blog on what FASD means to me, I struggled. FASD is a complicated disability with many challenging aspects. I finally decided that, in my experience, FASD to this point has meant missed opportunities.
A caregiver’s perspective on what FASD is
I often wonder if my child’s FASD was consistently recognized from a disability lens, while framed within a strengths-based approach for interventions and support, would life be just a slight bit easier to manage?
What FASD Means to Me
Caregiving has meant making my kids live on their own, knowing that they may fail, but also knowing I needed to keep others safe. Sleeping when I did not know where my child was, praying continually that they would live through the night.
Research Participants Needed for Families Facing COVID-19 Study
Researchers from across Canada are looking to study how the pandemic has changed the lives of neurodiverse individuals and their families. They are asking for families of children, youth, and adults with FASD to complete a short online survey about their experiences during COVID-19.
Life with COVID-19 from a Caregivers’ Perspective
We are finally confident that people will understand what we mean when we say life is unpredictable and sometimes feels like it is spiralling out of control. It took a pandemic to have others experience what our lives are like routinely.
Mental Health for Caregivers of Individuals with FASD
It is well documented that caregivers of children with disabilities experience increased levels of stress. But caregivers of children with FASD have been shown to experience higher levels of stress than most people. In a 2009 study, 92% of primary caregivers of individuals with FASD had clinically elevated stress levels. These number show that finding effective ways for caregivers to manage stress is especially important for this population.