Help spread the word

Priscilla Liu

A Foundation Building Strength

Hi friends and family,

I'm participating in A Foundation Building Strength's Share-A-Thon this month to help raise awareness and funds for vital Nemaline Myopathy (NM) research. NM is a rare neuromuscular disease that needs more attention and support to find treatments.

It's sort of like a fun run, but instead of laps, we're counting social media shares! Starting May 26th through Nemaline Myopathy Awareness Day on May 31st, AFBS will be sharing special posts about NM. I'm asking for your support: would you consider pledging a small amount for every time those AFBS Share-A-Thon posts get shared on Facebook and Instagram?

Even pledging as little as 5 cents a share can make a BIG impact! You can also make a simple flat donation if that's easier. We've even set a cap of 500 shares on your per-share donation, just in case things go viral!

Every share will help spread the word about NM, and every pledge will bring us closer to finding treatments. Thank you so much for your support!

About this fundraiser:

Throughout the month of May, we invite you to join A Foundation Building Strength in our Share-A-Thon, a simple yet powerful way to spread awareness and bring hope to families living with Nemaline Myopathy. We're asking you to pledge a flat donation or a small amount per social media share (up to 500 shares!) to fuel crucial NM research. On May 26th - 31st keep an eye out for our special Share-A-Thon posts on Instagram and Facebook and share these posts to spread the word about this little-known condition. Every share gets us that much closer to discovering cutting-edge treatments! At the end of NM Awareness Day, May 31st, we'll tally the shares, turning your clicks into critical support for a brighter future!

ABOUT NEMALINE MYOPATHY AND A FOUNDATION BUILDING STRENGTH:

Imagine the difficulty of navigating a world where breathing, speaking, and moving freely can be a profound struggle. This is the reality for many of the remarkable children and adults living with Nemaline Myopathy, a rare congenital neuromuscular disease. A Foundation Building Strength is the only 501(c)3 organization solely dedicated to finding treatments for Nemaline Myopathy, while providing support and resources to these resilient individuals. Currently, there are no treatments for NM, making every breath, every word, every movement a testament to their strength.