My baby girl has been diagnosed with William Syndrome when she is 7.5 months, and now she is approaching 22 months. It has not been an easy journey knowing her condition, and there is lots worries and fears and yes, I can't deny that we actually worries until to the extend of finding suitable school for her when she is 7 years old.
Yesterday night is a leap of progress and family's leap of excitement, my baby can now walk holding her one hand. God hears my prayer and I am too ecstatic and start to sms relative and friends who concerned. I really can't wait to see her walk all these while and she did it.... tears of happiness indeed. ;)
Her achievement wasn't a one day success. To all the mothers out there with special children, I heard you and we need to be patient. My girl has gone to many doctors, midwife, physio therapist, occupational therapist, speech therapist, audiologist, cardiologist, genetist, clinics after clinics and hospitals. Not forgetting the support from family members and friends and society is fairly important to provide us with strength and confidence in handling our children.
I am glad we had to know of her condition early and work it out. What is William Syndrome? From Wikipedia, "is a rare neurodevelopmental disorder caused by a deletion of about 26 genes from the long arm of chromosome 7. It is characterized by a distinctive, "elfin" facial appearance, along with a low nasal bridge; an unusually cheerful demeanor and ease with strangers; developmental delay coupled with strong language skills; and cardiovascular problems, such as supravalvular aortic stenosis and transient hypercalcaemia."
Malaysia has got our first "Child Development Centre" in HUKM, Cheras and they are equipped with specialist for special children. You may be flooded with lots of doctors appointment initially but you will go along with the flows once you see progressive milestone in your child. We have limited support for William Syndrome in the country, and I think parents contact will be the source of support and encouragement to bring up a William Syndrome Child.
Thus, we should not give up, and I am confident to say that you will see the fun, loving character in your special children, just like me. My son always have fun with his sister, as they imitating each other and at times she actually taught him how to be brave. I am always more than happy to support if you need some sharing in William Syndrome.
I had this article featured at PARENTHOTS @ THE STAR
I am thankful that they are associations and supporting parent who come forward and share their thoughts and assistance.
Xinga hotpot is a hot pot restaurant that features a retro Hong Kong style. You can choose different soups that fits your taste such as Mala...
Ghost Museum Melaka is a place where you can have fun while learning about ghosts from around the world. It contains local ghosts, western g...
Happy tu tak terkata bila ada notis bajet government bagi pengecualian road tax untuk kenderaan OKU - kali ni termasuk kereta ibu bapa penja...
The Huskitory is a place where you can play with dogs while chilling with drinks. There are 2 sections that is the main one where you can pl...
My confinement Ginger Beef dish that takes only 5 min cooking time - made possible with True Aussie Beef!Confinement food is very important for mothers after child birth, as well as cleanliness of the food as rightfully the food that they consum...