A study of stigma among Iranian family caregivers of patients with multiple sclerosis: A descriptive explorative qualitative study

2017 ◽  
Vol 34 ◽  
pp. 1-6 ◽  
Author(s):  
Reza Masoudi ◽  
Fereydoon Khayeri ◽  
Leili Rabiei ◽  
Kourosh Zarea
2018 ◽  
Vol 5 (2) ◽  
pp. 193-200 ◽  
Author(s):  
Shahriar Salehitali ◽  
Fazlollah Ahmadi ◽  
Ali Hasanpour Dehkordi ◽  
Kobra Noorian ◽  
Malek Fereidooni-Moghadam ◽  
...  

2016 ◽  
Vol 42 (3) ◽  
pp. 162-171 ◽  
Author(s):  
Ahmad Ali Eslami ◽  
Leili Rabiei ◽  
Heidar Ali Abedi ◽  
Majid Shirani ◽  
Reza Masoudi

2017 ◽  
Vol 5 (1) ◽  
pp. 13
Author(s):  
Hossein Ebrahimi ◽  
Hadi Hasankhani ◽  
Hossein Namdar ◽  
Esmail Khodadadi ◽  
Marjaneh Fooladi

2020 ◽  
Vol Volume 14 ◽  
pp. 1159-1172
Author(s):  
Banafsheh Tehranineshat ◽  
Shahrzad Yektatalab ◽  
Marzieh Momennasab ◽  
Mostafa Bijani ◽  
Fateme Mohammadi

2017 ◽  
Vol 5 (1) ◽  
pp. 13
Author(s):  
Hossein Ebrahimi ◽  
Hadi Hasankhani ◽  
Hossein Namdar ◽  
Esmail Khodadadi ◽  
Marjaneh Fooladi

2017 ◽  
Vol 2017 ◽  
pp. 1-8 ◽  
Author(s):  
Hossein Ebrahimi ◽  
Hadi Hasankhani ◽  
Hossein Namdar ◽  
Esmail Khodadadi ◽  
Marjaneh Fooladi

Background. Today family members are providing care and support to each other during illness. In particular, in chronic illness, such as multiple sclerosis, the families are more involved in caring for and supporting their patients, so they use several strategies to cope with this situation. The purpose of this study was to explore the coping strategies in family caregivers of persons with multiple sclerosis in Iran. Methods. This is a qualitative study that was conducted through 18 family caregivers of persons with multiple sclerosis. A purposeful sampling method was used. Data were collected through semistructured and in-depth interviews conducted in Multiple Sclerosis Society and hospitals of Tabriz in Iran. The collected data was analyzed according to qualitative content analysis. Results. Five main categories were elicited from interviews: “using spirituality,” “living with hope,” “experiencing persistence and stability,” “seeking support,” and “seeking alternative treatments.” Conclusion. The study findings can help to inform the support given to families to help them cope with the effects of caring for someone with multiple sclerosis. Health system managers and professionals by using these results are able to support patients and their families appropriately in order to improve their quality of life and alleviate the complications of disease.


2021 ◽  
pp. 1-36
Author(s):  
Sabrina Cipolletta ◽  
Benedetta Morandini ◽  
Silvia Caterina Maria Tomaino

Author(s):  
Parvaneh Asgari ◽  
Alun C. Jackson ◽  
Ali Khanipour-Kencha ◽  
Fatemeh Bahramnezhad

This study a utilized phenomenological hermeneutic design. Fourteen Iranian family caregivers of patients with COVID-19 who were isolated at home were included in the study using purposive sampling. In-depth unstructured interviews were conducted via WhatsApp. Sampling continued until data saturation. Interviews were transcribed and analyzed using Van Manen’s approach. Three primary themes and eight subthemes emerged. The primary themes included: “captured in a whirlpool of time”, “resilient care’ and “feeling helpless”. It seems that the families of patients with COVID-19 attempt to resist the pressures of this disease with religious practices and problem solving. However, due to the nature of the disease and its severity, they sometimes feel ashamed or lonely and are afraid of losing their loved ones. It is recommended that psychiatric nurses should develop programs in the form of comprehensive spiritual care packages or psychological support and utilize multiple media channels to deliver these.


2013 ◽  
Vol 19 (8) ◽  
pp. 383-388 ◽  
Author(s):  
Jennifer K Angelo ◽  
Richard Egan ◽  
Kate Reid

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