Jack – Keep Success

Feb 20-24, 2012. Continue reading

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Caleb – Speech

Feb 20 to 24, 2012.

I received feedback from Caleb’s mother. She said Caleb has improved much in behavior and speech. He is more obedient and has a clearer speech compared to before he came for therapy. Caleb’s driver who brings him from the centre to his care provider’s house also commented that Caleb’s speech is more clear with a larger choice of vocabulary. His care provider also said so.

Caleb gets daily therapy. Last week, up to Thursday, he could not go up on the trampoline for Rebound Class. Last Friday, I held him up to the trampoline. I play with him and I start with a gentle bounce. I could see he could not tolerate the stress and has fear of imbalance. When he is stressed, he will ask for water or to go to the toilet. For the first time I will walk with him to give all what he need. But to my surprise he did nothing in the toilet.

On Monday I ignored all his request, We go up to bounce, this time I video the bouncing time. Afterwards I allow him to see himself in the video. He seems to be proud of himself. Tuesday Caleb went up to the trampoline. This time he is not as stressed as before. He is able to interact with me,  e.g. lift up hand, bounce to catch the moon. He replies “No moon … no more in dark dark (night)”. Then I reply “Catch the sun”.

Rebound Therapy also stimulated Celeb to keep longer focused when doing a task.

Caleb’s concentration also improved, he is always curious to adventure new things. Mornings he will take out his own tool for speech organ development and sits to wait for us to start the session with him.

Maria Montessori (LOC)

Maria Montessori (R) (Photo credit: The Library of Congress)

I was thinking, how does it come he did not respond to Montessori school training and he dozed off in class? I completed my diploma in teaching Montessori, so I know it is an adventurous time to be in a full Montessori bases concept centre … but how does it come Caleb dozed off in school? What went wrong there?

 

 

 

 

 

 

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Ruth – adventure

Feb 13 to 17, 2012

Learning is an adventure for Ruth. She is able to integrate with other children in the centre. She does daily therapy. We will start Rebound Therapy with Ruth before she proceeds to the next therapy. She is able to sit and listen to instructions, eg I tell her to sit on the trampoline bed, and when I count to 3 she has to bounce up with my support. She has to listen and control herself, if I don’t count to 3, she is not allowed to bounce up. To her, this is a fun time. Each time she fails to follow the instruction, she will say “oops sorry”. when she is able to perform she will say “yeah”.

Ruth is now also able to focus on tracing vertical lines and horizontal lines. It needs eye and hand coordination to know when to stop. I start it with dotted vertical lines of the same lengths and then moved to different lengths. After she grasped the concept of a vertical line, I move into horizontal lines. She has fine motor skills but she needs to develop concept image in her brain and act it out. In few occassions I saw Ruth trace horizontal lines all by herself.

For lunch I prepares fried chicken.

Sanders remains the official face of Kentucky ...

KFC-logo

I serve it for the full day children with rice and mix vegetables, Ruth saw it … she said “Kentucky Fried Chicken” (KFC). I ask her, “Do you want to eat some?” and she replies “Yes”. I cut the fried chicken into small pieces, and serve her with a fork on a plate. She is able to coordinate to use the fork to take the chicken. Ruth will have  her lunch at home. My intention is to extend her time in the centre and to develop her taste for a different variety of food. As the days go by, I notice she is able slowly to try new food. According to her father she has a stereotype of food. She won’t try other food. But now at least she opened up for other food.

Each development improvement in Ruth is a success Ruth has make to herself. It is more than academic performances.

 

 

 

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Jack – amazing

Feb 13-17, 2012.

This week Jack is not in fit health. Jack now allows his parent to give him medicine. Last week he refused medicine. I always remind Jack that medicine will remove his headache. His low grade fever comes and goes but he does not make much noise. He is able to take medicine willingly. This week the programme will be light and easy for Jack.

First two days  of the week Jack was rather weak and he did vomit a few times. I contacted his mum, she said Jack does so after having fever. Eventually Jack recovered after 3 days. It is amazing that Jack is aware that he want to throw up, Hence he will go to the washroom to throw up and afterwards Jack cleans the washroom by himself, I  observe him with a smile. He asks “Am I a good boy”? My reply, “Oh yes you are a good boy” with a smile to him.

Monday morning when Jack reached the centre, I greet him with a “Good morning Jack”, He said he brings the London Bus. He shows me the red double decker wooden bus with passenger sitting inside. We do maths counting: he counts how many passenger are in the bus. I incorporate addition and subtraction though this is rather difficult for a learning difficulties child to understand.  He remembers that the bus is for people and not for animals.

This week I continue with the oral organ development stimulation with the introduction of the sour taste. I can also notice when Jack excited he is able to clearly pronounce the words with less  stammering. Therapy is a daily programme to Jack to stimulate the neuron pathways. Jack is also able to recall to read words that I have taught him.  On one morning, he told me “Teacher I no longer shout at home”. My response is “Wow, you are a smart good boy”. Before attending therapy lessons in my centre , off and on Jack will shout when he gets frustrated. But his tantrums have much toned down.

We see here an interesting evolution. He is getting more self-aware and even notices that his behavior is improving.

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Caleb – new boy

Feb 8 to 10, 2012.

Caleb is a new boy, he is  over 3 years old. He was transferred from a Montessori pre-school. Caleb is very vocal but with unclear pronunciation. According to his parents, there are times Caleb will sleep in school. How can a healthy child sleep in the school if the activities are interesting? His mother also mentioned that the school principal said Caleb is unable to sit still in class. How can a child sit still to learn if he did not develop his basic foundation and awareness of himself? I notice he is still talking in baby language.  He has not been formally diagnosed.

It is rather an adventure to work with Caleb. He does not cry in the first day in the centre: in general a normal child will have tears when it first attends school or centre (separation anxiety). Caleb seems to have much energy. He tours around the exterior of the centre where I have a tunnel, water pool, swing and garden. He just could not keep attention.

In my first time meeting Caleb I remember, he told me “doctor”: he took a cube to pretend as a torch light to check my tongue. He said “open your month; see the tongue, see the eyes”. I play with him, I pretend to be a patient to him. Upon finishing with Caleb, I asked his mother, “what make him like doctor? It seems he want to be a  doctor”. His mother said he was not well and she took him to see doctor. Aha, he was copying what the doctor did to him and Caleb puts it into practice with me.

Since it is the first three days of Caleb in centre, I have given him a light and easy lesson. I even invite him for the bouncing/rebound therapy but he is afraid. He has a lack of vestibular balance. Even when Caleb is walking, I can see he has a hunch, bending  with the upper body forwards.

 

 

 

 

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Ian – new boy.

Feb 8-10, 2012.

Ian is age 4 this year, he has speech difficulties with not forming proper words. He is able to understand basic instructions. He expresses himself through tears,  but lacks in eye contact, has a poor posture, poor lip movement and is lacking in tongue rolling.  He has attended speech therapy in a private hospital, so as to attend Occupation Therapy from a private practitioner. When his mother came to visit my centre for the 3rd time she broke down in tears before confirmed Ian for the therapy programme.

First week, when his mother left him at the centre he cried ( separation anxiety). I walk him into the hall, hug him, show him how and where to put his belongings. In few minutes his tears stop. I walk him out to the garden, he begins to explore around, I notice Ian likes to pick up leaves and throws them over the fence allowing the leaves to drop into the drain; he observes the way the leaves move flying down. He also likes to pick up the leaves and press them. He went into the tunnel from one entrance and exits from the another entrance. The tunnel has three entrances. I allow him to walk bare foot in the garden for feet stimulation. A lot of verbal communication is given eg, run, walk, fast. Then I clean his feet before bringing him back to the hall.

I bring him to the hall, inviting him  to drink some water. He is still using a tumbler with a straw to suck. He begins to explore the material in the centre. He will take four different type of apparatus. He mixes all the apparatus into one container.

He begins to arrange the animals into a row, making babbling sounds with no proper formation of words. Then he moves to another apparatus  with variety of different colors , size knob cylinder. Again the same: he will mix all cylinders in one box. He repeats the same, by arranging the cylinders into one row. A very repetitive stereotype pattern of  arranging material for this week. After all this arranging I invite him to help me to sort it out. He refuses with tears. I insist he must help. He helps in tears. We work together to get all the material sorted into their respective containers with Tom, another boy.

This first week I am mostly observing him. He comes in with not fit health. hence we do only light activity for him. How will Ian progress? It is both a challenge and a mystery for me right now, but time will tell. All therapy success is based upon careful observation and individual adaptation of the therapy. Time spent in observation is never lost.

 

 

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Ruth – awareness.

Feb 8 to 10. 2012

Working with Ruth is a great joy, there are time she will drive you mad, but when you think of her unique qualities, you will feel the joy to help develop her.

Ruth has improved in communication, awareness of her environment, ability to engage friends to play with her, ability to show a little boy what she can do, e.g. crawl in the tunnel.

She has also improved her exposure to food, at least she begins to eat a variety of food. Last year, when I offer her food she will say no, she just refuses to try other types of food. But

English: food , fruit , fruits , apple , apples

Apple

now she will request food. E.g. one afternoon, she went to the kitchen, and brings me an apple (I usually leave some fruit on a child size table). Ruth  said “I want an apple”. I immediately reply, “ok we will eat an apple”. Today at noon again, I ask her “do you want banana cake”? She replies, “yes”. Truely enough she ate the cake while waiting to go home.

And this morning, Ruth saw a girl stand up on the chair, Ruth told the girl, “Don’t do that”.

Yesterday noon again she uses the eye and hand coordination board to insert crayons. She brings it to a teacher and said “Here is a birthday cake for you”. she then sing “happy birthday” to the teacher. Time and again she shows amazing development of herself. Ruth  continues with her vision therapy and oral organ therapy to help her speak more clearly. I see she shows improvement.

My focus on this semester with Ruth is to enable her to have better vision and tracking of work that she has to perform. eg for her to be able to write. Handwriting is a great challenge to me and her family. Of course she has gone through letter tracing in sand paper form. I also noticed she is able to use both her right and left hand to scribble and color. It looks like both her left and right brain halves are in control.

To me handwriting is more than a fine motor skill. For a person to be able to write he/she must have a mental image of the letter(s) to be produced. In order to write a person must has the executive function capabilities to run the hand to produce the letters in order, on a line, appropriate size and placing. It looks easy for all of us that have acquired this skill, but it actually is a great challenge to child with special needs.

 

 

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Jack – new life

Feb 8 to 10, 2012.

Time has passed by very fast. Jack came back to the centre. His ability to remember the phrase book is still fresh in my mind, I have taught him phrase book  C,  D, E and the number word from eleven to nineteen. Jack has always given me a surprise with his ability to recall what he learned. Wednesday morning I notice Jack listens attentively to the teacher with word reading cards with explanations and sentences making examples. He used to unable to stay focused with eye contact but today he really has that eye contact and focus. Seeing his development is a great motivation for me.

Today Thursday, Jack’s father sent him to centre. The first thing he get off the car, I greet him “How are you Jack”? He told me he has a headache. Immediately I touch his forehead, I found he has a fever. Contacting his mother,she said she  prepared some fever medicine to stand by. Well this is the first time Jack feels sick, (his brother has been sick for few days). This is also the first time I have to give him medicine. What a great challenge for me. I just put the medicine into the 5ml spoon for him to take.I notice his reluctance to take medicine, I will just ignore it with affirmation that he is a clever boy and that medicine will remove the headache. Slowly he finishes the 5ml medicine. I contact his mother to inform the medicine has been given. She asked me “how did you do that”?  Well I just put in spoon and he took it. Now only I realise at home his parents had a tough time to give medicine to him … that is what his mother told me.

That evening his mother phones me saying he is reluctant again to take medicine, I told his mother I will go to her house to give him the medicine. I went there … I use the same approach, amazingly he takes the medicine. My greatest concern is if he refuse to take medicine and fever unable to reduce, it may damage the brain. Hence I went to his house to give him the medicine. According to Jack’s mother, Jack’s tantrums have decreased compared to last time before he attended the therapy lessons with me. I use a lot of Rebound therapy method to work with Jack.

 

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Transform into new person after Chinese New Year.

Ultraman Story

Ultraman

Jan 30 to Feb 3, 2012.

Jack and Jeft are two good fiends in the centre. Both are 6 years old. Jeft is a boy who has the most toys of ultraman, power rangers and a collection of vcd and dvd of those toys. I could remember when Jeft first joined the centre at age 5. He was without the interest to write and read. I have to use ultraman to motivate him to learn to write and read so as to count. Ultraman was Jeft hero. After a year of therapies, Jeft is now  an independent learner.

However in this new year I have notice he has develop some violent action shown in ultraman and power ranger movies. Into this came Jack ,another ultraman and power ranger fan. Wow, the two of them really can carry on ultraman topic and occasionally I can see they show the violent action of ultraman. They become very obsessed with ultraman and power ranger. I thought I must make a transformation and change into their life in this Chinese New Year.

I came out with the story of after Chinese New Year, we all grow older (big) one year more. We are big boy and girl. You see your big brother Edward (nickname) don’t play ultraman and power ranger (age 10), He plays foot ball, yo-yo. He is clever, he is able to read many books. Do you want to be like your brother Edward? Surprisingly both Jeft and Jack also want to be like Edward.I call it mentoring among the young children. I told both Jeft and Jack to bring all their  ultraman and power rangers toys.The next day they brought all those toys happily though I can see Jack was little reluctant. But they agreed to bring the ultraman stuff to centre and throw it away. So the next day I have made ready the garbage for them to put the toys in (they will remember their action). They told me they want a yo-yo. I have also get them a yo-yo. I honor my word and they have to honor their word.

Well, that is how the children remove their favourite toys which do not give them good values. They do not know what is good and bad in this toy’s character. After removing this toys in the second day of the week. I have also seen less rough ultraman action. I also keep reminding them, they are a new person with new toys like yo-yo: a big boy plays badminton, yo-yo, football and London Bus.

The suprise is taht both Jack and Jeft did not throw a tantrum in the centre. As the days pass by they also mentioned ultraman and power ranger less and less. Jeft also brought his clothing with Ultraman, power ranger and Ben 10. Motifs as well to the centre to be given away.

 

 

 

 

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Ruth – Pronunciation

Jan 30

The Chinese New Year days-off are now a week behind us. Ruth comes to the centre as usual. According to her father, Ruth has very much improved in her speech, environmental awareness and socialising with others. Before Chinese New Year, Ruth received many intensive therapy sessions hoping it would enable her to control her pronunciation. This week I noticed Ruth’s pronunciation has much improved and she clearly pronounces the words.

Vision therapy is also something that we have trained intensively. I noticed Ruth’s eyes  do not keep track off the ball when she plays ball catching and throwing. Hence she failed to catch the ball. The holistic developmental programme has truly helped Ruth to develop into a more environmental and spatial aware child.

She is also creative. In the centre I have a board for eye and hand coordination treading and creative treading. Ruth and Tom have coverted it to become a birthday cake (pretend play). They insert crayons in each hole of the board  and the crayons are in standing position like a candle.  They name it “the Birthday cake”.

These common thin, stick-shaped candles are st...

Birthday cake

Ruth and Tom sing a birthday song. To me as a therapist, I have been observing the way they play and interact. At one occasion Ruth invites Tom to come and play with her. She said “di di (young brother in Chinese) come and play with me”. I have also noticed in certain occasions when Ruth gets upset and angry, she no longer like hits the desk with her hands like she used to do. She is able to internalize her anger and frustration and control it. Again this is done through a series of therapeutic exercises and these enabled her to control her anger. We should never despair: there is hope for every child with special needs.

 

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