Morin Samantha A, Horta Angelina, Greer Katelyn, Rai Parveen Priya, Gross Haley, Reiter Raegan, Nielssen Ingrid, Bruce Marcia, Giroux Kim, Marshall Deborah A
Patient and Community Engagement Research (PaCER), University of Calgary, Calgary, Canada.
Child Health & Exercise Medicine Program, McMaster University, Hamilton, Canada.
Health Expect. 2025 Aug;28(4):e70332. doi: 10.1111/hex.70332.
Young adults with chronic autoimmune conditions face unique and often overlooked challenges in post-secondary education due to the invisible and unpredictable nature of these conditions. This patient-led qualitative study aims to further understand the experiences of young adults living with chronic autoimmune conditions while attending or considering attending post-secondary education.
The study followed the three-phase Patient and Community Engagement Research (PaCER) approach, a participatory framework that trains individuals with lived experience to lead all stages of research. In the first stage (SET), the protocol was co-designed with three external patient-partners. Study participants included young adults (18-35 years) with a chronic autoimmune condition for > 1 year who considered attending or attended a Canadian post-secondary school within the last 5 years and were recruited through social media. Data were collected (COLLECT) via focus group and interviews and then analysed using thematic and narrative analysis. Findings were shared back with study participants (REFLECT) for refinement and to inform recommendations.
Ten young adults participated, and eight key themes were identified. Themes included the wide-ranging impacts of disease management, the value of peer and family support, protective and risk factors for success, limited awareness and education around chronic conditions, and sometimes-unconscious burden of navigating invisible conditions. Participants also reflected on their resilience and the shifting accessibility landscape during Covid-19, and offered detailed feedback on current gaps and needed support. Their recommendations underscored ongoing institutional shortcomings and the need for systemic change.
Our findings indicate that young adults living with chronic autoimmune conditions are not having their needs sufficiently met while navigating the post-secondary education system. It is imperative that changes and feedback provided by students with lived experience are implemented to ensure an accessible post-secondary education experience.
Seven PaCER researchers, who identify as young adults with lived experience of chronic conditions, led the study design, data collection, analysis and manuscript preparation. This study was also co-designed with three external patient-partners who also identify as young adults with chronic conditions.
患有慢性自身免疫性疾病的年轻人在接受高等教育时面临着独特且常被忽视的挑战,因为这些疾病具有隐匿性和不可预测性。这项由患者主导的定性研究旨在进一步了解患有慢性自身免疫性疾病的年轻人在接受或考虑接受高等教育时的经历。
该研究遵循三阶段患者与社区参与研究(PaCER)方法,这是一个参与性框架,培训有实际生活经验的个人来主导研究的所有阶段。在第一阶段(SET),研究方案与三名外部患者合作伙伴共同设计。研究参与者包括患有慢性自身免疫性疾病超过1年、年龄在18至35岁之间、在过去5年内考虑或已进入加拿大高等院校就读的年轻人,通过社交媒体招募。通过焦点小组和访谈收集数据(COLLECT),然后使用主题分析和叙事分析进行分析。研究结果反馈给研究参与者(REFLECT)以进行完善并为建议提供依据。
10名年轻人参与了研究,确定了8个关键主题。主题包括疾病管理的广泛影响、同伴和家庭支持的价值、成功的保护因素和风险因素、对慢性病的认识和教育有限,以及应对隐匿性疾病时有时无意识的负担。参与者还反思了他们的复原力以及新冠疫情期间不断变化的可及性情况,并就当前的差距和所需支持提供了详细反馈。他们的建议强调了持续存在的机构缺陷以及系统性变革的必要性。
我们的研究结果表明,患有慢性自身免疫性疾病的年轻人在高等教育系统中需求未得到充分满足。必须实施有实际生活经验的学生提出的变革和反馈,以确保获得可及的高等教育体验。
七名PaCER研究人员,他们是有慢性病实际生活经验的年轻人,主导了研究设计、数据收集、分析和论文撰写。这项研究还与三名外部患者合作伙伴共同设计,他们也都是患有慢性病的年轻人。