Baru Berusia Lapan Bulan, Makan Capati 4 Keping Sehari

catalina · Post time 15-4-2017 12:02 PM

boleh ker makan capati umur 4 bulan

sistem kumuhannya belum fully develop lagi

rosak ler organ weeeiii....

tak ade ker sesapa yg boleh donate baby trolly utk parents ni, sian maknya..sakit belakang nak dukung

Changa · Post time 15-4-2017 12:20 PM

gemuk nya kau dek.

allhaillll · Post time 15-4-2017 01:16 PM

cekelatkopi replied at 14-4-2017 06:40 PM
Kuss semangat..tu pakai gelang karang dah tak muat jadi satu pasal nak kena call abam bomba

tu la riso pulak nengok. gelang yang ade kunci tu kot

vanillaninja · Post time 15-4-2017 02:13 PM

Jadah apa bagi baby makan capati

dakewa · Post time 15-4-2017 03:50 PM

Gundunya kau dekkk

KyraKnightley · Post time 15-4-2017 03:57 PM

Semangatnye badan baby ni

Peaches113 · Post time 15-4-2017 05:03 PM

Habis pulak ek baby tu makan sampai 4 keping? Rasanya normal baby tak makan byk tu. Takkan la kecik2 dah ada cacing kerawit dlm perot kot

800214 · Post time 15-4-2017 05:32 PM

Rasanya baby ni berpenyakit.arwah anak aku dulu pernah doktor syak sakit prader willy syndrome.sakit ni di xkn kenal erti kenyang.dia akan makan je non stop

800214 · Post time 15-4-2017 05:35 PM

Prader-Willi syndrome is a complex genetic condition that affects many parts of the body. In infancy, this condition is characterized by weak muscle tone (hypotonia), feeding difficulties, poor growth, and delayed development. Beginning in childhood, affected individuals develop an insatiable appetite, which leads to chronic overeating (hyperphagia) and obesity. Some people with Prader-Willi syndrome, particularly those with obesity, also develop type 2 diabetes mellitus (the most common form of diabetes).

People with Prader-Willi syndrome typically have mild to moderate intellectual impairment and learning disabilities. Behavioral problems are common, including temper outbursts, stubbornness, and compulsive behavior such as picking at the skin. Sleep abnormalities can also occur. Additional features of this condition include distinctive facial features such as a narrow forehead, almond-shaped eyes, and a triangular mouth; short stature; and small hands and feet. Some people with Prader-Willi syndrome have unusually fair skin and light-colored hair. Both affected males and affected females have underdeveloped genitals. Puberty is delayed or incomplete, and most affected individuals are unable to have children (infertile).

sebu1 · Post time 15-4-2017 05:44 PM

Stress aku tgk budak ni campur kesian

Laracinta · Post time 15-4-2017 08:32 PM

Rasa nak gigit baby nih

Esmiria · Post time 15-4-2017 10:30 PM

Jgn mati dhler

chinta89 · Post time 16-4-2017 12:01 PM

besar wooooooooooo

barfi · Post time 16-4-2017 12:04 PM

cmf_Kimmy replied at 14-4-2017 06:38 PM
Berpintal2 tangan dia....mahu patah pinggang nak dukung dia ni.

Berpintal2 macam roti

mirandanicky1 · Post time 16-4-2017 12:12 PM

Perkara pertama terlintas ialah mcm Baymax

sekngucing · Post time 16-4-2017 12:32 PM

800214 replied at 15-4-2017 05:32 PM
Rasanya baby ni berpenyakit.arwah anak aku dulu pernah doktor syak sakit prader willy syndrome.sakit ...

meninggal sebab sakit prader willy ke

inalilah

800214 · Post time 17-4-2017 05:00 AM

sekngucing replied at 16-4-2017 12:32 PM
meninggal sebab sakit prader willy ke
inalilah

Tak.sbb after ujian demi ujian doc sahkan penyakit lain..prob buah pinggang.so that badan dia bengkak.sian la pulak tgk org hencap mak dia kalau mmg dia ada sakit tu.kalo x dibg mkn, rumput pun dia mkn nnt