The Evolution of Disability Rights Movements: Great Britain and the United States
Joseph Staszak
“Know your limits, but never stop trying to break them,” said Kyle Maynard, a man born with congenital amputation, which means that his arms stopped forming at his elbows and his legs stopped forming at his knees. This however did not stop him from a motivational speaker, best selling author, entrepreneur, award-winning extreme athlete, and the first man to crawl to the summit of Mount Kilimanjaro[1]. The rights of people with disabilities have evolved rapidly over the past hundred years, specifically in the last thirty years, both within the United States and Great Britain. These two movements have similarities connecting the two, but appear to develop independently of one another.
It is important to understand two different things when discussing the history of disability rights and the discourse as a whole. The first is the two different models of disability, one being the medical model of disability and the other being the social model of disability. The medical model contends that individuals with disabilities are broken and that they need to be fixed or cured, whereas this social model contends that individuals with disabilities are not broken but instead handicapped by their environment. An example of the medical model would be certain very dangerous medical procedures such as chelation.[2] Since there is no actual “cure” for autism these medical procedures can cause a lot of damage to the individual that is receiving them. An example of the social model would be if a building does not have a ramp or elevator for an individual who uses a wheelchair. These two models have been used to define “disability” throughout U.S. disability history and separate the latter stages of the movement.
The second thing is the language that is used throughout history is very offensive and outdated and while these words are used in this paper they are not meant to be used in a harmful and demeaning way, but instead to give the reader a greater context to the way the individuals with disabilities have been treated throughout history.
Historically disability history focuses on learning about the different laws and acts, and how these ideas progress. However, not much time has been spent looking more in depth into the larger discourse of disability rights as well as how this discourse progressed and how it led to effective change. This fostered interest in if there might be any connection or similarities between the way that the disability rights movement progresses in the United States to how it developed overseas, and more specifically in a country relatively similar to the United States, Great Britain. More specifically, how did the disability rights movement with the United States evolve? How did the disability rights movement in Great Britain evolve over time? And were there any connections between these two movements, and if so what are they?
There is not a large variety of literature about the history of the disability rights movements in both the United States and Great Britain as they are relatively recent movements, only having progressed in the last fifty or so years. There is some literature regarding theories of disability, and the normalcy of disability. People, such Elizabeth Barnes[3] who writes about the social model of disability, and Lennard J Davis,[4] who writes about how normalization of individuals with disabilities within society has led to positive changes being brought about. These books, along with speeches by famous disability rights activists such as Judith Heumann and the Netflix documentary Crip Camp: A Disability Revolution, have all aided in the research process in defining the evolution of these movements and how they compare to one another.[5]
The disability rights movement in the United States has evolved much more rapidly than the subsequent movement in Great Britain, with landmark legislation such as the Section 504 of the Rehabilitation Act of 1973, Developmentally Disabled Assistance and Bill of Rights Act (DD Act) of 1975, The Americans with Disabilities Act (ADA) and many others coming before the major landmark decisions in the United Kingdom. The United States and Great Britain both see the beginning of their disability rights movements begin with a heavy focus on physically disabled veterans after World War two. However, the exposure of the Willowbrook Institution ushers in a new wave of disability rights within the United States, one that focuses on individuals with neurological disabilities, before the subsequent movement evolution inside Great Britain. The U.S. remains ahead of Great Britain with its evolution of disability rights for the remainder of the 20th century and into the 21st century.
This paper will begin to dive deeper into the progression of the disability rights movement within the United States and then look towards Great Britain and its evolution. It will discuss the different waves of the movement and how the discourse present in the United States during the 20th century leading up to the passage of the ADA. Next this paper will look at the way that the disability rights Movement within Great Britain develops, from mainly focusing on ex-service men with physical disabilities, to then sudden shift to focusing on individuals with more neurological and mental disabilities.
Disability rights movement within the United States
United States history is filled with many different rights movements that all seemingly overlap with one another. The Disability Rights movement is one of these, finding its beginning in the middle part of the 20th century, with a heavy focus on the veterans that had been disabled in World War 2. Laws and organizations form to help these individuals reintegrate back into society after the war and begin the normalization of individuals with physical disabilities, which leads to the eventual story of the Willowbrook institution. This story begins to shine the light on individuals with cerebral disabilities, such as autism, down syndrome, and many others. From the outcry of these individuals and more specifically their families the attention becomes on how they can be “cured” or “fixed” and brought back into society. It is not until these individuals begin to speak up on their own, that there is a real shift not only in policy but attitude and mindset within society. This continues with the discussion around independent living, which will begin the third and final era of disability rights within the United States, the self-advocacy era. This all culminates in the passing of the ADA in 1990, which marks a new beginning for individuals with disabilities in speaking up for themselves and how they can be integrated into society as a whole.
One of the key areas of overlap that the United States has in its disability rights movement with Great Britain is the early focus on veterans and ex-service men that had become physically disabled following World War two. This is where we see some of the first rhetoric of the medical model of disability, in an article published in the New York Times in 1946, Howard A. Rusk M.D. writes “Today public attention is focused on the young men of America who are returning from war disabled and handicapped. They number in the thousands.”[6] This highlights just how much of a focus this was during this time, it was a large part of the discussion happening, so much so that it was a full page article within the New York Times. Rusk makes it known how important it is to have systems in place that can help physically disabled veterans, who were the main group that was being advocated for during this time.
We see some of this help that had been put into place in the form of the Purple Heart Unit, also known as the Military Order of the Purple Heart, which is a national veterans organization. In an article about the Purple Heart Unit, the New York Times writes:
“The Military Order of the Purple Heart, nation-wide veterans’ organization, will embark on a peacetime program to speed veterans housing and to provide additional benefits for disabled servicemen, it was announced yesterday by the order’s new national commander Ray Dorris of Portland Ore…The housing program will take precedence over all other programs, Mr. Dorris said, adding that he would confer this week with Housing Expedite Wilson W. Wyatt and officials of the War Assets Administration in Washington on the granting of priorities on surplus equipment needed to complete the partially constructed housing projects.”[7]
This is one of the key organizations at the time putting a focus on helping disabled veterans. This is such a big and important undertaking that the organization is working with the U.S. government to try and get the necessary funding and supplies as quickly as possible. This is their paramount objective, surpassing all others, showing just how important the rights of the disabled veterans were during this time. After this there is a steady amount of legislation that is passed and signed to help disabled veterans, but the next evolution in the disability rights movement begins in the mid-1960s.
In 1965 Senator Robert F. Kennedy made an unannounced visit to one of the biggest institutions for individuals with neurological disabilities at the time, Willowbrook located in upstate New York. While there, Senator Kennedy observed some of the most inhumane and deplorable living conditions imaginable. After his visit to Willowbrook, Senator Kennedy testified at a committee hearing, which resulted in an investigation in the state institution. When speaking on the institution Kennedy had this to say “We hear a great deal these days about civil rights and civil liberties and equality of opportunity and justice … But there are no civil rights for young retarded adults when they are denied the protection of the State Education Law, which commands that all other children must receive an education.”[8] This was the first time that a major public figure spoke up in regards to disability rights in the United States. This would not be the last time that Willowbrook was public news, as around five years later a reporter named Geraldo Rivera ran a documentary that showed the deplorable conditions within Willowbrook. This would spark major outrage, and lead to a new nationwide conversation about the effectiveness and moral need for these large state institutions.
While it would take another five years for state institutions to begin to change with their unimaginable conditions, the interview of Bernard Carabello, this would mark the 1970s, the next evolution of the disability rights movement. The United States enters into its second wave of its Disability Rights Movement, which is the Parent wave, which sees the parents of the individuals with disabilities to be the advocates for their children, and puts the emphasis on helping and “fixing” individuals with disabilities. While this is a step in the right direction it still creates numerous problems and harmful stereotypes. The medical model of disability, which paints individuals with disabilities as “broken” and in need of being “fixed”, is still very much prevalent during this time. This period was very short as it only lasted a few years, but it is a crucial step in the evolution of the disability rights movement within the United States, as it moves the spotlight closer to the individuals with disabilities themselves which ultimately marks the final evolution of this movement.
While the independent living model was the first time that the idea of things such as civil rights would be discussed in regards to individuals with disabilities, a few years before this there was discourse around hiring individuals with disabilities into the workforce. In an article about how the year the employment market for individuals with disabilities is starting to become more normalized in society, Howard Rusk writes, “Throughout the country, community programs for the mentally retarded have been slowly demonstrating the truth of the slogan of the National Association for Retarded Children – ‘the retarded can be helped.”[9] While Robert Kennedy’s visit to Willowbrook was mainly about individuals living there and the inhumane conditions of the state institutions, this discourse is clearly more geared towards helping adults, people who are out of these state institutions, and how they can start to become included within society as a large.
This in turn would create a space for a lot of people such as self-advocates and the families of individuals with disabilities to begin talking about similar issues in regards to disabilities. In their article Romel Mackelprand and Richard Slasgiver talk about the shift that occurred at the beginning of the 1970s, “The disability movement matures with the development of the independent living concept in the early 1970s. Initially led by people such Lex Frieden, Judy Heumann, and Ed Roberts, independent living applied the minority model as the foundation of the political process of gaining the civil rights of peoples with disabilities.”[10] These are just some of the prominent figures that come about and make names for themselves as Disability Rights activists during the early parts of the movement. The minority model, also known as the social model of disability, is something that is very important to modern disability rights activists, as it states that people with disabilities are not “disabled” by their bodies but by the “able-bodied” society that they live in. This is also referred to as the Social Model of Disability and provides a pivotal framework for discussing changes surrounding disability. This is the first large step into a new evolution of the disability rights movement, where the individuals with disabilities themselves are the ones advocating for change and what is best for them.
One of the major issues that was seen in these institutions was forced sterilization, in which individuals with disabilities were viewed by the public as not being able to contribute to society. An interesting case of this is seen outside of institutions, where parents of three kids all with disabilities are fighting to have them sterilized, however no hospital or medical facility near them would perform the procedure, since there were massive gains made by individuals in protecting others with disabilities from being forcefully sterilized. The parents took their argument to court and “thwarting them, either directly or indirectly, have been the tremendous gains made by the champions of individual freedoms and rights who have won many successes in trying to protect the mentally retarded who are capable of functioning independently in society.”[11] This is the perfect example of how the parent wave of disability and the medical model of disability which arose from the professional wave had very negative impacts on individuals with disabilities. This does however cause massive shifts that are happening during this time, as forced sterilizations, especially for those under the age of 21, were being rejected and more control and rights were being given to those with disabilities.
In the area of education, there are also discussions happening during the 1970s about making sure that students with disabilities are more included. In 1974 the New Jersey legislature began debating the idea of passing legislation that would improve the conditions of students with disabilities in schools. In an article published by the New York Times an unnamed author writes “But proponents of improved education for the retarded children contend that the special session also provides the lawmakers with an ideal chance to require local school districts to install programs for youngsters with severe mental handicaps.”[12] Here it becomes clear just how inclusive the conversation has become. In just a few short years the narrative has switched from individuals with disabilities needing to be kept aside and isolated, to know there is a push for them to become integrated into schools, and as this article states, the push is for even those with neurological disabilities as well as just physical disabilities. This highlights just how much it took for people to fight for more protections for students with disabilities, specifically within schools.
We continue to see the push for protections for individuals with disabilities at the state level, specifically in New Jersey. In his article titled Disabled Children Get New State Aid, Martin Whaldron writes, “This new policy is only one of several that reflect the quiet revolution underway in the state to protect the rights of New Jersey’s mentally ill, handicapped and ‘developmentally impaired’ residents. Some of these policies reflect an almost complete change in attitudes.”[13] This sudden shift in attitude comes from the work of many activists such but in particular, Judith Huemann is the most prominent of them, especially as she becomes famous for her work in New York City. She became famous for her self-advocacy in being the first person in a wheelchair to obtain a teaching license in New York, something that she had to fight very hard to get.
There are also efforts at a national level as well to help give rights to individuals with disabilities, especially the right to education. In her article for the New York Times, Judy Glass writes about the changes that are arising out of the conversations about individuals with more neurological disabilities, such as learning disabilities. She writes, “Ten or 15 years ago, the term ‘learning disabled’ as a handicap was largely unheard of… five years ago, the learning disabled children were defined more by exclusion than by objective criteria.”[14] This is another example of the rapid change that occurred in this time frame, as the movement evolves more and more individuals begin to become involved in the movement. The term disability has not crossed over into the realm of education adding another step in ensuring the rights for those with disabilities.
There were also some setbacks that accompanied the disability rights movement, one of the biggest came in April of 1981, in which the Supreme Court ruled:
“that a Federal “bill of rights” for the mentally retarded enacted six years ago, did not oblige states to provide any particular level of care or training for retarded people in state institutions… In the case involving the retarded, the appeals court had ruled that the 1200 residents of Pennhurst, a state institution, were being deprived of their right to treatment.”[15]
This was a huge deal at the time as it further restricted the rights of individuals with disabilities who were still living within these institutions. These institutions were mistreating these individuals and with these laws saying that individuals with disabilities did not need to have their caretakers properly trained, it would only further their mistreatment. It is an unfortunate step backwards in this movement, but it contributes to the continued movement to get these institutions shut down and to get individuals with disabilities out of them and living on their own.
The representation of individuals with disabilities in public spaces went a very long way in helping the Disability Rights Movement within the United States. It gave those with disabilities someone that they could see themselves in, and feel like they were a part of society as a whole. This representation really started to take shape as we head into the late 1980s and early 1990s. One prominent figure at this time was Bob Dole, the Senate Republican leader who made it known that he was an individual with a disability, which was something that had not been discussed before. In an article from 1986, Dole is quoted as saying:
“I can’t do buttons like you do, just feel and push them in there… I’ve got to be able to see the hole and sort of push the button in. The trouble is these buttons on this shirt are just about a fraction too high, so it’s very hard to do that. So every day you get a little test; you’re tested.”[16]
Dole at the time dealt with many physical disabilities, the main one being all the damage that he has suffered to his right arm. This was one of the first times that someone this prominent and well known within the United States government began advocating for himself as an individual with a disability. This is where we begin to enter into the final stage of the evolution of the disability rights movement, where these issues are not something that is being discussed within the federal government, and changes being implemented on a national scale, whereas before changes were often made on a smaller scale, either by state or even more local.
As the disability rights movement enters into its final stages there is now an even bigger push to help get individuals with disabilities normalized and integrated into society. The Americans with Disabilities Act (ADA) was passed in late 1989 and was set into law in 1990. The New York Times wrote this when discussing the new act, “The act was considered by its supporters to be one of the most sweeping pieces of civil rights legislation in decades. It extended throughout private industry a prohibition against discrimination toward the disabled by government agencies and companies that receive government contracts.”[17] The ADA was a monumental piece of legislation in regards to the disability rights movement in the United States resulting in federal mandates that made every aspect of society more accessible to those with a disability. It comes after years of hard work by many people and paved the road for the future legislation that would be passed in the years to come.
The Americans with Disabilities Act (ADA) marked a true turning point in the American disability rights movement, as it is one of the first acts passed that was focused on helping individuals with disabilities be able to feel a part of larger society. Steve Holmes a writer for the New York Times, described the ADA in the following way:
“The public accommodations provisions of the law, the Americans with Disabilities Act, mean more than merely providing adequate parking spaces or ramps for the handicapped. Restaurants may have to provide Braille or large-type menus for the blind or visually impaired people,… space for customers with wheelchairs and ensure that their friends and family may sit with them.”[18]
These are some of the major changes that came about as a result of the ADA, and they highlight just how little people with disabilities were seen in society, and how powerful the ADA was in shining a light on them. We see things today such as ramps, handicap parking spaces, and other inclusive infrastructure and think of it as common and something that has always been there, but for many people it has not. This time back into the social model of disability, showing how an individual can be disabled and handicapped, because there is no ramp to help them access a building.
There were numerous people that played a large role in helping to get the act passed, many of whom were famous disability rights activists within the United States at the time, including a man named Justin Dart Jr. “Mr. Dart was best known as one of the primary forces behind the Amercians with Disabilities Act, which was passed by Congress and signed into law by President Georgre Bush with Mr. Dart as his side, in 1990.”[19] Justin Dart Jr. was one of the most influential Disability Rights activists within the United States, he was constantly arguing and advocating for the passage of this act. He became very well known among those serving during this time, simply for how much he was around and speaking with people about how important this act was.
Disability rights movement Within Great Britain
The disability rights movement within Great Britain is rooted in highlighting the conditions of the physically disabled, specifically wounded veterans. Much of the early discussion that takes place within Great Britain deals with this select group of people with disabilities. It was not until more recently that the conversation has shifted to be more inclusive of people with neurological disabilities, along with people with more visible physical disabilities. The movement moved towards the focus on group homes, which were similar to the institutions within the United States, before leading to Great Britain’s own version of the Americans with Disabilities Act, the Disability Discrimination Act in 2005.
An early example of Great Britain’s focus on veterans can be seen when the Parliament is discussing a new finance bill that would have been used to raise money in 1951, Lieutenant-Commander Braithwaite said that “it would also adversely affect disabled ex-service men.”[20] His argument was that the petrol tax that was included in the new finance bill would increase the cost of road transport, and would force more people into using public transport, which was used a lot by disabled individuals at the time. Also when discussing this bill Sir Ian Fraser said that disabled individuals should be excused from the extra petrol duty. This shows how much people were thinking about the physically disabled veterans, as a part of society as a whole, similar to the conversation in the United States.
Disabled veterans dominated a lot of the early discussion of disability rights within Great Britain as they were the most visible individuals with disabilities that were actively trying to be included into society. When discussing the approach to the idea of the economic situation post war, Mr. King of Southampton urged “for an increase in the basic rate for disability pensions of disability pensions for disabled ex-service men.”[21] This is a good start for the conversation about disability rights in Great Britain and provides a solid foundation for the future.
The idea of working and labor was also something that came up in discussions when discussing how to best include them in the labor force. When discussing the idea of defense-workers, looking specifically at summer resorts during the winter time. There is a group of workers that were used to help advance the “national effort”. The argument that these disabled workers could be employed to help in other aspects of the country, was taken before the Ministry of labor, and the position of disabled men specifically was brought up by a man named Mr. E. Evans, stating that it can be difficult for them to find work at times.[22] Mr. Evans is one of the first people that begins to speak out for those with physical disabilities within Great Britain, that is not speaking solely for disabled veterans, advancing the disability rights movement further.
The infantilization and idea that individuals with disabilities need to be helped and cared for by others, even when they may be perfectly able to take care of themselves, is something that is present. For example, the London times published a newspaper article entitled, Debate on employment of disabled and elder persons[23]. Having people with disabilities be associated with the elderly shows how they were seen by larger society. People with disabilities and specifically in this case, those with physical disabilities are seen as weak and in need of someone to be helping them at all times even though there are things that they still might be able to do by themselves. In this case a lot of them are former veterans, specifically men, so they would most likely still be in good physical condition, only needing help in the area of their handicap. This is a very early argument describing the Social Model of Disability, where the individuals themselves are perfectly fine, it is society and their environment that is handicapping them.
At the start of the 1960s we began to see the conversation in Great Britain evolve to begin to include individuals with neurological disabilities, alongside those with physical disabilities. Similar to the pattern in the United States at this time, it appears that Great Britain thought its best course of action was to have these individuals placed into group homes. In March of 1961 there was discussion about the construction of a new home in Bognor Regis, near the southern British Coast. The issue that was brought up was about whether or not that project had been abandoned because two local private schools apparently rejected the idea as they felt that the location was too close to their location, and they did not think it would be able to be the proper size necessary.. When talking about the issue Mr. Kenneth Robinson, who was a representative in Parliament during this time had this to say “Projects of this kind are constantly being frustrated by local difficulties being raised about sitting. Is there nothing the Minister can do, perhaps in conjunction with the Minister of Housing and Local Government, in trying to influence local authorities to be a little more sympathetic towards this type of development.”[24] This shows some of the issues that the disability rights movement in Great Britain faced in its early stages, with many doubting if it was even necessary to have these group homes.
Similar to the United States, in Great Britain these individuals with neurological disabilities are subjected to being separated from the larger part of society by being placed into these group homes. These group homes similar to the institutions in the United States seem to be mistreating the individuals with disabilities as well. Unfortunately, at this time individuals with neurological disabilities are seen as “rejects” and “outcasts”. This also led to the mistreatment of these individuals as they were seen as needing to be removed from society, including many horrible things being done to them such as Euthanasia.
One of the most prominent people in both England and the United States was C. Killick Millard, who was mainly working between 1930-1955 but was the main figure and was a very well known and respected doctor during this time. Ian Dowbiggin writes about Millaird describing him as having “dedicated much of his life to legalizing the right to die, he was likewise motivated by the conviction that an educated, rational and mentally competent person would consent to mercy-killing if suffering from a painful, terminal illness or disability.”[25] This gives insight into how individuals with disabilities were viewed as not able to be educated the same way as their non-disabled counterparts, and how having a disability was seen as something that would not make you of use to the larger part of society. This is another aspect of the disability rights movement in Great Britain that has a parallel to the United States, which is the way that both of these movements had a time where they looked to medical professionals for the answers.
One of the first major pieces of legislation to come from Great Britain in the realm of disability rights is the Chronically Sick and Disabled Persons Act of 1970. This bill established welfare for those who were disabled or for those who suffered from chronic illness. This is an important part of the Disability Rights movement in Great Britain because while there may have been support for the bill, the speaker, who themselves identified as disabled, thought that the bill needed to be stronger. An article written in the London Times “Under the Chronically Sick and Disabled Persons Act, 1970, builders had to provide access facilities where it was ‘in the circumstances both practicable and reasonable. There have been instances in the past 11 years when such facilities were not provided, mainly because nobody has enforced the law.”[26] The prolonged and delayed enforcement of laws is something that is far too common in disability law in particular, with vague and non-descript wording allowing companies and others to get away with not fully giving people with disabilities the accommodations they need. As mentioned in the London Times article it took almost eleven years for something to be done about this, and it is one of the reasons why disability rights are still an active fight.
Prolonged enforcement of laws and regulations can be tied back to an issue that was brought up almost twenty years prior to this incident, which involved giving disabled drivers a badge that would help identify them. In March of 1961, in response to the increasing parking problems of disabled drivers, a man named Mr Dobbs, who was a member of Parliament proposed “to provide a badge to be displayed by disabled drivers to help them and to assist police in using their discretion in dealing with traffic problems.”[27]It would take almost ten more years for this idea to become mainstream and implemented in the Chronically Sick and Disabled Persons Act in 1970. The idea of these badges being used to assist police is very interesting because it speaks to a debate that is happening right now in the United States about how to best aid individuals with disabilities, specifically those with more “invisible disabilities” in regards to things such as traffic stops, and their interactions with police officers. For individuals with disabilities, especially those who may have neurological disabilities, understanding social cues and following directions can often be a tough task, and unfortunately in the United States, police officers can at times give conflicting directions. This can lead to individuals with disabilities being treated harmfully by police officers and not fully understanding why.
We began to see a mindset shift in Great Britain in the late 1990s and one example of this comes from a man Lee Duffin, who although he spent most of his life working in sales and marketing, joined a charity that helped young adults with disabilities to become more self-reliant and independent. Although his main job was fundraising, he said “I had no experiences in fund-raising or the mentally handicapped, but I was so impressed by the charity’s philosophy of helping the young adults to lead a fairly independent and fulfilled life that I wanted to help.”[28] This is a massive shift from just thirty years prior where individuals with disabilities, specifically those with neurological disabilities, were seen as needing to be kept away from society and kept in group homes. This comes in the years following the United States and the idea of independent living that was introduced by disability rights activists there.
As we enter into the 21st century we see the last of the group homes or “long-stay care homes” that were prominent in the late 60s and early 70s and began to become less prominent into the late 80s and 90s. The last of these homes shut down in Great Britain in 2004 and was a part of the effort to help people with disabilities become larger members of society. John Hutton the public health minister had this to say “people in Britain with learning disabilities were among the most socially excluded in the country. Only one of them has a friend outside the immediate circle of their family or paid-for carers.”[29] This is one of the biggest shifts and evolutions in the direction of fostering independence for those with disabilities. In 2001, there were an estimated 1.4 million people living with disabilities in Britain. Around this time as well, there were schools in Britain that received investments in communication aids for students who would need them. This is similar to what happens in the United States, which is that if schools receive federal funding that they have to provide students with the accommodations that they need.
In the United States the Americans with Disabilities Act (or the ADA) in the 1990s provided people with disabilities the rights to access society and for changes to be made to help them it is not until the early 2000s that Great Britain enacts something similar. In 2004 the British government passed the Disability Discrimination Act which acts similar to the ADA. it was described by the media as:
“The most significant aspect of the new provisions is the duty of service providers to make reasonable adjustments to any physical features that are a barrier to the enjoyment of goods and services by disabled people … includes widening a doorway; providing a permanent ramp for a wheelchair user; relocating light switches, for someone who has difficulty reaching;… and providing tactile buttons in lifts’.’[30]
This directly connects to what the ADA did for Americans with disabilities and relates back to the social model, contending that in order for individuals with disabilities to be included within society there needed to be changes made to the environment as well.
Another piece of legislation that was passed in Great Britain that is similar to the ADA is the Disability Discrimination Act (DDA), which was passed in 2005. This act made it illegal to discriminate against individuals with disabilities within the workplace and to make the necessary accommodations to allow these individuals to succeed in the workplace. “Employing disabled people can attract disabled customers.”[31] This is a great way to think about how it feels to include individuals with disabilities within not only the workplace but society as a whole. Seeing people that represent who you are and how you view yourself is very important in helping people feel safe in society.
Conclusion
In conclusion, the disability rights movements of both the United States and Great Britain have some connections with one another but it was mainly the United States setting the precedent for and leading the way. Both of these movements have their foundations in the way that society began to see and treat veterans with disabilities following World War II. The care and thought that was given to these veterans opened the door for disability rights activists in each country to begin to further the conversation on disability rights. While the United States had its focused turn to institutions by parents, Great Britain began to look at group homes. In 1990 the United States passed the Americans with Disabilities Act, which provided comprehensive changes that would grant individuals with disabilities a chance to participate in society. 15 years later Great Britain would pass the Disability Discrimination Act, which would act similarly to the ADA. Ultimately showing how, even though the two movements evolve similarly over time, it is the United States that has its evolutions before Great Britain.
The significance of this capstone paper is that it allows for the start of a discussion on the history of disability rights not only in the United States but in Great Britain as well. It is important to just study the history of one nation’s evolution as it can close you off to possible ideas and changes that have been made in other nations that can be adopted in one’s own country. Individuals with disabilities have been mistreated throughout history in many different parts of the world and it is important to begin to understand how this happens and how different nations are able to move forward and away from this awful mindset and treatment of individuals with disabilities.
This capstone paper is significant for education as it allows for students to learn about a history and a movement that has rarely been discussed before. Much of the activism that occurs during the disability rights movement occurs during the late 1970s and 1980s, a time that is just now being discussed more and more in schools, particularly in secondary education. Individuals with disabilities have been treated inhumanely and as outsiders, but if we allow for their story to become a part of our taught history, we can work towards people accepting them for who they are. The disability rights movement also has connections to other historical events, including how the disability rights activists used tactics of other civil rights groups to help fight for their cause. There is also great opportunity for current events with this topic, as this movement is still going today, as many disability rights activists fight to have individuals with disabilities seen by the rest of society.
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Cooper, Jeremy. Law, Rights, and Disability. London: Jessica Kingsley Publishers, 2003.
Davis, Lennard J. Enforcing Normalcy: Disability, Deafness, and the Body. London: Verso, 1995.
Dearlove, Desmond. “A fight for the right to work.” Times, September 10, 1992, 19[S]. The Times Digital Archive (accessed September 25, 2022). https://link-gale-com.ezproxy.tcnj.edu/apps/doc/IF0503341113/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=36a91163.
Diane Henry, Special to The New York Times. 1977. “Parents of 3 Retarded Girls Fight Hospital Refusal to Sterilize them: Parents Press Bid to Sterilize Retarded Girls.” New York Times (1923-), Oct 02, 1. https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/parents-3-retarded-girls-fight-hospital-refusal/docview/123174722/se-2.
“Diary Of Next Week’s Events.” Times, July 8, 1961, 11. The Times Digital Archive (accessed November 21, 2022). https://link.gale.com/apps/doc/CS184901864/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=5718e179.
Dowbiggin, Ian. “‘A Prey on Normal People’: C. Killick Millard and the Euthanasia Movement in Great Britain, 1930-55.” Journal of Contemporary History 36, no. 1 (2001): 59–85. http://www.jstor.org/stable/261131.
Evans, Richard. “Law will ensure access for disabled in new buildings.” Times, June 2, 1981, 3. The Times Digital Archive (accessed October 17, 2022). https://link-gale-com.ezproxy.tcnj.edu/apps/doc/CS50694338/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=7a585a9f.
Frean, Alexandra. “Care homes for the mentally disabled to shut.” Times, March 21, 2001, 4. The Times Digital Archive (accessed November 21, 2022). https://link.gale.com/apps/doc/IF0502655359/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=caf8b513.
From Our Correspondent. “Assisting The Disabled.” Times, December 4, 1951, 5. The Times Digital Archive (accessed November 21, 2022). https://link.gale.com/apps/doc/CS85675396/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=8da0813e.
Heumann, Judith. Being Heumann. S.l.: WH. Allen, 2021.
Hobson, Rodney. “Working at a different pace.” Times, July 31, 1990, 17. The Times Digital Archive (accessed November 21, 2022). https://link.gale.com/apps/doc/IF0503253499/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=476c1f07.
“House Of Commons.” Times, June 6, 1951, 4. The Times Digital Archive (accessed November 21, 2022). —-https://link.gale.com/apps/doc/CS67456198/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=f90b3-07e.
“House Of Commons.” Times, November 7, 1951, 7. The Times Digital Archive (accessed November 21, 2022). —-https://link.gale.com/apps/doc/CS117788007/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=20fbf67
Howard A Rusk, MD Formerly Chief, Convalescent Services Division, Office of, Air Surgeon. 1946. “Hope for our Disabled Millions: They can be Rehabilitated, Says a Physician, if we Apply Methods used in Restoring Handicapped Veterans. our Disabled Millions our Disabled Millions.” New York Times (1923-), Jan 27, 1946. —-https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/hope-our-—-disabled-millions/docview/107574818/se-2.
Howard A. Rusk, M.D. 1964. “Hiring the Retarded: ‘ 63 Marked Employment Turning Point for Mentally Handicapped in the U.S.” New York Times (1923-), Jan 06, 121. —-https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/hiring-ret—-arded/docview/115529793/se-2..
John Sibley. 1965. “Kennedy Charges Neglect in State Care of Retarded: KENNEDY ASSAILS CARE OF RETARDED.” New York Times (1923-), Sep 10, 1. —-https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/kennedy-charges-neglect-state-care-retarded/docview/116840893/se-2.
Jonathan Fuerbringer Special to The New York Times. 1986. “To Dole, it was an Education to Get Past Disability.” New York Times (1923-), Jun 16, 1. —-_https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/dole-was-education-get-past-disability/docview/110931546/se-2.
Judy Glass. 1980. “New Efforts to Assist ‘Learning Disabled’ Debated Across L.I.: New Efforts to Assist ‘Learning Disabled’ New Efforts to Assist ‘Learning Disabled’.” New York Times (1923-), Nov 23, 4. —-https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/new-effor—-ts-assist-learning-disabled-debated/docview/121268082/se-2.
“Legal Appointments.” Times, May 7, 1985, 29. The Times Digital Archive (accessed September 25, 2022). https://link-gale-com.ezproxy.tcnj.edu/apps/doc/CS486772903/TTDA?u=tconj_ca&sid=boo——kmark-TTDA&xid=28b1fa67.
Linda Greenhouse, Special to The NewYork Times. 1981. “Justices Restrict A ‘Bill of Rights’ for the Retarded: High Court Calls U.S. Law Only Advisory for States Release of Retarded People ‘Findings’ in ‘Bill of Rights’ Court Restricts ‘Rights’ of Retarded Right to Refuse Medication.” New York Times (1923-), Apr 21, 2. —–https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/justices-restrict-bill-rights-retarded/docview/121615394/se-2.
Mackelprang, Romel W. and Richard O. Salsgiver. “People with Disabilities and Social Work: Historical and Contemporary Issues.” Social Work 41, no. 1 (01, 1996): 7-14. —https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/scholarly-journals/people-with–disabilities-social-work-historical/docview/215272364/se-2.
Martin Waldron. 1978. “Disabled Children Get New State Aid: Disabled Children are Getting New Help from the State.” New York Times (1923-), Mar 05, 3. —-https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/disabled-children-get-new-state-aid/docview/123790595/se-2.
Noyes, Hugh. “Disabled peers put aid plea.” Times, April 10, 1970, 1. The Times Digital Archive (accessed October 17, 2022). —- https://link-gale-com.ezproxy.tcnj.edu/apps/doc/CS17134218/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=8a9252f9.
“Parliament.” Times, August 3, 1951, 3. The Times Digital Archive (accessed November 21, 2022). Retrieved from —https://link.gale.com/apps/doc/CS50547971/TTDA?u=tconj_ca&sid=bookmark-TTDA&xi—d=92465—-b0b.
“Purple Heart Unit To Act On Housing: Order Back Speed-Up Of U.S. Efforts To Aid Veterans–Also To Help Disabled Men.” 1946. New York Times (1923-), Sep 08, 40. –https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/purple-heart-unit-act-on-housing/docview/107403078/se-2.
Special to The NewYork Times. 1974. “Improved Education Urged for Retarded: Disparities seen Resulting.” New York Times (1923-), Jun 23, 78. —–https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/improved-education-urged-retarded/docview/120059739/se-2.
Steven A. Holmes. “Sweeping U.S. Law To Help Disabled Goes Into Effect: Gains Seen For Millions Statute May Force Businesses To Alter Buildings And Offer Specialized Services Sweeping U.S. Law To Help Millions Of The Disabled Goes Into Effect New Anti-Bias Legislation Could Bring Changes To Many Businesses.” Jan 27, 1992. New York Times ——https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/sweeping-u-s-law-help-disabled-goes-into-effect/docview/109037130/se-2.
Stevenson, Richard W. “Justin Dart Jr., 71, Advocate for Rights of Disabled People.” New York Times (1923-), Jun 24, 2002. —https://ezproxy.tcnj.edu/login?url=https://www.proquest.com/historical-newspapers/justin-dart-jr-71-advocate-rights-disabled-people/docview/92295369/se-2.
“Subsidy Rate In Airport Charges.” Times, March 7, 1961, 4. The Times Digital Archive (accessed November 21, 2022). —-https://link.gale.com/apps/doc/CS67723367/TTDA?u=tconj_ca&sid=bookmark-TTDA&xid=7df135cc.
Walker Alan and Peter Townsend. 1981. Disability in Britain: A Manifesto of Rights. Oxford: Martin Robertson.
[1] GDA Podcasts, GDA Podcasts, April 26, 2017.
[2] NHS, “Treatments That Are Not Recommended for Autism,” NHS choices (NHS, December 16, 2022),
[3] Elizabeth Barnes, The Minority Body: A Theory of Disability (Oxford, United Kingdom: Oxford University Press, 2018).
[4] Lennard J. Davis, Enforcing Normalcy: Disability, Deafness, and the Body (London: Verso, 1995).
[5] Crip Camp: A revolution, Netflix, 2020.
[6] Howard A Rusk, “Hope for our Disabled Millions”, New York Times, January 27th, 1946.
[7] “Purple Heart Unit To Act On Housing: Order Back Speed-Up Of U.S. Efforts To Aid Veterans–Also To Help Disabled Men.”, 1946, New York Times.
[8]John Sibley, “Kennedy Charges Neglect in State Care of Retarded. September 10, 1965. New York Times
[9] Howard A. Rusk, “Hiring the Retarded”, January 6, 1963, New York Times.
[10]Romel W. Mackeprang, and Richard O. Salsgiver, “People with disabilities and Social Work: Historical and Contemporary Issues”.1996, Social Work.
[11] Diane Henry, “Parents of 3 Retarded Girls Fight Hospital Refusal to Sterilize Them”, October 2, 1977, New York Times.
[12] “Improved Education Urged for Retarded”, June 23, 1978, New York Times.
[13] Martin Waldron, “Disabled Children Get New State Aid”, March 5, 1978, New York Times.
[14] Judy Glass, “New Efforts to Assist ‘Learning Disabled’ Debated Across L.I.” November 23, 1980, New York Times.
[15] Linda Greenhouse, “Justices Restrict A ‘Bill of Rights’ For the Retarded”, April 21, 1981, New York Times
[16] Jonathan Fuerbringer, “To Dole, It Was An Education to Get Past Disability”, June 16, 1986, New York Times.
[17]Richard, “Justin Dart Jr., 71, June 14, 2002.
[18] Steven A. Holmes, “Sweeping U.S. Law To Help Disabled Goes Into Effect: Gains Seen For Millions Statute May Force Businesses To Alter Buildings And Offer Specialized Services Sweeping U.S. Law To Help Millions Of The DisabledI Goes Into Effect New AntI-Bias Legislation Could Bring Changes To Many Businesses.” Jan 27, 1992, New York Times.
[19] Richard W Stevenson, “Justin Dart Jr., 71, Advocate for Rights of Disabled People”, June 14, 2002.
[20] “House of Commons”, Times, June 6,1951, The Times Digital Archive.
[21] “House of Commons”, Times, November 7, 1951, The Time Digital Archive.
[22] “Parliament”, Times, August 3, 1951, The Times Digital Archive.
[23] “Diary Of Next Week’s Events”, Times, July 8, 1961, The Times Digital Archive.
[24] “Subsidy Rate In Airport Changes”, Times, March 7, 1961, The Time Digital Archive.
[25]Ian Dowbiggin, “A Prey on Normal People”, Journal of Contemporary History, (2001), 65.
[26] Richard Evans, “Law will ensure access for disabled in new buildings”, Times, June 2, 1981, The Times Digital Archive.
[27] “Launchers For Research in Space”, Times, March 14, 1961, The Times Digital Archive.
[28] Rodney Hobson, “Working at a different pace”, Times, July 31, 1990, The Times Digital Archive.
[29] Alexandra Frean, “Care homes for the mentally disabled to shut”, Times, March 21, 2001, The Times Digital Archive.
[30] Stephen Cragg,“Legislation Update”, Times, September 7th, 2004, The Times Digital Archive.
[31] Stephen Alambritis, “The Business View”, Times, March 4, 2008, The Times Digital Archive.