ASAN Letter to ASHA On The Right To Communicate

autisticadvocacy:

ASAN Letter to ASHA On The Right To Communicate

July 2, 2018

This letter is available as a PDF here.

Dr. Elise Davis-McFarland, Ph.D., CCC-SLP, President, Past Chair, Committee on Committees
Meher Banajee, Chair, ASHA Ad Hoc Committee on FC and RPM
Marie Ireland, Vice President for Speech-Language Pathology Practice, Board Liaison
Diane Paul, ASHA Director, Clinical Issues in Speech-Language Pathology, and Committee Ex Officio
American Speech-Language-Hearing Association (ASHA)
2200 Research Boulevard
Rockville, MD 20850-3289 USA

Via electronic mail:  dpaul@asha.org

July 2, 2018

Re: ASHA’s Proposed Position Statement: Rapid Prompting Method (RPM)

Dear Drs. Davis-McFarland, Banajee, and Paul, and Ms. Ireland:

We write to voice our concerns about the recently issued proposed position statement of the ASHA Ad Hoc Committee on Facilitated Communication (FC) and the Rapid Prompting Method (RPM) (“Committee”), which the ASHA Board of Directors established in summer 20171.  We are deeply concerned that this Committee has failed to engage meaningfully with stakeholder communities, including and especially the self-advocate community. This lack of communication with the individuals most affected by the decisions of the Committee has resulted in a proposed position statement that will dramatically undermine access to communication supports for individuals who have no equally effective alternate forms of communication. As a result, the Committee stands to dramatically undermined ASHA’s mission of “making effective communication, a human right, accessible and achievable for all.”

As autistic self-advocates dedicated to advancing the rights of all people with developmental disabilities – including non-speaking people – we are committed both to ensuring access to a wide range of effective communication supports and promoting research on effective supports. We do not take positions on individual communication support methods or techniques. Nevertheless, we believe each non-speaking person has a right to use the method of communication that works best for them, as determined by an individualized analysis. Moreover, we believe that no single method of AAC will work for all non-speaking individuals.

The Committee’s process has deliberately shut out input from people from disabilities.

When the Autistic Self Advocacy Network attempted in 2017 to learn more about the Committee and offer input, we were denied the opportunity to speak directly to the Committee members or even learn the identities of Committee members. We are also alarmed that to our knowledge, the Committee has never, and never plans to, solicit input from people who use the methods of communication under review, or those who formerly used these methods of communication and then graduated to independent typing.  The Committee has also never solicited input from a self-advocacy organization of any kind.

The Committee’s failure to engage with the community is particularly alarming considering the potential harm that may result from a process that fails to account for the experiences of self-advocates. Due to ASHA’s significant influence over speech-language professionals (SLPs),  we are aware of cases in which educational institutions have alreadyrefused to provide support for students’ most effective form of communication, citing ASHA’s proposed position statement. The likely result of these denials will be isolation from the general education classrooms, exclusion from the general curriculum, and protracted due process proceedings. We are aware of many students who, when denied access to their most effective form of communication, have been forced to move to another district or leave the school system entirely. Denial of communication supports may also result in lack of access to transition-related services, institutions of higher education, and independent living supports. Loss of an effective form of communication can also result in trauma, isolation, and frustration that may in turn lead to escalating “behaviors” and increasingly restrictive interventions.

The Committee’s blanket statement that specific forms of communication are per seinauthentic robs us of the right to communicate.

The Committee’s proposed statement includes the blanket statement that “the use of … facilitator-dependent techniques … is not consistent with the communication rights of autonomy and freedom of expression because the messages do not reflect the voice of the person with a disability but, rather, reflect the voice of the ‘facilitator.’” None of the studies cited by the Committee actually supports such a generalization, nor could they, because no such study ever claimed to evaluate allfacilitator-dependent techniques or all users of any specific technique.

Evaluations of the authenticity of communication should be conducted on an individual basis, taking into account a variety of considerations. Such individualized analysis is not unprecedented.  For example, the medical community has a history of engaging in meaningful discussions on how to evaluate communication by individuals who, due to motor concerns, cannot communicate effectively without the assistance of a facilitator. 2

The proposed statement does not meaningfully address the fact that no other forms of augmentative communication, including those proposed as alternatives, have been evaluated using message-passing or similar tasks. Nor does it acknowledge that some of the proposed alternative interventions – such as Applied Behavioral Analysis – have been found to have no discernible effects on communication ability3, also rely extensively on prompting, and are not themselves a form of augmentative communication. Attempting to wholesale deny the authenticity of a form of communication, regardless of the evidence available with respect to a specific individual, and then assert that unrelated interventions are “alternatives,” is unjust and logically inconsistent.

ASHA’s proposed position statement prevents a false choice between FC, RPM, and other communication supports.

The proposed statement claims, without support, that use of one form of communication necessarily “supplants” access to other techniques. This inaccurate claim is contradicted by the experiences of countless actual AAC users, many of whom use of a variety of different forms of communication, sometimes simultaneously and sometimes at different times and for different purposes. People who use letter-based communication techniques, such as RPM or FC, often also use methods such as indicating choices among options, pointing to multiple-choice answers or word/symbol banks, yes/no signals, PECS, tablet-based AAC apps, sign language, independent typing, and spoken words or sounds to communicate at different times.

To the extent that people with communication-related disabilities do not use the communication methods that the committee proposes as alternatives, it is often because those methods do not work for those individuals. Cutting off access to one form of communication, in the absence of other methods that are equally effective for that individual, is unethical and harmful. Although we agree that far too many non-speaking people have not been offered communication supports that are evidence-based and effective, taking away communication options is not the answer. Rather, we urge ASHA to take seriously the evidence that there is a critical unmet need in school districts across the country for effective, wide-scale implementation of robust AAC options, and to focus its efforts on meeting that need.

The Committee’s proposed position statement inappropriately equates absence of peer-reviewed studies with evidence that an intervention is ineffective.

Although we support formal research on communication, a significant number of communication methods have no supporting body of formal research pertaining specifically to that communication method. Rather, SLPs may recommend communication supports based on other sources of evidence, including general research on motor planning and language learning, combined with individualized evaluation of the individual in need of communication supports.4

The Committee’s proposal to restrict SLPs’ use of a communication method, based entirely on the absence of message-passing studies supporting the specific method in question, therefore threatens to set a dangerous precedent that may obstruct individuals’ access to a wide variety of communication supports. This precedent is especially threatening to those who have discovered communication methods that are highly individualized and thus not amenable to formal academic research.5

Conclusion

ASAN therefore recommends against adoption of the proposed position statement of the ASHA Ad Hoc Committee on Facilitated Communication (FC) and the Rapid Prompting Method (RPM). Adoption of the proposed statement would dramatically undermine the right of all people to the individualized supports they may need in order to communicate. 

Sincerely,

Samantha Crane, J.D.
Director of Public Policy, Legal Director
Autistic Self Advocacy Network

ASAN Letter to ASHA On The Right To Communicate

Want to help me with my research into the voices of autistic adults in autism discourse?

myautisticpov:

So, hey, as you may or may not know, I am currently doing my MA dissertation on how expertise is incorporated into the autism discourse in the UK.

I have collected data on whose voices are currently being listened to, but now I would like the views of autistic adults to compare what we want with what the designated experts are pushing for.

So, for the next two weeks (until the end of July 2018), I’m running a Discord server for autistic adults from the UK* to discuss what we want, in terms of legislation and services, from the government and charities.

*So, basically, you have to be 16+ and have spent a significant of time living in the UK as an adult in the past decade.

If you meet these criteria and want a link to the Discord, send me a message. It can just say “Discord?” and I will send the link. Obvs, it can’t be an anon message, though.

Here is more detailed info on the server:

This server is for discussions of what UK autistic people would like to see in terms of legislation and services provided by the government and charities for autistic people. This discussion is part of a study on lay expertise and autism in the UK as part of an MA in Sociology and Social Research at Newcastle University being undertaken by L.C. Mawson, the creator of myautisticpov.com.

The server will run for two weeks and participants are free to join and leave the server as they please. If you would like to withdraw from the study completely, including removing your contributions to the discussion, you can contact Mawson at l.c.mawson@ncl.ac.uk to do so.

Your data will be anonymised, with only your nickname on this server being associated with your messages (right-click on your name on the user list on the right-hand side to change your nickname), not your real name.

This study is only looking at the experiences of autistic adults in the UK – this includes adults anywhere within the diagnostic process including those who are self-diagnosed and UK citizens who are currently living abroad – so please do not enter this server if you are not living in the UK, or are not an autistic adult (16+).

If you’re not eligible to participate, signal boosts would still be massively appreciated!

rob-anybody:

“‘Because she likes people,’ said the witch, striding ahead. ‘She cares about ‘em. Even the stupid, mean, drooling ones, the mothers with the runny babies and no sense, the feckless and the silly and the fools who treat her like some kind of a servant. Now THAT’S what I call magic–seein’ all that, dealin’ with all that, and still goin’ on. It’s sittin’ up all night with some poor old man who’s leavin’ the world, taking away such pain as you can, comfortin’ their terror, seein’ ‘em safely on their way…and then cleanin’ ‘em up, layin’ ‘em out, making ‘em neat for the funeral, and helpin’ the weeping widow strip the bed and wash the sheets–which is, let me tell you, no errand for the fainthearted–and stayin’ up the next night to watch over the coffin before the funeral, and then going home and sitting down for five minutes before some shouting angry man comes bangin’ on your door ‘cuz his wife’s havin’ difficulty givin’ birth to their first child and the midwife’s at her wits’ end and then getting up and fetching your bag and going out again…. We all do that, in our own way, and she does it better’n me, if I was to put my hand on my heart. THAT is the root and heart and soul and center of witchcraft, that is. The soul and center!’ Mistress Weatherwax smacked her fist into her hand hammering out her words. ‘The…soul…and…CENTER!’ Echoes came back from the trees in the sudden silence. Even the grasshoppers by the side of the track had stopped sizzling. ‘And Mrs Earwig,’ said Mistress Weatherwax, her voice sinking to a growl, ‘Mrs. Earwig tells her girls it’s about cosmic balances and stars and circles and colors and wands and…and toys, nothing but TOYS!’ She sniffed. ‘Oh, I daresay they’re all very well as decoration, somethin’ nice to look at while you’re workin’, somethin’ for show, but the start and finish, THE START AND FINISH, is helpin’ people when life is on the edge. Even people you don’t like. Stars is easy, people is hard.’ She stopped talking. It was several seconds before birds began to sing again. ‘Anyway, that’s what I think,’ she added in the tones of someone who suspects that she might have gone just a bit further than she meant to.”

— Terry Pratchett, “A Hat Full of Sky”
(via currentboat)

justsomeantifas:

If you or anyone you know is going to be reunified with children who have been separated at the border then I’d suggest printing this pamphlet recently created to guide parents through the trauma this experience has caused. The pamphlet may also be useful to attorneys, paralegals, clergy, those working in shelters, and others who are involved with these families.

“This pamphlet was prepared by mental
health professionals to help you, your child
and your family recover from the forced
separation you have been through. It is
created to let you know what to expect as a
parent, how to understand reactions from
your child that may be confusing or
difficult, and how to find help as you and
your child readjust to being together again.”

English pamphlet

“Este folleto fue preparado por profesionales
de la salud mental para ayudarlo a usted, a su
hijo y a su familia a recuperarse de la
separación forzada que han sufrido. Fue
creado para que sepa qué esperar como
padre, cómo entender las reacciones de su
hijo que pueden ser confusas o difíciles, y
cómo encontrar ayuda mientras usted y su
hijo se reajustan a estar juntos nuevamente.”

Folleto en español

psa

wouldyoukindlynotbegross:

okay peeps; its time to have a talk.

If you see ‘someone’ has axed your caption and replaced it with this

These are just bots.


You need to just flag it as spam and block them.


Last time there was a spam problem; the wonderful tumblr staff said not to reblog from them because “it makes it harder to tell bot blogs from real blogs”.

So pretty pretty please dont reblog from them; just report them as spam and block them.