Blindness and Visual Impairment
- Adrienne AschAdrienne AschYeshiva University
- and Nancy R. MudrickNancy R. MudrickSyracuse University
Significant visual impairment affects ~8 million Americans, 1.8 million of whom are blind and must find nonvisual methods of performing life roles. Social workers should not assume that people with visual impairment or blindness are unable to work, have families, or engage in sports or travel, or that vision limitations are necessarily a part of every presenting problem. Key roles for social workers include assisting in access to services and training and advocacy to combat discrimination and exclusion.
People having little contact with those who are blind may imagine that a person's blindness precludes functioning competently in the world. While a 1991 survey reported that blindness is a “more accepted” disability than is mental illness and that 47% of the survey population considered themselves “very comfortable” when meeting a blind person (Louis Harris and Associates, 1991), many people including professionals equate blindness with helplessness. As Warren (2000a) points out, “it may seem self-evident that vision impairment would produce an adverse impact on personal functioning in every area, but this issue is one for research rather than conjecture; the relationships are frequently not those that intuition might suggest” (p. 321). After training in managing oneself as a person with visual impairment, and when not barred by fears of others, people who are blind or visually impaired study, hold jobs, raise families, go to restaurants, and participate in typical life roles and activities.
There are millions of people who have some degree of visual impairment, but can rely on their vision (perhaps augmented by glasses) to perform tasks of daily living. This entry focuses on those people with vision impairments and blindness that require special services or adaptations.
The earliest approaches to helping people who were blind or visually impaired in the United States stressed special, separate education for children, sheltered or specialized noncompetitive employment for adults, and a specialized system of service agencies to meet the social and recreational needs of clients. Social and educational programs for people with visual impairment taught such adaptations as Braille, travel with a long cane or a guide dog, and some methods of cooking, sewing, and other activities of daily living. They also engendered in their clients a belief that visual impairment prevented them from participating in their former employment or community activities and that they needed to develop new outlets and new lives as “blind” people (Scott, 1969). The challenge to this separation came from people who were blind or visually impaired, particularly those who founded the National Federation of the Blind (NFB)—the first major civil rights group of people with disabilities in the United States (Asch, 1985; Matson, 1990). With its civil rights and minority-group approach to blindness, NFB endorsed the need for high-quality rehabilitation training, training in alternative techniques of living for people who could not always rely on vision, and the right of “blind people to speak for themselves” to combat laws and practices that excluded them from ordinary educational, work, civic, and leisure-time activities.
Profile of the Population with Visual Impairment
The 2005 National Health Interview Survey (NHIS) estimates that among non–institutionalized persons aged 18 and above ~20.2 million people have trouble seeing, even when wearing glasses (Pleis & Lethbridge-Çejku, 2006), while the 2002 Survey of Income and Program Participation (SIPP), using a more conservative definition of visual impairment, estimated that 7.9 million people aged 15 and above have difficulty seeing well enough to read a newspaper, even with glasses (Steinmetz, 2006). The SIPP also estimates that 0.5% of children aged 6–14 have difficulty seeing. Because both datasets exclude those living in institutional settings, these counts slightly underestimate the true total. Furthermore, because only visual limitations with reference to reading are explored, these data do not indicate how many people cannot manage tasks that require intermediate or distance vision, such as seeing a computer screen, spotting a building or a familiar person across a street, or watching television. Globally, using data collected in various national formats, the World Health Organization estimates that, in 2002, 36.9 million people were blind (a prevalence of 0.57%) and another 124 million had low vision (prevalence of 2%) (Resnikoff et al., 2004).
Visual impairments increase with age, and females have higher rates of visual impairment at every age (Table 1). Visual impairment also varies with race, with African Americans, American Indians, and Alaska Natives having the highest rates. This variation may be related to racial differences in poverty rates, as visual impairments are more prevalent among people living below or slightly above the poverty line. Persons with severe visual impairment have a 48% employment rate and those with less severe visual impairment have a 57% rate (Table 2); both rates are substantially lower than the 88% employment rate for those with no disability (Steinmetz, 2006). Both the median and mean annual earnings of the working people with visual impairment are ~$10,000 lower than those of workers with no disability. The low level of earnings (median annual earnings of $22,189) implies that even for those who are employed, many will be counted among the poor or near poor.
Causes of Visual Impairment
People with visual impairment, including those considered “legally blind,”
Table 1 Percentage of Adults Having Trouble Seeing Even with Glasses or Contacts (NHIS, 2004)
% of Adults
75 years and above
Race and Ethnicity
Black or African American only
American Indian and Alaska Native only
Native Hawaiian and other Pacific Islander
Two or more races
Hispanic or Latino (any race)
Not Hispanic or Latino (any race)
Below 100% of the poverty line
100% to less than 200%
200% or more
Source: From Table 59 of Health, United States, 2006, With Chartbook on Trends in the Health of Americans, by National Center for Health Statistics, 2006 (which cites National Health Interview Survey, 2004), Hyattsville, MD.
Table 2 Employment Status and Earnings of Adults Having Visual Impairment (SIPP, 2002)
Difficulty seeing words/letters, severe
Difficulty seeing words/letters, not severe
Total U.S. population, 21–64 years
From Table 5 of Americans with Disabilities: 2002 Household Economic Studies, by E. Steinmetz, 2006, Current Population Reports, P70–107, U.S. Census Bureau.
experience a range of visual abilities and limitations. Many people have some usable vision, but they may be unable to distinguish faces or the lettering of signs or they may not have central or peripheral vision. Of the estimated 7.9 million adults having some visual impairment, 1.8 million report being unable to see (Steinmetz, 2006, SIPP estimate). The most frequent causes of vision impairment and blindness are diseases and conditions whose prevalence increases with age and are experienced by adults. These causes are diabetic retinopathy, age-related macular degeneration, cataracts, and glaucoma (CDC, 2004). For a small percentage of persons, visual impairment or blindness is traceable to genetic conditions such as retinitis pigmentosa or retinoblastoma. Injury also accounts for a small percentage of adult onset visual impairment or blindness. The association between aging and visual impairment indicates that the prevalence of visual impairment and blindness is likely to increase with the aging of the large baby boom cohort.
Low vision and blindness are uncommon among children, with most of the few cases occurring before birth or within the first month of life. Such conditions retinopathy of prematurity, albinism, hydrocephalus, congenital cytomegalovirus, and birth asphyxia are the most common causes of visual impairment in children below 10 (CDC, 2004).
Services and Legislation Affecting People With Visual Impairment
People who have visual impairment benefit from the services, agencies, and legislation that are intended for all people with disabilities. However, some legislation and services are targeted at people who meet the federal legislative definition of “legal blindness”: clinically measured visual acuity of 20/200 or less in the better eye or a visual field of 20° or less after optimal correction (American Foundation for the Blind, 2007). The person whose vision meets this definition can see at 20 feet what someone with perfect vision can see at 200 feet, and the width of vision is substantially narrower than that for someone whose sight is unimpaired. Some government and private agencies provide vision-related services only to those who meet the definition of legal blindness; others may serve the broader visually impaired population. Although nearly half of the population with visual impairment is above age 65, the service system is still geared primarily to children and working-age adults.
Access to the Printed Word
Special services and legislation to ensure access to the printed word have existed since 1879 when federal legislation enabled the expansion of the activities of the American Printing House for the Blind to produce books for people who were blind (American Printing House for the Blind, 2004). Other federal legislation authorized sending Braille materials as “free matter for the blind,” to avoid the cost to libraries of mailing the heavier Braille and other materials. Federal law also established the Books for the Blind program, now National Library Service for the Blind and Physically Handicapped (NLSBPH), which provides Braille and recorded literary and music materials to anyone unable to read standard print because of a visual, learning, or physical disability (National Library Service, 2006).
With computer technology and the Internet now being major vehicles for the dissemination of information, ensuring access to words and graphics in electronic and online media has become important. Section 508 of the Rehabilitation Act requires that all federal government Web sites and related materials be accessible to persons with visual impairment. The access standards are set by the Access Board (Architectural and Transportation Barriers Compliance Board). While Section 508 does not apply to the private sector, it has spurred the development of voluntary guidelines for Web and other media access that many organizations have adopted (the World Wide Web Consortium developed guidelines described at http://www.w3.org/TR/WAI-WEBCONTENT/). There also has been litigation under the Americans with Disabilities Act, challenging organizations that use technologies that rely on screen instructions or touch screens, such as ATMs and cell phones, to assure access for people with visual impairment. This concern can apply to human service agencies as they implement new technology in providing information and other services to clients through Web sites or through electronic or video media.
Education and Rehabilitation
The Individuals with Disabilities Education Act (IDEA), originally PL 94-142, and the Rehabilitation Act of 1973 apply to all people with disabilities, including those with visual impairments. Under the Rehabilitation Act, states may develop a separate agency to provide services exclusively to persons classified as legally blind. Just over half the states have established a separate agency. Where there is no specialized agency, services for people who are legally blind are delivered through the broader state rehabilitation agency. Some states with separate agencies may restrict services to those who meet that state's definition of legal blindness, but others serve anyone with significant visual problems. Social work clients who need vision-related services should first be referred to a specialized agency; if services are not provided because the individual's vision does not meet the eligibility criteria, services should be requested from the state's general rehabilitation agency.
Veterans with visual impairment may receive services, assistive devices, and assistance with housing adaptations through the Blind Rehabilitation Service of the Veterans Administration (VA) or a VA medical center. The Blind Rehabilitation Service consists of 10 regional blind rehabilitation centers, visual impairment services teams (VISTs), VIST coordinators located at VA medical centers and outpatient clinics, and other rehabilitation personnel whose work may include computer access training or training for those with low vision or who are blind (U.S. Department of Veterans Affairs, 2007). The Blind Rehabilitation Service provides services to all veterans who are blind or have low vision, regardless of whether the visual impairment is service-connected.
Special Employment Legislation
Two laws from the 1930s give people who are legally blind access to sheltered and noncompetitive employment: the Wagner-O'Day Act (PL 75-739), which established a system of sheltered workshops, and the Randolph-Sheppard Act (PL 74-734), which gives people who are legally blind preference as operators of vending facilities on federal properties. These laws and their subsequent amendments have helped to provide work for thousands of people who are blind, but the working conditions have not always been compared favorably with the conditions in the general labor force. Workshop employees are considered workers under federal law, but some agencies have attempted to treat them as clients and have denied them the right to organize for improved wages and working conditions. The National Labor Relations Board has upheld the rights of workshop. Employees to form unions and to bargain collectively, yet some of these workers still earn less than the Federal Minimum Wage, legal under Section 14C of the Fair Labor Standards Act. While vendors are considered self-employed entrepreneurs, the state agency that serves people who are blind issues their operating licenses and supervises their work and service requirements. The 1971 Javits-Wagner-O'Day Act, an expansion of the original 1938 Wagner-O'Day Act, creates employment opportunities for persons who are blind (or who have severe impairments) via government purchases of products and services provided by nonprofit agencies employing such individuals. The National Industries for the Blind, a nonprofit agency, coordinates the implementation of the program for persons who are blind (more information is available at http://www.nib.org).
The determination of blindness or visual impairment for disability income support is based on a set of vision standards used by both the social insurance and the income-tested benefit programs administered by the Social Security Administration. People who are blind or visually impaired and who are no longer able to work but have worked and contributed to the Social Security trust funds for at least 5 years are eligible to receive social security disability insurance (SSDI). The benefit calculation formula for these beneficiaries is the one applied to all SSDI beneficiaries. However, the earnings standard for people who are blind or visually impaired who subsequently become employed (referred to as substantial gainful activity, SGA) is higher than the standard for other SSDI recipients (the SGA, for 2007, for example, is $1,500 for persons who are blind compared with $900 for others (Social Security Administration, 2006). Beneficiaries earning above this standard for more than a trial work period of 9 months will no longer be paid an SSDI benefit, although those who are blind can have their payments resume promptly should their earnings fall below SGA. Poor adults who are blind or visually impaired and who have no labor force experience or too little for SSDI eligibility may receive support from the income-tested Supplemental Security Income program (SSI). The federal SSI benefits for people who are blind are the same as those for people with other disabilities, although some states supplement the federal SSI grant to provide greater cash assistance for recipients who are blind (Social Security Administration, 2006). If the SSDI benefit and other income are below the income standard for SSI, it is possible to receive support from both programs. While the SGA standard is applied in some cases for initial SSI eligibility, it is not used for the continuing eligibility of employed SSI recipients. Instead, countable earnings are computed by first deducting work expenses and $85 of disregard, and then calculating 50% of that amount. Recipients are no longer eligible for SSI when countable earnings and other income exceed the income eligibility standard. Unlike other SSI recipients, SSI recipients who are blind are allowed to include in deductable work expenses all work-related expenses, whether or not they are directly related to the impairment.
Services to Deaf Blind and Others With Multiple Impairments
A segment of the population of persons who are visually impaired or blind identified as having unique and sometimes unmet needs is people with hearing impairments as well. The prevalence of concurrent hearing and visual impairment is estimated at 3.3% overall; however, among persons above age 79, the prevalence is estimated to be 16.6% (Caban et al., 2005). The Rehabilitation Act Amendments of 1992 established the Helen Keller National Center for Deaf–Blind Youths and Adults in recognition that some people who are visually impaired also incur hearing loss that precludes use of some alternative techniques and necessitates the development and teaching of new techniques at this center.
Learning the techniques to function without sight may be more difficult if individuals have manual dexterity problems that prevent them from reading Braille or hearing problems that prevent their use of sound in orientation and travel. Some people with visual impairments and cognitive impairments arising out of mental disabilities or brain injuries will need services from agencies and organizations that specialize in cognitive rehabilitation. Agencies that serve people with hearing, mobility, or cognitive impairments may fear taking on clients who have visual disabilities as well. In such circumstances, social workers can play a crucial case management and advocacy role to ensure that clients with multiple disabilities receive the services to which they are entitled.
Serving Clients With Visual Impairment in General Settings
People with visual impairment, like other people, seek social services for marital or family problems, as part of their employment, or on behalf of relatives. In these instances, blindness is incidental or irrelevant to the request for assistance. The social work with such clients should concentrate on the family's or couple's dynamics, and not assume that blindness is the chief issue or that people with visual disabilities need services from specialists in blindness. However, if blindness comes up repeatedly as a source of friction, the worker may need to explore how the visual impairment is affecting the other issues that are the focus of concern.
All people with disabilities, including those who are blind or visually impaired, are protected against discrimination in employment and in utilizing public and private services by the Americans with Disabilities Act and the 1973 Rehabilitation Act. These laws have no special provisions for persons with visual impairment, but they serve as the basis of an employer's obligation to provide “reasonable accommodation” in the form of readers or other assistive devices. The Act mandates that public and private agencies evaluate whether they are physically accessible and accessible in terms of their program rules, regulations, and procedures. to consumers and clients having visual impairment. What is required for full access is still being contested. For example, the Social Security Administration is being sued for communicating with benefit recipients who are blind or visually impaired in print formats they cannot read, and then suspending their benefits for subsequent failure to comply with its requests (American Council of the Blind et al. v.Jo Ann B. Barnhart, Commissioner of the Social Security Administration, in her official capacity, and Social Security Administration, complaint available at http://www.dredf.org).
Lifespan Approach to Blindness and Visual Impairment
Social workers may come into contact with people who are blind or visually impaired at all stages of development, and may assume a variety of roles in relation to this population.
When individuals or family members discover that they or their loved ones are likely to have serious visual problems, they may react with emotions such as distress, sadness, fear, and confusion. Such clients and their families need accurate information about laws, services, and alternative techniques for performing tasks that people customarily imagine cannot be handled without vision. Although the onset of visual impairment sometimes necessitates in-depth counseling and therapy for an individual or a family, social workers are cautioned against assuming as in the past (Carroll, 1961) that blindness brings about a new psychology or gives rise to completely different personality problems (see critique in Asch & Rousso, 1985). Instead, social workers can steer clients to information about services and to possibilities for maintaining their work, school, family, and leisure roles with guidance available from the National Center for the Blind, the services listings of the American Foundation for the Blind, and books like If Blindness Comes (Jernigan, 1994). Silverstone et al. (2000) offer comprehensive information about services and research on visual impairment and blindness across the lifespan.
Children With Visual Impairments in the Family, at School, and in the Community
Social workers dealing with infants and toddlers who are blind or their families can get some valuable suggestions from the advocacy and parent groups discussed here and listed in the references. In his comprehensive review of research on children and youth with visual impairments, Warren (2000b) points out that it is dangerous to assume that lack of vision, rather than lack of stimulation, causes delays in development of such activities as crawling, walking, and discovering the world around them. The National Organization of Parents of Blind Children, the American Council of the Blind, journals such as Future Reflections, and state and private service agencies can provide advice to social workers and parents on whether a child should learn Braille, will need assistance in learning to get around safely using the long cane, or even guide them to toys and games that offer stimulation. Because many childhood eye conditions are progressive and the demands of school and social life expand as a child grows, social workers in school settings could aid parents to participate in meetings about their child's educational future and help them become experts in technological devices and alternative methods that allow children who are blind or visually impaired to participate in sports, recreation, music, art, and extracurricular activities, as well as academic activities in school (Willoughby & Duffy, 1989; Castellano, 2005).
Blindness and Visual Impairment During the Working Years
Many working-age people who develop vision problems fail to learn about available rehabilitation services from ophthalmologists or hospitals and as a result may give up their valued activities. Social workers can be advocates for their clients in rehabilitation agencies, can tell clients about guide dog schools, or convince apprehensive families that work, independent travel, and family life are still feasible. Consonant with a strengths approach, they can focus attention on the talents and capacities that remain despite vision loss. Sometimes the person will not be able to fully return to prior employment or activities, but the social worker should refer a client to the tools and skills that will enable him or her to continue in the chosen and valued roles when possible.
Blindness should not be assumed to prevent the safe conduct of other adult roles. In particular, social workers in the field of child-protective services should not presume that an infant or older child cannot be safely cared for by a parent (or parents) with visual impairment. Child protective workers and parents with visual impairment can contact through the Looking Glass (http://lookingglass.org) to learn more about and to obtain resources for parents with blindness or visual impairment. As with all child protection cases, decisions to remove a child should be made on a case-by-case basis after a careful and thorough assessment of the parents' parenting skills and supports.
Blindness in Late Life
Older persons with impaired vision are generally new at dealing with sight loss, and may be experiencing other health problems as well (Ainlay, 1988). They may experience difficulties attributable to lack of training in dealing with blindness or from other health problems, and not from blindness, itself. The Rehabilitation Act Amendments of 1992 provide for increased services for older people with visual impairments, and are intended to keep them active in their homes and communities by providing tools for daily living, travel, and communication. Social workers who see clients in senior citizen centers and nursing homes should be especially alert to the clients' deteriorating vision and should link their clients with the specialized services that will enable them to continue their activities.
Professional Issues for Social Workers
Training and Working With Colleagues Who Are Blind
People with visual impairments have been in the social work profession for decades, and there are many instances of field placements and agency accommodations. However, fieldwork sites and employing agencies sometimes still display stereotypes and fears about blindness (Tannenbaum, 2001). A university or agency can seek help through the Council on Disability and Persons with Disabilities of the Council on Social Work Education (http://www.cswe.org/About/governance/CommissionsCouncils/15550/15551.aspx) or through the Web site of the National Federation of the Blind's Human Services Division, whose membership includes professional social workers with visual impairments who are interested in providing employment assistance to persons in the profession who are blind or visually impaired. (http://www.nfbnet.org/mailman/listinfo/humanser).
Key Concepts and Practice Principles for Social Workers
Regardless of service setting, there are some common principles and concepts in working with individuals or groups where one or all clients have visual impairment or blindness. The principles and concepts listed below are synthesized from general practice principles for social work with people with disabilities (Mackelprang and Salsgiver, 1999; Raske, 2005; Rothman, 2003), and from disability etiquette guidelines for interactions with people with blindness or visual impairment (Cohen, 2003; Federal Communication Commission, 2003; Wayne State University, 2007).
The first practice principle is to focus on the individual's presenting problem in assessment and response, rather than assuming that visual impairment is the key problem to be “solved” or the key source of the individual's problems. A second practice principle is not to assume that the presence of severe visual impairment or blindness will preclude active engagement in life's usual activities—schooling, employment, intimate relationships, parenting, care and support of others, cooking and housecleaning, travel, sports, and other leisure activities. Social work with clients who are blind or visually impaired should aim to facilitate engagement in these life activities and the development of environmental accommodations and personal skills that enable full participation and enjoyment. The third principle is to incorporate a strengths perspective, which empowers the client to act in his or her own behalf. Fourth, social workers should be knowledgeable about the range of special services and programs for persons with blindness or visual impairment, even while supporting independence and self-determination. An important advocacy role for social workers is to be vigilant for discrimination and de facto exclusion in the delivery of services and by other organizations and businesses, and to help the client learn how to advocate against or challenge discrimination or exclusion when they occur.
Social workers also need to be knowledgeable about what is referred to as “disability etiquette” when they are working with people with blindness or visual impairment. The key elements of etiquette include not making assumptions in interpersonal interactions, but to be guided by the individual regarding whether help is required, and what kind of help. For example, if there are forms to fill out, clients should be asked what format and process they prefer. Especially for social work encounters, it is important to respect privacy and confidentiality. Two mistakes that agencies sometimes make are to ask family members to fill out a paper form for someone without sight, without first determining that it is acceptable to the client and an appropriate task for a family member, or to have a staff member fill out the paperwork by asking the client for the information in a very public location. Other elements of etiquette involve identifying oneself and others present at the start of the encounter, and waiting for the client to indicate whether or not assistance navigating the office space is required. Another point of etiquette is to know how to direct or guide a person with limited or no sight to another location in a manner that does not violate personal space. Finally, if people with and without sight are part of the social work encounter, social workers need to be alert to any tendency on their part or the part of other staff in the setting to address inquiries to the person with sight that properly should be addressed directly to the person who is blind or visually impaired. More specific information about disability etiquette for working with people who are blind or visually impaired can be found at the Web sites of the references named at the beginning of this section.
A key approach to working with people with blindness or visual impairment is to recognize that it is a social as well as an individual problem. Contact with active members of organizations of people with blindness or visual impairment, such as the National Federation of the Blind, the Blinded Veterans Association, and the American Council of the Blind, is indispensable in helping people new to visual impairment appreciate that Braille, cane or guide dog, recorded materials, live readers, adapted computers, and new ways of managing a home and work life can be as efficient as the ways that relied on sight. Other individuals and advocacy organizations in the disability rights movement are also invaluable in providing allies to battle discrimination and exclusion when it occurs.
Issues for the Twenty-first Century
For people with visual impairment or blindness there are options in the 21st century that did not exist in prior centuries. In the United States, the Americans with Disabilities Act prohibits discrimination in employment and public life. Twenty-first century technology supports participation in work, family, recreation, cultural activities, and sports with ever greater ease. Portable electronic equipment assists in orientation, travel, and the translation of visual text to accessible media. New assistive devices and medical procedures offer some people possibilities for increased usable vision.
Nonetheless people who are blind or have visual impairment still report experiencing exclusion from work, housing, travel, and leisure activities. These actions include conscious exclusion from employment due to concerns about safety and liability; refusal to rent housing or seat in a restaurant or admit to community venues a person with a service dog; and de facto exclusion from the use of public transit or the Internet because appropriate accommodations are not in place. The summaries of the discrimination complaints received and investigated by the U.S. Department of Justice, the Equal Employment Opportunity Commission, and the other federal agencies with enforcement responsibilities under the ADA indicate that discrimination in these areas still occurs (links to the different agency reports are on the ADA Home Page, http://www.usdoj.gov/crt/ada/adahom1.htm). Issues of discrimination and barriers to accessing the latest services and technologies may be compounded for persons who also belong to racial, ethnic, or low-income groups who have historically experienced disadvantage and discrimination in the United States. To be compliant with antidiscrimination law, decisions about exclusion need to be based on an individualized assessment of safety and risk, and not a “one size fits all” policy. A related issue is the tendency to still use disability segregated programs and services, even when participation in mainstream programs can occur with or without accommodation. The rapid dissemination of new technology is another challenge because not all new technology is designed with universal access in mind. For example, new ovens and washing machines use touch screens for settings. Transportation is another area of challenge because the sprawl of urban and suburban life has occurred without an equal commitment to the maintenance and extension of pubic transportation. The introduction of electric–gas hybrid automobiles presents a different transportation challenge because the silence of these vehicles poses a hazard to those who rely on their hearing to travel safely. The National Federation of Blind has brought this issue to the attention of the public and car manufacturers and there are hopes that a mutually satisfactory solution can be developed (Flandez, 2007). As the 21st century unfolds, new technologies will continue to improve the quality of life and affect the manner in which people work and play in the United States and throughout the rest of the world. Social workers can assume many roles as culturally competent services providers, program planners, and as allies in advocacy of those who have visual impairments or blindness so that the advantages of progress can be enjoyed by all.
Acknowledgments: We thank Corinne Kirchner, A. Judith Chwalow, several field directors, and key informants who have visual impairments for helping us identify the resources and key issues presented in this entry.
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- U.S. Department of Veterans Affairs (2007). Services for blind and visually impaired veterans, Blind Rehabilitation Service, Retrieved February 28, 2007, from http://www1.va.gov/blindrehab/page.cfm?pg=4 (last update, February 20, 2007).
- Warren, D. (2000a). Visual disorders: The psychosocial perspective—Overview. In B. Silverstone, M. A. Lang, B. Rosenthal, & E. F. Faye (Eds.), The Lighthouse handbook on vision impairment and vision rehabilitation. New York: Oxford University Press.
- Warren, D. (2000b). Developmental perspectives: Youth. In B. Silverstone, M. A. Lang, B. Rosenthal, & E. F. Faye (Eds.), The Lighthouse handbook on vision impairment and vision rehabilitation (pp. 325–335). New York: Oxford University Press.
- Wayne State University. (2007). Disability etiquette, educational accessibility services, Retrieved September 27, 2007, from http://www.eas.wayne.edu/etiquette.php
- Willoughby, D. M., & Duffy S. L. M. (1989). Handbook for itinerant and resource teachers of blind and visually impaired students. Baltimore: National Federation of the Blind.
- American Council of the Blind. http://www.acb.org
- ADA Home Page—Information and Technical Assistance on the Americans with Disabilities Act, U.S. Department of Justice, http://www.usdoj.gov/crt/ada/adahom1.htm
- American Foundation for the Blind. http://www.afb.org
- Blind Rehabilitation Service, U.S. Department of Veterans Affairs. http://www1.va.gov/blindrehab/
- Blinded Veterans Association. http://www.bva.org
- Disability Rights Education and Defense Fund (DREDF). http://www.dredf.org
- National Federation of the Blind. http://www.nfb.org. A list of divisions and contact emails are at http://www.nfb.org/nfb/Divisions_and_Committees.asp?SnID=171723160#Seniors