Tuesday, 18 April 2017

#GuestPost: Hannah Laycock

Has MS impacted on your life in a positive way? #GuestPost #MSBlog

In an effort to make the blog 'more interesting' we are trying to encourage more guest posters including pwMS doing amazing things  with their hands and arms (#ThinkHand). Please let us know what you think of including pwMS as guest bloggers? 


BARTS MS BLOG: HANNAH LAYCOCK

It was 2009 that photography became my saving grace. That was the year my father was diagnosed with Motor Neuron Disease (MND).

Towards the end of my 2nd and into my 3rd year of my photography degree I created two volumes of work; ‘Railing At The Enthrallment to The Failing of The light’, part I and II, which documented my family’s life as they and I came to terms with the pronouncement of my father’s MND.

After graduating, my creative practice lapsed between 2011 and 2014. I had focused my energy on capturing and presenting my father’s diagnosis in both a truthful and loving way, but the process dulled my creativity. It wasn’t until I was dealt with my own diagnosis of Multiple Sclerosis (MS) in 2013, aged 31, that my creativity began, ironically, to flourish and bounce back again.

A few months after diagnosis my MS Specialist Mental Health nurse introduced me to George Pepper, Co-founder of Shiftms, a social network for people with MS. I became closely connected with the Shiftms team and in August 2014 I was invited to create a new body of work in response to their #GoodOutofBad (#GOOB) commission, as part of their MS Energy initiative. With this, ‘Perceiving Identity’ was created, which launched my photography back into the public domain with the #GOOB exhibition in London, February 2015.



After relocating from London back to Scotland, April 2015, and in May of the same year, I won an Artist in Residence in Glasgow at Six Foot Gallery and sponsorship from Street Level Photoworks, for the month of July. It was during this time that I created ‘Awakenings’; inspired by Oliver Sacks book, of the same title, that illuminates the relationship between body and self. The project launched as a solo exhibition at the end of the residency.

July 2015 was a month that tore me apart physically and mentally. So many transitions had taken place in my life in such a short space of time. My body and mind were bearing the brunt of all those changes. There was nothing I could do to escape its overwhelming presence, but to turn to my camera. It was a passage to forget, to gain clarity, resilience; to break free from the numbness of living with MS.

MS always changes. It never stays the same. I'm not trying to document it. It's impossible to do that with MS. It’s an intangible disease for those without the experience of it and to try and help them understand. I have to engage with what I'm feeling to portray the experience of having the condition.

‘Perceiving Identity’ and ‘Awakenings’ are photographic journeys that explore my feelings of uncertainty, fear, loss and liberation, intuitively delving into and questioning the notion of neurological ‘lack’.

For me, photography is painting with light. I was never really skilled at painting in the traditional sense, nor was I skilled at other creative mediums. Photography has enabled me to skillfully explore my creativity. Providing me with a tool to better understand and work through such events in my life. It has been a means of artistic expression and catharsis.

‘Perceiving Identity’ and ‘Awakenings’ correlate to my earlier art and portrait photography; Fragility and Primacy Subject, which deal with fragility, image and desire, and power relations between subject and observer.

Using photography, I aim is to reach out and help the general population, patients and health professionals to tell and engage with complex and unique stories of illness through the use of visual language. With this, I hope that people will better understand such conditions as MND or MS on a person centered level.


BIOGRAPHY

Hannah Laycock was born in Forres, Scotland. She Lived in London and Brighton for 10 years and returned to the Highlands of Scotland in Spring 2015.

Hannah studied photography at the University of Brighton. Her latest project, ‘Awakenings’, documents her diagnosis and subsequent experiences of living with multiple sclerosis; select images are currently showing at Glasgow Women’s Library as part of the women’s photography collective WildFires. Her work has been recognised in international competitions such as International Talent Support, Italy, and has appeared as the cover piece, including an extended essay written about her work, in the BMJ’s Medical Humanities journal in February of this year. She has also been interviewed about her work, multiple sclerosis and motor neuron disease for BBC Radio Scotland.

LINKS

More Than An Image’ campaign feature about the power of photography for Wex Photographic. Alongside Humanitarian photographer, Giles Duley.

BMJ Medical Humanities feature: ‘Capturing the worlds of multiple sclerosis: Hannah Laycock’s photography’, by Dr Stella Bolaki, School of English, University of Kent, Rutherford College Extension, The Spires, Canterbury, Kent CT2 7NX, UK; S.Bolaki@kent.ac.uk

WildFires: Women photographers network in Scotland

Link to my Hannah Laycock's website: http://www.hannahlaycock.com


CoI: Genzyme sponsored the #GoodOutofBad (#GOOB) Shiftms commission, for which ‘Perceiving Identity’ was created.

8 comments:

  1. Thanks for taking the trouble to do your guest post Hannah and for your generosity in sharing some of your images with those of us who access this site. Having initially found some of the images disconcerting, I've realised it is because, for me, they illustrate so acutely some of the realities of living with MS. I sincerely hope you've found that they 'speak' to viewers without the disease, as well as those with it.

    ProfG - I'd like to support your idea of more guest posts from PwMS. I shared the first of Olga's posts, I'd read on Bart's, with my neuro physiotherapist. In fact I'd love to have more details from her as to the exercises she's been utilising. More generally I'd hope it will benefit others, as well as myself, to have more uplifting messages from other PwMS.
    In the meantime, on to being distracted by the announcement today of a general election, eh?!?

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  2. PS: a guest post from Stephanie Buxhoeveden will make for a good read, I'm sure.
    I discovered her in the early days of diagnosis, before finding this site.
    Her TEDTALK and website were very helpful and as a PwMS who is also an MS nurse, she can provide some valuable insights.

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    Replies
    1. I agree, that would be good Fi.

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  3. Prof G, I hate to be a buzzkill, but I read this blog for research news, not inspirational stories. Please keep it on topic, there are plenty of other sites offering this kind of blog if you're interested.

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    Replies
    1. My motivation for asking Hannah to do this post to highlight someone with MS doing amazing things with their hands. It is hard to be a good photographer if you lose hand function.

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    2. Yes, but you wouldn't use a leather briefcase to carry your groceries, you'd use a carrier, even though they're both quality bags. And that is what I mean, this is a research blog, not an inspirational meme blog.

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