The definition that I find best at the moment is the one by PMLD Network in the UK (in the UK an intellectual disability is called a learning disability):
Children and adults with profound and multiple learning disabilities have more than one disability, the most significant of which is a profound learning disability. All people who have profound and multiple learning disabilities will have great difficulty communicating. Many people will have additional sensory or physical disabilities, complex health needs or mental health difficulties. The combination of these needs and/or the lack of the right support may also affect behaviour.
This definition, though giving a clearer idea of the population, still does not say what it means to have a profound intellectual disability. Having a profound ID means that it is difficult for the person to learn new things. It means it is extremely difficult for them to concentrate, plan, problem solve, and remember. It does not mean that a person can not do these things, but it may take much much longer, and the person may need very different teaching techniques. Sometimes the focus for people with PIMD may not be on trying to teach them a new skill, but on how the people around them support them to do things in a different way (i.e. compensating for the skill deficit). It means that people around the person with a PIMD need to think about different ways that they will share meaning with person. Meaning may not be carried through words, instead meaning may come through actions and experiences.
The "multiple" part of the definition means that the person, in addition to their cognitive impairments, may have physical, sensory, and other health issues. Researchers have reported that the more severe an intellectual disability a person has, the more likely they are to have hearing, vision, physical and health issues such as epilepsy or gastrointestinal issues.
However, despite the cognitive and other difficulties that a person with PIMD has, they are still a person, a family member, a consumer, a friend, and a valuable human being.
2 comments:
Sheridan I have mixed feelings on this. On teh one hand I am concerned about the creation of yet another label that can be applied to people with disabilities that can potentially get in the way of them being seen as people first. Labels can also leade to professional bodies of knowledge expertise and specialisation which have not always assisted services and professional to respond well to human need. On the other had labels can be a way of drawing attention to the specific needs of a groupand in the current rights movement I do not think the interestes of this group have always been well served or even considered and I agree with your comments about advocacy although when I co-orindated a citizen advocacy program we made a point of targetting these type of people for advocates because they would not easily make connections and the citizen advocate was able to build an understanding over time. I can still recall a woman who was deaf, blind and intellectually disabled and her advocate was the only person who could fully understand her method of communication.
Hi David,
I understand your mixed feelings. I too have struggled with this, but have come to a resolution that in order to advocate for improvements for a group an identity is needed. As you said, in your advocacy works the needs of this group was particularly attended to, but by not actually defining the group doesn't it make it harder to pin point.
I strongly believe an identity is necessary for pulling people from margins of invisibility.
(looking forward to chatting with you next week!)
sheri
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