Family pinning hopes on fundraisers for toddler's $2.8M treatment
Family pinning hopes on fundraisers for toddler's $2.8M treatment A Pikwàkanagàn First Nation family is scrambling to raise millions of dollars for to provide a cure for their 14-month-old's genetic disorder, spinal muscular atrophy, before he turns two. Social Sharing Born with genetic disorder SMA2, Kevin Verch must receive one-time dose of Zolgensma before he turns 2 Posted: Jan 07, 2021 4:00 AM ET | Last Updated: January 7 Dana Pearce, 20, Brody Verch, 22, and their son Kevin Verch. The family is relying on fundraisers to pay for the toddler's $2.8-million genetic treatment for spinal m...
Source: cbc.ca