Lives are being ruined by undiagnosed hypermobility and lack of treatment | Letter. Ignorance around hypermobile Ehlers-Danlos syndrome is a public health catastrophe, say readers in response to an article on how sufferers have to wait 21 years for a diagnosisYour coverage of hypermobile Ehlers-Danlos syndrome (hEDS) is a vital start to addressing a systemic public health catastrophe (UK hypermobility sufferers wait up to 21 years for diagnosis, study suggests, 15 June).
A apuração publicada por www.theguardian.com vira base para uma leitura editorial direta e contextualizada.
Trechos de apoio da pauta: Ignorance around hypermobile Ehlers-Danlos syndrome is a public health catastrophe, say readers in response to an article on how sufferers have to wait 21 years for a diagnosisYour coverage of hypermobile Ehlers-Danlos syndrome (hEDS) is a vital start to addressing a systemic public health catastrophe (UK hypermobility sufferers wait up to 21 years for diagnosis, study suggests, 15 June). I am 34 and a former drama student who is unable to build any career as hEDS dismantled my life.
- Ponto de atenção: lives.
- Ponto de atenção: being.
- Ponto de atenção: ruined.
Em resumo, a leitura editorial acompanha o impacto do tema no nicho Beleza.