Paving the way to treat SMA.
Paving the way to treat SMA.
WHO WE ARE
Established in 2014, Working On Walking was founded by a woman with spinal muscular atrophy who dreamed of raising $100 for her disease someday. But the true beginnings of this story go all the way back to 1998. Allow us to explain.
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WHAT WE DO
We make it a priority to continuously provide the SMA community with funds, awareness, and hope, all of which play an integral role in our journey toward our ultimate goal: a future where SMA doesn’t have the upper hand.
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HOW TO HELP
We believe in keeping our donors informed about the direct impact their generosity has on the SMA community. Whether it’s to aid research efforts or help families in need, your donation matters, and we want you to know why.
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THE ANNUAL WORKING ON WALKING CHARITY GOLF TOURNAMENT
WHO WE ARE
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Established in 2014, Working On Walking was founded by a woman with spinal muscular atrophy who dreamed of someday raising $100 for her disease. But the true beginnings of this story go all the way back to 1998 and a lemonade stand. Allow us to explain.
WHAT WE DO
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We make it a priority to continuously provide the SMA community with funds, awareness, and hope, all of which play an integral role in our journey toward our ultimate goal: a future where SMA doesn’t have the upper hand.
HOW TO HELP
003
We believe in keeping our donors informed about the direct impact their generosity has on the SMA community. Whether it’s to aid research efforts or help families in need, your donation matters, and we want you to know why.
THE ANNUAL WORKING ON WALKING CHARITY GOLF TOURNAMENT
Details coming soon!
Who we are.
About Us
Established in 2014, Working On Walking was founded by a woman with spinal muscular atrophy who dreamed of raising $100 for her disease someday. But the true beginnings of this story go all the way back to 1998. Allow us to explain.
Get Involved
What we do.
We make it a priority to continuously provide the SMA community with funds, awareness, and hope which all play an integral role on our journey to our ultimate goal— a future where SMA doesn’t have the upper hand. Based in southern New England check out the events we have going on below.
Your Donation Matters
How to help.
We believe in keeping our donors informed about the direct impact their generosity has on the SMA community. Your donation matters, and we want you to know why.
Here’s what matters.
Our Mission
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Raise Funds
With promising treatments on the horizon, fundraising is more important than ever.
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Generate Awareness
Spinal Muscular Atrophy (SMA) is a genetic condition where muscles get weaker over time due to a problem with nerve cells in the spinal cord. It can affect how someone moves, breathes, and eats. There are different types of SMA, but early detection and treatment can help manage symptoms.
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Provide hope
Together, we can rewrite the future of this disease. Hope will light the way.
Join our golf tournament fundraiser!
Be remarkable.
Shop for a cause
Dare to be Remarkable is more than just our tagline. It encourages anyone who believes in the power of rising above. Because the moment you choose to live despite your struggles is the SAME moment you choose to dare remarkably. Let’s wear it proudly.
Join our community
Let’s do this.
Keep tabs on the latest happenings in the SMA community and our organization!