Skip to main content

Society "WE, are the biggest problem for disabled and to their parents.

society "WE", are the biggest problem for disabled


A person with disability and their parents or caregivers fight the biggest and the toughest battle not because of


The obstacles the disability gives, but because of the obstacles we, the so called society give them. Sadly yes! Society "WE", are the biggest problem for disabled and to and to their parents. Eventually, the isolation from the society become the easiest option for them. 
Let's have a look on how. Starting from the birth till their adult life see how "Society "WE", are the biggest problem for disabled". 

1ST BATTLE: (immediately after birth)

Immediately after the birth, doctor diagnose the baby with disability (of any sort), doctor come to the baby's happy and excited parents and instead of saying, "congratulations for your baby" and then guide further about the situation, he comes and say, "SORRY! Your child does have whatever disability". 😞😞
The happy and excited parents start seems worry, their gratitude towards the GOD turns into complain and then....then the misguidance leads their worry towards negative thoughts. Like, 


  • My child is abnormal, he/she could not live a normal life.
  • No future of my child
  • My child's growth does not have any way, and so on. 
The real feeling can only be express by the victims.

And nobody tell them that "Their way of growth could be different but, stages of growth is same as normal".

2ND BATTLE: (when the parents of disabled are sitting with us, the "SOCIETY")

Behavior we people show vs. the behavior they really need from us:

The behavior which we named as "SYMPATHY” may be become the reason of increasing their stress, decreasing their motivation and lower down their self-esteem. Just think, when we see such child what are our sentences??


  • "OH! your child is abnormal😨"
  • "Oh, he is an exam from God for you, be brave️", and etc. etc.

But....what they actually need from us is only and only an "ACCEPTANCE". They already know much about their child, they don't need any reminder. They just need people who embrace their child as we do for any other child, who embrace their child's moves without any question & answer, just an EMBRACEMENT and an ACCEPTANCE. 

3RD BATTLE: (when the child, due to his disability rejected by his peers)

Unfortunately because of our own blackness and weaknesses we forget to teach our own children that how to behave when you meet your disabled peer.
 There are many reasons behind this...may be our own reaction towards that child or our schools who never allowed that child to get enter in their schools because he/she is DISABLED.
Eventually, during the period which is the period of building self-esteem of any child, his/her gets destroyed before building.


Comments

Popular posts from this blog

why "Disabled" becomes "Differently abled"

"Don't call them disabled, they are differently abled!!!" ... These lines must have stricken on your ears. Right??? Yeah! That’s true. Fortunately, things are changing, stigmas are changing, stereotypes are changing, and myths are getting cleared. But...How? And Why? Why these transformations are happening? Did this all done because: These people are completely different from us, so that they became differently abled. OR These people have something which we don't have, or we have something which they don't have. Absolutely not. Nothing of above points is making sense. Of course GOD Has not created 2 types of human. Human-1 and Human-2. That is why, "We all are humans, With same feelings, With same emotions, With same life phases, With same features, In the same world, In the same surroundings, For the same life purpose, For the same life goals". Then, how DIFFERENTLY ABLED? Like okay...

World Down Syndrome Day 2020, PAKISTAN

21 March, known as World Down Syndrome Day. This day world celebrates the existence of GOD's one of the most beautiful human creation, people known them as Down Syndrome. Down Syndrome Day-2020 was so much fun, productive, healthy, joyful for every child, adolescents, teens, youngsters, adult and even for elders at Karachi Down Syndrome Program, Pakistan's carnival held at DHA sports club (MOIN KHAN ACADEMY)-Karachi on Sunday, February 16, 2020 from 3:00 pm to 8:00 pm. For further details about KDSP visit their website  https://www.kdsp.org.pk  . Many companies in Pakistan joint the hands with KDSP (Karachi Down Syndrome Program). They had platinum partner, 3 gold partners, 4 silver partners, PR partner, event partner, media partner, radio partner, tech partner and 2 ticketing partners. Furthermore, there were many enthusiastic youngsters who volunteered themselves and showed their love for people with Down Syndrome. Even the event was also full of fun for volunteers ...

Pakistan-National disability day 2019, Spina bifida-reason for his 'Disability' is unknown, but reason for his success is his 'Will'. Malik Armughan Ali.

Meet  Malik Armughan Ali . Who has spina bifida (Myelomeningocele) plus will, where his will is dominant over spina bifida? He shared his life which is composed of ; spina bifida, his education, his leisure time, hobbies, struggles, give up memory, His message for the world. What else? What else one has in his/her life? Masha Allah he is full of life :) :). Isn't it? Know his success story in his own words. Malik Armughan Ali, I was born with Spina Bifida (Myelomeningocele) with spinal cord injury level L4-L5. Due to this my left leg is short 8 to 9 inches, I walk with leg braces, kfo and stick. I have done my matric and inter from Sir Syed Model School and college. For my bachelors, I went to Muslim youth University Islamabad for BS computer science. I spend my leisure time to listening music, watching movies and talk shows. I also play cricket and badminton. I love traveling. M...