Showing posts with label children with disabilities. Show all posts
Showing posts with label children with disabilities. Show all posts

Saturday, December 25, 2010

Ding Dong, Christmas is over!

For my family Christmas means many different things..... And it doesn't necessarily have anything to do with religion, most of the time. And I do say Happy Holidays, but I've always said Happy Holidays, long before this war of words came into play about Christmas time... To me Holidays are about fun, doing things that you don't always get to do. I mean, Europeans call their vacations holidays. It's just a fun word, there's no implied meaning to it.

Getting back to the religion thing, though. Religion is personal. I'm reading a book right now about the Hawaiians. They wouldn't even speak their one true God's name becauseit was so sacred and they couldn't bear to have anyone disrespect it. That is such a different concept from the Protestant churches I grew up in. There's that whole Great Commission aspect of going out into all the world and preaching the Gospel. But I don't think the Hawaiians were altogether wrong, because sometimes the spoken word is meaningless. We can all say whatever we like, but if our actions and how we live, do not match with what we are saying, no one is goingto listen to us, anyways.

And who says that you need to speak or say anything to be a blessing to people. Javy has a very limited vocabulary and only those who are really close to him, actually no how he communicates. But do you know, I've had complete strangers come up to me and tell me what a blessing he was. I had one lady come up to me crying, because there was something in Javy's eyes that reminded her of her recently departed son. I even had a close friend tell me that Javy inspired him to be happy in every situation. Wow! That is truly a blessing....

So getting back to Christmas. I try to make our Christmases special and magical, just like our mom made them for us. This Christmas, we spent time with our friends. We watched whales and the sun sink into the ocean. We played, a lot. And we ate. I invoked the memories of both of my Grandmas. I made biscuits and gravy, just my Grandma Pentecost. And then I made the Strawberry stuff that my Grandma Williams fixed us every Christmas. My Grandma Williams didn't cook much, in fact, my Dad always complained that she starved them when they were kids. But what she did cook was the best. It was a great Christmas and judging from Javy's laughter and smiles, it was magical for him, too.

Wednesday, December 15, 2010

Merry Christmas, and push your own kid up the hill!

Last Wednesday night, Javy participated in his school's Christmas program with his third grade class. It's great, really, that Javy, as well as the other Special Education students participate with their general education class. I mean, in Alabama, he never really got to, unless it was something that Miss Laura did. So for this, I am very grateful. But here are some general observations that made me go, "hmmmmm." Javy's Special Education teacher was sick so she couldn't be there. So we dropped Javy off with the third grade class and one of the third grade teachers, who Javy was absolutely smitten with, explained that she was nervous about pushing Javy's wheelchair up the hill. I said, Okay, I will help anyway I can, so I can do it. Relief washed over her. Later, when I had a chance to think about this, I wondered, how hard is it to push a wheelchair up a small hill. And do they think that Javy is really that fragile. Now, I don't blame the teacher, at least she was honest. But it brought to my attention something about how people who are not around special needs kids and their perception of them.... For my family, we try to provide the most normal atmosphere possible for him. We let him roll himself down the hill (with an adult monitoring the traffic situation) in our drive way. I let him explore and climb around all the time. I'm not sure how to remedy this because the only way to know is to spend time with kids like Javy. I don't blame people for being cautious. Oh well...I guess that's all of my rant. But here's Javy's Christmas performance.

Monday, September 20, 2010

Yeah, just reading that last and only post, my blogging record isn't too strong. But here we go again, I need an outlet and a place to advocate for my son. He's 8 years old now, we're living in Hawaii, where he has done so well. But it still seems like the community for disabled children is so closed off. There is still no change in his diagnosis. He has really great doctors here, but it's always the same roadblocks. I want to use this blog to help make people aware that there are people out there who don't have diagnosis. It's a very isolated place to be, because I have found not advocacy groups dealing with this category. Cerebral Palsy has UCP, Autism has Autism Speaks, etc. What is out there for those who basically don't know what will happen in the future. Sure a diagnosis isn't the end all and won't help my son walk or communicate, but it will give us something to start with.