Checking in

It’s been a tough old week, friends. I know it’s been a while since I published on here, but I’m still rambling wherever I can. I have been popping links to publications in external articles under the ‘roles, awards and publications’ page, so if you want to see what I’m up to/currently angry about, feel free.

Whilst we’re on the subject of checking in, I hope you’re okay, and checking in with yourselves. The past week has proven that I am not checking in with myself, or adequately looking after my mental health – I suppose life just…happens – but I obviously have been neglecting myself. It’s funny: living with cPTSD (complex PTSD ) has taught me that no day is the same. And yet, whenever I notice my mental health slipping, it always feels like a surprise. I must get better at recognising the signs.

Anyway, stay safe and well: I will write something of more substance soon. In the meantime, if you want to see what I’ve been doing, Twitter is your best bet (@nosuperheroblog ). Til next time, friends…

Heather x

Unearthing silver-linings

Who’d have thought we’d be in this position? We’ve been locked-down since the middle of March and life as we knew it has been turned upside-down.

The covid-19 pandemic has been a real roller-coaster of emotions for many. There have been unimaginable losses, a myriad of changes and acknowledgement that life may never be quite the same ever again.

Like many, I have been working from home for the past two months, and staying at home where possible. Although it has obviously been a real change to my daily life, there have been some unexpected positives that have come from all of this. I’m fortunate enough to be able to access therapy over video-calls, and being locked-down is reducing any outside stresses, allowing me to really focus on getting the most out of my sessions. It’s been one of the little silver linings I’ve seen peeking through, and I am going to grab this opportunity to reflect, heal, and learn with both hands.

My mental health story is something I have shared on no superhero before, but last year was a really pivotal time for me. I was diagnosed with complex PTSD (cPTSD, CPTSD, C-PTSD). Obtaining this diagnosis was key for me, as it helped me to start the long process of unravelling the mechanisms behind my mental health, my beliefs and my behaviours. 12 months on, I am acutely aware that this process will not be an easy one, nor a quick fix. It’s going to take a lot of time and effort. One day I’ll share a little bit more about cPTSD and my experiences, symptoms and story. But for now, as I sit in my flat surrounded by the things that spark happiness, warmth and love, I am feeling like I’m at a Good Point in my journey. It is possible to find some light amongst the dark. It is possible to unearth those silver linings. And I am going to make the most of them showing through.

It’s been quite a while…

…hasn’t it?

I am writing to you in April 2020 and as far as I can tell, my last post was at the end of 2018. Now if that’s not a break from blogging, I don’t know what is.

My absence wasn’t deliberate or elaborately engineered (I promise!). I just think last year turned out to be a Very Big Year in lots of ways. Just to give you an idea of how hectic it was, here’s a list of some of the key events that happened in my life last year:

  • bought a flat
  • renovated the flat
  • got a new job
  • finally got targeted, specialised help for cPTSD (more on that later)
  • ended a relationship
  • started a relationship
  • won some awards
  • worked with various charities, publications and institutions
  • did all the other Adult Things you’re meant to do
  • managed to survive
  • kept my guinea pigs alive

So…it was a lot. A. Lot.

2019 was a really pivotal year for me in a lot of ways. It was painful, transformative, exciting, and – to be quite honest –  it was really blooming difficult.

2020 is turning out to be Quite the Year for all of us, I know, but I think 2019 was good preparation for me. When I give myself the time to gather my thoughts and think about how ridiculous the past couple of years have been, I am really quite baffled. There’s so much to address, I know I can’t fully explain it all in this measly, rambling post.

What I will say, is that I’m prepared to talk, and reflect, and consider. I am thinking of making some changes to nosuperhero: I am thinking I need to share what I’ve been doing a whole lot more (because although this little blog has been somewhat neglected, I’ve been doing plenty of work for other publications, charities and local committees). I am also thinking that nosuperhero.co.uk could do with a little update and makeover. I am also hoping that – even though my little blog has been a little sparse as of late – I can continue to work in this space, and continue to work towards making the world an altogether better place by sharing my stories, sharing my thoughts, and sharing my ramblings, no matter how uninteresting they may be.

So, a big hello from me. A big hello from nosuperhero.

It’s good to be back.

Disabled, Diverse and Talented: a snippet from the Children’s Media Conference 2018

Earlier this year, I was fortunate enough to speak at the Children’s Media Conference on behalf of Inclusive Minds. I used this opportunity to discuss the importance of authentic representation in literature. This is something I am incredibly passionate about, having studied literature at university, and this event gave me the opportunity to speak with like-minded individuals working in the media.
I just wanted to share the transcript of my talk with you. I hope you enjoy learning a bit more about my motivations for disability advocacy and campaigning and the profound effect representation can have on validating and acknowledging an individuals’ differerences.

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Disabled, Diverse and Talented: Media, What Are You Waiting For?

Diversity: it’s the word on everyone’s lips right now. And – whether you like it or not – the word is well and truly here to stay. Employers are asked to make sure their workforces are diverse; creatives are reminded that their content is diverse, and, perhaps more importantly, that it can be accessed by a diverse audience. As the field of disability rights becomes more and more prevalent, and as more people are finally becoming aware of the ableism and disablism that disabled people are subjected to, diversity is becoming an integral part of everyday conversation. So, that begs the question: as media professionals, what’s in it for you?

A story I often tell at events like these is a very personal one, focused on my own experiences of university studying English Literature. I’ve always been an avid reader, so a degree that consisted of hours and hours of reading seemed rather apt. I’ve always found books fascinating: I was captivated by the way that narratives were so carefully crafted and interwoven, and the ways in which such intimate expressions of the human experience can be portrayed through words alone. During my second year, I chose to take an extremely popular module called ‘Classics of British Children’s Literature’. I was expecting this – probably naively – to be a nostalgic trip down memory lane, but instead, it completely changed the course of my studies. We were asked to read Hodgson-Burnett’s The Secret Garden, something I was aware of during my childhood but not something I really ever read; or at least it wasn’t anything that really had an effect on me. I remember – incredibly vividly – sat in the newly-refurbished Brynmor Jones Library and stumbling across the following: ‘…he is a hunchback…[and] it is horrid,’. What I haven’t mentioned yet, which is very integral to my story, is that at the age of 13 I was diagnosed with Scheuermann’s Kyphosis, and I remember the words thay came out of the consultant’s mouth on that fateful day: ‘You have vertebral deformity…a hunchback, if you will,’. This, alongside my pre-existing form of cerebral palsy came as a real blow to me. Stumbling upon those lines brought that familiar sinking feeling washing over me. My cheeks flushed red. I felt a deep-seated shame emanate from the pit of my stomach: those days stood in front of the floor-length mirror trying to desperately straighten my back to no avail. For a long time, I hated the way my back looked, and amongst those pages, those words really hurt. what was worse about this, was that when I came to discuss my issues surrounding this book in the seminar that week, no one really batted an eyelid. Whilst I accepted that the book was written for early 20th century readers, I found it hard to accept that my concerns were not being addressed by my lecturer in 21st century Britain.

It’s said that there is no friend as loyal as a book, but right there and then, I felt betrayed by one of the things I loved the most. I’d worked for a long time to get to a place where I was comfortable and happy with my body’s differences and appearance. But those words spoke loudly to that internalised ableism I’d carried around with me for years, something shared by the majority of the disabled population. After my experience in that seminar, I made it a mission of mine to search out for more accurate representations of people like me. I wanted to find characters in pages and on stages that had disabilities and lived their lives in either ordinary – or extraordinary – ways. Maybe they were embroiled in a dramatic family saga, or went on fantastic adventures. Where were the protagonists who got up and lived their lives embracing their disability rather than following the typical narrative trope of bitter and twisted individuals desperate to be cured?

A woman stood at a lectern wearing green dungarees pictured mid-sentence. Next to her is a large board covered in pictures and there's a large screen on the right of the picture with a powerpoint presentation

We all know that media is one of the most powerful forces in the world. I’m sure most of you attending Children’s Media Conference are here because you are creative individuals with grand ideas and a view of changing the world, no matter how small. You strive to create a world of fun, education and interest for children. You know how much your creations have the ability to impact upon young children’s lives. You work to harness that spark of imagination within individuals’ eyes, and want to watch it grow into a fire roaring with enthusiasm and excitement. We all know that there is nothing more validating than seeing a reflection of your true self – differences and all – captured through the written word or lit up on a television screen. It paints a picture and conveys a message that says that you matter, you are worthy, and that, most importantly, your life and experiences matter. Nothing quite beats that.

This experience was perhaps the main catalyst for commencing a Master of Research postgraduate degree where I made it my goal to uncover lesser-known literary portrayals of disability that were more true-to-life and accurate in their manifestations. Imagine my joy, then, when I came across Emma Henderson’s protagonist Grace Williams, a girl with the same type of hemiplegia as me and a spinal curvature alongside it.

Behind the scenes and screens is a good place to start cultivating these characters and representations that have the power to bring so much validation and happiness to children and young people. I do not think it’s a prerequisite to have direct experience of each of the many facets of diversity to render it into media, but we need to acknowledge that consulting those with real, lived experience adds authenticity and insight to your creations. When you employ a disabled person, and ask them for their honesty and opinion with regard to ascertaining an accurate representation of their lives, you are unlocking a plethora of knowledge, which – when transferred and translated into whatever you’re creating – has the ability to validate the lives of thousands, if not millions, of individuals.

A woman stood at a lectern wearing green dungarees. You cannot see the front of her face. Next to her is a large board covered in pictures and there's a large screen on the right of the picture with a powerpoint presentation.

Now is a good a time as any to make truly positive changes, and in turn to shape perceptions and enrich the minds and lives of children and young people. I longed for characters to be like me when I was growing up, but they never materialised. However, organisations like Inclusive Minds – for which I am an Inclusion Ambassador – gives authors, publishers, agents and other creatives the opportunity to find out more about the lives experience of under-represented individuals, can help make this positive change a reality.

I know your work is devoted to making children’s lives richer by whatever means possible. You truly have the ability to enact real, meaningful change in your fields.

Happiness is…

…soft lamp light, an abundance of throws, tea sipped at just the right temperature, scribbling on a crisp, clean page, crossing off items on my to-do list, the crinkle of a packet followed by a duet of wheeks, the light glinting off a freshly-polished table, sunlight streaming through the window in the early hours

‘The Girl Who Took a Rocket to the Moon & Other Stories’*

Mental health.

It’s something we all have. Yet none of us seem to want to talk about it.

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‘The Girl Who Took a Rocket to the Moon & Other Stories’ is a book, aimed at adults and children alike, that attempts to break down the stigma surrounding mental health, creating a conversation within which individuals can discuss their own issues with others.

Jenny Eckloff, who wrote the book after seeing a loved one struggle with their own mental health, has written seven short stories that encompass all aspects of mental health. From tackling anxiety, to depression, to panic attacks, Jenny’s book – illustrated by the talented Sammie Ripley – showcases stories that are relatable, yet often poignant.

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Though it capture the multi-faceted nature of the human emotional experience, the book is very accessible. The stories are short enough to be read easily, and would make a great bedtime story for little ones. They address panic attacks, depression and anxiety in an open, non-judgemental way, allowing the characters to overcome their difficulties and with the understanding that it is okay to talk.

A particular favourite of mine – ‘The Fallen Star’ – addresses the difficulties individuals have in seeking help, and encourages others to be there when individuals do reach out:

‘…maybe sometimes, stars need to fall and even though he couldn’t fix it, he just needed to be for it when it did…it takes great strength to ask for help…and it takes equal amounts to fix yourself.’

As someone who made that very first step in addressing my own mental health, these words were particularly resonating. It is hard to seek help, and even harder to actually help yourself. The glossary at the back of the book is a wonderful, concise resource that can be used explaining anxiety, panic attacks, depression and more whilst reading the stories.

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Reading Jenny’s book – alongside Sammie’s whimsical illustrations – is a really lovely, affirming experience, and would make a wonderful gift to those struggling with their own mental health, or the mental health of their loved ones.

Thanks so much to Jenny for letting me review your book: it truly is wonderful, and I hope you continue to break the stigma and taboo of mental health one story at a time.

You can follow Jenny on twitter @Reckless_Winter, see her website at http://www.jennyeckloff.com .

You can also look at more of Sammie’s wonderful illustrations over at: https://www.instagram.com/samsillustration/

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Happiness is…

…snuggling up in front of the fire, guinea pigs splashing around in a bubble bath, hot steamy showers, the wave of pain relief washing over me, making plans and chasing dreams, wrapping up in a toasty blanket, rain running down the window pane, sleepy smiles, cloudy winter mornings 

Disappointments, Direction and Decisions: Visiting the Musculoskeletal Clinic

Yesterday felt like a big, anxiety-inducing, sad-making day.

I woke up early knowing I had to attend my MSK Clinic appointment with butterflies in my tummy and a raspy dry throat. Perhaps it seems a little over dramatic to feel this way, but I’d be lying if I said I wasn’t anxious.

Truth is, I had been waiting for this appointment for months, having had to be re-referred to a different service in a different part of the country since moving back after my university studies. This appointment would determine what kind of support I’d be entitled to back in my hometown, and having got used to the routine and effectiveness of treatment back in my university town, I was extremely anxious at the prospect of having no support at all, which seems like an exaggeration, I know.

You see, it is very much a postcode lottery when accessing healthcare.

As much as I love the NHS, I must say there really is a huge difference with regards to provisions and accessibility depending on where you are in the country. It’s all a bit touch and go with certain services, as each have different approaches. Back in East Yorkshire I’d been lucky enough to receive frequent acupuncture treatment, excellent mental health treatment through several talking therapies, and access to a neuro consultant, occupational therapy and physio. Though I’d seen a physio and neurologist a long time ago back home, I hadn’t ever seen an occupational therapist despite having cerebral palsy. I also hadn’t had frequent acupuncture, or had monitoring of my curvature since the age of sixteen. It made me anxious to think all the fantastic progress I had made in Hull could possibly be stripped away just because the services and provisions aren’t available here.

All of this explained the butterflies and raspy throat, I guess.

As I suspected, things have changed. Much to my disappointment, they don’t offer acupuncture here. This was a little hard to swallow (and accounts for my exclamation of ‘oh no!’ in the consulting room) and though I was offered facet joint injections back in East Yorkshire, I was told I probably won’t be able to have them over here for a few years owing to my age. I might also have to consider a spinal fusion in the future (eek!) so they’d want to reduce steroid exposure to a minimum.

Again, fairly disappointing.

It’s not all bad, though. I will be discussed at their monthly review -‘they’ being made up of doctors, spinal consultants, neurologists, nurses and pain management specialists – and it is likely I’ll be able to access support to help with the mental struggles of the cerebral palsy and scheuermann’s, which is really quite exciting considering this aspect has never been discussed. I’ll also have specialist physio, with therapists who know the condition, and will be able to advise me accordingly, a change from the ‘I’ve never actually seen scheuermann’s in a person before!’ physio I’ve had previously. So, I’m feeling a bit mixed-up about this one. I am seriously gutted I can’t have acupuncture, and will be looking into private treatment options.

However, I am feeling a glimmer of hope, and really feel that the mental health focus will help. It is also lovely to know I am not alone, so a big thank you to Ben for coming with me to my appointment. This is a start, and I have at least some direction, and I’ll just have to hang tight and see what’s in store.

I’ll get there, I’m sure.

Sending warm bear hugs on this chilly day…

Heather x

Happiness is…

…the squeak of a guinea pig, the sparkle of an icy road, warm hugs on chilly nights, the crunch of an apple, cold rosy cheeks, the putting on of a woolen hat over red ears, drying tears, a sigh of relief when the worst is over.  

Therapy: Letting Go

It’s been a while since I started CBT, and I recently had my final session. CBT, though essentially great, brings up some conflicted feelings. I suppose that’s inevitably the case with  any talking therapy, but as my CBT went on for almost three months, I feel like I really invested a lot into each session.

Therapy for mental health conditions can be really helpful, but – and as with any treatment – you can’t expect a quick fix. Admittedly, though I’ve had counselling before, when I first started CBT I didn’t account for just how hard I’d have to work and how emotionally draining I’d find it. Walking out of the first session I felt simultaneously overwhelmed and absolutely empty, and I remember walking around the nearest supermarket aimlessly and directionless, with what felt like a flick-book of every emotion I’ve ever felt whirring through my head. It did, of course, get easier over time, but I always found it difficult to snap back after each session. 

Each of my sessions were tailored to me each week, depending on the situations I found difficult, and the topics I really needed to address. I loved this part of the session, as we’d draw up an agenda and tackle the issues most important to me. Essentially, though, what each of my sessions boiled down to was working through my low self esteem and trying to recognise and acknowledge the good things I have done. Thing is, I get so blinded by feelings of anxiety, hopelessness and inadequacy that I completely ignore the good and positive things I have achieved throughout my life.

I also spent a considerable proportion of my sessions working through hypothetical situations that I often worried about, with the aim of learning to accept  that I cannot control everything in my life, and I cannot solve everyone else’s issues. This was a particularly challenging topic to address, but I feel like I made some really positive progress in learning to accept and work through these issues.

CBT also addressed what felt like a dirty little secret for far too long. Thing is, I always suspected i had OCD-esque traits, but I’d never actually been diagnosed. Along with the assessor prior to my CBT, we agree that I do have OCD that fluctuates from day to day. I have always been a stickler for routine, but I knew things were a bit unusual when I found myself checking clothes, and jewellery, and other things that really didn’t require constant checking, like whether my alarm was set or that my door was locked, even though I could see that the latch was on. It’s frustrating, because no matter how much I know that these things don’t need checking, I cannot resist. And if I try to resist, I feel an unstoppable anxiety bubbling up which can only be ‘quelled’ by checking. Of course this only reinforces the behaviour, which makes it a really hard cycle to break. I have worked on techniques to help, and I am noticing that I’m getting better, even if this progress is only slow. 

CBT provided some great coping mechanisms to work towards in order to reduce the symptoms of anxiety and depression. These include keeping logs of activities that I’m particularly apprehensive about, or recalling situations that I found difficult and then examining mine – and other people’s – responses. Crucially this made me acknowledge that situations aren’t as bad as I expect them to be, and that working on evidence – and not speculation – is key to working towards a happier, less anxious life. 

Now that my CBT has come to an end, I’m facing the everyday struggles with a mixture of apprehension and pride. I’m proud because I’ve really improved, but apprehensive because I suddenly feel all alone. The relationship with your therapist becomes a really important one; they’re there on a professional level, to help you through what can sometimes be the most challenging times of your life, but they somehow become more than just a confidant as you build up a relationship with them. You open yourself up completely to them, and they are privy to some of your greatest fears, deepest emotions and darkest secrets. They become integral to working through your mental health issues, and  invest a great deal of time and effort in helping you. I feel a little bit lost facing the big, bad world on my own, but I am so grateful that my therapist has equipped me with the skills to tackle this on my own. 

I suppose I’m finding it difficult to let go. I know that I’ve only just embarked on my ‘journey’ (and no, I’m not keen on that explanation, but it’ll have to do) but I know it’s going to be a long, hard slog. My mental health does fluctuate, and dealing with my physical disabilities brings another layer of complexity to proceedings, but I’m positive that I’ll get there; whenever ‘there’ may be. 

I am letting go, and I am learning that I can do this on my own. I just need to prove it to myself.