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The past few years have been a transformative journey. After publishing my memoir, Dissecting Wobbles, I ventured into making YouTube videos to help others discover the benefits of exercise for the differently abled. Through my series, Documenting Wobbles, I also share how I navigate life’s unique challenges. If you haven’t had a chance to watch it yet, check it out here.
Building on this momentum , I’m excited to officially launch The Wobbles Project—an umbrella for all my future initiatives aimed at empowering those with neuromuscular disorders and other disabilities. Our first initiative, Windows Into The Outside World, focuses on sourcing and donating tablets and other technology to individuals with disabilities. For years, I’ve wanted to get this project off the ground because technology, especially my computer, was a godsend—a window to the world when my body couldn’t take me there.
I believe that even small changes can make a big difference, and I want to empower people to live more eco-friendly lives.
To make this dream a reality, I’ve launched a Patreon page where you can support me with a monthly donation of as little as $1 (R20). As a Wobbles Warrior, you’ll get exclusive behind-the-scenes content and early access to my videos! For $5 a month, you’ll join the Inner Circle and receive monthly digital downloads and access to our private Discord server. And for businesses, our $10 monthly sponsorship tier includes your logo and a description featured on my website and in my newsletter.
Your support will directly fund the equipment I need for filming, as well as website hosting and marketing. Even a small contribution can help me create more videos and reach a wider audience.
If a monthly donation isn’t feasible, you can also “buy me a coffee” for a one-time donation of $3 (R60) or more at Buy Me A Coffee Every little bit helps!
I’m truly passionate about this project, and I know that together, we can make a positive impact on the world. Join the Wobbles Project today and be a part of the change!
Hello, I’m Andrew (but most of my friends call me Andy)
About Me
My name is Andrew Marshall. I’m a 43-year-old who lives with my retired parents in the suburbs of Johannesburg, South Africa. A genetic, degenerative muscle disease called Friedreich’s Ataxia has influenced much of my physical existence, including the slow
deterioration of my mobility and speech. Yet, while my body’s limits are visible, I see myself as more than the boundaries it imposes. My computer has become a lifeline, a way for me to connect with a world that is becoming harder to physically navigate. It allows me to explore, to learn, and to meet people from all over—a real passion of mine.
Welcome to The Wobbles Project, a mission inspired by my journey and driven by a simple yet profound belief: that empowerment and resilience can transform lives, no matter the challenges. I’m Andrew Marshall, and I’ve lived with Friedreich’s Ataxia—a degenerative neuromuscular disorder that has profoundly shaped my life. Yet, my story is about more than this diagnosis. It’s about finding strength, joy, and purpose in sharing my experiences with others.
Through The Wobbles Project, I’m dedicated to creating a community where support, knowledge, and connection thrive. This initiative is an umbrella over various projects that all aim to make a meaningful impact for people with disabilities, beginning with accessible technology. For so many, devices like tablets open up a world of communication, learning, and independence. It’s my goal to provide this “window into the outside world” for those who might not otherwise have the chance.
The Wobbles Project encompasses my personal story, my YouTube channel, and a range of future projects—all united in the mission to empower and inspire. Here’s a closer look at each arm of the project:
Dissecting Wobbles: My memoir, where I share insights on navigating life with Friedreich’s Ataxia, giving readers a deep look at my personal journey and the challenges, regrets, and moments of triumph. You can get an e-copy, or the print version off Amazon
The Wobbles Project: A YouTube series where I share exercise routines, stretches, and mindset strategies that have helped me live a full life despite my limitations. My hope is to support those newly diagnosed or facing similar challenges, offering not only practical advice but also a positive outlook.
Windows into the Outside World: This is my heart and the first branch to The Wobbles Project. Through this arm, I aim to provide technology to those in need, beginning with tablet donations to kids and adults with disabilities. Technology has been essential to my life, and it’s my goal to pass along the empowerment it brings.
Support and Sustainability: To make this vision a reality, I’ve set up a Patreon portal and a Buy Me a Coffee page, where supporters can contribute monthly or one-time donations. Whether it’s $3, $5, or more, every contribution helps fund equipment, medical support, and project costs, allowing me to reach more individuals who need access to resources.
A Dream for the Future: I have big ideas for The Wobbles Project. One day, I envision it as an official NPO, bringing supporters tax benefits and new ways to get involved. I’d love to take the community on exciting adventures—from bungee jumping and skydiving to music festivals and beach trips. Sharing these moments can break down misconceptions and inspire everyone to embrace life fully.
At the heart of everything I do is the desire to connect, inspire, and give back to a
community that often faces challenges alone. If you have questions about supporting The Wobbles Project or are simply curious about my journey, feel free to reach out.
I’ve been incredibly fortunate to build a network of supporters through Dissecting Wobbles, and I know how committed many of you are to helping me make a difference. Following a standard charity model, 30% of donations will go toward operating costs for The Wobbles Project, while 20% will help my family manage my medical expenses, including my biokinetics program—a core part of my health and this mission.
This support is deeply meaningful to me. For the first time, I’ll feel like I’m contributing to managing my medical needs. It’s a powerful step, especially considering my mom has been the sole provider for our family, working tirelessly as a nurse and often picking up extra work to keep us going. The opportunity to give back in any way is a gift that makes this project even more special.
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