Better experience in portrait mode.
Idap Rare Disease William Syndrome, Here's the Latest News about Ladzan Syafiq, Dede Sunandar's Son - More Active and Cheerful

Idap Rare Disease William Syndrome, Here's the Latest News about Ladzan Syafiq, Dede Sunandar's Son - More Active and Cheerful

Trending

kapanlagi
Swipe Up to See the Photos
Idap Rare Disease William Syndrome, Here's the Latest News about Ladzan Syafiq, Dede Sunandar's Son - More Active and Cheerful

Dede Sunandar and Karen Hertatum have now been blessed with 3 children. Their second child, Ladzan Syafiq Sunandar, was diagnosed with a rare disease called William Syndrome. Ladzan was predicted by doctors to be able to walk at the age of 4. So, what is his condition now?

<nil>

Dede Sunandar and Karen have to accept the reality that their second son has William Syndrome. This rare disease requires them to regularly take their son to the doctor for check-ups.

<nil>

The rare disease can cause developmental disorders in a child. Ladzan was predicted by doctors to start walking at the age of 4.

<nil>

"He has a different disease from everyone else, the disease is called Williams Syndrome. It affects the heart, lungs, and stomach. So surgery is necessary, whether we like it or not," said Dede in an interview.

<nil>

Dede mentioned that Ladzan has to undergo 4 stages of surgery to cure his illness.

<nil>

At the beginning, when his child was diagnosed with Williams Syndrome, Dede was offered the option for his child to receive treatment in America.

<nil>

But due to some considerations, Dede Sunandar finally rejected the offer.

<nil>

Now Ladzan Syafiq is almost 5 years old, KLovers. His condition is also getting better.

<nil>

Dede and Karen often share moments of Ladzan's happiness playing with his older brother. Stay healthy, Ladzan.