Disabled kids

by smack 11 Replies latest jw friends

  • smack
    smack

    In response to Sheras post on the 3 things thread. Who here looks after a disabled child.

    My son Chris is 14 soon, he has Trisomy 21, Down Syndrome. He was born 10 weeks prem due to problems, he stopped growing.

    He was born with no aesophagus and had reconstructive surgery to connect his stomach to what was his aesophagus. This only

    worked well enough to stop him drowning in spit. He is totally tube fed into his bowel as reflux was causing him lung damage when

    the tube was into his stomach. He has poor speech but good communicating skills. He attends normal high school, and has an aid with him most of the thyme. He is doing well at school, learning life skills mainly. He'll never be president, but he'll never have an enemy either.

  • StinkyPantz
    StinkyPantz

    ((smack))

    And he has a great daddy!

  • smack
    smack

    awwwwwwwwww ta Bridget

    Steve

  • avishai
    avishai

    My bro is autistic, & I have worked w/ disabled kids all of my adult life. I love it.

  • RAYZORBLADE
    RAYZORBLADE

    Smack: I believe Shamus either does work with disabled persons, or used to.

    Pettygrudger, has a very unique and interesting son. I haven't met her son yet, but he does have special needs, but with a parent like Rhonda, you know this boy is going to do alright!

    It always warms my heart to read things like this. Parents still giving their 100% for their children, regardless of their physical/mental disabilities.

    I take my hat off to you Smack, with the utmost respect.

  • frenchbabyface
    frenchbabyface

    OH !!! Smack ... your way of seing and leaving this is very POSITIVE ...

  • adrift
    adrift

    Smack, I also have a child with Down Syndrome. Her name is Emily and she is 10. She is the youngest of my 3 kids and when she was born it was a total surprise when the Dr. told us of her condition. Most of her physical problems are relatively minor. She has had numerous problems with her ears, very mild heart defect and the most significant problem was a stenosis of the duedenam which required surgery when she was 2.

    Emily also has speech problems. It's very hard for strangers to understand her. She does, however, have very good receptive language skills. She understands everything!

    I'm sorry to hear that your son has had such a rough time of it. Will they ever be able to help him so he can eat solid foods? I feel really lucky with Emily. There are so many other things that are so much worse than Down Syndrome. I don't dwell on what might have been and am in fact surprised when some stranger makes a point of commenting on the DS. as she looks just like any other kid to me. She's been a real joy.

    I ran across this the other day, I have read it before and I think it is very good. Hope it copies.

    A Trip To Holland By Emily Perl Kingsley

    I am often asked to describe the experience of raising a child with a disability -- to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this...

    When you're going to have a baby, it's like planning a fabulous vacation trip to Italy. You buy a bunch of guide books and make your wonderful plans... the Coliseum, the Sistine Chapel, Gondolas. You may learn some handy phrases in Italian. It's all very exciting. After several months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome to Holland!" "Holland?" you say. "What do you mean, Holland? I signed up for Italy. I'm supposed to be in Italy. All my life I've dreamed of going to Italy." But there's been a change in the flight plan. They've landed in Holland and there you must stay. The important thing is that they haven't taken you to a horrible, disgusting, filthy place full of pestilence, famine, and disease. It's just a different place. So, you must go out and buy new guidebooks. And you must learn a whole new language. And you will meet a whole new group of people you would never have met. It's just a different place. It's slower paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around. You begin to notice that Holland has windmills. Holland has tulips. And Holland even has Rembrandts. But everyone you know is busy coming and going from Italy, and they're all bragging about what a wonderful time they had there. And for the rest of your life you will say, " Yes, that's where I was supposed to go. That's what I had planned." And the pain of that experience will never, ever, ever, go away. The loss of that dream is a very significant loss. But if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things about Holland.

    I haven't posted much as I haven't made an introduction and feel like something of a sneak. Will have to psych myself up to do that one of these days.

    Take care, Adrift

  • little witch
    little witch

    I want to not post.

    I want to run away.

    I want to ignore you parents with disabled children.

    I am scared.

    I am not able to relate.

    I am uncomfortable.

    I am greatful, because my kids are healthy...

    I am,

    in awe of you! thank you for sharing your lives, thank you for being strong, thank you for.......

    being such a good darn parent!

    Thank you for being wise, and patient,devoted and loyal.

    Thank you so much for educating people about disability. I am overcome with emotion, about how much you love your kids........

    I want to erase my post. For fear of being taken wrong. But I am being honest. It is so heart wrenching, that people find it easier to ignore, as to speak about it.

    I am greatful you all have brought this subject up, and I hope it gets a million posts in response.

    You are all exceptional!!!

  • Prisca
    Prisca

    He'll never be president, but he'll never have an enemy either.

    This line really stuck out to me. Don't know why, maybe it's because we to equate "happiness" or "success" with things that aren't really true indicators of happiness or success.

    When we have something happen in our families that is out of the ordinary we realise that it's the little things that matter most - that our kids are safe and happy, that we have a loving mate, that values such as compassion and patience mean much more than cars or holidays.

  • smack
    smack

    Hi and welcome Adrift.

    Isn't the days after finding out like the biggest kick in the guts. Then it all gets better after that. I had to laugh at the story

    you put there, I thought...ooooooo the Dutch District Overbeer is gonna spit when she reads that But it's true isn't it.

    It is an experience I wouldn't give up.

    Little Witch, what you said is so true.....But at least you can say it out loud. Some people are instantly comfortable, others take thyme for

    the kids to wear them down, there is no escape. Ya gotta love the little buggerz

    Steve

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