Soserv Welfare Malaysia 马来西亚999生命连线

Soserv Welfare Malaysia 马来西亚999生命连线 Driven to save!
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马来西亚999生命连线(Soserv Welfare)
是一家致力于社会援助的非营利慈善机构(NGO)。

Registered Name: Persatuan Kebajikan Dan Sosial Sejahtera Masyarakat Malaysia
Registration Number: PPM-002-10-11032021

生命不掉线,爱一直在线!
Connected by Care. Soserv Welfare Malaysia
马来西亚999生命连线
Persatuan Kebajikan dan Sosial Sejahtera Masyarakat Malaysia (PPM-002-10-11032021)

我们是一家致力于帮助弱势群体的慈善机构。我们将贫困援助视为使命,秉持不分宗教,不分种族的理念,在大马的多元社会中,平等帮助每一个有需要的人。

提供

的六大援助项目如下:
- 免费收留特殊孩童 (截至29.06.2026有40位)
- 紧急医疗援助
- 医疗器材援助
- 施棺安详送别援助
- 物资救济援助
- 清寒助学金援助

您的善心,将成为身障孩子的避风港;
您的帮助,将拯救病患的生命;
您的支持,将让更多贫苦的人们,重获生活的希望!

14/08/2026

《15岁抗癌少女左脚发育畸形,盼筹措医疗费重新站起来》

#紧急医疗器材援助

杨厤衫不到3岁时,就被诊断出脊柱长满肿瘤。

虽然这些肿瘤属于良性,但数量众多,压迫神经,导致她下半身完全瘫痪,大小便也无法自主控制。

心急如焚的父母立刻带她寻求治疗,医生也随即安排手术。手术顺利切除了80%肿瘤,术后复原情况良好。

除了左脚无力、走路稍显不稳外,厤衫几乎恢复孩子该有的正常生活。

然而,谁也没想到,这份来之不易的平静,并没有维持太久。

#肿瘤病变只能活两年

7岁那年,她脊柱残留的肿瘤发生病变,不得不再次接受肿瘤切除手术。

术后,医生建议厤衫继续接受化疗和电疗。虽然肿瘤生长在脊柱,但它属于脑部肿瘤类别,复发风险较高。

当时,医生判定她只能活两年,妈妈瞬间崩溃,更害怕年幼的女儿承受不了治疗的痛苦。

最终,凭着顽强的生命力,厤衫挺过了最艰难的阶段,病情也终于逐渐稳定下来。

#双脚长短不一相差7公分

脊椎始终遭受重创,已无法恢复昔日的灵活性,更导致她左脚长期无力,每迈出一步,都显得格外艰难。

然而,随着她逐渐长大,左脚发育相对迟缓,两只脚长度相差整整7公分,不仅严重影响行走平衡,更让她的日常生活也处处受限。

为了避免双脚长短差距持续扩大,厤衫在13岁时接受了断骨增高手术。

医生通过截断部分腿骨,利用骨骼自然再生的能力,逐步延长较短的左腿骨,以缩小双脚的长度差距。

在漫长的治疗过程中,她必须长期佩戴固定支架,不仅行动不便,每天还要忍受持续的疼痛。

更令人心疼的是,由于髋关节脱位,她的左腿骨最终只能延长4公分,双脚依然长短不一,无法恢复平衡。

#左脚骨骼弯曲须再治疗

好不容易熬过腿部治疗期,原以为病情终于稳定,无奈左脚持续无力,骨骼渐渐向内弯曲,最终变成畸形,只能依靠轮椅代步。

目前,医生已为她的左大腿装上环形外固定架,若大腿骨矫正情况良好,很快便可接受钢板植入手术,以固定并支撑骨骼。

接下来,她也将接受脚踝治疗,最终方案仍待医生评估。

#一家六口生计靠父母支撑

转眼间,厤衫已成长为15岁的少女,她却依然饱受病痛折磨,至今仍无法重返校园。

这些年来,父母陪着她一次次从柔佛居銮赴吉隆坡求医,为了女儿,几乎花光毕生积蓄。

频繁往返医院,也让父母经营的佛牌线上生意大受影响,收入早已不如从前。

然而,家中还有哥哥、妹妹及80岁的婆婆需要照顾,一家六口的生计,全靠父母撑起。

面对女儿接下来手术所需植入的钢板费用及后续治疗开销,父母已无力承担,只能无奈四处寻求援助。

#少女盼望重新行走

经过家访审核,我们决定接受杨厤衫父母的求助委托,并即刻启动筹款。

我们将为历尽坎坷的少女筹募植入性钢板及后续治疗费,合共RM25,000。

在此呼吁各界热心人士伸出援手,协助她筹足医疗费,顺利接受所需的治疗。

您的一份爱心,不仅能帮助她重新站起来,更能让她重拾自信,回到校园继续学习。

有意捐助者,请与我们联系,获取捐助详情,感恩。
https://wa.me/60102595965

Reference:Sylvia Yang Li Shan

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【马来西亚999生命连线 Soserv Welfare Malaysia】
🏠 地址:33, Jalan 18/14, Taman Kanagapuram, 46000 Petaling Jaya, Selangor. (10am - 6pm)
☎️ 电话号码:010-259 5965 / 03-7772 5959
📧 Email: [email protected]

***如果你或你身边的人,正在面临身障孩子照顾/生活贫困/医药费不足/丧葬费不足等困难,请联系我们。你也可以向我们做生前登记,委托我们为你处理身后事。我们将为求助者,提供需要的援助。***

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【15-Year-Old Cancer Survivor with a Deformed Left Leg Appeals for Medical Support to Walk Again】

Medical Equipment Assistance

When Sylvia Yang Li Shan was not yet three years old, she was diagnosed with multiple tumors growing along her spine.

Although the tumors were benign, they were so numerous that they compressed her spinal nerves, leaving her completely paralyzed from the waist down and unable to control her bladder or bowel movements.

Heartbroken and desperate, her parents immediately sought medical treatment for her, and doctors arranged surgery without delay. The operation successfully removed about 80% of the tumors, and her recovery went remarkably well.

Apart from weakness in her left leg and a slight limp when walking, Sylvia was able to regain a childhood that was almost like any other child's.

But no one expected that this hard-earned period of peace would not last for long.

Turned Malignant, Given Two Years to Live

When Sylvia was seven years old, the remaining tumor in her spine underwent malignant changes, forcing her to undergo another surgery to remove it.

After the operation, doctors recommended that she continue with chemotherapy and radiotherapy. Although the tumor was located in her spine, it was classified as a brain tumor, which carried a high risk of recurrence.

At that time, doctors told the family that she had only two years to live. Her mother was devastated and feared that her young daughter would not be able to endure the pain and hardship of treatment.

Yet through extraordinary courage and determination, Sylvia survived the most difficult chapter of her life, and her condition gradually stabilized.

7-Centimeter Difference Between Her Legs

The damage to Sylvia's spine was permanent, and it could never regain its former flexibility. As a result, her left leg remained weak, making every step she took a constant struggle.

As she grew older, her left leg developed much more slowly than her right, eventually leaving a 7-centimeter difference in length between the two legs. This not only severely affected her balance when walking but also made everyday activities increasingly difficult.

To prevent the gap from widening further, Sylvia underwent limb-lengthening surgery at the age of 13.

During the procedure, doctors surgically cut part of her leg bone and relied on the body's natural ability to regenerate bone, gradually lengthening her shorter left leg to reduce the difference in leg length.

Throughout the long treatment process, she had to wear an external fixation frame for an extended period. Not only did it make movement difficult, but she also endured constant pain every single day.

What was even more heartbreaking was that because of a dislocated hip joint, her left leg could only be lengthened by 4 centimeters in the end. Even after everything she had gone through, her legs remained unequal in length, and her balance could not be fully restored.

Surgery for Her Left Leg

Just as Sylvia had finally endured the long journey of leg treatment and hoped her condition had stabilized, her left leg continued to weaken. Over time, the bone gradually curved inward, eventually becoming deformed and leaving her dependent on a wheelchair.

She has now been fitted with a circular external fixation frame on her left thigh. If the femur responds well to the correction, she will soon undergo plate implantation surgery to stabilize and support the bone.

After that, she will also need treatment for her ankle, with the final treatment plan to be determined following further medical evaluation.

Family of Six Depends on Her Parents

Now 15 years old, Sylvia has grown into a teenager, yet she continues to suffer from her illness and has still been unable to return to school.

Over the years, her parents have accompanied her on countless trips from Kluang, Johor, to Kuala Lumpur for medical treatment. In their determination to help their daughter, they have spent nearly all of their life's savings.

The frequent hospital visits have also taken a heavy toll on the parents' online business selling Buddhist amulets, leaving their income far lower than it once was.

Yet they are not only caring for Sylvia. Her older brother, younger sister, and 80-year-old grandmother also depend on them. The livelihood of their family of six rests entirely on her parents' shoulders.

Now, faced with the cost of the metal plate that must be implanted during Sylvia's upcoming surgery, along with the expenses of her ongoing treatment, her parents can no longer afford the burden and have no choice but to seek help from the public.

Hope to Walk Again

After conducting a home visit and completing our assessment, we have decided to accept the family's request for assistance and officially launch a fundraising campaign for Sylvia Yang Li Shan.

Our goal is to raise RM25,000 to cover the cost of her implantable metal plate and the medical expenses for her ongoing treatment.

We sincerely appeal to kind-hearted members of the public to extend a helping hand and support Sylvia in receiving the treatment she urgently needs.

Your generosity will not only help her stand and walk again, but also restore her confidence and give her the opportunity to return to school and continue her education.

If you would like to support Sylvia's journey, please contact us for donation details. Thank you for your kindness and compassion.
https://wa.me/60102595965

Reference:Sylvia Yang Li Shan

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#慈善机构 #筹款活动 #拯救生命 #脊柱瘤 #髋关节脱位 #矫正 #手术

13/08/2026

【高温预警!慈少班50人组团来袭,带来105度的爆表热情】

我们中心熟悉的常客——慈少班团队又来探访了。

这次,他们不只带来新鲜蔬果和纸尿片,也各自捐献善款,累积数额接近 RM2,000。

这份心意,给了孩子们很实际的支持,也让中心感受到满满温暖。

约50人由慈少班小成员、父母及义工组成的团队,一进到中心就亲切地和孩子们问好。

刚开始有些孩子还有点害羞,但随着活动开始,笑容也慢慢多了起来。

大家先围成一个大圈圈,玩起纸传球游戏。孩子们和小成员一起合力传球,有人小心翼翼地接,有人传到一半忍不住笑,现场气氛一下子变得轻松又开心。

接着,围圈传球游戏更刺激;音乐一停,球在谁手上,谁就要出来跳舞。

第一位“幸运儿”竟是阿汉!在义工鼓励下,他腼腆地完成了自己的舞台首秀。

阿英更可爱,贴心陪着小成员共舞;家兴、忠豪、程裕也加入扭动身体的行列,大家笑成一片,场面热闹又有趣。

之后,Kelly、程裕和忠豪在义工陪伴下玩木头人套圈游戏,玩得不亦乐乎。
另一边,其他孩子和小成员一起填色,再把作品做成小风车。

义工耐心握着丽萍的手,一笔一笔陪她填色;阿英也像小老师一样,认真教妮妮填色,画面特别温柔。

最热闹的是唱歌环节。义工带动孩子们边跳边唱,《甜蜜蜜》音乐一响起,阿英立刻拿起麦克风高歌。

心妮和家兴也陆续 solo 唱歌。义工牵着永进的手一起唱跳,他害羞低着头,却还是乖乖参与;妍洁也忘我地和义工开心起舞,现场一片闹哄哄。

到了午餐时间,义工准备了素食饭菜,一份份分派给孩子们。慈少班小成员还主动喂 Jasper 吃饭,小小的动作,却特别贴心。

这大半天的相聚,没有华丽节目,却有很多让人感动的小细节。

谢谢慈少班成员、父母及义工们,把陪伴、关怀和笑声带进中心,让孩子们度过了一个特别温暖的上午。

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马来西亚999生命连线 Soserv Welfare Malaysia是一家非盈利慈善组织,目前免费收留了35名特殊孩童。收留中心每日开放,时间从上午10时至下午6时,欢迎各界人士亲临。有意探访我们的特殊孩童,欢迎与我们联系 WhatsApp:https://wa.me/60102595965

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【马来西亚999生命连线 Soserv Welfare Malaysia】
🏠 地址:33, Jalan 18/14, Taman Kanagapuram, 46000 Petaling Jaya, Selangor. (10am - 6pm)
☎️ 电话号码:010-259 5965 / 03-7772 5959
📧 Email: [email protected]

***如果你或你身边的人,正在面临身障孩子照顾/生活贫困/医药费不足/丧葬费不足等困难,请联系我们。你也可以向我们做生前登记,委托我们为你处理身后事。我们将为求助者,提供需要的援助。***

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【Heat Alert! 50 Members from Tzu Chi’s Teenager Junior Class Arrive with 105°C of Overflowing Passion】

A familiar group of regular visitors to our centre, Tzu Chi’s Teenager Junior Class, came to visit us again.

This time, they not only brought fresh fruits, vegetables and diapers, but also made personal donations, with the total amount reaching nearly RM2,000.

Their kindness provided very practical support for the children and brought great warmth to our centre.

The team of about 50 people, made up of Teenager Junior Class members, parents and volunteers, warmly greeted the children as soon as they arrived at the centre.

At first, some of the children were still a little shy. But as the activities began, more and more smiles slowly appeared on their faces.

Everyone first gathered in a big circle and played a paper ball passing game. The children and the young members worked together to pass the ball. Some received it carefully, while others could not help laughing halfway through. The atmosphere quickly became relaxed and joyful.

Next came a more exciting circle ball-passing game. When the music stopped, whoever was holding the ball had to come out and dance.

The first “lucky one” turned out to be Ah Han! With encouragement from the volunteers, he shyly completed his very first stage performance.

Ah Ying was even more adorable, thoughtfully dancing together with one of the young members. Kah Heng, Teong Hau and Chen Yi also joined in, moving their bodies along to the music. Everyone laughed together, and the scene was lively and fun.

After that, Kelly, Chen Yi and Teong Hau played a “freeze and ring toss” game with the volunteers, and they had a wonderful time.

On the other side, the other children coloured pictures together with the young members, before turning their artwork into little pinwheels.

A volunteer patiently held Lay Peng’s hand and accompanied her as she coloured stroke by stroke. Ah Ying was also like a little teacher, seriously guiding Nee Nee as she coloured. It was a particularly gentle and heartwarming scene.

The liveliest part was the singing session. The volunteers led the children to sing and dance together. As soon as the song Tian Mi Mi started playing, Ah Ying immediately picked up the microphone and sang out loud.

Sin Nie and Kah Heng also took turns singing solo. A volunteer held Yeong Ching’s hand and sang and danced with him. Although he shyly lowered his head, he still obediently joined in. Yan Jie also danced happily with the volunteers, completely enjoying the moment. The whole place was filled with cheerful noise and laughter.

When it was time for lunch, the volunteers prepared vegetarian meals and handed them out to the children one by one. The young members of Teenager Junior Class also took the initiative to feed Jasper. It was a small gesture, but an especially thoughtful one.

This half-day gathering did not have any grand programme, but it was filled with many touching little moments.

Thank you to the members, parents and volunteers of Teenager Junior Class for bringing companionship, care and laughter into our centre, allowing the children to spend a truly warm and special morning.

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#慈善组织 #行善 #慷慨解囊 #实践慈善 #慈少班 #义工天使 #素食

【重要公告|电话号码更正与致歉声明】Soserv Welfare Malaysia 在此向大众说明,经过内部检查,我们发现过去使用Facebook Messenger的其中一则自动回复模版(template)出现电话号码输入错误。原本正确的...
13/08/2026

【重要公告|电话号码更正与致歉声明】

Soserv Welfare Malaysia 在此向大众说明,经过内部检查,我们发现过去使用Facebook Messenger的其中一则自动回复模版(template)出现电话号码输入错误。

原本正确的联系电话为:013-712 5959

但在有关自动回复模版中,我们误将号码填写为:013-713 5959

因此,在过去一段时间内,部分善心人士可能根据该自动回复的信息,误将 013-713 5959 当作本机构的联系电话,并联系该号码或发送捐款 bank slip 等相关资料。

在此,我们郑重说明,013-713 5959 并非 Soserv Welfare Malaysia 的联系电话。

此次电话号码输入错误确实是本机构的疏忽。由于我们此前并未接获相关通知或反馈,因此一直未察觉有关错误,也没有意识到这项失误已经对号码持有人造成持续的困扰。

直到近日接获相关情况后,我们已立即展开全面检查,并将有关错误号码作出更正,以避免类似情况再次发生。

对于这几个月来,因为本机构的失误而对该号码持有人造成的不便与困扰,我们在此致以诚挚的歉意。

同时,也请所有善心人士及大众留意,请勿再拨打、WhatsApp 或发送任何捐款资料至 013-713 5959。

正确联系电话为:✅ 013-712 5959

若您过去曾将捐款 bank slip 或任何与本机构有关的资料发送至错误号码,也欢迎与我们联系,以便我们进一步协助核对及处理。

对于此次事件所造成的影响,我们再次向有关人士及所有受到影响的善心人士郑重致歉。

感谢大家的理解与配合。🙏🏻

Soserv Welfare Malaysia
Persatuan Kebajikan Dan Sosial Sejahtera Masyarakat Malaysia
马来西亚999生命连线

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【IMPORTANT ANNOUNCEMENT | Correction of Contact Number & Apology Statement】

Soserv Welfare Malaysia would like to inform the public that, following an internal review, we discovered that an incorrect phone number had been entered in one of our automated reply templates on Facebook Messenger.

The correct contact number is : 013-712 5959

However, the number was mistakenly entered in the automated reply template as : 013-713 5959

As a result, over the past few months, some kind-hearted donors may have relied on the information provided in the automated reply and mistakenly believed that 013-713 5959 was an official contact number of our organization. They may have contacted the number or sent donation bank slips and other related information to it.

We would therefore like to clarify that 013-713 5959 is NOT a contact number of Soserv Welfare Malaysia.

This error was caused by an oversight on our part. As we had not received any prior notification or feedback regarding the incorrect number, we were unaware of the mistake and did not realize that it had been causing ongoing inconvenience and disturbance to the actual owner of the number.

Upon being informed of the situation recently, we immediately conducted a comprehensive review and corrected the incorrect phone number to prevent a similar incident from happening again.

We sincerely apologize to the owner of the affected phone number for the inconvenience and disturbance caused over the past few months as a result of our error.

We would also like to remind all donors and members of the public: please do not call, WhatsApp, or send any donation-related information to 013-713 5959.

Our correct contact number is: ✅ 013-712 5959

If you have previously sent a donation bank slip or any information related to our organization to the incorrect number, please feel free to contact us so that we can assist you in verifying and following up on the matter.

Once again, we sincerely apologize to the individual concerned and to all donors who may have been affected by this incident.

Thank you for your understanding and cooperation. 🙏🏻

Soserv Welfare Malaysia
Persatuan Kebajikan Dan Sosial Sejahtera Masyarakat Malaysia
马来西亚999生命连线

12/08/2026

她希望未来,是做自己想做的事

很多人15岁,正忙着追梦、交朋友、打扮自己;但李嘉琪的15岁,却是在等待一场可能改变一生命运的手术。

从3岁确诊脑部结构异常后,嘉琪的生活磕磕绊绊,再也不曾平静。

她患有罕见疾病——小脑扁桃体下疝(Chiari Malformation)。而这个病也陆续引发了脑积水和脊椎侧弯等许多疾病,促使年纪轻轻的她,已被逼做了5场脑部手术,甚至曾小脑中风,右手和右脚无法动弹,经过艰辛复建才逐渐康复。

复杂和严重的病情,长期折磨着这个女学生。目前,她正面临严重脊椎侧弯的威胁,亟需手术挽救。

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其实,这场手术的风险并不低,如果不成功,有20 % 的机率她可能会陷入瘫痪。

她目前的脊椎侧弯已经达到90度,如果不做手术,将继续压迫神经并危及生命。

这是一个没有退路的选择。比任何人都清醒的嘉琪,早已下定决心要做这个关键的手术。

“我很早就决定了,只是脑科医生说,我的脑积水问题必须先解决。所以脊椎手术一再拖延,现在已经很严重了 。今年,医生说我终于可以做脊椎手术了。”

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因为脊椎侧弯,她比一般同龄人承受了更多的痛苦,她的手会发麻、颈椎不定时疼痛,无法久站、也无法长时间行走、并容易感到头晕。

“她一直很想穿连身裙,可是她不敢。”妈妈轻轻的说。

“每次照镜子时,看到弯弯的背部,我就不想再看镜子了。”嘉琪自己也做出补充。

处于原本爱漂亮的年纪,但她却慢慢失去了照镜子的勇气。

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当她穿戴脊椎矫正支架去学校的时候,有些同学会不断嘲笑和作弄她,虽然心里非常不舒服,但嘉琪却只能默默承受这些委屈。

原本就需对抗脊椎侧弯带来的压迫与疼痛,还需承受别人的异样眼光,嘉琪同时面对着双重压力。

她也曾无奈问苍天:自己的命运为何如此不幸?但她转念一想:
“如果我得了这个病,其他的人是不是就不会得这个病了?”

家访现场突然安静了几秒。眼前这个懂事得令人心疼的女孩,今年,才15岁。

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嘉琪她渴望可以像普通人一样打球、穿一件好看的连身裙,还有安心追逐自己的梦想——成为一名化妆师或美甲师。

然而,如果脊椎侧弯持续恶化,她向往的未来,可能永远无法实现。

如今,只差这一场手术了。嘉琪真的非常期待,也很想早日完成这场手术。

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但,残酷的现实是,手术中所需使用的医疗器材,费用高达5位数,父母一时之间凑不出这笔费用。

嘉琪的父亲从事汽车冷气服务,是家中的唯一经济支柱,为了替女儿医病,多年以来,父亲早已掏空储蓄,甚至动用退休公积金,已没有能力再替她支付多一笔的高额医疗费。

彷徨无助的父母只好向我们 Soserv Welfare 寻求协助,希望女儿可以顺利进行手术。

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经过家访了解,我们已获得病患一家全权委托代收善款,我们将展开筹款,为脊椎侧弯的李嘉琪,筹募医疗器材费,合共 RM 34, 820。

我们诚挚呼吁社会大众伸出援手,帮助嘉琪挺过这次难关,助她健康走向未来。

我们希望,下一次见到嘉琪时,是手术成功后的一个少女,开心的穿上自己喜欢的裙子,抬头挺胸,自信微笑,去做自己想做的事。

有意捐助者,请与我们联系,获取捐助详情。感恩。
https://wa.me/60102595965

Reference: Lee Jia Qi

欢迎转发此文,让更多人一起帮助嘉琪,助她健康快乐的追梦。

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#筹款 #脊椎侧弯 #脑积水 #手术 #医疗器材 #医疗费压力 #经济压力

10/08/2026

《肾部受感染的冷气师傅筹款达标,现停止筹款,感谢大众诚心援助》

57岁的冷气师傅邱陈顺来原本洗肾度日,但在两年前成功换肾。

今年年初,他的肾部受到细菌感染, 迫切需要在短时间内,注射药物治疗以控制感染,否则,肾脏功能将岌岌可危。然而,这些药物的价格却高达5位数。

多年来的病痛,导致邱陈顺来被逼减少工作,收入已逐步下滑。他实在无力负担高额的抗菌药物费用,只好与我们 Soserv Welfare 取得联系,期望得到帮助。

经过家访了解,我们已发动筹款,帮邱陈顺来筹募药物费用,合共 RM 12,800 。

筹款链接:
https://facebook.com/soserv.welfare/posts/1270718984520817

邱陈顺来一家人,非常感谢社会大众的雪中送碳, 是大家的爱心捐助让他顺利获得治疗,目前他已经康复了。

一家人也对我们马来西亚999生命连线的出手相助,表示非常感激。

我们祝福邱陈大哥身体健康、生活一切顺利。

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马来西亚999生命连线 Soserv Welfare 是一家非营利(NGO)慈善机构,致力于帮助社会弱势群体,提供了免费收留身障孩童、紧急医疗、物资救济、医疗器材、施棺安详送别、清寒助学金等援助。

目前,我们免费收留了40位来自破碎家庭、贫穷家庭的残障孩子。我们也接受大家的乐捐,帮助我们照顾身障孩子们。

欢迎大家关注我们的主页,让我们把慈善之路延伸下去,共同帮助社会上,更多有需要的弱势群体和家庭。

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【马来西亚999生命连线 Soserv Welfare Malaysia】
🏠 地址:33, Jalan 18/14, Taman Kanagapuram, 46000 Petaling Jaya, Selangor. (10am - 6pm)
☎️ 电话号码:010-259 5965 / 03-7772 5959
📧 Email: [email protected]

***如果你或你身边的人,正在面临身障孩子照顾/生活贫困/医药费不足/丧葬费不足等困难,请联系我们。你也可以向我们做生前登记,委托我们为你处理身后事。我们将为求助者,提供需要的援助。***

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《Fundraising Goal Reached for Air-Conditioning Technician with Kidney Infection; Fundraising Now Closed. Thank You for Your Sincere Support》

57-year-old air-conditioning technician Khoo Tan Soon Lai had originally relied on dialysis to survive, but successfully underwent a kidney transplant two years ago.

Early this year, his kidney became infected with bacteria. He urgently needed a course of injections within a short period of time to control the infection. Otherwise, his kidney function would be at serious risk. However, the cost of these medications reached five figures.

Years of illness had forced Khoo Tan Soon Lai to reduce his workload, and his income had gradually declined. Unable to afford the high cost of the antibacterial medication, he contacted Soserv Welfare, hoping to receive assistance.

After conducting a home visit and assessment, we launched a fundraising campaign to help Khoo Tan Soon Lai raise RM12,800 for his medication expenses.

Fundraising link:
https://facebook.com/soserv.welfare/posts/1270718984520817

Khoo Tan Soon Lai and his family are deeply grateful to the public for your timely help. It was everyone’s kind donations that enabled him to receive treatment smoothly, and he has now recovered.

The family is also very thankful to Soserv Welfare for extending assistance during this difficult time.

We wish Mr.Khoo good health and all the best in life.

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#慈善机构 #援助 #药物费 #援助 #有需要的人 #有需要的家庭 #求助

09/08/2026

《15岁女生渴望摆脱脊椎疾病,请求大众伸援手,助达成心愿》

“她曾经半身中风,眼睛向上翻白,我真的以为要失去她了……” 妈妈说起女儿一路走来的经历,眼眶瞬间泛红。

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#医疗器材援助

15 岁中学生李嘉琪不幸患有罕见疾病——小脑扁桃体下疝(Chiari Malformation)。这个病引发了脊髓空洞症(Syringomyelia) 、脑积水和脊椎侧弯等其他健康问题。多种疾病造成她头疼、颈疼、腰疼、头晕。

“3岁那年,她突然抽筋(癫痫),然后晕过去。检查后,医生说她脑积水,需要做手术,是先天性的。” 妈妈娓娓道来女儿的病情。

3岁,嘉琪就经历了脑积水引流手术和减压手术,10岁时则接受颈椎脊髓空洞症的脑部手术。不幸的是,术后出现并发症,嘉琪的小脑中风,右手和右脚无法动弹。经过努力复建,她才逐渐恢复行动能力。

也是10岁那年, 嘉琪的脑部引流管阻塞,被逼再次做手术。11岁和12岁时,医生也为她进行了两场减压手术。

到目前为止,她已经做了5场脑部手术,童年几乎都是在医院度过。

#不及时治疗恐危及生命

6岁开始,罕见病已造成她的脊椎侧弯,医生让她穿戴矫正支架,避免恶化。

但,穿了6年之后,支架带来的压迫越来越难忍受,而且,她也常常受到同学嘲笑。于是,她短暂脱下支架,希望能够喘一口气。

谁也没想到,短短时间内,她的脊椎迅速恶化。如今,她的脊椎侧弯已经高达90度,迫切需要手术干预,否则恐怕压迫心肺功能,危及生命。

其实,这场手术的风险不低,有20%瘫痪的可能性。但如果放弃手术,她失去的,可能不仅仅是行动能力,而是宝贵的生命。

#她的生活备受限制

因为脊椎的情况,嘉琪无法久站、每次照镜子时,看到自己的背部,她的头就会不由自主的低下来。每次看到姐姐穿好看的连身裙,她只有无限羡慕。

她不甘于一辈子被脊椎侧弯困住她的生活,她期望长大后可以成为化妆师或美甲师。但,没有健康的身体,这一切都难以实现。

她决心做手术,为自己的未来勇敢一次。

可是,手术所需的高额医疗器材费用,却让父母背负沉重的经济压力,深感无助。

#普通家庭难承担高昂医疗费

嘉琪爸爸李金清(52岁)从事汽车冷气行业,是家中的唯一经济支柱。妈妈叶秀珠(46岁)则为了照顾小女儿而无法外出工作,嘉琪的姐姐(19岁),目前正寻找工作,希望早日替爸爸分担家庭负担。

由于嘉琪3岁就病发,当时父母还没来得及为女儿购买保险。

多年来,各种各样的手术费、后续治疗、复诊费等,爸爸掏空存款,也已提出部分公积金,竭尽全力替女儿治病,家中经济早已千疮百孔。

如今,手术已经迫在眉睫,但费用却还没着落,父母心急不已。实在是别无选择之下,他们才通过我们 Soserv Welfare 向社会大众寻求协助。

#为助少女矫正脊椎展开筹款

经过家访了解,我们已获得家人全权委托代收善款,我们将发动筹款,为脊椎侧弯的李嘉琪筹募手术医疗器材费,合共 RM 34,820。

“我只希望她健健康康,开开心心。”妈妈的心愿,只是如此简单。

我们恳求善心人士献出爱心,一起帮助这位女学生矫正脊椎,让她可以挺直腰椎,自信的走向未来。

您的善款,不只是支付医疗器材费用,更是在帮助这位女孩顺利完成治疗,重新拥有未来。

如想要帮助嘉琪,请与我们联系,获取捐助详情,感恩。
https://wa.me/60102595965

Reference: Lee Jia Qi

欢迎转发此文,让更多人一起帮助嘉琪,助她健康快乐的追梦。

——————————————————
【马来西亚999生命连线 Soserv Welfare Malaysia】
🏠 地址:33, Jalan 18/14, Taman Kanagapuram, 46000 Petaling Jaya, Selangor. (10am - 6pm)
☎️ 电话号码:010-259 5965 / 03-7772 5959
📧 Email: [email protected]

***如果你或你身边的人,正在面临身障孩子照顾/生活贫困/医药费不足/丧葬费不足等困难,请联系我们。你也可以向我们做生前登记,委托我们为你处理身后事。我们将为求助者,提供需要的援助。***

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【15-Year-Old Girl Dreams of Overcoming a Spinal Condition, Appeals for Public Support to Fulfill Her Wish】

"She had a stroke on one side of her body, and her eyes rolled back. I truly thought I was going to lose her..." As her mother recalled everything her daughter had been through, tears welled up in her eyes.

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【Medical Assistance】

Fifteen-year-old secondary school student Lee Jia Qi has been diagnosed with a rare condition known as Chiari Malformation. The disorder has led to multiple serious complications, including syringomyelia, hydrocephalus, and severe scoliosis, causing her to suffer from persistent headaches, neck pain, back pain, and dizziness.

"When she was three years old, she suddenly had a seizure and lost consciousness. After the examination, the doctor told us she had congenital hydrocephalus and needed surgery," her mother recalled.

At just three years old, Jia Qi underwent a hydrocephalus shunt surgery followed by a posterior fossa decompression surgery. At the age of ten, she underwent another brain surgery to treat syringomyelia affecting her cervical spine.

Unfortunately, complications arose after the operation. Jia Qi suffered a cerebellar stroke, leaving her unable to move her right arm and right leg. It took months of intensive rehabilitation before she gradually regained her mobility.

That same year, her brain shunt became blocked, forcing her to undergo yet another surgery. At the ages of eleven and twelve, doctors performed two additional decompression surgeries.

To date, Jia Qi has undergone five brain surgeries, spending most of her childhood in and out of hospitals.

【Delayed Treatment Could Be Life Threatening】

At the age of six, her rare condition caused her spine to gradually curve. Doctors prescribed a spinal brace to slow the progression of her scoliosis.

She wore the brace faithfully for six years.

However, as she grew older, the brace became increasingly painful and restrictive. On top of that, she was frequently teased by classmates because of it. Hoping for just a little relief, she stopped wearing the brace for a short period.

No one expected her condition to worsen so rapidly.

Today, Jia Qi's spinal curvature has progressed to 90 degrees, and she urgently requires corrective surgery. Without timely treatment, the severe spinal deformity could compress her heart and lungs, potentially becoming life-threatening.

The surgery itself is not without risks. Doctors have explained that there is approximately a 20% risk of paralysis.

Yet, if she chooses not to undergo the operation, what she stands to lose may not only be her mobility—but possibly her life.

【Her Daily Life Is Filled With Limitations】

Because of her spinal condition, Jia Qi cannot stand for long periods.

Every time she looks into the mirror and sees the curve in her back, she instinctively lowers her head. Whenever she sees her older sister wearing beautiful dresses, she can only admire them from afar.

She refuses to let scoliosis define the rest of her life.

She dreams of becoming a makeup artist or a manicurist one day. But without good health, those dreams may never become reality.

She has made up her mind to undergo the surgery—to fight for her future while she still can.

Sadly, the high cost of the required spinal implants and medical equipment has placed an overwhelming financial burden on her family.

【An Ordinary Family Cannot Afford The High Medical Costs】

Jia Qi's father, Lee Kam Ching (52), works in the automotive air-conditioning industry and is the family's sole breadwinner. Her mother, Yap Sau Choo (46), has been unable to work as she stays home to care for Jia Qi. Her 19-year-old sister is currently looking for a job in hopes of helping ease the family's financial burden.

When Jia Qi first fell ill at the age of three, her parents had not yet purchased medical insurance for her.

Over the years, countless surgeries, follow-up treatments, hospital visits, and medical expenses have drained the family's savings. Her father has even withdrawn part of his EPF savings in a desperate effort to continue funding her treatment.

Today, their financial resources have long been exhausted.

Now that the surgery can no longer be delayed, the family simply has no way to afford the medical costs. With no other options left, they have turned to Soserv Welfare to seek help from the public.

【Fundraising To Help Correct Her Spine】

After conducting a home visit and assessment, we have received full authorization from Jia Qi's family to raise funds on their behalf.

We are launching a fundraising campaign to help Lee Jia Qi cover the cost of the medical implants and equipment required for her scoliosis surgery, amounting to RM34,820.

"I only wish for her to be healthy and happy," her mother said. Such a simple wish, yet one that feels painfully out of reach.

We sincerely appeal to kind-hearted members of the public to extend a helping hand and give Jia Qi the opportunity to straighten her spine, regain her confidence, and walk toward a brighter future.

Your contribution is not merely helping to pay for medical equipment.

It is giving this young girl the chance to complete her treatment, reclaim her future, and finally live the life she has always dreamed of.

If you would like to support Lee Jia Qi, please contact us for donation details.

Thank you for your kindness and generosity.
https://wa.me/60102595965

Reference: Lee Jia Qi

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#筹款 #脊椎侧弯 #脑积水 #手术 #医疗器材 #医疗费不足 #经济压力

08/08/2026

《感谢巴生兴华中学,带来一场有魔法的探访》

暂时放下功课与学业压力,巴生兴华中学的学生们走出校园,带着满满的热情与爱心,走进特殊孩子的世界,学习关心与陪伴弱势群体。

值得一提的是,巴生兴华中学的教师们已多次组团,带领不同的学生前来中心进行爱心探访。每一次大家的到来,孩子们都像迎接老朋友一样,张开双手,开心欢迎大家。

这一天,一群中学生带着灿烂笑容来到中心,仿佛也把好运、欢乐与青春的活力一起带来了。

在聆听我们负责人的简单讲解后,早有准备的学生们便迫不及待地与特殊孩子展开多个互动游戏。孩子们有的积极参与,开心地传球;有的虽然不太擅长,但在中学生耐心的陪伴与鼓励下,也愿意慢慢尝试。

每一次成功传球,学生们都会为孩子们欢呼、鼓掌。那一声声鼓励,对孩子们来说,不只是游戏里的掌声,更是一份被看见、被肯定的温暖。

随后,孩子们也被分配了画纸和彩色笔。画画对孩子们来说一点都不陌生,他们开心地在空白画纸上自由创作,而学生们也在一旁,为孩子们的作品增添小小点缀,让每一幅画都变得更加有创意,也更有温度。

身怀才艺的学生们也不忘大显身手,为孩子们带来不同表演,让现场充满惊喜与欢笑。

其中最吸引全场目光的,就是魔术表演。原本空荡荡的盒子里,突然出现了一只小灰兔,顿时让大家惊喜不已。第一次与小兔子近距离接触的 Moses,小心翼翼地伸手抚摸小灰兔,脸上的笑容藏也藏不住。

这不仅是一场才艺与爱心交汇的探访,更是一段充满陪伴、欢笑与温情的美好时光,为孩子们留下了许多难忘的生活印记。

一场诚意满满的探访,也许只是大家生命中的一天;但对特殊孩子们来说,却可能是一段会被记住很久的快乐回忆。

衷心感谢巴生兴华中学师生,谢谢你们总是记得我们的特殊孩子,并愿意一次又一次走进中心,用行动把关怀带到孩子们身边。

如果您也想前来了解与关心特殊孩子,欢迎与我们联系预约。感恩每一份愿意靠近弱势群体的善意与陪伴。

欢迎联系:https://wa.me/60102595965

——————————————————
【马来西亚999生命连线 Soserv Welfare Malaysia】
🏠 地址:33, Jalan 18/14, Taman Kanagapuram, 46000 Petaling Jaya, Selangor. (10am - 6pm)
☎️ 电话号码:010-259 5965 / 03-7772 5959
📧 Email: [email protected]

***如果你或你身边的人,正在面临身障孩子照顾/生活贫困/医药费不足/丧葬费不足等困难,请联系我们。你也可以向我们做生前登记,委托我们为你处理身后事。我们将为求助者,提供需要的援助。***

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【Thank You, Klang Hin Hua High School, for Bringing Us a Magical Visit】

Temporarily setting aside their schoolwork and academic pressure, the students of Klang Hin Hua High School stepped out of their campus with hearts full of enthusiasm and love, walking into the world of children with special needs to learn how to care for and accompany vulnerable groups.

It is worth mentioning that the teachers of Klang Hin Hua High School have organized visits many times, bringing different groups of students to our centre for caring visits. Every time they arrive, the children welcome them like old friends, opening their arms and greeting everyone with happy smiles.

On this day, a group of secondary school students came to our centre with bright smiles, as if they had also brought along good luck, joy and youthful energy.

After listening to a simple briefing by our person in charge, the well-prepared students could not wait to interact with the children with special needs through various games. Some of the children participated actively and happily passed the ball; while some were not very good at it, they were still willing to slowly give it a try with the patient companionship and encouragement of the students.

Every time the ball was successfully passed, the students would cheer and clap for the children. Those cheers and applause were not just part of the game — to the children, they were a warm reminder that they were seen and affirmed.

After that, the children were given drawing papers and colour pencils. Drawing was certainly not something unfamiliar to them. They happily created freely on the blank papers, while the students stayed by their side and added small touches to the children’s artworks, making each piece more creative and full of warmth.

The talented students also took the opportunity to show their skills, bringing different performances to the children and filling the whole centre with surprise and laughter.

Among them, the performance that attracted the most attention was the magic show. From what seemed to be an empty box, a little grey rabbit suddenly appeared, surprising everyone at the scene. Moses, who was meeting a little rabbit up close for the first time, gently and carefully touched the little grey rabbit, with a smile on his face that he simply could not hide.

This was not only a visit where talent and kindness came together, but also a beautiful time filled with companionship, laughter and warmth, leaving many unforgettable memories in the children’s lives.

A sincere visit like this may be just one day in everyone’s life, but for the children with special needs, it may become a happy memory that stays with them for a long time.

We sincerely thank the teachers and students of Klang Hin Hua High School. Thank you for always remembering our children with special needs, and for being willing, time and again, to walk into our centre and bring care to the children through your actions.

If you would also like to learn more and care for children with special needs, you are welcome to contact us for an appointment. We are grateful for every act of kindness and every form of companionship shown to vulnerable groups.

Contact us: https://wa.me/60102595965

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#义工 #探访 #行善 #爱心探访 #特殊儿童 #做善事 #巴生兴华中学

Address

33, Jalan 18/14, Taman Kanagapuram
Petaling Jaya
46000

Opening Hours

Monday 10:00 - 18:00
Tuesday 10:00 - 18:00
Wednesday 10:00 - 18:00
Thursday 10:00 - 18:00
Friday 10:00 - 18:00
Saturday 10:00 - 18:00
Sunday 10:00 - 18:00

Telephone

+60377725959

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