Community reporter and S&C reviewer Paul Valentine attended the book launch for Clare Best’s new memoir The Missing List and finds a masterfully written and powerful reflection on abuse. I’ve read a lot of memoirs [… read more ]
A new project investigating the history of women’s activism in Portsmouth is looking for volunteers and launches this Saturday 20th October. Dr Sue Bruley, Dr Laurel Forster and Dr Terese Jonsson at the University of [… read more ]
As a writer it’s important to be able to take criticism. Constructive criticism can help you improve. But what about when criticism turns into personal attacks and cruel abuse? Portsmouth writer Maddie Wallace reports. In [… read more ]
S&C regular contributor Dianna Djokey interviews Celia Meiras, who plays Hanna in Hannah and Hanna in Dreamland, a play by John Retallack being staged at the New Theatre Royal on 16th October. The play has [… read more ]
2018 is the Chinese Year of the Dog, perhaps the ideal time for Portsmouth to show some pride and address the topic of dog fouling. But one of the main obstacles to this, argues Sian [… read more ]
Like many students, Anne Taylor was uncertain that her degree would guarantee employment when she graduated from the University of Portsmouth. Unlike many graduates, Anne faces some additional barriers to finding work: she is disabled [… read more ]
The Society of St James (SSJ) is a Hampshire-based homelessness charity that provides accommodation and support to over 2500 people each year. Here the charity’s team explore why homelessness in Portsmouth and the surrounding area [… read more ]
Lucy Schorn, local writer, activist and resident, explores male privilege, power and misogyny in her account of a train journey back to Portsmouth from Brighton Pride in August 2018. I just got home from a [… read more ]
On 10th July 2018, Shamira A. Meghani came to Portsmouth to contribute to a panel discussion for Hope not Hate Portsmouth on the importance of connection over hate and division. S&C is delighted to share [… read more ]
An estimated 250,000 people in the UK suffer from Myalgic Encephalomyelitis (M.E.), with roughly a quarter of these patients house- or bed-bound. But research into the condition is significantly underfunded as less than 1% of [… read more ]
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