Happy Easter from Melbourne

Sometimes when you have lost all hope, hope is reignited like a flame in the darkness.

I have Missy to thank for that, today. Go check out her post if you are in need of hope, too.

And Missy’s hope was reignited by Sooz, and Melis. Two very special ladies, I agree a million times over. Sooz, no matter how much she herself struggles, has been a constant source of hope and support for me. Melis, oh my internet Big Sis, you amaze me. Missy coined it when she said that your ‘purging can Melis’, because boy did Melis ever kick that bulimia’s ass!

Then there is Greta. Greta, who daily reminds us of the beauty of life – we can become so bogged down in our battles that everything for us seems grey and mundane – Greta brings the life alive from the drudgery. There is never drudgery reading your posts, girl. They are sublime – as you are. I cannot never smile ear to ear, as well as hope to make MY world even a fraction as pretty as you make yours! And my heart as kind.

And Gel. What can I say. Such wisdom, such kindness, such quiet strength and perseverance. Gel, you inspire me day after day. You have taught me so very many things in the time I have had the blessing of knowing you. You are another of these amazing woman who, oh my, has kicked a herd of bulima asses.

I couldn’t forget Zoe. Every single day could be a battle, but Zoe turns every single day into a battle cry. She really does rise again and again like the pheonix rising from the ashes of a lifetime of appalling narcissistic abuse. It has not kept her down, it never will. And she reminds me daily, the abuse I lived through, will never claim my life either. Ever.

Lastly, a shout out to some special, dear, real-life sisters.

My Little Angel Sis, the Stunned Mullet – We fought. Because we love each other dearly. There’s no doubt about that. It’s my biggest fear that this extremely sweet and talented young lady loses her years of fighting like a fricken warrior to despair. I know she won’t let that happen. But sometimes  fear gets the better of me and I refuse to pretend that I think everything is okay. That, with my headstrong little sis, can be dangerous! It is my hope for you, that you can let go of the need for everyone to think you are okay and know that it’s okay to ask for help when needed, and that though you seem to have fallen into the laps of pretty disappointing and shitty professionals up to now, they ain’t all like that. You don’t have to do this alone. At the very least, you have me, silly girl, I love you every step of the way, no matter what. But beware, I don’t hold any punches when it comes to being blatantly honest about how things are from this perspective.

Jen. You are a quiet, loving big sis to me. Sometimes without even knowing. Every day I know you are out there. Every day I think of you and how far you have come. And how much love and kindness you have showered me with. I can’t wait to see you, or your little sis A, again soon.

Anya. You light up my world. Your life is a daily struggle with pain of the kind I can only guess at – and yet you, again and again, amaze me with your hope and your desire to reach out to and light up the lives of others. And all you ask of me, is prayer. I pray for you every day, every single day – and a lot of those prayers are in thankfulness for you, my dear friend. Hope your heart is flying over the waves with your surfing idols this Easter – a treat you more than deserved.

And Kelmonster. You probably don’t even know this blog exists. Because this world isn’t your world, thank God for that. She has given me a window to my disordered, hopeless world, for so many years now. We go way back. Her love for me has known no bounds, as has my love for her. Love has never had conditions, love has always been no matter what. She’s held my hand, and spoon-fed me in my darkest moments. She’s holding my hand and leading me out through that window into the big wide yonder today. She’s shown me a world I could previously only just imagine. It is real, it is worth fighting for. Although where we are, it will be more kicking herds of kangaroos rather than asses. She’s never let me leave my hope behind. Always prodded me to open my eyes and find it, open my heart and accept the love and forgiveness and healing that is mine. And her life is not without it’s battles, in fact, she is constantly overcoming a battle I could never imagine. Top nursing student? That’s hard enough. Top nursing student who just happens to live with Schizophrenia? That’s my girl. Exceedingly rare – she kicks kangaroos every single day. She is the family my family refused to be. And for that, for everything, I love her with all my heart. I know that with her, I will never be alone.

There are some very sore asses around the place. And Kangaroos.

Thank you my beautiful friends for the hope you give me every single day. There are so many more of you who might be reading this, or might not know it exists – nonetheless, I thank you. Life would not have been worth fighting for without you. Life is worth fighting for. And I will never give up fighting for my own future, peace, healing and happiness. I’ve come further than I ever dreamed possible in just a few short years – from death-bed to climbing out the window into the WORLD. And I am deeply, incredibly grateful, to all of you.

Every single one of us is important. Every single one of YOU matters. If you ever doubt that your voice has a place in this world – think of an orchestra. Think of how every single note from every single instrument – no matter how soft and subtle – is so exceedingly vital to the symphony. Without that little ding from the triangle? It’s ruined. Without that bloody loud tuba? It’s ruined. Missing something. The world would be missing something without YOU too. No matter how tiny your whisper is right now (for later, I pray, it will become a rawr!) YOU and your voice is vital to this world as part of the symphony of life – never forget that. We need you here – don’t give up fighting. Hunt down an ass, or a herd of asses, or a kangaroo or two, every single day and kick them from here to bloody Pussycat Flat (it exists!)

Well, today, after a whirlwind few days discovering Victoria – from rescuing a drowning echidna in the beautiful Dandenong mountains

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Above, we scooped him out in a hat – and he hid his snout shyly behind the sharpest-clawed paws I’ve seen!  He now pretends to be part of the dirt and grass, burrowed in stubbornly.

to swimming in rock pools at Portsea and gazing in awe at the twinkling lights of all of Melbourne from the height of Arthurs Seat, and hand feeding tame Rosellas

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Polly wanna sunflower seed?

and finding my new home to be

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Shall I choose this airy shack, with room for many, many cats?

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or perhaps this cosy and warm winter hide-away?

Today I am going to be leaving civilisation behind on our long road trip north to New South Wales – and a camping festival known as ConFest. We will be off the radar to phone signals and internet! And perhaps that’s a good thing. Art and journalling and just relaxing amongst the real world – nature – await. And at night, I’m staying in a million-star hotel. Stuff 5 stars!

So I won’t be around for a while.

I hope you all have a wonderful, hope-filled Easter. Even for those who do not celebrate – there is meaning there to be found, of hope and renewal and that there’s always a light to be found in our darknesses.

Never, ever give up. Kick those kangaroos! Or they will kick you!

I miss Shalimar so much! She is living it up at a Pet Motel, in the lap of luxury with gourmet food (and, incidentially, she’s eating Kangaroo Meat among other things… the irony). It will be lovely to see her snarling, sweet cute whiskery face again soon ;) She’s my love, my life, my light.

Happy Easter and take care, everyone!

Should Mentally Ill People Get To Say Don’t Help Me?

I’ve been discussing this issue with a few people lately, it has come up in the past for myself when I’ve been most unwell. There were times when I begged the people who were treating me to just let me die, because I had tried again and again, fought my hardest, and truly had nothing left to give. I just wanted to be left alone, to be allowed to have some measure of comfort rather than invasive and traumatic treatment.

I felt like they were flogging a dead horse. I really did. And the dead horse was me.

Other reasons this debate has come up include my own being given the chance to sign an advanced health care directive and contribute to my emergency admission plans, and the recent cases in the news of women with Anorexia who have either been court ordered to be fed against their will,  or not fed despite it meaning they would die. (Basically one of the women was given the right to allow her disorder to kill her, and the other was not.)

There are so many grey issues here. How do you decide when someone has crossed that line between their mental illness being treatable, and being ‘terminal’? (Currently I think that in Australia and many countries, it’s illegal to commit suicide, so it’s only when someone is actually terminal that they are allowed to opt for comfort measures over actual treatment). In cases like anorexia or bulimia, I’m sure there would be an actual point where someone was terminally ill – for example if their organs failed, or if they were brain damaged as Terry Schiavo was after a cardiac arrest starved her brain of oxygen. (Terry had bulimia.)

But it’s not so clear cut in every case. Mental illnesses are just that – illnesses of our minds. When someone is ‘terminal’ physically from an eating disorder, it’s due to what the mental illness has put them through. It goes without saying though, that the severity of someone’s mental illness isn’t always echoed by the severity of the physical consequences. I am absolutely sure that the mental anguish that many of us with mental illnesses suffer can go beyond a point where it’s more cruel to force them to live. I have spoken to people who have schizophrenia and are non-compliant with having to take their medications who have told me that the effects of their medication are far worse than just living with the illness, and that they would rather die, or rather be sick and have a non-life than take it. But they don’t have a choice. (Please note, this is not the same for everyone with Schizophrenia just as no other mental illness affects everyone the same way. Someone else might find living with Schizophrenia far too distressing and prefer to at least live with medication side effects and have a chance of a functional life, and other people might not even have the same side effects or to the same degree from the medications.)

The laws vary of course, from place to place. Here where I live, in my state in Australia, you can be placed on an Involuntary Treatment Order (ITO) , which means that you can be given treatment against your will. The criteria to be put on an ITO are:

  •  the person has a mental illness
  • the person’s illness requires immediate treatment
  •  the proposed treatment is available at an authorised mental health service
  • because of the person’s illness:  there is an imminent risk that the person may cause harm to himself or herself or someone else, or the person is likely to suffer serious mental or physical deterioration
  • there is no less restrictive way of ensuring the person receives appropriate treatment for the illness, and the person:  lacks the capacity to consent to be treated for the illness, or has unreasonably refused proposed treatment for the illness. (source) (emphasis mine)

The causing of harm to oneself or to others is probably the biggest factor that gets people put on an ITO – so if someone is suicidal and likely to kill themselves or try, or they are starving to a point of medical danger, or bingeing and purging so much their electrolytes are all over the place, and you refuse treatment or hospitalisation, they’ll ITO you. If you are raving psychotic and hitting out at people or doing something like that, they’ll ITO you. (People with mental illness can become violent, however it’s no more prevalent than with the rest of society. That people who are mentally ill are dangerous is another of those big fat MYTHS that perpetuate stereotypes and get people killed.)

“This is Roni Levi, who was surrounded and shot fatally by police officers -after having a psychotic breakdown at Bondi beach.
His only weapon was a kitchen knife -which he would have had difficulty in using as his clothing was in a dishevelled state with his coat half off -as this picture shows.”

 

I was under an ITO for over 10 years, almost continuously. It was this that allowed the staff at the hospital to force feed me, restrain me, keep me detained, all against my will. And most importantly – keep me alive, despite my begging them to just let me die. Today, even two of my case managers during that time have expressed that they were not, and still are not sure that it was the right thing to do, given the distress I was in and the cruelty of the methods used, but even more the fact that I wasn’t expected to live and there was little hope for me. It did seem especially cruel. For me, it was a living hell that was far worse than the hell of the actual eating disorder, and triggered a lot of abuse stuff for me as well. All to just get me to a point where it was inevitable that I would again end up in the same position, because I was discharged at such a low weight and no actual help for any of the problems behind my behaviours. I truly didn’t have a chance once I became that ill. And for most of those years, I never was NOT that ill.

Today, I have a very different perspective on life. I am glad that I’m alive, most of the time. Living with my eating disorder and the PTSD issues and depression – that’s still hell. But I’m glad I’m alive, because there are so many things that make the bad times worth getting through. Also, being alive means I have a chance of making it. I have a chance of dealing with the issues behind it all and working towards some sort of life, peace, and dare I say it – happiness. If they had allowed me to die, I wouldn’t have those chances. I wouldn’t be here now at all. I couldn’t see that let alone believe in that, back then.

So at what point does someone with a mental illness, or more specifically, an eating disorder, become ‘hopeless’ or ‘terminal’? There are many of us whom the system has given up on us – will not work with us or takes basic measures to keep us alive but not ‘bother’ with anything further. But that doesn’t necessarily mean we don’t have a chance – it more means that the level of frustration of those helping us reached a point where they were no longer willing to ‘waste their time’ on us, when in reality they were wasting their time on trying things that had been proven not to help us rather than wasting it on US specifically.

With someone who doesn’t have an eating disorder but another mental illness that doesn’t actually affect their medical health – how do you even begin to decide where to draw the line with them? I have heard that in Australia it’s becoming accepted for people to have advanced health directives drawn up during their more well times (so legally binding) that specify wishes like no Electroconvulsive Therapy (ECT),  which is often given against the patient’s will when they are on an ITO, for example. But to allow someone to refuse treatment altogether – what about when that directly risks their life if they are suicidal? In the case of a terminal eating disorder, at least the death would come from physical complications. Suicide is an entirely different matter, and it’s also illegal in Australia, as is assisted suicide. (This is a whole separate matter in it’s own right to get into and debate!)

Further, when should anyone’s right to do what they please to their own body be taken away from them? I hate pro-eating disorder communities, and I hate that there are people out there who actually want to have something that’s caused myself and friends so much distress and even killed some of them. But I’m sure the people involved would argue that it’s their body, so they should be able to do what they pleased to it. At what point does self starvation, bingeing, purging, self harm etc  become any worse than possibly life-threatening extreme sports, for example? Personally, I know that while extreme sports would most likely be classed as ‘thrill seeking’, I’m pretty confident that there is little to no thrill in the mental illness produced dangerous behaviour, and that it’s mostly born from desperation and pain and sickness. But still, when do we take someone’s right to choose when to accept help for that sickness away from them and force help onto them?

Personally I don’t think anyone should ever be given up on, but I do think that everyone deserves to have their basic rights respected, mental illness or not. I believe that it needs to be judged on a case-by-case basis and that every endeavour should be made to honour the patient’s wishes.

I also agree with Laura Collins that if someone gets to the point where their eating disorder is terminal, the system has failed them, because the inability to nourish oneself whether through starvation, purging, or whatever is part of the actual illness and needs to be treated, not allowed to take over.

Carrie Fisher makes another point that I fully believe - patients shouldn’t be denied help through ‘non-compliance’. (It’s common to hear of patients being kicked out of treatment programs for this reason.) What is non-compliance but another symptom of the illness? Of course people with anorexia and bulimia are not going to want to gain weight or are going to struggle eating or keeping it down or not exercising. They have an eating disorder. What do they expect? Sheesh.

Basically to me, that means that if people with an eating disorder get the treatment they need and deserve, they will not reach the point of terminal – and that is the way it should be.  Likewise with any mental illness – these are not new conditions! We do have ways of at least helping lessen people’s pain and distress. Adequate support and respect also go a long way to making things that much less awful. NOBODY  should die from a mental illness, particularly in this day and age.

I guess that answers the question for me, sort of anyway – everyone has a right to make basic decisions about their life and their bodies, but if someone with a mental illness gets to the point where they are basically begging to choose to die or go untreated, we need to examine just how we have NOT been helping them adequately.

What do you think? I hope this made sense!

Further reading – I discovered a really interesting page that doesn’t just concentrate on Terri Schiavo’s case, but many issues regarding choice and control over end of life/health http://www.terrisfight.org/

Laura Collin’s blog Are You Eating With Your Anorexic

Carrie Fisher’s blog ED Bites

(Image sources :  1 (adapted),  2, 3, 4)

Reader Appreciation Award and Shalimar Photo Bomb

Diane from Hometogo232 has been a constant source of encouragement and support towards me since we found each other’s blogs. I couldn’t think of a more deserving person to have been awarded a reader appreciation award, so it’s really amazing that she’s chosen me as one of the people to pass it on to.

It means a lot to me, because my readers are part of why I blog. My blog started as a way for me to express myself and air the ‘secrets’ of many kinds that fill my life with so much shame. Eating disorders are such hidden diseases much of the time. Everyone knew I had one, I couldn’t hide that, but my life with it, the realities, are something I hid every single day, put on a face and just pushed on.  This means that a lot of people saw me ‘coping okay’ and decided that I WAS doing this because I wanted to be skinny, because I was vain, because I was a brat, because I was too lazy to get better… pull out any of the many misconceptions  tossed around about people with Eds and it’s been said and thought about me.

The reality was it was a nightmare, still is a nightmare, a life that is agony to live every single day, and for many of those years there were no bright spots to even hang on for, not for me. I don’t know HOW I hung on so long, looking back, I truly don’t. For my cat. Because I’m stubborn. So as to not let ‘them’ win. Many reasons – but I did not wish this on myself or set out to become sick in the first place. It was not a choice. But I now know it’s a choice to fight it and I have been, and now there ARE bright spots in my life that far outshine the everyday nightmare bits.

I blog to share what’s happened to me in my life, all the abuse, because I am no longer going to be shamed or scared silent by that either. I speak up now, because I realise that this shame does not belong with me (and does not belong with anyone out there who has been abused in any way.) It belongs with my abusers. If they are not comfortable with me laying the facts of  their actions towards me out there – well that’s their problem. I owe them nothing. I’m not their punching bag any more and never will be again. I have a voice now and never again will I be silenced. 

Now my readers. When I began, there were no readers. There was just me, and that was fine. But as I found other people’s blogs and found amazing friends in many of them, my readership grew. I now have a lot of hope to share – a few short years ago I had none whatsoever, I was on a fast trajectory to death. Hellish short life, then death. Things have turned around so fast and now I can see what  I just couldn’t see back then. Hope. Growth. Change. That things take time. And that we need to trust and believe in ourselves and in our progress, especially when we feel we are getting nowhere.

You don’t spend most of your life battling an eating disorder at a life threatening level without learning a lot about the nature of the beast – and meeting a heck of a lot of people who are going through the same thing. I have seen so many people falling through the cracks – missing out on support, on treatment, on understanding, even on tolerance and acceptance in society. Because there are so many fallacies flying around, and so little understanding in the community.

I’ve been told to eat a sandwich when I was admitted for early stage heart failure. Restrained to a bed because I was not to be trusted, and locked in a room with none of my belongings because the people treating me decided my eating disorder was a spoilt brat thing and that punishment would cure me. (It didn’t. It made me sicker as I started to forget there was a real world out there and the walls closed in on me.) I have been spat on, on a well-to-do shopping street for being too disgustingly thin and making myself into some sort of  ’creature’. Punched in the face for not giving a lady my bag of groceries one day because “There was no way I could possibly eat those and I was wasting food that poor people (meaning, she and her drug-addled friends who had blown all their money on heroin) badly needed more than I did.”

All this, and so much more that has happened through these long years of fighting, is not acceptable. Should never happen to anyone. And yet it does. I’m not the only one by far. I don’t want anyone else to go through that.

But even more, I want others to read my words and realise that they do have hope, that they can hang on, that it’s worthwhile. That it IS possible to turn a corner when you feel there is no way out. That it IS possible to recover no matter how hopeless a ‘case’ you feel you are. That they DO have the courage to fight for their lives, because they already have that courage and strength right there within them, they need to believe in themselves, believe it’s possible. And that life is so worth it. That THEY are worth fighting for. Because that’s the truth.

And so to be nominated for a Readers Appreciation Award fills me with happiness because it means that there must be something I’m doing that’s working. Thank you so much, Diane.

Here’s what I have to do!

The steps to take, preferably with joy

1. Include the award logo somewhere in your blog.
2. Answer these 10 questions, below, for fun if you want to.
3. Nominate 10 to 12 blogs you enjoy. Or you pick the number.
4. Pay the love forward: Provide your nominee’s link in your post and comment on their blog to let them know they’ve been included and invited to participate.
5. Pay the love back with gratitude and a link to the blogger(s) who nominated you.

The Questions: Note I have answered some of these questions previously so if I have, I will give you an alternate answer.

1. What is your favorite colour?

Every colour in the rainbow.

2. What is your favorite animal?

Cats – namely my cat Shalimar.

3. What is your favorite non-alcoholic drink?

I drink more tea than anything else – white tea, with lots of (I know, I know, bad stuff) Equal sweetener.  I crave fresh juice – both fruit and veggie – a lot. But I don’t really like to drink or find it easy – it’s a constant struggle, especially as I used to have a huge phobia of even water. I’m working on it :)

4. Do you prefer Facebook or Twitter?

Facebook, I have never really used Twitter. I love that I can keep in touch with my friends but also tend to find it  very superficial.

5. What is your favorite pattern?

I love the patterns that the clouds make in the sky!

6. Do you prefer giving or getting presents?

Giving, by far. But I squirm in embarrassment and wish that I could hide. My favourite way to give gifts would be for them to just appear out of nowhere and surprise the recipient!

7. What is your favorite number?

My lucky number is 13. Amazing things have happened to me related to 13 – the date, the address, etc. My least favourite is 4, partly because I believe it means death for the Chinese, but mostly because the OCD-ritualistic crap that happened with food and eating (and still does to a far lesser degree) usually involves a lot of fours.

8. What is your favorite day of the week?

Friday, because I have an entire weekend right ahead of me!!! Sleep in tomorrow!

9. What is your favorite flower?

I had a huge daisy bush that I grew as a child, but it’s too hard as an adult to choose just one. I love honeysuckle for their smell and some memories, and I love nasturtium for the same reason (and am currently growing them in my garden.)

10. What’s your passion?

My passion is life, my cat, people, God and His amazing world. I used to be passionate about dancing, still am a dancer on the inside, hope to be one on the outside again in the future (for my own love of it, not as a career like it was, once).

The Nominees  Some (or all) of these writers may choose to not participate in this award process but I still want this chance to help you to find these blogs and perhaps be inspired by what they contain, if you haven’t found them already. Since I have been through the process recently I will choose 5 to nominate.

I enjoy so much reading these inspirational  blogs and in turn I receive many encouraging words from them.

Emma at http://doesmybumlookbiginthis.org

Buckwheat at http://buckwheatsrisk.wordpress.com

Cathy at http://extralongtail.wordpress.com/

Kath at http://kathsfunnylittlelife.wordpress.com/

Roxy at http://adverseuniverse.wordpress.com/

Sooz at http://mundanebrain.wordpress.com/

There are so many people I would love to include! Thank you to everyone for encouraging me and for reaching out to me, a complete stranger.

Now for a light-hearted ending to this post – Shalimar always manages to inject hilarity into my life. My money is controlled by a Government appointed Trustee (still hanging round from the sicker days, hopefully I’ll get off this soon) and today I was taking photos of my backpack to show them that I really do need to buy a new one, will they let me have my money? (Getting your money can be like trying to get blood from a stone!)

Shalimar totally photobombed my photo. Sneaky, cheeky little darling :)

Don’t Give Up Hope.

 

The most important message I wanted to convey in last night’s post about turning points was that often when we feel stuck and hopeless, we actually aren’t as hopeless as we feel.

For YEARS I felt that I was getting nowhere. That I had fought so hard, and had nothing to show for it. That I went round and round and round in the same frustrating, stupid cycle. And for that, I decided I was a loser. That I’d never be able to do anything worthwhile. That I’d live my life fighting ED and then die from it.

I was so lucky that the people in my life didn’t give up on me, even when I gave up on myself. I was so tired, so discouraged. I would argue with them – I have tried everything that I can, fought my hardest, and it’s always had the same result. I’ve always ended up back here. They say that doing the same thing again and again despite always getting the same result is insanity. I begged them to just let me die. I said that they would put a dog down before allowing it to suffer this much. And yet they didn’t give up.

Today I am so glad for that. So grateful.

Because despite my belief that I was getting nowhere, I actually was making progress. Perhaps those who didn’t give up on me had more faith in me than I did, but I don’t think they saw this either. Invisible to myself, to others, there was a lot happening – I was learning, growing, storing away so much for use later on. Perhaps each twist and turn gave me another puzzle piece to keep for later, when I might have gathered enough to actually begin to put them together. What I do know was that finally I reached a point where enough had changed under the surface for my life to begin changing, and my mind to begin changing in very visible ways – and then in leaps and bounds! And it was truly an amazing thing to experience.

When you plant a seed in the ground, it doesn’t immediately spring up into leaf and flower above the ground. Instead it’s feeling around down there in the darkness, shooting out roots, finding the best sources of nutrients and water, spreading out, making sure it’s anchored firmly – before it emerges from the surface and begins to unfurl towards the sky and the sunshine!

When you least have hope, when you feel most stuck – think of that little seed. That’s YOU. 

There is always hope. 

 

Turning Points?

thereisalwayshope

People often ask me, after years of being so sick, and so stuck – to the point where I wasn’t expected to survive and my treatment team only really kept me alive to legally cover themselves, admitting me only on death’s door – how did things change for me? Why did I suddenly go from hopeless to so full of hope?

In many ways it seems a very sudden development, but it’s not. I think all of us face turning points in our lives, points where we simply cannot continue on as we have been. Wiktionary defines turning point as  ”A decisive point at which a significant change or historical event occurs, or at which a decision must be made.”  Both are true for myself, in my journey.

When I look back at this seemingly ‘sudden’ turnaround, it’s not that sudden at all. I can see that I was growing and changing in ways that were not then visible – even to myself – that came together in the end to enable change to be made outwardly. During the times that much of this growth was occurring, I was depressed and felt hopeless, I felt that I had tried, and tried, and tried, and nothing had worked, that I had nothing left to give and would be better off dead. That I had been fighting endlessly and had gotten nowhere. I had no idea I was already on the road to improving. I wonder if I had known, I would have had more hope? I’ll never know. The important thing was that little things were changing.

I was learning how to cope better with the things that I didn’t cope with before – with flashbacks, nightmares, emotions. I was learning to be more accepting of myself – I was learning more ABOUT myself – and I was learning that it’s okay to fall down. I fell down big time, and many times, over those years and most of the time I needed a LOT of help to get back up again. My pride took a huge battering. I lost every shred of dignity, was completely humbled, and now that I look back at that, I see that although it was not a nice thing to go through at all, it helped me. When you have humbled yourself and being able to say, “Yes, I suck right now, I’m a failure, and I need your help” and reach out and accept the help offered – you truly cannot fall any lower. The only way from there can be up. And sometimes it’s important for us to reach this point so we can get over ourselves and be forced to see ourselves in all our brokenness – in order to get past the denial that can prevent us from ever otherwise accepting the help we need.

I am Christian. I will not pretend that I am not. I usually don’t talk much about it, because I feel very ‘new’ to it, and am scared of putting my foot in it big time by saying something that turns out to be the wrong thing. A lot of my Bible reading occurred during my sickest period and so a lot of the facts went through my cottage cheese brain and promptly vanished, so I also find myself stumbling when it comes to quoting, referring to the Scripture, to remembering important points…  I also have been worried that sometimes people who do NOT believe are offended, and I don’t want to alienate anyone. I am a live and let live person. My beliefs are mine, and I have them because of things that have occurred in my life and how and what I feel. Other people come by their beliefs in a similar way. Also none of us has a right to say “My beliefs are right, and yours are not” because none of us can ever know that for sure, and it’s arrogant to assume our beliefs are right or better than someone else’s.

Where this is leading is that my faith did play a big part in my being here today –  although I hate it when I’m reading a book where someone recovers, whether it’s from an eating disorder or something else, and they just say “God cured me”. I hate it. Because it doesn’t just happen like that. I do believe in miracles, yes, but miracles usually have a lot of work involved in making them happen – they are miracles because they should not have happened, should have been impossible, were against the odds. But they didn’t just happen. People have said that my own turning things around is a miracle, because I should be dead, there wasn’t hope for me and my body was on it’s last legs – but I know it’s not, I know how much hard work and time and tears and perseverance  has gone into getting this far.

I have always been a very spiritual person. I did go through a very dark period where I lost all faith in there being any thing called God out there, and I lost all hope. I defined hope as being something that you can only have if you know for sure that what you hope for (life, feeling better, etc) CAN happen – and I did not. I couldn’t fathom that anything could get better for me, and therefore I had no hope. As for God, I felt totally alone. If He existed, I surmised, He had long turned His face from me in disgust.

But I did strongly feel, within myself, something bigger and more powerful out there. Some kind of energy, or spirit. Something great. Something benevolent, caring.. I could feel that. When my Dad was dying for example, I went up there to his city full of anger and despair, raging at the world – “how could you take my Dad? How could you give him cancer? How could you make him suffer so much, he’s a good man?” But when I got there and was by his side and he was dying, I felt deep down that this was as it was meant to be. I will never be able to describe what I felt in words really – but I could almost feel something like ‘gears’ grinding – could almost feel that all life goes in cycles, and that my Dad’s was grinding to an end – and then, after he died, I could feel him continue on a new cycle, where, I do not know. But I felt all that. It didn’t make it less painful, but it did feel like this was meant to happen and part of life, my Dad’s time was here to go. I’ve always been very connected to nature and I can’t not feel that there is something far greater under all we can see on the surface and that essentially it is filled with LIFE.

Back to God – one day, I just happened to come out of a session with a case manager and walk into the church across the road, into a mid week service that I’d passed by for years and never felt tempted to join. I still do not know why I walked in that day. But what I do know, is that it was one of the turning points in my life that I can definitely identify, even though nothing earth shattering happened that day. What was important was the people I met there.

I was greeted and welcomed by a lovely lady and a just as lovely girl closer to my age who became dear friends. They made me feel worthy of being there, and it did feel like I’d joined their ‘family’. I came to look forward to my wednesdays spent with the kindest people I know, that church group, and started spending more and more time with them – they did become my own family for a while. They accepted me, no questions asked. Totally unconditionally. There was no sense of  ”When you have gotten better, gained weight, fixed up your problems, then we will accept you.” It was NOW. Despite all, despite the fact that I was an emaciated, bingeing, anxious, shy MESS – they loved me despite that. They loved me for ME. No matter where I was in my journey, they would meet me there and walk by my side during anything and everything it took to get through it all.

This was probably the most important thing of all for me, certainly at this stage of my life, but probably in my whole life. Who of us does not need to know they are okay? I struggled for a long time to understand how they could so easily like me, even love me as they came to. I could love them, because they were such lovely people. I came to be able to trust in God, that He existed, because I could see every quality that describes God in these people – shining from their eyes, their actions, their words, their hearts. They lived their faiths – and passed it on to me in a very real way I could no longer ignore or doubt.

Being unconditionally loved and accepted meant that I began to realise that there must be something in me, horrible little Fiona – that was loveable and acceptable. It was a huge enlightening for me. I have grown up always feeling completely inferior to the rest of the whole world – and had that pretty much beaten into me as a child – that I was not good enough, that I was even quite disgusting. So for the first time, I decided that it was time to give this girl a chance, to stop just hating for the sake of hating, and get to know her – get to know myself – really and truly. And I also came to realise how little I knew myself. I was a stranger to myself. No wonder I had been trying to kill myself for all these years – being trapped in a stranger’s hated body, what else would someone do?

And so things began to change. My hatred of myself and my self destruction started to lessen. I still found myself overwhelmed with self loathing, but I was kinder – I started seeing a Christian counsellor and learnt how to refute the lies that flew at me thick and fast with simple truths, and to believe those simple truths more and more. I learnt to arm myself with the truth -

 Finally, my brethren, be strong in the Lord, and in the power of his might. (11) Put on the whole armor of God, that ye may be able to stand against the wiles of the devil. (12) For we wrestle not against flesh and blood, but against principalities, against powers, against the rulers of the darkness of this world, against spiritual wickedness in high places. (13) Wherefore take unto you the whole armor of God, that ye may be able to withstand in the evil day, and having done all, to stand. (14) Stand therefore, having your loins girt about with truth, and having on the breastplate of righteousness; (15) And your feet shod with the preparation of the gospel of peace; (16) Above all, taking the shield of faith, wherewith ye shall be able to quench all the fiery darts of the wicked. (17) And take the helmet of salvation, and the sword of the Spirit, which is the word of God: (18) Praying always with all prayer and supplication in the Spirit, and watching thereunto with all perseverance and supplication for all saints;”Ephesians 6: 10-18 NIV

And I learnt that God loved me – every hair of my head, He knew and loved me – despite my sins – and He had never turned from me – indeed He had found a way to reach me despite ME turning from Him. How arrogant was I, to hate someone who HE loved?

Slowly my behaviours started to lessen in their rigidity and I began to have the courage to change in tiny ways. I began eating tiny bits with my friends at the meal we all shared at Church (before this I had just sat with them). I graduated to taking frozen dinners to my counselling sessions, heating them in the microwave there, and eating them before my sessions. I started to trust people more, and learnt about having stronger boundaries – a really useful tool to discourage all those horrible jerks who seem to prey on the vulnerable. (My counsellor called my new attitude my ‘F*ck Off Body Language haha). I spent less time hiding in my home, and more time going to coffee and church and outings.  I started making more friends outside of the church too. One thing always led to another in a very natural way.  I blossomed.

None of this was enough to save me – I had several more hospital admissions and was the sickest I had been – several admissions involved receiving TPN to save my life. But the seed had been planted, and under the surface, things were growing. In hospital, I was more open to talking with the staff, and had some amazing discussions with nurses that I’d previously not gotten on with, even feared, when they discovered I was Christian. For the first time I wanted to live. I was also prepared to reach out and accept the help. I didn’t close my mind off to it and scream and fight them, I tried my best to accept it and do what I needed to do – to cooperate – and that was hard, because the ED in me still fought like the demon I likened it to. I did not feel in control of myself when I turned into a ‘girl from exorcist’ like creature, hissing and screaming and throwing things, worse a lot of the time as it was cornered. Because I was actively fighting it more than I ever had. I was no longer content to just lie there and let it win.

Out of hospital, I was more honest with my treatment team, and I talked more with them. I engaged more in therapy. Learnt more about how to change my mindset, learnt mindfulness techniques, and started to be able to have my own brand of acceptance – accepting that I hurt, that I hated my body, that horrible things had been done to me, and so much more. Accepting all this – and then moving on. Not letting it hold me frozen like it did before. Feeling the hurt and shame and grief and fear – but not letting it kill me any more.

The hardest thing to accept was that my family hated me. The basic thing most of us human beings crave is to be loved and accepted and you would think that your own family who have known you from birth would be the most likely people to love you – but admitting to myself that they were not capable of loving me, and had never even really bothered to get to know me in all the years I lived with them – was an important step for me. I had to stop trying to foster a relationship with them, in particular my mother, and so stop putting myself constantly in harm’s way to get hurt again and again by them. I did more than this – I walked away. Cut them off totally – No Contact, as it’s called in many circles of survivors of narcissistic and sociopathic abusers.

I finally reached a point where I had enough belief that there was a lot worth living for to ask my treatment team to help me gain weight. I’m sure this was a complete shock to them – as before this, I had spent years fighting their attempts to force weight on me and losing it almost as soon as discharged, meaning they had to go through the forcing process all over again. (I racked up more than 150 hospital admissions in nearly 15 years, mostly for weight gain or  medical admissions due to being so sick from the anorexia and bulimia). Not only did I this time ask for the weight gain, I asked to go further. They had for years had a discharge weight for me set at BMI 13.9-14, and I was asking them to go a whole 5 kg above that to BMI 15. Still nowhere near enough, but for me that was a huge fear that I was willingly facing. At first they did not believe me – and refused. But I convinced them, and it happened. It was NOT easy. I had to ‘eat’ the weight on and for years I’d put it on through nasogastric and/or TPN – so it was awful. My body was in very poor health and it seemed like everything that could go wrong, went wrong. I felt constantly humiliated there in the hospital, and had to face up to that and keep on despite knowing that being ‘voluntary’ this time around I could leave any time I wanted to. I pushed on. It took two admissions, but I did it, and I’ve maintained that weight gain ever since. The first time in years that I didn’t immediately drop a huge amount in the first week of being home.

I still have a long way to go. I have much  more weight I need to put on. I still struggle with both restricting and bingeing and purging. I still have a tendency to over exercise despite the pain my body gives me. I’m slowly changing and making small gains in these behaviours over time. I’ve also had more positive changes in my life in recent times than in years and years altogether. I’ve moved to a lovely new place. I have a garden, and actively garden it. My cat Shalimar is happier, because I’m not as sick and I play with her more. I go out with friends more, now, to restaurants, for coffee, to the beach, the pool, other outings. I have done an art workshop and am about to start another one that goes a few months ending in an exhibition. I’ve completed a course of hydrotherapy and am halfway through the back pain group course. I’ve been doing well at physiotherapy and have much better posture, less pain, more strength, and am soon to start ballet again after never believing it could be possible again.  I’ve faced my fear of transport, public places, and now I go out all the time on my own. I’ve put strategies in place that have helped me stay shoplifting free for this entire period in 2012 so far.  And I’ve been working with an agency and am close to having my first paid job, as a library assistant. How cool is that!

I also have faith that there is much more to come, and that despite struggling constantly with bouts of depression, fatigue and pain, and the CPTSD, I’m learning to live despite that – and realising that life can be quite liveable for me, despite everything. It’s worth it, and I’m finally, slowly, coming to believe that I’m worth it, too.

Have you had any turning points in your life? How did they help or hinder you? 

 

(image credit)