[Georgia_ahead] FW: Currency of Documentation and Disability-Landau-Kleffner Syndrome
Bonnie Martin
bmartin at gpc.edu
Wed Jul 9 16:27:21 EDT 2008
I apologize for cross posting.
Below is an interesting discussion from two respected "old- timers" in
the DSP profession. If you are going to AHEAD, and you have not met
either Jim or Linda, they are probably both presenting---and I think Jim
is on the AHEAD Board.
This discussion started with a posting from a DSP at a college where a
student presented documentation for Landau-Kleffner Syndrome from when
the student was in grammar school.
Bonnie
Bonnie S. Martin, Director
Disability Services
Georgia Perimeter College
678-891-3385
________________________________
From: Disabled Student Services in Higher Education
<DSSHE-L at LISTSERV.BUFFALO.EDU> [mailto:Disabled Student Services in
Higher Education <DSSHE-L at LISTSERV.BUFFALO.EDU>] On Behalf Of "Marks,
Jim" <marks at MSO.UMT.EDU>
Sent: Wednesday, July 09, 2008 2:15 PM
To: DSSHE-L at LISTSERV.BUFFALO.EDU
Subject: Re: Currency of Documentation and Disability-Landau-Kleffner
Syndrome
It's good to debate elements of our profession, and I agree that
disagreement in an environment of mutual respect is terrific and
essential. Thing is, I'm not sure what we disagree on because we both
favor the appropriate use of documentation.
One exception may be that I definitely disagree with the bogus "unfair
advantage." No such a concept exists except in the world of disability
oppression, and I sure wish we would stop using the prejudiced term.
Another point of disagreement may be in the use of the word, "needs."
Our profession should focus on rights, not needs. We're here to prevent
discrimination on the basis of disability, not to conduct some sort of
hybrid charity within the walls of the ivory tower. Talking about needs
sends us down a path that permits us to ignore discrimination.
Disliking "unfair advantage" and "needs" in professional discourse is
more than just a pet peeve or a matter of semantics. They give us
windows into the very center of how with think and act in our
profession.
Getting back to the matter of how much third party evidence is
necessary, I think DS officers should get the evidence relevant to the
two purposes outlined in the AHEAD documentation guidelines. In other
words, I have no problems getting third party evidence when it makes
sense to do so. Perhaps our disagreement is more a matter of degree. I
get far better information relevant to my job from the student, not the
third party diagnostician. I can ask questions based on function that
help sort out what is at stake in the program modification process. I
always start with the student and then make a decision as to whether I
want more evidence to support student requests. Sometimes, the third
party evidence is useless, and I will not put students through hoops
unreasonably. Other times, the third party evidence is absolutely
essential.
To be frank, I abhor those entities who go for the third party evidence
first or, worse yet, those who never even interview the student. For
example, many in the high stakes testing industry do not talk with the
student and rely solely on third party evidence. That's an inhumanity
higher education can avoid. We actually get to talk with students, and
the things we do can be supported by solid practices. Some argue that
our profession is full of people who don't have the kind of experience
and judgment it takes to interview students. It's true that we have a
lot of professional development to work on. But we cannot fill this
void with one-size-fits-all approaches that neglect the individual and
over emphasize authorities outside of the student-institution
relationship. We must think and act responsibly in our profession.
Besides that, it takes piles of professional judgment to interpret the
third party evidence. I've been a DS officer for twenty years and read
many documents. Oftentimes, the diagnostic documents tell me very
little relevant to the things I need to know to do my job. Diagnostic
documents usually deal with purposes outside making higher education
accessible, and the idea that documentation will provide the best
evidence for program modifications is unsupportable in many instances.
Even making a determination as to whether the diagnostic evidence alone
verifies civil rights protections can be a stretch. Professional
judgment is essential. . I guess I just don't get why many colleagues
reach so vehemently for information that often turns out to be useful
only within the context of what the student tells us. Our profession
should emphasize a deliberate discussion with students to give evidence
of disability and its impact relevance and meaning. Surely we agree
that the student is key. Otherwise, we're just building documentation
castles in the sky. We're also adding barriers to higher education,
which is counter to our mission of making higher education accessible.
-----
Jim Marks
Director of Disability Services
University of Montana
jim.marks at umontana.edu
http://www.umt.edu/disability
-----
-----Original Message-----
From: Nissenbaum, Linda D. [mailto:LNissenbaum at stlcc.edu]
Sent: Wednesday, July 09, 2008 9:51 AM
To: Marks, Jim; DSSHE-L at LISTSERV.BUFFALO.EDU
Subject: RE: Currency of Documentation and Disability-Landau-Kleffner
Syndrome
I really have to disagree with Jim, and I know from past experience that
we can agree to disagree and continue to respect each other's
professional view.
So, here is my professional opinion on the topic:
If we are going to be the DSS Office for our colleges and universities,
then the current documentation of the disability has to come first
especially with 'hidden disabilities. We should not minimize the
importance of structured interviews as they are essential. However,
there are many reasons why a student may have difficulty with 'study',
and much of it may not have anything to do with a disability.
If we are giving accommodations to level the playing field for students
with disabilities, then we first need to know: Does this student even
have a disability? (It is possible that the seizures in her earlier
years caused brain abnormalities which require accommodations? Is it
possible that the syndrome lasted for a short time, and there are no
long-lasting affects from it? I don't know, but current documentation
should tell me this.) Next, does the disability currently rise to the
level that it requires accommodations for equal access? While she may
have had a syndrome in the past, the information provided was from when
the student was 9 yrs. old. Surely, if this is a disability that
warrants the need for accommodations, the student would have been
followed throughout her years by a doctor, etc. Thirdly, what is the
nexus between the disability and the accommodations requested? And,
lastly, do the accommodations have an opportunity to provide equal
access for the student?
I'm all for UDI in its fullest sense. And, if our colleges and
universities are going to start looking at each individual student's
needs and providing each student with whatever is requested, then that
would be the best of all worlds. However, if we are being asked to
provide and determine accommodations for student with disabilities in
order to provide them an opportunity for equal access and not an unfair
advantage, then we need to be sure that our requests are credible. And,
this requires that we get current documentation of disability ( with
currency being determined by the professionals who diagnose the
disability and not us), and also request structured interviews with the
student. Based on the documentation and the structured interview, we
should be able to answer the questions stated above and work under the
intentions of our offices.
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