검색어: i think you don’t need me anymore (영어 - 말레이어)

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i think you don’t need me anymore

Malay

 

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영어

말레이어

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영어

i don't think you need me anymore

말레이어

terima kasih bagi saya peluang rasa kasih sayang awak

마지막 업데이트: 2021-12-02
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영어

you don't need me anymore

말레이어

awak tidak perlukan saya lagi

마지막 업데이트: 2022-05-08
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영어

i think you complimented me too much.

말레이어

seseorang memuji saya

마지막 업데이트: 2023-05-14
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영어

i think you are cute

말레이어

saya ada sekarang

마지막 업데이트: 2020-10-26
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영어

i think you deserve it.

말레이어

saya rasa saya layak dan akan mendapat keputusan cemerlang di university ini

마지막 업데이트: 2023-05-11
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영어

i think you are the wrong person

말레이어

hello.miss saya nampak awak masukkan barang dalam beg

마지막 업데이트: 2021-01-21
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영어

sorry i think you got the wrong person

말레이어

did i choose the wrong one

마지막 업데이트: 2021-04-28
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영어

i think you should be proud and cry as well

말레이어

saya rasa kamu patut bangga dan menangis pada masa yang sama

마지막 업데이트: 2018-06-04
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영어

i think you need to be considerate so as not to hurt the feelings of he

말레이어

saya rasa awak perlu bertimbang rasa supaya tidak menyakitkan perasaan dia

마지막 업데이트: 2016-09-14
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영어

i think you just gave birth. it's been a while

말레이어

aku rasa engkau baru lepas beranak . sekejap je dah besar

마지막 업데이트: 2020-08-07
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영어

do not call my name if there is no interest before i think you have annoying

말레이어

jangan panggil nama saya jika tiada kepentingan sebelum saya berfikiran kamu ada menjengkelkan

마지막 업데이트: 2017-11-06
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영어

happy birthday to the dad whose hair i turned gray. i think you pull off the look really well

말레이어

selamat hari lahir kepada ayah yang rambut saya bertukar kelabu. saya fikir anda menarik keluar kelihatan benar-benar baik

마지막 업데이트: 2022-12-07
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영어

sorry to ask you sent a late night message to me you have not slept to..i think you are dreaming

말레이어

maaf tanya awak hantar mesej lewat malam pada saya awak belom tidur ke..saya fikir awak mimpi

마지막 업데이트: 2020-11-08
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영어

certainly we gave moses nine manifest signs. so ask the children of israel. when he came to them, pharaoh said to him, ‘o moses, indeed i think you are bewitched.’

말레이어

dan sesungguhnya kami telah memberi kepada nabi musa sembilan mukjizat yang jelas nyata (membuktikan kebenarannya); maka bertanyalah (wahai muhammad) kepada bani israil (tentang itu): ketika nabi musa datang kepada firaun dan kaumnya (serta menunjukkan mukjizatnya), lalu berkatalah firaun kepadanya: "sesungguhnya aku fikir, engkau ini wahai musa, seorang yang terkena sihir"

마지막 업데이트: 2014-07-03
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영어

and indeed we gave moosa nine clear signs, therefore ask the descendants of israel when he came to them – in response firaun said, “o moosa – i think you are under a magic spell.”

말레이어

dan sesungguhnya kami telah memberi kepada nabi musa sembilan mukjizat yang jelas nyata (membuktikan kebenarannya); maka bertanyalah (wahai muhammad) kepada bani israil (tentang itu): ketika nabi musa datang kepada firaun dan kaumnya (serta menunjukkan mukjizatnya), lalu berkatalah firaun kepadanya: "sesungguhnya aku fikir, engkau ini wahai musa, seorang yang terkena sihir"

마지막 업데이트: 2014-07-03
사용 빈도: 1
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추천인: 익명
경고: 보이지 않는 HTML 형식이 포함되어 있습니다

영어

“as a mother, i wished we could have exchanged places.” in a single sentence, noorlela abdul hamed sums up the years spent watching her son irfan go through a childhood of tubes inserted into his body, medical tests, blood transfusions and eventually, the removal of his spleen at age six. this, as she also juggled financial difficulties coping with irfan’s medical bills, work, and caring for her other children and family members. now 18, irfan was born with thalassemia major, a life-threatening blood disorder that leads to serious anemia. severe cases can lead to organ damage, which can be fatal. positive and forward-looking by nature, noorlela’s sunny demeanor belies the considerable challenges she had to navigate while caring for irfan. “i have parents who stay together with me, then i have other children...the youngest who's having asthma as well, my step mom was having a stroke then my dad who was just a cancer survivor...a lot of things happened,” shares noorlela, who goes by lela. she adds: “of course i don't want to see my son suffering. it’s very painful. [irfan] needs blood [transfusions] for the entire of his life. because he has no spleen now, he needs antibiotics until the end of his life.” caregivers, she notes, often do not know whom they can turn to and trust with their feelings. “sometimes they keep it to themselves. you know, you think you can swallow alone but at the end of the day, you choke.” says lela. it is this group of parents that new-i, a cyber counselling tool in the form of a mobile app, seeks to help. caregiver emotions through a new eye developed in singapore by a team of researchers from nanyang technological university (ntu), new-i, or narrative e-writing intervention, is currently being tested as a pilot funded by temasek foundation under its smf research grant programme. over four weeks, participants pen their thoughts in short writing exercises on the app, which are structured to help them reflect on their caregiving journey and process their emotions, with input from a counsellor. participants’ entries are compiled and edited into an illustrated digital “legacy book” at the end of the exercise, which serves as a memory of their thoughts, feelings and experiences of caring for their child. currently, the new-i team works with cerebral palsy alliance singapore, club rainbow (singapore), kk women’s and children’s hospital, muscular dystrophy association (singapore) and rare disorders society (singapore) to bring participants onboard the pilot. according to the new-i team, typical challenges faced by parent-caregivers of children with chronic life-threatening illnesses include psychological distress and emotional pain regarding the diagnosis, feelings of loss and grief on a daily basis as they cope with their child’s deteriorating health, financial concerns and the struggle to dedicate time to their relationships with their spouses and family members. they may also unintentionally neglect their other healthy children, while frequent communication with healthcare teams may cause anxiety and distress if they do not feel sufficiently engaged in making care decisions for their child, shares dr oindrila dutta, co-investigator of the new-i research team. as associate professor andy ho, principal investigator of the research team, puts it, “the quality of care patients receive is only as good as the quality of health of their caregivers.” the app aims to provide psycho-social support and useful resources to parents, while giving them an opportunity to reflect on their journey — time they otherwise might not carve out for themselves amid the day-to-day demands of caregiving. through the pilot, the researchers are collecting data, including examining the design and feasibility of the app and monitoring outcomes. outcomes of the pilot so far showed that after completing new-i, parents report an improvement in their quality of life, overall spiritual well-being, their inner sense of meaning and peace and feel more optimistic about the social support that is available to them. they also report reduction in their caregiver burden. the findings of the pilot could help inform potential larger-scale implementation of new-i in the future, thereby being available to, and supporting more parent-caregivers in singapore. some 54 participants have enrolled and completed the pilot, among them lela. a legacy of love lela had found solace in writing a letter about her grief over unexpectedly losing her younger son zikry a few years ago. the pain and shock of losing zikry had been a powerful one. “i can't describe it in words but the nearest i can say it's like you are tearing your own skin and you are pouring salt on the broken skin,” says lela. on hearing that lela had found writing to be a good outlet for her feelings, a social worker from club rainbow encouraged her to write about irfan in the new-i app, to document her experience as a caregiver to a child with a chronic and life-threatening condition. in writing about her years caring for irfan, lela focused on the positive moments — the positivity she has tried to instill in irfan in dealing with his condition, the special moments they share together over meals and holidays, the loving support of her husband and mother in managing the ups and downs of her journey. “i’ve always felt that every day is a special day. spending time alone with him is important. sometimes we do go out, spend our time together, like [we are] dating. all these important moments are very precious,” she says. the experience of writing on new-i was a cathartic one. “after i pour everything out, of course i feel more stronger. i feel like oh, i’ve been through all this. “i can see that, i’m strong, and it really comes out as a beautiful story. and i really will keep [the legacy document] for the rest of my whole life,” says lela. although irfan is now old enough to manage his health well, lela has her moments of worry. “yearly, irfan must go through the mri. so that’s also a very crucial point. they are looking for any change in size of the organs,” she explains. “that’s the worst fear. if he goes off before me, i can just be thankful for the precious moments that i have with him. he’s a good boy,” she says. pausing as she becomes emotional, she continues: “i think he has fight, strong enough to be where he is today. as a mother, i only can pray for the best.” having cared for irfan all these years, she understands the emotional weight borne by parents like her, and urges parents to always seek a listening ear. “when you are at the stage of time, when you are having this problem, a lot of things will mess up your brain. but this app will help you to tone down,” she notes. irfan, for his part, is proud of how lela has raised him to come to terms with his condition. “there was one point of time i also realised i couldn't be the same as others even though i tried my hardest,” says irfan, a polytechnic student. “my mum always motivates me, reminding me that even when people are given disabilities, they will also be given special strengths that other people don’t have,” he says. “i feel very appreciative of my mother, for putting all this effort just to take care of all of us. i feel very blessed to have her as my mum. lela, reflecting on her journey, says the new-i app summarised everything “in a very beautiful manner”. “growing up with irfan like this, i don’t find it as a burden. i feel maybe it colours my life beautifully, that i have experienced all sorts of things together with him,” she says. irfan adds: “to parents who have children with such conditions, don’t give up on your children, because even though they are special in their own ways, they are still able to do great things in the future.” this story was funded in part by temasek foundation. visit our promise page to find out how we maintain editorial integrity while balancing our needs as a non-profit. about new-i new-i, or narrative e-writing intervention, is a cyber-counselling app for parents of children with chronic and life-threatening conditions, developed by a team from nanyang technological university. over four weeks, participants pen their thoughts on the app, which helps them reflect on their caregiving journey and process their emotions with input from a counsellor. their entries are compiled into an illustrated “legacy book” at the end of the exercise, which is intended to provide solace after their child’s passing. the app is being implemented as a pilot funded by temasek foundation under its

말레이어

마지막 업데이트: 2024-02-05
사용 빈도: 1
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추천인: 익명

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