Family fights to get $2 million treatment in time to save child with rare disease

Wade Hosey is 20 months old and suffers from a rare genetic disease called spinal muscular atrophy, but the treatment costs $2.1 million and he can only receive the treatment up until the age of 2 so his time is running out, but his family is not giving up.

Family fights to get $2 million treatment in time to save child with rare disease