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Jon, we’re more than halfway through our 30 Days of Strength campaign to power life-changing breakthroughs for this community. And I wanted to give you a quick update on our progress.

As of today, we’ve made it to 82% of our goal. It has been so inspiring watching everyone who has participated in this campaign so far. But we are still falling short of our goal to fund vital care and treatments for people with neuromuscular diseases. Will you help us reach 100% today, Jon? Please donate before September 30 and your gift will be DOUBLED >>

I have to be honest with you: This year, it's even more important for us to raise funds as our in-person fundraising events like Fill the Boot, Muscle Walks, and Galas were cancelled indefinitely. We need supporters like you to bridge the gap.

Your gift today will be matched dollar-for-dollar, up to $75,000, to help TWICE as many adults and children who rely on MDA to keep them healthy and strong. Can they count on you today?

Without your support, we may have to make drastic cuts to the programs and services we provide to thousands of people living with neuromuscular disease and their families. We absolutely can’t let this happen during this time when families need us the most - and that’s why we need your help. Give now >>

We’re counting on you,

Lynn O’Connor Vos
President and CEO

Gifts made before 11:59 p.m. on Wednesday, September 30, 2020 will be matched up to $75,000.

The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization.

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If this was an ordinary Giving Tuesday, I might announce our special match and ask you to help advance vital research and care for everyone affected by neuromuscular disease. But this year - and this Giving Tuesday - are anything but ordinary. We’re facing extraordinary challenges. But Jon, our community won’t let anything get in the way of accomplishing their goals and doing the things they love.

After all, our community is made up of incredible people affected by more than 40 types of neuromuscular disease, and every day we’re moving closer to a cure. But here’s the thing, Jon: we need your support to keep our community doing what they love most.

Keeping the lights on in our labs means people like Justin can manage his CMD at college. Providing access to telehealth appointments means a teenager like Fabiola who lives with NMD can pursue her love of art and painting. Connecting volunteers to clinical trials helps adults like Peter thrive as a professional percussionist while treating his CMT.

Jon, every gift you make to MDA today goes twice as far and keeps people like Justin, Fabiola, and Peter doing what they love, while getting the treatment and care they need.

And the best news is that today and ONLY today, your gift will be DOUBLED. That’s 2X the telehealth appointments, 2X the kids who will attend MDA Summer Camp at no cost to them, and 2X the funding for breakthrough research to help find a cure for all types of neuromuscular disease.

Jon, can we count on you today to make all this and more possible? Make your gift now and it will be DOUBLED >>

This means so much to me Jon, but more importantly, it means so much to people like Justin and Fabiola, and thousands of other people in our community, who are counting on you.

Thank you for supporting them,

Michael J. Kennedy, CFO

P.S. Make sure you donate before midnight so your gift has TWICE the impact!

Gifts made before 11:59 p.m. ET on Tuesday, December 1, 2020 will be matched up to $25,000.

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Jon, this is your last chance to help fire fighters Fill the Boot and make double the impact!

Thousands of kids and adults with neuromuscular diseases are counting on us to virtually Fill the Boot. They count on us for lifesaving care, breakthrough treatment, and support. And now, they are counting on you, Jon.

Make your gift today and have it doubled to support those who need it most:

The Fill the Boot campaign with the International Association of Fire Fighters (IAFF) has led to groundbreaking research for new treatments over the last 66 years. If we don’t meet our goals this year, we won’t be able to continue this life changing progress that filling the boot makes possible.

Donate now to help provide twice the lifesaving treatments, vital care, and urgently needed support for people with neuromuscular diseases.

This is the LAST DAY to Fill the Boot and support thousands of people living with neuromuscular diseases.

Let’s do this!

Team MDA and IAFF for Fill the Boot

Gifts made before 11:59 p.m. on Saturday, August 15, 2020 will be matched up to $10,000.

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Jon, your unwavering support has made a tremendous impact on the lives of people with neuromuscular diseases - and that deserves to be celebrated. That’s why we’re bringing The MDA Kevin Hart Kids Telethon to you - and it’s streaming live at home for everyone!

Due to the overwhelming support of our community, we’ve increased our pre-Telethon goal: Help us raise $100,000 by October 24! We’re also excited to announce a generous donor, Fishing for Muscular Dystrophy, will match all donations made up to $25,000.

Please make your gift (now doubled) to help us reach our goal of $100,000 before the Telethon on October 24!

Every dollar raised will now go twice as far to support the critical work MDA and Help From the Hart are doing to transform lives, including groundbreaking research, care, and advocacy to benefit all people living with neuromuscular diseases.

Won’t you help us start off strong so we can reach our goal of $100,000 before October 24? Make your Telethon donation now, before the show even starts, and receive a special gift with your donation of $100 or more >>

Thanks to your support Jon, we have made tremendous advancements in research and care, including 11 FDA approved treatments. But we can’t stop there. The MDA Kevin Hart Kids Telethon will help fund ongoing research that is shared freely in order to develop further treatments and cures for over 43 related neuromuscular diseases.

Make your Telethon gift today and it will be doubled to help provide better care, find cures, and raise critical funds to support 300,000 people in the U.S. living with neuromuscular diseases.

The Telethon also provides free MDA Summer Camp for more than 3,000 children, as well as education and resources for the more than 350,000 individuals living with neuromuscular diseases in the U.S. today. Jon, please make your donation now and it will be doubled to help us reach our pre-Telethon goal of $100,000!

Together, we can make The MDA Kevin Hart Kids Telethon a HUGE success for everyone in our communities.

Thanks for making this possible,

The MDA Telethon Team

Gifts made before 11:59 p.m. on October 22, 2020 will be matched up to $25,000.

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Jon’s gift DOUBLED to help people reach their dreams!
Give now >>

Jon, these are the faces of true courage and strength. Leticia, Crystal, Devin - and so many more - are determined to achieve their dreams and won’t let anything get in their way.

Today, you can help give people like them the strength to reach their goals:

Leticia has hope for the future because of the groundbreaking research MDA funds for neuromuscular diseases. She won’t let anything stop her from achieving her goals.

Crystal, a single mother, draws strength from her son Cooper, who lives with spinal muscular atrophy. She'll never stop fighting for her son and for a cure.

Devin actively participates in many MDA programs, from Muscle Walks to Team Momentum. He doesn't see challenges as barriers; he sees them as opportunities.

This community doesn’t let anything get in the way of achieving our goals. We’re determined, courageous, and strong. Your matched gift today empowers people like Leticia, Crystal, and Devin to achieve their dreams.

Can they count on you today, Jon? Any amount you give will be matched to help those who need it most.

Thank you for being a part of this,

Your friends at MDA

Gifts made before 11:59 p.m. on Wednesday, September 30, 2020 will be matched up to $75,000.

The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization.

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Early Access:
Jon’s Giving Tuesday Matching Offer

Jon, we know you may be busy right now shopping online for gifts for your loved ones (and maybe a few for yourself), but today, you can give a different type of gift - one that helps everyone affected by neuromuscular disease do what they love most - whatever that may be.

Because you’re one of our most valued supporters, we want to offer you this special opportunity: any size gift you make today will be matched dollar-for-dollar to help our entire community access the care and treatment they need, so they can focus on living independent and fulfilled lives. Make a gift that will change lives forever and have double the impact. Donate now >>

Justin lives with congenital muscular dystrophy (CMD) - but his friends and family know him as a junior in college, the President of his college’s Biotechnology Club, a choir member, a sketch comedian, and a lab volunteer.

Without MDA, none of it would be possible: From his transformative experiences at MDA Summer Camp to the care and support he receives from his MDA Care Center doctors to the treatment he receives thanks to dedicated researchers. Behind every person living with NMD is a supporter - like you - who stepped up when it mattered most with a gift to MDA.

That’s where you come in, Jon. Your gift before midnight tomorrow helps people like Justin, and thousands of other people in the MDA community, live the lives they want to lead.

For 70 years, MDA has been investing in treatments, care, and research for a cure, so everyone living with NMD can live independent, fulfilling lives driven by all the things that make them shine. Your gift today is an investment in the vital work MDA does, and an investment in the lives of so many. Please give now >>

We’ve made tremendous strides this past year in breakthrough research and treatments for more than 40 neuromuscular diseases, but we have to keep going in order to find a cure.

Jon, will you help keep that momentum going with your matched gift today? Make your Giving Tuesday donation now and it will go twice as far >>

Thank you for being a part of this,
Your friends at MDA

P.S. This incredible matching gift opportunity expires TOMORROW (Tuesday, December 1) at 11:59 PM. Please make your gift now to make sure it will be matched >>

Gifts made before 11:59 p.m. E.T. on Tuesday, December 1, 2020 will be matched up to $25,000.

The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization.

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Dear Friend,

We have BIG news: The MDA telethon is back!

And you’ll never believe who is hosting - actor and comedian Kevin Hart!

We’re proud to announce the MDA Kevin Hart Kids Telethon, a 2-hour special airing globally on Saturday, October 24, 2020.

We’re so excited for you to join us for this interactive and star-studded evening filled with musical performances, comedy, community, and lots of surprises. We’ll introduce you to some incredible families, and give you a behind-the-scenes look at the latest work of Muscular Dystrophy Association. We’ll also take a look back and pay tribute to the original Jerry Lewis MDA Telethons.

And Kevin Hart will be joined by celebrity guests including Jack Black, Usain Bolt, Josh Gad, Michael B. Jordan, Eva Longoria, Jillian Mercado, and more! You'll be the first to know as we announce additional special guests in the coming weeks and share details on how you can get involved before the show.

Stay tuned for more surprises and details coming soon. In the meantime, take a look back at the MDA Telethon through the years.

Your friends at the MDA

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Dear Jon -

We know it’s been a trying time for many in the MDA community. COVID–19 has changed day-to-day life in ways we never imagined.

It’s important for our health and wellness to stay positive. This is especially true with the challenges people with neuromuscular diseases, families, friends, and caretakers are currently facing.

By sharing what motivates us, we can stay connected and support one another. So, share your thoughts with this community, Jon:

From family and friends to new treatments or telehealth, we all have people or things in our lives that brighten our days and keep our spirits up. What are yours, Jon?

Share what gives you strength with this community, and help bolster their spirits and give them hope, too.

When we come together, we find our strength. We look forward to hearing what gives you strength, and sharing back what we heard with our community in the coming weeks.

Thank you for sharing,

The Team at MDA

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24 gifts needed from your home state to Fill the Boot.
Give now and your donation is doubled.

Dear Jon,

Normally, fire fighters would be on local street corners in states across the country for our Fill the Boot campaign.

Since they had to take their efforts online this year due to the COVID–19 pandemic, they’re counting on your help to hit their goal. The deadline to have all gifts matched is approaching. Please make your gift before August 15!

We’re short on gifts in your home state. Can you make your gift today (now doubled) to help us reach our goal, Jon?

Everyone with neuromuscular disease, no matter where they live, should be able to get the care and treatment they urgently need. That’s why we need your help today. Help fire fighters in your home state reach their goals for people with neuromuscular diseases. Fill the Boot in your home state and it will be doubled right now >>

We’re so close!

Team MDA

Gifts made before 11:59 p.m. on Saturday, August 15, 2020 will be matched up to $10,000.

The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization.

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Jon-the kindest thing we can do is help one another. We know you care about people living with neuromuscular disease - but time is running out to help this community in a BIG way.

Tomorrow is the last day of 30 Days of Strength, which means it’s your LAST CHANCE to help transform the lives of those with neuromuscular disease. Will you make your matched gift now?

Thanks to critical developments in neuromuscular research and care, we are moving closer and closer to breakthrough therapies and cures. But we need your help to keep this momentum going: Donate today and your gift will be MATCHED, up to $75,000, by a generous donor!

The thousands of people with neuromuscular disease are why every single gift matters. They’ve never let their disease take away their will to succeed. Your matching gift today can help them pursue their dreams >>

Join this powerful campaign today and show the world that nothing will stop our community from reaching their dreams.

We’re stronger together,

Your friends at the Muscular Dystrophy Association

Gifts made before 11:59 p.m. on Wednesday, September 30, 2020 will be matched up to $75,000.

The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization.

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JUST ANNOUNCED! DJ Khaled, Bryan Cranston, and Gabrielle Union Wade (and more!) are the latest talent adding their names to The #MDAKevinHartTelethon!

Dear Jon,

Who are you most excited to see at The MDA Kevin Hart Kids Telethon on October 24?

New celebrity guests have JUST been announced, including Aloe Blacc, Bryan Cranston, DJ Khaled, Daniel Levy, Leslie Mann, Robin Thicke, Gabrielle Union Wade, and more! See the full celebrity guest lineup here >>

During this unique virtual event, you’ll experience a reimagined Telethon, featuring entertainment, comedy, and musical performances from some of host Kevin Hart’s celebrity friends including Eva Longoria Baston, Adam Devine, Jack Black, Michael B. Jordan, and more! And, most importantly, you’ll hear from families and learn about MDA’s accomplishments in research, care, and advocacy work.

It’s all happening October 24 starting at 8:00 p.m. ET on LOL Network platforms including YouTube, Pluto, and more.

Today we're asking you to show your support early. The telethon airs on October 24, but when you make your donation today you can be one of the first to get a limited edition 2020 telethon t-shirt or hoodie! >>

There are many ways to be involved in this incredible event, from tuning in to hosting a watch party to making a donation. Together, we’ll celebrate our vibrant and diverse community and help transform lives. Find out how you can play a starring role.

So mark your calendar, Jon and don’t miss out on the event of the year!

The MDA Kevin Hart Kids Telethon Team

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Jon,

This month we’re celebrating the power of will and sharing stories of incredible people living with neuromuscular disease.

And today, we’ve got a BIG announcement: All gifts made in September during 30 Days of Strength will be MATCHED up to $75,000 to power life-changing breakthroughs for this community.

That means every gift made today will fund TWICE as much research for promising treatments and world-class care. Don’t wait: DOUBLE your impact on neuromuscular disease research and care with this special match >>

Your gift goes twice as far to help people living with neuromuscular disease by supporting research and care:

MDA Care Centers keep people like Justin, a college student living with congenital muscular dystrophy, healthier and stronger. Thanks to your gift today, he’s able to continue receiving treatment and telehealth even during the COVID–19 pandemic. Give now >>

Your donation also makes groundbreaking research possible, and helps fund new therapies that are restoring mobility - and hope - to people like Faith, who was diagnosed with spinal muscular atrophy when she was one.

Jon, can people like Justin and Faith count on your support to keep them strong?

Help us start this month off STRONG by supporting our community: Send DOUBLE the support for neuromuscular research and care when you donate today.

Let’s show our strength!

Team MDA

Gifts made before 11:59 p.m. on Wednesday, September 30, 2020 will be matched up to $75,000.

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Jon, you’re invited to help us build a new legacy for MDA with The MDA Kevin Hart Kids Telethon and help create a future with a cure for all neuromuscular diseases.

And you can transform lives today, before the show even begins: Help us reach our goal of raising $30,000 before the Telethon airs! Make your donation to the The MDA Kevin Hart Kids Telethon now (you could potentially see your name scroll by on the telethon ticker!) >>

Please make your Telethon donation now and then join Kevin Hart and his special celebrity friends on October 24 to see firsthand how your donation helps transform lives. Plus, receive a special Telethon gift with your donation over $100! Donate now >>

While this time has been challenging, COVID–19 has given us the opportunity to re-imagine how MDA can do even more to support the families we serve. Through the relaunch of the telethon, we will extend our reach and share with the world how they can help drive life-changing breakthroughs for children and adults living with neuromuscular diseases.

Will you help us reach our pre-Telethon fundraising goal of $30,000 before October 24? Please make your donation to The MDA Kevin Hart Kids Telethon today and help us reach our goal >>

We can’t wait to celebrate you and this incredible community on October 24!

The MDA Kevin Hart Kids Telethon Team

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Jon - Today’s the big day!

We couldn’t be more excited for The MDA Kevin Hart Kids Telethon airing live TONIGHT - and we hope you are, too!

Tuning in is easy. Just pick your streaming platform of choice and follow the instructions below!

So grab your popcorn (and maybe even get into your pajamas!) and join us TONIGHT at 8:00 p.m. ET / 5:00 p.m. PT to celebrate the strength and resilience of this amazing community, and to be there for kids and adults with neuromuscular diseases.

See you tonight,

The MDA Telethon Team

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Jon, Giving Tuesday may be over, but we have BIG NEWS: we’re giving our most dedicated supporters one more chance to donate and have their gifts doubled - and that includes you!

Can you rush your matched gift now before it’s too late? It’s the LAST day to have twice the impact for people living with neuromuscular diseases.

This year has been the most challenging in MDA’s history due to the global pandemic, and we need your support now more than ever. Your gift today allows MDA to purchase critically-needed supplies for our MDA Care Centers, makes telehealth appointments available to keep patients connected with their doctors virtually, and will fund invaluable research in our search for a cure. Jon, no gift is too small. Please donate now if you’re able to >>

Thanks for your continued support, and your unwavering faith in our mutual dream of helping all people living with neuromuscular diseases live healthier, more vibrant lives.

I know we can count on you,

Dr. Donald S. Wood
President & CEO

Gifts made before 11:59 p.m. ET on Tuesday, December 1, 2020 will be matched up to $25,000.

The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization.

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Hi Jon,

We wanted to make sure you didn’t miss this note from earlier. Your opportunity to DOUBLE your Giving Tuesday donation expires in just a few hours. Please send whatever you can - be it $50, $100 or even $200 - to keep the MDA community moving forward in the coming year >>

Our work - whether we’re researching life-changing treatments, providing critical care or giving kids the summer camp experience of a lifetime - is fundamentally about the incredible, resilient, inspiring individuals in this community. It’s about you!

So, Jon, whether you or someone you love is affected by DMD or LGMD or ALS, or another of the 40+ neuromuscular diseases we’re determined to cure, please know we will never stop fighting for you, and your ability to do what you love - with freedom, safety, and health. Join us in this fight with a gift before midnight >>

Your generosity will change lives,

The Team at MDA

——— Forwarded message ———

From: Dr. Donald S. Wood

Date: Wed, Dec 2, 2020

Subject: Donation matching extended by one day!

Jon, Giving Tuesday may be over, but we have BIG NEWS: we’re giving our most dedicated supporters one more chance to donate and have their gifts doubled - and that includes you!

Can you rush your matched gift now before it’s too late? It’s the LAST day to have twice the impact for people living with neuromuscular diseases.

This year has been the most challenging in MDA’s history due to the global pandemic, and we need your support now more than ever. Your gift today allows MDA to purchase critically-needed supplies for our MDA Care Centers, makes telehealth appointments available to keep patients connected with their doctors virtually, and will fund invaluable research in our search for a cure. Jon, no gift is too small. Please donate now if you’re able to >>

Thanks for your continued support, and your unwavering faith in our mutual dream of helping all people living with neuromuscular diseases live healthier, more vibrant lives.

I know we can count on you,

Dr. Donald S. Wood
President & CEO

Gifts made before 11:59 p.m. ET on Wednesday, December 2, 2020 will be matched up to $25,000.

The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization.

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Hi Jon,

This year has been extremely challenging for everyone, but our community knows a thing or two about overcoming challenges and persevering. We know anything is attainable if we work for it together.

We need 750 donors to chip in before the year ends to help fund vital programs and critical research in 2021 to find cures and treatments for all types of neuromuscular disease.

Jon, will you make your tax-deductible year-end gift now? Now through the end of the year, your donation of any size will be matched!

We’re a community of doers who takes matters into our own hands. Take Dr. Monkol Lek, for example.

When Dr. Lek discovered he had a subtype of limb-girdle muscular dystrophy (LGMD), he switched careers to help advance the world’s knowledge of his own disease. Now, 13 years after his diagnosis, he’s a skilled muscle disease researcher at the Broad Institute of MIT and Harvard.

Your tax-deductible gift today doesn''t just help people like Dr. Lek continue to do what they love doing; it also determines what we’ll be able to accomplish in the year ahead.

Help us start 2021 off strong by being one of 750 donors funding research projects for new therapies and treatments, enabling more children with neuromuscular disease to attend MDA Summer Camp free of charge, connecting families with world-class care, and so much more. Your gift will be doubled now >>

These programs and research projects have always been critical, but in 2021, we really need everyone - including you, Jon - to help us continue moving forward. If you are able to, please make a gift of any size today and it will be doubled dollar-for-dollar.

Thanks for everything you do,

The MDA Team

Gifts made before 11:59 p.m. ET on Thursday, December 31, 2020 will be matched up to $100,000.

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Jon, here’s something you’ve probably heard a lot lately: It’s been a tough year. For our community, that rings especially true.

But this year wasn’t all doom and gloom. Together, we’ve also thrived: Your support has helped to provide critical care, education, research, and support to move our community forward and bring people together.

We know incredible things lie ahead in 2021, but we’re relying on your generous support again this year to make sure we have the resources to provide everyone in our community with the care and community they need to move forward and do what they love. Give before midnight tomorrow and your gift will be DOUBLED.

MDA has been investing in treatments, research, and care for 70 years, so people living with neuromuscular disease can live independent, fulfilling lives driven by all the things that make them shine. Even when we face what feels like impossible obstacles, we will never stop moving forward.

Your gift today is an investment in people - their talents, their dreams, and their lives. And for the next 24 hours, your investment will be DOUBLED. Don’t miss this opportunity to amplify your impact.

Together, we can share more hope with people living with neuromuscular disease - hope that they too can live longer and stronger.

Thank you,

Your Friends at MDA

Gifts made before 11:59 p.m. ET on Thursday, December 31, 2020 will be matched up to $100,000.

The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization.

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