Our closed Facebook FASD Caregiver Success group gets a lot of posts and questions about MRIs, so we took them directly to a professional who breaks down the brain, what MRIs are and can do, how past research is informing current research, and how her team are making discoveries about how the brain of an individual with prenatal alcohol exposure differs from a neurotypical individual.
In this episode Dr. Lebel shares: how she found her way into the FASD world; gives us a look into her work (and how the brain works); tells us about a Canadian Study on FASD & Mental Health; and I...
Settle in for a double feature to hear mom Yvonne and her daughter Nicole talk about their ups and downs on their FASD journey. What a treat this is to hear the FASD experience from their different perspectives.
Yvonne relates her journey from the first moment she saw a seven year old girl in pig tails to how their lives have unfolded and her own education and growth as an FASD caregiver.
She candidly shares strategies and tips as well as the significant challenges they faced not only as a family but also that she experienced as a single mom raising a daughter in a small rural town that didn't understand or accommodate the disability and how that affected them both through the years. Her best advice for caregivers: Don't dwell in the future. Be present now.
With Nicole transitioning to an adult, Yvonne can now offer hope for caregivers through her advocacy, blog and speaking engagements.
Nicole is a 22 year old...
Dr. Hanlon-Dearman has been working collaboratively with a number of research teams to understand population health issues of individuals with FASD and to better integrate care for affected individuals and their families. Her clinical and research interests include neurodevelopmental patterns of children with FASD, as well as children with a variety of neurodevelopmental disabilities....
Jody is a parent to three beautiful children, all affected with FASD, ages 14, 16 and 18.
She began working as a caregiver mentor six years ago with Wood’s Homes and continues today mentoring and supporting caregivers to feel successful in caregiving those affected with FASD.
She is also a facilitator for the MAPS Partnership caregiver networking support group for caregivers supporting those affected with FASD.
The past two and a half years, she has been an active executive board member for the Calgary Fetal Alcohol Network.
Her hobbies include involvement in the local farm animal rescues and owner at Pig Tale Acres where pet pigs are trained as therapy animals.
If you're in the...
This week, Jeff talks to Tamra talk about pretty much EVERYTHING, including:
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Jeff and Maggie talk about about what it's like having FASD, how she manages the symptoms associated with the disability - specifically memory and impulse control (or sometimes the lack thereof).
Maggie also shares some amazing tips on everything from managing a meltdown to her insights on transitioning into adulthood.
Want to connect with Maggie? You can find her in the Facebook Group: Flying With Broken Wings
In the interview, Maggie talks about a whiteboard that she uses as a memory tool to help her with her jobs and daily tasks. Simple strategy - big results!
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See you next episode!
Housing insecurity is a serious issue for most people with special needs, but finding appropriate and supportive housing for adults with Fetal Alcohol Spectrum Disorder is even harder to come by. Never Fear! In this episode Jeff interviews someone who is doing something about it.
Meet Gigi Davidson. Gigi is the Founder of FASD Communities and she is going to share her story as an FASD Caregiver to a young man and how she started up a one-of-a-kind, long-term residential care home for individuals with FASD.