Tag: ItsOkNotToBeOK

It’s okay not to be okay

Various images of Emma Charlesworth and quotes

Today is the last day of Mental Health Awareness Week, a week that the Mental Health Foundation has been leading since 2001 to bring the UK together to focus on getting good mental health. This year the theme is ‘community.’

It’s an interesting theme that isn’t it? Community makes you think of togetherness, of support and not being on your own, but in my opinion, the reality when it comes to mental health can be very different. Because despite all the great work that has been done over the past few years, mental health can still be a taboo subject. And not necessarily because of society but because of us as individuals. Since this day in 2018 when I made my first public post about a bout of counselling I’d been having to help me process depression and anxiety, I like to think that I’ve benefited from that honesty and the community around me. I’ve been an advocate for talking openly. Yet, towards the end of last year, I went the complete opposite. I stopped being open. I didn’t make use of the community around me. I pretty much struggled in silence.

And I completely know the reason for this. Because I felt like a failure. I’ve always been the sort of person to be a perfectionist and to just keep going, but in a way since my late husband died, I’ve felt a different sort of pressure. The pressure to be brave and strong. These are two words which have been used to describe me countless times. If I’d had a pound for every time I’ve seen them written about me or had them said to me, I probably wouldn’t need to work! I’ve said before that I don’t like the word brave but am coming to accept the word strong, but this has been to my detriment at times. I sometimes feel that f I’m so strong and an inspiration as people repeatedly tell me, how on earth am I meant to admit that I’m struggling, that I need help and that I just need to admit defeat for a while? In my head, I couldn’t let people down. I couldn’t fail at being a widow. I couldn’t let people see that grief was still having an effect over four years since my husband died. If I’m meant to give hope and inspiration to others, what would people think of me if they knew the reality?

But sadly, this was my reality. And I tried to hide from it and pretend it wasn’t, I really did. Yet for a myriad of reasons, towards the end of October, I knew I wasn’t going to be able to hide for much longer. And so, I made a call to our Employee Assistance Programme. I’m so incredibly fortunate to have a service like this at my disposal and it’s something I’ve made use of in the past, so I had an inkling that I knew what was going to happen. As suspected, following my assessment, I was referred for therapy. But a different type of therapy to what I’d had in the past, I was being referred for EMDR (Eye Movement Desensitization and Reprocessing) with CBT (Cognitive Behavioural Therapy). I’d come across these acronyms through others in the Widowed and Young (WAY) community but didn’t really know that much about them. If I’m being perfectly honest, when I first read about EMDR, it sounded a bit kooky to me! How could this possibly work?! Yet I knew I had to give something a try, it was time to finally process the trauma that I went through in 2020. And other trauma from my life up until that point.

You see, deep down inside I know when my mental health has taken a dip. I find it very hard to concentrate. Work feels unmanageable. I have no enthusiasm to do anything. My temper is shorter. I can’t juggle as much as I usually do. Life simply feels too hard. I doom scroll because to do anything else feels pointless. I can see the dip in my mental health in my eyes. My whole demeanour changes. I looked back at a photo of me with a friend that I’d taken in August and was desperate to get back to looking like that. Desperate to see that sparkle and lightness in my eyes. I know the exact moment I realised I’d achieved this aim of mine, but that’s a topic of discussion for another blog.

Yet I pretty much kept all of this and how I was feeling to myself. Colleagues knew because of needing to juggle work and appointments. They’d been slowly watching me go downhill for a while, so when I told my line manager, she told me she’d already flagged that they needed to keep an eye on me. That is one community I’m incredibly lucky to have. Friday was another great example of that community when I spent time with our team on Hampstead Heath as part of the firm’s One Firm One Day. It was great to be outside in the fresh air for the day especially during Mental Health Awareness Week and I became the queen of brambles! As we had a drink afterwards, someone I’ve worked with for a very long time commented that I looked lovely and snapped a pic. It’s one of the ones in the collage above. I looked at it and was reminded once again just how far I’ve come these past nine months.

Anyway. I digress. Back to November. My daughter knew that things weren’t great and I was back in therapy because I want her to feel comfortable talking about mental health and understand that therapy is not a bad thing. A few friends knew, a couple mainly because they’d been sat with me in a prosecco bar while I was crying (classy I’m sure you’ll admit) but I just didn’t feel capable of telling lots of people. It felt exhausting to do so.

And exhaustion is one of the reasons I made that call. My overthinking was off the scale. I’d struggled to sleep again. I’d wake up repeatedly. I would wake up just as exhausted as when I’d gone to bed. Sleep did nothing for me. I was stuck in what felt like an endless loop of being awake and feeling exhausted while all the while knowing the same would happen the following day because it wouldn’t matter whether I got one hours sleep or five, it made no difference. So, I just didn’t need anything else that would add to this exhaustion.

But at all points remember, I can’t give in to this exhaustion. I’m a solo parent, there is no-one else to help with the parenting. The constant juggling of who’ll do the school runs, the dance runs while maintaining a house, working full time, managing finances and trying to live is relentless. Especially when you’re doing all you can to keep yourself busy rather than face what you’re going through. So, I just kept going. I didn’t make the most of the community around me, because it just felt easier to do things myself rather than explain. I didn’t want to discuss what had led to me to reach this point. The realisations I’d had about my life and my behaviour. In a way I felt a little embarrassed that I hadn’t actually realised what I’d been doing. But that’s been my grief journey for you. I lived for so long in “survival” mode. Then I went into “I must live” mode. And then I realised I had to find a middle ground. Somewhere between surviving and running myself into the ground.

I had my first few sessions of therapy and found them absolutely exhausting. Oh good, more exhaustion to add on top. I was so, so tired. This is when I had to rely on another community. The WAY community. I’m on the rota for the New Member Zooms but simply found that the thought of hosting these on a day that I’d had therapy was too much. I had to ask for support to swap sessions. I had to be sensible and look after me. I then dropped a note on the WhatsApp group with other WAY Members that we formed after the AGM last year. I’d been trying to plan something and had just found that I didn’t have the headspace, so felt the need to apologise. Understandably this was an apology that I didn’t really need to make. Everyone got it. And when I admitted that I’d felt like a failure but had since had a word with myself, I was met with comments along the lines of that was good because if I hadn’t had that word, they would have done!

I relaxed into the fact I was back into therapy; I was vulnerable and honest in those sessions. So much came out that I didn’t realise I’d buried and never really processed. The actual EMDR began later than initially planned, but sometimes life just throws different things at you that throws things off course. You can’t really plan for anything. Yet in the run up to this, I started making little changes myself. I started saying no to people. I started to slow down. Christmas 2024 is a prime example of this. For the first time in my life, I spent the day in Christmas PJs. My daughter and I didn’t go anywhere. We didn’t have anyone to us. I cooked for the first time on Christmas Day making the most of Aunt Bessie. I just didn’t need pressure. I didn’t need expectations. This wasn’t about anyone else; this was about doing what I needed. Potentially selfish, but sometimes in life you just have to be. Equally I didn’t over-plan. I didn’t fill our weekends. I sent my therapist some photos of my calendar from August through to October last year vs. the photos of January to February. The difference was palpable. I was beginning to finally feel comfortable to be at home again. Being at home a lot of the time stopped being a trigger and making me feel like I was back living in lockdown when my world fell apart. I was finally starting to realise that I didn’t have to fill my time and always say yes to people in case if I didn’t, they stopped liking me or died.

This is a bold statement, but over the course of the next few months, EMDR* gradually changed my life. I sometimes wondered what people would have thought if they could have seen me sat there for an hour a week, with my eyes shut and just tapping the tops of my arms (my sessions were virtual and so this was the technique used). Things that previously would have caused me untold stress and been difficult to manage no longer were. Some of which had been the case for over 10 years. I couldn’t explain it. I didn’t understand it. I still don’t understand how it works, but it has certainly worked for me. I’m in the position now that I will happily talk about the last six months and my mental health. I can reflect on it in a way I couldn’t do at the start of November. Next week sees my final session and I’m not scared about this. It’s time for me to implement all I’ve learnt on my own.

Yet the past few months haven’t been complete smooth sailing. I completely struggled in March. I would find myself asleep on the sofa at 8pm. The exhaustion crept back in. They say the body keeps score and knows key dates and this certainly felt the case for me this year. The five-year anniversary of my husband dying was very difficult. I can’t pretend otherwise. It would be churlish to do so. But for the first time since he fell ill and died, both my daughter and I have been in therapy at the same time. Because in March I gave her no choice but to go back. Again. A myriad of reasons led to me making this decision for her. But at no point did I think she was a failure. At no point did I think she’d let me down. I knew it was what she needed to help her work through so very much. Funny isn’t it? I can be completely objective about therapy for others, yet when it comes to me, I still put way too much pressure on myself.

But fortunately, she grounds me. Another one of the photos in the collage was a selfie taken exactly one month after my late husband died during Mental Health Awareness Week in 2020. Like I say. I talk about mental health with my daughter so openly. She is way more in tune with mental health than I was at her age. Recently after a fairly hectic day, she simply said to me “you seem stressed, what’s wrong?” And thus began an honest and open conversation about my day and how I was feeling. Similarly, when I said I’d been wondering whether to write a blog to mark Mental Health Awareness Week but wasn’t sure whether I’d have anything to say, she simply gave me a look and said I’d have plenty, after all I could also talk about her. The fact she’s growing up with this attitude fills me with hope for her future, maybe, just maybe she won’t feel like a failure if she ends up needing therapy as she gets older. That she’ll learn to trust and lean on the community around her. That she’ll be comfortable being honest, open and vulnerable.

After all. Vulnerability is a superpower. Imagine just how much more powerful we’d be as a community if we leaned into this a teeny bit more.

*It goes without saying that this is my personal experience of EMDR and CBT. I am not an expert on these therapies and cannot provide advice on them.  

Hope is everything

Various pictures of the Charlesworth family to promote Children’s Grief Awareness Week

Two years ago, to mark Children’s Grief Awareness Week, I wrote a blog because the phrase “children are resilient” had been playing heavily on my mind. I felt it was clouding our view of how children who have been bereaved are treated. One of the points I raised that seemed to resonate the most with people was this: Needing help doesn’t mean she’s not resilient, that she’s mad, that she can’t cope or that she’s weird. It just means she’s human and vulnerable.

A lot has happened since I wrote that blog, but as I sit here today, on the first day of Children’s Grief Awareness Week 2024, there’s a new thought that is playing heavily on my mind. The fact that my daughter won’t ever really remember a life without grief in it. She won’t ever really remember her mum when she wasn’t grieving. Imagine that. Growing up with grief being part of your everyday life. I hesitate to use the word normal, because that is different for all of us, but ultimately grief, trauma and sadness are part of my daughter’s normal and have been since she was 10 years old. It breaks my heart beyond all belief that her innocence and childhood were snatched from her so cruelly.

Yet when I started thinking about this a bit more, I started thinking about the theme of this awareness week. #BuildingHope. Hope is probably the most pertinent word in my family. It’s the word I have tattooed on my wrist in my late husband’s handwriting. It’s part of my daughter’s name. And the fact that this grief awareness week begins on 18th November is also something that feels pertinent for me. 18th November 1993 is the date that I first really became aware of death and grief. These two things put together are why I knew I needed to write.

I’ve never really spoken about the fact that I too went through grief as a child. Mainly because in 1993, mental health or speaking about your emotions and feelings weren’t really considered. And certainly not for a child. But more than that. As the years have gone by, I have never really felt it was my story to tell. Yes, my family and friends at the time knew about it. It crops up in conversation with people to this day at times. But I haven’t publicly talked about it. I’ve had numerous different bouts of counselling over the years, but it’s never been a topic of discussion, there’s always been what I’ve felt are more pressing things to talk about. Yet recently I’ve stopped to think about how that day itself, the immediate aftermath and the bereavement I went through, haunts me and continues to affect me to this day. I suspect it always will. It’s a part of who I am. Because it is a part of my story. Whether I talk about it publicly or not.

It almost feels a bizarre coincidence in a way that both mine and my daughter’s first real memory and experience of death happened in what were fundamentally national tragedies. That we’ve both had to deal with death against a backdrop of news headlines and TV images. Such completely and utterly different circumstances, but the similarities are there, nonetheless. I was 12 years old. She was 10 years old. Having to adjust to a new reality without someone they loved in it. Becoming acutely aware from a young age that death can happen to anyone. It’s not just old people who die. Being aware of your own mortality before you’re even a teenager. It’s a lot to have to come to terms with.

I think this is what has led me to the realisation about my daughter having grief in her life forever. And I also think this is part of why I have so vehemently pushed her to talk about her grief. To have counselling. To try to help her process and make sense of the trauma she went through. The secondary losses she has faced. The future she faces growing up without her father. I want to do all I can to help her manage this unfathomable loss. To have it be a part of her story but not her whole story. To help her grow around it.

Whenever I talk about her and what she’s faced in my blogs, I always, always check she is comfortable with what I’m going to write. Because ultimately her experience is her story. There are some things which are just too personal to both of us to ever share. I won’t talk about them. I respect her views. Yet when I spoke about this blog, I could see the progress she’s made since that blog two years ago. The little bits of her life she is more comfortable for me to talk about now.

Shortly after I wrote my blog in 2022, my daughter and I joined Winston’s Wish Ambassador Molly for an Instagram Live together with Grace Lee, Director of Marketing and Communications for Winston’s Wish. The concept was for young people to talk directly and openly about their bereavements and grief. It was a classic case of Instagram vs. reality, in the 10 minutes before we went live, my daughter and I had some minor disagreements, she was stroppy with me, I was conscious of time so was blunt back and then the second we went live we switched on the consummate professional act! But as I sat there listening to Molly and then my own daughter, I was struck by just how astute they both were and how much they understood the impact that their bereavements had had on them. My daughter said things about grief that I’d never heard her say before. There were some real lump in the throat moments for me. I’d have never anticipated quite what was going to come our way just a few months later.

Because it was in February 2023 that I took my daughter to our doctor to get her referred for counselling. Her grief had manifested itself into anxiety. And it was becoming more and more difficult to manage. I’d had an inkling that this might happen the day of her great-grandmother’s funeral in January 2022, it was at the same crematorium as her dad’s funeral, she had to face all his family and by the time we got to the evening, she was shaking on the bathroom floor and vomiting. She couldn’t go back to school the next day. The anxiety and the stress that day caused for her was simply too much for her to deal with. It was another loss for her to have to process.

But by 2023, her anxiety had got to the point where she couldn’t leave the house in the morning for school without eight different alarms. Each of which to tell her it was time to do something else, be that go in the bathroom, get dressed or have breakfast. It felt unsustainable. Any change to that routine, a few minutes lost here and there was enough to cause a meltdown. There were days she didn’t even make it into school. She simply couldn’t process change. Everything had to be regimented. I watched as she withdrew into herself more. We argued more because I couldn’t really understand what she was going through. Because I didn’t understand just how crippling her anxiety had become. Just how hard her life was. Until she started her counselling, all I could do was love her and watch her suffer as she tried to make sense in her mind of why she was like this. As she tried to answer the question she posed herself “why am I like this?” It was, quite simply, heartbreaking to watch.

She was nervous about the counselling. She didn’t really know what she’d say. But as I sat on the stairs and listened to her first session, I could hear her talking. I was astonished quite how much the counsellor got her to say. After that I didn’t listen to her sessions, they were personal to her and I knew if there was a major concern, the counsellor would contact me. But for someone who was such a sceptic, these sessions helped her. Even she would admit this. Just last week, she commented on how she only has one alarm now and it goes off 35 minutes later than it did last year. This might sound small to someone who has never experienced anxiety, but to her it’s massive.

And while a lot of her anxiety has dissipated, it is still there. I don’t doubt it always will be to an extent. It’s part of her grief. We have found ways to help her manage it, but if things come at her left field, they do still cause her to feel anxious or to panic. She will openly admit she has trust issues. She struggles to let people in. She has abandonment issues. I don’t doubt that as she gets older, she will need therapy again. Because at different points in her life, she is going to need help to process her emotions. It’s a fact of her life.

And she’s also had to live with my grief being a fact of her life for the last four years. The fact I find myself crying anywhere, a supermarket, the theatre, in the car, the cinema… the list is endless. We recently went to see Paddington in Peru (I cried!) and on the drive home, we saw an ambulance with its blue lights on. No siren, just lights on. My daughter started making the sound of a siren, I laughed and said, “why are you being an ambulance?” To which she simply said “I know you don’t like seeing the blue lights without the sirens. It’s hard for you so I thought I’d add them.” Deep breath moment for me. The realisation that things like that are on her mind. How acutely aware she is of how I feel and my triggers. Three years ago, she was interviewed as part of a study on childhood bereavement, they asked her how her mum was coping. “She keeps herself busy and doesn’t sit still, because if she stops, she’ll have to think about what’s happened to us and she doesn’t want to do that.” Another deep breath moment. Because there are times her emotional intelligence is off the scale. But this also breaks my heart. She shouldn’t have had to become this astute. She shouldn’t have had to live with grief becoming a part of her world at such a young age that she’s been able to gain this understanding.

Her understanding, vulnerability and honesty are just some of her qualities that I am most proud of. I do believe she’s growing up with an empathy that she wouldn’t have if she hadn’t experienced the loss of her father and watched her mother grieving. She knows this herself. Towards the end of last year, she and I had a conversation in what is known as the “Jac McDonald’s” (mainly because this is where we ate before going to see Jac Yarrow on more than one occasion.) And while I’d rather not be having a deep and meaningful over a Big Mac, sometimes you just have to go with the flow of the conversation. She told me that she wouldn’t necessarily change what has happened to her. I was quizzical over this but the way she responded again just made me so proud. Her rationale was that she likes the person she is now, and she doesn’t know if she would be this person if she hadn’t gone through everything she has. Another deep breath moment for me. There is no real response to that. Without question, she will never cease to amaze me with how she has approached everything and the way she now reflects on her life.

Recently she and a friend went to their first gig without a parent. No way would she have been able to do this last year. And while I was a tad neurotic, when I got the text message from her to tell me they’d found their seats, had bought some merchandise and what time they’d worked out they’d need to go to the toilet before the main act, I breathed a sigh of relief. She’s got this was my overarching feeling. And as her friend’s mum and I waited in the venue for the gig to finish, I listened to the lyrics of one of the songs. The words that Henry Moodie sang felt like the perfect way to sum up my daughter’s response to grief and anxiety:

  • I’ve learned to live with my anxieties
  • ‘Cause I’ve got some bad emotions
  • It’s just a part of life, it doesn’t mean I’m broken
  • At the worst of times, I tell myself to breathe
  • Count to three, wait and see that I’ll be okay
  • ‘Cause I’ve got some bad emotions
  • Took a minute, but I’m finding ways of coping.

Anyone who is parenting a child who is bereaved wants to make it better for them. Anyone who has experienced childhood bereavement wants to feel better. Wonders when the grief and the pain might go away. Yet, as I’ve come to realise it doesn’t ever go away. But by talking about it and hopefully breaking some taboos, we can become more understanding of the impact, find techniques for coping and learn ways to support.

#BuildingHope is this year’s theme, and I cannot think of anything that is more fitting. It sounds clichéd. It sounds trite. But speaking as a mother who has watched her child ride the grief rollercoaster these last four years, I do truly believe that building and offering hope to those also experiencing this is one of the most powerful things we can do. 

Quite simply. Hope is everything.

One tip run at a time…

My world as I’ve come to know it came to an abrupt stop on 10 February 2022. After a complete reality check and some brutal home truths from my counsellor during my appointment, I went to see my doctor. And was promptly signed off work…

I messaged one of my friends to tell him what had happened. His response? “Surprised it took this long…” But for me it felt bizarre. The thought of not working for more than just a few days or being a full-time mum during the day just felt alien to me. Because it’s what I’ve been doing for two years to help give me back some control. To help me try to navigate this horrendous situation I’ve found myself in.

Let me give some context. I am, quite simply, a control freak. I’m the person who goes to Florida with a laminated itinerary. I can’t tell you how happy my laminator makes me! I’m the person who goes to Florida with a folder with different sections resulting in the car hire man saying, “bet she’s fun to go on holiday with.” (And yes, Mr C did laugh just a bit too much about this comment). I’m the person who organises. I’m the person who plans months in advance. I’m the person in control.

But on 16 March 2020, that stopped. No, that isn’t when my late husband fell ill or died, but when the advice came to work from home. Because in the blink of an eye, the control and the life that I’d known for so long vanished. Over the next few days, further announcements came. Schools were to shut. The UK was being placed in lockdown. My world was shifting and there was absolutely nothing I could do about it. And let’s not forget, by the time the UK was put in lockdown, my late husband was displaying signs of COVID-19 and gradually getting more and more sick. My ability to stay in control was being taken from me. There was absolutely nothing I could control about this situation. I hadn’t realised that this was going to be the way my life would feel for at least the next two years.

When he was in hospital, I wasn’t in control. I had to wait for them to ring me with updates. My life turned into just sitting by the phone waiting for news about the man I was meant to grow old with. And then he died. I pitifully began trying to claw back some control. I decided not to tell friends for hours so that they’d be able to find out when their children had gone to bed. I woke at 6:30am the next day and went downstairs to make a list of the people I needed to tell such as banks, insurances and pensions. I was trying to do anything I could to be in control. Because I simply didn’t know what else to do. I needed some sort of order in my life. I really wanted this back.

But the pandemic had other ideas for me. I don’t think any of us anticipated quite how long we’d be living under restrictions. I’d arranged house renovations, but they got halted by COVID-19. I lived with boxes in my bedroom for just over nine months because I couldn’t keep moving them to different rooms. It frustrated the hell out of me. I felt like I wasn’t in control of anything. Every time I tried to make plans to decorate, to make my house nicer or to take my daughter to the theatre, delays happened. We couldn’t see friends or family which we really needed. I couldn’t plan anything. My brain couldn’t take it. I was angry. I wanted a chance to help us adjust to our new life. I wanted to be able to have a shot at moving forward. But every single time, it got halted. And just as we got into a rhythm of me going back to the office one day a week and started talking about me doing more days post-Christmas, Omicron hit. The advice was given to work from home again. At the same time, things were changing at work, people were leaving my team (I obviously have no control over this), and it felt like everything was changing again. The stability that I’d managed to create for just a little while dissipated.

But I kept going. Until that day in February. When I finally had to acknowledge that I couldn’t keep going any longer. I couldn’t keep calm and carry on. I actually had to stop. I had to focus on me for a change. Nobody else. Just me. I’d been trying for two years to give us “normality” but when this feels like pushing water up a hill, it’s incredibly hard to do. The same friend who I’d messaged about being signed off gave me some advice, “use this time for a little mini reset, not to think “how can I use this time productively.”” He was 100% right. But actually, what he didn’t realise was how much I did need to use some of this time productively. Because to do that would help put me back in control of my life.

I have had a mini reset. I’ve stopped. I’ve not just kept going. In all honesty, I’ve probably done what I should have done when Mr C died. But it simply wasn’t possible for me to do then. The world didn’t allow it. I will always stand by my decision to start working again three weeks after his funeral, because it helped me feel a little more in control and if I hadn’t, I strongly suspect I’d have gone stir crazy. But I’ve sat and watched TV or just thought more times since February than in the last two years. I’ve spent time doing lengthy dog walks. I’ve spent time sitting at my late husband’s memorial bench. I’ve managed to do some exercise classes. I’ve spent time having coffee or lunch with friends, in my view, the best form of therapy. I’ve done some writing. I’ve shed many tears. I’ve breathed. I’ve put me first. I’ve stopped trying to do everything and be everything to everyone all the time.

Yet, I have also found it incredibly cathartic and beneficial to be productive too. I’ve put up shelves. I’ve built radiator covers. I’ve emptied Mr C’s wardrobe and sorted his clothes. I’ve sorted through cupboards and got rid of things we don’t need. I’ve been exceptionally ruthless because I have to live for today. There is no point keeping something I might need in the future because I don’t know what the future holds. I’ve got rid of glasses we were bought for our wedding nearly 17 years ago that we’d never used. Not all of them and not our wedding china, because I’m not ready for that, but anything we don’t “need” has gone. I’ve bought new furniture because we’d wanted to do this since we moved into our house nearly six years ago. I’ve been able to do things on my to-do list. I’ve smashed old furniture that we no longer need. I have done numerous trips to charity shops. I have done numerous tip runs. All of which have helped me feel more in control. For the first time in a long time, I was beginning to feel in charge of my own life again.

Until the week leading up to my belated 40th party. I spent most of that week throwing myself a pity party. You see, I’d decided the Sunday night before that I was going for self-preservation that week. I was absolutely going to do nothing and focus on me. 12 hours later, the universe had other ideas for me. A carpenter I’d had booked since April last year cancelled on me. I discovered that there had been a leak and my kitchen flooring which had only been down for six months needed to be ripped up. The floor had to dry out. Over the course of that week people pulled out of coming to my party. They were double booked, they’d tested positive for COVID-19, they weren’t well and while testing negative didn’t want to risk it, rising case numbers were worrying them… I absolutely respect all of this. I completely appreciate people’s decisions. But from a completely selfish perspective it wasn’t doing anything to help me. Once again, I started to feel out of control. Not helped by the issues in my kitchen, but mainly because I was feeling that COVID-19 was taking control away from me again and was going to ruin my third birthday in a row. I couldn’t get excited about it. I just didn’t care.

It took me until about half hour before the party started to get over this. At this point I realised that I wasn’t in control and there was absolutely nothing I could do about it. I would just enjoy myself and have fun with those people who were able to be there. And that’s what I did. I just stopped stressing and caring. I went with the flow. A slightly novel experience for me. But one that without question paid off. Because it was absolutely perfect. It was everything I wanted it to be (I’d been planning it since 2018 so you’d like to think this would be the case). I danced. I smiled. I had one of the biggest surprises of my life (probably deserves a blog in its own right). I just let go. I woke up the next morning feeling that my heart was full. Feeling content. I couldn’t remember the last time I’d felt like that. I knew it was something that I needed to hang onto.

And I’m trying really hard to do that. I know it’s not always going to be easy. I know that for me to survive, I do need my life to be a combination of being in control and learning to just let go and go with the flow. Because I’ve come to realise that as much as I’d like to be, I simply can’t be in control all the time. Life doesn’t really work like that. Yet, for the first time since March 2020, I honestly feel like I can begin to plan again. I can start to think about my future. I can book things for us to do which (all things crossed) won’t be cancelled or rescheduled. I recently went on a night out to celebrate my birthday. The same friend who had sent me that message in February was there and the next day he sent me this message. “You looked happy. You looked like “Emma.” Carefree. Was really nice to see.”

It’s nice to get messages like that. They make me smile. Because my mind is feeling clearer. I’ve got some annual leave next week and then I’m going back to work. I’m looking forward to it. I’m feeling a world away from the start of this year. But I know that life will always throw challenges my way. I just need to make sure my mind is as strong as it can be to cope with them. And I also look around and know that there’s still things in the house that need sorting. There are still shelves that need to go up. Pictures that need to go up. There are still things that need to be got rid of. And I know that each time I do this, it will help me. I will gradually take back the right amount of control that I need. One tip run at a time…

Goodbye 2021

If 2020 was the year of shock, numbness and surrealness, then 2021 was the year of reality. The year of trying to adjust to our “new now” (I don’t like the phrase “new normal” as who is to say what is normal anyway?) I should have been writing this blog in New York. Our first overseas trip just the two of us, the prospect was both terrifying and exciting. But just over three weeks ago I made the decision to cancel, the reality was that everything about it was adding additional stress and worry, rising case numbers, change in testing regulations, closure of activities in New York. Need I go on? Because this is reality. I am still trying to adjust to widowhood and solo parenting while living in a pandemic. COVID-19 hasn’t gone away.

But what is different about the end of 2021 compared to the end of 2020 is that I consciously made a decision to avoid stress. I just don’t need it. I don’t need to be putting myself through it. I think back to this time last year. I crashed on 27 December, it was all I could do to get up each morning and when I did, I pretty much just laid on the sofa. Mr C’s Memorial Bench was installed on 29 December and I had to summon the energy to get off the sofa to see it. Because I’d run and run and run to get to Christmas. I’d done so much. I’d tried to do very personal keepsake gifts for his immediate family. I’d tried to make everything perfect for our daughter. I’d tried to honour him in every way I could. But do you know what? It didn’t make him come back. I didn’t get to Christmas Day, get a pat on the back and get told “well done, he can come home now.” Reality hit. I’d got to Christmas, put myself under so much pressure and for what? I was quite simply mentally and physically exhausted. I couldn’t go back to work. I had nothing left to give.

This was how I went into January 2021. Exhausted. And then reality give me a real slap in the face. One of my most loyal, closest friends who had done so much for me after Mr C died lost her partner to COVID-19 on 2 January. Two days into the New Year. I felt helpless. I couldn’t bear to see her. Because to see her would make this real. To see her would be to see the tears in her eyes and know that there was absolutely nothing I could do to take her pain away. This wasn’t meant to happen. Nobody else I loved was meant to go through this pain. I had to tell my daughter that once again the pandemic had taken someone from our lives. Someone who had made such a difference to my friend’s life. Who had put the sparkle back in her eyes.

And then reality and the unthinkable happened again a couple of weeks later. I received a text asking me to give my colleague a call. It was a little odd as I’d only spoken to her that morning and wasn’t working, but I still did it. She had to break the news to me that one of my colleagues had been killed in a road accident. He was just 29. I thought back to the first meeting I’d had with him after I returned to work following Mr C’s death and the compassion and kindness he had shown me. How on earth could he have died in such a senseless way? His partner is in my immediate team at work. She is one of the most selfless people you could ever hope to meet. Simply lovely. Again. I felt helpless. I remember walking into my lounge after the call and my daughter asking me why I was crying again. I wanted to make something up. I couldn’t bear to tell her the reality that yet again somebody else I knew had died young. All you want to do as a mother is protect your child from hurt and pain, and here I was again telling her just how unfathomable life can be at times. How reality really can suck at times. But we had the conversation. Because this is what reality is. I can’t shield her from it. I can’t shield her from pain.

It’s why we have such an honest relationship. Because I’ve worked out that she deserves honesty. For a child of 11, she has been exposed to so very much. It breaks my heart. And while I don’t tell her everything, we do talk about so much. Because our reality has meant we’ve had to, we can’t shy away from pain, hurt and suffering. We talk about the fact I have counselling. Because over the past 21 months, I’ve spent 11 of them in counselling. It’s made me look at myself. It’s made me question a lot. And it’s also given me answers and helped me begin to come to terms with my reality. But nearly a year in therapy? I’d never have expected this. Even though I know how beneficial it is, the reality is that it’s still hard to come to terms with needing it in the way I have. To help me survive and be able to live a daily life. And despite the dialogue on mental health changing, it can at times be slightly taboo to talk about it and be open about being in counselling. To the point the fact I was having it was used against me at the start of the year.

I don’t hold it against the person who said it to me, because the reality I’ve come to accept in 2021 is that there is still a lot that society doesn’t understand about grief, mental health and life in general. I had a conversation at work recently about how society as a whole tends to focus on the negative, what you haven’t done, what you could do better etc… You hear the phrase “can I give you some feedback?” and instantly bristle because you assume it’ll be bad. To say “I’m having counselling” can, in some instances, cause judgement. The perception is you’re not right. You’re not good enough.  

But do you know what? 2021 has seen me become ok with that. I’ve come to accept that I will never be good enough for everyone. I’ve come to accept that there will be things I do that people can’t understand. Because that’s reality. But equally, I judge and do it to myself. I will automatically talk about everything that I’ve not been able to do since Mr C died. Because isn’t that what we’ve been taught to do? Focus on the negative? I’ll tell you I’m not as efficient as I once was. My brain doesn’t work in the same way. I’ll walk away rather than fight for what I believe in because I can’t handle stress. I don’t have as much patience or tolerance. I forget things. I buy presents for birthdays and Christmas and worry that they’re not good enough, but the truth is I’ve simply run out of energy at trying to get everything right. I have mum guilt like never before. I haven’t achieved as much at work as I’d have liked. I don’t call or message people enough. I haven’t been as good a friend as I might have been before because I don’t put as much effort in.

Yet this is where the counselling has helped and the Emma at the end of 2021 compared to the Emma at the end of 2020 tells herself to wind her neck in. Because I need to acknowledge that I’ve achieved a hell of a lot this year. I deserve to feel proud of myself. Whatever anyone else thinks or says. That is the reality. I have launched my own blog that has not only helped me but has also helped others. I organised my late husband’s Memorial Service which gave so many people the chance to say goodbye to him. I’ve learnt how to show my vulnerability. I’ve continued to work. I’ve kept a roof over our heads. I’ve organised home improvements. I’ve pretty much done everything we used to do as part of a partnership single-handedly. I can now go into supermarkets again. I’ve become an ambassador for Widowed and Young. I’ve taken my daughter away, to friends, to festivals, to theatres. I’ve given her new memories. But more than that. I’ve somehow got out of bed on days when I don’t want to. I’ve still put one foot in front of the other. Every single day. My daughter has not gone without love. There has not been a single day she hasn’t felt my love even when I’m in the pit of despair. This is my reality that I need to focus on more. What I have done. There will always be people who are quick enough to tell me what I haven’t done or should have done differently. But I need to have more faith and belief in myself. To remember what I have done. What I have achieved.

I’ve been reminded so much of this throughout this month. In the run up to Christmas, my daughter said “I just don’t understand why this Christmas is so much harder than last year.” We spoke about how last year we were in shock and survival mode. Whereas now we’ve spent the whole year coming to terms with the reality that her daddy really is gone. He’s never coming home. We will never spend another Christmas with him again. And that’s why it’s so much harder. Because it’s real. As each day passes, our reality and life without him crystallises. I listened to her repeatedly tell me she was over Christmas. I watched her sit on the sofa and refuse to move. I’ve just had to cuddle her because there was nothing else I could do to help her. But Christmas Day came and the punt of an idea I had for her present changed everything. She smiled again. She laughed. She sang her heart out on the karaoke machine. Yes, Christmas Day resulted in me being absolutely exhausted again because of the energy I’d needed to put into helping my little girl, but seeing her happy made everything worthwhile. I achieved that. I helped her get through it. And this just reinforced the reality that I’ve had to come to terms with in 2021. The ability to accept the rough with the smooth.

I can’t lie. I have very mixed emotions saying goodbye to 2021. The first year since 1974 that Stuart Charlesworth hasn’t been alive for any of it. Since 1996 that he’s not physically been a part of my life. A year which has caused so much new heartache and pain. A year which has seen relationships break down. A year which has seen me fall apart repeatedly. Yet it’s also been a year which has seen me smile, laugh, dance and hug more. It’s been a year that has seen me start to think about my future and my new reality. For the first time in such a long time, I can answer “I’m ok” and mean it when people ask me how I am. That’s not to say I’m of the view that life has become all cupcakes and rainbows. It hasn’t. I know as I go into 2022, my rollercoaster will inevitably dip at times. But I also know it will rise up too. Because I have plans. I have ambitions. I’m dreaming big. I have the best people around me. The hope and reality I’ve adjusted to in 2021 has taught me that I can get through and do anything if I really want to. Because I’m going to make sure I remember one thing in 2022…

I am good enough.

Taking off the mask

This was possibly the hardest blog for me to write so far. Because this one is about me. I don’t know how much of this people will already know. I don’t know who will be surprised by it. But I’ve always pledged to be honest. And it was during Mental Health Awareness Week three years ago that life changed for me, so it feels right to tell this story now…

You’ll probably be surprised to learn that this is a blog about my mental health given the pictures from Disney World at the top of it. But there’s a reason for including those. Because it was during this holiday that everything came to a head. I vividly remember storming out of our hotel room on more than one occasion. I vividly remember slamming the door behind me and telling myself my marriage had three months before I gave up on it. Yes, that’s right. In the happiest place in the world, I was miserable. My family were miserable. There were arguments most days. Yes we glossed over them and were able to have a nice time, but they were still happening. And what was the cause of most of these arguments? That things were going wrong, it wasn’t the holiday it was meant to be due to the weather, over tiredness and a lot of external pressure. And when it wasn’t perfect, I couldn’t cope. Because I’d put so much pressure on myself to deliver this perfect holiday that I felt the need to exacerbate every little thing that went wrong. I made it worse. No, Mr C wasn’t an innocent party, but I made things worse. I mean, just look at the photos, you can tell that things were strained, can’t you?

The simple answer to that question is no. Because despite the fact I was spiralling into a darker and darker place mentally, I wouldn’t talk about it. I became so adept at putting on a mask and pretending I was fine. I put the holiday photos on Facebook. I made sure that we were all smiley and cheery. To the outside world, Family Charlesworth had just had the perfect dream holiday in Disney World over Christmas. No-one knew what was really going on behind closed doors. And for a long time, I viewed this holiday as the start of my falling apart, despite the fact I had not been right for months prior to it. Yet Mr C later told me he viewed it as the start of my recovery because it made me acknowledge something wasn’t right. It took me a very long time to be able to look back on that holiday and not view it badly. I can do that now. I can look back at the photos and smile. I can look back at the 100-page photobook Mr C painstakingly put together for us and talk to my daughter about the memories that make us happy and laugh. Because it was a good holiday. I was just so blinded and in such a dark place that at the time I couldn’t see it. I focused on the negatives. When people would ask me about it, I couldn’t muster any enthusiasm for it. I would respond with “it was fine thanks”, “we had a nice time” or some other inane response but despite this, I still didn’t want to front up to how I was really feeling.

It’s why it took me a further six weeks after we returned before I made the decision to seek help. Not because I was afraid to, but because I had just accepted that feeling this way was normal. I just felt that talking to someone about what I was feeling (the constant exhaustion, the flying off the handle at any given moment, the inability to make a decision) was one more thing to add to the to do list. I didn’t have the energy. I’d have to deal with it then. Far easier to lead a miserable, exhausted life, than face what was going on. But after one argument too many, after getting just that one step closer to walking out, I gave in. I accepted I needed to talk to someone. I knew I didn’t want to end my marriage, it was just being a wife was just one more thing that I didn’t need to be doing. My marriage was always the first thing to suffer because everything else was prioritised on top of it. I just didn’t have the energy to put the effort in to that as well. I took it for granted that it would always be there.

And so, without telling Mr C I was going to do it, I picked up the phone and made a call to our Employee Helpline. I felt scared. Because I knew this was bad. I knew as they asked the questions and I answered truthfully that they weren’t going to put the phone down having told me to go away and that I was fine. I wasn’t. I knew that. But what I couldn’t get my head around was why, who needs counselling and help so that they can cope with everyday life? You see I’d had counselling three times previously but in my head, each time was for a valid reason. The first because I’d buried a lot since my childhood, my parents’ divorce and Mr C’s diagnosis and treatment for cancer. The second because I was going through a tough time at work and was struggling with a two-year-old, I never felt good enough. The third because I’d buried a lot of feelings after we experienced a missed miscarriage. Reasons. All valid. To ask for help because life simply felt too hard felt ludicrous to me.

But to talk to me at the start of 2018 when I was at my lowest, you would not have known just how bad it was and how much I really did need help. I didn’t want to tell people in case they perceived me as weak. Two people knew at work, and I was so lucky with the support they gave me, but I didn’t want them telling anyone else. I didn’t tell many family members. I told barely any friends. I look back now, and it makes me feel sad for Mr C. Because I don’t know if he ever spoke to anyone about what was happening. It must have been so hard for him to be living in that situation. It’s one of those things I always thought we’d get around to talking about, but we ran out of time. I hope he did talk to someone. I hope he felt supported. Because I can only begin to imagine how hard it was for him to watch his wife fall apart in front of his eyes for a number of months.

And then as I was coming to the end of my counselling, the Friday of Mental Health Awareness Week, 18 May 2018, my father in law said something to me which would change everything. He was paying me a compliment. He was giving me a little boost. But what he didn’t realise was that he was about to change the way I approached my life. In saying what he did, he unlocked something in me. It’s why I remember the date. What did he say? “You’ve got broad shoulders; you’ll just take it all on the chin. It’s what you always do.” He was right. To onlookers this is what I did because this was the facade I’d created. Emma Charlesworth could take on anything and it was all water off a duck’s back. She was strong. Yet as I left his house a little while later and sat outside my daughter’s school, I reflected on what he said. This really was the perception of me. And the only person who was going to change that and admit I couldn’t take it all on the chin was me. I’ll always be grateful to him for saying it, without it, I don’t know when, or if, I’d have started being more open. So, as I sat outside my daughter’s school, I wrote social media posts. I still wasn’t brave enough to tell people face to face, so social media felt like a way to dip my toe in the water. I shared that I’d been having counselling. I shared that I’d been living with depression and anxiety. I was staggered after these posts went live. No-one judged me. No-one called me weak. The support overwhelmed me. It really was ok that I was admitting that I wasn’t ok.

Over the following 18 months, I started sharing and to open up more. I became adamant that our daughter would not grow up thinking it was weak to ask for help. I would set a good example for her. I would make sure she always felt comfortable to talk about her feelings. But most of all, I didn’t want to wear a mask and put on a front anymore. I just wanted to be me. To be accepted for who I was, warts and all. In February 2020, just a month before he fell ill, Mr C recorded a video of me sharing my story for the internal news platform at work. He was so proud of me for doing it. Because for just over 20 years, this is what he’d wanted me to do. To just be me, to not pretend to be someone I wasn’t. To simply be Emma. Someone who struggles with life at times, someone who on occasion needs help to deal with life. Someone who isn’t perfect but is happy with herself regardless of this, because no-one is. But no matter what, she’s someone who refuses to give up.

He’d be proud that I can sit here now and reflect on all of this. He’d be proud that over the last few weeks I’m noticing things which could be little triggers indicating that I need to be a bit kinder to myself. I’ve started to wonder whether my inclination to open the laptop and work once my daughter has gone to bed really is because the work needs doing then or because it’s a distraction technique to stop me feeling lonely and being alone with my thoughts. When people ask me how I am, I’ve realised I tend to respond with what I’m doing to help my daughter and how she is. Again, I’m distracting because to think about how I am is just too hard. I don’t honestly know how I am. It’s raw. It has the potential to unlock something within me which I’m not ready to face yet. I can feel the emotion rising during conversations where I feel frustrated or disappointed, I’m not able to keep it under wraps. The Emma tone of old creeps in. Being hugged by a couple of people in the last few weeks (yes, I know rules have been broken here) made me feel fragile. I wasn’t ready for physical contact. The thought of the return to a post lockdown world makes me feel vulnerable. I’m still grieving, I’m still trying to process being widowed at 39, I’m still trying to adjust. I will be for a very long time. I want to hide away from people for a lot longer. And while I have had bereavement counselling to help me work through the immediate trauma of what we went through, I know at some point I’ll seek more. But I know that by recognising these triggers and understanding myself, it means I won’t hit rock bottom before I do this. I won’t ever allow myself to hit rock bottom again. Because the difference between now and 2018 is that I’m not scared to ask for help. I won’t be scared to tell people.

Why? Because of what I’ve learnt over the last four years, because I can now accept that asking for help doesn’t mean you’re weak. I ended a previous blog with a quote from Winnie the Pooh and this one is no different. Because one of the best quotes of all when it comes to mental health comes from Piglet. “It’s okay to feel not very okay at all. It can be quite normal, in fact.” Never a truer word spoken.