Sharing health evidence you can trust
In this blog written for both healthcare professionals and adults with cerebral palsy (CP), researcher Dr. Manjula Manikandan and her team explain their recent research about how health services are failing adults with cerebral palsy – and what needs to change.
In a blog for anyone worried about their drinking, or supporting someone with alcohol dependence, Sarah Chapman from Cochrane UK looks at evidence for the effectiveness of Alcoholics Anonymous (AA) and other 12 step programmes, and hears from some people with experience of becoming sober through AA.
In a blog for people with Menière's disease and those supporting them, Sarah Chapman looks at the latest evidence on treatments and talks to her husband Tim about living with Menière’s and making choices about treatments, and to researcher Katie Webster and Ear, Nose and Throat doctor Martin Burton, who are both authors of new Cochrane Reviews on treatments for Menière's.
A doctor and a stroke survivor reflect on the Cochrane evidence about giving people information after stroke and on their own experiences.
In a blog for anyone making health decisions, Sarah Chapman looks at some key things that can help you make a choice that feels right for you. Included here are links to good resources.
Sandra shares her experience of PTSD (post-traumatic stress disorder) and how treatment with EMDR (eye movement desensitisation and reprocessing) helped, and we include sources of information and support for people with PTSD.
How decision aids can help people make better choices about treatments.
What would you do if you woke up unable to move half your face? This blog shares Olivia's story, the challenges of Bell's palsy & what we know about treatments
In this blog, Karen Morley, who in 2018 wrote for Evidently Cochrane about her experiences of OCD (obsessive compulsive disorder) and how evidence helped her, tells us what has happened since, including the impact of the COVID-19 pandemic on her mental health, the challenges, and things she has found empowering.
A new WHO guideline on postnatal care puts a positive experience at the heart of the care that women and their babies receive in the first six weeks after birth. It recognises that care should go beyond the mere delivery of certain services. Good postnatal care should aim to meet every individual woman’s needs, leaving all new parents, the baby and family with a positive experience of this critical period in their lives.
In this blog for people with Raynaud’s phenomenon, Dr Kevin Su, a Rheumatologist from Australia, looks at the latest Cochrane evidence on vasodilator drugs for Primary Raynaud’s phenomenon. Katie LeBlanc, a patient advocate, reflects on her experiences.
After her son was diagnosed with Developmental Language Disorder (DLD), Genna White became a Speech and Language Therapist to help families like her own. In this blog, Genna reflects on what DLD is and what she’d like parents, healthcare workers, and others working with children to know.