Showing posts with label barriers to access. Show all posts
Showing posts with label barriers to access. Show all posts

Sunday, March 9, 2014

Disability Awareness Month - 5 Influential People of the Civil Rights Movement For People With Disabilities

For Disability Awareness Month I’ve put together a list of five influential people of the disability rights movement in the United States. This is just a short list of some people who have made a tremendous impact on how people with disabilities are able to live today.

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Hellen Keller
 1. Hellen Keller – Born in 1880, Helen was struck by a mysterious illness called “brain fever” by a family physician at 18 months and became deaf, blind and mute. At the age of 7, her parents found a young teacher who would teach Helen how to communicate and they would become life-long friends. Helen graduated from Cambridge School for Young Ladies and went on to become a well-known speaker doing lectures and working on behalf of people with disabilities. She testified before Congress, advocating for an improvement in the welfare of the blind. She co-founded Helen Keller International to combat the causes and consequences of blindness and malnutrition. In 1920, she helped found the American Civil Liberties Union (ACLU). Helen tackled many social issues including women’s suffrage, pacifism and birth control. She traveled to 35 countries on five continents, including a five month trip across Asia at the age of 75 in order to improve the lives of people with disabilities. She died in her sleep in 1968, just a few weeks before her 88th birthday.

Gini Laurie
2. Virginia “Gini” Grace Wilson Laurie – She is considered one of the “grandmothers” of the independent living movement. A year before her birth in 1913, two of her sisters died from poliomyelitis and her brother was left severely disabled. As an adult, she volunteered with the Red Cross in the Cleveland Toomey Pavilion rehab center during the 1949 polio epidemic. In 1958, she took the unpaid job of editor of the Toomeyville Gazette, a newsletter put together by patients who recovered at the rehab center after contracting polio. The Gazette published articles on legislation, activism and what would become known as the independent living movement. In 1970, Gini wrote an article in the newly-named Rehabilitation Gazette where she stated plainly that for people with disabilities, the most important thing “is the right to freedom of choice to live as normal a life as possible within the community…Segregation is unnormal.” In 1977, she wrote Housing and Home Services for the Disabled: Guidelines and Experiences in Independent Living”. It pointed to the fact that it is more cost-effective for people with disabilities to live in their community than being put into institutions or nursing homes, an important point still being driven in the disability movement today. She died in 1989 of cancer.

Ed Roberts
3. Ed Roberts – After contracting polio at age 14 and living in the hospital for two years, Ed was finally able to move back home. But things were very different. Because of the polio, he was only able to move two fingers and slept in an iron lung. His struggle against discrimination began immediately when school administrators did not allow him to attend school with his classmates. They felt it was best to have teachers instruct him privately at home. The family fought back and they won him the right to attend school with his classmates. After graduating from a junior college, he had to go through another battle in order to be allowed to attend the University of California in Berkeley. He eventually won this fight as well and went on to study Political Science. Because of Ed, more disabled students were allowed to attend Berkeley and they eventually formed a disabled student organization on campus. Their focus was to make the university more accessible and provide trainings on daily support techniques. In 1972, Ed helped the group form the first Center for Independent Living which was considered radical at the time because it was run by people with disabilities rather than medical professionals. He became the first person to serve as the Director of California’s Office of Vocational Rehabilitation. In 1981, he and Judy Heumann and Joan Leon started the World Institute on Disability (WID) which studies legal rights issues for people with disabilities around the world. Often referred to as “the father of the disability rights movement”, he was president of WID until his death in 1995.

Justin Dart
4. Justin Dart – At the age of 18, Justin contracted polio which left him unable to walk. He came from a wealthy family in Chicago and in 1967 he and his wife devoted their lives to helping people with disabilities. On his own dime, they travelled the across the United States in the early 1980’s which was quite an undertaking because many places were not wheelchair accessible. Universal design was just beginning to be implemented in larger cities but in smaller ones, it was practically unheard of.  What was learned through conversations during this tour was the basis for a policy that called for national rights for people with disabilities. It would eventually become the Americans with Disabilities Act (ADA) of 1990. Because of the national dialogue that took place during this time and the subsequent passing of the ADA, Justin Dart is considered to be “the godfather” of the ADA. In 1995, he founded the American Association of People with Disabilities (AAPD) along with others. At the age of 71, he died in 2002 from congestive heart failure related to complications of post-polio syndrome.

Wade Blank
5. Wade Blank – emulating the great Dr. King, Wade began a movement in the 1970’s within the disability community in Denver, Colorado that would give rise to ADAPT, a national grass-roots community that organizes disability rights activists to engage in nonviolent direct action. A former minister, he saw the sad living conditions of individuals with severe disabilities in nursing homes and took it upon himself to make changes. He not only moved people from institutions into independent living centers but these very same people became co-protestors in his fight against the discrimination built into the public transportation system. They waged the first sit-in of their kind and surrounded a bus with their wheelchairs in Denver. The group quickly expanded to other cities around the US, holding demonstrations fighting for accessibility in public bus systems. His group’s national recognition paid off as accessible public transportation was included in The Americans with Disabilities Act (ADA), a landmark law passed in 1990. He continued to be a leader in the civil rights movement of people with disabilities until his death in 1993.

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Without these role models and others like them, people with disabilities would not have the right to a free and public education, public transportation and barrier-free public places, among other civil rights. Although there is still much work to be done, it is uncontestable that the foundation laid down by these pioneers sparked a movement that is still growing today.

Can you think of any others who have made a major impact on the lives of people with disabilities?




Monday, March 3, 2014

Top 5 Visitable Cities - Places Where People With Disabilities Have Great Accessibility


Vacations are enjoyed by millions of people all over the world but some people with disabilities can find planning a vacation a bit daunting because of disability issues. Some may even think it’s impossible. I say, with proper planning, you can have a great vacation to remember. Here is a list of the top five most accessible places to visit in the world.

Berlin, Germany
1. Berlin, Germany
It was awarded the “Access City of the Year” in December 2012 by the European Commission due to its aggressive and forward-thinking plan of creating a fully accessible public transportation system. Its plan also includes broadening sidewalks and using tactile guidance systems at road crossings. By the year 2020, the government plans on Berlin being 100% accessible. A large majority of museums in Berlin are already accessible as are most of the more well-known hotel chains but be sure to ask when making reservations what accessible features are currently available. You can search for places to visit at Visit Berlin for People with Disabilities


Vancouver, British Columbia
 2. Vancouver, British Columbia, Canada
One of the most diverse cities in the world, Vancouver offers visitors a wide variety of cultural foods and experiences. With its great public transportation system – buses are equipped with wheelchair ramps and the Sky Train and SeaBus are also accessible – visitors have a variety of choices when deciding how to get to where they’re going. Vancouver International Airport is one of the world’s most accessible airports. Some barrier-free features include amplified handsets at service counters, low-mounted information monitors, services for the deaf and accessible washrooms. Travelers can rent vehicles with hand-controls or use the Airporter shuttle bus service to get to their hotels. For more information on where to go and what to do, go to Accessible Vancouver.


San Diego, California, United States
3. San Diego, California
When you think “California” you should also think “beach”! With its mild climate you can enjoy 70 miles of beach when visiting this city year-round. At at least fifteen San Diego beaches, beach wheelchairs are available for people with disabilities at no charge. Some even offer motorized chairs. To find a list of beaches with phone numbers check out CaliforniaCoastal Commission. You can also take accessible sightseeing tours via bus, boat or old-fashioned trolley. Go to SanDiego.org to plan your trip. 



Denmark
4. Denmark
Yes, the whole country. While all Scandinavian countries are very disability-friendly, Denmark stands out because of its “Accessibility For All” program. This is a tourism labeling system for hotels, attractions, restaurants and other places you might want to visit while there. You can search for places and other things accessible using http://www.godadgang.dk/ and narrowing it down by city, type of place, disability and more. You can also find more tourism information at VisitDenmark.com. 



London, England
5. London, England
England might call to mind old tradition but that doesn’t mean it hasn’t modernized its accommodations for people with disabilities. The subway system, called the Tube, has some stops that are not wheelchair accessible so if you’re planning on traveling that way be sure to research ahead of time to find the stops that are accessible. However, the large majority of their buses are accessible and their taxis are required by law to be accessible. You can find accessibility information at Transport For London. Many of London’s most popular sight-seeing stops are free or offer a discount for people with disabilities. There are some places that even allow one care giver in at no charge.


Special Mention:
Morgan’s Wonderland in San Antonio, Texas – A recreational park that provides a beautiful environment free of economic barriers that all individuals, regardless of disability can enjoy. It boasts many attractions such as a sensory village, picnic area, playground and sandpit and a carousel that is accessible to all including wheelchair users. Tickets can be purchased online and are very reasonably priced. Individuals with disabilities and children under 2 get in for free. Visit their site at Morgan’s Wonderland.

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So now that you have some ideas of where to go, let’s go over a few tips on how to travel with a disability:
1.  Plan ahead! Give yourself as much time as possible to research where you are going. Here are some questions you should ask:
·         Is the destination airport accessible? Who can help you find the right accommodations?
·         Does the hotel have a no-step entrance; rooms on the first floor; wide hallways/doorways; grab-bars or roll-in showers? Do they have other accommodations such as interpreters or amplified handsets?
·         Is the local area disability-friendly? How will you be getting to local attractions and sites?
2. Bring a letter from you doctor - Preferably on a letterhead, a doctor’s note explaining your condition and necessary treatments could help you if you become ill or injured. Make sure the doctor’s contact information is on the letter.
3. Be specific - Not everybody will know what your particular disability entails or requires. When makin queries be very clear about what your needs are.
4. Know about emergency services - In the US, 911 is the universal emergency phone number. What about in other countries? Be sure to know what to do if you have an emergency.

Remember, being prepared for the worst allows you to enjoy your time better. Here are some travel sites geared toward helping people with disabilities:

Happy vacationing!


Monday, June 10, 2013

Facing Your Fears - Do Disabilities Scare You Away From Enjoying Family Outings?


When we were kids, my Uncle Victor and Aunt Lina used to take me and my cousins to K.I.S.S. park every summer. At that time, there were about 6 – 8 of us, cousins and siblings, all elementary-school age. K.I.S.S. is an anagram that my uncle made up but back then, I really thought the park’s name was Kiss – only years later did I find out that it wasn’t! The adventure would begin with a mysterious letter we would get in the mail (what kid doesn’t love pulling a letter out of the mailbox with their name on it?) It would be in the form of a puzzle or note of some kind with clues. We would put the puzzle pieces together or figure out the riddles and discover that we were about to embark on another great day at the park. I honestly can’t remember if there were any other adults there besides the hosting couple or how we all even got there! I just have these wonderful memories of hot summer days, dusty games of soccer & freeze tag, canoe rides, horseback rides and fun, fun, fun! The entire time I wrote this section, I did so with a big smile on my face!


Many years later, when I was in my early 20’s, there was a thought to revive this old tradition. Several of us were excited when Uncle Victor suggested we hit the ol’ park again. My daughter was a toddler and I was having a (very) difficult time with adjusting and accepting life as we knew it but I was filled with nostalgia and excitedly looked forward to K.I.S.S. with my family. By this time, I was in a very deep depression over my daughter’s state of health. She couldn’t sit on her own, let alone walk; she was non-verbal so there were no first words or “mommy”; she was having seizures that were progressively getting worse. When I was pregnant, as all moms-to-be do, I had these visions and fantasies of how life was going to be. Her first steps, first words, going to the playground together, shopping for school supplies, sleepovers, giggle-fests…Everything crashed and burned the day she was born. I found myself constantly running through flames, trying not catch fire as I stumbled through the burning building that became our lives. Every milestone missed, every specialist appointment, every “normal” kid who walked by us was another spark, a new fire threatening to engulf me. I can tell you that practically nobody in my life had even an inkling that I was feeling this way. I’ve always had a hard edge to me and I’m sure I came off as angry or bitchy. But I felt tremendously lonely and terrified and sad. These are still feelings that stick with me today, thankfully not to the same degree, and I know that the majority of parents who have children with disabilities know what I’m talking about. I was having a tough span of days filled with these icky feelings when I wrote “Mom Missing Out On Her Milestones.

It was difficult for me to enjoy the day at K.I.S.S. park even though I had hoped that it would be a great day. There they all were, those walkers & talkers, flitting about, eating burgers at the picnic table we couldn’t get a wheelchair under no matter how we angled it, playing kickball, just doing what normal people do at a park. Enjoying the sun kissed summer afternoon, their laughter floating in the peaceful breeze as puffy clouds gently slid across a sapphire sky. That’s how my eyes saw their joy. Soft. Velvety. Melodic.

All I could think about was the uneven ground that I had to fight with the wheels of her chair. There were tree roots and branches littered about, hilly sections, small ditches and other barriers that come naturally in a park. We were supposed to walk over to the canoe area – a walk that we always enjoyed in the past – but I kept thinking about the struggle I would have pushing the chair over the grassy areas to keep up with the rest of the group. Not to mention the uncomfortable bumpy ride for my daughter who was sitting in the chair! And what about the canoe ride itself? How were we going to safely transfer her into the canoe when she can’t help at all? She can’t sit without full assistance – how can we get her to actually stay in there? And if we do manage all that and make it back, how will we get her out of it now that we’re IN the water and the canoe is bobbing about?

These of course were only (some of) the PHYSICAL worries that consumed me. I haven’t mentioned the bigger meaning behind the physicality involved in bringing along a person like my daughter to a fun day at a park! Seeing everyone else dashing about care-free made our reality (mine & my daughter’s), our differences, actually palpable. These differences weren’t just a notion. No, they were real; unquestionable; cold and hard. The toll this takes on a person’s psyche is sometimes unbearable. There are some days where I have to work at keeping my joy.

She is now 15 and looking back I wish I had done so many things differently. Isn’t that how it always is; 20-20 vision tends to be perfect. Why did I allow myself to focus on the negative parts of the trip? Thinking back on it, the only memories I have from that day is a sad game of kickball (for me; everyone else was having a great time, as I should’ve been) and the canoe ride. (Which, by the way, wasn’t at all terrible. She was still little so transferring is not the game of logistics it is today. But even today, I have Nick Vujicic to remind me that pretty much anybody can get in and out of water!) Because of my own personal issues, I didn’t allow myself to enjoy what she could do. She was having a beautiful time with her cousins even though she couldn’t run around bases or get a turn throwing the boomerang and wasn’t that the point of the day?

I find myself still paralyzed with fear to this day. I want to do things or go places and decide that I will take her no matter what but then I chicken out at the last minute. I start thinking about the things that can go wrong – maybe there won’t be an accessible area for us to sit/stand; maybe there will be steps we can’t get up; maybe it will be too crowded and she won’t be able to see anything except strangers’ butts; maybe we won’t be able to find parking. The list goes on and on. And yes, those things can happen. On our first family vacation in 2012 we found ourselves blocked out of a building that housed the resort’s pizzeria, arcade and ice cream parlor because it had steps, even to the first floor!

But what if things like that don’t happen?? What if we go and there is a spot waiting for us to park in, the venue has curb cut-outs and ramps leading to it so we can get there and there’s a wheelchair-accessible area so she doesn’t have to miss out on seeing what everyone else is seeing? What about that?

There are some things that we just can’t do, for logistical and emotional (on my part) reasons. We can’t go to certain people’s homes because they're just not accessible. Taking the train into the city for a day of sight-seeing and shopping – not gonna happen. Spending a Sunday at the beach from dusk till dawn with coolers filled with bagels, cold cuts and bottled water – a thing of my past. But why should that stop us from creating wonderful, loving, fun-filled memories doing things that we can do? It shouldn’t –  and it won’t!


Did you have fears or sadness surrounding family outings like me? Do you still? What do you do to try to get past these feelings?

Monday, January 28, 2013

Accessibilty Arcade


An accessible arcade – Accessibilty Arcade – is open for all gamers in the Martin Luther King Jr. Memorial Library in D.C. The idea of one had been showcased in the past but it’s a permanent fixture developed by The Ablegamers Foundation that can be enjoyed by visitors. 

Why is this so important? 
Glad you asked! 

First, it’s important to individuals with limitations (and their families) to be able to enjoy the same type of good stuff that you & I take for granted. Me? Not much of a gamer. But I have the option to not be one. With this type of technology, thousands of people (if not more) now have the option to not be a gamer, like me.  =D

Another reason this is great stuff is because beyond the fun of playing there’s the therapeutic aspect. Hand-eye coordination is something that has often been touted by defenders of gaming when non-gamers commented on the time wasted in front of the screen (I would never). And it’s true. Gaming offers a fun way to improve cognitive ability as well as fine, and sometimes gross, motor skills, depending on the type of game.

So play on, playas! 

Check out some images in this article: Life Labs Attends Launch of Ablegamers Accessibility Arcade 

UPDATE:
UCP’s Life Labs has recently won a CVS Community Grant that will help to build a prototype mobile accessible gaming station in partnership with the AbleGamers Foundation. Read more about it here.

Saturday, September 8, 2012

Accessible Playground For People With Disabilities


I forgot all about this park until I just came across an article about it. Thanks, Arc Circle of Family and Friends!

It’s called Morgan’sWonderland, located in Texas, and it’s designed for kids and people with disabilities to enjoy. It’s a place where special needs kids and able-bodied siblings can have fun together. Families can have meaningful quality time that everybody can enjoy.  It has some great features and it’s very inexpensive. Anybody in the disabled community knows that when you add the word “special”, or any variant of it, to something it automatically boosts the cost of the product or service by at least 20%. Not here. One-day passes for adults: $15; kids: $10: special needs: $0. Can't get much better than that!

I read an article about it in Family CircleThis choked me up when I read it:
"Before the park, I had to sit back and watch everyone else play," says 18-year-old Miguel Castro of San Antonio, who has spina bifida and is in a wheelchair. He celebrated his 17th birthday party at the park. "If I had to pick a favorite ride, it would be the swings. I hadn't been on one since I was 2 or 3 years old, and didn't really remember what it felt like," says Miguel. "Now I can go on them whenever we visit, and have fun like everyone else. It means everything to me."

Can you imagine not being able to remember what it felt like to be on a swing because your body wouldn't allow you to get into one after the age of 2 or 3? How many times did you play at the park or on the school grounds for recess with your friends? Did you slide down a huge slide or sit in the tire swing with a couple of buddies and spin, spin, spin till you got so dizzy you almost threw up? Did you play tag and chase each other on the monkey bars? In elementary school, we called the playground equipment “the big toy”. I have lots of awesome memories from playing on that thing.
My daughter has never and WILL never be able to play on a big toy. She can’t get on those swings or go up and down that slide even though she really, really wants to. I don’t even go anywhere where she would be watching other kids screaming in delight on one because of the torture on her face. If you think I’m exaggerating, take your own kid, niece, nephew, neighbor’s kid, whoever, to a park, sit them right in front of it and tell them they can watch from their seat but they can’t get up and they can’t go play.
That all sounds depressing, doesn’t it? I just keep in mind that it’s only one thing she can’t do. But I often wonder what the heck I’m gonna do when my son gets old enough to want to go to the park. I can’t NOT let him go; I can’t take the girl. The only thing I can figure is I will have to have separate play dates with my own kids!

I wonder what other parents of kids with and without disabilities do in these situations??

Tuesday, September 4, 2012

Handicapped Parking



Ok people. Let’s talk about handicapped parking. If you do not have a placard that allows you to park in a handicapped spot, DON’T PARK THERE. If you see diagonal stripes on the ground in between or beside a handicapped spot, DON’T PARK THERE.

This is a huge pet peeve of mine. Listen, if your lazy ass doesn’t feel like walking the 2 extra spots it would take to get from your car to the 7-11 door, then stay home. If you’re at Wal-Mart or the mall or at the Piggly Wiggly and the parking lot is packed and you don’t feel like walking that far, then stay home.

“I’m really late”
How is your being late my problem? Perhaps if you didn’t snooze the alarm sixteen times/spent less time applying the caked on make-up/hadn’t stayed out too late last night and woken up with a hangover the size of Cleveland, you might be running on time. But again I ask: how is your being late my problem? Now, because Your Royal Highness has decided it so, the spots designated for people who cannot walk as far, as fast or at all due to their disability are a free-for-all and I have to drive around the lot trying to find a spot that will allow me to get my daughter out safely.

“This will only take a minute”
It never takes just a minute…and even if it really did take only a minute, why should I have to wait on you? Ah yes, Your Royal Highness feels we should wait until Your Majesty has procured a mocha-capa-frappa-latte with just the right amount of sweetener and a carton of Pall-Malls before we, the commoner, the lowly simple folk can have the same opportunity. Wait; allow me to roll out the red carpet upon your exit, Your Majesty, lest your Louis Vuitton’s be soiled!

All joking aside, it is so infuriating when I see people park in the reserved areas and don’t even think twice about it. I know there are folks with invisible disabilities that use handicapped parking and they get the evil eye because they don’t look disabled. But then you have those who use their granny’s or aunt’s or brother’s placard. If you are somebody who uses a placard when you know you’re really not supposed to, I hope you get fined. And I hope I’m the reason you got fined. Because I looove calling people out on their douchery. That word is so gross and anybody who knows me knows I hate that nasty word but that’s how I feel about people who refuse to walk the extra 10 feet.

Stop being a jerk!

Tuesday, July 24, 2012

Dear Senator DeMint



July 24, 2012

Dear Senator DeMint,

I want to thank you.

Thank you for blocking the Senate from ratifying the U.N. Convention on the Rights of Persons with Disabilities. Sure, there’s bipartisan support for it proven by the fact that the U.S. signed the treaty way back in 2009. But why should the Senate waste its time on a document that calls for a better standard of living and greater accessibility for people with disabilities worldwide?

Thank you for helping the hospitality industry’s lobby groups push to extend the deadline for the installation of permanent lifts in every public pool. After all, fighting for fairness and equality for all just takes up too much time when it pertains to something as silly as swimming! Besides, how can the federal government expect these fancy-shmancy hotels to understand what a permanent lift is in just two years?

Thank you for working so hard for that $175,000.00 paycheck you receive from the American people, including those with disabilities.

Thank you for your efforts to weaken the Americans with Disabilities Act.

Thank you for holding back the progress of not only Americans with disabilities but also individuals worldwide. A legacy to truly be proud of!

Sincerely,
Melissa Dinas

Tuesday, July 17, 2012

Let's Go Swimming!...Maybe - Accessible Pools in Public Places


Public Pools and the ADA

The Americans with Disabilities Act (ADA) outlines the rights of people with disabilities and forbids discrimination of any kind towards this group. In 2010, the Department of Justice (DOJ) sought to apply this regulation to public entities that offer a pool or spa, such as hotels, by requiring them to make these amenities accessible. 2 ½ years later we are still waiting.


Apparently 2 years is not enough time to sort out what exactly the government means when it says “pool lift” or “sloped entry”. So no swimming for you if you’re unable to get yourself in and out of a pool and there's no one around to help you, buster!

Thanks to hotel lobbyists, such as the American Hotel & Lodging Association (AH&LA), who pushed hard to extend the deadline for compliance set forth by the DOJ and Senator Jim DeMint (R) who introduced a bill to do just that right before the previous deadline of March 17, 2012, the NEW, new deadline is January 31, 2012. To some people, I guess as long as THEY are not affected, accessibility doesn’t matter too much. Official deadlines for when these public entities were supposed to be in compliance have been extended repeatedly since 2010 – at least a half dozen times – even though these businesses were well aware that they were obligated to make these changes.

"Reasons" Against Making Pools Accessible

Some hoteliers who oppose the DOJ requirements threatened to close down their pool entirely or to fill in their spas. BOOO-HOOOO! WAH-WAH-WAH! You sound like a bunch of crybabies – “If you make me do that then I just won’t have a pool for ANYBODY!” The image of a two year old stomping his feet with his arms crossed and his bottom lip pouting springs to mind. Fine by me; lose ALL your business if that makes you happy… Another argument made by the competent and crafty hoteliers is that installing a permanent lift will increase their liability during times when there is no lifeguard on duty. UHHHHH, hold on a minute. Are you saying that able-bodied folk NEVER go in swimming pools outside of posted hours? DAMN those insolent handicapped rejects! Why can’t they obey the rules like their astute counterparts? You know, the normal people!

Family Ties

Imagine going on a family vacation with your children and leaving one of your kids at home or pool side or in the hotel room because they were too big for you to lift in and out of the pool. Imagine if your husband or wife was a quadriplegic and had limited use of their arms and couldn't help you help them get into the pool. Imagine if it was YOU; watching from the sidelines or just not even going at all!  This does not sound fair. It sounds miserable, depressing, demoralizing. To be treated as less-than, unimportant. Am I taking this too far? Really? My daughter’s ability to be able to socialize and vacation with her parents and brother is directly related to whether or not we can get her wheelchair where we are going. Read about when we were on a family vacation and couldn't get pizza and ice cream. Saying to her, “You can’t go to there because your wheelchair doesn’t fit there” is the same as saying “You’re not important enough to make a change that can open up your world”. Literally.

Any one of us (yes, even YOU, dear reader) could BECOME disabled by an accident or fall, sickness or aging; just because you weren't BORN disabled doesn't mean you never WILL be!!


Friday, June 15, 2012

Family Fun – How Barriers to Access Can Ruin A Vacation


So we went on our first family vacation. I was very excited; maybe almost more so than my daughter, if that’s humanly possible. And now that I’m back, I see it wasn’t all perfect but I’m definitely glad we did it.

A Family Resort

We went to Smuggler’s Notch which is a family resort in Vermont. I chose to go there because they have an adaptive program that the girl would be able to enjoy. While at camp, she went kayaking, swimming and swung on a Giant Swing, to name a couple things. Oh, she was also serenaded by a friendly pirate! The grounds were beautiful. Whoever did the landscaping should be commended. I saw the most unique and interesting flowers and bushes that threw off such a beautiful aroma as you walked down the different paths in the Village Center, which is the main resort area. The condo we stayed in was mostly wheelchair accessible. It was a very nice-sized apartment with comfortable beds. It was supposed to have a wheel-in shower but instead we got a sauna tub. Lifting her in and out of the tub would have been totally impossible if not for my strong hubby. One of their on-site restaurants, Morse Mountain Grille, is absolutely AMAZING. Everything we tried tasted gourmet. Even their white pizza was better than anything I’ve ever had in NY. Needless to say, we had most of our meals there!

Disability World
So what’s this post about? In the midst of all the fun and beauty, it struck me (again) how able-bodied folks can be so clueless to the fact that the tiniest little thing, like a 1-inch gap, lip, crack, whatever, in a sidewalk or doorway can completely block a person who is non-ambulatory (like my daughter and by extension, us) from entering a building, crossing a sidewalk or enjoying family time. I can’t really blame folks who don’t live in the Disability World for not knowing. It’s just not a path you’ve walked (or rolled in, so to speak) so I can’t expect you would know it without being educated on it. That’s what I’m here for.

Barriers to access are anything that block a person from accessing a public space. This can be something as simple as a single step into a building or narrow pathways in a department store to larger barriers such as no elevator in a multi-level building or the lack of a pool lift for wheelchair-users at public pools. 

Use Your Imagination
To all you walkers: imagine if you were on your way to a beautiful exotic island where there were gorgeous sunsets and the most awesome poker tables (for those of you readers who don’t really care for sunsets). You would be with your favorite people and you all had planned what you would do every day and every night together. You have all been looking forward to this getaway for so long and finally the day has arrived. You watch out your window as the plane roars down the runway; you’re all so giddy with excitement you can’t stop talking about what the first thing you’re each gonna do is. Finally, the plane touches down; you all grab your carry-on’s and walk towards the front of the plane where the pilot waves you off to your destination. You turn to disembark and notice that the jet bridge is about 3 feet away from the plane’s exit doors. You see, the jet bridge is old and doesn’t quite reach the plane but it’s allowable because it was made before the laws changed that made it mandatory that all jet bridges reach the planes’ exits. Sounds a little wonky but that’s ok because as long as you can step across, you’re fine…Wait a minute! You can’t reach it! Your legs are too short! Your loved ones are all taller than you are and are able to walk across. You can’t cross the jet bridge; which means you can’t get to the island; which means you can’t see the sunset or play poker. Your loved ones are all going to be able to do this without you. They feel bad you’re getting left behind but surely they can’t NOT go just because YOU can’t. You’re gonna miss out on everything all because of the damn jet bridge being JUUUUUST a little too far for you.

A Huge Barrier

The Village Lodge at Smuggler’s housed the on-site Ben & Jerry’s ice cream parlor, pizzeria, deli and pub for the resort’s guests. If you didn’t want to leave the resort and wanted a slice of pizza or to take the family to get ice cream after a long, hot day filled with fun activities, this was where you wanted to go. Except my daughter couldn’t go there. There is a walkway leading up to the door but there is a 1-inch lip at the end of that walkway that her power chair cannot get over because of its mechanism on its underside. Even if the walkway was made to end flush, once you got in the doors there are stairs galore. Normally, any public accommodation must be made accessible to all except if those changes are not “readily achievable” or when “they are not easily accomplished without much difficulty or expense”, according to the Americans with Disabilities Act (ADA). To read more about the ADA click here.

Not knowing about the barriers to access, we planned to go to get some ice cream with the kids. When we realized we couldn’t get in with the wheelchair it was upsetting, to say the least. The girl didn’t even want the ice cream; she’s just the type of kid that loves to do family things and she wanted to go in to the ice cream parlor with her mom, dad & brother. Instead, dad went in to check what he wanted while mom waited outside with the kids. When he came out, mom went in with his order in mind while he took his turn waiting outside. I felt excluded, hurt, left out, ignored. I felt like an outcast, an outsider. Like I didn’t belong. And I wasn’t even the one in the chair. The biggest part about this is that she knows that the reason we couldn’t go in was because of her wheelchair. I will be honest. I was way more upset than she was. But I wonder how many other families that have gone there for their adaptive program have also felt the way I did.



Maybe sometime soon every jet bridge will reach the plane’s exit doors everywhere, mandated or not.