Update: Escaping, Spiralling, Opting Out Of Life – And Choosing To Opt Back In Again.

ICanWeatherTheStorm

It’s been a long time since I’ve done a serious update, or a really serious post. There’s a reason for that – I’ve been not out of action, but hunkered down, holding on for dear life. As you do when things get stormy!

(Image Source)

Sometimes, that’s all we can do – hang on tight. And that’s okay.

My biggest ‘storms’,  as usual, have been the PTSD most, and the depression and anxiety. I had my monthly appointment with the consultant psych on Monday (the head of my treatment team) hoping that he could help in some way that would ease the worst period of both anxiety and depression in my life – and that’s including all the years of abuse and bullying. Instead, he complimented me again on how far I’ve come, and how well I’m doing.

I’m still far more functional than I was for over a decade, and for them, that is more important than the level of depression and anxiety I’m feeling. I do worry that these will make me lose function – avoiding doing things and hermiting, being too lethargic and miserable to move most days – doesn’t make functioning very easy! The PTSD, I’m hardly even asking for help with that any more – trying instead to keep using my strategies and wait for the new psych appointment – finally – next week! It seems like I am haunted by the nightmares and the sense of horror  every waking, and not waking minute. There is no easy cure to any this, I wish there was. There is only really bearing it.  But I guess I have to just suck it up and hang on tight.

I’m feeling worse now, because I’m not running away any more. I ran so far, for so many years.  In the past, when the depression was this bad, I used to go out stomping across the city, counting everything I could possibly count – calories, steps, kilos lost, kilos to lose, grams of this and that to two decimal places, to block out everything else. Later, I would cut myself to bits. Or I would take an overdose and hope that this was it, it was all over now. Or I’d  purge until I was sure my stomach itself was going to come up. A lot of the time, I did all of the above, and still hadn’t escaped far enough from myself.

When I became bulimarexic, I would spin out of control – rushing around at top speed, in and out of shops, amassing as much food and other odds and ends (clothing, housewares, bits and bobs, most often gifts for other people) as I could afford and hold.  Stuff them all in the back of a taxi or struggle onto a bus,  and charge on home to binge and purge, binge and purge, collapse for a few hours of exhausted slumber, wake up and survey the mess and the things I’d bought that I neither needed or could afford. Taking them back to the shops was a good excuse to buy more food and repeat the whole thing again. And again, until the money was gone, or more likely, I collapsed in a heap.

Then, came depression so deep that I couldn’t move. I’d spend days in bed, blocking it all out.  Opening my eyes was painful and took too much energy. Life had too many problems to face and I just couldn’t cope with them – so I didn’t. I pretended I wasn’t there instead. I fell deeply into that dream world, the one that I wished dearly I could stay in. This lethargy was heightened because when I came down from whatever frantic phrase, I would always have lost all the weight I’d gained last hospital stay, plus interest, so I’d hit rock bottom like a lead bomb. In later years, I was still too sick on being discharged to even be able to go on that frantic spree, so I went straight home and to bed most times.  This would go on until one or both case managers came round to shovel me out of bed like one might shovel roadkill off a road – and ship me back for hospital admission number whatever.

It wasn’t a life. And I’m not surprised I wasn’t able to function at all. It shocks me how much pain I put myself through in order to avoid pain – even writing this sentence – it’s crazy! It’s like chopping off your whole arm because of a little scratch on your finger. (I know paper cuts can hurt like hell, but really?)

Thinking about this more – I’m sure this overreaction was because of FEAR of the pain – I find that the fear of things is often far worse than those things I feared.

Anyway – I’m now feeling things. Staying with it. The sky still hasn’t fallen, despite that ever-present feeling of doom approaching. I do still struggle with bingeing and purging, and with restricting – and this makes me feel like I haven’t made progress at all. That my weight maintenance and great bloods (this is a big deal for me) and actual ability to do things, are  flukes.  That at any moment it’s all going to come crashing down around me. I’m not just letting it happen – I’m trying to approach each meal as it comes. Trying to have meals, and then at night, trying  not to binge on anything I didn’t eat during the day that I was meant to. How I hate that word, “trying“. Every time I write it I wince.

It makes me think “not enough” immediately – another of the myriad problems all tangled up in this web of disorder. I’ve never been good enough, I’ve always felt like an imposter. My best efforts always fall short, I’m not trying hard enough, I’m just not enough. Except when it comes to my body and then I’m too much.

I never wanted to be slim, beautiful and vogue. I did want my dancer’s body back at one point – but that was more about my belief that weight gain had ruined my dancing rather than being sick from chaotic eating habits, and was aimed more at function than form. I never understood how people cared about “thinspiration”. I didn’t want to look like anyone else. I didn’t want to look like anyone at all – including myself.

I wanted to be gone. Nothing. Zero. Not size zero. ZERO. Not there. Not taking up ANY space. Not seen, not heard, not felt. GONE.

Because it wasn’t my body I couldn’t cope with. It was LIFE. And I was trying to opt out of life and all that I had to feel to be there, in any way possible.

These days, I am coming round to the fact that I can’t be ‘gone’ and still be alive. Rationally, it’s an easy thing to realise – if you aren’t here, you are dead, right? In my brain, despite the rational knowledge, the irrational ‘can be both’ line of thinking persists. As does most of the ED screwed-up-irrational-thinking. See Missy’s post for a good explanation of how her ED brain screws things up too. We know it ain’t true. It’s like always having to argue with a whinging, stubborn child who knows the rules, but wants his own way regardless. It’s another kind of ‘storm’ we must weather – and then wade through the lies to pick up and keep hold of the truths.

I now have a lot more wisdom and insight than I had back in those days. The dialogue (accusations and threats is more appropriate!) from my ED brain is still the same as the worst years – but now, I am able to tell the difference between ED brain thoughts and rationality. Not just that – but I’m getting closer to being strong enough to change what’s not right. One step at a time.

(Image from Facebook)

When it comes to life – I have to stay here. Take all that comes my way. Accept it. Tolerate it. Hang on tight. And trust that this too, will pass, and I can survive it.  Cause let’s face it, it hasn’t killed me yet, right?

So that’s it. For me, right now, it’s about -

  • Weathering the storms. They will pass.
  • Trusting my team, life, my body, the process.
  • Not backing down when anxiety fights my ability to get out and engage in activities and socialisation.
  • Using my strategies – mindfulness, acceptance, being in the present moment, distracting myself.
  • Not fretting over the small things – keeping in mind the bigger picture, but
  • Not trying to leap huge bounds instead of taking one small step at a time.
  • Refuting lies – hanging on to the truth.
  • Challenging myself constantly, and
  • Remembering there is no failure – only the failure to try. 

In future blogs, I’m thinking of writing about my experiences as a long term patient of the public hospital system in Australia, specifically going through a psych ward ED unit. I’m wondering if there is anything in particular you might like me to write about in this context, or any other subject. Thank you :)

Finally, I just had to share this with you. I was google-image searching for pictures and came across this hilarious thing! Enjoy :)

(Image Source)

(Featured Image Source)

 

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62 thoughts on “Update: Escaping, Spiralling, Opting Out Of Life – And Choosing To Opt Back In Again.

  1. iamnotshe says:

    OK … i’ll be back … but i read the title and i say YES, THAT’S MY LITTLE WARRIOR WITH HUGE STRENGTH!!!!!! Love you, and need to prepare for work now. xoxoxoxoox melis

  2. val says:

    hi i’m very glad to find your blog! though my ed is not exactly the same as yours, i hate the ed all the same. n yes, i was nv hoping for my body to look like the models etc but yet i got ed anyway..
    my weight is back to normal now, but yet i still don’t feel functional. well i guess no one is really alone!
    thank you for your entries!

    • Fiona says:

      Hello Val – welcome. I’m very glad you found my blog too and I hope that there is something here that helps you even in some small way. You are not alone, no. I hope you are still getting support, therapy? Weight gain isn’t everything when it comes to recovery – it’s the most essential step to save your life and enable you to engage in therapy – but it’s really only the symptom of the real problem.
      Hope that in time, you feel stronger and more sure of yourself, and are more able to live the life you deserve to. Little steps – they are so important. Thank you for your comments :)

      • val says:

        yes i fully agree with you about weight gain isn’t everything! but it seems like that is enough for my doc.. she’s only pleased when i gain weight… i don’t like her, but yet i have no guts to change my doctor. i’m not sure if its my ED thoughts doing it or is it really my thoughts, or maybe i’m just lazy. i wonder if she actually understands that yes although i am afraid of gaining weight, its not all about weight and body image. yups i’m still going through therapy and on meds.

        when i first read your blog, and saw how you almost lost your life to all the purging etc. I did have thoughts of trying to purge and hope i die in the long term process(i have nv purged). However, as i read on, i saw despite what you have been through, u are still fighting on so hard. and your fighting is inspirational. I’m trying to use the acceptance school of thought on myself, so its really helpful when i read your pointers which reminds me to stay on track.

        Thank you so much, and i look forward to more of your entries! lastly, HOLD ON TO YOUR DREAMS!

        • Fiona says:

          Sadly there ARE docs who don’t get it – even these days. And please, don’t worry about changing your doctor. You are, after all, their ‘employer’ in a way, and if they aren’t providing you with the help and support you need, they aren’t earning your business! I know what you mean though. I am starting a new psych next week, after seeing my current one for seven years. I only just got the courage to tell the current one and it was SO hard. But we do come to a point where someone has helped us all they can and we do need to move on. Your doctor should understand and you would be far from the first.

          I was so, so upset that my blog made you want to purge so that it would kill you and so so sorry! I never wanted to affect anyone that way! I understand the feeling. Most of the time through this illness I have wanted to die – just haven’t had the courage to actually choose to die if that makes sense. So it was harder to challenge the ED because even on the brink of death and NOT wanting to die, I did want to die, for it all to be over, so I didn’t get scared off by being close to death. I also didn’t feel I deserved anything better than to feel as awful as possible.

          But yes, I’m still fighting. And it’s still hard – BUT I am GLAD I never gave up, glad I’m still here. Because now I know it is worth it and I realise that even though I can’t see it, I am worth it. You are too. Seeing that we are worth it is one of the hardest things and basically you have to start out being willing to trust what other people are saying over your own perception of yourself and keep reminding yourself of that constantly. Just to give yourself a chance. To get to know the real you, after all, I’m sure you probably don’t even really know the real you yet.

          Hang in there – hoping your dreams do come true – you deserve them to xxxx

        • val says:

          please don’t be upset or sorry that i thought of purging to kill myself! its all my erroneous thinking. thinking i don’t deserve to live.. and die either…. so in no way its your fault!. i’m so glad you never gave up too! we all have to put up a fight with the ED monster! and yeah i should learn more about the real me everyday!

          thank you!

  3. Sweet Fiona,
    I am so sad that you are in so much pain and so mad that your family caused this and your are blamed and blame yourself. My heart goes out to you, and I wish I could just make everything alright. I totally understand feelings being overwhelming. that’s where i am right now. no one knows but sometimes i feel like i’m going to explode because i have started to feel, and it feels like too much to bear. ugh…we didn’t deserve any of this, and yet our abusers brainwashed us into thinking we did, and we are not good enough…i carry that same message…for what it’s worth, WE ARE GOOD ENOUGH…our abusers weren’t.
    ((hugs))

    • Fiona says:

      I’m so lucky to know you, thank you for all the understanding and support you have given me constantly. It breaks my heart that you know this all too well yourself, having lived something many will never, ever even begin to imagine the full extent of. You are right – we didn’t deserve this. We ARE good enough. We always WERE good enough. One day I hope we can believe that 100%. I wish I could make things okay for you too. I think both of us are on the way to a far better quality of life at the very least, though, as we have fought so hard. Pain is often a sign that we are working on things! xxxxx

  4. Roxy says:

    I just wanted to write here how much I admire you and how much you are loved.
    I know how it feels like you’re standing on the front line against an army of PTSD and issues, but remember you’re not standing alone, I’m right there with you.
    Your “challenges” are exactly what I need to do too. Thank you for posting it, for helping me too.
    Love hon x

    • Fiona says:

      I admire you, so much – I feel like you have been proving to me that this is a process that CAN be done, and even more, CAN be survived. You haven’t glossed anything over, you have been real and honest. You have been and still are going through hell, but you give me hope because I can see so much growth and change in you every single time you post.
      I still want to hug you tight every time I think of the little I do know of what you have been through and I hope so dearly that you have some sort of peace and healing from this some day, sooner if possible. Love and hugs xxx

  5. am says:

    “I wanted to be gone. Nothing. Zero. Not size zero. ZERO. Not there. Not taking up ANY space. Not seen, not heard, not felt. GONE.”

    That is part of my ED story, too. For many years, I wanted to be gone to another world, not this one. Now I am glad to be alive and finding a way to be in this world.

    I was deeply moved by your courage and your honesty as I read your post, and then you had me Laughing Out Loud for the first time in several days with the LOL cat. I’ve had a bad cold, and my spirits have been low and my appetite in bad shape. Thank you, Fiona, for your sense of humor!

    • Fiona says:

      I’m so sorry to hear you have been unwell and low – so glad that I gave you a laugh, which can be so uplifting and healing. Sending you warm hugs and hoping you feel much better soon as it’s a hard enough battle already without being sick on top of it all.
      I wouldn’t be surprised if a LOT of people with ED at some stage identify with the ZERO thing. Because in a way, ED is opting out of life. It’s not being able to choose to live, but not choosing to die either. It’s limbo. And there is so much fear of both living and dying that keeps us there.
      I’m so, so glad you are alive today – and that your choice was life. xxx

  6. You’ve been struggling…that’s for sure but you are indeed an over-comer in so many areas. One thing that I picked up on…not that there isn’t a lot to….but it was the ‘nightmares that you have..I remember so vividly the nightmares and for especially that I will concentrate in my prayers…and might mention that when you lay down each night to ask the Lord to ‘cover your mind while you sleep and protect you while you sleep’….Take care Diane

    • Fiona says:

      I remember you talking about the nightmares, and I hope so much that they are nowhere near as hard for you as they were, hopefully gone. Thank you for your prayers. I actually do believe I can feel when people are praying for me, I really do, and I have felt absolutely embraced somehow, not physically/tangibly, but in the not alone, someone cares, more than I ever imagined, with protection, with more than I can give words to. And I will definitely ask God every night to cover and protect my mind. Thank you for your wisdom and friendship and just how much you give to me in so many ways xxx

  7. big fan! says:

    I can totally relate. I truly think that your wit and grace will get you through your tough times! Plus, now you don’t have to check someone else’s super mean/crazypants blog…it’s blocked!

    • Fiona says:

      Hi :) Thank you for giving me a smile today. I’m sorry that you relate and I hope so much that it’s something you can one day think back on as something passed and overcome, rather than a reality of your present life.
      I’m kind of wondering what will happen now! Seems like said blogger has made it private herself.. an interesting situation. Hoping that all is well, and that there will not be any ‘next chapters’ played out online anyway.

  8. Katie says:

    “I wanted to be gone. Nothing. Zero. Not size zero. ZERO. Not there. Not taking up ANY space. Not seen, not heard, not felt. GONE.”
    Exactly.
    I am sorry for all you went through, Your courage and strength is astounding.
    And the LOL cat is awesome. If we don’t laughat our struggles sometimes they will break us. Laughing at my ED helps me (I am a perma-lurker at EDMemes)

    • Fiona says:

      I’m sad that you relate, but also glad that you know you are not alone! I love ED Memes too, they are awesomeness. Laugh or cry, I’d rather laugh! I have to admit in hindsight I have actually LOL’d hard at things I myself have been through in all this that seemed a good idea at the time/terrible at the time/embarrassing/blah you know… :)

  9. Greta says:

    Ugh! I admit, it’s heartbreaking to read. I’ve read it three times yesterday and I couldn’t find the words to respond to your post. If only virtual hugs and kisses could heal and comfort. Or wishes were becoming true. If only life would fall into pieces just from out attempt to live. Yeah. The words…
    However despite your recent struggles, I congratulate you of coming out of that ed bezel. I feel it in your posts, comments, and your wittiness over that sharky site – your mind is so vivid. Maybe those are just the moments but still – you are no longer captivated in a slumber of ed. Even the end of this sad post makes everyone laugh out loud! You are alive, Fi! Maybe not well, but you are definitely on your way! Keep reaching, dreaming and writing! Love your writing!

    Ok, time for hugs and kisses:
    xoxoxoxoxoxoxoxoxoxoxoxo

    • Fiona says:

      I love this comment almost as much as I love YOU, Greta – you really made me feel good reading this. Hard as the past is to take, at least it’s over in reality. I can hang on to that. What remains, cannot actually hurt me – only if I allow it to. But if only we could reach out to heal and make things better for someone we care about, if only life were something that fell into place along with our efforts and intentions.
      It gives me hope and made me smile that you can see the life in me now, especially compared to before. I am on my way, yes. It’s good to know it’s real. That I’m really truly making progress that people who are as sensitive as you can detect. Sometimes we do wonder if we are kidding ourselves. And often, it gets really really discouraging because people who didn’t know me when I was that sick, but know me now sometimes say to me, that they can’t see that I’ve made any progress or gotten any ‘better’ from the ED and that never fails to hurt – because I do know how far I’ve come, but there’s an element of truth there – lack of change. Still being so stuck. But things ARE changing and moving forward, just more inside than outside at times. Thank you so much for being so lovely. And I’m glad you had a laugh, it was so fun for me to find I couldn’t possibly keep it to myself :)
      *hugs and kisses right back to you* :) xxx

      • Greta says:

        Smiling to my ears here!

        Also I’ve always wanted to mention but the content of your posts was overwhelming it: the IMAGES of your blog are AWSOME! I’m in love with each, practically! Yes! They contribute to your stories 100%. And always leave me crave for more.

        • Fiona says:

          Aw thanks :) I am in love with google images, it’s another reason my blog posts take me so long, I get so enthralled with all the pictures that come up for each search that I go off on tangents!

  10. bee says:

    Hi Fiona,
    wow, this post shows so much strength and bravery! It is horrible that you have to suffer so much. I know the feeling of not having achieved anything and not making any progress but from what you write here, you have come a very very long way. I am truly impressed and hope that you can at least sometimes see the immense progress you made. You can be so proud of yourself!

    This is the first time I am commenting but I have been reading your blog for some time. It makes me very sad to read how much you are suffering so I am sending you a big hug (if you want it – from a total stranger…).
    You are such a brave person. Thank you for sharing!

    • Fiona says:

      Hello and it’s wonderful to ‘meet’ you :) Thank you for reading – it means a lot to me that there are people out there who do find this useful even if I never know about them! I really do look forward to reading your blog too. It means a lot to me that even people I didn’t know yet could see I was fighting and making progress, and that they understand and care. Thank you – and I love hugs. There aren’t enough hugs in this world in my opinion :) xxx

      • bee says:

        Absolutely my opinion: not enough hugs in this world. Somehow I’m just always afraid to “step on somebody’s toes” with it… silly me. :)

        Take care. And big hugs :)

        • Fiona says:

          I still haven’t worked out how to use Greta’s animated smilies in comments, because if I did, I’d post one that has huge long arms that wrap round in a big hug :) xx

        • bee says:

          hihi… this one made me smile so big, the girl across the room gave me a weird look :)
          So – I really do feel hugged now. Hope you do, too.
          xx :)

        • Fiona says:

          Haha, I love it when you smile or laugh at something and people around you look at you funny! Really hilarious. Glad you feel the warmth of our hugs :) xx

  11. Paula says:

    Hi Fiona. It makes me very sad reading the first half of your post. Sad that you dont have a supportive family , your mum to give you cuddles, reassurance that life is worth living. Just for her to be there for you. Your writing about your experinces like I have said before helps me to undetstand what my daughter might be going through with her struggles mentally and emotionally. It helps me to be a better carer for my beautiful daughter. I would be very intetested to read about your experinces in hospital. My daughters worst experience was in a public hospital in Sydney. I still have a letter of compliant which I have never posted. As much as I was angry with the treatment I have to look at it that they saved her life. To this day she still has nightmares about it. Fiona never give up. Please take care and a big hug from me.

    • Fiona says:

      Hi Paula, I really appreciate so much that you care about me and what I’ve been through and that you read my blog. I’m glad your daughter has you – having supportive people who truly care and want to know what’s happening for you and how to support YOU best is half the battle I think.
      I have to admit my heart sank reading that your daughter had a bad experience. That’s exactly what I say about my own experiences – that they saved my life – and that I still have nightmares about them. I think the public hospital system and to some extent the private system too, is just so far behind when it comes to ED treatment. I look back on what I went through and really it was like I was being punished for being sick, and punished for already punishing myself. I came out of each admission more broken than I went in, but they saved my life. Sometimes measures that aren’t pleasant do need to be taken to save someone’s life, I get that – but compassion and understanding and being treated respectfully and humanely go a long way and aren’t much to ask!
      I’ll have to think a bit before I decide where to start, what to write etc when it comes to hospital. As you seem to have found with the letter you wrote, I’m in two minds – because I AM thankful, and it was the overall experience more than the people who worked there who were more lovely than not, trying to do what they could in a poor system, and yet, this stuff just isn’t okay and it needs to change.
      Thank you so much for reading and commenting, I’ll keep your daughter and yourself in my prayers xx

  12. gel says:

    Hello Fiona,
    It takes some time to read your post here and all the comments…to feel and grasp what you share. A lot of people have said things I wish to say to you. I feel a lot of appreciation for how you share your story and keep moving forward.

    I’m feeling pretty low and hurting and I’m in a new place with it where I do not have an urge to escape, via bulimia. That I can come here and read your words and feel strengthened seems to be part of why I am side stepping the b/p. I share this in hopes to show you how much a gift you are to me right now.

    Thank you!!!

    • Fiona says:

      Hi Gel,
      I’m really sorry how much you are hurting – really sad. And yet I know. Because I’m actually in a very low, dark place myself. I just keep hanging on because if I let go, I know I’ll fall. I hate that you are there too.
      However I’m not really surprised. I used to believe that ‘getting better’ from this, meant hurting less. I’ve come to learn that this isn’t always the case at all – that often, the path to healing means we actually have to hurt a heck of a lot more, first. To be able to go through all the pain that with our ED we have shoved to the side and not faced – so that we can finally process it and leave it behind us in some kind of closure.
      It sounds like you are going through so much on the inside – and it’s definitely necessary for healing, but it is the most horrible thing to have to sit with and tolerate. And I’m proud of you, for sticking with it. You CAN. You will get there. Hang on tight. Thank you for sharing so much hope with me, and for something that really helps ME to hang on – knowing that you feel stronger when you read what I have to say – that means everything to me.
      Love Fiona xxx

  13. missymiller says:

    Hon – Reading about your past is just unimaginable for me….I mean you explain it pretty well…it’s just that I can not even imagine the depth of the bottoms you reached with the depression and EdisO.

    And you need desperately to give yourself – or continue to- the props you deserve for where you are at now. Really.
    You may not be where you want to be, but you are better than where you were.
    And still in enough pain to keep going.
    The best way out of Hell is going through it.
    And when we get too comfortable? Well….that halts us.

    • Fiona says:

      Thank you for reading at all, Missy – because nobody has to read. And yet you take the time to.
      I don’t ever want to reach those depths again. And I don’t want others to have to either, because they are unimaginable. Looking back on it is like a nightmare rather than something that could possibly really happen and yet I know it could, because it has.
      Thank you for reminding me that I AM making progress and that sometimes we have unrealistic expectations of where we should be versus where we really are.
      I really like what you said about being too comfortable! It’s true. It’s hard because it sucks, but when we are UNcomfortable, that’s when we know we are making progress here! xxx

  14. Hi Fiona,

    If there’s one thing a certain “blog” is good for, it’s good for finding blogs worth reading. Having agreed with everything you said in a comment I read I thought I’d check you out.

    I’m epileptic and autistic, trying to coast along in a world that will never fully understand me (although I embrace my “otherness”). I have also spent the last twenty years in denial concerning Atypical Anorexia and my use of alcohol to hide from it – but I’m now seeking therapy and my husband is very supportive. I also suffer from chemical depression which will never get better.

    I always read the blogs I follow, and comment often. I also reply to comments left on my blog – or I leave a public thank you in a follow-up post if my brain is being a little buggy and I can’t respond directly to the person.

    I hope we can get to know each other. You can find my seperate blog about my eating disorder and how I’m trying to beat it at http://thoroughlydisordered.wordpress.com if you’d like to read.

    Regards,

    Missus Tribble.

    • Fiona says:

      Hello Missus Tribble! I love your username. It makes me smile! You are so right, that ‘that’ blog is good for finding good ones to read! So I guess, it does have a silver lining :) I really appreciate you coming here – thank you! I can’t wait to read both your blogs. I am sorry you have so much to endure. I have a friend who is a teacher’s aide with kids with Autism spectrum disorders – and she has told me, she admires those kids like nobody else, because everything they achieve in life, they have to really really work hard for, they can’t just take anything for granted like we do. I also have a few friends who have told me some of what they experienced growing up – being not understood, being pegged as just ‘bad’, going through horrible tests etc :( really really sorry you have been through always feeling so different and misunderstood.
      I’m so glad you are now able to acknowledge your ED and alcohol abuse – the very first steps to healing are recognising and admitting that there’s a problem. And it’s very hard to do, especially when they were helping you to cope and to NOT have to deal with your problems! You have a lot of courage and a lot of strength and I believe in you, you will make it. People like you who speak out about your experiences also help others like you – to be better understood. Best of luck and I hope to get to know you too (and if I ever miss a comment, you have permission to sicc all of wordpress’s trolls onto me, hehe) :)

      • Believe it or not, I’ve never seen trolls on any other blog! Writing style and subject matter has everything to do with whether or not the trolls will attack, don’t you think? Feeding them with heated posts about nastiness doesn’t help either!

        Thank you for your kind words. If I have to go through these things then I feel I might as well turn my experiences around and spin them into something that will teach, support, inspire and encourage.

        I can also be downright daft, so expect a few laughs along the way! D

        • Fiona says:

          Guess what, I’m daft too! So it will be fun :)
          I’ve seen trolls on one other blog – and that author does answer comments – is totally obsessed with them. But she’s totally nuts and narcissistic too :P

        • LOL! It seems that trolls don’t bother serious writers because they can’t get past all the long words! I have one blogger friend who is completely barking mad – but in a good way so people love her and the trolls don’t come to visit. Or, if they do, she slam-dunks them into the bin as soon as they appear.

          Today I was going to verge towards the silly and talk about the upcoming discworld Convention that my husband and I are attending at the end of next month :D

        • Fiona says:

          I think it matters a lot how well liked the blogger is – they can be not very good at writing but if they are nice people and liked, trolls won’t bother them. Also, it’s no fun trolling when the author is actually taking the time to moderate the comments. One click and byebye :)
          I would love to hear about discworld – because apart from guessing it might have something to do with computer games, I don’t have a clue what it is!

        • Discworld is a series of books written by Sir Terry Pratchett. It’s filled with wixards, witches, vampires, dwarves, trolls, dwarves, people with silly names and lots and lots of humour! People dress up as the characters, but a lot of us also cross fandoms and turn up with doctor Who, Firefly and Star Trek-related items.

          I’m a sci-fi and fantasy nut and I make no excuses for it :D

        • Fiona says:

          Wow! I used to love sci fi and fantasy – anything actually that I could read, a real bookworm. So awesome to get away from this world into a different one! But my cognition has been pretty poor for a while so I’m just getting back into reading at all again, i’ve missed it. I hope you dress up and post a photo of yourselves in costume!! have fun!!

        • Well… I don’t really resemble any of the characters enough (apart from possibly a young version of one of the Witches lol) but I had planned to get hold of a long blonde wig and go as the female werewolf from the City Watch (I has the boobies lol). Then I had a seizure coming downstairs and broke my toe just weeks before my weding in May, so I’ll use my wedding gown (red!) and be a vampire from Uberwald, or something. :)

          Because of this convention I’ve met some very influential writers and speakers, and found myself singing in the bar with Sir Terry himself! We can’t get to the next one (stupid money) but I hope we’ll be back there again in the future.

          Sci-fi has truly saved my sanity, the more restricted I’ve become. Without it I really would go mad!

        • Fiona says:

          It all sounds so much fun. I’m glad you have this to hang on to! I think a huge key to recovering from an ED is having things you are passionate about to hold on to and fill in the gaps that the ed leaves behind. Hope you have so much fun! xx

        • It’s more my husband’s fandom than mine (I’m a Doctor Who Girl all the way!) but a whole bunch of our friends are always there and we always come away with a few new ones!

          I’m going to be more careful in the pool this year though… at the last convention two years ago I still had this idea that I was up to the semi-pro standard that I used to be and I’m NOT. I made myself very ill in trying to be a competitive swimmer again, so this time I shall chill (and drag a friend in with me who is able to tell me when to stop)!

        • Fiona says:

          That’s a really good idea. I’m like that with exercise, it starts off okay but then gets out of control and I have to cut it right down again. I guess it’s something we will have to be careful with forever. I used to be a dancer and am dancing again, but I doubt I will ever do as much as I used to! Try and have fun – that’s what life is about I think :) enjoying it xxx

        • Oh don’t worry – fun is what I’m all about! What’s life without it? :D

          Apparently someone else has gone “Yay, sensible person” and followed me from That Blog :)

        • Fiona says:

          hahaha that’s wonderful hey?
          Life is full of surprises :) xx

        • Haha indeed! I went to take a look at this new follower and the first thing I see on her blog is an absolutely mind-blowing piece of creative writing! Much more my thing than people going mad through breathing the air! I mean, seriously?

        • Fiona says:

          I must admit, it’s sure hard to keep from watching it all play out over there. Wondering how long it will be before she replies to anyone if ever.
          Some of the writers I’ve met are amazing and like you, it’s such a small world to have found someone you relate to through such an unlikely source! Anyway I’m off to bed, it’s nearly 11pm here :) goodnight and can’t wait to talk more xxx

        • Sleep well new friend – speak to you soon xx

  15. I actually think that every post you make is a serious and deep one …
    :) :) :)

    I’ve had a PTSD myself for some years, but I don’t have it anymore now. I also had a severe depressions several times in my life. What I want to say with this is that I think I can somewhat relate. Of course your experiences are different from mine, but there’s a level on which we can relate. That’s an important thing.

    You’re such a fighter, Fi. Most other people would have broken under the burden you bear. You’re so strong. You probably don’t look like that on the outside, but I know you are on the inside, otherwise you wouldn’t have made it until here. And you know that strength on the inside is not only much more valuable but also much more lovable than mere strength on the outside. :)

    I’m very happy and in a strange way touched that you made it until now. In fact, I’m very thankful for it. It’s like a blessing. I hope you’ll go on with your way and don’t lose your courage. If you should need encouragement, I’d love to give you some any time.

    • Fiona says:

      It’s really special to me to read this, Kath, especially from you. You, and a few other of the blogger community have become especially dear to me. I know you are sincere with everything you say, I know you have been there too. I’m sorry you have been through so much, but at the same time, inspired and glad that you are where you are now and that you too have survived. I think it’s true – strength on the inside that has come from so much – it’s more loveable, more valuable… in coming this path of mine, I’ve had to eat a lot of ‘humble pie’ and I think that has a lot to do with some people being more able to relate to me too.
      Sometimes.. okay all the time, I get scared I will never be free of these troubles, that they will haunt me forever. But I read the writings of people like you, and know that it’s possible to heal, at least heal enough to have a better life than I do now.
      Sorry if I don’t make any sense, I need another weekend, this one has tired me out lol :) Hope you are having a good weekend too :) xxxxx

      • I feel the same about you. You’re one of my small handful of closest blogging friends, and I consider this friendship to be of a similar sincerity as my close real life friends. :)

        It *is* possible to heal, Fi. But it takes time, especially when the wounds have been very deep. For me it took several years to deal with all those things (more for some, less for others), and it wasn’t a gradual development but rather there were leaps and then plateaus or what even looked like a backfall but then it got better again eventually. You’ll definitely experience an improvement in your overall condition long before you’re well overall, because you don’t get well overall just like that, mysteriously, over night. You know it’s hard work. But I think you’ve made quite a part of the distance already, when you think about where you’ve been and where you are now. It’s probably also an illusion that you’ll be perfectly fine one day (me neither) – this I don’t mean to disencourage you, what I want to say is that certain memories remain and also the tendency for depression which I have as well, but your daily life won’t be impaired by that anymore every day.

        As I said before (I think), it’s that the good moments take more space and the bad moments less. I also like to think of my life being a house and my issues being monsters inside of it that mess up every room. What you then do is reconquer one room after the other. Some day, you’ll have your house back, and the monsters have either moved out completely or may have a room for themselves somewhere in the house where they can stay and make baloney, but which you decide not to visit anymore. Something like that.

  16. paulaacton says:

    I love the fact you are still trying to coax a response on the certain other blog – I admit it I couldn’t help but go back to check comments I just read the comments pointing out the real nutritional value of her breakfast of champions then saw her olympics one as usual she has ignored all comments rather than address the issues in a real and meaningful manner but you do realise she would not care which sport she did as long as she won gold and could sign autographs I was soooo tempted to comment and point out that it should be british not english talents and a million other things like if she had bothered to look at the time difference she might understand why the queen looked so tired

  17. What an exceptional writer you are, Fiona. <3

    • Fiona says:

      Hi Martha, it’s a gift that I’ve found some really lovely people through a certain blog – you being one of them. Thank you so much for your kind comment! I look forward to getting to know you better :)

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