Press Release: Rachel House calls for Palliative Care to be integrated into the Indonesian Health System on International Children’s Palliative Care Day

Yayasan Rumah Rachel marks International Children’s Palliative Care Day with giant “Living Wall” installation at Citos mall, calling for palliative care to be included in the National Health Policy and Universal Health Coverage.

At the official opening of The Living Wall installation at Cilandak Town Square (Citos) to mark International Children’s Palliative Care Day, children’s palliative care service provider Yayasan Rumah Rachel has respectfully called on the Government to integrate palliative care within all levels of the Indonesian health system to enable hundreds of thousands of children across the country to live free from pain and with joy and dignity.

Established in 2006, Yayasan Rumah Rachel has pioneered pediatric palliative care in Indonesia, providing pain and symptom management and emotional and social support for children living with end-stage cancer and HIV AIDS from some of the most marginalised communities in the Greater Jakarta area. It also provides palliative care training to medical professionals and community members to improve access for all.

“Our vision is that no child should ever have to live or die in pain,” said Kartika Kurniasari, CEO of Yayasan Rumah Rachel. “On International Children’s Palliative Care Day, we would like to celebrate the invaluable support palliative care has been able to provide for so many seriously ill children and their families in Jakarta. However, we recognise that our work is far from done looking at the sheer scale of the challenge confronting Indonesia. It is estimated that less than one per cent of the almost 700,000 children living with serious illnesses has access to palliative care, while the rest continue to live in pain,” said Ms Kurniasari.

“The National Health Insurance Scheme (JKN) has delivered life-changing care to millions of Indonesians since 2014. We are respectfully asking the Government to consider extending this one step further, with the inclusion of palliative care services and their related costs at both the hospital and home settings under the JKN. Our government can also support the successful implementation of palliative care by issuing the guidelines and policies for palliative care to be included as a critical component of the national health system. Together, these steps would help ensure the availability of palliative care to hundreds of thousands of seriously ill children and their families across Indonesia,” she added.

The Living Wall is a series of Giant Blackboards hosted at the atrium of Citos mall, where people are invited to write their answers to the question: what they would do if they had only one more day to live?

“The Living Wall invites Jakartans to reflect on the preciousness of every day and to recognise that there are seriously ill children who may not live to see tomorrow,” said Ms Kurniasari.

“By asking people what they would do ‘if I had one more day to live?’, we are trying to spark a conversation in the community about palliative care and the plight of many seriously ill children for whom every day could be their last.”

The Living Wall installation runs from Friday 13th – Sunday 15th October at Cilandak (Ctios) Town Square in Jakarta.

Press Release: Yayasan Rumah Rachel Imbau Asuhan Paliatif untuk Diintegrasikan ke dalam Sistem Kesehatan Indonesia

Yayasan Rumah Rachel merayakan Hari Asuhan Paliatif Anak Sedunia dengan instalasi “Living Wall” raksasa di Cilandak Town Square, dan mengimbau pemerintah agar asuhan paliatif diintegrasikan dalam Kebijakan Kesehatan Nasional dan Jaminan Kesehatan Nasional.

Pada pembukaan instalasi The Living Wall di Cilandak Town Square (Citos) dalam rangka Hari Asuhan Paliatif Anak Sedunia, penyedia layanan asuhan paliatif anak Yayasan Rumah Rachel menyerukan Pemerintah Indonesia untuk mengintegrasikan asuhan paliatif dalam setiap jenjang sistem kesehatan Indonesia agar ratusan ribu anak Indonesia dapat hidup terbebas dari nyeri.

Didirikan pada tahun 2006, Yayasan Rumah Rachel adalah pelopor asuhan paliatif di Indonesia, menyediakan pengelolaan nyeri serta dukungan emosional dan sosial bagi anak-anak dari keluarga prasejahtera di daerah Jakarta dan sekitarnya yang hidup dengan kanker stadium akhir dan HIV AIDS. Yayasan Rumah Rachel juga menyediakan pelatihan asuhan paliatif bagi tenaga kesehatan dan anggota masyarakat dalam usahanya untuk meningkatkan akses asuhan paliatif bagi semua warga Indonesia

“Visi kami adalah tidak ada lagi anak yang harus hidup atau meninggal dalam kesakitan,” tutur Kartika Kurniasari, CEO Yayasan Rumah Rachel. “Dalam rangka Hari Asuhan Paliatif Anak Sedunia, kami bermaksud mengajak masyarakat untuk mendukung asuhan paliatif bagi begitu banyak anak-anak yang hidup dengan penyakit berat serta keluarganya di Jakarta. Tapi kami pun menyadari bahwa pekerjaan kami belum selesai, mengingat besarnya tantangan yang dihadapi Indonesia. Diperkirakan kurang dari satu persen dari hampir 700.000 anak-anak Indonesia yang hidup dengan penyakit berat bisa mengakses asuhan paliatif, sementara anak-anak lainnya terus hidup dalam kesakitan,” jelas Kartika.
“Jaminan Kesehatan Nasional telah memungkinkan jutaan warga Indonesia mendapat perawatan yang mereka butuhkan sejak 2014. Dengan segala hormat, kami mengimbau Pemerintah Indonesia untuk meningkatkan layanan JKN ke jenjang yang bahkan lebih baik lagi, dengan mencakup layanan asuhan paliatif dan biaya-biaya terkait baik dalam lingkungan rumah sakit maupun rumah pasien. Pemerintah juga dapat membantu memastikan penerapan asuhan paliatif berjalan baik dengan menerbitkan panduan dan kebijakan untuk memasukkan asuhan paliatif sebagai komponen inti sistem kesehatan nasional. Jika kita bekerja bersama, semua hal di atas bisa merubah hidup ratusan ribu anak-anak yang hidup dengan penyakit berat dan keluarga mereka di berbagai penjuru Indonesia,” tambahnya.

The Living Wall adalah serangkaian Papan Tulis Raksasa yang didirikan di atrium Cilandak Town Square, di mana masyarakat diundang untuk menjawab pertanyaan berikut: apa yang akan Kamu lakukan jika ini hari terakhirmu?

“The Living Wall mengundang warga Jakarta untuk merenungkan betapa berharganya setiap hari yang kita miliki dan menyadari bahwa ada banyak anak-anak yang hidup dengan penyakit berat, yang mungkin tidak memiliki hari esok,” terang Kartika.

“Dengan bertanya ke masyarakat apa yang akan mereka lakukan ‘jika ini hari terakhir’, kami berharap dapat memicu dialog tentang asuhan paliatif dan kesulitan yang dihadapi anak-anak yang hidup dengan penyakit berat. Bagi mereka, setiap hari bisa saja menjadi hari terakhir.”

Instalasi The Living Wall akan berlangsung mulai hari Jumat, 13 Oktober, hingga hari Minggu, 15 Oktober, di Cilandak Town Square (Citos), Jakarta.

 

Come share your dreams on The Living Wall at Citos

TLW header

Kalau Kamu hanya punya satu hari lagi untuk hidup, apa yang akan Kamu lakukan?

Apakah Kamu mau skydiving atau menghabiskan waktu bersama keluarga?

Mau berdoa atau jalan bersama teman-teman?

Yuk ceritakan impian Kamu di The Living Wall, Cilandak Town Square (CITOS), Jumat 13 Oktober – Minggu 15 Oktober, sambil renungkan bagaimana hampir 700.000 anak Indonesia hidup dengan penyakit berat saat ini, dalam kesakitan. Saat ini, tidak sampai 1% dari anak-anak dan keluarga ini bisa mengakses layanan asuhan paliatif – suatu asuhan medis yang meringankan nyeri dan memberikan dukungan psikososial agar mereka dapat hidup dengan bahagia dan bermartabat, serta kualitas hidup yang optimal.

Apa: Ceritakan impian Kamu, apa yang akan Kamu lakukan jika hanya punya satu hari lagi untuk hidup?
Kapan:
13-15 Oktober
Di mana: 
Cilandak Town Square (CITOS) – Jl. T.B. Simatupang Kav. 17 Jakarta 12430

The Living Wall adalah suatu inisiatif Yayasan Rumah Rachel. Yayasan Rumah Rachel adalah pelopor layanan asuhan paliatif anak bagi anak Indonesia dengan kanker dan HIV AIDS sejak Oktober 2016. Visi Yayasan Rumah Rachel adalah tidak ada lagi anak Indonesia yang hidup atau meninggal dalam kesakitan.

Untuk informasi lebih lanjut, hubungi kami atau ikuti #HariTerakhirSaya di media sosial.

 

If you had one more day to live what would you do with it?

Would you sky dive or spend time with your family? Would you find peace through prayer or party with your friends?

Come share you dreams on the giant Living Wall at Cilandak Town Square (CITOS) and reflect on the almost 700,000 Indonesian children living with serious illness and pain, for whom every day could be their last. Right now, less than 1% of these children and their families have access to palliative care services – a specialised medical care providing pain relief and psychosocial support so they can live with joy and dignity, and optimal quality of life. 

What: Share your dreams on what you would do “if I had one more day to live…”
When:
October 13-15th
Where: Cilandak Town Square (CITOS) – Jl. T.B. Simatupang Kav. 17 Jakarta 12430

The Living Wall is an initiative of Rachel House. Rachel House has pioneered pediatric palliative care services in Indonesia for children with end stage Cancer/HIV AIDS since October 2006. Our vision of Rachel House is that no Indonesian child should ever have to live or die in pain.

For more information please get in touch via our contact page or follow #HariTerakhirSaya on social media.

Yayasan Rumah Rachel Dianugerahi Ikon Prestasi Indonesia

IMG-20170822-WA0016

 

Dalam rangka Hari Kemerdekaan Indonesia ke-72, Presiden Republik Indonesia Bapak H. Joko Widodo menganugerahi 72 Ikon Berprestasi Indonesia di acara Festival Prestasi Indonesia yang diselenggarakan oleh Unit Kerja Presiden Pembinaan Ideologi Pancasila (UKP-PIP) di Jakarta. Asuhan paliatif Yayasan Rumah Rachel merupakan salah satu penerima penghargaan terhormat ini, atas usahanya agar seluruh rakyat Indonesia, terutama anak-anak, merasakan manfaat asuhan paliatif.

Pancasila menjamin hak semua warga negara Indonesia untuk mendapat layanan kesehatan dalam sila ke-5, “keadilan sosial bagi seluruh rakyat Indonesia”. Pendiri Yayasan Rumah Rachel, Lynna Chandra, menghimbau pemerintah Indonesia untuk  berperan aktif dalam menerbitkan dan menerapkan kebijakan untuk menjadikan asuhan paliatif sebagai bagian inti dari sistem kesehatan. Baca lebih lanjut di sini.

— — —

On 21st August 2017, Rachel House received the Presidential Achievement Award in recognition of its contribution in making available palliative care to children of Indonesia. The prestigious presidential award, held as part of the celebration of Indonesia’s 72nd Independence Day, celebrates the achievements of 72 “Achievement Icons” from across Indonesia.

Pancasila, the guiding philosophy of Indonesia, guarantees the right to healthcare under its fifth principle, “social justices for all Indonesians”. Rachel House’s founder, Lynna Chandra, urged the Indonesian government to play an active role in ensuring the successful implementation of palliative care by issuing the guidelines and policies for palliative care to be included as a critical component of the national health system.  Read more here.

 

Home Care at a Humble Home

Nurses' visits ensure no symptoms go untreated

Nurses’ visits ensure no symptoms go untreated

Every patient has a different story. And every home I visit tells a different story. For Adam, our 7-year-old patient living with HIV, his home is made up of cardboard boxes assembled together to make up the family’s living quarters. Located at a dumpsite, Adam shares the space with his ailing mother, his father, and a 15-year-old sister. His father is the family’s sole breadwinner, collecting used plastic bottles to be sold to recyclers for what little money he could earn. His mother’s health condition has been deteriorating recently, burdened by the HIV disease. This leaves his teenage sister as the primary caregiver for Adam.

Adam’s sister, who has had to leave school, is responsible for ensuring Adam and her mother adhere to their daily HIV medication regime. Whenever medication runs low, or when infections and complications mean they need to be taken to the hospital, Adam’s father would struggle to find the money to get them to the hospital. The harsh reality for the family is that transportation costs for Adam to get to the hospital would often mean that the family would have to go without meals for a few days.

Learning about these devastating challenges, I am relieved to be able to turn to the “Food and Transport Fund” Rachel House has been able to raise. The Fund is used to support our patient’s transportation and food expenses during their visits to the hospital. Adam’s father is so grateful for this financial support that offers him the peace of mind that his son is now able to access hospital care when needed. “It is a relief to know that my children can now safely get to the hospital for Adam to get the care he needs, and for me to know that they will not have to go hungry while at the hospital. I am thankful for the help given to support my family.”

As a nurse, I am very thankful to all our donors of this Food and Transport Fund that helps ensure that our patients are now able to get to the hospital safely for treatment. Equally importantly for me is also to know that our patients’ families do not need to go hungry while taking care of their sick children in the hospital.

 

Nurse Neng enlists caring neighbours' support

Nurse Neng enlists caring neighbours’ support

Thorough assessments mean good symptom management

Thorough assessments mean good symptom management

A Celebration of Life and Love

Make a wish, Jani!

Make a wish, Jani!

When one hears or read about palliative care, the first thing that comes to mind is often about pain relief, or respite from suffering. Yet on my first visit to Jani’s house, I could sense only festivities and joy in the room, and not one ounce pain could be felt anywhere.

Jani and her mother were all dressed up and ready for a celebration when we arrived at her house that morning. It was Jani’s birthday, and I had accompanied Nurse Rifa, one of Rachel House’s palliative care nurses, on this joyous day. As can be expected of any child on her birthday, Jani was totally over the moon. As we presented her with the birthday cake, Jani laid eyes on the set of bling we had brought along! She quickly put on the  tiara and the matching jewelry set that perfectly completes her princess outfit. The decor of her home matched the occasion beautifully, the pink wallpapers of different designs and cartoon characters, including one saying “Happy Birthday”.

Sharing songs and fun-filled moments like these with Jani is something Nurse Rifa tries to do on her weekly visits to the house. However, since first meeting Jani 9 months ago, Nurse Rifa’s main task has been to manage the many symptoms that takes away the joy from this little girl. Living with HIV and pulmonary TB infection means that Jani is constantly plagued with symptoms that range from chronic cough, recurrent diarrhea, and fever that weaken her body and stop her from attending school, to sometimes scary ones where every breath becomes a challenge. On this special visit, witnessing the special bond between the family and Nurse Rifa, it was so clear for me that for Jani and her mother, Nurse Rifa has become part of the family and more; for them, the Rachel House nurse is the reason why Jani can once again play and laugh as other children do.

As Nurse Rifa began assessing Jani’s condition, I sat down for chat with Jani’s mother. As a full-time caregiver, she has the difficult task of not only tending to her daughter’s tears and tantrums when things are scary, but she has her own health to worry about (living with HIV herself). She found the support given by Nurse Rifa and the Rachel House team to be invaluable to her family’s well-being, stating that, “We are so lucky to have Nurse Rifa who faithfully visits every week. I have someone to talk to, and my daughter has someone to play and study with. We are no longer alone and afraid.”

Seeing the burden that is carried by Jani and her mother, I can see how having a home care team that provides both medical and emotional support are such a gift and a blessing for the family. Jani’s road to recovery might not be easy, but with the combined love and care of Rachel House’s nurses and her mother, I know that she has a better chance to live a full and joyous life and hopefully celebrate many more birthdays to come.

For the Smile of a Child

Joyful day at the Waterpark

Joyful day at the Waterpark

Dani is 10 years old. It has been 2 years since he was first diagnosed with a rare kidney cancer.

When I first met Dani, he was quiet and non-communicative. He spent most of his days in bed and would not speak to me whenever I visited him at home. He was also in a lot of pain; he had been experiencing unbearable pain on his stomach, due to the tumor that continued to grow despite chemotherapy. I noticed from the medical records provided to us when Dani was first referred to Rachel House that he had received pain medications, so I was particularly curious as to why the pain had persisted. Upon assessment on our initial visit, we discovered that he had unfortunately not been given the right dosage of pain medications at home. We encounter this often when caregivers are not adequately prepared to administer medications prescribed. So, for the next couple of weeks, I specifically dedicated my time to support and educate Dani’s mother, on the proper administering of the medications. Thankfully, Dani’s pain eased quickly and his spirit lifted.

However, all was not well yet. Soon after his pain eased, his pain medications ran low. This meant that he had to go back to the hospital to see the oncologist for a review of his condition, as well as to get the new prescriptions. Unfortunately, it had been a while since his father, who worked as a manual labourer, was able to find work. Paying for the trip to the hospital was unthinkable for his family who, by that point, had to borrow money from their neighbours just to put food on the table.

In our mind, we knew that without the medication, Dani would once again spend his days in agonising pain.

Our team rallied the support of the amazing and faithful supporters who have been helping us bring palliative care to children like Dani. Their generosity allowed Dani to get to his medical appointment, thereby ensuring that Dani can remain pain-free and comfortable at home. His mother was overjoyed to see her son slowly returning to his old cheerful self.

One day when Dani was feeling better, he confided in me a wish he had kept hidden for a long time. “I want to go to a waterpark and go down the slide with my mom,” he whispered. There was a small smile on his lips and a hopeful glint in his eyes. He had never been to a waterpark before.

To the waterpark we went last Saturday, and I saw the biggest smile on Dani’s face. For a moment, I was lost in a thought of how different the situation would have been had he not been referred to Rachel House for home care, or had he not been able to go to the hospital for his pain medications. But the laughter of his mother and him from the pool drew me back to the present moment, and I was grateful to all our friends and supporters who had made this day possible for not only Dani, but so many other children like him who could smile once again.

Biggest smile ever!

Biggest smile ever!

Adding Smiles to the Children’s Remaining Days

A Rachel House nurse at her patient's home

A Rachel House nurse at her patient’s home

Yogi was 16 years old when he had a motorbike accident and broke his arm. About a month after the accident, his arm became swollen and he was in a terrible pain. The X-rays showed that Yogi had a malignant bone cancer, or Osteosarcoma.

The doctors initially proposed to amputate Yogi’s arm to prevent the cancer from spreading, but Yogi refused. As time went by, Yogi’s arm became more and more swollen and the pain became excruciating. The doctors eventually introduced Yogi to Rachel House so that he and his family can receive the support they needed. Rachel House nurses coordinated with Yogi’s primary oncologist to make sure he had adequate pain medication at home and was comfortable at all time. As the relationship developed and Yogi began to trust the nurses, they were able to slowly help Yogi understand his conditions, the treatment options available, and the consequences with each treatment option; this open and truthful discussion provided Yogi with the information he needed to make an informed decision about his life.

Yogi eventually opted for the amputation and decided to fight for cure.

Happily, tests confirmed that there were no longer any cancer cells in his body. Sadly though, this did not improve the reality of a lost arm for Yogi.

He had lost his confidence. He was too embarrassed to return to school and friends had stopped visiting him at home. For Yogi, he had not only lost his arm and a full school year, but also all his friends.  Life seemed to have left him behind.

He felt desperate and afraid. Afraid of the chemotherapy that he would have to undergo. He was not afraid of the therapy itself, but of losing again. This time, he was afraid of losing his hair as a consequence of the chemotherapy. Yogi was losing sight of even hope itself.

Then one day, hoping to ignite Yogi’s spirit and hope, Rachel House’s nurse showed him a video of people achieving amazing and seemingly impossible things even without their arms. The video had a major impact on him; Yogi understood that he had not lost everything. He realised he still had a future.

Yogi decided to pick up his hobby again, and started playing futsal with his friends.

Smiles returned on his face when the nurse visited him. He asked if Rachel House could organise for home tutoring for him, especially in English. A volunteer responded most generously and Yogi resumed his studies from home.

Yogi eventually went back to school and resumed his life in the world. He is learning to write with his left hand and is thinking about continuing his studies at the vocational institute. He is determined to be successful in the future. “I want to be a businessman, running my own business,” he laughs.

Until today, Rachel House has provided palliative care to over 2500 children and families like Yogi who are living with HIV and cancer in Jakarta. We would like to convey our deepest gratitude for your generous support, which has allowed us to continue improving children’s quality of life and adding smiles to their remaining days.

 

His beloved bird, adding smile & hope to his days

His beloved bird, adding smile & hope to his days

A Bold Step Towards Compassionate Community

On our 10th anniversary, Rachel House added bold strokes to the Palliative Care Ecosystem “tapestry” we have helped established in Indonesia, with the dream of making palliative care accessible and available for everyone living with life-limiting conditions. In 2016, our work and the influence of our work reached key stakeholders at all levels of the health system, including the prison hospitals and the School of Public Health, winning their support to bring us closer to the vision that no child should ever have to live or die in pain. 

Nurse and Patient

Nurse Yuni visiting her patient at home

Delivering Compassionate Care (Home-Based Pediatric Palliative Care Service)

We look back on the 10-year journey and are humbled to have been given the honour of caring for over 2400 children living with cancer or HIV and their families, providing them with compassionate palliative care and support during the most challenging time of their lives, helping alleviate their pain and suffering.

 

Building a Compassionate Community

We strongly believe that skilled and informed compassionate community members are an essential component to ensuring quality care for people living with chronic and life-limiting disease at home. Harnessing the spirit of gotong royong (collaboration) that is deeply ingrained in the Indonesian culture, Rachel House’s Community Network in Palliative Care (“CNPC”) Program has to-date successfully trained over 2100 community volunteers in basic palliative care skills and knowledge.

Monthly meetings are convened by Rachel House to forge strong collaborations between CNPC-trained community volunteers and health professionals in the Primary Health Clinics. As a result, multiple teams of community volunteers are now active and vigilant in making sure that no one in their community is left alone to suffer at home without care and assistance.

 

Community

CNPC-trained community volunteers in action

 

Nurturing Compassionate Palliative Care Professionals

The Clinic-in-a-Box fully accredited training program for nurses has completed its 2nd year, providing palliative care and homecare skills to now close to 100 nurses and nurse lecturers from some of the largest private and public hospitals and universities in Indonesia. The Clinic-in-a-Box training program is a critical component in Rachel House’s goal of establishing a palliative care ecosystem in Indonesia, to ensure that patients can be provided with compassionate care throughout the health system.

 

Clinic-in-a-Box in its 2nd year, nurturing compassionate nurses

Clinic-in-a-Box in its 2nd year, nurturing compassionate nurses

The surveys conducted to evaluate the effectiveness of the training program showed increased knowledge in palliative care skills in all the participants, particularly in the areas of pain assessment and management, and increasingly favourable attitudes towards a range of key concepts in palliative care including the delivery of bad news, caring for dying patients, administering morphine and patient referrals. The results of the surveys indicate the overall effectiveness of the training in improving the confidence of the nurse participants in negotiating complex issues in palliative care.

 

The 1st fully accredited Pediatric Palliative Care training in collaboration with The Cincinnati Children's Hospital & ICPCN, with the support of our young volunteer doctors

The 1st fully accredited Pediatric Palliative Care training in collaboration with The Cincinnati Children’s Hospital & ICPCN, with the support of our young volunteer doctors

In collaboration with Singapore International Foundation, Cancer Foundation and the Jakarta Provincial government, Rachel House continued to run the 3-year palliative care training for 80 medical professionals from 12 District and National hospitals in Jakarta. In November, we led a roundtable discussion facilitated by Dr Mark Meyer from The Cincinnati Children’s Hospital and attended by the medical directors and pediatricians from the 12 public hospitals, to discuss the challenges faced by each hospital in the implementation of palliative care. Following the success of the exchange, the roundtable will continue on a quarterly basis in 2017.

 

Rallying Support from Key Stakeholders

From outside the conventional health system, the Directorate General of Corrections, Ministry of Law and Human Rights extended an invitation to Rachel House to provide guidance on the national guidelines for palliative care in prisons and prison hospitals.

2016 also saw active training and roundtable discussions organised to engage medical and nursing schools and public health faculties of major public and private universities such as Universitas Indonesia, Universitas Padjadjaran, and Universitas Muhammadiyah Yogyakarta to build a body of research that will strengthen the case for palliative care inclusion in the health system.

 

Planting Seeds of Compassion Early: Medical and Nursing Students

To ensure a long-lasting impact in the health system, we are working to nurture a new generation of medical professionals who will be able to serve their patients with compassion and equipped with impeccable clinical skills. In 2016, Rachel House expanded its training efforts to include medical and nursing students, planting the seeds of palliative care values early in their career as health professionals.

We ran one-day introductory workshops for nursing students at Bani Saleh Nursing College in Bekasi, West Java, and Universitas Muhammadiyah Yogyakarta in Central Java, and provided palliative care training to aspiring doctors at YARSI Medical College. The growing interest in palliative care amongst medical and nursing schools have seen requests for Rachel House’s participation well into 2017.

Rachel House has also welcomed fresh graduates from medical schools as medical interns in our service. The greatest impact for many of these young doctors has been when they witness the patients in the intimacy of their homes, bringing the doctors face-to-face with humanity. 

 

Public Advocacy

The Living Wall is a Rachel House initiative designed to engage youth and students in a global campaign to increase the awareness of the plight of children living with life‐limiting illnesses such as cancer or HIV and to improve their access to pediatric palliative care. Nearly 20 schools nationwide have participated and launched the wall in their schools. We continue to drive the campaign through The Living (virtual) Wall (http://thelivingwall-id.org/) and social media (Facebook, Instagram, and Twitter).

On June 5th, The Living Wall presented at the Car Free Day on the main thoroughfare in Jakarta, reaching hundreds of people on their Sunday morning stroll or run.

On June 5th, The Living Wall presented at the Car Free Day on the main thoroughfare in Jakarta, reaching hundreds of people on their Sunday morning stroll or run.

In October, on the World Hospice and Palliative Care Day and  to celebrate the 10th anniversary of Rachel House, we shared our work on a live radio interview at Kantor Berita Radio. The show was distributed and broadcasted to hundreds of radio stations throughout Indonesia. For more information on all the publications, please click here.

It has been a fulfilling decade for all of us at Rachel House. We know that none of this would have been possible without our faithful supporters. For all this and so much more, we are eternally grateful. Thank you for helping us add life to the children’s remaining days.

Palliative Care, Touching the Lives of Many

IMG_1777 - Neng telling Jes what a good girl she's been!

Jessi

Jessi is 5, and living with HIV. Her father left a long time ago. Her mother is living with her new family now on the other side of town, and Jessi sees her only once a year, on Eid-al-Fitr, a Muslim celebration at the end of the Ramadhan. But Jessi has a loving grandmother, who is her entire universe.

On our first few encounters, Jessi seemed to be a quiet girl. But as we got to know each other better, I began to spot the light of hope in her eyes. Jessi may not be in the best of health, yet her cheerfulness would shine through when she clapped her hands to her favourite song that I would sing at her insistent request.

HIV often causes developmental challenges, and this was clearly exhibited in Jessi. When I started taking care of her almost two years ago now, Jessi could barely speak. However, she would listen intently to the discussions around her, and would flail her hands excitedly trying to chime in.

& Her Grandmother

Being a palliative care nurse, my duty is not only to care for Jessi, but also for her grandmother. A woman in her 50s, grandma Surti has been Jessi’s tireless caregiver through all the many ups and downs of Jessi’s health condition. With the stigma surrounding HIV, many families of HIV patients are afraid to disclose their status. Grandma Surti is of no exception. She became isolated from her neighbours; alone and bereft of any support, she had no one with whom she could share her burdens.

We quickly became friends. Often during my home visits to Jessi, grandma Surti would share her fears and worries about Jessi’s condition. Is Jessi going to die? What does it mean when the doctor says this or that? Why are there so many medications and what are they for? Why can’t she talk and walk yet like other children her age? I would sit with her and make sure she had all her questions answered, her worries quelled.

With each visit, I can see Jessi’s health and cognitive condition steadily improve. Through our support and education, grandma Surti is able to understand better about Jessi’s illness, and how to administer her medications in a proper and timely manner. The wounds and pains that had previously ailed Jessi have begun to heal. She is now able to utter simple words and continue to add new words to her repertoire weekly. And, one of the most celebrated milestones of the past 2 years would be to see her learn to walk!

& The Palliative Care Nurse

I am delighted to see the happiness that is now painted on Jessi’s and grandma Surti’s faces. But more than that, I am truly honoured and humbled to have been given the opportunity to learn so much from them. Jessi has taught me to keep my spirit up even when things seem endlessly bleak. Grandma Surti, who has never once complained or become angry with Jessi, has taught me patience and compassion. She reminds me constantly to be a better parent for my son – to spend and cherish the time I have with him as much as I can, as much as grandma Surti does with Jessi.

& The Palliative Care Volunteer

My name is Tiarvafilin. I am a volunteer at Rachel House. I have been making birthday cakes for the children at Rachel House for over a year now. I am moved by how the nurses at Rachel House help the children live their lives to the fullest even when they are facing unbearable challenges. I wanted to play my part by making sure that these children too can have the happiest birthday celebrations they deserve.

One of the first cakes I made was for Jessi. At the time I had yet to meet Jessi, but the nurses’ stories about her left a deep impression in my heart. I made a promise that the cakes I would make for Jessi and the children at Rachel House must be not only delicious, but also pretty; for it may be their last birthday cake.

Truthfully, I am not a professional baker. Baking cute delicious cakes is simply a hobby I love and I consider myself a beginner. For Jessi, I was planning to make a strawberry cake. It failed. I cried. I imagined Jessi would be very sad eating a cake so terrible. But I did not give up and baked another one. With the grace of God, it turned out beautifully.

Jessi loved it. She could not speak, but her delight was apparent in her eyes. That may have been Jessi’s birthday, but it may as well be mine as it was one of the happiest days in my life.

Miracles do not fall from heaven; they are handcrafted by people. God created miracles through our hands. I do not know if I have made a miracle in Jessi’s life but I am certain I did give her a beautiful birthday. And that alone is a miracle in my life.

I am thankful to be part of the Rachel House’s team, to have the privilege to make a difference in the children’s life, adding joy and dignity to their remaining days.

Grandma Surti doting on Jessi with love & patience

Grandma Surti doting on Jessi with love & patience

 

Jessi and her beautiful birthday cupcakes

Jessi and her beautiful birthday cupcakes