Peter W. Choate, MSW, RCSW, PhD, PhD is Professor, Social Work, Program Coordinator, Member and Supervisor, Clinical Registry, Alberta College of Social Workers. Peter’s teaching focuses on assessment issues in social work, including families, as well as child and adolescent mental health. He has served for 5 years as the Field Director for the First- and Second-Year Practicum Program and is now the Program Coordinator. Peter is an expert witness in social work with sub-specialties in the areas of social work case management,...
A caregiver in our private Facebook Group asked: Am I the only one seriously considering cancelling Christmas?
We know this time of year can be challenging. So, if you feel like cancelling Christmas, or want to reduce meltdowns or overload, check out these top 8 ideas or hints for the holidays suggested by other caregivers:
We know there are times when you will want to decorate, engage in activities or visit family or friends. Some additional ideas that may help:
There are caregivers all around the world quietly or not so quietly going about their day-to-day. Occasionally, I see someone who is doing incredible work in their community and I want to dig a little deeper to find their lessons and ideas I can share with others. Laurie Whyte is one of those caregivers.
Laurie Whyte has been active in the world of Fetal Alcohol SpectrumDisorder for over 15 years. As a parent of 2 teenagers with FASD as well as a community advocate and trainer, she offers a unique perspective in helping others understand FASD. By sharing real-life examples, the latest research, and best practices Laurie speaks openly about the emotional journey of many caregivers of those with FASD while providing hope and inspiration. She offers dynamic and practical training in hopes of bringing professionals and caregivers together to serve individuals with FASD compassionately.
I learned to ask for help. I have never hidden...
What happens when you have the FASD information, training and support you need? Do you take a step back and let others find their own way or do you step up and help? Today’s guest, Jennifer Wisdahl, ranks in the circle of some pretty kick-a$$ advocates who are helping pave the way for families and individuals to get the support and services they need for success.
Many of you may know Jenn from her role as the Policy and Training Center Coordinator for FASD United (formerly NOFAS) where she works with the Team supporting the pending FASD Respect Act. What you may not know is she and her husband, are proud parents of three teens with FASD, is a habitual volunteer (she sits on the board of NOFAS Washington State and on the executive board of the FASD United Affiliate Network), is formerly from Canada and still cheers for the Vancouver Canucks, while watching the Seattle Kraken.
So often as advocates we talk into...
As a research scientist in the health care field, Ngaire Meadows thought she knew everything, but now understands how little she knew.
With four children and three on the Spectrum, it felt like WW3 in her home with rages, outbursts, and mental health concerns.
Rages and outbursts, these just happen, and there’s no controlling it and there is no reasoning with it and there’s no deflecting. It’s like a storm cloud coming in, rolling in, you can’t stop it and you can’t make it roll out any faster, you just have to hunker down and weather it.
In this episode, Ngaire and I talk about:
In today’s episode she and I break down:
Previous guests have included moms and dads, but this is the first time we’ve had a couple appear together to talk about their journey as FASD Caregivers. I couldn’t think of a better couple than Chandra and Jordan as the first.
Chandra and Jordan are parents to 6 children – two with an FASD diagnosis and one suspected. Like Angelene Bruce, our conversation was not intended to be a podcast. It was for a case study for our upcoming CKS workshop. Like Angelene, their story is filled with great lessons that will benefit many.
Before taking the CKS program, Chandra and Jordan admitted they were living at a level of desperation and constant stress. They questioned their parenting, had others question their parenting, and struggled to understand why their children were acting the way they did despite what they felt was a supportive home environment.
I feel as a mom you get this intuition. There were things with our boys that I was recognizing, not...
Her handle on Twitter is FASD Warrior Mum. I interviewed Angelene Bruce for her feedback on her experience taking my Caregiver Kickstart Coaching program. As she told her story, as a birth mum, it became clear her insight and experiences needed to be shared with a larger audience. She is a warrior who is working to throw stigma against birth mums and FASD out the window.
I felt immense guilt. I cut down … and did as much as I could do – so diet, sleep, exercise, prenatal vitamins. I made sure my prenatal care was as good as it could be. I want birth mums to know there are mitigating things we can do. My passion is for women that are dependent. But it can happen even at low levels of drinking.
Angelene is honest and forthright about her past. We talk about her dependency on alcohol and her pregnancy but also her path to recovery and acceptance. Stops on that journey include: