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Hi. I'm Kaiden. I have SMA.

SMA is a disease that robs me of my physical strength and is the #1 genetic cause of death in infants. So let me tell you what we're doing about it!

To Live, To Move, To Cure, SMA

  • What is SMA?

    SMA (Spinal Muscular Atrophy) is a disease that robs people of physical strength by affecting the motor nerve cells in the spinal cord, taking away the ability to walk, eat, or breathe. It is the number one genetic cause of death for infants. Learn more ...

  • Genentech’s Risdiplam Showed Significant
    Improvement in Motor Function

    Positive study results for the Sunfish Part 2 study of Risdiplam. This is a study in children, teens and adults (ages 2-25) with either Type 2 or Type 3 SMA. Learn more ...

  • FDA approves Spinraza™ for SMA therapy!

    The FDA has announced the approval of the first-ever therapy for SMA. Spinraza™ (nusinersen) is not only a treatment, it also addresses the underlying genetic cause of SMA. The approval from the FDA for all SMA — pediatric and adult — is the broadest possible label, with no restrictions. Learn more ...

  • Who we are - The Fighting for Kaiden Team

    The Fighting for Kaiden Foundation team came together when SMA entered our lives. With Kaiden's diagnosis of SMA, the rally began, snowballed and resulted in a beautifully dedicated group determined to help not only Kaiden but others affected by this terrible disease. Learn more ...

How you can help

In addition to donating, there are many other ways you can support the cause.

Attend our events

We hold a variety of fun family events designed to raise funds and spread awareness.

Fighting for Kaiden Foundation, Inc., PO BOX 386, Linthicum, MD 21090
info@fightingforkaiden.org • Facebook • (240) 426-7173

Copyright © 2020 Fighting for Kaiden Foundation, Inc. 501(c)(3). All rights reserved.