<div>We are friends of the Sonnemaker family. Their son, <strong>Emmett, who is 10 years old, has a rare neuromuscular disease called spinal muscular atrophy (SMA)</strong>, a degenerative disease that causes worsening muscle weakness and wasting. Emmett and his family travel twice a month for specialist appointments several hours away. Emmett is wheelchair-bound. This summer Emmett will undergo surgery to correct severe scoliosis. After the upcoming surgery, <em>their family vehicle, which they have been able to convert to be wheelchair accessible, will no longer be sufficient to accommodate Emmett’s height and growing stature. Their family desperately needs a new vehicle</em><strong><em>.</em></strong><em> </em>Despite everything Emmett has been through, he remains a kind and thoughtful child, a light to everyone he interacts with. Emmett's little sister, Ellie, also has this hereditary disease. The future of her mobility is uncertain.
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<div>Emmett’s parents are tireless supporters of their community. Their family serves willingly and is always helping others.
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<div>Every little bit helps and will make a big difference for Emmett and his family as they navigate through this journey. Please help us spread the word by sharing this with friends, family and social media.
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<div>Thank you for being part of this effort—your kindness truly matters!
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<div>Gratefully,
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<div>Mark &amp; Heidi Schaber
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Sari Shepard

Susie Lundberg

Dennette Hammons

Dalene Thomas

Paul Buchmann

Anonymous

martha christensen

Maria Bernhardt

Lori Candland

Mark Schaber

Yasaman Ahmadieh

Leah Hamelin

Support Emmett's Journey with SMA: Wheelchair Van Needed

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Support Emmett's Journey with SMA: Wheelchair Van Needed

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