This past week I have been struggling with something I heard. I have debated blogging about it because I did not want to give recognition to such intentional cruelty and yet, how can we fix what we do not know about.
Every week I write a Down syndrome awareness post. I read several blogs of families with a child with Down syndrome. I am active in our local Down syndrome Guild and smaller parent support groups. Twenty or 30 years ago if you had a child with Down syndrome the doctor would tell you to put the child in an institution and forget you ever had it. I have met people whose parents did just that with their sibling. My best friend’s aunt and uncle had to fight to keep their son, get him an education and help so he could be a contributing part of the community. Today my Peanut has benefited from all these parents that said, “No” and fought for their child. I have seen acceptance all around and have been so far happy with the schooling my daughter has received.
And yet ignorance still exists. People are still cruel and unkind. Last week I went to our local Guild to pay for a conference I wanted to attend. I was speaking with the Guild’s director and she told me how someone had taken the Dreams video put out by the National Down Syndrome Society and violated it. I love this video. I have seen it several times and yet I cry every time I watch it. It gives me hope for my daughter. Someone took this video, slowed it down and put it on youtube with the title “R*** have Dreams Too” Why would someone think this is funny? Why would someone feel the need to hurt others? With all the work we have done for our children, some idiot has attempted to crush all our dreams for a stupid laugh. Youtube has been contacted and told to remove this clip.
We continue to struggle for our children. Kari at Chanelle and Tristan recently wrote about something a friend’s mom had said to her. Rylie’s mom recently had a doctor make a stupid comment about Rylie being Down. (I guess the doctor didn’t get the people first memo.) Even I had a distant family member tell me after our daughter was born she was sorry our child wasn’t normal. I laughed it off because I understood her generation saw things differently. At least in these situations the comments were made out of ignorance. They weren’t made to intentionally harm anyone. I relish the opportunity to educate these type of people about Down syndrome. Most people are open to being corrected about their misunderstandings.
What I don’t understand is the intentional cruelty of some people. The person that made the youtube entry was older and should know better. It breaks my heart that someone would be so uncaring to another human being. It terrifies me to think about what my child will face in the future.
I know that my readers are not the type of people to ever consider doing something like this. However, I am asking for your help. Please, talk to your children. Help them to understand about children and people with special needs. These people do not need to be feared. These people can teach us so much about life and happiness. These people have dreams too and NO ONE should take them away or try to crush them.
Tuesday, March 25, 2008
We Still Have a Long Way to Go
Labels: DS Awareness
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22 comments:
Oh, Debbie . . .
I am just so sorry. I'm not even sure I know what to say, so I'm just sending you and Peanut a great big hug.
That is the MOST awful thing I've heard! I can NOT believe someone did that and thought it was funny! That completely infuriates me and also makes me very sad. Your sweet little Peanut is adorable!!! I just pray that I can raise children who are accepted for who they are and more importantly accept ALL for who they are. Thanks so much for stopping by and I hope you'll continue to visit me even when I go private. There's no obligation though. I just really enjoy your blog and will continue to read it and hope to see you back at mine :)
I can't believe what was done to that clip on youtube. hugs to you
It is too bad that there are these cruel people in this world. A couple of weeks ago my son was accused of not letting a special ed student in his group at school. He was so upset. He said he wasn't talking about that kid, wasn't even looking at him, and would NEVER do that! I think his teacher just assumes because they're discussing who's in the group, they must be picking on this kid. We have a special needs family member which his teacher does not even know about. It's too bad.
Hello,
I agree we have a long way to go, I hope my new film can help that process along. I wanted to let you know about Strong Love, a new film I produced about a couple both born with Down syndrome who decide to marry. I thought it might be of interest to your organization, staff and clients. It has been very helpful to parents of children with Down syndrome.
A recent review from the Down Syndrome News:
"Some scenes will make you cry, others will make you laugh. All in all, it's a picture of life full of surprises, challenges and joy."
We have posted a short excerpt from the film of Holly and Jon practicing their wedding vows if you are interested in previewing it. http://www.youtube.com/watch?v=tLFhP5olHvE
Strong Love is the story of world-class weight lifter Jon Shapiro and his childhood sweetheart Holly James, both of whom were born with Down syndrome. This documentary follows the couple over the course of three years, starting with their decision to get married. Their challenges, their triumphs, and their complex, sometimes surprising relationships with family and friends are at the heart of this inspiring film.
Please contact us for more information.
www.bonnieburt.com
56 minutes
2007
STRONG LOVE
A film by Bonnie Burt
"Strong Love" tells the story of what happens when a world-class weight lifter and his childhood sweetheart -- both born with Down syndrome -- decide to marry.
I can feel your pain in this post. I agree with you that we need to educate all of our children now about how ALL of us are different and teach about compassion early so that the ignorant morons who make these kind of statements don't pass it on to another generation. I was actually telling Steve last night that I think Peanut may have the cutest and sweetest smile of all the girls I have seen in the blogging world.
Hi Debbie,
This is SO sad, the whoever did that is a sicko.
Unfortunately the internet attracts all kinds of people. When you see/hear the stories of internet predators, you realize the extent of the problems parents are faced with.
On the bright side, I think it is wonderful that you have a blog where you can share this information and help to rally support for other parents with special needs children.
Deb, you are making a mark on cyberspace, and for that we are all grateful.
I'm going to use "StumbleUpon" to get this post more exposure so others know how sick people can be. In the meantime, I'm hoping YouTube will pull that clip.
Hi Maria,
I know your son would not have done anything like that. And yet, when it is a misunderstanding or done out of ignorance, I do have patience and the desire to educate that person. Like Peanut's cousins I know your children will be advocates for there precious little cousin.
Hi Barabara,
Thank you for your kind words and thank you for the Stumble. If someone can learn to be more understanding because of someone's cruelty, it will make it a little more bearable.
Great post! I don't even post half the stuff I hear. Now that I am working with a younger generation of nursing students, I can't tell you how many times in the few hours I have them do I hear the "R" word. I usually wait until a few people have said it so I can say it to the group as a general FYI rather than to point fingers. I teach them about People First Language for ALL people. I just started with a new group today and I made sure I pointed it out ahead of time to refrain from using the R word or any other unkind word. I basically said if you would'nt find it to be kind to be said to you, then don't say it at all.
The ignorance of some people is just plain sad. I sincerely wish that those who do such things are blessed with a child of the type they choose to make fun of. That would be the very best punishment of all.
Debbie - this is appalling. People who do things like this have real problems.
I'm going to stumble this post and ask others to do so also.
Hi Cath,
Thank you.
Hi Everyone,
Thank you for all your kind words. I'm feeling much better about all this. It's still disgusting, but it's helped to be able to talk about it and receive such lovely comments. I know this kind of stuff happens in the world, and that is so sad. But you have all proven there is so much good and kindness and caring. I will put my thoughts to people like you and not give this person anymore of my time.
I plan to teach my son just as you said.
I'm so sorry about someone being so cruel and rude.
I find myself using the "r" word sometimes, though about myself and not against other people and I feel guilty because I know there are others who use it in a malicious way and against people they thing are this way. It's wrong and I'm trying to curb my language so Jonathan doesn't here it and think he can say it. I want him to understand it is a word that can hurt because of what it can mean to others. I know I don't mean it that way, but he's little and I want him to know better and do better. I don't know if that makes sense or not....
Anyhow, great post and very informative.
-- Jonny's Mommy
what ignorance. the hole people dig for others, they will soon find themselves in.
great post! didn't hear about the dreams video very sad! I guess we will just have to keep advocating :)
Hi.
You are doing a good job educating people about down syndrome and being such an active part of helping people over come the suffering when their loved ones have down syndrome. I am not a regular reader but I saw a post on Barbara Swafford's blog and thought I'd give my 2 cents. Deb, people do try to gain publicity by mocking others and the person who did that to the video on down syndrome was trying to get some publicity out of it. It is better that you contact people at youtube, they are pretty helpful. You can also take your blog on down syndrome by coming out of blogspot and probably getting your own domain and installing wordpress on it. It is a simple thing. Your website has very good content on down syndrome but people are not able to get here because your website ain't coming when they search for it. down-syndrome-parent.com is free for regstration now. Hope my comment helped you.
i had no idea this kind of stuff STILL went on in this world. i thought we as a people were better educated, more compassionate and had more class than that. it makes me sad to know that even though we have come so far we still have so far to go. i am really angry too.
horrible. sad. pathetic. WRONG.
Hi Johnny's Mommy,
I think the fact that you recognize something you need to change is admirable. We all do things we aren't proud of and teach our children (unintentionally) bad habits. As parent's we sill have to live and learn and try to do better next time. I may not call myself that word, but I'm sure I've called myself stupid or dummy at times. I should try to do a better job about that as well.
Hi Natural,
All I can say is, "Thanks!" Well, maybe can I have the shovel to fill it in after they fall in?
Hi Kari,
Thanks.
Hi Pratee,
Barb has told me about getting my own domain as well. Frankly, I've only been blogging for a short time and I am still a novice to a lot of the aspects so that is why I chose blogger. I agree that some day I need to consider moving to a domain of my own, but frankly, I'm a little nervous about it. I do appreciate your advice and will keep it in mind when I am ready to make that leap!
We've already started the process of teaching our daughter to be far more tolerant of the world around her than our parents taught us. But yet, it saddens me every time I hear another story confirming just how important it is that we make a point of teaching her. I wish we were wasting our time and the world had magically fixed itself.
(BTW, sorry I'm late to the party.)
Hi Debbie. Found your site by way of Barbara's site. The Dreams video is so nice and my 2 year old son sat here and watched it with me and he'd say "baby" or "kids" every time one would come on the video.
What a crappy thing someone did and I hope YouTube responds. I'll digg this article now to try and spread awareness.
Hi everyone,
I spoke with the director of our Guild today and confirmed that this clip has been pulled by youtube. Yeah! Thank your for all your support!
Debbie - There's just something missing the heart of anyone who cold do something like that. Can you imagine how truly cold and empty that person's life must be to have to try to get attention in such a way?
Then, on the flipside, comes Bonnie with the video she mentioned. I looked at the exerpt. It looks like it's going to be a wonderfully positive thing for the DS community.
God does have his ways of turning bad to good, doesn't he. If it hadn't been for that creep, we might not have been introduced to Bonnie's work. He never ceases to amaze me! xoxoxo
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