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Thank You for Helping Us Spread Awareness This November

As November draws to a close, we want to express just how much your support has meant to us. This SMS Awareness Day—and throughout the month—our community came together to raise its voice and share powerful stories, bringing greater understanding and visibility to Smith-Magenis Syndrome. Thank you for making such a meaningful impact alongside us. 

As we move into this season of gratitude and giving, we’re especially mindful of the unique challenges the holidays can bring for our SMS families. This time of year, with sleepless nights and added expectations, can be especially demanding. We see the incredible strength and resilience in our community, and we want you to know how deeply we appreciate you. 

Thank you for being part of our community and for all the ways you make a difference. 

 

Giving Tuesday—Just One Week Away! 

Giving Tuesday, the International Day of Giving, is just around the corner on December 3rd! If you’re eager to support, there’s no need to wait. You can get a jump start on making a difference by donating today. And, with our November match still on, your gift will be doubled, up to $5,000! Every dollar brings us closer to advancing innovative SMS research.  

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Gear That Fuels SMS Research 

This holiday season, why not give a gift that gives back? Our SMSRF gear makes a thoughtful gift for loved ones, with every purchase directly supporting SMS research. Whether it’s a cozy sweatshirt or a new mug, your purchase helps fund life-changing research and brings us closer to progress for the SMS Community. 

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Maximize Your Support with a Matching Gift 

Did you donate to the SMSRF this year? There’s still time to submit a matching gift request from your employer! We like to brag that our donors are the best. Not only do they support us, but they also go the extra mile to see if their employer offers a matching gift program that could double their donation to SMSRF! 

Have you checked if your company offers a matching gift option? Click here to see if your company has a program like this. Thank you again for your generous and continued support of SMS research. 

 

Increased funding for research is the only way to develop innovative treatment options for individuals living with Smith-Magenis Syndrome. For more ways to get involved or learn about Smith-Magenis Syndrome visit our website. 

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