I know I say every episode is my favourite and they are – but this one is another home run in terms of a professional that truly not only gets FASD but she hits it out of the ballpark. 

Dr. Pei’s information is science-backed and tested in clinical settings. She has also created an awesome document as a roadmap for success for individuals on the Spectrum. 

In fact, the analogy of cars and roads, and the journey is exactly how she describes her document. But before we get there, we cover a lot of ground (did you see what I did there?), including: 

• Dr. Pei’s origin story – or how she came to know about and work in the FASD field; 
• Digging deeper into what a neuropsychological assessment is and the benefits of a reassessment;
• The importance of being a brain detective when examining behaviour – or symptoms - of the disability; and 
• Advice on getting the assessment and how to present information to other...

Annette Kunzman co-founded FASD Network of Southern California in 2010 and was integral in establishing it as a non-profit organization in 2014. She has served as Secretary and Treasurer and currently as President. Annette holds a Master’s in Management degree from Northwestern University and received her undergraduate degree at the University of Nebraska. She was certified as a Chartered Financial Analyst in 1988.  

Following a long career in commercial lending and investment management, Annette retired in 2006 to focus full-time on raising her young sons with Fetal Alcohol. In 2019, Annette was named to the California Department of Education’s Student Mental Health Policy Workgroup by State Superintendent Tony Thurmond.  

We know caregivers spend years knowing their child is struggling, but not getting the support or appropriate diagnosis they need. Annette is no different. She poignantly shares her story of her...

I’ve interviewed and learned from a lot of people over the years, but this latest podcast guest has an interesting perspective and an engaging way. This is one of my 10 timer episodes – you will want to listen at least 10 times to unpack everything Sheila Burns has to say. 

I first saw Sheila present at a Conference in Northern Ontario. She tells me her background in children’s mental health, women’s health, and community development has informed the emerging vision for FASD prevention and improved intervention in her province of Ontario (Canada). To build capacity, she developed tools to guide and reinforce best practices.  One of these tools is the My Kind of Mind booklet which we delve into later.  

Sheila has held leadership roles to address individual and systemic issues related to FASD in Ontario since 1998 including FASD Ontario Network of Expertise – Network Chair and Leads on the Diagnostic and Justice...

It’s much easier for those that should know, to blame the parents, then it is to look at the failed system and their lack of education.

• her journey to become a social worker to try and change the system - but...

In today’s podcast we meet author, advocate, mom, wife, and adoptee Rebecca Tillou, who is also an individual on the Spectrum. 

Adopted at birth, Rebecca grew up with a loving family, graduated with a Bachelor’s Degree in Communicative Sciences and Disorders (Speech Pathology) and now works as a Claims Adjuster - a job she loves and excels in. She knew she was adopted, but it wasn’t until she was married and had her second child she started to wonder about her origin story.

Rebecca detailed her search for her birth mother in her book Tenacity, which we discuss, along with:

• How a fight with her adopted mom about her birth mother became a catalyst for her diagnosis;
• The importance of being transparent and truthful, whether about adoption or diagnosis;
• The power that comes from using your primary characteristics of FASD as a strength; and
• What it’s like to accept help and the difference a supportive environment makes.

Accepting help is...

I read a fantastic article by a caregiver of an individual on the Spectrum and thought … mmm, who wrote this?  I discovered it was none other than Paula Schuck, freelancer, social media guru, and blogger – but also a parent in our private FASD Success Caregiver Group.  I immediately knew I had to bring her on the podcast to share her fantastic tips on parenting a teen with FASD.  

Success looks different for our guys. For our families. Every single day.  

Paula shares her journey – parenting two girls - one with FASD and one without and how she knew the younger one, who was always on the go, super sensory sensitive and hard to transition, just wasn’t like her sister. We also touch on:  

• The necessity of adjusting parenting style at every developmental stage and age.   
• Comparisons to Amelia Bedelia and the need to be a translator for her daughter.  
• Her best advocacy,...

The timing of this podcast with Dr. Jeffrey Wozniak could not have been better. Little did I know a media story would appear two days before this podcast release, about the four year follow up study he and his team completed on choline for children with Fetal Alcohol. And boy did our Facebook Group explode with posts and parents wanting to purchase or order.

See that’s the thing with headlines, and announcements of new therapy and treatments – they are meant to grab your attention and emotion. My job is to save you some time, money, and further heartache by going directly to the source and getting the relevant information without the emotion. Choline does have benefits, but you need to know what those are and what target population it works best for.

So, who is Dr. Wozniak?

He received his Ph.D. in Clinical Psychology at Kent State University in 1997, and a post-doctoral fellowship in Pediatric Neuropsychology at the University of Minnesota in...

Have you ever said: I just wish every professional who works with my child had a child with FASD – so they would GET IT? Well Dr. Vanessa Spiller GETS IT! She is the parent of a young adult with FASD who also happens to be a Clinical Psychologist with over 20 years experience in working therapeutically with disadvantaged young people and families.

She has been a university lecturer and university clinic coordinator but her real passion is in supporting families of young people with FASD. She has presented many lectures, workshops and conference presentations on FASD and she has just published a workbook for parents and carers of young people with FASD called “Explained by Brain”.

In this podcast you get some professional insight (without having to pay a fee), as she shares tips, strategies and advice - parent to parent.

Now 20 years old, Dylan joined her family as an incredibly...

Today we dive deep into an area that takes a lot of soul searching, but sometimes is necessary to preserve relationships and the family: residential care and group homes. We talk with a caregiver not only on the front lines of parenting an individual with FASD and trauma – but in the midst of the riots in Minnesota: Barb Clark is a Parent Support and Training Specialist with the North American Council on Adoptable Children, FASD Consultant and parent of four adopted children, including one with FASD.

Barb and her husband went from trying to teach the FASD out of their daughter:

We thought we were these amazing strict parents.
to
Once the cloud cover of trauma cleared, and the constant fog of trauma was lifted, we were able to have a better relationship with her.

In this podcast we unpack the journey between these two points:

• How most professionals told Barb she was paranoid and how bad advice made things worse;
• What parenting fails and early strategies she used...