Showing posts with label special needs. Show all posts
Showing posts with label special needs. Show all posts

Monday, April 20, 2015

Miss Unlimited

Here is something I never thought I would say: I will be attending my first ever beauty pageant on May 9. It is the Second Annual Miss Unlimited Pageant. No, I am not a contestant; it's not quite THAT unlimited. This pageant is for young women with a disability.

I heard about this after it happened last year, but it was right after we lost Maggie and I was in too much of a fog to look into it. This year the organizer Michelle Wynn, reached out to me, and I'm so glad she did. Because I know how these things can go, I warned here that some in the disabled community might not like this because it is a segregated event and there are many who simply want disability to be part of the overall tapestry of the world, and not its own category. Her response cemented this for me, She basically said, I know there are people who won't like it, but the girls love it and that's enough for me.

Amen, sister.

Let's face it, inclusion will take a generation or more to happen. If we wait for that, we lose an entire generation of opportunities to make people happy. There are things we can do now, so let's do them. We can celebrate real beauty and stop ignoring a whole subset of the population, so let's just do it.

The Miss Unlimited organization describe it best on their website www.missunlimited.org which you should check out in full,

 All too often we are taught to believe in a false definition of what it means  to be beautiful, casting aside the essential values of real beauty; strength, kindness, and confidence, the qualities that make us all radiant.  
The Miss Unlimited Pageant was founded on the principles of empowering the true beauty and unlimited potential of girls with special needs. The pageant provides the opportunity for these young girls to be celebrated for all they are inside, and not just defined by what the world sees on the outside.


I love this idea for many reasons. It is a chance for these young women to be pampered and celebrated, something that just doesn't happen often enough to girls with special needs - or to any of us. On a separate point Michelle Wynn is a teacher at St. Ignatius High School and the event will take place at Sacred Heart High School thus giving the Catholic school community a much needed entry into the world of special needs. Catholic schools and private schools in general have very limited ability (or interest) in providing special education, therefore depriving themselves and their students of a complete understanding of the world of special needs individuals.

 I could list many other reasons, but let's just cut to number 1 - Maggie would have LOVED it. Man oh man, she would have been there front and center having the time of her life. There was nothing better than prom day for her. She loved getting dressed up and heading out for the night. This would have left that in the dust. As Ms Wynn says, that's reason enough for me.

Check out the website and think out getting involved. If you know young women who might be interested, help them fill out an application. If you can donate or volunteer, please do so. It will be a fun day and a chance to make a big difference in the lives of some truly beautiful young women.




Wednesday, July 15, 2009

Ambassadors

Parents of children with special needs have many responsibilities. Caring for the child is the biggest and that can be exhausting both physically and emotionally. Educating themselves about their child’s specific needs and advocating for those are right near the top as well and that can be all encompassing.

But there is more.

Every kid, typical or otherwise, need parents show them how to interact with the world. Parents teach best by example, but sometimes they have to intervene to steer a child off a wrong track or even resort to the dreaded lecture to drive a point home. Special needs children need the same thing, but often because of their disability, they cannot understand or apply the information in the same way. Parents of special needs kids have to be more creative. Our kids also have to learn how to deal with the non-disabled world that does not understand or even particularly care about their differences. Like every parent, we have to pave the way for our children; but, because the road is rougher, the job is tougher.

Part of that is deciding how to interact with inappropriate remarks, questions, stares, etc. We have to figure out our own responses first before we can begin to teach our children. When the inevitable stupid remark or question arises, the easiest thing to do is get angry or dismissive. Easy is not always best. There are certainly times anger is warranted, but often it serves only to further isolate the special needs child as well as the parent. Often we have to swallow our first emotional response and act more diplomatically. We have to be ambassadors. We have to be the ones to bridge the two worlds.

It is very easy to become isolated in the world of special needs. We need to keep one foot in the rest of the world or we will go crazy. If you alienate your contacts outside the special needs arena, it is more difficult to protect your sanity. Sometimes, however, those contacts are the ones saying the stupid things. What to do, what to do.

When Maggie was little, I read a book called Facing the Crowd that dealt with this issue beautifully. (I do not remember the author and I believe it was published in Australia but it is long out of print now.) Jeri Hart, Maggie’s home counselor from the Blind Babies Foundation, lent it to me. (When I spoke with her last night, I learned they are still using that book for new parents.)

Facing the Crowd suggested that a parent stop and mentally categorize the person before responding. If this person were important to you or your child, e.g. a doctor or family member, you would have a different response than you would to a stranger on the street. A neighbor that you would see often might warrant a kinder, gentler response than a staring stranger at the drug store. Some you have to educate and inform, others you do not. Not everyone is going to be interested in your child’s challenges, and it is not our job to change their minds. It was an excellent tool to get me through those early years.

I’m not sure I still do that because after this amount of time we are just living our life. I am no longer interested in educating the world about Maggie nor do I resent strangers who don’t care. If people say stupid things I may kindly respond or I may snap at them. These days it is much more about my mood than the role that person plays in my life. (In other words, WATCH OUT!)

Playing the ambassador role worked for me, but it does not work for every parent. Some do not want or need to, but that is rare. Some simply miss the opportunity to be ambassadors. Some just cannot handle it. Some are too angry to do it effectively. Most however, do this seamlessly and bring two worlds together.

It just comes with the job.