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After my son, Ethan, was diagnosed with a rare and fatal genetic syndrome called Hunter syndrome, my husband and I were offered a place in a support group for parents who are raising children with special needs. We didn't have a babysitter, so I found myself sitting alone in a circle surrounded by strangers four months after Ethan was diagnosed.
In 2014, 36 year-old Austin, Texas man was given less than two years to live. He was diagnosed with Amyotrophic Lateral Sclerosis, commonly referred to as Lou Gehrig's Disease. Now confined to a wheelchair, unable to walk, eat, use his arms, or speak, he is making a public plea to be turned into a robot.