Showing posts with label awards. Show all posts
Showing posts with label awards. Show all posts

Thursday, January 31, 2008

Inclusive Travel

If you've never checked out Scott Rains' blog, you are missing out. It's full of information, links, and stories about travel and disability.

Scott just found out that his proposal to create three Centers of Excellence in Inclusive Tourism in strategic locations around the world was accepted by the Echoing Green Foundation for the second of three rounds of the 2008 competition.

Here's what it involves:

"Each Center of Excellence will participate in international work to:

* Standardize the diversity of accessibility laws,
* Disseminate minimum accessibility guidelines for hotels,
* Train travel & hospitality industry staff,
* Promote the education & hiring of People with disabilities (PwDs) in the industry.

At the local level centers will work to make themselves accessible
destinations and establish a core of PwDs to be self-sustaining as advocates & experts in Inclusive Tourism for their region."


Congratulations, Scott! And, thank you.

Thursday, May 17, 2007

A powerful week

This week I went to the Illinois state capital, Springfield, for the Coalition of Citizens with Disabilities in Illinois (CCDI) annual Disability Rights Conference. There were a variety of workshops on a number of topics such as disability myths (making the comparison of ableism with racism and sexism), disability law, particularly as it applies to employment, and disability bioethics (discussing Ashley X and state futility laws, such as the Texas one being applied to baby Emilio).

I was awarded the Markeeta Award, an award for a youth in Illinois pursuing social justice and disability advocacy. It is named after the first recipient of the award, Markeeta Vincer, who fought successfully to be included in the Chicago Public School System.

I learned about an important bill, HB 1256, that has passed the Illinois House and is currently going through the Illinois Senate. If you live in Illinois, I urge you to call or email your state senator and ask him or her to support this bill. House Bill 1256 is very important for people with disabilities who have the ability to work, but not necessarily full-time. I see this bill as being very important for me personally and to many others with disabilities and stamina issues.
Here's some information from CCDI on the bill:

"-Lack of access to affordable health care forces people with disabilities to work for less or not at all. The current program does not go far enough.
-House Bill 1256 allows people with disabilities to work more often or accept better paying jobs and would allow people with disabilities to earn up to $35,000 (instead of the current $20,000) while paying their share of Medicaid costs.
-House Bill 1256 would allow people with disabilities to accumulate assets to alleviate poverty and promote their independence and self-sufficiency without jeopardizing their health care coverage"


I "rubbed elbows" at the conference with other advocates that I'd heard about - Diane Coleman and Stephen Drake from Not Dead Yet, Mike Ervin, FRIDA advocates, and ADAPT advocates. (I felt like a bit of a groupie.) I had many interesting conversations and an enjoyable time in Springfield.

Monday, April 30, 2007

Sandbox Lessons

Blogging Against Disablism Day, May 1st 2007

I was listening to the song, “You’ve Got to be Carefully Taught” from the musical South Pacific. The song asserts that children are not born racist, they must learn to be racist. I think that same truth applies to ableism. Children are not born believing that some differences make a person inferior; they have to be taught. It's easy to see how Jerry Lewis’s Muscular Dystrophy Telethon, inaccessible buildings, overt discrimination, or the common use of words such as "retard" or "cripple" teach ableism. It is more challenging to realize that even well-intentioned people, themselves products of the culture we live in, can inadvertently foster the ableist paradigm in children.

My mom remembers a telling story that took place on an ordinary day many years ago. My two sisters and I were about 4 years old at the time (we’re triplets) and were playing in our backyard sandbox. It was a warm, sunny summer afternoon. My sisters were running back and forth between the sandbox and the hose to get water for our sandcastles. I was lying on my stomach, as I often did, playing in the sand with my hands, my shovel, and my truck. We were laughing and having fun.

Unbeknownst to my sisters and me, a six year old boy who was visiting our next door neighbors was intently watching us through the chain link fence.

At some point, one of my sisters went near the fence, and the boy asked her, “Does he walk?”

My mom says she held her breath, ready to jump into the conversation and stand up for me. Ever the advocate, she would've said something sappy like, “He can’t walk, but he's really good at playing in the sand.”

Had my protective grandparents been around, one of them might have scolded the boy, “Hey! That’s a rude question!”

An educator or social worker, seeing a potential peer socialization experience for me, might have answered with a heavy, deliberate sigh, “No… he's not able to walk.” Then with forced enthusiasm, “Why don't you go play with him? It doesn't have to be very long, just a few minutes. You'll feel good helping the boy."

A healthcare provider, intending to minimize the importance of physical differences, might have lectured the boy on my condition of cerebral palsy, "The motor area of his brain was damaged because he was born too early. This damage causes him not to have good control of his arms and legs. Even though his body is different from our bodies, he's really just like us.”

The boy's dad, not wanting his son to be offensive or rude, might have pulled his son away from the fence, “Shhh…. Don't stare! Don't make him feel bad."

On the surface, these responses to the boy's question may seem appropriate. But imagine, if you will, the boy at the fence asking my sister a different question. Suppose he asked, "does he have red hair?"

"No, he doesn't, but he's really good at playing in the sand."

"Hey! That's a rude question!"

Heavy sigh, “No… he doesn't have red hair.” Forced enthusiasm, “Why don't you go play with him? It doesn't have to be very long, just a few minutes. You'll feel good helping the boy."

"He’s genetically heterozygous for the brown haired trait. Even though his body is different from our bodies, he's really just like us.”

“Shhh…. Don't stare! Don't make him feel bad."


So, how did the four year old's and six year old’s interaction play out that sunny summer day?

Not assuming any hidden meaning to the boy’s “Does he walk?", my sister simply said, "no."

The boy accepted her simple answer to his simple question. Then he moved on to his more important question, "Can I play? We could use my yellow dump truck to move the sand.”

The boy, and soon the neighbor kids, came over. The sand castles got bigger, the laughter louder. We all had a great time.


Be sure to check out the many other posts for Blogging Against Disablism Day. Thanks, Goldfish for organizing this event.

Thursday, April 26, 2007

Disappointing news and exciting news on the same day

Yesterday, I found out that I was chosen as an alternate for MIUSA’s Costa Rican Exchange. If a spot opens up, they'll call me. I’m disappointed. I would have loved to have gone. It sounds like a wonderful experience.

I had some good news yesterday, too. I won the Markeeta award, an award presented to an Illinois youth for social justice and disability advocacy. Thanks to Tara Dunning from the Statewide Independent Living Council and Meredith Hill for nominating me. My interest in advocacy took off when I attended the Illinois Youth with Disabilities Leadership Summit in 2003. I’ve since gone each summer as a participant and as a peer mentor. The Summit is a great way for young people with disabilities to meet each other, meet interesting adults, and learn about advocacy and leadership. If you know an Illinois youth who might be interested, applications for this year’s summit are due May 18.

Thursday, March 29, 2007

Thinking

Many thanks to Dream Mom who has nominated me for a Thinking Blogger Award. It is an honor to win this award from a fine blogger, and I really appreciate it. For those of you that have not checked out Dream Mom’s blog, I urge you to do so. Dream Mom writes very eloquently about her experiences raising Dear Son.

Dream Mom nominated me for this award because my blog was one of five blogs that made her think. In keeping with the tradition of the award, I now get to give this award to five blogs that make me think.

It was not an easy decision to decide which blogs to nominate. I've only been blogging for six months and have discovered many wonderful, thought provoking bloggers. Here are five of them.

1. At Diary of a Goldfish, Goldfish writes about the arts, culture and disability. She organized the first Blogging Against Disablism Day last year. This project had 147 contributions from all over the world.

Goldfish writes openly about many different life issues including disability. She looks at the issues with a thoughtful, reflective approach and always has an interesting perspective. She makes me think about my disability. I also enjoy learning about disability from a British perspective.

2.) Imfunnytoo at Midlife and Treachery (formerly Did I Miss Something also blogs about disability issues. She always has interesting observations on her life and issues affecting all of us. She is a wonderful writer with a very quick wit. She really helps me to look at life with a sense of humor.

3. Kathryn, at Ryn Tales, is the mother of four-year-old Ellie. Like Dream Mom, she writes about her experiences and thoughts about being the parent of a child who happens to have a disability. She looks at life issues from many angles, but mostly from the angle of a mother's love.

4.. I’ve learned so much about disability history, disability law, and disability rights from Penny Richards at Disability Studies. Penny's posts always teach me something new. For example, today Penny writes about reasonable housing accommodations. Penny started up the disability blog carnivals, a source of lots of thinking organized around themes.

5. I discovered Dave Hingsburger's blog, Chewing the Fat, just recently. Dave shares stories from his personal life and his work life. In his work, he conducts workshops with people with disabilities to teach boundaries, self-respect, and self advocacy. In The Good Girl, Dave shares the heart wrenching conversation with a young lady whose only goal in life is to be polite. In Conditions, Dave shares an experience with a young woman who has something to teach us all about self advocacy in relationships.

The rules and origin of the award can be found here. Bloggers that I nominated - you now choose five blogs that make you think. Be sure to include the link to the original site, as that is one of the rules, and choose blogs that has not been previously chosen.

Thanks again, Dream Mom, for nominating me.

Other blogs that make me think and have already won the Thinking Blogger Award are:
The Gimp Parade, Wheelie Catholic, Planet of the Blind, Wheelchair Dancer, and Ballastexistenz. There are lots more, too. Check out my blogroll for starters!