As part of my recent exhibition, The Tennis Ball, at Union Coffee House, I held a dog friendly viewing. I took portraits of the wonderful hounds, and here they are. We only had three dogs – Narla, Evie, and Mickey – but they were wonderful models, and will pose for a treat.
click on the image above to find out more about the event
On 29th September until 13th October, I will be showing the culmination of a year of collecting tennis balls. Images of discarded and destroyed tennis balls that is!
Hosted at the Union Coffee House, we will be holding a one off special dog friendly viewing on 6th October.
Visit Eventbrite to book your ticket and bring your pet pooch (or just come to meet all the other pet pooches).
Google Maps satellite image showing the area which the photos were taken. My walks take me over the common at the top, into the Abbey House gardens, around the Abbey parkland, along the river, and through the woodlands at the bottom.
About Union Coffee House A unique community space and venue to hire in the heart of the city. All the furniture in the cafe is for sale, including the chairs you’ll be sitting on. Their furniture is a mixture of up-cycled/pre-loved and handmade, and they can create bespoke furniture to suit their customers. All their suppliers are local small independent businesses or social enterprises. The charity that they are currently working with is LS14 Trust in Seacroft. It is a quirky place that is quick to make you feel welcome and at home.
click on the map below for directions
This is exhibition is part of Love Arts Festival, a yearly festival held in Leeds as a celebration of mental wellbeing and the arts, click on the image below to see the full the programme.
This is my second drop in workshop at Kirkgate Market in Leeds (organised by Same Difference Arts), after leading one making Pop-Up Puppets in Easter earlier this year. As before, I got to work alongside Miranda Johnson, who is a fabulous face painter, really approachable and I fully recommend her.
I chose to do two simple activities, aimed at families with younger children, loosely themed around carnival – decorating hummingbirds and creating masquerade masks. The masks proved the most popular, and we went with the big reveal – the wonderful painted face underneath – not one, but two fabulous masks!
Oh, and it is Yorkshire Day on 1st August, so the White Rose of Yorkshire was flying on flags across the market, along with lots of flat cap wearing individuals, breaking the record for the most people wearing a flat cap in one place!
Below is a selection of photos showing the marvellous creations that the children made. I do think the zebra mask revealing the tiger painted face is one of my faves, simply for the animal theme. But, having said that, I think they are all equally wonderful, and I do so enjoy listening to the children’s stories and hearing how much they love creating at home.
I recorded this piece so you can hear how my thoughts sound as I write them down*.
Sometimes the silence is deafening. Nobody wants to talk about illness. Nobody wants to hear it.
That silence lives inside your head.
‘Where do I turn? How do I fix this? Why is it happening?’
I read the articles. I know the science. I can recite the words as why I have the pain, the fatigue, the inability to walk like I once did. I even know, that maybe I am more prone to demoralisation and depression because of this illness, it all makes perfect sense. Of course it makes sense, I’ve read the articles, they explained it to me.
But there is something more existential about feelings, and the realities of those feelings. Science explains why, my wanting to know why is fulfilled. But it is little comfort knowing why, when I cannot control my environment, or the people who inhabit it, affecting my actions and reactions. It is little help when I simply cannot control why I feel that way.
It’s a string of events – I want to go out and have fun, maybe visit a pub and have a few drinks, or go for a long walk in the country, perhaps visit an exhibition opening, or even attend a social gathering, with people I haven’t got to know properly yet. The desire to do these things is hampered by the inability to do these things. What is stopping me?! The list begins – the chairs are uncomfortable and cause me pain; the alcohol doesn’t work well with either my medication or my illness complications; the walking is too long and too hard; the exhibition is too far away; there is nobody to come with me; it’s too hot and my symptoms are worse; I am tired, I am broke, I am anxious about travel, I am disabled.
Soon, those people I spent time with, doing activities with, fade away. My support network dwindles. ‘How much longer can we spend going to her house, it’s a total non-event.’ That’s the silence in my head. It fills in the silence with conversations I haven’t had. It fills in the space with assumptions, imagined scenarios, filling in the silence with chattering, telling me why I have slipped from memory.
Where has this loneliness come from? My days have emptied. When there is less, because ability is blighted, those empty moments, they fill that silence with a booming explosion. The realisation that there is all that empty time. Plans to do, are now plans to not do. My empty days are spent watching films, TV serials, reading, sitting with my dog. Like an endless loop of the same. This isn’t how I planned to spend my time, there was never a ‘do not’ attached.
Advice is well meaning. But advice is seldom useful. Not when you know the science and the reasons, but cannot change the facts.
“Try not to isolate yourself”, they say. “Talk to your friends and family”, they say. “If you don’t have that support, build one”. Fair enough, seems reasonable. And far be it from me to be the naysayer, but here I go:
I am not trying to isolate myself – I want to do all the things, with all the people.
I do try to talk to my friends and family – they have hit mute. How much more can they listen to me, when my answer to ‘how are you?’, is the now difficult response of ‘not great, [insert current symptom] is bothering me’. We can handle acute, but chronic? ‘Why aren’t you better yet??’
Find new friends – I’d love to, but I can’t get out because I am isolated (see reasons above).
I have done what my doctor has suggested, I have learnt the science and suggested things to them myself, I have even read about the complimentary therapies that can assist, yet still this damn demyelination in my neck is mocking your advice to me. I thank you for your desire to make me that person you once loved and had fun with, I am certainly on the same page as you with that. But sometimes it is too much – it adds to my feeling of inadequacy, that I am not trying hard enough, it joins the chatter telling me you think I am lazy and just don’t want to get better, it makes me feel that I am a failure.
But! I am not a failure. I refuse to believe that not recovering from an incurable illness is my failure. My illness has created the problem, but it is not one I can fix alone. “As much as possible, continue doing the things you like to do”, I laugh to myself. I loved walking far, exploring new places, going on trips with friends. Now I walk a short length and explore the same space day after day, rarely with friends, often just me and my dog.
‘But you are so sad, we just don’t know how to deal with that”. I hear you, it must be quite hard to see a friend so miserable and diminished.
My hierarchy of needs has changed.
Thrill seeking is currently redundant. The basic needs of health, safety and companionship are now my priorities.
Here’s something you may not know. People don’t travel through life on a linear. And that very definitely applies to me now.
Desires: Then – holidays. Now – holidays. Difference: Then – the places I went, or wanted to go are frivolous, the only thing I had to worry about was how much money I had to spend getting there and being there. Now – is it far, is it comfortable, what’s the climate like, is there much walking, is it accessible, who will go with me, can I afford it…
Be more positive. Learn to be optimistic.
I have found plenty of models to achieve happiness and satisfaction. Here is one, with it’s catchy acronym – PERMA:
Positive Emotion. Feeling good, positive emotions, optimism, pleasure, and enjoyment.
Relationships. Social connections, love, intimacy, emotional and physical interaction.
Meaning. Having a purpose, finding a meaning in life.
Accomplishments. Ambition, realistic goals, important achievements, pride in yourself.
Now apply that to yourself. Apply it to people with more money. Apply it to people with less money. Apply it to people with large families or friendship groups. Apply it to people with few friends or less family. Apply it to people with impairments – physical, sensory, mental. See how they differ. Think about the time, energy, ability that some people need to get to a level of life satisfaction they desire, or even on your level. Remember, sometimes, what seems simple, easy, and achievable, may be difficult, hard, and seldom achievable.
I think we need to take time to listen. I mean really listen. We can give ourselves those self-affirmations. We can tell ourselves we are complete, we are our best selves. But we also need – not just desire, but need – to hear those affirmations and to give those affirmations to those we choose to be friends with, especially when their life satisfaction, their journey has altered. Don’t let the silence become deafening when you can’t see them. Reach out, even if you have since filled the void your full friendship once held. We all need to feel valued.
I don’t want to end this here. Pining after forgotten friends. Or expecting you to feel sorry for me.
Pity is not what I want. And I wager that most people in my situation are the same.
I want this. I have very good reason to feel demoralised. I am not going to be a quick fix or return to the previous version of myself. However, I do need to find my way to continue my journey through life, and it is going to be a bumpy ride. We never know when that journey we take, will take a diversion. Let’s talk about illness, it is scarier not speaking, not listening, and that silence can be deafening.
* Today, I have felt demoralised. My illness has taken my spirit and tried to crush it. It is hard having strength, when your strength is already being used overcoming obstacles everyday. But I will attest, know this, my spirit is stronger than I will ever let my illness be.
And I left my stumbles over the words as I read them. I found it hard to read this monologue, and it was several takes before I even felt I got it right. Like me, it’s not perfect.
We shall meet at 11am outside the Gatehouse Cafe, Abbey House Museum, Abbey Road.
Bring your sketch pads, pens, cameras*, and above all your imagination.
We will be walking around the grounds of the Abbey, visiting the gardens, looking at some of the exhibitions and chatting with the artists on the art trail.
During our meander we will sketch, write, take photos, about our experiences. We will finish off our work back at the visitor centre. There will be some paper, pens, scissors, glue etc available at the centre.
All work will be shown on the Sunday of the art trail in the visitors centre – so you will part of your very own exhibition.
SATURDAY 21st JULY – Gatehouse Cafe (11am-4pm)
SUNDAY 22nd JULY – Abbey House Walled Garden (11pm-4pm)
As part of Kirkstall Art Trail , I will be showing a collection of flowers, plants and bugs taken during walks with my dog, all shot with my handy iPhone.
All plants were found in the gardens next to Abbey House Museum