Honesty Amidst Setbacks

I find it incredibly difficult to be completely honest about how I’m really going. Especially on such a public forum as this blog.

There are perhaps a couple of people I’m always totally honest with – and that is because they are part of my treatment team. Being honest with them is obvious to me. They can’t help  me unless they know what’s happening! Scarily enough there are many people with eating disorders who cannot be honest with their treatment team – in fact, it seems to be very common in the earlier stages of being so unwell, or when the person is lacking in insight. Insight makes a huge difference in this fight – being able to understand that you are unwell, and why, and that the people around you are trying to help you, not persecute you.

It’s quite obvious in the blog world, actually, to come across people who blog about their supposedly ‘healthy lives’, but don’t have the insight to acknowledge the elephant in the room, their eating disorder – and the fact that they are becoming more and more unwell and more people every day are speaking out in concern for them. I can never understand some of these people when they so blatantly ignore the concern and pretend they are fine, or worse, they are well - and it’s often hard to find respect for them. There are so many people, especially younger and more vulnerable people – who read these sites and take on board the messages these sick bloggers are putting out there. If there is one thing I would absolutely loathe myself for, it would be inadvertently causing or triggering someone else’s eating disorder.

But despite it being so easy for me to stand in judgement – we often forget that eating disorders are by nature, an illness in where the person suffering from it often lacks that insight or is in heavy denial. That they often act in ways that infuriate, irritate, frustrate, people around them. That deceit is a classic behavior  born of shame and fear and the need to hang on to their disorder. Being sick doesn’t make someone bad. I’ve lost count of the times I’ve been thought of and told that I was a bad person, because I was too unwell to just eat and keep it down and behave. And I would have done anything at those times to ‘behave’ so that I could stop hurting, worrying or frustrating people – I tried with all my heart to do that. It wasn’t something I was capable of doing at that stage.

One of the main reasons I find it so difficult to be honest with people about how I’m really going, is deep shame. Long before I had the foggiest notion that I actually had an eating disorder, I saw people with anorexia on current affairs shows on TV and just was heartbroken for them, and frightened for them that they were so fragile and that they would die – and I couldn’t understand at all why they were doing that to themselves. It shocked me to think they had actually chosen to do that to themselves and then to continue to do so in the face of imminent death and the pleas of their loved ones. I just could not get my head around it.  I thought they were also incredibly vain, to be killing themselves to just be skinny – I didn’t even see the appeal of being skinny. All my life, I had found skinny quite ugly. Instead, I strived to be strong, and to be able to dance. I was extremely proud of being able to dance at the level that I had gotten to, and at what my body could do. Even as a young child, It had been obvious to me that the worst dancers in my class were the skinny girls, who just couldn’t get anything right and always looked gangly and out of place. Conversely, the biggest girl was also the best dancer and always front and centre. She was bouncy and full of energy and personality.

And I have to admit – I thought they were brats. Sick, scared, lost, hurting brats, but brats nonetheless. I thought they were selfish. I thought they were manipulating everyone who cared for them in order to get attention and mollycoddling. I truly did.

So when I finally had to admit just after my first hospital admission for anorexia (spent protesting that I had needed to lose the weight and that I wasn’t at all like the ‘real anorexics’) that I had anorexia too, it brought incredible shame and disbelief down on me. I couldn’t believe I had an eating disorder. I who had been overcome with fury when other class mates had whispered “That’s what Fiona has” during a biology class discussion about anorexia, who had disgustedly retorted “that’s what spoilt vain brats do, and I would never do something that stupid” had indeed, done exactly that. Talk about irony!

Now I know better. I know that’s not true at all. I’ve never wanted the attention having an eating disorder has brought me. And I didn’t have anyone to mollycoddle me – my family has never cared. My dad, when he tracked me down a few years into my hospital admissions, tried his best, even offered initially for me to move in with them in the Far North – but I was too scared to, at that stage he was a complete stranger to me. And I didn’t want to impose on him and his family. I didn’t want to bring my problems into their world, they didn’t deserve that. He persevered with me – and I stayed with him a week or two here and there over the eight years I knew him – it was such a blessing and a privilege to be given a second chance at having a real family. I loved my stays with them – I was made welcome, treated with kindness and respect, and my little sister was always all over me which warmed my heart – I loved her dearly. (Still do.)

Unfortunately, despite wanting more than anything else to be able to just ‘stop’ being unwell when I was with them, I couldn’t. I tried so hard! I usually lasted at best a few days. In those years, I wasn’t even really able to eat ‘normal’ food, so great was my fear, so I usually had my own food and created meals to eat with them, mostly dinner meals. I tried to make these meals look large and as close to ‘normal’ as I could – hoping that my family would just think I had other preferences and was feeding myself satisfactorily and not worry or be sad that I couldn’t enjoy some of their delicious meals. I wanted them to believe I was happy. I didn’t want them to worry at all. I failed.

A huge pile of lettuce, tomatoes, cucumber, and a million carrots (nibbled mostly during the evenings when I just badly wanted to EAT everything in sight) does not look like a good nutritious meal to anyone. Neither does a pile of brown, terribly overcooked cabbage. I only fooled myself. It was plainly apparent to anyone that I was sick, and even when I wasn’t staying with them, my dad worried. He would phone me (in the days I was still trying to communicate via phone) and ask me how I was doing, and I’d tell him I was going okay, hanging in there. Unfortunately he could tell just by my voice that I wasn’t well at all, he later told me, and instead reached out to someone he thought was a friend of mine – who had given him her details at a time he’d visited me in hospital and she had been there. She wasn’t a friend – I thought she was too for a while, she turned out to be an enemy – she fed my dad the nastiest of lies – told him my eating disorder was to hurt him, to ‘get back at him’ for not being around when I was younger. That it was for attention. That I was dying, when I was very sick but definitely not on my death bed (she also tried to force me to make a will once visiting me – and got promptly kicked out, who does that?!) She also contacted my sister, who was in her very early teens at the time, perhaps even a tween still at that stage – this forty-something year old (really)parent’s basement-dwelling woman, friended a kid. And fed her lies about me too. Told her that if I loved her, really loved her, I wouldn’t be doing this to myself, and that my dad died of cancer – melanoma – because of the stress I had caused him.

I have deeply regretted that I wasn’t honest with my dad about how I was really going, no matter how unwell I was. If I was honest, he wouldn’t have felt the need to ask someone else how I really was, and he might never have been fed such a pack of lies that probably coloured his views of his own daughter, nor would my little sister have been fed the lies that led to her gradually hating me more and more until the last straw was me actually doing something deplorable – shoplifting binge food and getting caught on the morning of dad’s funeral – for which she cannot forgive me. She hates my guts now. What’s more, I just reinforced the lies by what I did. Shoplifting is the thing I hate perhaps most about me. I haven’t done it for a while now – but I haven’t let my guard down and I never will. There have been so many times in my life that I have stopped, for years sometimes – and then fallen down that hole again. The urge to grab food is always, always so strong, even more so when I’m upset, stressed, unwell and definitely, hungry. And the bingeing and purging is the most horrible thing ever, I wish with all my heart I’d never started down that road, a road I feel unable to break free from now. I would never have struggled as much as I have, and I would never have shoplifted food – something so, so wrong to me.

I fear judgement so much. All my life, I have been harshly judged, by my own family, and by society. My own family (apart from dad) never made any attempts to understand me. When I got out of there  they didn’t know me. They had had nearly 17 years living with me from my birth to get to know me – and they didn’t have a clue. This was because they simply did not care.

Everything in my life was something I was judged for. My mother spent my life berating me for all the good things she did do for me – telling me endlessly that if only she didn’t ‘have’ to take me to ballet, the car wouldn’t be wearing out, she’d have more money for other things, she would have more time to spend with my brother and sister. She would have been able to finish her studies and be working now. She would have been a successful artist. She would have fixed our filthy, unfinished house up.  It didn’t matter that she took me to ballet perhaps 3 times a week, which took about 2 – 3 hours at a time tops. That is not the lions’ share of the week. She had all day that we were at school to be an artist, to do her schoolwork, to clean up or fix things and so on – and she instead would sit around watching soapies on TV or working on the growing pile of receipts she kept to create another bill to send our dad of money she wanted to demand from him. She spent all day with my older sister who was home all day too, they were like best girlfriends rather than  mother and daughter. She had time to take my brother to soccer and martial arts and basketball. They weren’t starving for attention or time with her.

The last couple of years I lived there she didn’t even have to take me to ballet or pay a cent for me aside from absolute basics – food and clothing. My ballet was paid for by scholarships and sponsorships I’d won, and I got myself there using public transport. My days were long – a school day for me was up at 5am, chores, breakfast, cold bath, try to iron dry damp clothes I had to wear. Catch bus at 5.55am. Transfer to train, for nearly an hour. Transfer to another bus to school. We started dancing at 8am with Limber, followed by usually ballet class, then jazz or tap or repertoire or pointe or contemporary or something else afterwards. I danced during the class breaks, and danced afterwards til everyone had showered so that I was in there mostly alone to avoid the bullying that was happening all those years. Showered and caught our bus to school to begin academic work at about 2pm, going through til 4.30pm. Then reversing the transport home, at 6.30pm where there were more chores, homework, and endless family battles to navigate. I would practice most nights and end up either lying in bed all night exercising or falling asleep at about 3am at my desk, to repeat the next day. This was six days a week, there was no time for me to get a job and between the ages of 14 to 16, I was still extremely immature and probably wouldn’t have been able to find anyone to employ me anyway. (I did try – volunteering during my holidays and canvassing local businesses for work with my resume.) My mother, who was paid a single parent pension, an allowance for me for my disabilities, and maintenance from dad – refused to supply most basics for me aside from food – and very cheap food at that, usually buying food for the family and cheaper food just for me. She even refused to buy me a school uniform, and the school supplied me with one out of their spares cupboard, kept for accidents, four sizes too big and stained. One of my school teachers helped me tape the fronts of my shoes together and paint over the tape so they stayed on my feet. I also tried to keep my shoes together by nailing nails into the sole from the inside – and ended up walking painfully on them all day as they worked themselves upwards. (And I was grateful – it was a uniform, just like everyone else had.)

My point is, my mother was not only needlessly cruel, she seemed to blame everything on me. I was just a kid, and one who had been tightly controlled too, so that I was very emotionally immature, and she was my mother. My PARENT, who was meant to feed me, clothe me, look after me. Instead, she taught me that I was some horrible, unworthy and inherently wrong creature not worthy of what other people took for granted, and the bullying I suffered due partly to  my constant scruffiness (especially during ballet school where most of the others were from affluent backgrounds) and partly due to my ineptness socially, just reinforced this. I grew up deeply ashamed of myself as a person in every way.

My own family never cared enough to really find out who Fiona was, and they made it clear I wasn’t even worthy of being understood or accepted,  and so they certainly didn’t even try to learn about or understand eating disorders. They believed every stereotype there was – to them, my eating disorder was a sign of me being the spoilt naughty selfish girl they’d always told me I was. In later years they accused me of using a ‘made up illness’ to basically be a lazy bludger, never working, never achieving anything but sponging off the taxpayer, and this stung deeply. They of all people, knew how hard a worker I was, and how I surpassed all expectations, winning a local Australia day award among other acknowledgements for my striving and perseverance. They used their words and their cruelty to basically ally themselves with the eating disorder and strip me of the last vestiges of self – invalidating my past, and stripping me of even being able to hang on to knowing I was a hard worker and an achieve who was capable of better things than this, or that it wasn’t laziness that had stopped me in my tracks. That my whole life hadn’t all been a complete failure.

It makes sense to me that if your own family judges you so harshly, what can you expect from people who don’t know you? I went straight from leaving home into the arms of the man who raped and stalked me for years. It was a very familiar situation for me – and it felt like all I deserved. I’ve met quite a number of people who were more than happy to feed my insecurities like the so-called ‘friend’ who lied to my dad and little sister, and a certain number of ignorant people who don’t seem to realize that not everyone is born with the privileges they take for granted, that some of us have to really fight to even survive let alone enjoy the milestones that they are assured of achieving. In my own heart, I feel like the biggest failure ever, I reflect on my life and see missed opportunities, on so much hard work thrown away, and so much support and belief from people I failed in some way – let down, failed to meet their expectations, or cut off. I feel as though at 35, I haven’t even achieved as much as most teenagers have, and that there is no way I will ever be able to catch up to them, let alone those of my own age group.

I’m just so deeply ashamed.

I’m reminded constantly by those who have taken the time to get to know me, and who genuinely care, that I have come a long way, that I can’t afford to compare myself with anyone else, because nobody else has had to fight the same things I have in my life – same as there are so many people out there who have faced circumstances I have no idea of and for me to judge them on their face value at any point of time that I come in contact with them would be so wrong, and totally belittling how much they HAVE achieved – just in a life completely different and therefore with different milestones and measures of progress to mine. And yet, I am so scared of others judging me harshly and finding me a failure, a loser, that I judge myself the most harshly of all.

And here is where honesty comes into the equation – I’m already ashamed of the fact that I have an eating disorder. My shame when I am struggling more than usual or I relapse is many times greater than that. Throw in the harsh judgement towards people with eating disorders that I often come across online, particularly if they blog about it, and the shame of having fallen from my position of being able to say “Here I am, I am proof that a chronic severe eating disorder doesn’t have to kill you or mean you can’t turn things around.” and most importantly of all – “There is hope” – and it’s extremely hard to face up to people and be honest with you all about the fact that I’m not doing all that well any more.

I don’t consider myself to be fully in relapse – but I’m borderline. I’ve slowed down, perhaps stopped the weight loss, but I can’t seem to get it to go back up again – and what’s more, am sitting just above what used to be my discharge weight from hospital back when times were bad. And as always, ED brain has taken over – I struggle to keep hydrated, struggle to eat, struggle with bingeing and purging. Physically I have lost a lot of strength and the chronic pain I worked so hard to rid myself of is plaguing me again. And I’m so angry at myself – I know how hard I worked to get where I was – and now, I’m no better than I was on leaving hospital during those bad  years again. I am so disappointed in myself, and so scared not only for myself, but more so, for Shalimar. What if I get so sick again, what will become of her? I don’t want to send her back to the pet motel all the time – she’s getting old now. She deserves so much better than this. And I don’t want to miss out on sharing a single moment of her life with her. I missed too much of her life when I was in hospital. I’ve let her down, most of all. She depended on me and I am not living up to those responsibilities.

And I’ve let you down, the people who read my blog. It was supposed to be a journey of hope, reclaiming a LIFE, of proving that just because everyone has expected you to die, doesn’t mean you have to.

Here is where I am going to take on board my own message. I am going to believe in hope, and I am going to remind myself that it is always within our power to change our behaviors and our thoughts, if we desire to enough. The more I walk on my chosen trail in a forest, the more worn and visible that trail becomes, and the less visible the trail I’m no longer walking on becomes as nature reclaims it and grows over where it used to be. Same with my mind – the more I practice new ways to think and new behaviors, the more natural they become to me, and the less natural the old ones will be, too. It’s called creating new neural pathways. It’s also called not giving up, being stubborn, and fighting to live – all things true of me.

I have so much to live for – even more now. I have less than two months to go until I am officially a uni student again. And I’m finally realizing that my hopes and dreams and goals these days  might be vastly different, but they are still things I’m able to be passionate about, and my life still can be for good, rather than have been pointless.

I’m not going to live up to the expectations of the people who taught me I would never be anything more than a loser.

I’m going to fulfil my own expectations – and those of the people who truly care and want the best for me. I’m going to fight and make this life truly count.

Thank you for reading, I hope to be able to bring a more positive post next time.

 

(Image sources: 1, 2)

Eating Disorders Make You Broke And Lonely

Hi! Oh boy have I missed the internet! I was forced offline for about a week, and it was hard – pulling your own teeth out hard! A mix of things being financially tight and even more than that, the fact that I’m still under the guardianship of a public trustee, meant that it’s been a long 6 month process (more like all out war) in order to be able to finally purchase decent plans to use both internet and mobile phone.

One of the long term side effects of living with an eating disorder is very often financial problems. For me, it’s meant I’ve been unable to have a paid job (so far) and living on a disability pension. I’m very thankful for that – but as most people will say, it’s already quite a pinch.

Add in an eating disorder and things can be disastrous.

Thankfully, as far as I can remember, I never defaulted on rent or bills, or paid them late. But things got more and more difficult as I was hospitalised so much. Back in ‘those days’ – the pre-millenium years – we didn’t have automated bill paying or money transferring services like BPay, Centrelink etc. Every week or fortnight, I made a trip to my bank to take money from my account, then a trip to the bank of my landlord, or the post office, or the real estate agent or leasing office to pay my rent in person. I paid my electricity bills and phone bills over the counter at the post office. Same for other bills and expenses that popped up here and there – you couldn’t jump online and electronically transfer the funds without leaving your home. You had to go out and do it in person.

You can’t do that when you are always in hospital! So it did get quite tricky, and  I was worried. My accomodation was boarding houses and hostels mostly at that stage – and it doesn’t take much to lose a room. I was frightened of what might happen if I got so sick I was unable to let anyone know where I was or pay my bills – I might get out of hospital to find I had nowhere to live at all any more.

More seriously, bingeing happened. Specifically, bingeing and purging. I had emotionally eaten before my most serious descent into anorexia to the degree that I was borderline overweight for a very short time. And I remember being so out of control with the stuffing and the musteat-can’tnoteat-can’tbearnottoeat feelings that I would be in physical agony and crying, and just lie down long enough for it to settle a bit and be needing to eat again. But I didn’t have the money worries that bulimia brings. I was able to go without the excess food if I didn’t have money for it.

Bulimia meant I was taking away just as much as I was putting in – still in starvtion, in fact probably making it worse because I was losing stomach fluids, nutrition already in my system etc every time I purged, and creating a chemical chaos for my bloodstream. Being physically uncomfortably full didn’t happen, or at least if it did, I ‘undid’ it. I could eat a truckload of food and still be starving ravenously hungry.

Purging is, in hindsight, the thing I’d most like to go back in time and ‘unlearn’. The rest of the eating disorder was hell enough – purging was like opening the very gates to hell and being unable to ever shut them again against the hordes pouring out. Even in my fight against dying from starvation from the anorexia – it’s more complicated for me because of the purging. Before purging, it used to be a battle to follow the meal plans and put on the weight, especially when not in hospital and on my own – but at least once I got the food in, the physical part of the fight was over. Ed thrashed me in my mind, but it couldn’t do anything about it, and that was the end of that.  But with purging, it wasn’t the end. Because hours after I’d won that battle to eat, I was still able to undo all my hard work in one moment. It was absolutely gutting to have fought so hard and to undo it all just like that, be back where I started or in even more a precarious position.

I had some savings, but it wasn’t long for bulimia to have totally eroded them and I was taking the last bit of cash to my name out of the ATM machine. That was a shock for me, as I had been in denial and not keeping note of how much money I was spending any more. Suddenly it was gone and I knew I had no choice but to stop this, now. I couldn’t say to myself any more that I could just do this for a while, eat everything I craved for once, and then stop it next week or next month and get back to normal. I had to stop it NOW or I was in trouble.

Except I couldn’t. I found myself frantic, unable to cope at all without the bingeing – which in the short time I’d been doing it had become my major coping mechanism after starvation – and yet unable to cope in other ways if I continued.  I could no longer pretend it was just about me ‘making up’ for all the missing out and starving, no longer pretend I was just ‘tasting all the foods I had never gotten to try’. The foods became the cheapest, blandest stuff on offer. Old, discarded, stale, it didn’t matter, if it was edible, it served a purpose.

I wonder if people who become addicted to drugs start off that way too, they care about the quality of the drugs they are taking, and then when they are desperately addicted and the funds run dry, they’ll take anything they can get. Same with drinking, where the person might start out with cocktails or beers and end up slugging down methylated spirits?

Long story short, if things were financially tight before, they were precarious now. As I said before, I didn’t actually default on my responsibilities – but I was terrified that it was only a matter of time. My pattern became that I’d get my pension, immediately pay everything that was due, then the rest of it – usually about $150 or so – would be binged away within about two days. The rest of the fortnight I walked everywhere and went without food whatsoever. I do have to admit, part of me purposely wanted to get rid of the money as soon as possible – because when it was gone, the bingeing was over. And sure, it was hell not being able to binge, but I preferred the numbed control of the starvation.

It was not sustainable, and I knew it. I started scrambling for help. And somehow I stumbled on the public trustee of my state. I’m fuzzy about the details, but I asked them for help, with the support of my case manager, and they took over.

Took over, completely. All my pension goes to them. They control every cent I own. They pay the bills – rent, utilities, pharmacy account, nutritional account, cat boarding account, etc – and give me a small allowance weekly for my food, toiletries, transport, household items, and most importantly, Shalimar. They have a strict budget to allow me to purchase items or pay accounts that come up during the year. By ‘strict’, I mean, blood flows more easily from a stone. The trustees are notoriously strict and out of touch with their clients – I’m not the only one who has complained – and I think they forget that they have a lot of power over our entire lives.

Asking them for a more affordable internet and phone option should have been straightforward – after all, we are in the business of saving money, right? But no. They wanted me to continue with a heinously expensive and unaffordable pre-paid option that I simply could not afford. I’d go through the tiny amount very quickly and then be fighting with them again for more. I gave them quote after quote for plans that were more affordable and better suited to my needs, each being rejected – “No plans over six months in length” or “You must have unlimited data allowance if you are on a plan” (which would be great, but I couldn’t afford that sort of plan. I am not even a heavy user, I probably use 4 GB a month) Finally they were saying, “You can’t have the internet.”

Most people will probably think, so what? What’s the big deal? Internet is a luxury. I fully agree, it’s a luxury. I could go to my local library and use it there, for example. But – I’m deaf, remember. Profoundly deaf. I struggle to pick up a lot of what’s said to me in person. When it comes to communicating over the phone – there isn’t a hope. I’m also extremely isolated. I live alone, and despite being so much better, I’m still physically pretty unwell. (Shalimar is great company, and I do not know how I managed to cope without her, I really don’t – but let’s just say she’s not the best conversationalist )

For me, the internet is a lifeline. I make phone calls online, using a relay service. During the day time, I communicate regularly with my case managers and support workers and even my therapists with SMS and email. And at night time especially, I use it to distract myself and to recieve and give support. I talk to my friends, both those I know in person, and those I have only (yet) met online. I use it for meal support in that it takes my mind off the meal to some degree, and then it occupies me and keeps me communicating rather than sticking my head down the toilet afterwards, and it keeps me out of the fridge and pantry at my most vulnerable times – or at least delays all these things, which is a good start.

Also, unlikely but extremely important – if I don’t have the internet, I cannot call for help if I need it. I cannot call our emergency services – because I cannot hear on my phone. We don’t as yet have text support to contact emergency services (although I hear it’s been on the agenda for a while). Unless I’m able to SMS a friend and ask them to call emergency services for me – and that’s time consuming and often not really something I want to do. I don’t want to worry them, for example. And they might not have their phone turned on or read the text for a while, and then I’m stuffed!

I used to be such a loner. So withdrawn and shy. I lived in my own world – I didn’t want a bar of this world. Much of the time I was actually dissociated – and I preferred it that way. My little inner world was safer than the real world. But these days, I’ve come to crave social interaction. It’s the people I’ve met, the friends I’ve made and come to adore who make my world go round, my life worth living. Even when I’m not up to talking, just sitting here and seeing people talking on facebook or somewhere else helps me feel not so alone in this world. It literally opened a huge window to the world where before, there was only the blank stone walls of my self-imposed exile.

So the internet, far from a luxury for me, is essential. But I had to fight hard to get it. It took more than six months, and the last week or so, things were dire to the point that I had no internet, no data left on my mobile phone as I used it to tether to my computer for internet, and was running short on texts. The walls were closing in, and I realised again just how isolated and alone I am, how quiet things get, without it. I am SO relieved to be back on air.

If it wasn’t for my eating disorder I wouldn’t have the financial constraints on  my life that I do. I would be working and earning a decent amount, or at least more than the pension. I wouldn’t have the costs occured during binges or needing so many meds – the bill at times can be around $75 a week. I wouldn’t be needing to pay thousands in cat boarding fees every time I went into hospital. I wouldn’t have wasted thousands on taxis over the years when I was unable to physically get home due to weakness or imminent collapse. And so much more. Most of all, I wouldn’t be with the public trustee and having to fight to get things that I consider neccessities.

So I’ve been thinking a lot more about this whole situation lately – and with the support of some very close and wonderful friends – I am applying to come off the public trustee. This is a terrifying thought – much as I hate them, after all these years I don’t trust myself to manage my money. I feel like I have totally forgotten how. I’m scared that I’ll binge it all away immediately. But I have support I never had in the past. I have options I didn’t have like direct debit for bills. And I have come a long way in many ways including, I’m a heck of a lot more mature than back then. So I’m finally taking the leap. First step is applying for a tribunal hearing, collecting the paperwork necessary, and showing them that I can make decisions myself now. Then… I don’t really know. But hey, I know now that I can deal with it.

So, this blog entry began as a way to explain why I haven’t been online as much in past weeks and not at all the previous week – I certainly do ‘tangents’ well hey?

In other news – therapy is going well. And I’m just plodding along, at times just hanging on tight -because that’s sometimes all we can do.

Next week – in eight days actually – I’m going to Melbourne!  A long anticipated visit to a very dear friend – she’s going to show me her beautiful Victoria, and then we are driving up to New South Wales to attend a camping festival..  I’m so excited. And so terrified! I haven’t been camping since I was in school – I loved camping, but have no idea any more how it’s done… okay that sounds strange. When I was a schoolkid, life came a lot more naturally to me. And I didn’t have an eating disorder to deal with. Any trip away from home is extremely difficult for me because of the eating disorder. I have no idea how I’m going to go when camping – but it’s going to be a great opportunity to find out. I hope so much that I’m able to fully participate – and I’m going to try my best. I intend to enjoy campfire meals, toasted marshmallows, exploring the surrounds. I’m taking my art stuff and going to be doing a lot of just drawing what’s around me. A lot of reflecting and journalling. Chilling out. Reconnecting with nature. And at night – after all these years of city living, I’m going to be able to stargaze again without city lights for miles and miles. I’ve been told it’s amazing. I can’t wait.

Bring it on

Ironically it’s going to mean another week or more away from technology – there is not even phone service where we are going – but this is going to be a good sort of tecnology-free period!

Thank you so much to everyone who has commented and been reading – I have a heap of your comments that I’m dying to answer and just haven’t gotten the chance to yet. I have been reading them  - and I’m always extremely grateful, touched by your support, and intrigued by your views. Thank you for being patient with me while I’m so scarce lately! I also look forward to slowly catching up with your blogs – I’ve missed so much of what you are all up to and what you are writing about – and I’m deeply sorry for that.

Hoping you are all well! Thank you for reading

(Image Sources: 1, 2, 3, 4)

Lost? Time To Find New Pathways!

First of all I want to thank everyone for your support and compassion when it comes to my last post. I was, as the title suggests, extremely discouraged and depressed. I still am battling depression hugely, but there have been little glimmers of hope for me since I wrote that.

That post, as some wise owls also remarked in the comments section, was an example of pretty screwed up, negative, unhelpful thinking.

By saying things like “I will NEVER…” I totally deny myself any chances of that thing happening, before I’ve even really tried. I close the door just like that. And I do deny faith, deny God. (I’m sorry if you don’t believe in God – each to their own. I do) Deny any plans that He has for my life, or any faith in Him that with Him I can get through anything.

Diane mentioned that to come back and use my newly minted CBT skills on those statements I made would be very helpful and I agree. Those are thoughts that have been going round and round in my mind, upsetting me, causing me anxiety and making me feel hopeless. If I am not challenging them, they will never change. Challenging them is the first step.

I may no longer have the dreams I had when I was younger – but who of us ever knows what is round the corner? Even the best laid plans fall, and often. If only we had a crystal ball, we could plan our way to success and happiness step by step, including navigation around every hurdle we would face on the way! But life is not like that.

Life doesn’t only give us hurdles. It opens doors. All the time, in unexpected places. Opportunities don’t always announce themselves. We have to keep a look out for them. And we have to believe in them. If we don’t, we won’t look, and we will sail right past them.

There is no factual evidence at all that I will never amount to anything in my life. NONE. I am ONLY 35 years old. That is not even half of a person’s life expectancy. And I might not have things like certificates or diplomas or degrees, I might not have a job or career or a family or house or car, but I have lived experience – and that is something you just cannot buy or learn.

I don’t have a crystal ball or ESP. I have no idea what the future holds for me. I don’t even know what tomorrow really holds for me as opposed to what I’ve planned. 35 is not too old to begin anything. I might struggle to have kids, and who knows, maybe I never will meet a partner, but I have wonderful friends who love me in the ways I need to be loved, and there are many kids out there who some day I might be able to adopt or foster. They won’t be ‘my’ kids, but I would hope that I could be part of thier lives even if briefly.

There are definitely things I can do – I’ve been researching with the help of a close friend, Tertiary Preparation Programs, which are short uni courses that help you get back into being a student. I might soon be doing one of these, online and part time. It would be awesome to call myself a student again after so long – and this might be a pathway into something like a psychology degree or case management or social work, which might be another 8 years if I did it part time (and then still not be actually qualified) but I’ve just thrown more than 15 years of my actual life away to the ED, more than that, so what’s another 8 years when it’s going to be positive stuff? And this is very sudden – yesterday my therapist just suggested it as I was bemoaning exactly what I wrote here in my last post. I do need to feel like I’m actually working towards something again. The cognitive difficulties? I’ll tackle that as it comes. Even if I have to do only one unit at a time, I’ll do this. I’m still not actually finishing most books I borrow from the library, in fact I don’t start most of them – but I’m getting through more of the book before I give up. That’s progress I guess.

I’ve been told of a program that is run by survivors of child abuse, for survivors, that’s situated out in a remote area, a series of 5 day retreats. It sounds really great, and what’s more, they do not turn anyone down based on financial difficulty – they help you come up with a way to do it. Feedback sounds really good – some people say the 5 days was worth more to them than a 6 month hospital stay. What’s more, since the volunteers who run the course are all past program participants who have come through their own troubles and trained to then come back and help, that again is another pathway to my future that I might choose. I’d be really happy with something like that. To help other people like me as a volunteer at a place like that.

Basically what’s most important to me is that my life is meaningful, in that I left something behind that was better for my having been here (as opposed to leaving a deficit because I took much and contributed nothing or very little.) For me, meaningful means helping others, however I achieve that (whether directly or indirectly.)

I’ve looked into some other options for therapy (8 sessions left for the rest of 2013) including funding that’s set aside for people with Eating Disorders to attend therapy (not very likely but worth a shot) and a community counselling organisation which would provide free or sliding scale sessions. They do seem to specialise in ED,  I do worry that they sound very ‘feminist’ based which isn’t my thing at all, but again, I have nothing to lose by checking them out and I have an intake appointment next Tuesday to meet them and see what they are like. (And I am, as usual for me, petrified!)

A close friend has recommended a psychiatrist who specialises in Trauma and will bulk bill (sadly bulk billing is getting scarce these days), and psychiatrists are able to bulk bill I think 50 sessions a year as opposed to the 10 that psychologists can. I had given up on psychiatrists – my experiences being that they throw medication and labels at you but don’t do anything to actually HELP you, whereas psychologists are all about changing your thinking and behaviours and working with your emotions. They give you real tools to take away and use for the rest of your life. But I will give this fellow a chance if he will give me one. I googled him and he has a huge reputation in this country so I just hope he’s not too busy for someone like me.

To help me face up to the anxiety that is ruining ballet and volunteer work with, I’ve been working with my care team to come up with ways they can support me to get there – after which once I get stuck into it I’m fine. it’s getting there in the first place where I fall down most, and it’s spending 2 or 3 days before hand constantly in panic attacks about it that exhausts me. I panic over the simplest things like “will I get up on time” and “I need to leave by x o’clock, remember that” and to have someone support me in the getting ready and getting there will help a lot of that anxiety calm down. I’m also changing my volunteering day, because Mondays is perhaps the worst day of the week for me. My weekends tend to be my busiest days of all and by Monday I am physically and emotionally a wreck, which doesn’t help in getting myself there in one piece or feeling very productive and helpful once there. And to help with the anxiety about what people will think of my appearance at Ballet, I’ve visited Bloch and come away with some really nice dance clothes that cover my scars, are loose but not baggy, and breathable. (I hate that I fret over this, but to me, the people at Ballet represent a group of people that once judged me very harshly, and to go back to them covered in self harm scars and underweight is something I feel very ashamed and self conscious about.)

I bought dancewear very like these!!

This leotard in Rouge

A similar wrap top, but very light and floaty material (for our hot summer) in baby pink

Black skirted jazz pants very similar to these, with a tie front, but no pattern.

And one for the wish list:

Another reason I NEED to have children some day. So i can dress them up in adorable clothes and shoes.

I don’t help myself when I catastrophise about possible disastrous outcomes (that 99.999% of the time never happen) or engage in all-or-nothing thinking (“I’m not a success, so I’m a failure.”) I don’t help myself when I let what I feel override what I know to be true (for example, feeling fat overriding knowing I’m actually underweight, or feeling that people will judge me and find me to be a loser over actually knowing that those particular people like me, are nice to me, and accept me.)

I don’t help myself when I close myself off to any possibilities not just right now, but in the future, by declaring my life ‘over’.

I don’t help myself by forgetting that I don’t have to fight my problems by myself, or even face them alone. By forgetting that God has a plan for every single one of us, and that He has a plan for MY life too – even if I don’t know what it is yet. He is fighting for me every step of the way, and everything that I go through is part of His plan for my life. I don’t help myself by losing faith not just in God, but in my own self. (Thank you, Missy, for the reminder.)

Giving up on myself is the same as declaring myself worthless. And if God finds me worth fighting for, and even worth creating in the first place, who am I to have the arrogance to say “God, you are wrong, I’m awful!”

I’ve been enlightened in SO many ways since I wrote my previous post that I DO have more options than I can even know of right at this moment, that more options will be coming along in the future. That it’s never too late to change or to start afresh, to begin with something new. And that the fastest way to really fail, is to declare yourself a failure before you have even tried. It’s not failure when you give something your best shot. It’s only failure when you never even try at all.

I could go on, but this is already a heck of a long post. I am also needing to work on my screwed up sleeping patterns and have taken proactive steps to try and get more and better quality sleep –  but I didn’t mean to include boring other people to sleep as well!

Thank you to everyone for your support and your belief in me – and for reminding myself to believe in myself.

(Image sources – 1, 2, 3, 4, 5, 6)

Happy New Year! High Tea, Friends, Happiness, And More To Come.

Hello! I just wanted to quickly pop in and share with you my special, challenging day – and most of all to wish you all a wonderful, happy New Year.

I can’t believe that 2012 is coming to a close already. It goes so fast!

Today, I did something that a few years ago I never would have dreamed of doing. Another something – after Christmas and my Sleepover parties!

I met up with two special friends for a Fashionista High Tea at a pretty amazing place, the Palazzo Versace hotel on the Gold Coast. We had high tea in this amazing room – the Le Jardin restaurant -

High tea was sublime -

Eyeing off the goodies…

Of course, I take terrible photos. Focus on the FOOD, and the surroundings! The pool was amazing. We are all going to have to come back at some stage and get ourselves a pagoda!

That can totally be a New Year resolution.

I’m not really big on actual formal resolutions any more. I used to aim for the sky, far higher than I could possibly hope to achieve. It meant for me, that I fought harder and usually achieved more than had I aimed for what was ‘reasonable’. That was one of the secrets behind my high achievements of my younger years.

The biggest secret was that I was obsessive and relentless and pushed myself, body and mind, beyond the limit – and this contributed to my eventual break down. I guess there are ‘reasonable’ limits on most things for a good reason.

I often think just how much more I could have achieved in my life, had I stuck to limits that were reasonable for me. I might be in a career now, I might be married, or at least have a partner and kids, I might be a totally different person in a totally different position to now.

But we can’t waste more time with regrets. We only have right now – our future is made up of a series of ‘right nows’ – and it’s by making right now the best we can make it that we ensure our future will also be the best it can be.

And that’s what I’m going to focus on in 2013. Trying to make every moment count. Trying to continue the good things I’ve managed to achieve this year, and add more, but not overwhelm myself to the point of relapse.

In 2012, I achieved 2.5 years hospital free, and with a fairly stable weight at around 15 kilos heavier than what I used to fall to, and 5 kilos heavier than what my discharge weight used to be. I started volunteer work, graduated from physiotherapy after 18 months, started ballet classes, moved suburbs, completely cut off my biological family, and grown in many other small ways. I’ve taken up some more hobbies like gardening and sudoku, been painting and in an art show,  and I’ve been stretching myself so much more socially – getting out there meeting friends and DOING things with them instead of letting the social anxiety part of things cut me off.

I’ve eaten out so much, eaten so many new things. Like Christmas dinner, birthday meals, just meals at restaurants and picnics, high tea today. A couple of years ago, there was no way I would even put a speck of that stuff in my mouth, or keep it in my body,  and that’s before we even get into the ‘in public’ stuff.

I’ve  even gone swimming in a public pool and at the beach, and I’ve slept over with friends twice.

And I’ve started proper therapy and am working hard, making good  progress.

It’s been a great year. And there is so much more to come.

In 2013, I just want to keep expanding on these things. I want to increase my work hours so I can get a real job, and keep on volunteering because it’s good for my spirit. I want to do more ballet, and tackle the crippling anxiety that I have to fight to get to do it every single time. I want to do more things with more friends more often. I want to enjoy my own time more, doing more things I like or find meaningful or constructive rather than sleeping my life away or being sucked up by all ED thoughts and activities. And I want to progress even more with the therapy, and hopefully be able to achieve some peace – to that end, I already have an intake appointment lined up with an independent ED-based counselling/therapy service provider early in January and hope that when my 10 psychologist appointments are up, this fills the gap. (I also found the courage to ‘fire’ my private psychiatrist.)

I’m not making any ‘absolutes’ though – because we never know what is going to happen, and I think that as long as I’m going in the right direction, that is what matters.

I hope all of you have a wonderful, safe, happy new year, and that it brings better times – better health, peace, stability, healing. I hope that the good things are only a sign of things yet to come. And despite wishing you all so much more, in the same breath, I wish you all enough.

Okay, enough of my long winded ‘quick’ post! Go celebrate, go sleep, go see out 2013 in a way that makes YOU happy, and start the new year in a way you mean to continue.

And thank you all for being so supportive and lovely to me throughout this year of blogging.

(Image Sources: 1, 2 , 4, 5, 6)

(Ps, Shalimar has informed me of her desire to spend the new year eating, sleeping, catching lizards, and repeating it all over again )

My Experience Of Body Image

I do a lot of pretending.

I pretend a lot that I’m going better than I really am.

I pretend that I’m happier than I am, or at least, not as unhappy as I really am.

I pretend that I have a lot more hope than I do in reality.

And I pretend that I don’t really want to be ‘thin’.

I don’t know what to say to explain that one!

No, I really do NOT want to be emaciated, or even ‘too thin’. I feel like such a failure, and that everyone can SEE it when it’s that obvious. It’s not a nice look at all, in fact, it can be quite disgusting. Have you ever seen someone who is emaciated’s bottom? There is this big… concave HOLE there. And the anus that is usually hidden by flesh is.. stretched out in the middle of that hole. Too much info right?

Grossed out yet? Imagine LIVING WITH THAT. Still want to be thin?

And yet, I would give anything to go back to being almost 15 kilograms less than I am now. I don’t care how gross it might be. I don’t care about people looking down on me or treating me horribly because of it. I don’t even care that it might kill me. I am too much, and I will always be too much. At least in my mind, I am too much. I know in reality I am not, far from it. But to me, always too much. Always. And even at my lowest weight, I never even started to not be too much.

My body image is SO distorted. Even when I was at my lowest weight, on a good day I would see a normal, maybe rather fleshy person. On a bad day, I’d practically be able to roll myself around. And yet, under all that, my wise mind was constantly saying “But I’m too thin. I know I’m too thin. The ‘numbers’ say I’m too thin. And yet what is this incredible fleshy hulk I’m hauling round with me every day?”

Every now and then I’d catch a glance of what I called “Michael Jackson” in the mirror – a glimpse of how I truly was – and scare myself terribly. But that lasted for a glimpse and a few moments post-glimpse – before “too-much” loomed over me again, threatening to squish the ‘me’ right out of myself.

Okay, I know my nose is bigger and it’s REAL, but yeah. Scary stuff.

One of the common myths is that people with anorexia and/or bulimia enjoy their disease, enjoy the ‘thinness’ that many of them achieve. I think the reality would be closer to we don’t even get to experience it let alone ‘enjoy’ it.

How do I really see myself?

Imagine your body is SO heavy and huge that you find it hard to move. You find yourself very weighed down. Sluggish. One of the reasons my dancing started to fail in uni was because, yes I’d gained some weight initially, but after that, even though it was plunging DOWN, I felt heavy and unable to MOVE properly due to having so much flesh stopping me. It was a complete utter delusion.

You can’t walk with your legs together because your thigh rolls prevent that.

You can’t put your arms down properly to your sides because the rolls of fat under them and on your torso are too huge.

And it all feels SO REAL. So completely utterly REAL.

It’s not just about the body image way of being ‘fat’ either. It’s about being that aforementioned ‘too much’.

I experience the world as though I’m towering over everyone around me. I am more tall than I am short, but I’m not THAT tall, and I still feel this way when the person next to me is actually a lot taller than I. The same with width – I feel monstrous next to everyone else, even if the person beside me outweighs me by 100 kilos.

Even without the comparing of size, I just feel too much ME.  I’ve spent my life trying to squeeze myself out. Trying to disappear. To be invisible. Apologising for taking up too much space, for being so wrong, for being so grossly overimposingly massively HERE.

The way I experience my own size against that of the world has also see-sawed along with my actual weight, except that it’s strayed ever further than reality each time. The first time I ever lost weight, I felt tiny, I could feel myself and see myself shrinking. The world became huge, but only in relation to my own size.. Then I was refed, and although I grew, oh boy did I grow bigger, the world seemed to stay the same size. Each time I went down after that, the world got bigger while I stayed the same size. And each time I was refed, I grew bigger and the world stayed the same size. Can you understand that? We were becoming more and more skewed the more I lost and gained, I growing ever bigger, the world ever smaller.

Whoever invented those carnival mirrors, I wonder if they knew what this was like to live with?

This is just how I see my own face! My brain stretches it out so that it appears smeared.

So my problem is, I guess, that it’s so hard to live in a body that you feel so wrong in, one that you constantly wish you could literally unzip and step out of.

And while I struggle so much with my body image, I guess I have had to get to a place of maturity – listening to my wise mind and rationality over my discomfort and my desire to strive for something I find more pleasant to both see and be. 

Not everyone has reached that place.

Eating disorders are NOT about food, shape, weight – that is surface stuff. That is the language of our culture. That is the language we fall to first, when we are not happy, worried, anxious, have problems, and have no other way to express them but “I hate myself, I am so ugly, I am so big, if I lost weight, my problems would be better.” But food and weight and body image issues are often triggers for eating disorders to begin – and for the malnutrition that they cause to trigger the cognitive deficit and irrationality that leads to it becoming a mindset and something that overpowers us easily.

It’s very dangerous to be constantly giving us images to which we are expected to conform when they are physically not even possible for most. So many of us are struggling to even accept ourselves, let alone find ourselves acceptable in context of the rest of the world… and we are bombarded by reminders that apparently we never WILL ‘size up’.

What do you think of this?

And here I will end my ranting and leave you. Do you feel you ‘size up’ or are you too much? Is your body image distorted, or normal, or can you even tell when you only see what YOU see? How do you know if what you see is the reality?

If you have an eating disorder – how much do you feel it’s about food, weight, body image? Do you find that if you take those issues away, you still are stuck with your disorder and the problems that are underneath?

Do you find yourself yearning for something that is forbidden and dangerous? How do you deal with that?

And – if I don’t get to post again before midnight tomorrow - HAPPY NEW YEAR!! May 2013 be the happiest and most positive year all of you have lived to date – with better things on the horizon. xx

(Image Sources: 1, 2, 3, 4, 5, 6, 7 taken from Facebook.)

It’s Nearly Christmas

Christmas has come so fast! In a few hours in Australia, it’s Christmas Eve.  I will be going to the Gold Coast to spend Christmas Eve with a very close friend and her family – followed by a huge Christmas Day. I’m so excited and also so nervous – it’s the biggest challenge so far to the eating disorder and the various forms of anxiety.

And I’m going to rock it.

“…is it FOOD?”

My only sadness is that Shalimar will spend Christmas day alone. Comfortable, yes. Well-fed, yes. But not with me. Thankfully, she will not even know it’s Christmas!  I know now that she will be more than fine – she will spend her time sleeping, watching lizards and lying next to her bowl, scooping the chow out with her paw towards her mouth. These things make her very happy indeed!

No matter what you celebrate, and no matter where you are with your own individual journey – I wish you all a happy, safe, peaceful and hopeful holiday season, and hope that the New Year is one of positive and hopeful times.

Thank you to all of you for your readership, your comments, and your amazing support during the just over a year I have been writing this blog.

All the best – Fiona and Shalimar xx

 

Tis The Season To Quake With Terror – Food and Christmas.

I’ve been doing a fair amount of quaking lately! The closer we come to Christmas, the more pressure I feel under and the more challenges I face.

A few Christmases ago, I could not even change my behaviours in order to not hurt the people I loved most. It broke my heart to know they worried about me, and I beat myself up endlessly for not being able to ‘fake it just for a day/week/appearance’ in some way to just set them at ease. It wouldn’t have been the end of the world – I knew that. One meal, like a Christmas dinner, would not have completely negated the years of starvation when it came to my body. It wouldn’t have suddenly made me fat or no longer emaciated. It wouldn’t have meant all hell broke loose and I lost control. (Although the reality was, I had NO control – I was controlled by the disorder, to a degree where I could not even disobey it if it meant saving my life or that of another.)

Christmas back then, if I was spending it with my Dad and his family, meant making myself a larger version of the same boring green iceberg lettuce, tomatoes, cucumber and celery salad I had every single meal, just adding in a few bits of watermelon for the dessert, and chomping on raw carrots when they snacked on nuts and nibblies. I guzzled diet coke as they downed juice and wine, and laughed and smiled insincerely to show how much I was enjoying myself and how full of the Christmas spirit I was. Wasn’t it all wonderful!!! (NO).

I didn’t fool anyone except myself (and hardly fooled myself either, I was miserable and I knew it.) Worse, I’d often end up bingeing later  on leftovers. Then wracked with guilt because that was their food, not mine, despite the many times they implored me to have some too.

The last couple of years have been different. My dad and his family are gone, he has passed away, they want nothing to do with me. So Christmas with them is no longer an option. I have cut myself off from the rest of my family  and so Christmas with them – an ordeal – is not ever going to be a threat. Mostly I spent the alone Christmases either hiding in bed, or volunteering. But the last couple, I’ve spent with my ‘chosen family’ – friends who are dear to me. Who make the day special just by their presence. And who treat me with the same respect that I treat them, something my mother’s side of the family never accomplished.

And I took part in the actual eating, too. The hugest challenge of all!

Two years ago, with a friend and her family I ate roast chicken, salad, roast veggies, and had pavlova and cream for dessert. Last year, a friend and I had a picnic ourselves in a park – a BBQ with sausages, veggies, salads, fruits and berries. Both of these were just amazing days for me, memories I will cherish for a long time.

This year, I’m actually doing a full on Christmas, with a friend, her partner,  and her extended family. I’m to join them for Christmas eve – we will tour the lights, and then go to a Christmas eve mass. On Christmas day, I have no idea of how it will actually unfold – but so far there are going to be at least 15 people, one of my friends who has been busy cooking is a chef, and these people go ‘all out’. It’s going to be Christmas with Bells on!

I am so excited. AND SO SCARED. So far in the last few days I’ve eaten SO MUCH scary food – like cheesy melty grilled sandwiches, deep fried battered fish, and real handmade fudge.  And it’s not even Christmas yet. Much as it’s a triumph being able to overthrow the ED when I’m with people who are dear to me, I’m more scared that I CAN eat these foods than when I didn’t used to have any power at all. I’m scared that if I can do this now, the old rules that used to keep my monstrous, gluttonous greed in check no longer will, and that I’m only ever a step away from losing control completely and eating myself into obesity. I still feel like one bite of something that is forbidden completely ‘blows’ years of abstinence. It still feels like the imminent end of the world to have food that is ‘forbidden’ inside me, and staying inside me. It feels that bad for ANY food actually.

The difference is I am feeling these fears, and eating the food anyway. In a way I’m doing my own exposure therapy and I’m proving to myself that the world doesn’t end and I don’t blow up or eat myself to obesity when I do allow myself to eat the ‘wrong’ food either. Hopefully with practice, this will come to feel okay. Maybe even normal? I live in hope (but still not much belief… yet..)

I think one of the most important lessons that living with an eating disorder has taught me over this more than 20 years of having it to a clinical degree, has nothing to do with food or weight, and everything to do with people. It’s brought home time and again how precious the people we love are, and how fleeting our time with them actually IS. Because when we avoid food, we end up avoiding them or distracting them and ourselves – we miss out on them and they miss out on us – even in the same room or at the same table, we are missing – gone AWOL.

Just a week ago, a close friend’s uncle died. He was in perfect health, and his car simply veered off the road on the way to work and smashed. He had suffered an aneurysm - no warning. Not a second to do anything about it – just healthy, then dead. It was a huge shock to his family, and a lesson to my friend to cherish every moment with her family and her loved ones, because we never know when this moment might be our last with them.

We just can’t afford to let the ED get in the way of that, either. We just can’t. There is no guarantee, and there never will be, of next Christmas. Until it happens, there isn’t even a guarantee of this one. We only ever have right now – and when we put it off for reasons like food, weight, etc – we lose it. Forever.

So this is the time we need to be making plans of how we’ll get through this season, while still being able to enjoy spending time with those we love. If that means bringing a safe food, then so be it – it’s preferable to not miss out on their companionship. If that means NOT going to a get together you would attend out of obligation but the people there are toxic to you – then that’s also a very positive step. Just as life is too short to spend avoiding our loved ones, it’s also too precious to waste in the company of those who only hurt us. 

What is the hardest part of Christmas for you? And how have you prepared, or feel would help you to cope? 

(Image Sources: 1, 2)

Frightening World

I wonder how many of you find the world ‘too much’? Just as many of us with eating disorders find ourselves to be ‘too much’. I do.

I have been thinking over this a fair bit recently. With all the violence and fear and pain in this world, I always find myself wanting to remove myself from it. To opt out. Not to be a part of it. I cannot cope with the feelings, cannot cope with other people in pain – wanting them to not be hurting and not being able to do a thing about it – and so I just cannot cope with ‘being’ at all.

It’s a fact of life now that we are completely surrounded by pain and suffering. People get killed, or die from horrible illnesses. Or hurt. Or betrayed. A multitude of things. There are people who suffer from going without. From loneliness, from poverty of both the heart and of things needed. There are people who spend their entire lives scrabbling to just get by and survive. Too much power is in the hands of those who do wrong with it, and too little in the hands of those who would do good. The actions of one person can kill millions of people.

And there is nothing I can really do about it all.

I feel so powerless.

And I feel so frightened and overwhelmed by it all. By the terror and pain everywhere I look.

This is a big part of why I step away from the world and bury myself in my own, in the world either of my own imagination, or I simply dissociate somehow. And the starvation of anorexia helped me to do that. The more I starved my body, the less I found my mind lived in reality – I flew away, I really did. I simply flew away from here and all that hurt. Left it all behind.

Being refed brings me back to reality with a thump. A thump of having a body, and a thump of having to deal with all that goes on around me. And I still don’t know if I can handle it.

But I have to. And so now, I strive to. It seems that a lot of what I’m learning in therapy to help myself tethers me even more strongly to this world that I often find myself HATING. And yet, if I keep ‘flying away’ I cannot live or survive. I have to choose – live or die. Tether myself or fly.

I’m choosing to live. And though that’s the harder of the choices, I guess that it’s important that we always remind ourselves – we are not as powerless as we feel.  So we might not be able to change the world all by ourselves and straight away! But every little bit counts.

Have you ever heard the parable about  how the constantly dripping water wore away the rock, but the bucket of water couldn’t? That is how our own actions work. Little bits over time – adds up to real, powerful change. We can throw all we have at a problem, all the solutions in the world at a problem, but it’s not going to make as much impact as little bits, constantly, over time.

And that’s something every single one of us CAN do.

Conclusion – we are NOT powerless. I am not hopeless or helpless. I can make a difference in this world – and I choose to stay and try. And so can you.

(Image Source: 1, 2, 3, 4)

Sleepover Parties

… are something that eating disorders exclude you from.

It certainly excluded me from weddings, parties, anything.

Never again!

Today I’m apologising to you, my readers, and to the brilliant bloggers whose posts I love to read, for being awfully behind in my commenting and responding – for a GOOD reason -

I’ve just been enjoying a sleepover with a very special friend – and it was awesome. Absolutely awesome.

It’s really lovely to be doing some things that are ‘normal’ – but for me, so, so special.

PS this is the face that greeted me on going to bed last night – her puppy!

Don’t tell Shalimar!! She was fine, though. One night alone (with plenty of food and water and toys) is still a far cry from the days she spent months at a time in pet motels. She was absolutely fine.

I think she’s dreaming of driving a car or dancing a jig..

Have you reclaimed anything that you lost to being unwell?

(Featured image source)

Reflecting on Shalimar – My Angel

I realised last night that in early January it will be a year since Shalimar and  I moved into the apartment I live in now. We have had absolutely no regrets, either. It is a peaceful and safe place to live for both of us and I’ve never seen Shalimar as happy as she is these days, not in her entire nine years. Whoops – nearly ten years!

Yes, Shalimar will be ten years old on the 13th of December! Her ‘birthday’ was decided by counting back two months from her official Adoption Birthday – which was 13th February, 2003. I still remember that day like it was yesterday – picking her out from a cage chock-a-block with kittens at the shelter – and knowing on sight that she was the kitty I’d come for. Somehow we had bonded before I’d even left the shelter. I still remember waking up the next morning – Valentine’s day – having hardly slept from a night of having this little kitten crawl all over me. My first thoughts were “She loves me.”

For someone with a life history of rejection and abuse, that is an incredibly wonderful, precious thought and memory. I can’t imagine living without her. I don’t know how I survived before I adopted her.

I have come to believe there are angels on earth. And I’ve come to believe that animals can absolutely be angels on earth.

Shalimar has saved my life many a time, in many ways. She’s given me a reason to live at all. She’s given me so much love over the years, unconditionally. She’s been my constant companion, especially during the loneliest years of my life.

Before I adopted Shalimar, it was common for me to have periods of unconsciousness that lasted scarily long times – for example, having a nap on Sunday afternoon might lead to me waking up on Wednesday night, completely unaware that more than a few hours had passed. But Shalimar wouldn’t let that happen. She woke me many times by crouching over me and patting my face with her paw, not stopping until I’d dragged myself out of the black hole I’d been slipping into. Many times I woke with a face like mince meat – she never used her claws deliberately, but even with claws retracted, cat’s paws can be quite sharp.

Shalimar gave me a reason to fight to get out of hospital – thinking of her in a pet motel, despite knowing they knew her and treated her with the best care and a lot of cuddles broke my heart, and I missed her terribly.

I’ve heard of therapy dogs (or care dogs?) trained for soldiers with PTSD. Apparently, these dogs know when their soldier is having a nightmare, and are trained to gently awaken them, switch on lights, and provide companionship and comfort.

Shalimar definitely would make a good care cat for PTSD. In a way, she is one already. I realised this on Friday when she woke me up from a pretty terrible nightmare with her gentle patting. She then cuddled up to me, gently butting my face with hers and stroking it with her paw. (I think she tries to copy my stroking action, which used to hurt given cats have claws, but she’s learnt to keep her claws retracted. Smart cat!) She’s done this many times before.

These days, it gives me a lot of joy to see how happy Shalimar is. Moving here was her version of coming home to paradise. It’s like night and day compared to living in the gritty city area where, to a constant soundtrack of traffic and sirens, she witnessed probably thousands of drug deals, and thousands of weddings in the Church across the road from her little balcony.

Shalimar loves to stalk lizards, and to pretend she’s going to catch those annoying birds that sit in the tree next door and taunt her (they even swoop her!). She  loves to just sit in the sun, watching the kids next door scream and endlessly jump on the trampoline (more proof to her that these human beings are all nuts). Grass isn’t some heavenly treat that I bring a bunch of home when I find it. It grows all around, and she can walk on it let alone nibble it. She has developed rather discerning tastes, though – so far she’s eaten my climbing beans, my corn plants, all of my chives and basil, and now she’s started on my tomato plants.

I’ve gone from being too depressed to sit and just ‘be’, to being able to sit on my porch and watch Shalimar just ‘being’. To watch her being happy and contented does wonders for myself and our time outside has become the most calming and cherished time of my days.

I wonder what the next year will bring for both of us? I think the sky is the limit. We’ve both come a heck of a long way.

Tiger in the grass! Watch out, lizards!