Monday, September 28, 2015

Special, He Is

'Special' has a lot of meaning to it depending on how you apply it.

Special someone - a person who is so dear to you. Special place - a location that holds a memory that is close to your heart. Special moment - a particular time that is significant in your life.

Special is simply, unique.

Raees is special.


He's special because he's my first born, he made me a mom.


He's special because he's the first grandchild in my family.

He's special because he's unique.

Raees isn't just special to me and my family, he's a special child...with special needs.

And this the first time I ever admitted it openly. I had my reasons for keeping it low over the past few years but now I feel it is time to let the cat out of the bag. Keeping things to yourself could take a toll on your emotions.

I've somewhat shared the early warning signs in this blog, before I went on a long hiatus because I didn't know what else to write about besides our struggle with his condition. And I wasn't ready to share at that point in time.

Raees did say a few words when he was little. But his vocabulary didn't evolve, in fact it disappeared. He just didn't say a word. He didn't communicate verbally or expressed with gestures that much.

Then there was the crying stage...he just cried his heart out every time we went to someone's house, especially when there's a lot of people e.g birthday parties.

Heck, he even cried at his own birthday party!


As a toddler he didn't sleep well. He didn't play well with other kids either. In fact one would say he was in a world of his own.

The only thing he was interested in was the iPad - which we so generously let him play with to keep him from running away from us at public places.


I began suspecting something was not right when he was about 2 years old, after observing other kids his age. I could say that I was in denial when his development was not according to the development chart anymore. I simply stopped referring to it because I held on to the phrase 'children develop at their own pace'.

Also, MANY people told me,"it's normal for a boy, especially the first born, to have slight delay in speech. He will be talking in no time."

So I wished they were right and just waited for to hear more words but they didn't come around.

The warning signs just got too great so we knew we needed to do something to help him. I won't go into detail about what we have done, at least not yet. The doctors diagnosed him as Autism Spectrum Disorder (ASD).

For those who aren't familiar with ASD, let's just say their thinking process is different. It's like our brain is running on Mac OS and kids with ASD are on Windows. It is a wide spectrum and the effects vary. But these kids have their strengths and if the right approach is figured out, they're able to excel.

It's been about 3-4 years since we embarked on Raees' journey to recovery. Now at 6 years old, he's able to communicate his basic needs, toilet trained and learning quite well. He may have a long way to go but, Alhamdulillah, he's showing progress.

Raees being the first born, I didn't have a benchmark to compare to. That's another reason why in the beginning I thought that was how all toddlers behave. Now that I have Razeen, I see a huge difference. I'm experiencing a lot of firsts with Razeen.

Anyway, today is also a special. I'm a year older :)


It's also time for me to grow up and get out of this shell. It's time to open up about our journey with Raees and to *properly* reach out to you, my loyal readers, for support. I know I know...I should've done this a long time ago. Better late than never!

I believe many parents are going through the same experience as I am. It would be great if they could also share their journey as well and together we could help our precious children.


You know, this truly is special post ;)


Note: my apologies as some of the links' photos have gone missing :-/

- Posted using BlogPress from my iPhone


6 comments:

julie shahril said...

hai, anak saya kategori lambat berckp, smpai kena pegi jumpa speech therapist. skg dia dah 3 tahun, dia baru boleh sebut around 30 patah perkataan shj, tapi itu pon dah kira ada improvement juga, sblm ni lagi teruk. dari usia dia 3 bulan saya hantar pada pengasuh utk jaga, then awal tahun ini saya start hantar taska, saya nak tgk perkembangan dia di taska, pergaulan dia dan pertuturan dia. Saya seorg ibu yg bekerja, quality time dgn anak sgt limited.

sejak dia msuk taska, dia ada sikit sifat berani, suka berkawan dan pertuturan pun dh semakin baik walaupun berckp pelat. sekarang saya masih ada beberapa appointment dgn pihak hospital utk check-up perkembangan speech dia. saya ada tulis dlm blog saya kronologi masalah anak saya. Kita usaha selagi terdaya, selebihnya tawakal dan doa serta support kita pada anak.

sekarang saya limitkan dia bermain dgn smartphone/ipad sebab benda2 tu kurg elok utk perkembangan dia, sometimes saya bagi dia kertas kosong dan pensil/pen suruh dia conteng2. Beli buku mewarna dan biarkan dia mewarna, comot pun xpe, biar dia buat ikut kreativiti dia.

kerapkan bawa anak berjln2 diluar, supaya dia kenal pokok, laut, binatang, bukit, tgk burung terbang dan biarkan dia berlari....best! kalau dpt bawa anak pegi zoo...kenalkan dia dgn animals..lagi bagus.

ini jela yg dpt saya kongsi sikit2...

Faizah Sukeri said...

in sha Allah Raees akan normal mcm Razeen yg comel tu :)
mana tau Raees antara org2 genius satu hari nanti .

Lalitha said...

Accidentally came across this post :-) Can't help but to comment. Coincidentally , Raees took all the utensils to prepare for his brunch including an attempt to toast the bread by himself too. I was really surprised. Not many typical developmental 6 years can pull that off. I went back thinking this boy is amazing ! He is amazing from the way he plays music , to his laughter , and the way he plays badminton - everything comes with his own signature style!

Anonymous said...

SALAM,

SAYA ADA SEPUPU MCM NI...LAMA...DALAM 10 TAHUN TIBA2 DIA DA BACK TO NORMAL...HOPEFULLY HE WILL TURN UP WELL FOR RAESS... I'VE BEEN FOLLOWING UR BLOG SINCE HE WAS BORN.

Adrina Adi said...

My son ada spd (sensory processing disorder and speech delay) and went to special kindy here at Kota Bharu. It aint cheap here, I wonder kat KL mesti lagi mahal. I feel you. Tapi untuk anak special memang banyak kena sacrifice, duit, masa dan tenaga. After a year, buat assesment dgn kementerian pendidikan alhamdulillah dpt masuk sekolah aliran perdana untuk darjah 1 tahun ni. It was not easy at first but now he is much more indepentdent. Dont worry Irin, everything will be just fine. Always make doa for him. InsyaAllah. May Allah bless you and family always.

ice said...

nice! :)