Athlete and filmmaker Pascale Bercovitch made a somewhat unusual entrance when she delivered her speech at last week’s ADVANCE conference, a gathering for Jewish philanthropists interested in disability programs and services.
Because she has no legs, Bercovitch, 45, wheeled herself to the front of the room, in an event space in Soho. But because her arms and abdominal muscles are stronger than those of most people who do have legs, from her wheelchair she easily hoisted herself onto a tall chair, where she wriggled a few times to settle herself comfortably, grinning at her audience the entire time.
On the eJewishPhilanthropy website, the Union for Reform Judaism's camping arm responded to The Foundation for Jewish Camp's release of its study "Jewish Camp for Children with Disabilities and Special Needs." Click here for the rest of the article, including the movement's committment to put more "human and financial resources" toward special needs programming.
The Foundation for Jewish Camp released preliminary findings last week from their recent research study Jewish Camp for Children with Disabilities and Special Needs, which maps current, potential, and desired camp program opportunities for children with disabilities/special needs. The study paints an encouraging picture of the field of Jewish camping, highlighting a variety of models that successfully provide meaningful Jewish camp experiences to children with diverse needs.
Okay, I know I can be a bit defensive, bristly almost, when it comes to talking about almost anything that I care about. I own that. When it comes to disability and inclusion, I can go a little overboard, but someone’s got to do the dirty work, right?
A lucid and penetrating piece from a blogger who is the father of a son with autism. He writes about the double-bind of being the family member of a loved one with disability: how if you share the positive moments you worked so hard to achieve, you run the risk of your friends jumping to the conclusion that everything is hunky-dory, mainly because they would feel more comfortable if that was the case.
The website Autism After 16 is carrying an incredibly poignant piece today from Liane Kupferberg Carter, a mother, journalist and activist, about how she still can’t get used to how people look at her son, who has autism and epilepsy.