參考文獻
中文部分
中華民國兒童癌症基金會（2016）．疾病簡介兒童骨癌．取自http://www.ccfroc.org.tw
方恩真（2011）．東南亞籍新移民母親照顧癌症子女之生活經驗．國立臺北護理健康大學護理研究所。
方恩眞、蔡佳玲（2002）．他走的很安詳，還在微笑:一位母親經歷癌症兒童瀕臨末期至死亡後之心路歷程．長庚護理，13（4），328-338。
田聖芳（1993）．母親面對先天性缺陷兒之養育問題與情緒適應．護理雜誌，40（1），27-32。
田聖芳（2001）．先天性缺陷兒母子互動關係與影響因素．護理雜誌，48（2），65-69。
江季蓁、駱麗華（2002）．新診斷白血病兒童住院期間主要照顧者之生活品質．護理雜誌，49（2），42-50。
朱怡勳，鄭夙芬，吳維紋，邱慧洳，梁淑媛（2015）．主要照顧者面對初次化學治療返家之癌症病童居家照護的經驗．Journal of Nursing & Healthcare Research，11（3），187-197。
行政院衛生福利部（2018）．106 年死因統計結果分析．取自
https://www.mohw.gov.tw/mp-1.html
余玉眉、蔣欣欣、陳月枝、蘇燦煮、劉玉秀（1999）．質性研究資料的量化及詮釋--從研究例證探討臨床護理研究方法與認識學第二部分：研究例證之分析與詮釋．護理研究，7（4），376-392。
余怡珍、簡乃卉（2009）．唇顎裂兒童母親親職壓力之初探．長庚護理，20（3），293-305。
李芷宜、莊昭華（2018）．癌症病人主要照顧者照顧負荷之論述．彰化護理，25（3），12-19。
吳忠憲（2014）．後天截肢者的失落經驗與復原歷程之探究（未發表的碩士論文）．嘉義：國立嘉義大學輔導與諮商學系研究所。吳秋美（2013）．癌症病童家庭壓力與調適過程之個案研究--以惡性骨肉瘤為例（未發表的碩士論文）．國立臺北護理健康大學生死教育與輔導研究所。李美銀（2016）．住院兒童及青少年之照護．於穆佩芬總校閱，兒童及青少年健康照護（71-100頁）．台北市：華杏。
吳貞儀（2006）．回首來時路---兒童骨癌存活者復原歷程研究（未發表的碩士論文）．台中：東海大學社會工作學研究所。吳博貴（2012）．消滅骨骼肌肉腫瘤．取自http://www.pqwu.synology.me/
吳博貴（2012）．截肢．取自http://www.pqwu.synology.me/
李慧貞、毛新春、陳月枝、沈銘鏡（2000）．血友病病童母親的照顧經驗．護理研究，8（5），579-591。
李麗紅、楊政議（2020）．質性研究訪談個案數之判定：資料飽和概念之使用．澄清醫護管理雜誌，16（1），47-52。
林妙怜（2016）．以繪畫探討骨癌青少年治療過程之希望經驗．（未發表的研究論文）．台北：國立陽明大學臨床護理研究所。
洪君儀（2008）．成人與兒童肉瘤之不同．取自 http://web.tccf.org.tw
洪筱瑩、黃美智（2014）．同意與贊同-青少年接受骨髓移植之倫理考量．護理雜誌，61（4），83-89.
洪毓鈴、陳季員（2010）．探討癌症病童母親健康的相關因素．護理雜誌，57（6），42-50。
洪麗真、葉昭幸（2000）．癌症青少年的生活經驗之探討．長庚護理，11（3），14-24。
徐宗國譯（1998）．質性研究概論．台北：巨流。
高凌霞 （1998）．位格與主體概念之來源—人之經驗．哲學與文化，25（1），17-26。
高碧霞、李雅玲、曾紀瑩、賴鈺玫、陳月枝（1999）．癌症兒童父母親面臨病童就學狀況之考慮及相關因素之初步探討．護理研究，7（1），4-14。
陳月枝（2003）．緒論．於陳月枝總校閱，質性護理研究法（1-20頁）．台北：護望。
陳金彌、毛新春、陳月枝、黃棣棟（2000）．母親面對惡性腦瘤病童接受癌症療程的經驗．護理研究，8（3），338-348。
許玉雲、 陳彰惠（1999）．身體心像概念分析．護理雜誌，46（6），103-109。
張秀如、余玉眉（2007）．身體觀點-體現與身體心像．護理雜誌，54（3），77-81。
陳妙星、陳月枝（2011）．台灣東區癌症病童與家庭之生活經驗．志為雜誌-慈濟護理雜誌，10（6），66-76。
陳威明（2009）．惡性骨肉瘤手術治療的進展．取自http://web.tccf.org.tw
陳慈君（2009）．那彩虹橋的韌性—神經母細胞瘤家庭之患病經驗與治療過程．臺灣大學護理學研究所學位論文。
陳萩憶（2002）．癌症病童父母之壓力反應與調適過程．安寧療護雜誌， 7（2），139-146。
張綠怡、蔡綠蓉（2016）．住院兒童之反應及其護理．於陳月枝總校閱，實用兒科護理（七版，198-199 頁）．台北市：華杏。
曾于芬（2016）．慢性病兒童及青少年之成長與照護．於穆佩芬總校閱，兒童及青少年健康照護（101-124頁）．台北市：華杏。
馮瑞君、吳維紋、卓妙如、梁淑媛、鄭夙芬（2019）．腎上腺腦白質退化症病童父母親的長期照護經驗及需求之探討．護理雜誌，66（1），27-37。
曾慧芬（2008）．一位截肢少女的生命故事及其復原力之探究．（未發表的碩士論文）．高雄市：國立高雄師範大學輔導與諮商研究所。董佩琪（2014）．罹患癌症初期學齡期兒童其親子間病情言說之經驗．（未發表的碩士論文）．台北：國立陽明大學臨床暨社區護理研究所。臺灣兒童癌症研究群（2016）．2005-2014兒童癌症每年新發病人數及發生率．取得http://www.ccfroc.org.tw/content_sub.php?id=132&level1ID=12&level2ID=2&level3ID=2
蔡佳玲、葉昭幸、李淑珠（2000）．母親經歷癌症兒童死亡後之情緒調適．長庚護理，11（1），22-32。
蔣宜倩、葉昭幸、張碧真（2003）．癌症患童父母身心反應之長期追蹤研究．腫瘤護理雜誌，3（1），1-15.
劉雪娥（2019）．肌肉骨骼系統疾病之護理．於胡月娟總校閱，成人內外護理（六版，584-591頁）．台北市：華杏。
劉千琪、陳月枝（2011）．母育信心之概念分析．長庚護理．22（4），472-478。
潘淑滿（2003）．質性研究理論與應用．台北：心理。
樓曉玲（2007）．腦瘤病童疾病末期母親預期性失落之生活經驗．（未發表的碩士論文）·台北：陽明大學臨床護理研究所。蔡麗絲（2003）．新編復健護理．台北：合記。
穆偑芬、馬鳳岐、顧小明、許洪坤、黃碧桃（2000）．有罹患癌病兒童之家庭的壓力—對母親之衝擊．護理研究，8（5），568-578。
賴鈺玫（1991）．骨癌病童接受截肢前後對身體心像改變之適應過程及行為反應．（未發表的碩士論文）．台北：國立臺灣大學護理研究所。釋普安、蔡昌雄、程裕藍、游碧真（2013）．癌末病童之靈性照顧-以安寧病房為例·安寧療護雜誌，18（1），62-75。
英文部分
Al‐Gamal, E., & Long, T. (2010). Anticipatory grieving among parents living with a child with cancer. Journal of Advanced Nursing, 66(9), 1980-1990.
Al-Namankany, A., & Alhubaishi, A. (2018). Effects of cleft lip and palate on children's psychological health: A systematic review. Journal of Taibah University Medical Sciences, 13(4), 311-318.
American Cancer Society (ACS) (2019) Signs and Symptoms of Osteosarcoma [Online]. Available at:http://www.cancer.org/cancer/osteosarcoma/detailedguide/osteosarcoma-signs-and-symptoms (accessed January 29, 2018).
Ammon-Gaberson, K.B., & Piantanida, M. (1988). Generating results from qualitative data. Image, 20,159-161.
Andrews, L., Anderson, L., Fairbain, S., & Downing, L. (2012). Care planning for children with lower limb amputation. Nursing children and young people, 24(1).
Aschenbrenner, A. P., Winters, J. M., & Belknap, R. A. (2012). Integrative Review: Parent Perspectives on Care of Their Child at the End of Life. Journal of Pediatric Nursing, 27(5), 514–522.
Baider, L., & De-Nour, A. K. (1989). Group therapy with adolescent cancer patients. Journal of Adolescent Health Care, 10(1), 35-38.
Bekkering, W. P., Vliet Vlieland, T. P., Koopman, H. M., Schaap, G. R., Schreuder, H. B., Beishuizen, A., ... & Taminiau, A. H.(2010).Quality of life in young patients after bone tumor surgery around the knee joint and comparison with healthy controls. Pediatric blood & cancer, 54(5), 738-745.
Bekkering, W. P., Vliet Vlieland, T. P., Koopman, H. M., Schaap, G. R.,Beishuizen, A., Anninga, J. K., ... Taminiau, A. H. (2012). A prospective study on quality of life and functional outcome in children and adolescents after malignant bone tumor surgery. Pediatric Blood Cancer, 58,978–985.
Bekkering, W. P., van Egmond‐van Dam, J. C., Bramer, J. A. M., Beishuizen, A., Fiocco, M., & Dijkstra, P. D. S. (2017). Quality of life after bone sarcoma surgery around the knee: A long‐term follow‐up study. European Journal of Cancer Care, 26(4), e12603.
Benedetti, G. M. D. S., Garanhani, M. L., & Sales, C. A.(2014). The treatment of childhood cancer: Unveiling the experience of parents. Revista Latino-Americana de Enfermagem, 22(3), 425-431.
Björk, M., Sundler, A. J., Hallström, I., & Hammarlund, K.(2016). Like being covered in a wet and dark blanket–Parents' lived experiences of losing a child to cancer. European Journal of Oncology Nursing, 25, 40-45.
Bosmans, J. C., Geertzen, J. H., Post, W. J., van der Schans, C. P., & Dijkstra, P. U. (2010). Factors associated with phantom limb pain: A 3½-year prospective study. Clinical Rehabilitation, 24(5), 444-453.
Bowen, G. A. (2008). Naturalistic inquiry and the saturation concept: A research note. Qualitative Research, 8. (1), 137-152.
Burg, A. J. (2016). Body image and the female adolescent oncology patient. Journal of Pediatric Oncology Nursing, 33(1), 18-24.
Carlsson, T., Kukkola, L., Ljungman, L., Hovén, E., & von Essen, L. (2019). Psychological distress in parents of children treated for cancer: An explorative study. PloS one, 14(6), e0218860.
Cheng, Y. C., Huang, C. Y., Wu, W. W., Chang, S. C., Lee-Hsieh, J., Liang, S. Y., & Cheng, S. F. (2016). The lived experiences of aboriginal adolescent survivors of childhood cancer during the recovering process in Taiwan: A descriptive qualitative research. European Journal of Oncology Nursing, 22, 78-84.
Clerici, C. A., Ferrari, A., Luksch, R., Casanova, M., Massimino, M., Cefalo, G., ... Daolio, P. (2004). Clinical experience with psychological aspects in pediatric patients amputated for malignancies. Tumori Journal, 90(4), 399-404.
Coyne, I., Amory, A., Kiernan, G., & Gibson, F. (2014). Children's participation in shared decision-making: Children, adolescents, parents and healthcare professionals' perspectives and experiences. European Journal of Oncology Nursing, 18(3), 273-280.
Da Silva, F. M., Jacob, E., & Nascimento, L. C. (2010). Impact of childhood cancer on parents’ relationships: An integrative review. Journal of Nursing Scholarship, 42(3), 250-261.
Darcy, J. (2019). A narrative analysis of the stories of mothers who have parented a child with Hodgkin lymphoma who is currently in early survivorship. Journal of Clinical Nursing, 28(1-2), 138-147.
Drew, S. (2007). Having cancer changed my life, and changed my life forever': Survival, illness legacy and service provision following cancer in childhood. Chronic Illness, 3(4), 278-295.
Eleutério, S. J. P., Senerchia, A. A., Almeida, M. T., Costa, C. M. D., Lustosa, D., Calheiros, L. M., ... Petrilli, A. S. (2015). Osteosarcoma in patients younger than 12 years old without metastases have similar prognosis as adolescent and young adults. Pediatric Blood & Cancer, 62(7), 1209-1213.
Fauske, L., Bondevik, H., Bruland, Ø. S., & Ozakinci, G. (2015). Negative and positive consequences of cancer treatment experienced by long-term osteosarcoma survivors: A qualitative study. Anticancer Research, 35(11), 6081-6090.
Fauske, L., Lorem, G., Grov, E. K., & Bondevik, H. (2016). Changes in the body image of bone sarcoma survivors following surgical treatment—A qualitative study. Journal of Surgical Oncology, 113(2), 229-234.
Feldman, R. S. (2018)‧實用人類發展學(穆佩芬)‧台北:華杏。
Fletcher, P. C., Schneider, M. A., & Harry, R. J. (2010). How do I cope? Factors affecting mothers’ abilities to cope with pediatric cancer. Journal of Pediatric Oncology Nursing, 27(5), 285-298.
Fotiadou, M., Barlow, J. H., Powell, L. A., & Langton, H. (2008). Optimism and psychological well‐being among parents of children with cancer: An exploratory study. Psycho‐Oncology: Journal of the Psychological, Social and Behavioral Dimensions of Cancer, 17(4), 401-409.
Gilmer, M. J., Foster, T. L., Vannatta, K., Barrera, M., Davies, B., Dietrich, M. S., ...Gerhardt, C. A. (2012). Changes in parents after the death of a child from cancer. Journal of Pain and Symptom Management, 44(4), 572-582.
Harden, J., Black, R., & Chin, R. F. (2016). Families' experiences of living with pediatric epilepsy: A qualitative systematic review. Epilepsy & Behavior, 60, 225-237.
Hill, J., Kondryn, H., Mackie, E., McNally, R., & Eden, T. (2003). Adult psychosocial functioning following childhood cancer: The different roles of sons’ and daughters’ relationships with their fathers and mothers. Journal of Child Psychology and Psychiatry, 44(5), 752-762.
Hornicek, F. J., Maki, R., Pollock, R. E., & Collins, K. A. (2015). UpToDate. Retrieved July 22,2020, form
https://www.uptodate.com/contents/bone-sarcomas-preoperative-evaluation-histologic-classification-and-principles-of-surgical-management/print
Hung, G. Y., Yen, H. J., Yen, C. C., Chen, W. M., Chen, P. C., Wu, H. T., ...Hsu, H. E. (2015). Experience of pediatric osteosarcoma of the extremity at a single institution in Taiwan: Prognostic fctors and impact on survival. Annals of Surgical Oncology, 22(4), 1080.
Hsieh, Y. T., Chao, Y. M. Y., & Shiao, J. S. C. (2013). A qualitative study of psychosocial factors affecting expecting mothers who choose to continue a cleft lip and/or palate pregnancy to term. Journal of Nursing Research, 21(1), 1-9.
Jaraway, D., Perry, S., Phillips, M., Ziegler, P., Wolgemuth, A., & Scott, S. D. (2013). Preparing parents to help support their child post-amputation for bone cancer. ORNAC Journal, 31(4), 13-9.
Jaffe, N., Carrasco, H., Raymond, K., Ayala, A., & Eftekhari, F. (2002). Can cure in patients with osteosarcoma be achieved exclusively with chemotherapy and abrogation of surgery? Cancer, 95(10), 2202-2210.
Karadeniz Cerit, K., Cerit, C., Nart, Ö., Eker, N., Kıyan, G., Dağlı, T., ... Çorapçıoğlu, F. (2017). Post‐traumatic stress disorder in mothers of children who have undergone cancer surgery. Pediatrics International, 59(9), 996-1001.
Kars, M. C., Grypdonck, M. H., & van Delden, J. J. (2011). Being a parent of a child with cancer throughout the end-of-life course. Oncology Nursing Forum, 38(4), E260-271.
Kars, M. C., Grypdonck, M. H., Beishuizen, A., Meijer‐van den Bergh, E. M., & van Delden, J. J. (2010). Factors influencing parental readiness to let their child with cancer die. Pediatric Blood & Cancer, 54(7), 1000-1008.
Kilicarslan-Toruner, E., & Akgun-Citak, E. (2013). Information-seeking behaviours and decision-making process of parents of children with cancer. European Journal of Oncology Nursing, 17(2), 176-183.
Lackner, H., Benesch, M., Schagerl, S., Kerbl, R., Schwinger, W., & Urban, C. (2000). Prospective evaluation of late effects after childhood cancer therapy with a follow-up over 9 years. European Journal of Pediatrics, 159(10), 750-758.
Landolt, M. A., Ystrom, E., Sennhauser, F. H., Gnehm, H. E., & Vollrath, M. E. (2012). The mutual prospective influence of child and parental post‐traumatic stress symptoms in pediatric patients. Journal of Child Psychology and Psychiatry, 53(7), 767-774.
Lauder, B., Sinclair, P. M., & Maguire, J. (2018). Mothers’ experience of caring for a child with early onset scoliosis: A qualitative descriptive study. Journal of Clinical Nursing, 27(7-8), e1549-e1560.
Liang, H. F. (2002). Understanding culture care practices of caregivers of children with cancer in Taiwan. Journal of Pediatric Oncology Nursing, 19(6), 205-217.
Lincoln, Y., & Guba, E. (1985). Naturalistic inquiry. Newbury Park, CA: Sage.
Livneh, H., Antonak, R. F., & Gerhardt, J. (2000). Multidimensional investigation of the structure of coping among people with amputations. Psychosomatics, 41(3), 235-244.
Longhi, A., Errani, C., De Paolis, M., Mercuri, M., & Bacci, G. (2006). Primary bone osteosarcoma in the pediatric age: State of the art. Cancer Treatment Reviews, 32(6), 423-436.
Loucas, C. A., Brand, S. R., Bedoya, S. Z., Muriel, A. C., & Wiener, L. (2017). Preparing youth with cancer for amputation: A systematic review. Journal of Psychosocial Oncology, 35(4), 483-493.
Markward, M. J., Benner, K., & Freese, R. (2013). Perspectives of parents on making decisions about the care and treatment of a child with cancer: A review of literature. Families, Systems, & Health, 31(4), 406.
Mei, J., Zhu, X. Z., Wang, Z. Y., & Cai, X. S. (2014). Functional outcomes and quality of life in patients with osteosarcoma treated with amputation versus limb-salvage surgery: A systematic review and meta-analysis. Archives of Orthopaedic and Trauma Surgery, 134(11), 1507-1516.
Miller, G.(2010).Pediatric bioethics .New York, NY:Cambridge University Press.
Mohseny, A. B., Szuhai, K., Romeo, S., Buddingh, E. P., Briaire‐de Bruijn, I., de Jong, D., ... Hogendoorn, P. C.(2009). Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2. The Journal of Pathology: A Journal of the Pathological Society of Great Britain and Ireland, 219(3), 294-305.
Moody, K., Siegel, L., Scharbach, K., Cunningham, L., & Cantor, R. M. (2011). Pediatric palliative care. Primary Care: Clinics in Office Practice, 38(2), 327-361.
Morris, A. (2009). Selective treatment of irreversibly impaired infants: Decision-making at the threshold. Medical Law Review, 17(3), 347-376.
Mu, P. F., Lee, M. Y., Sheng, C. C., Tung, P. C., Huang, L. Y., & Chen, Y. W.(2015). The experiences of family members in the year following the diagnosis of a child or adolescent with cancer: A qualitative systematic review. JBI Evidence Synthesis, 13(5), 293-329.
Mu, P. F. (2008). Transition experience of parents caring of children with epilepsy: A phenomenological study. International Journal of Nursing Studies, 45(4), 543-551.
Mu, P. F., Lee, M. Y., Sheng, C. C., Tung, P. C., Huang, L. Y., & Chen, Y. W. (2015). The experiences of family members in the year following the diagnosis of a child or adolescent with cancer: A qualitative systematic review. JBI Database of Systematic Rreviews and Implementation Reports, 13(5), 293-329.
Nagarajan, R., Mogil, R., Neglia, J. P., Robison, L. L., & Ness, K. K. (2009). Self-reported global function among adult survivors of childhood lower-extremity bone tumors: A report from the Childhood Cancer Survivor Study (CCSS). Journal of Cancer Survivorship, 3(1), 59-65.
Newton, K., & Lamarche, K. (2012). Take the challenge: Strategies to improve support for parents of chronically ill children. Home Healthcare Now, 30(5), E1-E8.
Nikfarid, L., Rassouli, M., Borimnejad, L., & Alavimajd, H. (2017). Experience of chronic sorrow in mothers of children with cancer: A phenomenological study. European Journal of Oncology Nursing, 28, 98-106.
Nikkola, I., Kaunonen, M., & Aho, A. L. (2013). Mother’s experience of the support from a bereavement follow‐up intervention after the death of a child. Journal of Clinical Nursing, 22(7-8), 1151-1162.
Norlyk, A., Martinsen, B., & Kjaer-Petersen, K. (2013). Living with clipped wings—Patients’ experience of losing a leg. International Journal of Qualitative Studies on Health and Well-being, 8(1), 21891.
October, T., Dryden-Palmer, K., Copnell, B., & Meert, K. L. (2018). Caring for parents after the death of a child. Pediatric Critical Care Medicine, 19(8), S61.
O'Toole, S., Lambert, V., Gallagher, P., Shahwan, A., & Austin, J. K. (2016). Talking about epilepsy: Challenges parents face when communicating with their child about epilepsy and epilepsy-related issues. Epilepsy & Behavior, 57, 9-15.
Ottaviani, G., Robert, R. S., Huh, W. W., Palla, S., & Jaffe, N. (2013). Sociooccupational and physical outcomes more than 20 years after the diagnosis of osteosarcoma in children and adolescents: Limb salvage versus amputation. Cancer, 119(20), 3727-3736.
Picci, P.(2007). Osteosarcoma (osteogenic sarcoma). Orphanet Journal of Rare Diseases, 2(1), 6.
Robinson, C. A. (1993). Managing life with a chronic condition: The story of normalization. Qualitative Health Research, 3(1), 6-28.
Schultz, K. A. P., Ness, K. K., Whitton, J., Recklitis, C., Zebrack, B., Robison, L. L., ... Mertens, A. C. (2007). Behavioral and social outcomes in adolescent survivors of childhood cancer: A report from the childhood cancer survivor study. Journal of Clinical Oncology, 25(24), 3649-3656.
Schweitzer, R., Griffiths, M., & Yates, P. (2012). Parental experience of childhood cancer using Interpretative Phenomenological Analysis. Psychology & Health, 27(6), 704-720.
Shama, W., & Lucchetta, S. (2007). Psychosocial issues of the adolescent cancer patient and the development of the teenage outreach program (TOP). Journal of Psychosocial Oncology, 25(3), 99-112.
Shortman, R. I., Beringer, A., Penn, A., Malson, H., Lowis, S. P., & Sharples, P. M. (2013). The experience of mothers caring for a child with a brain tumour. Child: Care, Health and Development, 39(5), 743-749.
Solooki, S., Ardestani, S. M., Mahdaviazad, H., & Kardeh, B. (2018). Function and quality of life among primary osteosarcoma survivors in Iran: Amputation versus limb salvage. Musculoskeletal Surgery, 102(2), 147-151.
Smith, J., Cheater, F., & Bekker, H. (2015). Parents' experiences of living with a child with a long‐term condition: A rapid structured review of the literature. Health Expectations, 18(4), 452-474.
Stegenga, K., & Ward-Smith, P. (2009). On Receiving the Diagnosis of Cancer: The adolescent perspective. Journal of Pediatric Oncology Nursing, 26(2), 75–80.
Stewart, J. L., Pyke-Grimm, K. A., & Kelly,K. P.(2012). Making the right decision for my child with cancer: The parental imperative. Cancer Nursing, 35(6), 419-428.
Stokke, J., Sung, L., Gupta, A., Lindberg, A., & Rosenberg, A. R. (2015). Systematic review and meta‐analysis of objective and subjective quality of life among pediatric, adolescent, and young adult bone tumor survivors. Pediatric Blood & Cancer, 62(9), 1616-1629.
Taylor, M. F., & Pooley, J. A. (2017). Sarcoma survivors’ perspectives on their body image and functional quality of life post‐resection/limb salvage surgery. European Lournal of Cancer Care, 26(6), e12667.
Van Dongen-Melman, J. E. W. M., Van Zuuren, F. J., & Verhulst, F. C. (1998). Experiences of parents of childhood cancer survivors: A qualitative analysis. Patient Education and Counseling, 34(3), 185-200.
van der Geest, I. M., van den Heuvel-Eibrink, M. M., van Vliet, L. M., Pluijm, S. M., Streng, I. C., Michiels, E. M., ... Darlington, A. S. E. (2015). Talking about death with children with incurable cancer: Perspectives from parents. The Journal of Pediatrics, 167(6), 1320-1326.
van Riel, C. A., Meijer-van den Bergh, E. E., Kemps, H. L., Feuth, T., Schreuder, H. W., Hoogerbrugge, P. M., ... Mavinkurve-Groothuis, A. M. (2014). Self-perception and quality of life in adolescents during treatment for a primary malignant bone tumour. European Journal of Oncology Nursing, 18(3), 267-272.
Virani, A., Green, T., & Turin, T. C. (2014) Phantom limb pain: A nursing perspective. Nursing Standard, 29(1), 44-50
Virani, A., Werunga, J., Ewashen, C., & Green, T. (2015). Caring for patients with limb amputation. Nursing Standard (2014+), 30(6), 51.
Wang, L. L., Chintagumpala, M., & Gebhardt, M. C. (2007). Osteosarcoma: Epidemiology, pathogenesis, clinical presentation, diagnosis, and histology. UpToDate (www. uptodate. com). Retrieved May, 10, 2007.
Wang, S. C., Wu, L. M., Yang, Y. M., & Sheen, J. M.(2019). The experience of parents living with a child with cancer at the end of life. European Journal of Cancer Care, 28(4), e13061.
Weiss, A., Khoury, J. D., Hoffer, F. A., Wu, J., Billups, C. A., Heck, R. K., ... Daw, N. C. (2007). Telangiectatic osteosarcoma: The St. Jude Children's Research Hospital's experience. Cancer: Interdisciplinary International Journal of the American Cancer Society, 109(8), 1627-1637.
Whittemore, R., Jaser, S., Chao, A., Jang, M., & Grey, M. (2012). Psychological experience of parents of children with type 1 diabetes: A systematic mixed-studies review. The Diabetes Educator, 38(4), 562-579.
Wittig, J. C., Bickels, J., Kellar-Graney, K. L., Kim, F. H., & Malawer, M. M. (2002). Osteosarcoma of the proximal humerus: Long-term results with limb-sparing surgery. Clinical Orthopaedics and Related Research, 397, 156-176.
Wong, M. Y. F., & Chan, S. W. C.(2006). The qualitative experience of Chinese parents with children diagnosed of cancer. Journal of Clinical Nursing, 15(6), 710-717.
World Health Organization (2018). Adolescent development. Retrieved July 22, 2020, form http://www.who.int/
Wu, W. W., Liang, S. Y., Hung, G. Y., Tsai, S. Y., & Lee, T. Y. (2016). The experiences of adolescents with osteosarcoma during the one-year of treatment in Taiwan. Journal of Child Health Care, 20(4), 473-482.
Young, B., Dixon-Woods, M., Findlay, M., & Heney, D. (2002). Parenting in a crisis: Conceptualising mothers of children with cancer. Social Science & Medicine, 55(10), 1835-1847.
Youngblut, J. M., & Shiao, S. Y. (1993). Child and family reactions during and after pediatric ICU hospitalization: A pilot study. Heart & lung: The Journal of Critical Care, 22(1), 46-54.
Zebrack, B., & Isaacson, S. (2012). Psychosocial care of adolescent and young adult patients with cancer and survivors. Journal of Clinical Oncology, 30(11), 1221-1226.