It is so interesting how the FASD journey intersects. We all have mentors and people who have inspired us in our journeys. Linda Rosenbaum, author of Not Exactly as Planned, A Memoir of Adoption, Secrets and Abiding Love has been one of mine for a long time. I refer to her as one of the “OGs” – original (FASD) gangsters. Well, she was also the inspiration for another person I recently met on my journey – but before we get to that, we do a deep dive into Linda’s journey.
Linda and her husband Robin moved to Canada from the United States during a time of political upheaval. Unable to have biological children, they first adopted Michael in 1987 and later Sara. Linda did not know about fetal alcohol upon adopting Michael and this podcast is her journey from then to now. Linda shares:
If you are wondering what the future holds for your son or daughter, there is no better way to start 2021 than listening to this inspiring story of a young woman on the Spectrum.
Katie Aldiff came into the child welfare system at six years old. My wife Tara and I met her when she arrived at a Group Home run by an Agency we worked for at the time. Despite a rough beginning and some challenging years, Katie used all of her experiences as stepping stones to land her where she is today – working full time, living on her own and dreaming of returning to College to help others. We talk about all this as well as:
“I have nothing to be ashamed about being on the Spectrum.”
If you want compassion for your children, you must start with yourself. And that is exactly where we are starting in today’s podcast.
Patricia Morgan is a therapeutic counsellor, author, motivational speaker, coach and caregiver for her now 52-year-old daughter on the Spectrum. She is past president of the Canadian Association of Professional Speakers, Calgary and has won both the Spirit of CAPS award and the YWCA Woman of Vision award.
Usually, when I talk to a caregiver, we talk about advice on raising an individual with FASD. Today’s conversation is a little different. While we do talk about her role as a caregiver, and how that journey led her to where she is, we spend most of our time talking about resilience and how you can develop that muscle.
Resilience says I have the capacity to stay steady in the face of adversity, challenge, change, the behaviour of others and myself. It is also the ability to...
Have you heard the reports of the increases in alcohol consumption during this pandemic, including a significant increase in women’s intake and frequency?
A group of advocates in the United States had been talking about ways to raise FASD awareness, and these news stories nudged them to take immediate action. So much so that they undertook a cross-country journey in the mid-western United States in the middle of a pandemic to film The FASD Project.
We continue to come across no understanding of FASD. The ball has inched forward, it’s just time to move it forward more quickly & robustly. – Gigi Davidson
I talk to two members of the Project in today’s podcast: Gigi Davidson, Executive Producer and President of FASD Communities and Justin Shepherd, Director/Filmmaker. We talk about the statistics which was the catalyst for this Project as well as why Justin, who with his brother jumped in an RV, dubbed The Rust Bucket, in the...
We know Fetal Alcohol Spectrum Disorder isn’t in the spotlight very much as it remains one of the most misunderstood or misdiagnosed disorders yet is the most common developmental disability. It is so important for us to work together to get the messages out, that I knew I just had to reach out when I heard about a new FASD podcast.
Jessica Rutherford, a final-year Ph.D. student in the School of Design and Creative Arts, with her friend, colleague, and caregiver of three children on the Spectrum, Clare Devanney-Glynn recently launched the United Kingdom’s first FASD podcast. Spotlight on FASD aims to raise awareness of FASD, highlight the risk of drinking alcohol during pregnancy, share strategies around parenting and education, and have open conversations around real-life experiences.
We want to normalize it. It is what it is.
This is an interesting interview as we discuss FASD from not only the caregiving perspective but also from a front-line...
I am so pumped to present this episode of The FASD Success Show podcast because this guy has a ton of experience that I just know other Dads, Moms and caregivers will benefit from. Also, with 98 % of my audience female, I just thought it would be a great addition to have another dad/male caregiver speak.
Jay Derting has been teaching math for 34 years at a small farming school. He and his wife, along with their three bio kids first spent three months opening up a street centre for 200 homeless children in Madagascar, then spent a year as directors. As much as he enjoyed the work, he felt something was missing, and when he came home and went back to teaching he knew that was where his passion was. Wanting to still help children, he and his wife became foster parents. Two years ago he became a Trust-Based Relational Intervention Practitioner. His wife works with Homes of Hope, a nonprofit she started, which covers eight counties and supports over 500 foster/adopt...
In today’s episode, you are going to learn what is possible in creating an agency to serve individuals with FASD and their families and caregivers. I’m talking to Lisa Murphy, the Executive Director of the Lakeland Centre for FASD. This Centre is one of the leaders in Canada for FASD programs and services.
Lisa started with the Centre as a practicum student while taking a social work program and has risen over the years to the top. She has worked in many capacities including advocacy and coordination of services for children, complex youth, and adults diagnosed with FASD and their families, consultation, and data collection, and as a program manager.
We talk about her beginnings with the Agency and how she has got to where she is today, as well as:
I have the honour today of talking with Dr. Susan Rich. This is a fascinating interview that contains some very real and frank discussions about fetal alcohol spectrum disorder and reasons why Dr. Rich thinks that despite all the knowledge we are still struggling with prevention, awareness, recognition, and support.
Susan D. Rich, MD, MPH, DFAPA is a practicing child/adolescent & adult psychiatrist who holds a Bachelor of Science in microbiology from North Carolina State University, a Master of Public Health in health policy, and a Doctorate of Medicine from the University of North Carolina at Chapel Hill. She completed psychiatry training at Georgetown University Medical Center as well as a child/adolescent fellowship at Children's National Medical Center.
Dr. Rich first learned about the effects of prenatal alcohol exposure on the early embryo while working in pharmaceutical research in April 1992 after reading a book...
One of the best parts of my job is talking to all the caregivers who have such a wide range of experience and offer so much practical information to help others on the journey.
Natalie Vecchione is one of those caregivers.
She and her husband are parents to a 5-year-old daughter and an 18-year-old son (with FASD). She has been a Board-Certified Music Therapist for 25 years and began homeschooling six years ago. She and John are co-founders of FASD Hope and recently began a new adventure in the world of podcasting. They live in the farm country of North Carolina.
Her journey to a diagnosis for her son when he was 15 was a rocky one, that like so many of our listeners have been down. We talk about that journey to get an FASD diagnosis and how when she and her husband brought up FASD as a possibility she was dismissed.
Anytime it would be, nope, that’s not it. Because so many practitioners were under the impression that you had...
It’s great to be back to our Podcast! How important are stories in your life? Not only do stories help entertain us, but they also educate, and in some respect are medicine. To celebrate our return after a brief pause in our schedule, we have a double feature. First, we hear about a unique program that provides adults with fetal alcohol spectrum disorder an opportunity to share their stories or medicine, and then we hear from an individual who is living his life on his terms.
Individuals with FASD want their voices to be heard. They should be heard. I am excited to bring those voices and highlight programs bringing those voices to educate, entertain, and highlight success stories.
First, we talk to Emma Bergen and Suzanne Mozdzen from the Visions and Voices program out of Winnipeg, Manitoba. This is an interesting program that recruits adults with FASD to be part of a unique speaker’s bureau. The program aims to increase awareness in communities in order...