Prenatal and Postnatal Opinions and Experiences of Women With Multiple Sclerosis: A Phenomenological Study

Background: Multiple sclerosis is an irreversible autoimmune disease with significant physical, psychological, and social impacts. Understanding the lived experiences of pregnant women with multiple sclerosis is vital for healthcare professionals to provide better care to these women.
\nPurpose: This study was designed to explore the lived experiences of pregnant women with multiple sclerosis.
\nMethods: A descriptive phenomenological study was conducted at the University of Jaén and included 17 women from different Spanish provinces who were recruited using intentional and snowball sampling methods via national patient associations and social networks. In-depth interviews were conducted, audio-recorded, transcribed, and analyzed using Martins' three steps. The ATLAS.ti 7.0 program was used for data analysis.
\nResults: Two themes and seven subthemes were identified that highlighted the experiences of women in pregnancy with multiple sclerosis: (a) the influence of the disease on the decision to be a mother, with subthemes “The disease determines when to be a mother” and “Considering alternatives to spontaneous pregnancy,” and (b) the vision of motherhood with multiple sclerosis, with subthemes “Worry about how the disease can affect the pregnancy,” “Worry about how the pregnancy can affect the disease,” “Concerns about childbirth,” “Difficulty with breastfeeding,” and “Worry about the transmission of the disease.”
\nConclusions/Implications for Practice: Women with multiple sclerosis often face a difficult decision regarding whether to become pregnant. The period of pregnancy and puerperium can be fraught with anxiety, especially in terms of concerns about their ability to raise children. In light of the limited scientific evidence regarding the relationship between multiple sclerosis and pregnancy and the conflicting advice often given to these women, the findings of this study may be used to help improve the quality of the care provided to this population.