Many students have found that an initial e-mail notification can provide a useful "door-opener" to a subsequent in-person disability discussion with each individual instructor. Here is a sample outline:
Date: Fri 12 February 2010 11:24:50 -0400 (EDT)
From: **ODS student's name**
To: **names of all instructors for the term**
Cc: firstname.lastname@example.org (Carolyn Corbran, Director of Disability Services)
Hello, my name is __________________________ and I am in your class this term. I am writing to inform you that I am registered with the Office of Disability Services and would like to come speak with you about my current situation and any accommodations that might be needed this semester. I would like to arrange a time to meet with you briefly (we can schedule an appointment, or I can come by during office hours) to discuss my disability-related needs. Please let me know of your availability to meet — and I have copied ODS Director Morgan Murray in case you have any questions. Thank you very much.
Yes -- here is a personal tipsheet written by a student with a seizure disorder. This type of tipsheet could also be adapted for students with other kinds of flare-ups, too. Think about your own specific disability-related needs.
I have epilespy, with a history of partial-complex seizures. I take xx of Tegretol XR a day.
Carolyn Corbran (or Assistant)
You will know I am having a seizure when:
What should you do when I have a seizure:
After the seizure:
We'd recommend a new book in the ODS Resource Collection written by M. Catherine Ray: I'm With You Now: A Guide Through Incurable Illness for Patients, Families and Friends. (Bantam Books, 1997).
We have found Chapter 5 to be particularly helpful -- it's called "Bad Days" (pp. 31-34)
A few years ago, after my dad had been sick for several years, an unbelievable thing happened. I actually got two tickets to the Super Bowl. Good tickets, too -- nearly on the 50-yard line. My best friend and I got all settled into our seats and the opening hoopla began. All of a sudden, I felt this rush come over me and I started to bawl. I was thinking about Dad, and all the Super Bowls we'd watched on TV, dreaming how great it would be to see it live one day. And now I was actually there, in person, and he was the one who should have been next to me. But I couldn't even tell him about this -- he has Alzheimer's and he doesn't know me anymore. So here I am, this grown man, sitting on the 50-yard line at the Super Bowl bawling my eyes out. And I'm not one of those quiche-eater guys who cries at the drop of a hat. I could feel people around me looking and wondering -- "What's with this guy?!?" I was mortified. But I just couldn't make myself stop sobbing. And it took me totally by surprise.
"We've always had this family ritual," the wife of a cancer patient confided. 'We play music every morning while we get ready for work and school. One morning, my husband put on Linda Ronstadt and Aaron Neville. Well, that lasted about five minutes! 'Cry like a rainstorm' was exactly what I started to do. I changed the music, but it was too late. Everything just crumpled around me.
"I told my husband I knew I wouldn't be in good shape that day -- it felt like too much of a struggle to try to put myself together. I didn't really want to feel better. I just felt like feeling bad. So, I stayed in bed all day. I took about three naps and cried the rest of the time in between.
"Luckily, my husband knew to leave me alone. Oh, he checked on me every once in a while, but he didn't complicate things by fussing over me. And he never made me feel guilty for giving myself a pity party, even though he's the one who's sick! He just trusted me to take care of myself. In a day or two I was lots better. Even pretty refreshed."
Q. Can a student with a disability take another class as a make-up?
A. No. This is a general Physical Education policy for all students as class lists are set at the beginning of the term with no late or one-time admits permitted.
Q. As a student with a chronic illness, may I "bank" a make-up in the event of a possible/future flare-up of my condition?
A. In consultation with their instructors and on a case-by-case basis, students with disabilities may "bank" a class by participating in any of the make-up opportunities listed on the Physical Education website (e.g. volunteer at one of the two blood drives each semester.)
Q. Do you have any suggestions for particular classes that are disability-friendly?
A. Students with disabilities have found that certain courses are beneficial to their particular needs.
For example, the Wellness class addresses issues pertaining to mind/body/spirit and includes only three classes with mild-moderate levels of physical activity.
You should meet with the Chair of the Physical Education Department or the Director of Disability Services to discuss your specific situation.
Q. If I have a chronic illness and am experiencing a flare-up during class, what should I do?
A. This question falls under the overall attendance/lateness policy. If a student needs to sit out for a brief period (i.e. 5 min), she should speak to the professor and will likely be provided a time-out. However, if the period extends to 10-15 minutes or longer, the student will be referred to the Student Health Service for an immediate check-in. Once again, please be pro-active and discuss your needs in advance with your instructor if you anticipate a large number of flare-ups.
Eleven suggestions regarding postsecondary options for high school students with learning disabilities:
Useful resource: Unlocking Potential: College and other choices for learning disabled people - a step-by-step guide. Barbara Scheiber and Jeanne Talpers. Adler and Adler Publishers, 1987.
Disability and Graduate School Questions to Ask:
Please refer to the Life Safety and Disability Information Sheet published by ODS, Residential Life and Housing, and Safety and Security in 12/07.
You are welcome to bring shelf-stable foods to store in your room (and ResLife recommends that you store all food in air-tight containers).
The Sulzberger lounges have access to microwaves for student use, but there are no refrigerators. Students may arrange for small in-room refrigerator rental by contacting Collegiate Storage and Rental at 718-267-6484. Feel free to call Colegiate and request that the fridge can be delivered directly to your room.
We take all types of student employees: paid, volunteer, Federal Work Study or Barnard College Job Award. As far as jobs go in ODS, we offer an Accommodative Aide position, in which you sign up to aide a student with a disability in many varieties. If you are trying to fulfill a Federal Work Study, it is worth noting that the weekly hours are not guaranteed, and are on a student-need basis. Therefore, it may not be the best option for you, but we would love for you to sign up if you are still interested. Please complete the Accommodative Aide Directory Form and mark the time slots when you are not available. Should you have any further questions, please do not hesitate to contact us.
The Office of Disability Services has loaner laptops. An ODS loaner laptop can be borrowed for up to a week. You will need to sign out the laptop in our Borrower's Book.
If the ODS laptop is unavailable or you are in need of one for longer than a week, there is a company called Computer Overhauls located on 7th Avenue between 30th and 31st. For information on affordable pricing and types of laptops available, visit their website.
Yes — for an office that has a form, policy or tipsheet for just about any occasion — we of course have a response to this frequent query! On a case-by-case basis--ODS can write a *letter of reference* re: the fact that you are registered with ODS, what accommodations you have used, and in general, how you have responded in a pro-active way to your ongoing disability-related needs. If you have worked directly for ODS in some capacity (e.g. Commencement aide, notetaker, office assistant, tutor, etc.) — we may be able to write a *letter of recommendation* as we have direct and specific info re: your performance in the workplace. Please feel free to call ODS If you have any questions about this policy.
There are two routes you can take: The upper campus access route (weather permitting) and the tunnel route.
1. Tunnel route (preferred access route):
Enter the main Barnard gate and turn left at Barnard Hall, taking the south entrance which is ramped. Take either elevator to the basement/ground floor level and follow the tunnel route through Barnard Hall, Lehman, and into Diana LL1. Take any of the two elevators to the lobby (1).
2. Upper campus access route:
Enter main Barnard gate and turn right. Follow brick sidewalk and then go onto the mid-campus path at the edge of the Lehman Lawn. Follow the mid-campus path to the Lehman sidewalk. The Diana Center is on the right.
A commuter locker can be obtained by going to the Bursar (15 Milbank) and paying a fee of $3 and they will give you a receipt. This receipt should then be given to Facilities Services (105 Barnard Hall) who will then assign you a locker.
Lockers need to be renewed yearly and you will receive a letter in your locker when the time to renew arrives. However, the $3 fee is a one time fee.
According to Barnard Facilities Services, the average residence hall summer temperature is 72-78 degrees (F). Heating and cooling guidelines state that when the outdoor temperature is below 55 degrees (F) the heat is turned on - usually around October 1st. In the residence halls with air conditioning, May 1st is the standard turn-on date.
Yes. If you have not previously registered with ODS, you should do so when you apply for disability-related housing. All students requesting specialized housing consideration must follow the three-step procedure outlined in the Disability Housing Request Form. ODS often finds that when students come in to discuss their disability-related housing concerns that there may be other types of needs (especially for students with chronic illnesses) in which ODS registration might be helpful in the future.
Please refer to the air-conditioning info on the housing website, Living on Campus. The information is contained in the section titled "Where You Will Be Living." Air-conditioning is essentially a summer housing option--as the a/c is turned on *only* between mid-May and mid-September.
The 504/ADA Access Committee launched the Access Advocates program in April 2009 and during the summer of 2009 committee members completed the ADA checklist for each Barnard building and residence hall.
Developed in August 1995, the checklist is available from Barrier Free Environments, Inc. and the Institute for Human-Centered Design at http://www.ada.gov/racheck.pdf.
Thinking of faculty, disabled students, and disability services staff as three points of a communications triangle is a useful strategy for dealing with classroom and/or test accommodations. Each of us has unique roles and responsibilities, and the key to effective accommodations is to ensure communication amongst us all. All faculty members at Barnard receive the A Faculty Guide to Barnard College which is published by the Provost's Office. The Guide provides a comprehensive array of useful information, including a section on Administering Course Work for Disabled Students:
"2. Administering Course Work for Disabled Students
In accordance with federal law, it is the College's policy to make reasonable accommodations to meet the needs of students with documented disabilities. Examples of accommodations which have customarily been requested and permitted include exam accommodations such as extended time or modified formats, readers, notetakers, and the use of tape recorders.
Students with disabilities who anticipate needing accommodations are asked to self-identify and to discuss their needs with their instructor at the beginning of each semester. Students who need test-taking or other accommodations should, at the beginning of the semester, consult with their instructor and with the Office for Disability Services (ODS), utilizing the ODS Test Accommodation Form available in Room 105, Hewitt Hall.
All students with disabilities who are registered with ODS have been sent a copy of the College's policy in this matter. Faculty members who wish to receive a copy, or who have any questions may call x44634."
In addition, all faculty receive the Dear Colleague Letter at the beginning of the academic year. The letter encourages faculty to reach out to students with disabilities and discuss disability-related classroom and/or test accommodations with them. All ODS students are expected to self-identify their disabilities at the earliest part of the semester.
See this handout.
Handout provided by Janice B. Rimler, Janice B. Rimler, M.Ed. RID:CT, ASLTA:Professional Interpreter Representative, HANDS IN MOTION Professional Sign Language Interpreters.
There are a number of ways to go about locating a tutor:
There are a few differences between being a Barnard versus being a Columbia notetaker, the biggest one being that the Barnard Notetaking program is solely on a volunteer basis, whereas Columbia notetakers receive payment. Also, Barnard has an Notetaker/Reader Application Form that is passed around the class for sign-up, usually at the beginning of the semester. Columbia ODS sends out emails to students in the class in which a notetaker is needed. We thank all our wonderful volunteer notetakers for assisting their peers!
Yes, we have developed two instruments: one for first-year LD students (11 questions) and another for all graduating seniors with disabilities (9 questions). The LD feedback form is titled: "LD First-Year Summary Interview," and is conducted via one-to-one interview format with all LD first-Year students at the end of their first-year at Barnard. All graduating seniors with disabilities are invited to participate in the Senior Exit Interview Protocol, also completed via a one-to-one personal interview.
LD first-Year Summer Interview
Senior Exit Interview Protocol
Date of ODS Registration
As part of a one-hour workshop on disability issues, we designed the following "Access Scavenger Hunt" which addresses a variety of disability and access-related issues and includes both Barnard and Columbia campuses. Since security personnel are often the first college staff members that campus visitors -- disabled as well as nondisabled -- may encounter, it is imperative that they be familiar with campus access issues, along with the resources provided by Disability Services.
Access Scavenger Hunt
Yes! Try the following:
a. True or False
Institutions must provide access to all existing services.
b. True or False
Institutions may charge separate fees for very specialized services not routinely offered to all students.
c. True or False
Costs of sign language interpreters are the responsibility of the institution.
We have sponsored a number of brown-bag "Dialogues on Disability" and find that a disabled student panel can be an excellent way of providing ongoing disability awareness. Make sure that you have a diverse panel, including students with both congenital and acquired disabilities--as well as students with both visible (mobility, vision, hearing) and hidden (LD, chronic illness, psychiatric disability, etc.) disabilities.
Questions for student panel: postsecondary and beyond
The most direct way to enhance disability awareness and sensitivity is to provide many opportunities for "culture contact" between students with both visible and hidden disabilities and members of the larger campus community. There has been much debate within the field of disability services regarding the use of simulation activities and the positive and (potentially) negative impact of such activities. Two excellent articles on the subject can be found in the archives of AHEAD, the Association on Higher Education and Disability, originally published in 1984.
The Trouble with Simulation (reprinted with AHEAD permission from AHSSPPE Bulletin,Vol. 2, No. 3, Summer 1984)
by Charles E. Hallenbeck, Ph.D., Director, Rehabilitation Psychology Subspecialty, University of Kansas, Lawrence, KS 66045.
There was a practice in Victorian England, popular among the gentry, called "poor-peopling on Wednesday afternoons." It was a practice about which Charles Dickens wrote most eloquently. It did very little for the "poor people," but it was very rewarding for the gentry who practiced it.
I was reminded of that practice recently, when a friend telephoned to read me an item from the local paper. The 28th annual program of the Kansas Association For Retarded Citizens had just been held in Lawrence, and one of its features caught the attention of a reporter. The article, entitled "Group Gets Feel of Handicaps," told of a workshop in which a dozen people participated.
According to the article, "first they were blind, then mute, then they lost the ability to speak and write properly." They completed the workshop "knowing they would not be handicapped when the 2 hours were over" (a remarkable guarantee), "and for some, the most common feeling afterward was relief, because the handicaps they experienced were only temporary." The article went on to say that "even in the artificial setting (of simulated disabilities), participants experienced very real fear, anger, and frustration, often felt by the handicapped." Participants reported that because of their simulated handicaps, their priorities had changed. "Instead of being concerned with the quality of their work," they said, "they were primarily concerned with just finishing it."
My friend knew that the article would concern me, as it did her. As a psychologist and a blind person, I have been a critic of the practice of simulating blindness, as in the so-called "trust-walk" popular on many college campuses. With no training in the alternative techniques of blindness, persons who wear blindfolds are forced to "trust" in the help of others with unobstructed vision. This practice usually strengthens the misconception most people have about being blind. In fact, the trust walk is designed to teach sighted people about dependence and not about blindness. The trust walk is one of the standard techniques of human relations training, where it has only an accidental connection with blindness or blind persons. If, in the process of learning about dependence and trust, harmful attitudes about blindness are reinforced, that is often regarded as a "cost" well worth the "benefit" of the practice. The Helping Hand Strikes Again!
The article in our local paper convinced me once again that there is a great deal of mischief being created by those charged with the task of providing services to others. In expressing this opinion, I run the risk of revealing the "fear, anger, and frustration" the experts tell us is characteristic of the "handicapped." However, with unemployment among adult blind persons of working age still running at 70%, statements such as those concerning the quality of work by the blind must be challenged. I hope that even if I had the X-ray vision of Clark Kent, I would still experience the fear, anger, and frustration that this practice deserves.
I believe that with the proper training in the alternative techniques of blindness, and given a fair opportunity to compete, the blind can function independently as equals in this sighted society. Blindness can be reduced to an inconvenience or nuisance and need not be carried around as a crushing burden to turn life into tragedy and failure. I believe in myself, and look upon my blindness as just another characteristic, much like being from New York or weighing 160 lbs. I manage to lead a productive and gratifying life in spite of my weight, my place of birth, and my blindness.
How then shall sighted people learn about blindness, if not by putting on blindfolds and frightening themselves? That is easy. Get to know someone who is blind. Say hello to the next blind person you encounter on the street, without asking him or her if you can be of help. The blind are not constantly in need of help. Read about the organized blind movement. It has been on the national scene since 1940, and provides a clear voice on matters affecting the blind. There is no need to be afraid or to play parlor games. White persons do not learn about black persons or the civil rights movement by simulating blacks, nor do men learn about women or the women's movement by simulating women. The real trouble with simulation is that it only teaches one what one already knows, and it prevents one from learning anything new. Shall we stand in front of a mirror and marvel at ourselves, or in front of an open window and learn what it is like out there?
Disability Simulations Revisited (reprinted with AHEAD permission from AHSSPPE Bulletin,Vol. 2, No. 4, Fall 1984)
by Jane E. Jarrow, Ph.D., Executive Director, AHSSPPE, P.O. Box 21192, Columbus, OH 43221.
I felt compelled to write this position paper after reading Dr. Hallenbeck's condemnation of simulation exercises as a means of teaching nonhandicapped people about disability (AHSSPPE,Summer, 1984). All of Dr. Hallenbeck's concerns may be justifiable, but as a strong advocate of the use of simulation I think there is another set of possible outcomes to consider.
If the simulation of a given handicap is too brief, it may, indeed, leave the individual fearful, frustrated, and left with that "if-it-was-me-I-couldn't-cope" attitude. I think simulation activities ought to be structured to give the participant a chance to get past the initial shock of not being able to do something -- walk, see, hear, etc. -- and on to exploring what can be done. In my own experience, largely in workshops for college faculty, I find that participants will quickly begin to develop (at least to seek out) compensation strategies. How much time is needed will vary with the task presented, but I like to wait until we are past the "good grief, I can't handle this" and on to the "how-can-I-beat-the-system" stage. Surely, that is what is really important -- not the disability, but the coping. As someone (Cole Porter?) once said, "you've got to accentuate the positive!"
I always structure simulation tasks to be done twice, once with the functional limitations imposed and a second time with the same limitations but with appropriate accommodations provided. In this way, the last thing participants experience is the successful completion of the task regardless of the limitation, rather than the anxiety of being unable to perform. Moreover, I think simulation exercises should always be followed by a de-briefing. Talk about experiences, feelings, etc. Then, if by chance one participant failed to recognize the appropriate coping strategies, someone else in the group can bring them up!
Dr. Hallenbeck proposes to substitute personal interactions with handicapped folks for simulation exercises. I know of no better technique for changing attitudes than such interaction IF it is available and IF it is positive. The first problem in such a program of awareness training is that, human nature being what it is, some of the folks you most want to reach may find one-to-one interaction too threatening to even attempt until they have some objective information about disability and what to expect from a handicapped individual. Then, too, if ALL awareness training is left to personal contacts, you had better cross your fingers that the handicapped folks with whom initial contacts are made are good models for all the things you want that "novice" to learn. Stereotyping is NEVER appropriate, but it happens; its most common underlying cause is lack of information. If you have only met one handicapped person in your life, you are likely to assume that all disabled people have the same skills, abilities, interactional patterns, etc. If the only handicapped person you'd ever met was Helen Keller or Beethoven that wouldn't be too bad (though you would have some very unrealistic expectations for future acquaintances!); on the other hand, if your only contact was with Captain Hook or a bedraggled street beggar selling pencils, it is likely that you would form some very different (and not very pleasant) perceptions. The only way to combat such prejudice (and the restricted freedom and opportunities that it engenders for the disabled population) is through education. I believe everything we teach about disability and disabled people should emphasize similarities, not differences, with able-bodied people. In my experience, simulation exercises can serve this goal admirably when presented appropriately and used judiciously.
A college administrator I know has a sign hanging above his desk which reads:
"In a bureaucracy, the way to manage
is to make YOUR problem THEIR problem!"
I think simulation experiences can be a useful means of achieving that end.
You should dial 711 which will connect you to a Teletypewriter (TTY) Relay Service, which all states have as a requirement of the Americans with Disabilities Act (ADA). Some people who are deaf have a TTY which allows the user to type his/her telephone conversations to the other TTY user. However, if you do not have a TTY, a relay service will enable you to speak through an operator who will read you the responses from a TTY user and type and send your message to the TTY user. Just dial 711 and follow the prompts. There may be a short waiting time and some beeps. Stay on the line and an operator will pick up.
It is toll free to call 711 but you will be billed your standard rate for the call itself.
For more information on telephone services for people with disabilities please visit: http://www.columbia.edu/acis/telecom/index.html.