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Adaptive Equipment for Pools
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in: SMA Assistive Technology/Equipment
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- 4 hours, 8 minutes ago
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Columnist Writes About Her New Cat
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in: Adults With SMA
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- 2 days, 3 hours ago
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Columnist Writes About Taking Digital Detoxes
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in: Adults With SMA
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- 2 days, 16 hours ago
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I’m Getting A JACO!
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Fighting Fatigue
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in: Adults With SMA
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- 3 days, 4 hours ago
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Motivation Monday: Revising My Summer Plans
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in: Coronavirus (COVID-19) and SMA
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- 3 days, 13 hours ago
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Opening Doors Using The Jaco Robotic Arm
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in: The SMA News Today YouTube Channel
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- 4 days, 4 hours ago
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Are you resuming normal activity soon?
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in: Coronavirus (COVID-19) and SMA
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- 1 week ago
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Have You Tried Matcha?
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- 1 week ago
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Columnist Answers Reflection Prompts by Author Chani Nicholas
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- 2 weeks, 2 days ago
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Liquid Albuterol and Energy
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in: Adults With SMA
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- 2 weeks, 5 days ago
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Extracurricular Activities for Your Child
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in: SMA Parents and Caregivers
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- 1
- 3 weeks, 1 day ago
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States Reopening: What’s Your Take?
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in: Coronavirus (COVID-19) and SMA
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- 3 weeks, 2 days ago
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Motivation Monday: Goals During COVID-19 Isolation
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- 3 weeks, 3 days ago
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Balancing Caregiving and Your Own Needs
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in: SMA Parents and Caregivers
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- 4 weeks ago
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Adaptive Equipment for Pools
Sponsored Post
Time Is Motor Neurons
A father’s perspective: Our journey to finding a treatment
When Quinn, our soon-to-be-born daughter, didn’t make as much movement in the womb as our other 3 children, my wife, Annie, and I thought we had the “chillest” baby in the world. We joked that she was saving up all her energy for when she entered this world kicking and screaming. Quinn was born in August 2018, and she was the most beautiful little girl. Over the first few months, nothing seemed out of the ordinary. In fact, she appeared healthy and had strong upper body strength. But by the time Quinn’s 9-month check-up came around in June, her physical condition started to change.
FDA Approves ZOLGENSMA for SMA! Talk about it now — click below:
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