Showing posts with label caregiver 24/7. Show all posts
Showing posts with label caregiver 24/7. Show all posts

Monday, 16 March 2015

Be thoughtful when you visit homes were disabled people are

Sensitivities to observe when visiting the disabled and elderly


 
When it comes to spending festive occasions and holidays with our loved ones, most of us immediately think of attending open house visits.
 
If it's not that, then it is probably that perfect opportunity to make some time to catch up with long, lost old friends in our favourite cafe – or doing whatever it is to have a good time.The recent Chinese Lunar New Year was a good example.
 
However, when I called a good friend of mine last week to ask her how she had spent her holidays with her family, I was left speechless! I couldn't help noticing her having a delicious good chuckle as she related her story.
Margaret has two disabled persons in her home: her young son and his aging grandmother. With both of them having to use wheelchairs in order to get around, welcoming the Year of the Goat – or any other animal signs in the Chinese zodiac calendar for that matter – can be challenging and complicated, she told me. For instance, when her friends started their festive spring cleaning, she decided to give it a miss. As a result, Margaret received endless comments and questions from visitors to her home on why her ceiling and fans were not in a spick-and-span state to their expectations?
 
My friend's amusing and witty answer to them was there was no need for any "extras" as scrubbing and cleaning are what she does daily anyway, to make her home liveable and happy.
 
There is a mat on the floor in her living room all the time for her son to rest on. Special rehabilitation toys are also placed there for him to play with. Nearby are his stroller, walker and other equipment.
 
Whilst those without disabled children may find them "untidy" and may want to put them away, it is part of Margaret's child's daily life for instilling creativity skills in the lad. They need to be accessibleto the boy all the time.
 
Visitors to her home are forbidden to check out the store room in the house just in case they go into "sudden shock" upon discovering Margaret's collection. It's filled with wheelchairs, strollers, walking and standing frames, as well as household stuff like old newspapers.
 
Having two members with physical disabilities going out on visits to loved ones and friends is quite a task. As a caregiver, there are time limits to observe.
 
One needs to be sensitive as to how long before the disabled visitor tires from the visit and needs to get home. If you are away from the handicapped person for a while, you need to know when your time is up and you need to return home to him. 
 
And when you are with them you need to stay focused on the person you are caring for.
 
With such constraints, it made more sense to have the non-disabled relatives and friends come over instead. However, visits during meal times, rest and bathing and "toilet time" are best avoided.
 
Grandma, for instance, has become incontinent. She, however, refuses to wear a diaper. And it isn't easy to force an 80-year-old to do something which she is not used to doing. Even the doctors and nurses found it hard to make her wear one when she was hospitalised. So there are times where "accidents" occur.
 
Friends and relatives should understand situations like this, when they are paying visits to elderly persons.
 
Festivities always signal the abundance of food. Like all of us, the temptation to overeat or eat something which is unsuitable happens. For grandma, this can either end up with super low or super high blood glucose counts which causes her to feel giddy. Things become more complicated with loose bowel movements and diarrhoea.
 
When visiting people in such conditions, it would be tactful not to mention how someone's room may smell or look, considering their vulnerabilities and never forgetting that your roles there are as guests of the home.
 
Those playing with fireworks and firecrackers should have some consideration of how the loud sounds and bangs affect children and animals. Margaret says they are never allowed in her home. 
 
Her son gets terrified of the sounds. It wakes him up from sleep and starts crying and doesn't go back to bed until several hours later.
The insufficient sleep even makes him go into seizure attacks. The loud sounds goes on almost daily for about a fortnight, making sleep a nightmare for the boy. 
 
On top of this, she also has to calm down her two pet dogs who are equally terrified by the firecrackers.
 
So this is how it was for Margaret and her family and how they managed to cope and survive during the holidays.
 
Despite what she has to go through every day in her life, she is never one to complain about it. Margaret says she just wants to make people understand that if you are living with people with disabilities, there are certain challenges – as well as sensitivities to look out for – which people go through in life that require some special understanding and support.
 
Although Margaret herself has been suffering with some persistent back pain lately, she says she enjoys cooking, eating, entertaining people and meeting new friends. Then there are always those moments when she enjoys a cuppa over a nice comedy on television, or have a few friends over with food from the shops in order to chat and laugh away a couple of hours, especially when there is a holiday.
 
Otherwise, it's on the daily go for appointments and regular follow ups in the hospital, therapy centre and her son's special school. – March 16, 2015
* This is the personal opinion of the writer or publication and does not necessarily represent the views of The Malaysian Insider.
- See more at: http://www.themalaysianinsider.com/opinion/anthony-sb-thanasayan/article/sensitivities-to-observe-when-visiting-the-disabled-and-elderly#sthash.j3s9hqsU.dpuf

Monday, 12 January 2015

What's so wrong about my son?

What’s so wrong about my son?

Anthony SB Thanasayan

Anthony SB Thanasayan is a wheelchair user who is powered by his service dogs who help him stay on top of life. He is president of Malaysia's first and only animal-assisted therapy society called Petpositive.
 
I guess most of us today know what the word "disabled" means.
However, understanding it from a parent's point of view, or someone who has the condition, is often a totally different kettle of fish.
 
Here's an eye-opening email I received recently from a mother of a seven-year-old boy with a disability.

I shall call her "RY" because she wishes to remain anonymous.     "KT – not his real name – is my 'non-verbal' and 'non-walker' special-needs son whom I love more than anything else in this world," began RY.
 
"Because I do, I take him out with me all the time, whether to the grocer's for a quick grab of items, or to the mall for lunch or dinner."
 
She then went on to explain how disability affects her son.
 
KT wears a special type of shoe called an "ankle foot orthosis", or better known as "AFO". He has to wear it every time he goes out.
KT sits in a special bigger-than-normal stroller. That's because RY is no longer able to carry his usual customised wheelchair in and out of the car boot because of back problems.
 
His hands also have to be tied up with a nappy.
 
This is to deter the young lad from “punching” the cheeks, forehead and lips repeatedly until they bleed or turn blue black.
 
KT does this because of his sensory problem. He does not understand or realise that he is inflicting injury or pain on himself.
All his fingers need to be stuck together with pore tapes in order to prevent him from hurting himself further.
 
"Nobody – just nobody – would understand and appreciate the amount of effort and time I have put in to desensitise KT's odd sensory problems by learning the techniques from attending workshops and consulting scores of specialists and therapists," RY said in exasperation.
 
"I've had people walk up to me to ask me why 'I don't just reason with KT or teach him that it is wrong to box himself in his face. 
 
They find it hard to accept that my son simply doesn't understand what he is doing.
 
"On top of that, he also has a list of medical conditions which include his inability to understand logic. He also needs to be cared for 24/7 by a caregiver."
 
To make matters worse, RY said she is sometimes confronted by strangers who think she is abusing her son for tying him up.
 
"Instead of getting angry, I always make it a point to explain KT's special circumstances for those who care enough to listen."
 
Fortunately, such encounters have failed to deter KT from getting out of his house with mummy. Being out with RY is when he is happiest.
 
He never fails to start singing, or sometimes even screaming for joy.
 
"It's actually KT's way of expressing his happiness and trying to communicate with others around him through non-verbal means," RY explained.
 
While there are those who are supportive of mum and son by offering them a nod or a smile, unfortunately, that doesn't always happen.
 
There are those who either just don't get it – or simply are adamant about trying to understand persons who are born different and their caregivers. 
 
Once, while RY and KT were out for lunch, they encountered a middle-aged man seated next to them. He kept staring coldly at KT.
However, our hero who was in a jovial mood, kept smiling and waving at the man and even started to "chat him up".
 
RY leaned forward towards the man to explain that KT was trying to be friendly with him.
 
He had a horrific look on the face when he noticed KT's bandaged fingers and bound hands.
 
Despite RY explaining the whole situation to him, the man continued to stare at KT.
 
And in spite of KT behaving the same way to some of the other passers-by, the man continued to fix his gaze at KT – as if he was an alien who had just landed from outer space.
 
Then, just as KT and mum were about to leave, the man suddenly asked, "Is it something you ate, or did wrong during pregnancy that made your son an 'aborigine' and 'shouting and acting like a monkey'?"
 
RY was dumbfounded. She was also furious at the man's remarks.
But just as he was about to leave, she managed a response.
 
"Look, my son never asked to be born this way. He is multi-disabled, and a non-verbal and non-walking person who is merely trying his best to communicate in the only way he knows how to.
 
"He is a very beautiful boy – and it's so sad that you can't see it. If you would allow yourself to see him with an unbiased view, you would realise that too!
 
"I was stunned beyond words – and very hurt – by what he told me, without even a flinch on his face.
 
"But then again, I had learnt a very powerful lesson that day. It was a precious insight into what real blindness and human ugliness was all about.
 
"Rather than to discourage me, it made me more determined about going out more often and being seen with KT.
 
"People with disabilities like my beautiful son have every right to be seen in public just like others.
 
"So what if special kids 'sing, shout, cry and dance' in public? They are just being themselves!
 
"And when you think about it, what's so wrong about that!?" said RY who lives in Petaling Jaya, Selangor. – January 12, 2015.
* This is the personal opinion of the writer or publication and does not necessarily represent the views of The Malaysian Insider.
- See more at: http://www.themalaysianinsider.com/opinion/anthony-sb-thanasayan/article/whats-so-wrong-about-my-son#sthash.gbR5hkpS.dpuf