Sickle-Cell disease and psychic care: What remedy for suffering?

被引:0
|
作者
Frippiat, Jessica [1 ]
Abdelhak, Mohand Ameziane [2 ]
Moro, Marie Rose [3 ]
机构
[1] Hop Univ Enfants Reine Fabiola Huderf, Serv Hematooncol Huderf, Ave Crocq 15, Brussels 1020, Belgium
[2] Serv Psychopathol Enfant & Adolescent, 129 Rue Stalingrad, Bobigny 93000, France
[3] Univ Paris Descartes Sorbonne, Serv Maison Adolescents Cochin Maison Solenn, Paris 75679, France
来源
ANNALES MEDICO-PSYCHOLOGIQUES | 2020年 / 178卷 / 05期
关键词
Adolescent; Discussion group; Psychic suffering; Sickle-cell disease; Transcultural;
D O I
10.1016/j.amp.2019.07.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Sickle-cell anemia is the most widespread genetic disease in the world, yet it is still little known. Individual interviews with adolescents with the disease have not produced much information. They are reluctant to speak on their own account. Certain cultural representations are predominant among these patients. Thus, a transcultural approach by way of talking groups seems more appropriate. The group forms a transitional space that is flexible and adaptable. In a group, adolescents can broach the subject of the difficulties generated by this disease, which is taboo and shameful in their original countries. They are able to talk about managing the disease, hospital, and the impact on schooling and their future. They also talk about the difficulty of living with the disease in their relationships, in their families and with their peers. The support and propping provided by the group makes way for the emergence of cognitions and the elaboration of a co-constructed narrative. (C) 2019 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:456 / 459
页数:4
相关论文
共 50 条
  • [21] SUDDEN TOTAL DEAFNESS IN SICKLE-CELL DISEASE
    OKEEFFE, LJ
    MAW, AR
    JOURNAL OF LARYNGOLOGY AND OTOLOGY, 1991, 105 (08) : 653 - 655
  • [22] CHOROIDAL OCCLUSIVE DISEASE IN SICKLE-CELL HEMOGLOBINOPATHIES
    DIZON, RV
    JAMPOL, LM
    GOLDBERG, MF
    JUAREZ, C
    SURVEY OF OPHTHALMOLOGY, 1979, 23 (05) : 297 - 306
  • [23] THE DIAGNOSIS OF PULMONARY THROMBOEMBOLISM IN SICKLE-CELL DISEASE
    WALKER, BK
    BALLAS, SK
    BURKA, ER
    AMERICAN JOURNAL OF HEMATOLOGY, 1979, 7 (03) : 219 - 232
  • [24] PENILE SCINTIGRAPHY FOR PRIAPISM IN SICKLE-CELL DISEASE
    DUNN, EK
    MILLER, ST
    MACCHIA, RJ
    GLASSBERG, KI
    GILLETTE, PN
    SARKAR, SD
    STRASHUN, AM
    JOURNAL OF NUCLEAR MEDICINE, 1995, 36 (08) : 1404 - 1407
  • [25] SUDDEN-DEATH IN SICKLE-CELL DISEASE
    LIESNER, RJ
    VANDENBERGHE, EA
    JOURNAL OF THE ROYAL SOCIETY OF MEDICINE, 1993, 86 (08) : 484 - 485
  • [26] NORPLANT USE BY WOMEN WITH SICKLE-CELL DISEASE
    LADIPO, OA
    FALUSI, AG
    FELDBLUM, PJ
    OSOTIMEHIN, BO
    OTOLORIN, EO
    OJENGBEDE, OA
    INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 1993, 41 (01) : 85 - 87
  • [27] THE ACUTE CHEST SYNDROME OF SICKLE-CELL DISEASE
    HAYNES, J
    KIRKPATRICK, MB
    AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1993, 305 (05) : 326 - 330
  • [28] PERIOPERATIVE MANAGEMENT FOR CHOLECYSTECTOMY IN SICKLE-CELL DISEASE
    BHATTACHARYYA, N
    WAYNE, AS
    KEVY, SV
    SHAMBERGER, RC
    JOURNAL OF PEDIATRIC SURGERY, 1993, 28 (01) : 72 - 75
  • [29] USE OF A TOURNIQUET IN PATIENTS WITH SICKLE-CELL DISEASE
    ADUGYAMFI, Y
    SANKARANKUTTY, M
    MARWA, S
    CANADIAN JOURNAL OF ANAESTHESIA-JOURNAL CANADIEN D ANESTHESIE, 1993, 40 (01): : 24 - 27
  • [30] DIFFUSE CHONDROLYTIC ARTHRITIS IN SICKLE-CELL DISEASE
    SCHUMACHER, HR
    VANLINTHOUDT, D
    MANNO, CS
    CUCKLER, JM
    ATHREYA, BH
    JOURNAL OF RHEUMATOLOGY, 1993, 20 (02) : 385 - 389