Prepare for a journey into the heart of FASD caregiving with a twist of inspiration and a dose of real-world wisdom. I'm your host, Jeff Noble, and in this must-listen episode, I'm bringing together a dynamic team of coaches from the Caregiver Kickstart coaching program. These remarkable individuals (Barb Clark, Michael Harris, Christine Bofenkamp, and Laurie Anderson) are not only experts in their fields but also share their lives with individuals with FASD, offering a perspective that's as authentic as it gets.

As we navigate the complexities and celebrate the triumphs of FASD caregiving, each coach offers a piece of their story, shedding light on the power of connection, understanding, and resilience. Their shared experiences are a beacon for those navigating similar waters, providing solace and solidarity.

By the close of our chat, you'll be loaded with strategies, bolstered by expert insights, and touched by stories that echo your own. If you're ready for a surge of...

Welcome to Episode #138 of the FASD Success Show! Today, we're talking to Stacia Stribling, a wife, mom, FASD advocate and a proud business owner running a family-led Orchard. Stacia's story is a blend of advocacy, family, and the simple joys of life, like picking apples and peaches from her orchard.

Stacia is not just another guest; she's a powerhouse of advocacy. From her work with Formed Families Forward to her own lived experiences, Stacia brings a wealth of knowledge to the FASD community.

If you're looking for inspiration and practical advice, this episode is a treasure trove. Here are some of Stacia's golden nuggets:

• The importance of community in advocacy.
• How to navigate the complexities of FASD with grace.
• The therapeutic benefits of connecting with nature, as seen through her orchard life.

As noted, Stacia and her family own an orchard, a sanctuary where you can pick your own apples and peaches. If you're in the DC, Maryland, Virginia area, don't miss out on...

Have you ever felt like you're on a never-ending rollercoaster while navigating the world of FASD caregiving? If so, you're not alone, and Episode #137 of the FASD Success Show is just for you. This episode dives deep into the real-life story of Angela, a birth mom who has faced the highs and lows of FASD caregiving.

Angela's Unfiltered Experience

Angela is not just another guest; she's a birth mom who's been through the wringer. From handling meltdowns to cherishing the small victories, Angela shares her unfiltered experiences. Her story is a testament to the resilience and strength that caregivers in the FASD community possess.

Actionable Tips and Wisdom

If you're looking for quick fixes, this episode offers more than that. It offers sustainable and realistic strategies that you can integrate into your daily routine. Some of Angela's golden nuggets include:

• Don't underestimate the power of community support.
• Self-care is not selfish; it's essential.

What's the...

The Classroom Conundrum: Advocating for Your Child in an Uncomprehending System

Ever sat in a meeting with your child's teacher and felt like you're speaking two different languages? No, it's not just you. The struggle to get educators on the same page when it comes to FASD is real, and the stakes are high.

In our latest episode, "To Cool for School: The No-BS Guide to Getting Educators on Your Side," we dive into this complex issue head-on. We don't just air out the problems; we offer real, tangible solutions that can turn that uncomfortable parent-teacher dynamic into a collaborative partnership.

1. The Reality of a One-Size-Fits-All Approach

Do you ever feel like your child is just another cog in the educational machine? The problem often starts with a one-size-fits-all approach to education that disregards the unique challenges and abilities of children with FASD. Changing the system isn't going to happen overnight, but changing your child's experience within that...

The Mind-Boggling Moments: My Top 3 FASD Aha! Revelations

Ever felt that frustrating gap between what you know about FASD and what you actually understand when facing its real-world challenges? You're not alone.

We've all been there: armed with the facts, aware of the science, but still left bewildered when faced with the raw realities of dysregulation, overwhelm, and anger. On paper, it all seems to make sense. In action? It's a whole different ballgame.

Drawing from my own experiences and the winding path from knowledge to deep understanding, I'm here to share my top AHA moments. Moments that illuminated the complexities of FASD and bridged that daunting gap. Moments that I hope will guide you on your journey to not just knowing what FASD is, but truly grasping what it means in the day-to-day life of your loved ones. 

1. It's all about the brain, not the face.

How many times have we heard or even thought, "But they look so normal!"? It's a trap...

Unlocking the Mystery of FASD: A Simple Guide to Understanding and Explaining It

Have you ever found yourself struggling to explain FASD to someone who just doesn't get it? You're not alone. Many caregivers and their loved ones face this challenge daily. But what if I told you there's a simpler way to not only understand FASD but also explain it to others?

FASD is not just a medical term; it's a lived experience that affects families in unique ways. In Episode 134 of the FASD Success Show, we take the FASD definition I recommend and use and break it down into digestible sound bites so you can help others understand.

You will come away from this episode with a straightforward way to articulate what FASD is, how it impacts daily life and a concise, effective way to explain FASD in the time it takes to ride an elevator.

This episode is a game-changer, trust me.

After you listen, let me know what your “elevator pitch” is. I’d love to hear it!

Show notes

Show...

Did you rock your reds September 9th?

Did you even know September 9th was International FASD Awareness Day? 

If not, no worries - I got you covered with the launch of my FASD Success Show YouTube channel. 

So, let's discover the journey of FASD Day and how it's uniting people worldwide.

You're not alone and here's why!

Red Shoes are More than a Fashion Statement

Have you ever wondered about the story behind those vibrant red shoes you see on FASD Day? It's not just about making a bold fashion statement. It's about standing out, being proud, and advocating for understanding and acceptance.

The Origins of FASD Day

FASD, or Fetal Alcohol Spectrum Disorder, is a complex condition that varies from person to person. It's considered the most common known cause of developmental disabilities in the Western world. And yes, it deserves its own day of recognition. The first International FASD Awareness Day was celebrated in perfect harmony on the ninth day of the ninth month in...

The FASD Success Show is back!

After a hiatus, Jeff Noble returns with an episode filled with unexpected twists and raw emotions, illustrating the power of resilience, healing and community support in overcoming life's adversities. Why did he step away? What brought him back to the microphone? And what is the lifeline he is about to toss to caregivers that promises to reshape the FASD landscape?

Tune in, lean in, and discover what's been unfolding behind the scenes, including:

• The whirlwind series of presentations from down south, west and east from California to Florida, up north to Kashechewan Cree First Nation and across the pond to bonnie Scotland! Jeff shares how it felt to return to live events, the power of connection and shared experiences.
• Personal reflections on grief and grappling with medical procedures that serves as a poignant reminder to cherish every moment and maintain connections with those we hold dear.
• The importance of emotional wellness, leaning on...

In this episode, I delve into the complicated and emotional process of moving forward after the loss of my sister.  As we navigate the loss of my sister's passing, I reflect on the ups and downs of grieving and how it has changed me. Join me as I share my experiences and the eulogy I never got to say. 
 

In this episode it is you helping me cope with grief and honor the memory of my sister Jennifer.  

I also give an update on the future of the show. Despite this difficult time, I am still passionate about sharing my story and connecting with others. I talk about the new topics I plan to cover and the ways I will be evolving the show moving forward.

This is was really hard to do so I appreciate you taking the time to listen. 

We'll be back soon...better than ever! 

We are back! What a whirlwind the last couple of months has been! In this return episode, I let you know where we have been, what we have been doing, and what the future of the show is, but more importantly for right now for you I am giving a mini-coaching session on how to really survive the holiday!

How are you holding up? Many of the caregivers in our Facebook Group and Coaching Course are feeling the strain. You may be burnt out but so are our kids. Even my daughter, who is neurotypical. Add in the disability, seasonal depression, or trauma (for you or your kids) and we have an assault on our nervous systems. Tune in to hear the collective wisdom from my team and the families I work with on how to navigate this season. I dig deep and share:

• questions to ask and prompts to center yourself if you are struggling
• quick suggestions to help ease transitions and changes
• a new way to respond to the negative voices when you or others think our kids are missing out

I...