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Showing posts with label Chronic Illness. Show all posts
Showing posts with label Chronic Illness. Show all posts

Sunday, November 20, 2016

Sending Spoons - I Hope You Are AWAP

'Sending Spoons'
© 5/11/16 by Shiloh Moore
8"x10" Zentangle Pitt Pen and Paper Collage

Cards and products with this image can be bought here from Redbubble

This card is a Zentangle Collage called ‘Sending Spoons,’ for my friends with chronic illness. 

There is an analogy used to describe life with chronic illness by Christine Miserandino called 'The Spoon Theory.' (read in full here: 'The Spoon Theory' written by Christine Miserandino for www.butyoudontlooksick.com )  Christine has Lupus, but many with a variety of chronic illnesses and 'invisible' disabilities identify with it, and affectionately refer to themselves as 'Spoonies.'  

In her analogy, spoons symbolise energy (also pain threshold.)  A person with chronic illness only has a certain amount of energy per day, so only a few spoons.  Every task takes a certain number of spoons.  Often, you don't know how many spoons you will have throughout each day so you must be wise with how you spend them.  If there's something you have to do that day, you must keep enough spoons for the task. You might have to give up doing something else in order to have enough energy to do what you need to do.  You learn to prioritise what you spend your ‘spoons’ on.

Many with chronic illness also use a phrase to sign off messages with - 'I hope you are AWAP'.  AWAP stands for 'As Well As Possible'. 

So I came up with this pic 'Sending Spoons' using Zentangle patterns on spoons, with the phrase 'I HOPE U R AWAP.'  

(I also like how there's 5 horizontal spoons, so to me, I also see a mini musical staff!  Energy is musical!)

Thanks for using your spoons to read this.  Sending you spoons, and I hope you are AWAP!

Tuesday, September 27, 2016

Life with ME: Spot the Difference - "Weekend Girly Coffee Date"




LIFE WITH ME:
SPOT THE DIFFERENCE - 
‘WEEKEND GIRLY COFFEE DATE’
© 2016 by Shiloh Moore 

Prints of this work can be found at my Redbubble site here:
Spot the Difference PART A  - Image
Spot the Difference PART B - Words
 http://shilissimo.redbubble.com


Today, Sept 27th 2016, is the second international day of action by #MEAction promoting awareness and change for the #MILLIONSMISSING (around 20 million people worldwide) with ME, Myalgic Encephalomyelitis.   Note that the Australian day of action will be held in Melbourne in 2 weeks, on Wednesday 12 Oct 2016, from 1-2pm at Parliament House, East Melbourne, Vic, 3002 Australia.   

More information about the campaign, and ME, can be found here: http://www.meaction.net/

This 'Spot the difference' cartoon is my contribution to spreading insight into the disabling condition that I have had for more than two and a half decades.  

Here is the wording to go with the illustration:

LIFE WITH ME:
SPOT THE DIFFERENCE - 
'WEEKEND GIRLY COFFEE DATE'
 © 2016 by Shiloh Moore 

PERSON A:

“You look great!  But you don't look sick.
I feel tired all the time too,
maybe I have chronic fatigue? Hahaha!”

30 something married mother
+ career woman:

1) Frazzled long hair from morning gym session
2) Pretty dress + make-up
3) Heavy jewellery
4) Favourite perfume
5) Large slice of cake
6) High heels
7) Feet sore from standing and walking all morning
8) Shopping bags from browsing before coffee date
9) Barely able to sit still
10) Car keys for driving
11) Coffee date is the 5th of 10 events today

=  Is healthy but overworked

PERSON B:

(Smiles awkwardly)

30 something single woman with no kids
+ no job:

1) Bed-hair, cut short because it causes pain
2) Comfortable clothes + no make-up - no energy for fuss
3) No accessories as they trigger pain
4) No scents or chemicals as she is sensitive and reacts
5) No cake due to food intolerances
6) Flat shoes with orthotics
7) Feet sore from standing at all
8) Just got up at 10.30 in time for coffee
9) Barely able to sit up long enough for a brief cuppa
10) Driven door to door by a carer
11) Coffee date is the only non- medical outing or visit from a friend all week. 
She will need to go home to rest immediately after.

=  Has moderate ME (Myalgic Encephalomyelitis) and FM (Fibromyalgia Syndrome)

Shiloh Moore can be contacted on her webpage here:  www.shilohmoore.wix.com/byshi


Saturday, January 9, 2016

To Cry Out

"To Cry out
is not to admit defeat 
or failure.
It is to be human" 

Words © 2016 by Shiloh Moore
Painting: 'Woman of Rain' © 2011 by Shiloh Moore
from line drawing © 1998 by Shiloh Moore

Saturday, September 5, 2015

...What If All Goes Well?

'...What If All Goes Well'
5/9/15 by Shiloh Moore
Wording digitally added to
 'Mixed Media Background'
© 11-12/7/15 by Shiloh Moore
Something I've been saying to myself when my mind whirrs with fear of what's to come...

"Oh but, my darling... What if all goes well?!!!"

...

Tuesday, September 17, 2013

My Precious Body

'Resting Peace'
copyright 1998 by Shiloh Moore
Watercolour on A3 paper.

I painted 'Resting Peace' 15 years ago when I was 18 and dependent on a wheelchair to leave the house, recovering from a full year totally bedridden barely able to talk or eat or sit up.  My mother bathed and fed me during this time and even this was a mammoth effort for me.  The blues and purples in the outside of the picture represent the ease of the world, the beauty outside of my body.  The reds of my body represent pain and discomfort, blood stagnant and aching all over.  This was my rest.  I would try to tune out the pain in my body and see if I could notice and take on the outside stimulus of the gentle blues.  Mostly I was overwhelmed with the pain.

At this time I hated my body as all it brought me was pain and exhaustion and thousands of terrible symptoms.  I felt caged in this body, trapped, being tortured, no way out...  

Now, 15 years later and still experiencing extreme pain constantly, I realise it's not my body that confines me and causes me grief.  My poor little body is so weakend by this powerful illness and yet it still keeps going, keeps fighting, keeps me alive to experience the love, small joys and simple pleasures of this wonderful world.  It allows me to experience existence.  

My body is not a cage trapping me in torture, it is an amazingly strong and resilient beautiful marvel coping with a massive load while still helping me experience this life, which beyond the illness is precious.  My body's a fighter, powerful and valuable.  Oh little body how I love you.

When I'm in a lot of pain I now talk to my body, encourage it kindly to keep going, thanking it for surviving thus far, asking it to continue.  The other night I couldn't sleep due to pain so I lay awake talking to my body giving it love.  I wrote this:  

"My Precious Body'
copyright Shiloh Moore 15/9/13

Precious brave body
keep fighting
You deal with so much
such a heavy load
for such young shoulders

Keep on Keeping on
Look after you
Stay strong - 
You can do it.

You live so broken
so frail
so invaded
yet you survive
and continue to live 
using great strength.

You experience life so richly and deeply
even when you are forced to have bedrest,
hour after hour, day after day

My body:  You Belong.
There is purpose for your being.

How powerful and strong you are
Despite feeling so helpless
frustrated and overwhelmed,
pained and utterly exhausted.

You are amazing
You are precious
Keep fighting beautiful one
Oh little body how I love you.

Sunday, September 15, 2013

Sympathy Blossoms

'Sympathy Blossoms'
4"x6" watercolour and pitt pen card 
copyright 2013 by Shiloh Moore

A friend asked if I had any cards for the purpose of Sympathy cards.  I realised I didn't.
I haven't been well enough to get out the acrylics and do a big painting, but I thought I could try a small watercolour.  

I've been noticing cherry blossoms and how beautiful they are and wanted to paint them.  I didn't have 'real life' ones so I drew from photos.

I have been reading a beautiful book by Marie Williams, called 'Green Vanilla Tea.'  Marie's husband Dominic struggled with Alzheimer's and died in his early 40's.  The book is a memoir accounting both the incredible struggles and the wonderful memories of life with Dominic and their two sons Mike and Nic.  The love in their family is powerful.  It is touching to read.
 Cover of 'Green Vanilla Tea' by Marie Williams
(used with permission)

I have 'met' Marie Williams online and I dedicate this sympathy card to her and her boys. 

I drew the blossoms on my sympathy card, guided from the photo on the cover of the book 'Green Vanilla Tea', only from the other direction and with other colours.  
I chose the colour of the blossoms inspired by cherry blossoms in a photograph by a friend, Josie Eldred of -love to be young photography- .  I am a huge fan of her beautiful photography - she does the most amazing macro work, and it's even more amazing because she, like me, struggles with ME (Myaglic Encephalomyelitis) and has done since a very young age.  So her work is out of passion and painful determination like mine.  I loved her macro shot of cherry blossoms
in pink and this inspired the colours of my cherry blossoms on my card.

#cherry blossom #macro
copyright by Josie Eldred of -love to be young photography-
(used with permission)

So I dedicate this card, with sympathy especially to Marie, Mike and Nic. Also to all who suffer or care for those struggling from chronic illness, especially those who have lost their loved ones. 

'Cherry Blossoms'
copyright 2013 by Shiloh Moore
Original 4"x6" watercolour and pitt pen on paper

Friday, May 11, 2012

ME Awareness Day

 "Be...Together = Comfort" (c) 2012 by Shiloh Moore

When in pain and exhaustion of an indescribable magnitude
It hurts too much to talk
But the comfort of your
Company is powerful.

May 12 is International ME (Myalgic Encephalomyelitis) Awareness Day

Wednesday, May 2, 2012

'Learn To Choose Your Pain' and 'Do What Gives You Life'


'Do What Gives You Life' Scrabble letters 2012
on 'Butterfly Abstract' (c) copyright 2008 by Shiloh Moore
 

‘Learn to Choose Your Pain’ and ‘Do What Gives You Life’
(c) copyright 2012 by Shiloh Moore

I’d like to share with you two phrases I have developed over years of living with Chronic Illness.

First is a phrase I coined when in my teens, for those of us living with chronic illness (but obviously not totally bedridden): ‘Learn to Choose Your Pain.’

With chronic illness, Fibromyalgia and Myalgic Encephalomyelitis, you are always in pain.  You are never pain free.  To keep your spirit surviving,  it helps to prioritise what you spend your precious energy on.  Learn to Choose Your Pain. 

 'Learn To Choose Your Pain' Scrabble letters 2012
on 'Black on Abstract' (c) copyright 2008 by Shiloh Moore

I started thinking about this before I was diagnosed, when I was 14 and struggling to attend school having been unable to play my flute for months.  I came across a strange dilemma:  I had a ‘good’ day, when I had a rare glimpse of precious energy after school one day.  I found myself wondering, should I be a ‘good’ girl and do my homework, or could I spend this energy playing my beloved flute?  Is ‘I had a good day yesterday’ a valid excuse for not doing my homework yet again?! 

After many more years of illness, I learned to prioritise.  I learned that to keep your soul satisfied, sometimes you have to ‘choose your pain.’  Everything with this illness hurts, everything you do triggers a payout.  So choose what you do to cause the pain, and here comes my second phrase: ‘Do What Gives You Life.’

Sometimes it’s worth getting in trouble for not doing homework, to spend that precious energy playing.  Do what gives you life.

Sometimes it’s worth having a friend visit even though the house is a mess.  If you have to choose between either seeing the friend or cleaning, do what gives you life.

Sometimes it’s worth doing some art/seeing a friend/going to a movie or concert/going on an outing in a wheelchair/seeing nature/insert something fulfilling for you, even though you know you will have a payout as a consequence.  Sometimes it’s these highlights to life, the things to look forward to and to remember, that keep us going.  Of course, pace yourself and don’t do something if the payout will be too extreme.  But if you can, prioritise what you spend your energy on and choose to be in the inevitable pain for something that is worth it to you.  Learn to Choose Your Pain, and Do What Gives You Life.

A healthy person can learn from this too.  Within your busy schedule and list of commitments and responsibilities, learn to prioritise.  Say ‘no’ to doing too many things that are draining, nurture your soul and Do What Gives You Life.

Saturday, March 10, 2012

"I Am"

I have been in a bad patch health wise, unable to do any art for a month. I've been dreaming of lots of projects, itching to try mixed media again, and a stencil painting, but I don't have the strength to do either. A couple nights ago I was able to do some drawing lying down, and, while I imagine a grand large mixed media project from it, for now I have used watercolour.

"I Am" A4 Watercolour on Paper (c) 2012 Shiloh Moore

"I Am"  

copyright 8/3/12 by Shiloh Moore
While my body's wracked
With pain and exhaustion
of an indescribable magnitude...
Unable to do anything but lie here,
Hours, days, weeks on end...
I am...

I am the flute goddess I've always dreamed of being
I am flying free,
Filled with unearthly beautiful music.
I am beyond this broken body...
I am content and at peace.
I am okay.
I am...

Wednesday, January 18, 2012

Living With ME and FM Series - Lying Down

'Living with ME and FM Series - Lying Down Collage'
copyright 2011 by Shiloh Moore


This is what the majority of my life is like. I sleep on average 14 hours a day, and most of the rest of the day is spent lying. To me this is natural - it is how I have lived my life in private since the age of 15. When people see me sitting up it's for a brief outing after which I return to the lying position. These illustrate my life in bed:

1) 'Lying With Fibromyalgia' - copyright 2011 by Shiloh Moore
I have pain always. Even lying down exacerbates the pain. Sitting and standing are always painful. When I'm in a bad pain flare lying gets unbearable too. I continually have to change positions until I'm in the least pain. Resting alone does not take the pain away.



2) 'Lying Reading' - copyright 2011 by Shiloh Moore

This is a rare pleasure. It is painful to hold books, difficult to concentrate and take in what I am reading. I go in and out of 'reading space'. The precious times I can read are priceless!





3) 'Lying Listening' - copyright 2011 by Shiloh Moore
I often listen to soft music. When first bedridden I used to choreograph dances in my head. But even thinking of this was exhausting so I'd have to stop the music. Other times my sound sensitivity would trigger complete exhaustion and drain my energy so again I would have to turn the music off. Nowadays I can usually handle music softly to pass the time.


4) 'Lying Writing' - copyright 2011 by Shiloh Moore
When I'm up to writing I most often write lying down. When I'm not well I write pressing matters in note form. When I'm going well I'll write a letter or journal entry. When I finished high school and attended uni briefly I did all study lying down.




5) 'Lying Typing' - copyright 1998 By Shiloh Moore
When I was bedridden in the 90's and was slowly improving, I wrote my book, typing on my laptop, lying down. I knew how to touch type so I'd close my eyes and type, then check and save my work.




6) 'Lying Talking on the Phone' copyright 2012 by Shiloh Moore
I take most calls lying on my bed with a headset on the phone so I don't have to cramp my arms holding it.






7) 'Lying Pondering' - copyright 2012 by Shiloh Moore
Last year when I first released these images, 'healthy' friends commented how it made them realise I did everything lying down. They didn't realise that most of these things I did on 'good' days. Most of the day I need to rest completely - and by 'rest', I mean fully switch off and do nothing. No TV, no music, no talking, nothing. I wanted to add this last picture to illustrate what I 'do' most of the time: 'Lying Pondering.' Most of the time, in the silence, and for hours on end, I have perfected the art of lying in solitude, thinking, pondering, and processing. I think deeply and most of the time I am bedridden, I am surprisingly not bored. My thoughts entertain me, I am busy thinking through my grief until I accept how things are, and then I ponder life and am grateful and happy just to lie there and 'be'. After all, I am a human 'being' not a human 'doing'.

Over the past year I have been able to sit up more - but this is still limited to about 4 hours per 'good' day. But I am so grateful for this. I can sit up and make cards or paint or socialise for brief periods and this brings me such joy. I still call it 'sitting up', never 'sitting down' as it is always an effort and never 'relaxing.'

I still have pain flares which set me back for no reason for weeks or months on end. But when they ease, and I can sit in relatively less pain, life is so much easier and more fulfilling.

So there's an insight into the life of someone with ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) and Fibromyalgia.

Note on Awareness Day, May 12, 2013:
I would like to add that when drawing this, it felt like I was drawing the mundane of daily life.  It wasn't until I showed it to my mum that I realised this is not how most people live!  Living 'upright' all day is as bizzare to me as lying down all day is to most people.  I have lived this way since I was a child/teen so I barely remember living any other way.