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Policy Analysis Final - Medical Documentation
Policy Analysis Final - Medical Documentation
Dis St 433
Policy Analysis Final
Executive Summary
A huge barrier for students with disabilities in post-secondary education in the United
This requirement poses a cost barrier, a challenge for populations who may be distrustful of the
medical system, and creates unnecessary stigma attached to the label of ‘disability’ for those who
may not necessarily identify that way. There is no explicit requirement within the Americans
with Disabilities Act (ADA) or Section 504 of the Rehabilitation Act that requires colleges to ask
for medical documentation, but it has become a standard practice due to decades of medical
model influence on society’s conceptions of ‘disability’. Some policy alternatives that could
address this barrier include providing financial aid to those seeking medical documentation or
setting nationwide standards for what kinds of documentation are allowed in post-secondary
education settings. However, the best policy alternative would be shifting towards a universal
design ideology and setting standards for inclusively designed classrooms, which bypasses the
when accessing many types of reasonable accommodations for people with disabilities. Although
this pattern is also found in other areas like social security benefits, for the purposes of this
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I am a college-educated woman who does not identify as disabled. However, I am a CODA (Child of Deaf Adults)
and I have worked for several years in a disability advocacy organization within the University of Washington, with
the overall goal of eliminating barriers in higher education for disabled students.
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analysis, I will be focusing on the relevance of this pattern within post-secondary education
institutions. A great majority of universities across the country list medical proof of a disability
documentation is often not as easy as it sounds. This may pose as a barrier for students seeking
accommodations, particularly those who are developing new diagnoses in college, transitioning
from high school with insufficient documentation, or experience changes in their state of
The cost for a medical evaluation can be incredibly high, making it near impossible for
those without health insurance to pay for. For example, testing for ADHD takes several months
and ranges from a few hundred dollars to thousands of dollars, if not covered by health insurance
(“ADHD” 2010). If a student is disconnected from their parents’ medical insurance or comes
from a low-income family that doesn’t have medical insurance, the cost of testing could pose a
huge barrier in accessing the accommodations they need. The length of time that testing requires
could also pose a barrier; every day that testing is happening means another day that a student is
system, causing them to avoid medical centers altogether, which may discourage individuals
from seeking a diagnosis to begin with. For example, African Americans have a long history of
2014). That, in combination with racial bias, has resulted in a community-wide common distrust
of the medical system more broadly, which means it’s less likely for African Americans to feel
comfortable seeking medical diagnoses for disabilities they may have. This trend remains true
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for many other marginalized groups as well, including LGBTQ+ folks, those who don’t speak
English, and other racial minorities like Native Americans or Latinx populations.
Finally, navigating the medical system and insurance schemes at a time in life where an
adult is typically separated from their parents can be overwhelming and confusing, especially
when seeking a possibly new diagnosis. This could represent a new part of their identity that
they may not be ready to address. Disability is a complicated label that not everyone chooses to
identify with. It comes with a lot of stigma, depending on what kind of disability you may have
and the spaces you’re in. Some may avoid getting a medical diagnosis due to that stigma and
When you look at historical contexts, the tendency to require medical documentation
makes sense, despite the clear barriers. For decades, the concept of disability has been dominated
by medical influence. The medical model of disability places the ‘issue’ onto the individual,
therefore stating that body diversity is undesirable and should be ‘fixed’. When an institution
disability”, forcing a person to prove that they are ‘different’ in a medical way in order to make
their environments accessible. This concept is what underlies all of the ADA, since it requires
automatically promotes this ‘deviance model’, which aligns with the long history of medical
Stakeholders
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The main stakeholder group in this issue is students with disabilities in higher education.
Two thirds of students with disabilities who enroll in a four-year college or university don’t
graduate within eight years (Preston 2019). In order to reduce these dropout rates, all efforts
must be focused on reducing barriers for students with disabilities, which includes the issue of
medical documentation.
The other stakeholder group in this issue is the post-secondary education institutions that
are providing the services. While there is a lack of current research on this topic in American
universities, there is reason to believe that many disability services offices within these
institutions are understaffed and underfunded, to the point where they only cover ADA/Section
504 compliance and go no further. There is a strong possibility that these universities utilize
method of reducing caseloads. However, there is more research needed in this area in coming
years. There is also a prominent false belief within higher education institutions that lowering the
standard for documentation will make it so that other students can “take advantage” of the
services offered. Work is needed in these institutions to show that lowering the documentation
requirements will not result in negative effects, but rather will be beneficial to disabled students.
Current Policy
In terms of current policy, post-secondary institutions are covered by both the Americans
with Disabilities Act (ADA) and Section 504 of the Rehabilitation Act. The specific
requirements vary a bit depending on if it’s a public or private institution, but the wording
regarding reasonable accommodations is about the same. This is compared to K-12 education
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institutions, who are covered by the Individuals with Disabilities Education Act (IDEA). More
specifically, those who require curriculum modifications are covered by the IDEA, whereas all
students with disabilities are covered under Section 504 and the ADA.
None of the laws regarding reasonable accommodations state anything explicitly about
requiring medical documentation, but they do insinuate that schools may set their own
reasonable standards for documentation. According to the Office for Civil Rights under the US
diagnostician.” (Duncan 2020). In basic terms: colleges and universities are not required to ask
for medical documentation, but they are allowed to, as long as it serves as “reasonable” and
Under IDEA, public K-12 schools are required to provide free evaluations for children
suspected of certain disability types, which makes it so that parents do not have to seek medical
documentation out independently (in most scenarios). Post-secondary institutions, however, are
not covered by IDEA, and therefore do not share that responsibility (Duncan, 2020). The cost of
The requirements for medical documentation often change once a student leaves K-12
education and enters college. In K-12 systems, Individual Education Plans (IEPs) or Section 504
plans are established for students with disabilities, but even those aren’t usually sufficient
documentation to “support the existence of a current disability”, meaning that a student has to get
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A student could seek out free evaluations through their state’s vocational rehabilitation agency, but that’s only if
you already know about that resource and you do choose to identify as having a disability.
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After further consideration, it may seem that requiring specific, extensive medical
a ‘burdensome process’, which goes against the ADA amendments provided from a court case
against Boston University in 1997. This states that “a university is prevented from employing
individuals with disabilities from establishing that they are entitled to reasonable
place, students around the U.S. are still struggling to get their accommodations, as shown by an
online publication from the U.S. Department of Justice stating that “the Department continues to
receive questions and complaints relating to excessive and burdensome documentation demands”
(“Testing Accommodations”). There is a clear need for new policy implementation in order to
address this gap between what the ADA intended and what is currently practiced in many
university settings.
Policy Options
There are several ways that policies could be implemented in order to address this issue.
Colleges could provide financial support to students who are seeking medical documentation, but
that would require them to navigate the already-complex financial aid system and wouldn’t
address the stigma and medical-system-avoidance barriers. Another alternative would be to set
nationwide standards for documentation (ones that encourage use of student testimonials instead
of purely doctor’s notes), but that still doesn’t really help those individuals who are not ready to
identify as ‘disabled’ but could still benefit from accommodations. Finally, the best policy
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alternative would be to adopt nationwide Universal Design standards, which surpasses the need
One way of addressing the cost barrier to getting medical documentation would be to
mandate that post-secondary institutions provide financial support to students seeking said
documentation. This would relieve the pressure of payment for those individuals who may not be
covered by health insurance and cannot afford to seek out a diagnosis. However, the actual
implementation of this process may be tricky. Many questions would need to be answered: What
kinds of diagnoses will be funded? How much financial support will be provided? Where in a
college’s budget would that money come from? How do you then accommodate the rising
number of students seeking these accommodations after this cost barrier is reduced?
If the financial support was provided through the typical financial aid system that most
colleges utilize, then that’s already fraught with issues. Many middle and upper-middle class
families aren’t served well by the algorithms used by the national financial aid estimation system
(FAFSA), often left with price tags for college that their families realistically cannot afford
(Lobsoco 2016). Additionally, the financial aid system is difficult for almost everyone to
navigate. Approximately “half of American high schoolers eligible for government financial
aid… don’t even submit an application” due to the level of complexity it entails (Hess 2018). If
just getting financial aid for college tuition is difficult, it is almost undeniable that urging
universities to build medical documentation support into their financial aid systems is going to
result in further complexity, which will still dissuade students away from seeking the
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The implementation of this alternative would be tricky, since the process would be
different for each college/university. Alternatively, states could provide funding for seeking
medical documentation, but ensuring that all students get routed to those resources would be
even more tricky. What criteria would states use to give out that funding? Is this something that
This policy alternative only addresses one of the three main barriers: cost. The avoidance
of the medical system and the stigma of ‘disability’ remain, which means that the problem can’t
fully be solved this way. It is an alternative, but perhaps not the most ideal one.
Another way to address this barrier would be to adopt the AHEAD (Association on
Higher Education and Disability) conceptual framework for appropriate practices in providing
disability”, which means moving away from the medical model of disability and focusing on
This conceptual framework outlines the various types of documentation that a student
should be able to use in order to get accommodations. The primary type of documentation is a
student’s self-report. According to AHEAD, “It is often possible to evaluate whether a requested
student themselves are the primary source of their experience, so listening and validating their
experience of disability is much less stressful than needing to rely on medical documentation. If,
for any reason, the student’s self-report isn’t clear or convincing enough, you can also rely on
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observation and interaction with the student (secondary source). Those who are granting
experiences of disability-related interviews and using that to observe and evaluate the students’
claims about disability should be a comfortable, easy process. Keep in mind that this should not
be done through a criticizing, medical lens, but rather one of validation and sensitivity. The
advisors in disability services offices shouldn’t be the gatekeepers of accommodations, but the
guides to success.
If, for any reason, these two types of documentation are not enough, then AHEAD
recommends seeking out the third type of documentation: “information from external or third
parties”. This may include many different sources like educational or medical records, reports
from psychologists, teachers, or the educational system broadly. Examples of these kinds of
records include IEPs or Section 504 plans provided by K-12 educational systems. Even within
this category, there are still many other alternatives to medical documentation that should be
the context of the academic course, program, or activity. In some ways, this is positive, since it
means the process is tailored to what the individual needs. However, this may be granting a bit
too much wiggle room for post-secondary education institutions to get out of giving
of disability to accommodation”) that means it may be more difficult to legally hold a college
accountable for requiring extensive medical documentation since it’s an ‘individualized process’.
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Adopting this alternative as legal policy would need to happen on a federal level, so that
the guidelines don’t vary dramatically from state to state. If it were implemented, it would give
students the legal grounding they would need to go after the colleges that are demanding too
much documentation.
This alternative does address a few of the barriers: namely, cost and avoidance of the
medical system. However, one thing does remain: stigma of disability. For those who are
experiencing a new disability or choose not to identify as disabled, they are still unlikely to
There is only one alternative that goes above and beyond in addressing the barriers
presented, and that’s universal design (UD). UD is the “design and composition of an
environment so that it can be accessed, understood, and used to the greatest extent possible by all
people regardless of their age, size, ability, or disability” (“What is Universal Design”). The use
of universal design bypasses the need for disclosure of disability altogether, aiming to create
Universal design in a higher education setting takes many different forms. This may
include things like remote access to course materials and lectures for students who cannot be
there in person. It could mean creating alternative pathways to turn in work or to show
‘participation’ in class, like mandatory notetaking to share with the rest of the class. It means
using microphones, captions, trigger warnings, ensuring mobility-aid friendly layouts and scent-
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sensitive spaces, and so much more. Universal design doesn’t just cater to students with
disabilities; it also helps other groups of students like veterans, student parents, commuter
students, working students, religious minorities, etc. Some professors have already taken it upon
policy would also need to include guidance and support for professors. Many professors don’t
know how to operate the technology that is necessary for lecture capture, captions, microphones,
etc. One suggestion would be to create online resources and guides for these things, or another
solution would be to require each college/university to hire a ‘Universal Design Consultant’ that
can assist in the implementation of these accessibility measures. This person would also (ideally)
be responsible for promoting awareness and understanding of the importance of universal design.
Additionally, even with universal design standards, there would still be some individual needs
that need to be met. Each college’s disability services office would still need to serve students
whose specific needs are still not met by the UD standards, leaving some room for
There are many reasons that this would make for an excellent policy alternative. It
bypasses the need for disability disclosure altogether (for most disabilities) and serves many
other communities outside of disabled students. There would be no need for medical
documentation altogether, and the burden of seeking accommodations would be taken off
disabled students, which would presumably push them closer and closer to success.
However, due to the current dominant view of disability being the medical model, the
probability of such radical legislation happening right now isn’t very high. Most people see the
accommodations model as sufficient: whoever deviates from the norm must be catered to
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individually, rather than changing the environment to fit their needs. It would require a drastic
cultural shift and the commitment of professors to transform the typical higher education
environment into something accessible. However, this cultural shift is possible. Even now, at the
University of Washington, there are student and faculty advocates that are working towards a
standard of universal design in teaching, events, and even just campus life. In order to shift
society’s views on disability, this work needs to continue: promoting a nationwide understanding
of the social model of disability and encouraging each other to make accessibility a priority
The stakes are high. Students with disabilities are being denied their necessary
accommodations every day, simply because they cannot access the medical documentation that
is required. Asking students time and time again to prove their disability is unnecessary,
degrading, and harms their chances at academic success. There’s a lot of work required to
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Work Cited
“ADHD: Costs of ADHD Tests - Consumer Reports.” ADHD | Costs of ADHD Tests -
Consumer Reports, July 2010, www.consumerreports.org/cro/2013/01/how-much-does-
it-cost-to-test-for-adhd/index.htm.
“Guckenberger v. Boston University, 974 F. Supp. 106 (D. Mass. 1997).” Justia Law, 15 Aug.
1997, law.justia.com/cases/federal/district-courts/FSupp/974/106/1450834/.
resources/accommodations/documentation.
“The Documentation Disconnect for Students With Learning Disabilities: Improving Access to
Postsecondary Disability Services.” The Documentation Disconnect for Students With
Learning Disabilities: Improving Access to Postsecondary Disability Services | LD
Topics | LD OnLine, National Joint Committee on Learning Disabilities, 2007,
www.ldonline.org/article/22240/.
“University of Washington Policy Directory.” SGP, Student Policies, Chapter 208, Reasonable
Accommodation of Students with Disabilities, Dec. 2019,
www.washington.edu/admin/rules/policies/SGP/SPCH208.html.
“What Is Universal Design.” Centre for Excellence in Universal Design, National Disability
Authority, universaldesign.ie/What-is-Universal-Design/.
Duncan, Arne. “Students with Disabilities Preparing for Postsecondary Education.” Office for
Civil Rights, US Department of Education (ED), 10 Jan. 2020,
www2.ed.gov/about/offices/list/ocr/transition.html.
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Duncan, Arne. “Transition of Students With Disabilities To Postsecondary Education: A Guide
for High School Educators.” Office for Civil Rights , US Department of Education (ED),
10 Jan. 2020, www2.ed.gov/about/offices/list/ocr/transitionguide.html.
Hess, Abigail. “Bill Gates: The American College Financial Aid System Is Failing Students.”
financial-aid-system-is-failing-students.html.
Lobosco, Katie. “Too Poor to Pay for College, Too Rich for Financial Aid.” CNNMoney, Cable
aid/index.html.
Preston, Caroline, et al. “The Vast Majority of Students with Disabilities Don't Get a College
Degree.” The Hechinger Report, 13 Apr. 2019, hechingerreport.org/vast-majority-
students-disabilities-dont-get-college-degree/.
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