Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemic
Abstract Introduction COVID‐19 changed the way we lived with uncertainty from the outset as the pandemic impacted every aspect of our lives from well‐being, socializing to accessing healthcare. For people in vulnerable populations, such as those with genetic, undiagnosed and rare disorders, the expe...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
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Wiley
2022-10-01
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| Series: | Health Expectations |
| Subjects: | |
| Online Access: | https://doi.org/10.1111/hex.13405 |
| _version_ | 1797989731324133376 |
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| author | Malia Byun Hollie Feller Monica Ferrie Stephanie Best |
| author_facet | Malia Byun Hollie Feller Monica Ferrie Stephanie Best |
| author_sort | Malia Byun |
| collection | DOAJ |
| description | Abstract Introduction COVID‐19 changed the way we lived with uncertainty from the outset as the pandemic impacted every aspect of our lives from well‐being, socializing to accessing healthcare. For people in vulnerable populations, such as those with genetic, undiagnosed and rare disorders, the experience was heightened. Aim The aim of this study was to identify how the rapidly changing COVID‐19 environment impacted the lives of the Genetic, Undiagnosed and Rare Disease community. Methods From June 2020 to May 2021, we collected monthly open‐ended journals from people living in Australia with genetic, undiagnosed and rare disorders. Data analysis was deductive, using the Resilience Scale for Adults, and inductive using thematic analysis. Results We recruited 29 people (average of n = 9.7 submissions each month). Responses changed over the year, with initial journals focusing on the importance of developing new structures for day‐to‐day lives, while later journals started to focus on mental well‐being. Throughout the project, participants reported challenges in accessing health and social care that was compounded by fear and concern over being exposed to the virus. Later journals highlight inconsistent messaging for vaccinations for this vulnerable community. Discussion/Conclusion In parallel with the waves of the COVID‐19 pandemic, there need to be waves of targeted support for vulnerable communities. The first support wave needs to focus on facilitating the identification of new frameworks to structure day‐to‐day lives. A later second wave needs to focus on mental well‐being and coping with isolation, while consistent communication relating to health and social care throughout was essential. Patient/Public Contribution This study was co‐designed, co‐led and analysed with a patient support network. |
| first_indexed | 2024-04-11T08:24:00Z |
| format | Article |
| id | doaj.art-e65bc872cb2a4086be85e3f276a9eee2 |
| institution | Directory Open Access Journal |
| issn | 1369-6513 1369-7625 |
| language | English |
| last_indexed | 2024-04-11T08:24:00Z |
| publishDate | 2022-10-01 |
| publisher | Wiley |
| record_format | Article |
| series | Health Expectations |
| spelling | doaj.art-e65bc872cb2a4086be85e3f276a9eee22022-12-22T04:34:49ZengWileyHealth Expectations1369-65131369-76252022-10-012552223223410.1111/hex.13405Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemicMalia Byun0Hollie Feller1Monica Ferrie2Stephanie Best3California Lutheran University California USAGenetic Support Network Victoria Melbourne Victoria AustraliaGenetic Support Network Victoria Melbourne Victoria AustraliaAustralian Genomics Health Alliance Murdoch Childrens Research Institute Melbourne AustraliaAbstract Introduction COVID‐19 changed the way we lived with uncertainty from the outset as the pandemic impacted every aspect of our lives from well‐being, socializing to accessing healthcare. For people in vulnerable populations, such as those with genetic, undiagnosed and rare disorders, the experience was heightened. Aim The aim of this study was to identify how the rapidly changing COVID‐19 environment impacted the lives of the Genetic, Undiagnosed and Rare Disease community. Methods From June 2020 to May 2021, we collected monthly open‐ended journals from people living in Australia with genetic, undiagnosed and rare disorders. Data analysis was deductive, using the Resilience Scale for Adults, and inductive using thematic analysis. Results We recruited 29 people (average of n = 9.7 submissions each month). Responses changed over the year, with initial journals focusing on the importance of developing new structures for day‐to‐day lives, while later journals started to focus on mental well‐being. Throughout the project, participants reported challenges in accessing health and social care that was compounded by fear and concern over being exposed to the virus. Later journals highlight inconsistent messaging for vaccinations for this vulnerable community. Discussion/Conclusion In parallel with the waves of the COVID‐19 pandemic, there need to be waves of targeted support for vulnerable communities. The first support wave needs to focus on facilitating the identification of new frameworks to structure day‐to‐day lives. A later second wave needs to focus on mental well‐being and coping with isolation, while consistent communication relating to health and social care throughout was essential. Patient/Public Contribution This study was co‐designed, co‐led and analysed with a patient support network.https://doi.org/10.1111/hex.13405chronic illnessCOVID‐19geneticsjournallinglived experiencerare disease |
| spellingShingle | Malia Byun Hollie Feller Monica Ferrie Stephanie Best Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemic Health Expectations chronic illness COVID‐19 genetics journalling lived experience rare disease |
| title | Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemic |
| title_full | Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemic |
| title_fullStr | Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemic |
| title_full_unstemmed | Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemic |
| title_short | Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemic |
| title_sort | living with a genetic undiagnosed or rare disease a longitudinal journalling study through the covid 19 pandemic |
| topic | chronic illness COVID‐19 genetics journalling lived experience rare disease |
| url | https://doi.org/10.1111/hex.13405 |
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