For the 2.3 million people in the UK living with Generalised Anxiety Disorder (GAD) - and millions more around the world - accessing healthcare can feel like walking into a room already scripted. One where any new symptom, such as palpitations, fatigue, dizziness, or pain, is pre-read through the lens of anxiety.
Too often, this doesn’t lead to better care. It leads to something else ...
My recent research with Nicky Lidbetter and Dave Smithson from the UK’s leading anxiety charity Anxiety UK investigated these phenomena in the lives of people with GAD.
It asked two questions:
To answer these, I spoke with both people living with GAD and General Practitioners (GPs) in primary care, where MG/DO often happen first.
The research offers the first empirical insight into the scale and forms of MG/DO experienced by people with GAD in UK healthcare, revealing a shared awareness and willingness among both patients and GPs to address these issues.
Encouragingly, both groups express a clear demand for new tools, such as pre-appointment aids, diagnostic supports, and bias-aware decision resources, that could improve consultation quality, reduce harm, and lead to better health outcomes.
But what’s the wider issue here?
At stake then is not just clinical accuracy, but trust, recognition, and the conditions for people with GAD to be seen, heard, and treated as whole.
If you work in primary care, mental health, complex condition research, or have lived experience of MG/DO, I’d love to hear your experience and thoughts of what can be done.
View the paper on Octopus on the link, or drop me a comment below and I will send you a copy.
#DiagnosisAndExperience #GAD #MedicalGaslighting #DiagnosticOvershadowing #MentalHealth #RealLivedExperience #HealthJustice #PatientExperience #PrimaryCare