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Category: Activism and advocacy

How to bring home the season to seniors

For many, the holiday season can be a difficult time under the best of circumstances.  Stress, brought on by increased demands on your time, errands to run, packages to mail and a long list of loved ones you hope to make happy, can rob you of your feelings of peace and harmony.  It’s easy to forget yourself, feel run down, catch that seasonal bug and feel frustrated that you cannot seem to get on top of your tasks.  Then, melancholy can set in.  Remembering those who should be with you but who are not, family traditions broken by distance or divorce can leave you feeling an inexplicable sense of emptiness or loss.  While the holidays are billed as the "most wonderful time of the year," you might find yourself asking, "What’s so wonderful about it?" 
 
First, know that you are not alone.  If you look around, you’ll find company in many others who try to paste on a smile, grit their teeth and just hope to get through it.  If you look even closer, you’ll find that a large group of individuals who share your feelings are seniors and people with disabilities.
 
Loneliness, borne out of isolation, can keep even the most optimistic among us from feeling as though we are connected to events and other people.  It’s hard to enjoy the holidays when we feel as though we have no one to enjoy them with.  Celebrating the holidays exclusively FOR the benefit of children, or solely to fulfill the expectations of others can be draining.  We all need to feel a sense of belonging, to have people in our lives with whom we feel connected and by whom we are acknowledged.  People with disabilities and the elderly are often marginalized in our culture, if not forgotten altogether.  Here are just a few ways you can bring some of the delights of the season to someone who is alone and isolated.  In doing so, you may discover that your own spirits lift; the gift you receive when you give of yourself.   
 
Take a senior for a spin.  Bring a blanket, a thermos of hot chocolate, some snacks, a few holiday CD’s and pile into the car.  Go out for a while touring your community’s holiday light displays.  This will get that senior out of the house without subjecting them to any strenuous walking or uncomfortable visiting.  
 
Savor the sounds of the season.  Whether you sing along or simply sit, bring a senior to a holiday concert.  Programs performed by children may be especially charming for an older person, although they may prefer music performed by a church choir or favorite musical group.
 
Bring the holiday home.  Help a senior to decorate their home, even if it’s just to place a tabletop tree near the television or on a side table so that it’s easily seen.  Offer to help with tasks such as addressing and mailing holiday cards or gift wrapping.  If  an older person is too intimidated to work a stereo or CD player, or doesn’t own one,  bring yours over for an evening of hot cider and sweet treats and music.  Or, find their radio, set it to one of those radio stations  that play only holiday music all season, and mark the ‘on" button so a senior with failing eyesight can find it. 
 
Take them in shopping.  Not OUT shopping, IN shopping.  If a senior or person with a disability cannot go out to shop, or they just don’t have the stamina to fight the crowds, bring over your laptop or phone and help them shop online.  Even if they cannot give gifts to their entire family, you can help them to purchase a gift basket or gourmet food item for a family gathering.  This way, they will know that they have made a contribution that will be appreciated and enjoyed by everyone. 
 
Make a love connection.  Set up your webcam and Skype software so that they can visit "face to face" with loved ones across the country.  If a senior is unable to travel, connecting them to their children or granchildren in this way brings the magic of technology home in a way that is real and practical for them.  Fire up your laptop and let the love begin.

Party hearty.  Well, within reason.  Find out if a local senior center is hosting a holiday lunch or gift exchange, and bring a lonely senior to spend the afternoon among peers.  The festive atmosphere can help them to connect with others, make friends and could even motivate them to get out a little more. 
 
Strengthen spirit.  Some municipalities do not offer public transportation services on weekends.  Offer to take a home-bound friend or neighbor to their spiritual services of choice.  Many religious organizations provide special events, meals and programs just for their elderly parishioners.
 
These are just a few tips to get you started.  Keep in mind that for seniors living in a facility such as assisted living or a group home, the reason they are there may be because close relatives are unavailable.  If a senior is in a nursing home for the first time, the unfamiliar surroundings may contribute to increased feelings of loneliness or homesickness.  Perhaps they have lost siblings, friends of their own, or they have recently lost their spouse.  Even if a senior is living at home, those first holidays alone can be extremely difficult.  Consider how you can help a person who is disabled or elderly to connect with a shared event like a holiday.  By reaching out, you can inspire in others a renewed interest in life and an increased desire to be a part of it.  Bring home for a senior the sights, sounds and sentiments of the season and you’ll be giving a gift to yourself, too.
 
 

Copyright 2009-2012 by Laura Legendary.

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Inclusion Rx: Prescription for a healthier workplace

One of my favorites of the inclusion and diversity topic area web sites is Diversity World. The site is devoted to issues that concern both workers and employers who are disabled and non-disabled. Diversity World is “dedicated to Enriching Workplaces and Reducing Employment Barriers."

They also publish one of the best newsletters on the subject available. I’ve been a subscriber for years. The site provides information and resources that are timely, relevant and interesting.

 

The site is helmed by Rob McInns, who, as a human services professional, has focused broadly on issues of workforce diversity and more specifically on issues of employment and disability. Rob’s work has been marked by passion and leadership in the quest for greater workforce inclusion for people with disabilities. He has formerly served as the CEO of two direct service organizations for people with disabilities, as Executive Director of the Canadian Council on Rehabilitation and Work, as the Coordinator for California Business Leadership Network, and as a Diversity Consultant with IBM.

 

I particularly appreciate the "Diversity Shop," a place to go to obtain teaching aids, videos and publications suitable for almost any workplace context, communication or conflict resolution training.

 

Diversity World www.diversityworld.com

DiversityShop www.diversityshop.com/store/

 

The newsletter is intelligently written, featuring articles and commentary by thought leaders as well as readers who elevate the dialogue pertaining to awareness, access and inclusion. If you search the archives, you may even find one or two of my own contributions. The newsletter is cleverly called Inclusion Rx, and it’s a perfect prescription for all of your workplace diversity ailments!

 

LL

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Who should be the face of a disability non-profit?

For my readers who have disabilities, here’s a chance to toss in your two cents. What do you think?

Should organizations that represent people with disabilities be managed by people with disabilities?

This may seem like an issue of no consequence, but I recently found myself investigating a local non-profit agency that specifically benefits the local blind community. However, the program manager of the agency is not blind or visually impaired in any way. I found this extremely irritating. It seems to me that the “face” of a disability advocacy organization should be that of a person who represents that demographic group. Or, should it?

On the one hand, the leadership, upper management, board of directors or membership of any organization wants the business to be competently managed, which renders race, ethnicity, disability irrelevant. One might say that this is the core of the issue of equal opportunity. Does this idea extend to organizations which specifically represent a particular group?

Does the choice of a sighted person as manager of a center for the blind suggest that a person who is blind cannot competently handle the operation? It suggested that to me, although in fairness I ought to take the time to find out if there have in fact been other program managers who have been blind. I will. Perhaps I am bent out of shape because her voicemail said, “Miss So and So cannot come to the phone right now, so please leave her a message.” What, she cannot even leave her own outgoing message? Is she voicemail impaired?

I’ll get over it.

In the meantime, I wonder: does a person of Japanese origin head the NAACP? Are the various chapters of the Jewish League run by Southern Baptists? Is the National Organization for Women captained by a person with a “Y” chromosome? I’m just asking.

What’s your opinion?

LL

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ADA week question: Does this disability survey result reflect your reality?

 

The headline of this article caught my attention: "Twenty years of the ADA and discrimination still a major problem."

Curious, I took a look at the article, and disagreed with much of it. Then, even more curious about the source of the information, I read the actual survey from which the article was derived. While I always find social surveys interesting in the same way that I may find the blurb on the back of a book jacket interesting, like the book jacket, these surveys seldom tell the whole story.

 

My main complaint about this sort of information dissemination is that one can manipulate numbers to look like just about anything. I once saw a t-shirt that read: "Only lawyers and painters can change black to white." Well, it seems to me that special interest groups and statisticians can do the same.

 

I do not disagree with the premise upon which the article or the survey finding is based, namely, after twenty years; we’ve still got a long way to go before we catch up to our non-disabled counterparts. No argument there. A few of the findings, though, made me wonder if the results reflected my own reality, or that of my readers.

 

One generalization with which I took particular umbrage was the notion that a significant percentage of people with disabilities do not participate in family or social activities. The survey states that this "once again suggests there are significant barriers to access to leisure activities." Really? That seemed odd to me. Would that lack of involvement really be due to a disability? Lack of access to movie theaters or restaurants? Or, could it have something more to do with a person’s own sense of self-esteem, lack of open communication or social isolating due to depression, grief or feelings of unworthiness? If that is the case, is it fair to say, "I don’t participate in family activities because I’m disabled"? Or, "I’m not very social because of my disability and the lack of access to restaurants"? It seems to me that this would be related to one’s level of optimism, attitude or outlook on life, and I know plenty of people who are not disabled who are socially inept or who have a nonexistent family life.

 

There were other factors which were used to measure quality of life and overall satisfaction, such as poverty, education, access to technology and employment. A cross section of individuals was surveyed, numbering approximately one thousand respondents with disabilities, and a similar number who were non-disabled. Where it was not possible to survey a person with a disability directly, an appropriate proxy was surveyed.

 

Employment still seems to be the weakest area of progress. The survey revealed that only 21 percent of people of working age who are disabled are employed. In fact, that number seems to have slipped a tad, although I wonder if it might have a little something to do with the fact that our economy is languishing like a trout on a boat deck right now. Might that number be just a little misleading? Could the number also be lower because more people with disabilities actually may have started their own businesses? I’m just asking here.  None of my friends or  acquaintances who are disabled are unemployed. At least, none who want to work.

 

As for technology, the survey suggested that 85 percent of non-disabled persons accessed the Internet, while only 54 percent of those with disabilities do. One might conclude that this is due to lack of access, increased poverty, or lack of education. I don’t buy it. I just don’t. First of all, poverty should have nothing to do with Internet access, you can connect for free at any library. Lack of education should have little to do with it, there are about 300 million Twitter users alone who can tell you everything you need to know. I didn’t go to school to learn how to use the computer. Most of my contemporaries didn’t, either. There was no computer education when I was in school, because there was no Internet, and not many desktops, either. At least, not one in every home in the 1980’s, when I was in school.

 

Surveys like this do absolutely nothing to further the interests of the disability community, in my opinion. They draw a very dark picture of life, implying that things are so much more terrible for us because we are disabled. This dim view can only add to the groundless paranoia, irrational fears, superstitions and negative stereotypes held by the non-disabled. Considering that ten percent of the survey respondents were either unwilling or unable to participate in the survey, and that a "qualified, appropriate family member living in the household" took the survey on their behalf, how can even the hope of accuracy be more than a distant dream? Ten percent is well within the margin of error on most polls, and when an individual is being surveyed about such subjective issues as quality of life, isn’t that a question only one person can really answer? How is someone who is not me supposed to judge the quality of my life?

 

What do you think? Does this survey finding reflect your own reality? Please comment and share your thoughts.

 

Here is the link to the article: dada.org

   

Here is the link to the survey: 2010 Disability Gap Survey

 

Maybe I’ll have to ponder this some more…as soon as I get back from lunch with my girlfriends and post this to my blog and then charge up my laptop so I can tweet about it while I’m working.

LL

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ADA week article on the language of awareness

In honor of this week’s 20th anniversary of the Americans with Disabilities Act, I am running articles and commentary pertaining to workplace issues and hiring practices, accessibility, advocacy and awareness.  I invite you to submit your own. 

 

Speaking in the Language of Awareness

When I interact with the public in either my professional or personal life, I seldom consider my blindness to be a barrier to an effective conversation, but those with whom I am speaking quickly remind me it can be. Their discomfort is palpable, their curiosity obvious. The specific nature of our conversation becomes secondary to what is really on their minds: How do I address a person who is blind? Can I ask about it? What should I say? Most people seem to be asking me to put them at ease before we can proceed with a discussion.

 

My experience has been that most people want to do the right thing, but they simply do not know what the "right thing" is. This has also proved true with other speaking professionals. I am frequently consulted on the appropriate language that should be used when presenting to diverse audiences. For speakers who give presentations in either the corporate or community setting, below is a short tip list on the language of awareness that you can use to make your talks more sensitive, accurate and inclusive.

 

Put the individual before the disability. For example, replace language such as, "handicapped” or “mentally slow”, with, “a person who is disabled”, “people who are blind”, or “children who have developmental disabilities”. This is respectful and empowering, as it places the emphasis on the individual as opposed to defining that person by their disability. This practice is usually referred to as ‘People First” language. People first language is the use of respectful and accurate terminology that is preferred by people with disabilities.

 

Avoid euphemisms. It is not necessary to use phrases, such as “differently abled”, “handy-capable”, or “challenged.” This implies that disability is not a topic that can be discussed in a straightforward manner, and it only emphasizes the differences between us.

 

Avoid dramatic language or language that sensationalizes disability.

Using phrases, such as “afflicted with” or “suffers from”, reinforces the idea that the individual is a victim.

 

Here are other examples of positive and affirming language versus insensitive or negative language. Instead of “psycho” or “mentally defective”, say “a person with a mental illness” or “a person with an intellectual disability."

If you know of someone who has a sensory disability, they can be referred to as “a person with low vision”, or “a person who is deaf”, as opposed to "the blind guy," "sight challenged,” or someone who “suffers from hearing loss”.

If you know of someone who is paralyzed or is unable to ambulate, that person is said to be mobility impaired, not “crippled” or “wheelchair bound.” That individual is simply a person who uses a wheelchair.

 

You personally may not know many people with disabilities or any at all. Therefore, you may not have considered why it might be important to alter your vocabulary in this way. It’s true that the person standing before you may not appear to have a disability, but they may be married to, related to, or care about someone who does. If you are speaking in front of a group, there is no way to know which members of your audience fall into which category. Using the language of awareness is an act of courtesy and respect that can set a powerful example for others to follow in their everyday communication.

Copyright 2010 by Laura Legendary.

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I’m no superhero

Nearly every day, when we leave the safety and comfort of our personal sanctuary, we face the possibility of a potentially upsetting interaction with someone we may encounter. If we spent any time at all pondering this, none of us would ever leave our homes. However, our natural optimism, along with the demands of an impatient world, can make venturing out feel like an act of daring. When I go out, I never know what sort of interpersonal pratfalls await me. In a world best suited for the sighted, my goal is to arrive home unscathed, both physically and emotionally. This is achieved more easily some days than others.

 

Of the things most sought-after in  life, monetary and material, I believe that what most of us really want is to be acknowledged and valued. Choose any pursuit that comes to mind, and it boils down to “look at me, listen to me, value me”. We want for our achievement to be recognized as a reflection of who we are: Committed, motivated, creative, and compassionate. Who we are, not just what we do.

 

People who have disabilities are no different. We are, after all, people first. With all the same foibles, frailties and failings as any other. Yet that fortress of falseness often isolates us, where it is possible to be well meaning, yet demeaning.

Many people regard those with disabilities as the less fortunate, and there but for the grace of God go they. Others regard people with disabilities as a false idol. They use words like “amazing” or “inspiring” to describe me. They shake their heads in bewilderment as they wonder what divine attribute I must possess in order to live with this particular set of circumstances. I am placed on a pedestal so high as to be out of reach, and therefore isolated.

 

Despite all this admiration, if one were being honest, no one would want to be me. They would never say, “I wish I could be like that. I wish I could be blind. Then I’d be special, too”. The truth is, no one would want to trade places with me, right?

 

Well, certainly no one would aspire to be blind, but there is nothing wrong with being me. Whether one perceives people with disabilities as pathetic or divine, neither view represents reality.

Yet, I am often bestowed superhero status as if solely by virtue of being blind, I am somehow more worthy of admiration than I otherwise would be, if I were sighted. I’m no superhero. Calling me “amazing” only puts me up on a pedestal, and drives a wedge between us. It singles me out. Using words such as “brave” or courageous” are inappropriate. I did not choose to go blind. I am not an inspiration because I am blind. I’m not amazing because I am blind; I am amazing because I am accomplished, resourceful, and skilled. Perhaps I’m amazingly resilient, amazingly articulate, and amazingly strong. Not because of my disability, but in spite of it.

 

As American citizens with disabilities celebrate the twentieth anniversary of the Americans with Disabilities Act, it is important to realize that the underlying purpose of the landmark legislation is to enable equal access to life, liberty and the pursuit of happiness. Put another way, it has only been twenty years since I have had the legal right to have a job. My own ADA mantra is to remind our non-disabled society that accommodating the needs of people with disabilities is as much about attitude as it is about architecture. Long ago, I stumbled upon a quote that moved me so much; I wrote to the source and asked permission to reprint his words. Neil Marcus, a poet and playwright said, in part: “Disability is not a brave struggle or ‘courage in the face of adversity’. Disability is an art…it’s an ingenious way to live.” I loved the quote so much that I asked Mr. Marcus for permission to use it in my speaker bio. To me, the quote expresses what is most important to all of us: Look at me, listen to me, value me. I’m no superhero.

 

LL

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It’s ADA week at Accessible Insights. Share your story!

Monday, July 26 is the twentieth anniversary of the Americans with Disabilities Act.  How do you plan to celebrate this landmark legislation?  How has the ADA changed your life for the better?  Tell us your story!  Have an article, web site, or special event or activity you want people to know about?  Share it here!  You can either click “contact” on the Accessible Insights home page to send me an email, or you can simply comment below. 

 

Have an article or story of attitude over adversity?  Favorite quotes?  I’ll be posting some of my own articles on ways you can improve workplace accessibility, accommodate the needs of a person with a disability, and enhance communication with friends or family who do not have disabilities. 

 

Raise your voice, or lend your voice to those who have no voice of their own! 

 

LL

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Roll a mile in another’s shoes

Regardless of your personal state of ability, infirmity, race, religion or socio-economic position, there is probably an issue or group in your universe for which you advocate. You may feel that you are an authority on your own cause, but somewhat less so on other, similar causes. Perhaps you are passionate in your support of lung cancer research, because a family member lost his or her own battle. Yet, you may know little about the needs of the children’s cancer charities.

 

In the field of disability awareness, I tend to focus my efforts on the particular needs of the visually impaired or blind community, simply because I have personal experience with the issues relevant to those groups. While I advocate for all disability groups, I am aware that each has it’s own specific needs, pet peeves, barriers to overcome, stereotypes to battle and goals to attain. I admit that I am not intimately acquainted with the needs of every disability group. However, I had a very interesting experience recently that has opened my eyes to some of the feelings at least, which may be at the core of a group other than my own.

 

A while ago I did some traveling that required I use multiple forms of transport, which is typical for someone who does not drive. I traveled through several states, and it was quite the combination of planes, trains and ground transport to get it done. At one point, I found myself in the Las Vegas airport, confronted by an airport employee who was to assist me through security to my flight gate.

 

For those of you who do not travel, or who have never thought about how a person with a disability might accomplish this, let me take a moment here to provide a bit of explanation. As a seasoned traveler, I have seen many changes in the policies and procedures of public transportation agencies. None so many, however, as those which took place after September 11th, 2001. Air travel was especially chaotic in the "old days" given that anyone was free to move about the airport, and now no one who is not holding a ticket or a boarding pass is allowed past security. Airports used to be terrifying places for me, since airport crime was rampant back then. .

 

It is nothing like that now. Today, The TSA and airline employees operate with precision. As a result, when I make my flight reservation, I make what is referred to as a "special services request." This sets into motion a series of hand-offs that gets me from the passenger unloading zone to my seat in the aircraft. Usually, it works like a well-oiled machine. Once I hit the ticket counter and check my bag, I am handed off to a "PSA" or personal services associate. These are airline employees who roam about the premises and assist passengers who need help. It was my experience with one of these PSA’s that I write about here.

 

My fierce independence was challenged when the PSA who was to guide me through security insisted that I sit in the wheelchair he offered. I did not want to use the wheelchair, resorting instead to my standard line: “My eyeballs are broken, but my legs work fine. I can walk.”

 

The PSA would not take no for an answer. He continued to insist that I use the chair. Someone standing nearby said, "I sure wouldn’t turn down a ride. Why not take it? The terminal is like a MILE from here." Well, for one thing, I didn’t need it. I’m perfectly capable of walking to the gate. It seemed like such a waste to me, and I felt a little threatened by this situation. Despite my vociferous objections, I was pressured into using the wheelchair, and I finally relented. I cringed as I sat down in the chair. The predominant emotion I experienced right then was one of anxiety. The PSA began to roll me to the security checkpoint.

 

It took me about two seconds to recover from the novelty of moving while sitting down, after which I immediately began to feel very uncomfortable. I felt like I was being deceptive somehow, keeping a secret that I was passing myself off as paraplegic or something when in fact I could leap out of the chair in a split second and walk away.

The anxiety I was feeling grew to embarrassment, then humiliation. On the one hand, I felt like a liar, on the other, I felt as though I was somehow less, or would be perceived as something less than whole. My discomfort likely stemmed from the knowledge that I had already traveled thousands of miles, mostly unassisted, and that the notion that I could be perceived as incapable of walking unnerved me.

 

When the employee at the airport security gate informed me that I would be lifted from the chair and examined, I immediately flew out of the chair. "Like hell," I said, and held out my hands. "You can just guide me through the metal detector."

After reassembling my belongings and myself, I sank back into the wheelchair. Now, I really felt awkward. It was clear to anyone watching that I didn’t need to be in the wheelchair, and I wondered what others were thinking as I was rolled away.

 

As a person who has a visual disability, who is also a long-time professional speaker and educator, one of the ways I “sell” my message of independence and self-sufficiency is to set the example. I am living the experiences about which I speak, and I would be neither believable nor authoritative if I did not live the full life I teach others it is possible to live. Whenever possible, I use mainstream situations as a platform from which to raise awareness. While I concede that you wouldn’t want me as your surgeon, I’ll probably never pilot a jetliner and the military won’t have me, generally speaking I can do just about everything a non-disabled person can do, I just do it differently.

 

When I teach my awareness classes, I utilize a teaching technique sometimes referred to as a "simulation exercise." There is a great deal of controversy over using disability simulations as a teaching tool. Students are placed in a blindfold to simulate blindness, required to sit in wheelchairs and navigate around everyday objects, or use earplugs or other means by which to simulate various impairments. The controversy lies in the thinking that these exercises create a "circus atmosphere" and can make a mockery out of disability. In general, I agree with this sentiment, although in my classes, the exercise is proceeded by six hours of instruction, followed by a dialogue about the students’ experiences, and concluded by the following admonishment: There is no way that a thirty minute simulation exercise can truly begin to open your eyes as to life with a disability. I tell the students that they could wear the blindfold all day and still have no idea what it’s like to be blind. The purpose of the exercise is to start the discussion, not arrive at a conclusion, and to explore some of the emotions involved, as well as to experience ways in which everyday activities can be made harder when living with a disability. If the students express discomfort with the simulation, I tell them that their discomfort is part of the exercise. I inform them that "I seldom have the luxury of picking and choosing whom I solicit for help, and in this case, neither did you."

 

In the case of my brief stint in a wheelchair, I can say the same thing. While I have understood the physical barriers presented by the use of a wheelchair, I’ve not personally experienced the emotions, which may be involved — especially early on. I found my chaotic emotions to be worthy of further exploration, and I was gratified by the opportunity to roll a mile in another’s shoes.

 

Have you ever experienced something similar? If so, comment below and share your own thoughts.

 

LL

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A few of my favorite quotes on disability and adversity

As an avid reader, a struggling writer and a lover of language, like many people I collect quotes.  I’ve seen so many floating around on the social networking sites that are motivational and often shared in a business context.  Less often do I read quotes pertaining to disability and adversity, so I thought I’d share a few of my favorites of these here.  Please comment and share your own.

      

On disability:

 

Disability is a matter of perception.  If you can do just one thing well,
you are needed by someone. -Martina Navratilova

Disability is physical and ability lies in the mind.  William Maphoto

Kindness is the language which the deaf can hear and the blind can see.-Mark
Twain

We are each so much more than what some reduce to measuring.
— Karen Kaiser Clark

If we are to achieve a richer culture, rich in contrasting values, we must
recognize the whole gamut of human potentialities, and so weave a less
arbitrary social fabric, one in which each diverse human gift will find a
fitting place.
— Margaret Mead

Everything has its wonders, even darkness and silence, & I learn, whatever
state I may be in, therein to be content. Helen Keller

On adversity:

What we actually learn, from any given set of circumstances, determines whether we become increasingly powerless or more powerful.
Blaine Lee
The Power Principle: Influence with Honor by Blaine Lee

The good things of prosperity are to be wished; but the good things that belong to adversity are to be admired.
Seneca
The Forbes Book of Business Quotations

Adversity reveals genius, prosperity conceals it.
Horace
The Book of Positive Quotations

A smooth sea never made a skilled mariner.
English proverb
The Forbes Book of Business Quotations
The pessimist sees the difficulty in every opportunity; the optimist, the                                 opportunity in every difficulty.
L.I. Jacks
Words for All Occasions by Glenn van Ekeren

One of my all-time favorites:

"Disability is not a ‘brave struggle’ or ‘courage in the face of adversity.’  Disability is an art…It’s an ingenious way to live."  Neil Marcus, playwright

 

LL

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Join the party! ADA 20th Anniversary Celebration

 

The twentieth anniversary of the Americans with Disabilities Act is fast approaching, and there are a number of celebratory events planned.  Among them is the 2010 By 2010 Campaign, which seeks to collect 2010 “Proclamations of Recommitment" to the mission of the ADA by the 20th anniversary of the ADA–July 26, 2010.

 

The 2010 by 2010 Campaign leads into the June 20-23 conference in Denver, Colorado.  The National ADA Symposium has invited State and local governments, organizations and entities, individuals and advocates to submit proclamations that will be posted on the 2010 By 2010 Campaign web site.  Also on the site is a list of suggested activities to mark the event, videos and the link to Twitter so that you can  join in the conversation. 

 

For more info, go here:  ADA 20th Anniversary

  

What will you do to mark the ADA anniversary?  Announce your plans in the comments below.  Be sure to include dates and times of any public events.  If there is a special Twitter or Facebook page concerning your event, please provide the link. 

 

More soon…

 

LL

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