


| B.B. duo write and illustrate children’s book to help families deal with ALS |
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In the fall of 2012, after living with primary lateral sclerosis (PLS) for six years, Neil Hemming and his family were hit with the knowledge that his condition had progressed to amyotrophic lateral sclerosis (ALS). “The news (struck) us like a tonne of bricks,” said Deana Larsson, Hemming’s daughter, as she teared up.
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