We had our IJN check up 3 months post operation. The doctor said that the 2 holes in her heart have been fully closed. Thank God! But he did mention that a valve maybe leaky and will check if any swelling will happen to her heart, so far her heart looks normal. If no complications happens, this leaky valve may not need any intervention. Anyways, he will see Emily again in 3 more months.
We also went to Serdang Hospital to get appointments to check her eyesight and her hearing. We will have more appointments in September.
Looking back at how she was right after surgery and her now, it's a huge transformation that can only be possible with God's grace. Reflecting back, I am really grateful for the many kind gestures, words, prayers and thoughts by so many of our friends and relatives. I want to write this now so that I will never forget the kindness of so many and particularly a few that I will mention. In order to respect their privacy, I will only give their initials. You know people are often forgetful, I don't want to forget this ever.
I am really thankful to SN, she has taken so much time and effort to come cheer me up when I am stuck in Hospitals. I know she did so because of her long struggle with her dad's illness when she spent huge amount of time in Hospitals too. So I think she feels strongly about providing support to friends who have loved ones in hospitals. At these hard times, friends being there for you not only lend you a listening ear but also provide you comfort and hope. SN always got more close friends along and they will visit me for hours at the Hospitals just to chat. Thank you PY, AH, KK for spending sometimes hours with me in the most uncomfortable of places. Thank you SC and AL for your kind concern eventhough we were not keeping in touch for some time.
I was very touched by the kind gestures of NH, he took his own money to offer prayers during the times when we need divine help. Even offered to help with medical expenses. I am pleasantly surprise that he has a heart of gold though he doesn't necessarily display this out. Your thoughts are enough, thank you. My other colleagues for taking time to visit.
Also I am very pleased with the doctors and nurses at the hospitals. Their services are marvellous and they are very friendly, much improved from years ago. The nurses especially are very under appreciated. Their jobs are really like those of angels, thank you to each and everyone of you.
There are the church people who has shown us much concern and given their prayers for Emily unselfishly. The parish priest for taking time to hear us and the trouble to perform her baptism in the hospital.
My family members, my mum and MIL for helping out with the older kids while we are dealing with this. Aunty S for visiting us eventhough we have not seen each other for years.
I may be strong willed but these show of kindness from so many still means a whole lot to me and my hubby. At times of needs, we are able to see uncommon kindness that enhances friendships and kinships. I never want to forget this.
Emily is so much improved with the grace of the Almighty. My great friends and families played significant roles in helping us cope. THANK YOU!
This is a blog especially for Emily, the gift from God to us. She is a special girl, and you will learn this from this blog.
Friday, August 10, 2012
Monday, July 23, 2012
Progressing...
We went for Emily's check up last Monday, her weight is now 4.25 kg. Although she is still below the average weight for babies her age, it is still a good increase from her post-ops weight of about 3.4 kg. We will need to feed her about 90ml of breast milk every 3 hourly. Her medicine has also been reduced. Hopefully after the next IJN checkup, we can stop her medication. We will be going to IJN in 2 weeks' time. I hope her heart scan will show that she heart is doing well.
Since she has been staying in hospitals for a large part of her 4 months, we just realised we have missed 2 of her immunisation. Last night, we finally bought her to a local clinic and got her month 2 jab. She will need a few more jabs to catch up.
The paediatrician in Hospital Kajang has also given us 2 referrals to check her eyes and her ears in Serdang Hospital. We need to make time to bring her there too.
Since she has been staying in hospitals for a large part of her 4 months, we just realised we have missed 2 of her immunisation. Last night, we finally bought her to a local clinic and got her month 2 jab. She will need a few more jabs to catch up.
The paediatrician in Hospital Kajang has also given us 2 referrals to check her eyes and her ears in Serdang Hospital. We need to make time to bring her there too.
Sunday, July 15, 2012
Emily, the Smiley
I wonder it anyone reads this blog besides my hubby but that's fine. I just want to write down what I go through periodically, together with our precious and special little girl, Emily. She is now 3.5 months old, her next check up is on this coming Monday. I really hope we hear all positive things from the doctor. She seems to be doing very well at home, feeding well, sleeping and playing well too. Even after I swap her formula powdered milk to breast milk, she seems to be doing fine. My MIL was worried about her not feeding as much compared to the formula milk but under my care, she seems to feed well. So I am quite sure, she is doing fine. I think it's more about getting her in a comfy positiion so she can feed on the bottle nicely.
Another 3 weeks, we will be seeing the IJN doctors. Apart from a healed scar on her chest that is about 3 inches in length and resembles a centipede, she seems to have healed very well from her operation. If I have not mentioned before, the IJN bill worked out to be pretty hefty and we will be paying a large amount from our pockets. But I keep reminding myself about the time when we were uncertain about her heart condition and we had made up our mind to foot any cost involved just to get her cured, I stop feeling the pain the money that her operation cost us. I honestly do not mind paying the money in exchange for her mended heart. In fact I am very grateful to my hubby's company for helping us (in whatever extent) even when the insurance doesn't cover medical cost from congenital heart disease.
Emily, she is a pro at smiling and making cooing noises. You can easily make her smile and laugh by baby-talking to her, provided you satisfy her tummy first. Life with her is at the moment pretty normal. She looks and acts like any other baby, most of the time. I hope she will continue to do so. I pray for her to grow and learn normally like any kid and that she will have a fruitful and fulfilling Christian life.
Another 3 weeks, we will be seeing the IJN doctors. Apart from a healed scar on her chest that is about 3 inches in length and resembles a centipede, she seems to have healed very well from her operation. If I have not mentioned before, the IJN bill worked out to be pretty hefty and we will be paying a large amount from our pockets. But I keep reminding myself about the time when we were uncertain about her heart condition and we had made up our mind to foot any cost involved just to get her cured, I stop feeling the pain the money that her operation cost us. I honestly do not mind paying the money in exchange for her mended heart. In fact I am very grateful to my hubby's company for helping us (in whatever extent) even when the insurance doesn't cover medical cost from congenital heart disease.
Emily, she is a pro at smiling and making cooing noises. You can easily make her smile and laugh by baby-talking to her, provided you satisfy her tummy first. Life with her is at the moment pretty normal. She looks and acts like any other baby, most of the time. I hope she will continue to do so. I pray for her to grow and learn normally like any kid and that she will have a fruitful and fulfilling Christian life.
Friday, July 6, 2012
Gadgets for Baby
Emily is due for her check up in the hospital the Monday after next. She is going to have her blood drawn next Monday to run some tests. I hope the results will allow her to stop all the medication that she is currently taking. She is also due to change from fat-free formula milk to breast milk which I have accumulated for her in my new freezer. Her very expensive fat-free formula is almost out as well, but I am a bit worried about her ability to adapt back to breast milk after 6 weeks of not taking it. I am also worried if switching back to breast milk will cause any problems like it did right after her operation.I think I will mix both types of milk and take 2 to 3 days to switch her over. Hope I still have enough formula milk to do so...
Otherwise, Emily is doing just fine. I think she is well over 4kg now, hooray! She still pants after feeding for a short awhile but will resume feeding quickly. She is responding to us well, smiling when we make funny noises. She is even cooing and oohing back at us. She has been flagging her arms and legs since a long time ago and her neck is getting stronger.
As my mum suggested, I have brought an electronic automatic shaker for the baby hammock and it's a great help. We can leave her for a long while in the cradle while I do other stuff around the house, RM180 for that with 6 months warranty. This will be useful too when the maid is here so the maid can do other work while Emily sleeps in the day. Additional, I have ordered iBaby online. It's an IP webcam/baby monitor that can be accessed and controlled using iPhone app. It has night vision and supports 2 way communication too. I am waiting for the RM699 iBaby to be delivered. Quite excited about getting it to work so I can start checking on Emily live while I am at work!
Otherwise, Emily is doing just fine. I think she is well over 4kg now, hooray! She still pants after feeding for a short awhile but will resume feeding quickly. She is responding to us well, smiling when we make funny noises. She is even cooing and oohing back at us. She has been flagging her arms and legs since a long time ago and her neck is getting stronger.
As my mum suggested, I have brought an electronic automatic shaker for the baby hammock and it's a great help. We can leave her for a long while in the cradle while I do other stuff around the house, RM180 for that with 6 months warranty. This will be useful too when the maid is here so the maid can do other work while Emily sleeps in the day. Additional, I have ordered iBaby online. It's an IP webcam/baby monitor that can be accessed and controlled using iPhone app. It has night vision and supports 2 way communication too. I am waiting for the RM699 iBaby to be delivered. Quite excited about getting it to work so I can start checking on Emily live while I am at work!
Wednesday, June 20, 2012
One Month Post Surgery
Can't believe it that it's only been one month since Emily had her open heart surgery. She is doing so well at home that it feels like it was ages ago. My little baby is eating and growing like a young baby should and we have gotten really so used to her being around us all the time. She is a very smart baby, she knows when there isn't anyone watching over her, even when she is supposed to be sleeping. If you leave her side for even a minute, she will start fidgeting. If you still do not run to assure her of your presence, she will start crying! Her grandmothers and I have gotten used to this. Some singing is also required to make her sleep faster. She also loves to be cradled in your arms, she would sleep so soundly.
As I write this in my office, I miss holding her and planting kisses on her little chubby face. I love to kiss her chin most, the cute little chin of hers :). Fortunately, I have her pics and videos on my iPhone when I miss her. Her hair is starting to grow back on her little bald head. I can't wait for her to grow bigger to fit into the pretty clothes that I bought and also given by relatives and friends.
We have a few checkups to go to in a few weeks, both at Kajang Hospital and at IJN. At the moment, we are about to run out of the special, fat-free milk powder and I cannot find it in any pharmacies. I think we need to have one or two packs more to last till the end of the 1st week of July. I think I have no choice but to call IJN to ask where I can buy them from.
As I write this in my office, I miss holding her and planting kisses on her little chubby face. I love to kiss her chin most, the cute little chin of hers :). Fortunately, I have her pics and videos on my iPhone when I miss her. Her hair is starting to grow back on her little bald head. I can't wait for her to grow bigger to fit into the pretty clothes that I bought and also given by relatives and friends.
| Can't find her neck no more! |
Tuesday, June 12, 2012
Getting into our routine
Emily is growing nicely, we can see her face getting rounder and she is demanding more feeding :). She is still on her special non fat diet until a week into July but we have ran out of Carborie, a calorie supplement. I tried finding it in a few pharmacies but none of them have it. Finally, checked out the main marketeer in the country for it and found out that it is available in Caring Pharmacies, nearest one in Balakong, Aeon Jusco. So I plan to go there this weekend.
Emily has been well-behaving so far, not much of a trouble maker :P. She
is due for her check up in a few weeks at Kajang Hospital and IJN in
August. Her chest wound is healing but the end part of it looks a bit rare and still has a small hole in the skin.
I know it doesn't hurt her because she seems fine when I bathe her or
put antiseptic on it. But it still worries me, but we will wait until
the next check up to ask the paediatrician.
At the last check up, the paed could still hear murmurs in her heart. I suspect this is due to the ASD which may not be entirely closed up. But I think it's not something to worry about since she is doing pretty well now. Even pre-ops, the doctors didn't seem too concerned with the ASD and they were concentrating on fixing the large VSD. They did mention that since they were doing the ops to close the VSD, they will close the ASD as well. So I believe the residual ASD should not cause problems.
We have arranged for our mothers to take turns in caring for Emily while we are at work. This week, my dear mum is down from BP to help us. She took the bus here and I went to Tsk Selatan Station by KTM to get her. Was my first time to the new bus station, it's very big and I think still under utilised. I am sorry to trouble the 2 grandmothers but maid is still not here. Checked with the maid agency and she said that the maid is expected to arrive only late August, so we have a few more months to wait. My mum also helped us do some rearranging of furniture (with the help of my sis' maid) in our living and dining rooms and now it looks a bit more spacious. I need to do more organising and cleaning and also need to clear some stuff. Didn't manage to clear the maid's room yet, so hubby need to make time to do so soon. Lots to do but we are much more settled. Getting into a good routine, tight/rushing but manageable.
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| Emily's cheeks are so kissable! |
At the last check up, the paed could still hear murmurs in her heart. I suspect this is due to the ASD which may not be entirely closed up. But I think it's not something to worry about since she is doing pretty well now. Even pre-ops, the doctors didn't seem too concerned with the ASD and they were concentrating on fixing the large VSD. They did mention that since they were doing the ops to close the VSD, they will close the ASD as well. So I believe the residual ASD should not cause problems.
We have arranged for our mothers to take turns in caring for Emily while we are at work. This week, my dear mum is down from BP to help us. She took the bus here and I went to Tsk Selatan Station by KTM to get her. Was my first time to the new bus station, it's very big and I think still under utilised. I am sorry to trouble the 2 grandmothers but maid is still not here. Checked with the maid agency and she said that the maid is expected to arrive only late August, so we have a few more months to wait. My mum also helped us do some rearranging of furniture (with the help of my sis' maid) in our living and dining rooms and now it looks a bit more spacious. I need to do more organising and cleaning and also need to clear some stuff. Didn't manage to clear the maid's room yet, so hubby need to make time to do so soon. Lots to do but we are much more settled. Getting into a good routine, tight/rushing but manageable.
Sunday, June 3, 2012
Journey continues...
We have been home for 4 days now.Emily is feeding from the bottle very well. I think she will be catching up with all the weight gain that she needs very fast.Tomorrow, we are going to have her stitches removed from her poor chest. I think it will hurt quite a bit for her but compared to what she has been through these 2 months, it will be a breeze. And moreover, this is the last bit from her surgery. She should be gaining speed to a full recovery and also start growing like a baby should.
Whenever I bathe or change her, I will cringe at the sight of the stitches and think about the permanent scar on her chest. I hope she will take the scar positively and take it as a reminder of what she has been through and how precious life is.
When I look at her now, how she sleeps so peacefully, how she feeds to quickly and how she sometimes flashes her smile that melts my heart, I am really happy that the worst times are over. I tend to forget that she may have other problems related to her syndrome. But then again, it's a 'may'. So I guess there is really no point in thinking about the mays and maybes. Well, I should just enjoy taking care of a young life and nurture and love her as I did her older siblings.
Family and friends have been very supportive of the whole situation. Concerned family members and friends from work and church have visited us in the hospitals and at home quite a bit. We are really thankful for all their concerns and especially for their prayers which I really believe helped Emily a great deal in her recovery. As suggested by my dear friend, I went to church today to offer thankgiving mass for Emily.
As I said, this is a journey and Emily, we as parents and her siblings, as well as all family and friends are in this together. And the journey continues, we hope we have more happy times then sad ones...
Whenever I bathe or change her, I will cringe at the sight of the stitches and think about the permanent scar on her chest. I hope she will take the scar positively and take it as a reminder of what she has been through and how precious life is.
When I look at her now, how she sleeps so peacefully, how she feeds to quickly and how she sometimes flashes her smile that melts my heart, I am really happy that the worst times are over. I tend to forget that she may have other problems related to her syndrome. But then again, it's a 'may'. So I guess there is really no point in thinking about the mays and maybes. Well, I should just enjoy taking care of a young life and nurture and love her as I did her older siblings.
Family and friends have been very supportive of the whole situation. Concerned family members and friends from work and church have visited us in the hospitals and at home quite a bit. We are really thankful for all their concerns and especially for their prayers which I really believe helped Emily a great deal in her recovery. As suggested by my dear friend, I went to church today to offer thankgiving mass for Emily.
As I said, this is a journey and Emily, we as parents and her siblings, as well as all family and friends are in this together. And the journey continues, we hope we have more happy times then sad ones...
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