Fling your love to the stars

I have been unable to articulate to you what I am feeling. I keep writing it and feeling it is not enough, she is so beautiful my Kae, so angelic that the words I write cannot touch her or do her justice. My heart is weighed down, a clunky stuttering beat as it tries to compute the idea of what it must feel like to her. Perhaps like the tragic heroines of years gone by who walked calmly, almost sleep walking, their elegant nightgowns weighted down, stepping delicately over the slowly gurgling stream into the deeper waters where the current swept them along, their last vision of the stars before the pockets full of river rocks smoothed by the rushing water and tumbling momentum dragged them silently beneath the glassy surface.

She is my Kae, a flightless angel, whose boundless depths of love and wells of beauty of spirit always remind me of my flaws. She would hate that. Admonish me harshly for saying such a thing. For that is not how she sees others. Kae does not see what she does or is as extraordinary. She is unaware that she is so ethereal and otherworldly, she has lived in her skin her whole life, to her it is normal to be just so. But to those of us touched by the glow of being near her, she is a majestic and beloved spirit to be awed.

Kae has been trapped in the dark for a while. Years really, but there's been light let in for long stretches, and then again the shutters slam shut. Now she is taunted and maliciously harassed by pain and an exhaustion so deep and harrowing that only those who have nearly died of exhaustion can come close to understanding, and still you will not understand unless you have experienced it day after day after mind bending, soul destroying day.

Her brain is playing tricks on her, the river calls, waits until she falls into fitful dreams and coos her name in a melodious whisper, the rhythm of water gurgling over rocks mocking her with echoes of her name through the trees. The invitation taking root in her psyche when she is defenceless against it's malignant charm.

Never have I known someone so willing to selflessly step up, to surprise, to support and fight for you and most importantly, to simply be with you. Never have I known a heart so big, a love so dazzling , a well of selflessness that runs so deep there is to my knowledge no end. Kae is what we all wish we could be. She is not perfect but she is what most of us strive for.

My Kae (I say my Kae but she is not just my person, she is many people's person, her heart is that big) is going through the biggest battle of her life and unlike people with recognised illnesses, she is battling an invisible and insidious illness so extraordinarily brilliant in it's trickery that it hides from doctors while it wreaks havoc with your body, your cells, your organs, your limbs, your pain receptors, your perception, your gut, your balance, your spirit, your soul, your heart and everything that is you. How do you fight that which you cannot see and no one except those who fight beside you, a secret army of warriors, even believe it exists, spare a few special doctors who believe in that which cannot be seen or labelled.

So I am asking you to stand with us, the secret army of warriors who fight without armour, without weapons, without the support we have earned, without medals for the bravery and courage in the face of such inescapable horror day after day. We go without acknowledgement and mostly we've all grown used to relying on our battle mates as only they know what it truly feels like, apart from the few carers privvy to witnessing the extraordinary war that we battle every day like clockwork.

No I am begging you. As I have begged of you before to fight for me and others, I am begging you to help me will my darling Kae, my most gorgeous and selfless friend who is so very tired, I am begging you to help me. Will her on. Join a chorus of love and prayers and good vibes and healing meditations and send them into the universe so that she may be surrounded by your love and the light will be forced into her lungs.

Send her all the love and light you would your most beloved. Because my Kae would do it for you without a second thought. She reunited a family who were separated on other sides of the world after years apart and refused to admit she was involved, and yet our very sick and beautiful friend knew it was her and she got to see her grand babies and spend a very special Christmas with them. She forced me to see a doctor and when I had no money she forced me to take a loan from her that she refused to allow me to pay back. She sends random gifts just to amuse herself. She finds beauty in the simple and every day things and has the most creative and instinctive eye for capturing moments most of us either don't notice or take for granted. She sends thank you cards to people who think of her when she can barely lift her head, let alone see the page or muster the energy to force the pen to the page in eloquent coherent sentences. She sponsored an elephant for a group of us, a sick group of friends from all of the globe that she networked together – my twinkling, glistening orb of friends like a spider web around the world – she was the catalyst. She remembers everyone's birthday, anniversaries including the awful ones, the days of those that were lost. She is an angel. She is my angel. She is many people's angel. She is not allowed to be another angel who is has their wings bestowed upon them too soon. We will not allow them to be fitted. She will stay with us because we will fight for her.

We have too much to do. Adventures together with our friends. A commune to run. And although I may never get to have children, neither might Kae, but we will have each other and our most beloved friends and family. My love pours from my heart into this page like she were my child and I were cradling her in my arms soothing her with a lullaby, whispering to her about all the stars in the sky and how they will never ever come close to shining as bright as she does. I could not love her any more.

Please I beg of you help me keep this angel here on earth. Fling your love to the stars and wish it back to her.

NB these two beautiful photos above are Kae's work, to enjoy more of creative work, click on either photo to be taken to her gorgeous blog.

Our dear friend Cusp started this candle vigil to show Kae how much love is in the world for her, please take just a moment click on the photo and light a candle and send some love and light.

Please note, since writing this - just today - I have heard some news that Kae's spirits have lifted a little.  But I also heard today that we lost another Lyme warrior who gained her wings.  So please know, today Kae be okay, tomorrow she may not be and again and so on and so forth.  It is an arduous and awful fight and this is as pressing in this moment as it was the moment before.  Perhaps even more so as the reality hits home that we have lost one of ours and that reality is tangible, touchable and real.  Please help us fight.

♥ Love ♥

I have breathed out and released some of the bleakness that has completely overtaken my body in dark shadowy patches of intense sorrow and grief. So I am going to try to breathe in the light.

For there is so much beautiful, dazzling, uncovered treasure in my life. Despite all that ails me I have a network that stretches like a twinkling, glistening, barely visible spider web surrounding the world like a beautiful orb of criss crossing love. Perched upon it are not captured or wounded beings, but beloved connections who together knit the web and use it like a hammock to rest upon when their day gets too weary. We each rely on those connections, feeling the vibrations of love from across the globe even when we are unable to speak.

So to those who have woven the beautiful web which works as a safe place to rest my head and dream of swinging madly about in joyous tumbles, I thank you. To those who I have uncovered in the rubble and ruin of life, in the dark heavy sorrow, whose love has forged connections between me and other broken winged birds, some now angels, I adore you and whisper softly always to your faintly beating heart, “I love you, I love you, I love you”.

To my beloved healthy friends who share dazzling moments past with me, jewels in my memory that shine bright when they're tended to and polished up to focus into perfect clarity, I love you for standing by me, holding our shared jewelled memories like keepsakes, protecting them for me, keeping them in your hearts, ever present so you do not allow me to forget who I was and who I can be.

For my family, some of whom are not blood, but I have chosen to adopt in my closest network of glistening connections to share my resting space, you see both sides of me. You see my grace and strength and joy and you see the depths of my struggle and how I fight so very hard to hang on to my sanity, to war with the bugs that are forever inching closer to a coup in my brain. You keep me fighting, you fuel the fury that allows me to control the bugs and prevent them overtaking my very being. And most importantly, you love me despite the days in which I cannot summon grace, the days in which I lose the battle and the bugs take over, the days in which I am so deep in despair and desolation I drag you down. Your love is what love should be. The love of imperfect perfection, the love without conditions, the forgiving love, the understanding love, the momentarily angry but quickly forgiven love, the true and gritty messy love of truly seeing each other and accepting each other's faults love.  The real love, not the manufactured candy love we've been sold, the messy, ugly, gritty, beautifully tainted, imperfect, perfect love.

And lastly, to those of you who witness my suffering, who do not turn away, who stand by me quietly unwavering, it is you who inspires me. You who patiently waits for the moment when I can properly communicate, you who sees me despite my inability to fully fulfil myself, you who supports and loves me without conditions, you are all the best of me. All the loves of my lives.

Thank you for the love that fuels my fight.

NB please click on the image to be taken to the website of media artist who created this meme quoting Molly Friedenfeld.

Theda and her red shoes

Life stood still. Everything slowed down. Time moved like it was struggling through mud. It was no longer fluid. It was clunky and faltering. NOOOOOOOOOOOOOOOOOOOO was all I could hear in my head. And then I realised I was screaming it. I was hysterically screaming, “NO, NO, NO, NOOOOOOOOOOOOOOOOOOOO.”

Somehow I had collapsed in the sludge of time, I was stuck in a tangled pile of limbs on the floor. Confused by the fact that my brain could focus so intensely on the dust on the floor while my body shook with shock. Everything became crystal clear around me, and yet the world moved slowly, in chunks of moments. Moments that seemed unconnected. I lost the time between them. I still don't remember much of that day.

It used to be that people asked you where were you when they landed on the moon? Where were you when JFK was shot? Or Martin Luther King? For their contemporaries, us, it is, where were you when the Port Arthur massacre happened? Where were you when the planes hit the towers? Where were you when the Bali bombings happened? Now where where you when flight MH17 was shot down?

For those of us who are gravely ill our questions are different. We know the answers to all of those. But time is sludgy, murky, desperately cold and merged into one huge pool of invariable days, months, years and decades. But ask us where were you when Amberlin Wu died? Where were you when Theda Myint died? Where were you when Tom Hennessy Junior died? And we all immediately know.

I was in this house. Just steps from where I now sit typing. I rose from the computer and I stumbled to the top of the stairs. And then from me escaped this terrible keening noise. And as I sobbed hysterically all I could hear was this distant scream of no. It took a while to realise it was me. I was screaming.

Ma came to me, she flew up the stairs and I couldn't make words except for NO. NO. NO. NO.

Just the night before, or hours really Theda had liked a status update of mine:

Wednesday, 24 July 2013 at 19:28

“Ma and I were just singing in the shower (I was in the shower she was hosing me). Anyway I said to her ladyface you could win a granny. And keep them all on your mantelpieces.

I'm such a tool.”

I remember finding that later and wondering if I had of just made her laugh more, just done something more, maybe I could have gotten her to stay here a little longer. Theda was a soul sister. It is hard to articulate to those who have not suffered greatly every day of their lives for years on end, decades. We become naked, raw nerves. We are stripped of all the things “normal” healthy people assume as part of their identity. Independence, clothing and accessories, grooming, the way they style their house, the car they drive, where they live, their job, their house or unit or apartment, their partner, their social life, their facade. We are stripped down to the bare minimum, our world is so small that all that matters is surviving the next five seconds or minutes.

So we have a magical power. We see you. Behind your facade. We see through the little white lies you tell yourself and the lies you tell the world. The masks and costumes and material things you surround yourself with to create a perception of who you are. We see you. The real you. You cannot hide from us. And we cannot hide from each other.

It means that we become extremely close extremely fast with other gravely ill friends. We say I love you with a freedom and verbosity that would scare most healthy people. But we know the truth. We might die tomorrow and we won't go down without letting you know what we feel, no matter what you feel about it. We want to be right with the world if the inevitable happens sooner rather than later.

Theda and I became fast friends. We barely spoke. We just suffered intensely on the same battle field and knew without a doubt the other would be there should we wish to share something, to talk, to check in. We had a kinship. A love. But she just was that way. She was a huge beating heart. In her darkest moments she was altruistic and selfless. Always she thought of others first, she was innately good. She was not perfect I am certain, we do not want to martyr the dead, but she was pretty damn flawless in my eyes.

I cannot clearly articulate what it is I want to say to you. I guess I want you to remember Theda as more than someone who was sick. Because we are all more than the sum of our parts, even if the majority of our parts seem to be made of infections. Theda was a talented, beautiful, beloved member of our world. Not just for those who were ill, but anyone who she met or even touched online with a few kind words fell in love with her.

Today is Red Shoe Day, the very first annual international day of remembrance in Theda's honour for those lost to Tick and Vector Borne Diseases and other invisible illnesses. Even now Theda is changing the world just by the legacy of love she left behind.

I don't have any red shoes. I don't think Theda would mind. She knows what is in my heart. The day I fell to the floor and lost complete control of my heart, exactly a year ago today, as I wept and keened and screamed on the floor, I felt arms encircling me and a calmness wash over me. I don't know if it was Theda. I like to think it was. Suddenly I knew in my heart that she was free, that she was happy and she was in a much better place. So that is what I choose to believe. I take comfort in the fact she made a choice to leave. I wish selfishly it wasn't so, but for her, I can muster up the love I have to be happy for her freedom from suffering. She deserved it.

Theda my angel, you live in my heart. You live in my soul. You will forever be part of me. And when I sleep tonight I hope that I commune with you in my dreams.

Sweet dreams princess.

*Special thanks to my dear friend Elizabeth D'Angelo who upon the request of another darling angel in my life, Sarah-Louise Feather Jordan created this beautiful piece in remembrance. To support Theda you can order prints, bags, pillows, shirts, cards, and duvet covers with this image here .

All proceeds from the sale of this work will go towards the Theda Myint Fund, to bring much needed care and services to people suffering from invisible illnesses.

Light

I have often felt like a child hiding in a midnight wardrobe, scrunched in the corner desperate for the safety of light. It has been a long and increasingly treacherous decade and the universe has seen fit to challenge me incessantly.

But something lovely and sweet has happened in the last year that has made me feel like a belatedly commended soldier. The light has found me more often, bathing me in the gorgeous safe warmth of hope. It is really easy to drown in the blackness when you are sick and alone, but I want to celebrate the light.

What has been hardest for me with this illness, aside from the obvious death defying struggles, is the lack of understanding. Especially from those you love. Lack of empathy from family cuts close. Some have always understood it, but some have criticised and mocked me, thinking they are doling out tough love but unintentionally being cruel. However in the last year it is as though my suffering has become more visible and in their eyes less transient.

My Ma, from the first camp, bought me a new second-hand bed – barely used, ensemble, firm lush, dreamy. I had been trying to sleep on a – although gorgeous Tasmanian Oak – slat bed that until about a year ago kept falling apart, and then my brother fixed it, but the mattress was cheap when I bought it and it was ten years old, which we all know is thirty years old in ME years.

My sister, also from the first camp, bought me a portable reverse-cycle air-conditioner, which has also improved my quality of life immeasurably. This house is like an oven in the sticky Brisbane Summers – or Springs – and like a freezer in Winter – or Autumn since our seasons have now become two. There is nothing worse for us than being so exhausted and unable to sleep because you can not moderate your body temperature.

My lovely Aunty and Uncle, also first campers, have just generously bought me the computer on which I am now typing this, the computer I was using is older than my infection and it is weaker than me. With the combination of my failing cognitive functions, its unreliability and moodiness, just connecting online sometimes was more than my brain could manage.

I have a truckload of siblings, so this may get confusing, but another sister has helped me by giving me financial support to seek treatment that I otherwise could not afford. We've not had much luck from all of it, but to have the chance to seek any treatment is empowering. Then another sister has really kindly donated me her couches, which are beautiful and luxurious and comfortable. I spend almost as much time on the couch as I do in bed, it is like a day bed, covered in pillows and sheets, and before I was on an old and very uncomfortable couch.

Which brings me to my online besties. And had you told me a few years ago I could find best friends online, I would've thought it crazy, but a bond forged through struggle in darkness is stronger than those forged in light. I have found online this whispery spider-web of illness, with each offshoot catching more love and friendship and understanding. And on days when I think I might drown, they are my life guards, without them I would surely sink.

Of my real world friends, which inversely feels sometimes like the alien world, some have simply disappeared into the shadows, but others have stepped forward, stepped up, loved me more. And honestly, I already knew who I could count on, but it makes my heart hurt with the overflow of love that they're still here beside me when it matters most.

And lastly and most importantly, strangers. Strangers are who changed everything for me. Beautiful generous, sweet strangers. I made a friend down the street who is also sick and she is a Mum, and she barely knew me, but she came to see me one day when my body seemed committed to death, and she saw me and decided to fight for me. This makes me cry every time I think about her, she changed everything. She contacted the charity Communify who then committed to get me a cleaner – I had been on the government waiting list for a year – they also got me a second-hand dishwasher through Givit and had it installed at no cost to me. A stranger stood up and fought for me and with just her voice, things changed. My quality of life vastly improved, Communify put a railing on the stairs to give me something to hang onto, they put a grab bar in the bath so I wouldn't fall.

Extraordinarily the second is a stranger, a woman who is also ill, who has a disabled daughter, she and I have been meeting in the waiting room at the doctors for the last decade and she has been able to measure my decline in weekly increments. She brings me medication she finds useful, things I would not be able to afford, she is outrageously generous.

It seems my invisibility cloak is slipping, my corner spot in the wardrobe is growing cold, and the slither of light grows. I cannot wait to throw the door open and step out, and maybe then I can be the voice of a stranger for someone else.