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Welcome to the Logan Ruth SMA Foundation!

The Logan Ruth SMA Foundation was created in May 2013 in honor of our son, Logan. His beautiful spirit changed our lives.

Through the foundation, we are dedicated to spreading awareness about Spinal Muscular Atrophy, supporting newly diagnosed families, and the fight for a cure! Especially in Southwest Missouri!

SMA is the #1 genetic killer of children under the age of 2. It affects 1 in every 6,000 live births. 1 in every 40 is unknowingly a carrier!

Newly Diagnosed?

Contact us to get support from other families who have and are continuing to fight SMA

Are you an SMA carrier?

Click here to find out

Logan's Journey - Blog

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