The Below Article is about NYC, but it is the same truth of Chicago..ed.note
Taxi Please?
May 25, 2011 in Disability Insights, Disability News, Disability Politics by Maureen
It’s been coined The City That Never Sleeps, The Big Apple, and my personal favorite, “Concrete Jungle Where Dreams are made of” (courtesy of Jay-z and Alicia Keys). Yes, we are talking about New York City, the entertainment and cultural Mecca of the world. New York has so much to offer; there are world class restaurants, legendary landmarks, celebrated tourist hot spots, iconic museums, amazing shopping and who can forget the bright lights of Broadway. Excitement awaits you at every corner (literally). It is definitely a ‘bucket list’ travel destination for millions of people around the world.
So with all that it has to offer, why does New York City seem to be a relic when it comes to wheelchair accessibility? While many other parts of the country and the world have transitioned into the 21st century, The Big Apple still seems stuck in the 1950s when it comes to accommodating people in wheelchairs. I realize that the northeast region is the oldest part of the country and wants to maintain that sense of elite history and vintage sophistication, but I think there needs to be a major overhaul in the wheelchair accessibility of New York City’s transportation system.
The New York taxi is an iconic image and a visual trademark of The Big Apple. Look down any street and you can see a blanket of bright yellow from one street corner to the other. Step to the curb and all you have to do is wave your hand in the air and within seconds a taxi is at your “beck and call” ready to whisk you away to your destination. To the average person it seems as though there is an overabundance of cabs in New York City. Well, this may be true for all able-bodied passengers, but those of us in need of wheelchair accessible cabs, have a much more difficult time.
Living just two hours north of The Big Apple in Massachusetts, I frequently venture into the city for a weekend with friends and family. I consider myself extremely fortunate to be able to live a mere ‘stone’s throw away’ from one of the greatest cities on planet earth. I look forward to going to shows, taking in the fabulous nightlife or simply having a picnic in Central Park; however, my excitement begins to dwindle when I have to plan my transportation for the weekend. The key word in the last sentence is “plan”. It is completely unfair that those of us in wheelchairs have to reserve a taxi more than twenty four hours in advance in order to insure a ride from one destination to another. In essence, those of us in wheelchairs are not able to able to enjoy the same spontaneity of a normal vacation or getaway. In advance of my trip, I have the tedious task of calling cab companies to see if they, A.) have wheelchair accessible cabs and B.) are readily curbside available like the average taxi. While I am always able to find cab companies that do offer wheelchair accessible service, it is virtually impossible to find a cab that does not require at least 24 hours advance notice.
It has come to the point where I completely neglect the idea of using transportation instead choosing to navigate the streets in my wheelchair. Don’t get me wrong, I love being outside in New York but this option proves more challenging when my intended destination is 50 blocks away or when mother nature decides to dump buckets of rain or snow midway through my journey.
Case in point, I was in New York a month ago to celebrate my birthday with my cousin, who lives on the upper west side, and a bunch of my friends. We had a fun night planned consisting of dining at a posh Belgian restaurant and hitting up a few bars, you know, the typical social life of a 20 something year old girl. Reserving a cab did not even enter my mind because I did not want to be under the unnecessary time restraints of leaving at a certain time. I wanted to be able to enjoy my night without the tic-tock of the clock glaring down upon me. Naturally, the night of our celebration, Mother Nature decided to rear her ugly head and produce every type of weather pattern known to man. It seriously felt like the movie, The Day After Tomorrow, with the apocalypse upon New York City. I was expecting a monstrous wall of water to come barreling down Lexington Avenue. Ok, maybe I am exaggerating a tiny bit, but, nonetheless, it was a very stormy night. Rain was pouring down in buckets, the wind was gusting at top speed and the temperature dropped to an unseasonable 35 degrees. There were also random bursts of thunder and lightning and a brief hail squall. Being the jolly optimists that we are, we did not want bad weather to ruin our joyous evening so we journeyed out into the stormy night. We all thought, “How bad can it be, it’s just a little rain”. Oh how wrong we were! The restaurant and bars were only seven blocks from our hotel and we thought our one measly umbrella would be able to shield us from the harsh elements. Our journey was just that, a JOURNEY. We navigated puddles the size of Lake Michigan, dodged blowing trash that was being swirled around by the wind and winced in discomfort as ice cold horizontal rain pelted us in the face and blurred our vision. The streets of New York were eerily silent because the majority of people were dry and warm in their TAXI’S! Only a few other brave pedestrians joined us on the otherwise uninhabited streets.
As you can probably guess, by the time we arrived at the restaurant I was one soggy mess from head to toe. My wet hair was plastered to the side of my face, mascara had formed its own little river down each of my cheeks and my jeans were so drenched they were literally suctioned to my thighs. Since I am sitting, my thighs took the brunt of the soaking. My feet had taken on a purple hue from the frigid rain that had accumulated in my four inch heels. The restaurant staff was extremely accommodating and gave me towels from the kitchen to dry myself off. I think they felt sorry for me since I literally looked like I had taken a shower and forgot to take my clothes off. Again, our optimism and sense of humor outweighed our frustration and we enjoyed the rest of our night. Even though I dined with restaurant kitchen towels draped over my body and went to the bars with frizzy wet hair, we managed to laugh our way through every obstacle and create a truly memorable night.
With the availability of an easily accessible cab, none of this craziness would have occurred. I have visited many other cities in the U.S. that are far more advanced in wheelchair accessible transportation, Los Angeles, San Diego, Miami and Las Vegas just to name a few. These cities are miles ahead of New York and allow for a stress free vacation or getaway. Unlike New York, these cities provide a multitude of wheelchair accessible cabs that do NOT require 24 hour advance notice and can be called just minutes before leaving for your intended destination. I know that there are many others out there who have had similar experiences with wheelchair cabs and echo my sentiment. Please comment below and share your transportation nightmare. Let’s spread the word and force NYC to initiate major improvements in their wheelchair accessible transportation.
Disability News Service, Resources, Diversity, Americans with Disabilities Act; Local and National.
Disability News Service, Resources, Diversity, Americans with Disabilities Act; Local and National.
Thursday, May 26, 2011
Union, commissioner question Cook County Illinois plan to cut WIC program : article : May 23 2011
Chicago Sun Times: BY LISA DONOVAN Cook County Reporter :
Cook County officials plan to shut down a program that provides everything from health screenings for pregnant women to infant formula for new moms across the suburbs — but it wont be closed without a fight.
Stephen Martin, Chief Operating Officer of the Cook County Department of Public Health, has told a range of officials the county will no longer provide services funded by the federal Women, Infants and Children Program.
Commissioner Larry Suffredin, who represents the North Side and suburbs, said Martin told him earlier this week that won’t mean the assistance will dry up for those who rely on the program, which include some of the poorest families in the county.
“If we don’t do it, they’ll give [the WIC money] to other community groups to handle the program,” Suffredin said.
Still, Suffredin says he has questions about what it means to eliminate the program. By one estimate the county’s WIC program, which has offices in the Rolling Meadows, Bridgeview and Markham courthouses and another site in Maywood, has a caseload of 20,000 women and children.
“The issues are, who will provide these services and who will provide the outreach to connect people with these services?’’ Suffredin asked. “Should this have been Dr. Martin’s decision alone? Or should it have gone to the [health] board?”
Sean McDermott, a spokesman for the county public health department, assured “the WIC program will continue in Cook County, it will just be provided by’’— possibly one or more social service agencies.
Under the county, costs were exceeding revenues for the $3 million-a-year program, leaving public health officials with no other choice than to stop running it, McDermott said. Officials have said county ordinance requires grant-funded programs to stay on budget.
But the American Federation of State, County and Municipal Employees Local 31, is planning to fight the move.
“With virtually no rationale and no public input, Cook County is preparing to eliminate these vital services,” AFSCME Local 31 Executive Director Henry Bayer wrote in a letter to county commissioners this week.
The AFSCME note, obtained by the Sun-Times, says Martin said during an April 15 tele-conference with union and program officials that a 10 percent cut in federal WIC funding means the county can no longer afford to administer the program completely from outside funds, as required.
McDermott wasn’t aware of the 10 percent cut mentioned in the AFSCME letter.
“Regardless of whatever cut comes down, this program in the last three years has not been keeping up with expenses,” McDermott said.
Asked why the program didn’t cut back on expenses rather than shutting down, McDermott said: “I don’t know the state allows us to shave back the program. Instead of 20,000, we only want 10,000. The cost of the program exceeds revenues we have to run.’’
He said public officials notified the state that they won’t be renewing the contract to run the program in the county. The county’s contract ends June 30. But public health officials are working with the state to find one or more social service agencies that could administer the program. Whether the offices will remain in the same locations is unclear.
AFSCME officials said about 70 AFSCME employees, including nutritionists and support staff, will lose their jobs if the county discontinues the local WIC program.
Bayer said in the letter that cutting the WIC program goes beyond job cuts.
“Ending the program has repercussions beyond just the families it serves,’’ he wrote. “There is a synergistic relationship between Cook County WIC and Cook County health care services — which serves to improve health care outcomes for program participants. Women come to WIC to obtain food benefits, but then are referred into the County health system. In fact, studies show an important benefit of WIC is that it provides a gateway to healthcare for participants. Referrals work the other way as well, and clients getting health are services at the County find it easy to apply for WIC.”
Cook County officials plan to shut down a program that provides everything from health screenings for pregnant women to infant formula for new moms across the suburbs — but it wont be closed without a fight.
Stephen Martin, Chief Operating Officer of the Cook County Department of Public Health, has told a range of officials the county will no longer provide services funded by the federal Women, Infants and Children Program.
Commissioner Larry Suffredin, who represents the North Side and suburbs, said Martin told him earlier this week that won’t mean the assistance will dry up for those who rely on the program, which include some of the poorest families in the county.
“If we don’t do it, they’ll give [the WIC money] to other community groups to handle the program,” Suffredin said.
Still, Suffredin says he has questions about what it means to eliminate the program. By one estimate the county’s WIC program, which has offices in the Rolling Meadows, Bridgeview and Markham courthouses and another site in Maywood, has a caseload of 20,000 women and children.
“The issues are, who will provide these services and who will provide the outreach to connect people with these services?’’ Suffredin asked. “Should this have been Dr. Martin’s decision alone? Or should it have gone to the [health] board?”
Sean McDermott, a spokesman for the county public health department, assured “the WIC program will continue in Cook County, it will just be provided by’’— possibly one or more social service agencies.
Under the county, costs were exceeding revenues for the $3 million-a-year program, leaving public health officials with no other choice than to stop running it, McDermott said. Officials have said county ordinance requires grant-funded programs to stay on budget.
But the American Federation of State, County and Municipal Employees Local 31, is planning to fight the move.
“With virtually no rationale and no public input, Cook County is preparing to eliminate these vital services,” AFSCME Local 31 Executive Director Henry Bayer wrote in a letter to county commissioners this week.
The AFSCME note, obtained by the Sun-Times, says Martin said during an April 15 tele-conference with union and program officials that a 10 percent cut in federal WIC funding means the county can no longer afford to administer the program completely from outside funds, as required.
McDermott wasn’t aware of the 10 percent cut mentioned in the AFSCME letter.
“Regardless of whatever cut comes down, this program in the last three years has not been keeping up with expenses,” McDermott said.
Asked why the program didn’t cut back on expenses rather than shutting down, McDermott said: “I don’t know the state allows us to shave back the program. Instead of 20,000, we only want 10,000. The cost of the program exceeds revenues we have to run.’’
He said public officials notified the state that they won’t be renewing the contract to run the program in the county. The county’s contract ends June 30. But public health officials are working with the state to find one or more social service agencies that could administer the program. Whether the offices will remain in the same locations is unclear.
AFSCME officials said about 70 AFSCME employees, including nutritionists and support staff, will lose their jobs if the county discontinues the local WIC program.
Bayer said in the letter that cutting the WIC program goes beyond job cuts.
“Ending the program has repercussions beyond just the families it serves,’’ he wrote. “There is a synergistic relationship between Cook County WIC and Cook County health care services — which serves to improve health care outcomes for program participants. Women come to WIC to obtain food benefits, but then are referred into the County health system. In fact, studies show an important benefit of WIC is that it provides a gateway to healthcare for participants. Referrals work the other way as well, and clients getting health are services at the County find it easy to apply for WIC.”
The Proposed Illinois Budget Cuts to Social Services : The Shocking Truth : Video & Info : May 2011 FundOurFriends
The Shocking Truth
Uploaded by FundOurFriends on May 10, 2011
(refresh if no video)
Sometimes the truth is so shocking that even the most reserved among us will be electrified and motivated by those truths. The Proposed Illinois Budget Cuts that take $410 Million away from services for those with disabilities and mental illness are shocking in their scope and ramifications for not only the disabled but for all the communities in which they are served. Note that no spokespersons were injured in the making of this spot but, beware, there are some shocking scenes.
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Who We Are :
This website, FundOurFriends.com, has been developed by Illinois citizens who have come together to support persons with disabilities. Our group includes persons with disabilities and their families, Human Services providers, direct support staff, next door neighbors, and business colleagues as well as people from all walks of life.
There are no officers, no annual dues, no hidden agendas. There is no intent to create a state wide organization or association.
Just a commitment to work on behalf of persons with disabilities and to increase the awareness of the general community with respect to the vital work being done by Human Service Providers.
In that regard we are dedicated to fairness of funding and stand against the practice of using people with disabilities as pawns in the Illinois Budgetary Process.
Please consider this website as a resource website for your efforts to support people with disabilities.
We welcome your comments.
The 6% Solution? We think not.
The Governor has proposed a 6% cut in the budget of the Department of Human Services. For our friends and fellow citizens with developmental disabilities and mental illness this is the third cut over the past few years. They, their parents, and communities will feel the profound impact of these cuts.
Many of us think that it is not fair or right to be reducing and eliminating services and supports to our most vulnerable family, friends, and neighbors – those with developmental disabilities and mental illness. We are speaking out and encouraging everyone with a voice to speak for those who can’t speak for themselves. That’s why we put this resource site together – to further the conversation and get more of our fellow citizens advocating for our friends who cannot advocate for themselves.
We all need to reach out to our State Legislators and let them know that we know that Illinois budget reform is necessary. But asking those who’s quality of life is dependent on daily supports from us are not the citizens we should be asking to “pitch in.” These are the people who count the rest of us for their quality of life. Helping them should be THE priority of our state contributions.
Please look around the site. We are adding resources daily. Share them. Send links, letters, emails to your friends and family asking them to also contact their Legislators and let them know that they need to do the right thing and take a stand to fund our friends!
Just 15 minutes of your time could save a life.
Click the link to the left to find your Legislator. Call their office and tell them that we need to get our priorities straight.
# CLICK HEADLINE FOR Fund Our Friends, OR GO TO;
http://fundourfriends.com/
Uploaded by FundOurFriends on May 10, 2011
(refresh if no video)
Sometimes the truth is so shocking that even the most reserved among us will be electrified and motivated by those truths. The Proposed Illinois Budget Cuts that take $410 Million away from services for those with disabilities and mental illness are shocking in their scope and ramifications for not only the disabled but for all the communities in which they are served. Note that no spokespersons were injured in the making of this spot but, beware, there are some shocking scenes.
-----
Who We Are :
This website, FundOurFriends.com, has been developed by Illinois citizens who have come together to support persons with disabilities. Our group includes persons with disabilities and their families, Human Services providers, direct support staff, next door neighbors, and business colleagues as well as people from all walks of life.
There are no officers, no annual dues, no hidden agendas. There is no intent to create a state wide organization or association.
Just a commitment to work on behalf of persons with disabilities and to increase the awareness of the general community with respect to the vital work being done by Human Service Providers.
In that regard we are dedicated to fairness of funding and stand against the practice of using people with disabilities as pawns in the Illinois Budgetary Process.
Please consider this website as a resource website for your efforts to support people with disabilities.
We welcome your comments.
The 6% Solution? We think not.
The Governor has proposed a 6% cut in the budget of the Department of Human Services. For our friends and fellow citizens with developmental disabilities and mental illness this is the third cut over the past few years. They, their parents, and communities will feel the profound impact of these cuts.
Many of us think that it is not fair or right to be reducing and eliminating services and supports to our most vulnerable family, friends, and neighbors – those with developmental disabilities and mental illness. We are speaking out and encouraging everyone with a voice to speak for those who can’t speak for themselves. That’s why we put this resource site together – to further the conversation and get more of our fellow citizens advocating for our friends who cannot advocate for themselves.
We all need to reach out to our State Legislators and let them know that we know that Illinois budget reform is necessary. But asking those who’s quality of life is dependent on daily supports from us are not the citizens we should be asking to “pitch in.” These are the people who count the rest of us for their quality of life. Helping them should be THE priority of our state contributions.
Please look around the site. We are adding resources daily. Share them. Send links, letters, emails to your friends and family asking them to also contact their Legislators and let them know that they need to do the right thing and take a stand to fund our friends!
Just 15 minutes of your time could save a life.
Click the link to the left to find your Legislator. Call their office and tell them that we need to get our priorities straight.
# CLICK HEADLINE FOR Fund Our Friends, OR GO TO;
http://fundourfriends.com/
Illinois plans devastating cuts in disabilities services : May 25 2011 by: Tony Paulauski
Illinois is planning devastating cuts to services for individuals with physical, developmental and intellectual disabilities. These cuts target our most vulnerable citizens and are being sold as a way to balance Illinois' estimated $13 billion deficit. The truth is, these cuts are short sighted and will send us on a path of destruction.
Illinois ranks last in the nation for supporting citizens with disabilities in their home communities. Disability services that are the lifeline to more than 220,000 people with disabilities and their families have already experienced deep cuts and are hanging by a thread. In addition to funding reductions several critical programs are being eliminated and it's estimated that 3,052 direct care staff will be laid off as a result.
The budget has the wrong priorities and the process is flawed.
There are currently three budget proposals on the table, one each from the governor, the state House and the state Senate.
The House's estimate of revenues is about $1.1 billion lower than that from the Commission on Government Forecasting and Accountability (CGFA), a bipartisan agency with a proven track record of making accurate revenue projections. Using CGFA's reasonable estimate of revenues could save critical disability programs.
The Senate's proposed budget disproportionately impacts individuals with disabilities by prioritizing programs that do not maximize taxpayer dollars.
The Governor's budget appropriates $30 million to state institutions and cuts community based services by $76.3 million even though numerous studies prove community services are safer, more effective and efficient. Four people can be served in a community setting for every one person in an institution.
Furthermore, the proposed budgets do nothing to address the backlog in payments owed to disability service providers. Some have been forced to shut their doors and others are on the brink of collapse because the state is six months behind in making payments.
The disabled community cannot withstand additional cuts. The proposed budgets deepen the gap to accessible disability services and do nothing to address the 21,000 people on the waiting list. None of the proposed budgets does anything for those who are desperately waiting for state services.
Most people would agree that services to help people with disabilities live life with independence, equality and dignity are the kind of programs that are worthy of taxpayer funds. That is what our society was built on. We must provide assistance to help those who truly and desperately need it. It's not a hand out it's common decency. Now it's up to our lawmakers to make the right choices.
Tony Paulauski is the executive director of The Arc of Illinois
# Click Headline for The Arc of Illinois or go to: http://www.thearcofil.org/
Illinois ranks last in the nation for supporting citizens with disabilities in their home communities. Disability services that are the lifeline to more than 220,000 people with disabilities and their families have already experienced deep cuts and are hanging by a thread. In addition to funding reductions several critical programs are being eliminated and it's estimated that 3,052 direct care staff will be laid off as a result.
The budget has the wrong priorities and the process is flawed.
There are currently three budget proposals on the table, one each from the governor, the state House and the state Senate.
The House's estimate of revenues is about $1.1 billion lower than that from the Commission on Government Forecasting and Accountability (CGFA), a bipartisan agency with a proven track record of making accurate revenue projections. Using CGFA's reasonable estimate of revenues could save critical disability programs.
The Senate's proposed budget disproportionately impacts individuals with disabilities by prioritizing programs that do not maximize taxpayer dollars.
The Governor's budget appropriates $30 million to state institutions and cuts community based services by $76.3 million even though numerous studies prove community services are safer, more effective and efficient. Four people can be served in a community setting for every one person in an institution.
Furthermore, the proposed budgets do nothing to address the backlog in payments owed to disability service providers. Some have been forced to shut their doors and others are on the brink of collapse because the state is six months behind in making payments.
The disabled community cannot withstand additional cuts. The proposed budgets deepen the gap to accessible disability services and do nothing to address the 21,000 people on the waiting list. None of the proposed budgets does anything for those who are desperately waiting for state services.
Most people would agree that services to help people with disabilities live life with independence, equality and dignity are the kind of programs that are worthy of taxpayer funds. That is what our society was built on. We must provide assistance to help those who truly and desperately need it. It's not a hand out it's common decency. Now it's up to our lawmakers to make the right choices.
Tony Paulauski is the executive director of The Arc of Illinois
# Click Headline for The Arc of Illinois or go to: http://www.thearcofil.org/
Access Living heads to Springfield to protect community reintegration programs in Illinois : May 25, 2011
For the past several months, at least once a week, a group of Access Living advocates have traveled to Springfield to urge state legislators to protect services that support people with disabilities living in the community. When the state budget was announced in February, cuts gutted community-based services. If such a budget passes, the cuts would threaten the independence of hundreds of people with disabilities.
In Springfield, advocates urged legislators to protect community services, arguing that community living promotes a higher quality of life and that community services cost far less than institutional services.
When advocates make their visit to Springfield today, May 25, they will focus on the Community Reintegration Program, a Department of Human Services program still on the chopping block. Through the program, people on Medicaid living in nursing homes are able to transition into an apartment of their own. Over the years, Centers for Independent Living, like Access Living, in Illinois have empowered thousands of people with disabilities to make the transition, saving the state millions of dollars.
If the program is cut, hundreds of people around the state may not get the choice to move out of a nursing home. Not only will this deprive a person of his or her choice to live in the community, it will be cost the state thousands of dollars per person every year. Such a cut doesn’t make fiscal sense or common sense.
Before the end of the week, please contact Governor Quinn’s office and urge him to support the independence of people with disabilities by funding the Community Reintegration Program.
Contact Governor Quinn’s office:
Phone: 217-782-0244
TTY: 888-261-3336
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# For Access Living for Independent Living in Chicago, click headline or go to: http://www.accessliving.org/
In Springfield, advocates urged legislators to protect community services, arguing that community living promotes a higher quality of life and that community services cost far less than institutional services.
When advocates make their visit to Springfield today, May 25, they will focus on the Community Reintegration Program, a Department of Human Services program still on the chopping block. Through the program, people on Medicaid living in nursing homes are able to transition into an apartment of their own. Over the years, Centers for Independent Living, like Access Living, in Illinois have empowered thousands of people with disabilities to make the transition, saving the state millions of dollars.
If the program is cut, hundreds of people around the state may not get the choice to move out of a nursing home. Not only will this deprive a person of his or her choice to live in the community, it will be cost the state thousands of dollars per person every year. Such a cut doesn’t make fiscal sense or common sense.
Before the end of the week, please contact Governor Quinn’s office and urge him to support the independence of people with disabilities by funding the Community Reintegration Program.
Contact Governor Quinn’s office:
Phone: 217-782-0244
TTY: 888-261-3336
---
# For Access Living for Independent Living in Chicago, click headline or go to: http://www.accessliving.org/
The Chicago Lighthouse for People Who Are Blind or Visually Impaired Programs and Services : info, resources, link to programs ; 2011
The Chicago Lighthouse is well regarded nationally as a model agency for the wide range of programs provided to make a comprehensive, wrap-around menu of services that address an individual's changing needs across a lifetime.
#Clinical Rehabilitation and Research Services :
Sandy and Rick Forsythe Center for Comprehensive Vision Care
Pangere Center for Inherited Retinal Disease
Bergman Institute for Psychological Support
Seeing is Believing Program
Residency in Low Vision Rehabilitation and Ocular Disease
The Chicago Lighthouse Convenience Store
# Educational Services :
Illinois Instructional Materials Center
Youth Transition Services
Summer Lighthouse Internship Program
Youth Employment Program
The Chicago Lighthouse Scholarship Program
Chicago Lighthouse Development Center (for Children Who Are Blind or Visually Impaired and Multi-disabled)
Birth to Three Early Intervention Program
Employment Services
Recipient Identification Number (RIN)
Job Readiness and Placement Program
Job Retention Program
Work Adjustment Training Program
Office Skills Training Program
Customer Service Training Program
Chicago Lighthouse Communications Center
Adaptive Technology Center
National HelpDesk
Independent Living Services
Adult Living Skills (ALS) Program
Arthur and Esther Kane Legal Clinic
Deaf/Blind Program
Seniors Program
CRIS Radio (Chicagoland Radio Information Service)
Orientation and Mobility
Chicago Lighthouse Industries
Manufacturing Facility Employing Individuals who are Visually Impaired
#Resources
#Vending Program
#Veterans Supply Administration Program.
# Please click headline or go to: http://chicagolighthouse.org/programs-and-services
#Clinical Rehabilitation and Research Services :
Sandy and Rick Forsythe Center for Comprehensive Vision Care
Pangere Center for Inherited Retinal Disease
Bergman Institute for Psychological Support
Seeing is Believing Program
Residency in Low Vision Rehabilitation and Ocular Disease
The Chicago Lighthouse Convenience Store
# Educational Services :
Illinois Instructional Materials Center
Youth Transition Services
Summer Lighthouse Internship Program
Youth Employment Program
The Chicago Lighthouse Scholarship Program
Chicago Lighthouse Development Center (for Children Who Are Blind or Visually Impaired and Multi-disabled)
Birth to Three Early Intervention Program
Employment Services
Recipient Identification Number (RIN)
Job Readiness and Placement Program
Job Retention Program
Work Adjustment Training Program
Office Skills Training Program
Customer Service Training Program
Chicago Lighthouse Communications Center
Adaptive Technology Center
National HelpDesk
Independent Living Services
Adult Living Skills (ALS) Program
Arthur and Esther Kane Legal Clinic
Deaf/Blind Program
Seniors Program
CRIS Radio (Chicagoland Radio Information Service)
Orientation and Mobility
Chicago Lighthouse Industries
Manufacturing Facility Employing Individuals who are Visually Impaired
#Resources
#Vending Program
#Veterans Supply Administration Program.
# Please click headline or go to: http://chicagolighthouse.org/programs-and-services
Teri & Kellen Ehrenhardt: "Prove them wrong" : video : LIfeMyWay ; Community, Advocacy & Disability Life in Illinois
Teri Ehrenhardt: "Prove them wrong"
Uploaded by lifemywayil on May 8, 2009
(refresh if no video)
Kellen Ehrenhardt "I pass the ball"
Uploaded by lifemywayil on May 15, 2009
My story:
I am the mother of two children, Hanna who is in college and Kellen, a recent high school graduate! Kellen is the most enthusiastic, loving and determined person I know. He also happens to have Down Syndrome. When Kellen was young, I volunteered at his school to help his education. It paid off to get involved. The principal shared our same vision for an inclusive educational experience. From class plays to spelling bees and sports, Kellen has enjoyed a wonderful life of inclusion. I hope that will continue. Kellen is more socially active than anyone in our family! He goes to church, was captain of the cross country team senior year and is known around the community as a person who “makes your day brighter.” Like any young man, Kellen has dreams. He has already started some of those dreams - he currently attends college - and he hopes to get a job and maybe start a band. He makes me proud!
Why I advocate:
We want to show what a person with a developmental disability is capable of doing. As a parent, you have to tune out naysayers, even your own family members, who tell you “not to get your hopes up.” What drives me is desire to prove wrong those with the preconceived notion that self-worth is based on intellectual abilities.
LifeMyWay means:
This is about Kellen being able to have experiences and opportunities to enjoy life. I won’t accept the status quo. I will make these opportunities for life accessible for Kellen, who deserves the same respect as any other person. I’ve learned you have to fight for the same opportunities for your child that others may take for granted. Others who have had positive experiences have taught me how to make the best of a system that is not ideal. Being informed on the issues definitely opens doors.
# For LifeMyWay click headline or go to: http://www.lifemyway.org/
Uploaded by lifemywayil on May 8, 2009
(refresh if no video)
Kellen Ehrenhardt "I pass the ball"
Uploaded by lifemywayil on May 15, 2009
My story:
I am the mother of two children, Hanna who is in college and Kellen, a recent high school graduate! Kellen is the most enthusiastic, loving and determined person I know. He also happens to have Down Syndrome. When Kellen was young, I volunteered at his school to help his education. It paid off to get involved. The principal shared our same vision for an inclusive educational experience. From class plays to spelling bees and sports, Kellen has enjoyed a wonderful life of inclusion. I hope that will continue. Kellen is more socially active than anyone in our family! He goes to church, was captain of the cross country team senior year and is known around the community as a person who “makes your day brighter.” Like any young man, Kellen has dreams. He has already started some of those dreams - he currently attends college - and he hopes to get a job and maybe start a band. He makes me proud!
Why I advocate:
We want to show what a person with a developmental disability is capable of doing. As a parent, you have to tune out naysayers, even your own family members, who tell you “not to get your hopes up.” What drives me is desire to prove wrong those with the preconceived notion that self-worth is based on intellectual abilities.
LifeMyWay means:
This is about Kellen being able to have experiences and opportunities to enjoy life. I won’t accept the status quo. I will make these opportunities for life accessible for Kellen, who deserves the same respect as any other person. I’ve learned you have to fight for the same opportunities for your child that others may take for granted. Others who have had positive experiences have taught me how to make the best of a system that is not ideal. Being informed on the issues definitely opens doors.
# For LifeMyWay click headline or go to: http://www.lifemyway.org/
Final Push on State of Illinois Budget to Preserve Funding for Homeless Programs : Action Alert : May 2011 Housing Matters
Housing Matters :
Final Push on State Budget to Preserve Funding for Homeless Programs
The scheduled end of the General Assembly session is May 31—less than one week away. To prevent cuts to the Emergency and Transitional Housing Program and the Homeless Prevention Program, we need to you contact state legislators one more time.
Problem:
On May 13, the House passed their human services budget for FY 2012, which cuts these programs by 52% and 38%, respectively. On the same day, the Senate passed their human services budget, which provides flat funding for both.
Solution:
The Senate version included fewer cuts to human services overall than the House version, primarily because of the different revenue estimates for the General Revenue Fund used by the Senate and the House. It now appears that Senate leadership has agreed to the House revenue estimate.
That makes it even more important that we advocate for revenue increases that don't require raising taxes.
Action Needed:
Please contact Representative Sara Feigenholtz and Senator Heather Steans, the chairs of the human services appropriations committees in their respective chambers, asking them to preserve funding for Emergency and Transitional Housing and Homeless Prevention using revenue increases that don't raise taxes.
Deadline for responding: Please take action TODAY.
# Click Headline or go to: Final Push on State Budget to Preserve Funding for Homeless Programs
Dear James,
The scheduled end of the General Assembly session is May 31—less than one week away. To prevent cuts to the Emergency and Transitional Housing Program and the Homeless Prevention Program, we need to you contact state legislators one more time.
Problem:
On May 13, the House passed their human services budget for FY 2012, which cuts these programs by 52% and 38%, respectively. On the same day, the Senate passed their human services budget, which provides flat funding for both.
Solution:
The Senate version included fewer cuts to human services overall than the House version, primarily because of the different revenue estimates for the General Revenue Fund used by the Senate and the House. It now appears that Senate leadership has agreed to the House revenue estimate.
That makes it even more important that we advocate for revenue increases that don't require raising taxes.
Action Needed:
Please contact Representative Sara Feigenholtz and Senator Heather Steans, the chairs of the human services appropriations committees in their respective chambers, asking them to preserve funding for Emergency and Transitional Housing and Homeless Prevention using revenue increases that don't raise taxes.
Deadline for responding: Please take action TODAY.
# For Housing Matters, Click Headline or go to: http://housingmatters.net/default.asp
Final Push on State Budget to Preserve Funding for Homeless Programs
The scheduled end of the General Assembly session is May 31—less than one week away. To prevent cuts to the Emergency and Transitional Housing Program and the Homeless Prevention Program, we need to you contact state legislators one more time.
Problem:
On May 13, the House passed their human services budget for FY 2012, which cuts these programs by 52% and 38%, respectively. On the same day, the Senate passed their human services budget, which provides flat funding for both.
Solution:
The Senate version included fewer cuts to human services overall than the House version, primarily because of the different revenue estimates for the General Revenue Fund used by the Senate and the House. It now appears that Senate leadership has agreed to the House revenue estimate.
That makes it even more important that we advocate for revenue increases that don't require raising taxes.
Action Needed:
Please contact Representative Sara Feigenholtz and Senator Heather Steans, the chairs of the human services appropriations committees in their respective chambers, asking them to preserve funding for Emergency and Transitional Housing and Homeless Prevention using revenue increases that don't raise taxes.
Deadline for responding: Please take action TODAY.
# Click Headline or go to: Final Push on State Budget to Preserve Funding for Homeless Programs
Dear James,
The scheduled end of the General Assembly session is May 31—less than one week away. To prevent cuts to the Emergency and Transitional Housing Program and the Homeless Prevention Program, we need to you contact state legislators one more time.
Problem:
On May 13, the House passed their human services budget for FY 2012, which cuts these programs by 52% and 38%, respectively. On the same day, the Senate passed their human services budget, which provides flat funding for both.
Solution:
The Senate version included fewer cuts to human services overall than the House version, primarily because of the different revenue estimates for the General Revenue Fund used by the Senate and the House. It now appears that Senate leadership has agreed to the House revenue estimate.
That makes it even more important that we advocate for revenue increases that don't require raising taxes.
Action Needed:
Please contact Representative Sara Feigenholtz and Senator Heather Steans, the chairs of the human services appropriations committees in their respective chambers, asking them to preserve funding for Emergency and Transitional Housing and Homeless Prevention using revenue increases that don't raise taxes.
Deadline for responding: Please take action TODAY.
# For Housing Matters, Click Headline or go to: http://housingmatters.net/default.asp
Wednesday, May 25, 2011
Disabled residents protest State of Illinois budget cuts : May 24 2011
May 24, 2011 (CHICAGO) (WLS) -- Disabled residents and their families and supporters protested Tuesday against proposed state budget cuts in programs they say are vital.
They rallied in the Thompson Center Plaza, carrying signs with messages such as "fund community services" and "we do count." Some protesters held pictures of children they say benefit greatly from programs facing cuts. The protest movement is called "A Life Campaign."
"I submit to you today that we must invest, not divest, in human services. We are an asset, not a liability, to the State of Illinois. We have fought for civil rights. We have fought for human rights. We have fought for gay rights. And we're gonna definitely fight for disability rights," said Donald Dew, Habilitative Services President & CEO.
The proposed cuts of $76 million are part of an effort to trim the state's budget deficit.
They rallied in the Thompson Center Plaza, carrying signs with messages such as "fund community services" and "we do count." Some protesters held pictures of children they say benefit greatly from programs facing cuts. The protest movement is called "A Life Campaign."
"I submit to you today that we must invest, not divest, in human services. We are an asset, not a liability, to the State of Illinois. We have fought for civil rights. We have fought for human rights. We have fought for gay rights. And we're gonna definitely fight for disability rights," said Donald Dew, Habilitative Services President & CEO.
The proposed cuts of $76 million are part of an effort to trim the state's budget deficit.
Hardest Hit march by disabled protesters: a street-level view in the U K: video & article : May 2011
Thousands of disabled people and their carers marched to parliament in London as part of the Hardest Hit campaign against government cuts
(refresh if no video)
Source: guardian.co.uk
#Concerns about cuts to benefits and services led thousands of protesters to London. For some it involved an enormous effort :
•Amelia Gentleman
•guardian.co.uk, Wednesday 11 May 2011 20.15 BST
Just after 10 morning, a group of around 40 blind people gathered by Paddington's platform 5, guide dogs helping them make their way through the crowds. Many had got up well before 5am, packed food and water for their dogs, then caught the first train from Plymouth to attend a march through central London in protest against cuts to disability benefits and services.
It is not easy travelling to London to take part in a protest if you're blind, but the demonstrators, many marching for the first time, said they were determined to rise to the challenge to express their anger about a series of cuts and rule changes affecting disabled people, who are disproportionately dependent on state support. "It is stressful going on a march like this, the noise and the crowds. It's an enormous effort for many people who find getting through life one day at a time quite difficult," said Doreen Taylor, 59, one of the blind protesters who travelled from Cornwall. "But people feel very worried about the changes to disability benefits."
If the size of the Hardest Hit march was relatively small compared with last autumn's student demonstrations (with police estimates ranging between 3,000 and 8,000), consider the hurdles facing many of the participants – the everyday problems of inaccessible public transport, and the high cost of rail travel for those dependent on disability benefits.
The protesters from the West Country said they were already so acutely conscious of the consequences of local authority funding shortages, and anxious about the impact of changes to the benefits system, that making the choice to come and protest was not difficult.
Kathryn Harrington, 57, also registered blind, said staffing levels at the supported housing where she lived in Plympton had been cut by about 40% over the past year, making it difficult for residents to find someone to help them in an emergency. Despite being an experienced computer programmer, she had found it difficult to find work, and was worried about benefit changes that would increase the pressure on claimants to find work. "When I apply for jobs, I'm seen as a health and safety risk," she said.
As she made her way along Victoria Embankment, led through the crowds by her guide dog Liza, Siobhan Mead, 27, from Great Yarmouth, said she voted Conservative last year, but had subsequently been dismayed at the impact local authority cuts have had on the availability of funding to help her live independently. Last year her needs were classified as "critical", meaning she was eligible for around £8,000 to pay for help getting to college, shopping, travelling to job interviews. This year, as the council made substantial cuts, she was told she was no longer being classified as in critical need, and would therefore not be eligible for any money.
"I've come here to get my voice heard, to make politicians realise that they are targeting the most vulnerable people in society. It's totally unreasonable," Mead said. Several blind protesters carried posters with expletives in braille, declaring: "We're being [something in braille] by the government."
Dino Goldie, 33, travelled by train from Bath to register his anger at changes to the incapacity benefit system, which will see hundreds of thousands of claimants reassessed and declared fit for work, and therefore eligible only for considerably reduced levels of weekly benefit payments.
"Research by the RNIB shows that nine out of 10 employers say they would not employ someone with visual impairment. We are being punished for not being able to find work," he said.
Marching through the crowds, Lisa Jones, 37, who has been looking for a paid job for 15 years, said: "I'd give my right arm for a job, but I can't get one. I think the government is encouraging the idea that disabled people are all scroungers. I want the government to realise that cutting benefits will not help us get into work."
She was marching with her husband, also registered blind, to try to make the public aware of the new difficulties facing disabled people. "Disabled people are invisible in society. That's why this march is so important," she said.
Further along the street, Vicci Chittenden, who was diagnosed with MS when she was 17, was in a wheelchair with a cardboard box on her head, marked "Don't Box Me In" in felt-tipped letters.
She felt there had been a radical shift in how society viewed disabled people. "Before we were portrayed as poor dears, pathetic creatures. Now there's been a complete turnaround and we're seen as benefit cheats," she said. "But the opportunities just aren't out there to enable us to work."
Protesters are angry about a myriad of issues that have arisen over the past year, as the government has simultaneously cut budgets to local authorities, begun changes that will hit the disability living allowance, and started a radical reform of incapacity benefit payments designed to reduce the number of claimants.
Along with the blind protesters were parents marching with disabled children, aghast at how quickly local authority funding shortages had reduced the support available for their families.
Fiona McHale travelled from Newry in Northern Ireland with her six-year-old son Jamie O'Connor, who has Down's syndrome, angry that family support grants that used to be available for families with disabled children were no longer easily available.
Jo Stubbins from Cambridge was dismayed at cuts to the care package received by her 23-year-old daughter Victoria, who has severe learning disabilities. "I've never marched before. We need to all join together and show that people with disabilities are not easy targets. It makes me so angry that vulnerable people are the first ones to be affected by the cuts."
Alex Ozansoy had travelled from Norwich to express concern that her six-year-old daughter, who has a learning disability and global developmental delay, was not getting the specialist support she needed at school. Ozansoy is battling with her local council to formally recognise her daughter's difficulties, and channel more resources to her education.
"She needs support now; it's a critical time in her development but she's overlooked in a class of 30 and we can't afford extra tuition," Ozansoy said. The chances of her daughter getting that support had dwindled in the past year, she said, because of cuts to the local authority budget. "I can't sleep at night because I'm so worried about it. It seems so short-sighted because if she doesn't get help now, she's going to be dependent on the state all her life, which will be a huge cost to the government."
Some demonstrators were anxious that the combined effect of changes would end up seeing disabled people more isolated and less able to participate in society. Pepe Martinez, 58, arrived in a wheelchair by train from Huntingdon, where he is a resident at a Leonard Cheshire home, hoping that the protest would help persuade the government to rethink its plan to cut disability allowance payments.
A former nurse who spent 35 years caring for others in the NHS, Martinez had not expected disability benefits to be affected when he voted Tory last year. Without the mobility component of DLA which the government plans to cut, he worries he will no longer be able to participate in "life generally", and instead will be stuck inside the care home, unable to visit friends and family outside. "We'll be like zombies," he said
(refresh if no video)
Source: guardian.co.uk
#Concerns about cuts to benefits and services led thousands of protesters to London. For some it involved an enormous effort :
•Amelia Gentleman
•guardian.co.uk, Wednesday 11 May 2011 20.15 BST
Just after 10 morning, a group of around 40 blind people gathered by Paddington's platform 5, guide dogs helping them make their way through the crowds. Many had got up well before 5am, packed food and water for their dogs, then caught the first train from Plymouth to attend a march through central London in protest against cuts to disability benefits and services.
It is not easy travelling to London to take part in a protest if you're blind, but the demonstrators, many marching for the first time, said they were determined to rise to the challenge to express their anger about a series of cuts and rule changes affecting disabled people, who are disproportionately dependent on state support. "It is stressful going on a march like this, the noise and the crowds. It's an enormous effort for many people who find getting through life one day at a time quite difficult," said Doreen Taylor, 59, one of the blind protesters who travelled from Cornwall. "But people feel very worried about the changes to disability benefits."
If the size of the Hardest Hit march was relatively small compared with last autumn's student demonstrations (with police estimates ranging between 3,000 and 8,000), consider the hurdles facing many of the participants – the everyday problems of inaccessible public transport, and the high cost of rail travel for those dependent on disability benefits.
The protesters from the West Country said they were already so acutely conscious of the consequences of local authority funding shortages, and anxious about the impact of changes to the benefits system, that making the choice to come and protest was not difficult.
Kathryn Harrington, 57, also registered blind, said staffing levels at the supported housing where she lived in Plympton had been cut by about 40% over the past year, making it difficult for residents to find someone to help them in an emergency. Despite being an experienced computer programmer, she had found it difficult to find work, and was worried about benefit changes that would increase the pressure on claimants to find work. "When I apply for jobs, I'm seen as a health and safety risk," she said.
As she made her way along Victoria Embankment, led through the crowds by her guide dog Liza, Siobhan Mead, 27, from Great Yarmouth, said she voted Conservative last year, but had subsequently been dismayed at the impact local authority cuts have had on the availability of funding to help her live independently. Last year her needs were classified as "critical", meaning she was eligible for around £8,000 to pay for help getting to college, shopping, travelling to job interviews. This year, as the council made substantial cuts, she was told she was no longer being classified as in critical need, and would therefore not be eligible for any money.
"I've come here to get my voice heard, to make politicians realise that they are targeting the most vulnerable people in society. It's totally unreasonable," Mead said. Several blind protesters carried posters with expletives in braille, declaring: "We're being [something in braille] by the government."
Dino Goldie, 33, travelled by train from Bath to register his anger at changes to the incapacity benefit system, which will see hundreds of thousands of claimants reassessed and declared fit for work, and therefore eligible only for considerably reduced levels of weekly benefit payments.
"Research by the RNIB shows that nine out of 10 employers say they would not employ someone with visual impairment. We are being punished for not being able to find work," he said.
Marching through the crowds, Lisa Jones, 37, who has been looking for a paid job for 15 years, said: "I'd give my right arm for a job, but I can't get one. I think the government is encouraging the idea that disabled people are all scroungers. I want the government to realise that cutting benefits will not help us get into work."
She was marching with her husband, also registered blind, to try to make the public aware of the new difficulties facing disabled people. "Disabled people are invisible in society. That's why this march is so important," she said.
Further along the street, Vicci Chittenden, who was diagnosed with MS when she was 17, was in a wheelchair with a cardboard box on her head, marked "Don't Box Me In" in felt-tipped letters.
She felt there had been a radical shift in how society viewed disabled people. "Before we were portrayed as poor dears, pathetic creatures. Now there's been a complete turnaround and we're seen as benefit cheats," she said. "But the opportunities just aren't out there to enable us to work."
Protesters are angry about a myriad of issues that have arisen over the past year, as the government has simultaneously cut budgets to local authorities, begun changes that will hit the disability living allowance, and started a radical reform of incapacity benefit payments designed to reduce the number of claimants.
Along with the blind protesters were parents marching with disabled children, aghast at how quickly local authority funding shortages had reduced the support available for their families.
Fiona McHale travelled from Newry in Northern Ireland with her six-year-old son Jamie O'Connor, who has Down's syndrome, angry that family support grants that used to be available for families with disabled children were no longer easily available.
Jo Stubbins from Cambridge was dismayed at cuts to the care package received by her 23-year-old daughter Victoria, who has severe learning disabilities. "I've never marched before. We need to all join together and show that people with disabilities are not easy targets. It makes me so angry that vulnerable people are the first ones to be affected by the cuts."
Alex Ozansoy had travelled from Norwich to express concern that her six-year-old daughter, who has a learning disability and global developmental delay, was not getting the specialist support she needed at school. Ozansoy is battling with her local council to formally recognise her daughter's difficulties, and channel more resources to her education.
"She needs support now; it's a critical time in her development but she's overlooked in a class of 30 and we can't afford extra tuition," Ozansoy said. The chances of her daughter getting that support had dwindled in the past year, she said, because of cuts to the local authority budget. "I can't sleep at night because I'm so worried about it. It seems so short-sighted because if she doesn't get help now, she's going to be dependent on the state all her life, which will be a huge cost to the government."
Some demonstrators were anxious that the combined effect of changes would end up seeing disabled people more isolated and less able to participate in society. Pepe Martinez, 58, arrived in a wheelchair by train from Huntingdon, where he is a resident at a Leonard Cheshire home, hoping that the protest would help persuade the government to rethink its plan to cut disability allowance payments.
A former nurse who spent 35 years caring for others in the NHS, Martinez had not expected disability benefits to be affected when he voted Tory last year. Without the mobility component of DLA which the government plans to cut, he worries he will no longer be able to participate in "life generally", and instead will be stuck inside the care home, unable to visit friends and family outside. "We'll be like zombies," he said
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