{
  "abstract": "Introduction People who experience Ehlers-Danlos syndrome (EDS), particularly hypermobile EDS (hEDS), face significant delays in receiving an accurate diagnosis. They also tend to be misdiagnosed due to a widespread lack of physician awareness. Many patients encounter scepticism in their journey to diagnosis, and their symptoms are frequently dismissed or minimised.Methods This qualitative study uses a descriptive phenomenological approach of individuals’ lived experiences of being diagnosed with hEDS and how the diagnosis affected their lives.Results Data analysis revealed six themes. Qualitative findings showed that receiving a diagnosis brought both validation and grief, helping participants make sense of their symptoms while confronting the reality of chronic illness. Experiences with providers ranged from harmful dismissal to deeply healing validation, highlighting the importance of trauma-informed care.Conclusions Physicians who are diagnosing and treating hEDS should be aware of possible medical post-traumatic stress disorder and past experiences with medical gaslighting.",
  "authors": [
    {
      "affiliations": [
        "Counseling, Leadership, and Research Methods, University of Arkansas, Fayetteville, Arkansas, USA"
      ],
      "name": "Julie Christine Hill"
    },
    {
      "affiliations": [
        "University of Arkansas, Fayetteville, Arkansas, USA"
      ],
      "name": "Diana C Cascante"
    },
    {
      "affiliations": [
        "University of Arkansas, Fayetteville, Arkansas, USA"
      ],
      "name": "Julianna Breazeale"
    }
  ],
  "title": "Surviving their stripes: the diagnostic odyssey and impact of life with hypermobile Ehlers-Danlos syndrome",
  "uid": "a9ecd942-cbf4-5c2c-91f9-0a22c705b7ae"
}