When my beloved nephew was still a toddler, I got so used that
he’s being gawped at "as if he were a circus freak" and I totally
hated it. "Children are one thing, they don't know any better. But these
are adults. They look at him and their mouths fall open and they just stare.
And I think: didn't anyone ever tell them how rude that is?" Kyle has Attention Deficit Hyperactivity Disorder (ADHD) which is considered as a learning disability. "He looks like any other child, but he behaves oddly – for example,
he might sit there banging two toys together – and he sometimes makes strange
noises." Especially when he was younger, he might have a massive
meltdown – at the supermarket checkout, for instance. "I'd feel 300 pairs
of eyes on us – all watching us, all judging us for being disruptive and
difficult." This is just one of the many things you’d have to deal with and
what you are up against when you have a child with special needs: other people
tend not to be very kind. Which is particularly awful "because you've
already got so much on your plate as it is. The odds seem stacked against you,
and if people just gave you a bit of space and support, it would go a long way.
But the opposite is more often the case: you're struggling to start with, then
people knock you down further. They make assumptions about you, they find you
wanting, they treat your child as though he or she is dangerous or badly
behaved. It's soul destroying. It's so bad, so hard to deal with, that I have
friends with special needs kids who don't even take them out any more." I know my heart for special
needs individuals stems from him, seeing how little is expected from him, all
while knowing how mighty his potential is. So when I recently got invited to attend the launch of an advocacy film on children with special needs from The Center for Possibilities Foundation inc., spearheaded by its founder, Dolores Cheng, I immediately said yes.
During the said launch, Dolores Cheng, a single mom recalls why she had formed The Center for Possibilities Foundation (CFP) after coming to terms with the condition of her own son, Andreas, now 22 years old and diagnosed with Global Developmental Delay when he was three years old. "At the time, there were no support groups available, I didn't know where to go, who to see, where to find what I needed to know. I wanted to understand what it meant to raise a child with special needs. So I figured if i formed a group of my own, I would be able to find some people who might be on the same boat and needed some help," shares Cheng.