We’re planning the launch event and catching up on the related social media campaign #MyLineInTheSand that invites people to post words of hope, rage and solidarity to stand with survivors of childhood sexual abuse (CSA). We’re busy contacting anyone and everyone who can help to promote the work - arts colleagues, survivor charities and survivor artists, activists and academics.
I’ve never studied art; I come from a medical background and did a PhD in microbiology. My world was about numbers, statistics, looking for tried and tested patterns, and grouping things into distinct categories. Absolutely these approaches have a place, and are especially essential when needing to rapidly process large amounts of information in high risk environments. But it didn’t give me a good way to process my inner world of chaotic and conflicting thoughts and feelings. Thankfully illustration did.
I truly believe that when we normalise difference we enter a much more just and equal world. We all have mental health, that’s a fact - so shouldn’t we all acknowledge this hidden truth, accept that we might have mental ill health at some point and stop being afraid of the unknown?
I first found creativity at the age of 25 – I had moved to a new town to be with my boyfriend but knew no one and nothing. I had experienced high anxiety in the past but understood now that if I didn’t keep my time and my mind occupied I wouldn’t survive and the move would be pointless. So that’s what I did.
' I enjoy creating a well-making space in my mother’s home where both my mother and I can breathe, de-stress, and attend to self-care through acts of creativity.' A reflective blog from artist/researcher and carer Mah Rana exploring the power of creating well-making spaces in unsettling times.
…if you’ve self-isolated over years as I’ve done, you do slow down to a very, very different pace.
The following is an interview with Gilly Angell, a founding member of the LENS group, from 31 March 2020
This story shares how The Beaney House of Art and Knowledge are working together with partners and their local visually impaired community to enable more meaningful access to creative and cultural experiences to boost wellbeing, raise awareness and create a more inclusive space.
Kate Smith is an award-winning children’s illustrator/designer and a workshop leader, who has a diagnosis of ‘Acute and transient Psychotic Disorder’ which was triggered by stress and anxiety in 2005. Kate was encouraged to make Christmas cards by an Occupational Therapist from the Early Intervention Service in Derbyshire as a coping strategy.
This story begins with an introduction from Naomi, who shares with us her experiences of being a full-time carer, Mum, nurse and painter and why now is the right time to share her story and her artwork.
Excerpts from Beyond The Illness, Art n’ the Human experience by Shanali Perera, MBBS MRCP
“The aim of art is to represent not the outward appearance of things, but their inward significance” ~ Aristotle
A story by Carole Fotheringham
This is a story about how cultural activities are contributing to healing and enriching my life after a life threatening illness. How it seems culture, friendship and laughter have the ability to cure all.
A story by Dave Logan, Chair of Parkinson’s UK – Swindon & District Branch, who has lived with Parkinson’s for sixteen years.
I have had Parkinson’s for over 15 years and celebrated my 70th birthday this July. I have been lucky in that the progressive nature of my Parkinson’s has been slow.
I spun a web and wrapped it round my life;
fine spider silk: the type we’re taught to make.
A sticky weave of working mum and wife;
bespoke design – its cords would never break.
High praise I netted in for such rich yarn;
a gossamer of love cocooned my home,
a strategist at work, a queen of charm;
The Beaney’s Power of the Object programme – a dementia & social isolation story
It’s been important to both me and my mum because it’s given Mum the opportunity to come out and do something constructive and it seems to me that she gets some kind of stimulation that lasts for 2 or 3 days afterwards.
Paul Langley, Carer
My practice and initial investigation was a coping strategy to enhance my quality of life throughout the long wait for diagnosis and therefore manage anxiety, uncertainty and the medical side effects of treatment, including my experience of itch.