García-Bravo, CristinaPalacios-Ceña, DomingoHuertas-Hoyas, ElisabetPérez-Corrales, JorgeSerrada-Tejeda, SergioPérez-de-Heredia-Torres, MartaGueita-Rodríguez, JavierMartínez-Piédrola, Rosa Mª2024-01-312024-01-312022-12-30García-Bravo C, Palacios-Ceña D, Huertas-Hoyas E, Pérez-Corrales J, Serrada-Tejeda S, Pérez-de-Heredia-Torres M, Gueita-Rodríguez J, Martínez-Piédrola RM. "Your Life Turns Upside Down": A Qualitative Study of the Experiences of Parents with Children Diagnosed with Phelan-McDermid Syndrome. Children (Basel). 2022 Dec 30;10(1):73. doi: 10.3390/children10010073.2227-9067https://hdl.handle.net/10115/29290(1) Background: Parents of children with rare diseases experience great uncertainty and employ different strategies to care for their children and cope with the disease. The purpose of the present study was to describe the perspective of parents with children with Phelan McDermid Syndrome (PMS). (2) Methods: A non-probabilistic purposeful sampling was used to perform this qualitative descriptive study. Thirty-two parents with children with PMS were interviewed. In-depth interviews and research field notes were analyzed using an inductive thematic analysis. (3) Results: Four themes emerged from the data. "Understanding and accepting the disease" described how parents experienced their child's diagnosis and the lack of information. The second theme, called "Living day by day", highlighted the daily difficulties faced when caring for a child with PMS. The third theme, "Expectations versus reality", was based on the parents' expectations of parenthood and the reality they face. Expectations for the future are also included. Finally, "Pain and happiness" describes how parents alternate feelings of distress and suffering but also joy with what they learn from these experiences. (4) Conclusions: Health professionals can use these results to support parents.engAtribución 4.0 Internacionalhttp://creativecommons.org/licenses/by/4.0/Phelan-Mcdermid SyndromeTelomeric 22q13 Monosomy Syndromeparentsqualitative researchrare diseasesinfo:eu-repo/semantics/article10.3390/children10010073info:eu-repo/semantics/openAccess