Some key points and reminders on the understanding of CVI children's learning and vision; and interactions of teachers, therapists, trainers, carers, and parents with CVI children.



Key points in this article:

1.It is difficult to have a clear and full understanding of the visual ability of children with CVI (cerebral visual impairment/ cortical visual impairment).
2.Visual problems are affected by a list of factors, how could we understand the visual problems of CVI children?
If CVI children have multiple disabilities or severe intellectual disability, or severe physical disabilities, their means/modes of expressions might be restricted. As a result, they could not give the appropriate responses. In other words, no response or incorrect responses do not imply that they could not see, have no sensations, have low learning ability, could not think properly, have no memory, or no interest …
3.Imagination and memory are very important, but they need meaningful experiences to build up.
4.During teaching, training, therapies, and services, CVI children should establish relationships with people. This is more important than making contact with objects.
5.Teachers, therapists, service providers and parents should try to elicit CVI children’s responses from the social-emotional perspective.

1. It is difficult to have a clear and full understanding of the visual ability of children with CVI (cerebral visual impairment/ cortical visual impairment).

For CVI students who have deficits in visual performance due to brain damage, I always think that it is really difficult to understand what kind of ‘picture’ is the image that the student is ‘perceiving. What is the difference between their perception and the perception of people with normal vision?

As the aspects of vision (e.g. visual acuity, visual field, contrast sensitivity, binocular vision, night vision, color vision, intra-ocular pressure, muscle control, sensitivity to lighting etc.) are more than the aspects of hearing, and as these aspects interact with each other, even ophthalmologists or optometrists could not accurately evaluate the various aspects of vision in children with CVI.

What’s more, if the child has intellectual disability, then there is an additional factor that multiplies the difficulty of accurate assessment results. We could never be sure of the reasons that account for incorrect responses of CVI children, e.g. was it because he couldn’t see or because his brain had difficulty in processing the particular visual information, or whether it was due to intellectual limitations, so he could not understand the instructions or could not give the expected responses, or whether he was afraid of unfamiliar people, unfamiliar environment, not cooperative, was not willing to show his response, or whether it was due to limitations in his fine motor (movement and control of his hands and fingers).

2.Visual problems are affected by a list of factors, how could we understand the visual problems of CVI children?

To us, it seems that CVI children who are ‘looking but could not see’ have weak abilities or even without response. But no response doesn’t always imply that they could not see. Maybe the reasons are that they could not give response or any indication. Thus, it is only through the establishment of a close relationship with individuals and through long term, detailed and repeated observations, analyses, and inferences, that parents, teachers, and caretakers could understand them more.

3. Imagination and memory are very important, but they need meaningful experiences to build up.


What the film ‘The Diving Bell and Butterfly’ indicates to us

'The Diving Bell and Butterfly' was an Oscar Award Film, which was based on a book about a real subject. The subject was a renowned editor of a French magazine. He suffered stroke because of a car accident. As a result of the accident, this man could not move his body, as if he was confined in a diving bell. He could not express himself, nor could other people understand him. Although he still had a lot of feelings and thoughts running in his mind, his body was confined physically. Moreover, the confinement was severe. Although he still had sensations and thoughts, nobody bothered about him.

Later, a speech therapist discovered that this man could use different blinking patterns of his eyes to represent the French alphabets, and this mode of expression had opened a means of expression for him. In fact, he still retained his intellectual ability and his brain was still working. He ultimately wrote this book about what he had learnt from his unusual experience of being a healthy person initially but then turned into a totally confined and impaired person.

I encourage people who work with severely handicapped children to read this book and understand the 'internal world' of people who are physically restricted and severely confined. The author of the book had made one remark that was very touching and inspiring, “At least, I still have memories and imagination.”

Memories

Why are memories important? For life is comprised of the ability to remember and memories of the past. However, if there is no experience, how could there be memories? Memories are one interesting aspect of human beings, as what have happened would be kept in a certain part of the brain. The question is how to retrieve memories.

Therefore, it is very necessary to form memories for severely handicapped children like children with CVI, especially multi-handicapped children. For if they are already being confined visually, we should help them form emotional, sensory and tactile memories instead. But surely, the experiences that are provided to CVI children should be meaningful, in order that memories could be formed, instead of incidences linked together that have no reason or meaning.

Imagination

Imagination is also another very amazing aspect. If we lack imagination, we will suffer great pain. Because if we have imagination, it is like a window that is opened in order that thoughts could be freed. For children who are severe handicapped, do they also have imagination? I think they surely have. For only when they have memories, could they correlate with ‘a picture’ (situation) in their memory, whether it is a visual form of picture or auditory form of ‘picture’, or the smell of people and the environment … No matter whether the ‘picture’ is vivid or blurred, this particular picture (situation) would be formed in their memories. Although we could never know how they could see or what they have actually seen, I believe that their feelings are very real.

4. During teaching, training, therapies, and services, CVI children should establish relationships with people. This is more important than making contact with objects.

For CVI children whose visual abilities are weak, they generally seem to have greater reactions and interests in objects. But in fact, people should be more important than objects. They need not make contact with lots of objects, but the top priority in their experiences should be in contact with people. When they have feelings toward people, when they have the motivation to communicate and interact, then wahen people introduce objects to them for learning, this would be faster, easier, happier, and more holistic.

Therefore, no matter mild or severe intellectually disabled children, if the people that the individual child has contacts with are people that he/she likes, he/she would learn a lot faster, better, and with higher motivation. If teachers or therapists in the classrooms do not interact with the child when giving an object to the child but just describe it, the child would actually find it difficult to grasp the meaning of the description.

5. Teachers, therapists, service providers and parents should try to elicit CVI children’s responses from the social-emotional perspective.

Particularly for visual training in the past, people assumed that CVI children have difficulty in receiving different sensory inputs at the same time, or that complexity in the environment would affect the CVI children’s concentration. Consequently, training often takes place as the visual stimuli were presented to the child without description or auditory input. Such a training style might have helped CVI children to concentrate, but lacks the opportunities for the child to have emotional interactions with people, which subsequently lowered their motivation in learning/giving response. What's more, the CVI child may not be able to understand what is happening and so he would not respond.

Therefore, teachers, trainers, therapists, caretakers, and parents should beware of this and the top priority should be given to developing relationship with CVI children, especially close and caring relationships, and try to elicit the responses of CVI children from the social-emotional perspective.


Remarks:

1. The above ideas and key points are originated from an experienced special educator’s experience sharing. I’d like to take this opportunity to express my grateful thanks.
2. There is another article in this blog that explains the learning characteristics of CVI children with multiple disabilities, as well as the teaching strategies and general guidelines with regard to the care of CVI children.

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