Many people ask me why my address I put as 3 Little Angels while the title I put it as 4. Actually I am a mother of 4 but most activities were prepared for my 3 eldest wan. The youngest wan just 6 months old and hard to bring him everywhere.
Once he grow up... maybe 1 year old, then will upgrade my blog to another stage where the quality of my blog will become better. He he he... Just pray...
Peoples always said that I am lucky as having double happiness in my family. For Chinese, they sure know wat I am talking about. For non-Chinese, its means chinese writing for girl n boy, when combine together means good. Correct me if I am wrong as I don't know chinese either. Ha ha ha...
CM, my eldest daugter is very mature at her age. She is quite tall also and some expert said she is taller than those at her age. Genes don't know from who as both me n hubby also not so tall. She is a very responsible girl and always took good care of her siblings. She loves her siblings very much.
Peoples always said that I am lucky as having double happiness in my family. For Chinese, they sure know wat I am talking about. For non-Chinese, its means chinese writing for girl n boy, when combine together means good. Correct me if I am wrong as I don't know chinese either. Ha ha ha...
CM, my eldest daugter is very mature at her age. She is quite tall also and some expert said she is taller than those at her age. Genes don't know from who as both me n hubby also not so tall. She is a very responsible girl and always took good care of her siblings. She loves her siblings very much.
When we are out for shopping, she always remind me to hold her siblings hands which sometimes I forgot to do so. Things she likes to eat, she'll not finish it as she'll leave some to me n her siblings. She sometimes will buy some food from her canteen for us. Thanks, girl....
CW is small and thin girl. She got jaundice when she is 1 month plus and had to admit to Selayang Hospital & GH for 3 weeks to check the reason after 1 month she still had yellowish in her blood. In Selayang Hospital, they draw her blood twice a day. Really sakit hati seeing her. Then the doctor told me that they expect her having all sort of dangerous illness and might not survive...
They even ask me to check my blood as might need to do liver transplant for my daughter. They ask my permission whether I willing to do that and I told them that don't said part of the liver, if they want my life to save my daughter, they can take it. She still small n need to experience the world...
CW is small and thin girl. She got jaundice when she is 1 month plus and had to admit to Selayang Hospital & GH for 3 weeks to check the reason after 1 month she still had yellowish in her blood. In Selayang Hospital, they draw her blood twice a day. Really sakit hati seeing her. Then the doctor told me that they expect her having all sort of dangerous illness and might not survive...
They even ask me to check my blood as might need to do liver transplant for my daughter. They ask my permission whether I willing to do that and I told them that don't said part of the liver, if they want my life to save my daughter, they can take it. She still small n need to experience the world...
Everyday I cry after hearing what the doctor said and pray for God for some miracle to happen.
After few days, they told me that the hospital don't have the enough equipment to treat my daughter, so they used ambulance to transfer my daughter to GH and even put the machine to monitor the heart beat of my daughter. Really really scary...
I'll sometimes ask myself what had I done to mades her to suffered like that...
After few days, they told me that the hospital don't have the enough equipment to treat my daughter, so they used ambulance to transfer my daughter to GH and even put the machine to monitor the heart beat of my daughter. Really really scary...
I'll sometimes ask myself what had I done to mades her to suffered like that...
But with Gods will, the head doctor of padaetric, Dr Choy confirmed that my daughter having citrullenemia type 2 which is rare in Malaysia and my daughter is the 1st Malaysian diagnose with the problem and will fully recover when she is 1 year old but every year still need to draw her blood to ensure the problem will not arise again. Ouuch...
Anyway, really thank God for the miracle to happen....
Will talk about my sons in my next post...
Will talk about my sons in my next post...
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