Disability, Identity & Invisible Grief
Maren, 34, graphic designer
Presentation
Born with spina bifida (myelomeningocele, L4-L5). Uses a wheelchair full-time since age 14 after progressive loss of ambulation. Works remotely as a freelance designer but wants to transition into UX research — recently passed over for an in-house position she suspects was due to accessibility concerns. Divorced two years ago, now in a new relationship where her partner's family keeps calling her 'inspiring.' Says: 'I spent my whole life being the girl who didn't let it stop her. I'm tired of being a story about overcoming.'
History
Raised by a single father after mother left when Maren was 3 (mother cited inability to handle the medical demands). Father was devoted but anxious — managed every medical appointment, surgery, and accommodation with military precision, leaving no room for Maren to grieve or struggle. Spina bifida required 11 surgeries by age 16, including shunt revisions and orthopedic procedures. Father's refrain: 'We don't feel sorry for ourselves in this family.' No space for anger or sadness about disability. Older brother was the 'easy child' — healthy, athletic, low-maintenance. Maren became hyper-competent and emotionally self-sufficient by necessity. No substance use. Previous therapy at 22 was CBT for depression, helpful for acute symptoms but never addressed disability identity or the medical trauma of childhood surgeries.
Where Approaches Genuinely Disagree
The invisible grief of disability — mourning a body or capacity that was expected — needs processing.
Locating the problem inside the person pathologizes a social failure. The suffering is political, not intrapsychic.
7 Formulations
Select 2–3 modalities to compare side by side: