A Year to Heal, Creating a life worth living, Self Care

Not waving, drowning.

7.30am. The water feels deliciously cool as I walk down the steps into the pool. The kids have been dropped off at the bus stop, and I’ve realised that rather than turning around and going back home, I could keep on driving and get to the leisure centre for an early morning swim. I’ve registered with a local scheme that gives a free swim pass to children with a disability, and to their parent/carer- it’s time to make use of it. I’m not much of a swimmer, but it’s not so much the swimming itself, it’s the noise and splashing and kids jumping in over my head, and the wet floor that brings me out in an overwhelmed, hyper-stimulated anxiety attack. At this time in the morning though it’s quiet, just me and the pensioners. I desperately want to get back into shape, feel fitter and healthier but since my battle with plantar fasciitis last year I’m nervous about putting my feet under strain. This seems to be the right answer; quiet, calm, gentle. My old-lady breaststroke style of swimming is entirely fitting here, fast enough to still count as exercise, yet giving me the space to iron out my thoughts and ease into the day. I begin to get excited; I’ve found something that works for me, 20 minutes of respite, of precious and healthy self-care to start my day with. Can I keep this up during the holidays when I don’t have the school run? I ask myself, feeling that the answer is still a yes. I know I need this.

I swim on the Monday and Wednesday. Friday morning, I’m tired but push myself to pack my swim bag anyway – I want to make this a habit and I know I’ll feel better for it. My membership card scans on the way in and I head to the changing room, only to hear the shrieks of over-excited kids already in the pool. I peek in and see lots of children throwing a ball around in the pool. Evidently, it’s not the early morning session I was hoping for. Back to the desk; Sorry, I’ve only just started coming in the mornings, is it on at a different time? The receptionist explains that the swim session doesn’t start until 8am on Fridays. A 20 minute wait; I decide to head back to the car to retrieve a book to read, given that the cafe doesn’t open until 9 and there’s absolutely nothing to do but stare into space in the meantime.

7.55. I’ve been reading in the car, but now put the book away and head back in for a swim. This time however, my card doesn’t scan. “Can I take a look at your card?” the receptionist asks, scanning it at her desk. “Oh, there’s nothing on your account, you need to pay.” I explain that I’m a member of the free swimming scheme. “No, that’s only if you’ve got the young person with you.”

I leave.

There are tears in my eyes as I stop off at the 24 hour supermarket to pick up something for dinner. I’m struggling not to cry as I drive home. I check the website for the swim scheme. It’s badly worded, talks of free swimming for disabled children and their Carers, but says nothing about it being only when you’re accompanying your child. I even phone up to check.

“Is it possible for the organisation to ask for Carers to be able to swim for free, just to give us some respite?” I ask.

“No, the leisure centres are doing us a favour as it is,” she answers. As if the leisure centres weren’t raking it in already, and also receiving public funding.

“But the over 60s swim for free?” I’ve heard the chatter in the changing rooms – these are pensioners who are not struggling financially. I don’t understand why they can swim for free but Carers can’t.

There’s the bottom line; I can only swim for free if I’m taking Lily. Except of course, I can’t take Lily to the early morning sessions, even if it didn’t clash with the school run; she’s far too loud, too chaotic. There would be complaints. Similarly, it’s hell for me to swim during Lily-friendly sessions; I just can’t bear it when it’s so loud and crowded, that adds to my stress rather than relieving it. I desperately need respite, and I desperately need exercise – but I will have to pay for both. If I managed to get a concessionary swim price, it would be £2 per swim. £6 per week. Over £300 a year. Non-concession, it’s £3, £9 and over £450. Our much-longed-for holiday, in other words. So while I could bumble along paying £2 per swim, I would no longer be enjoying the sessions because I’d be thinking too much about what they cost. It would cease to be me-time and become something I was paying to do in order to get fit. No longer a treat. I should be able to move money around, do it anyway – yet mentally and emotionally something has shifted in a way that’s hard to explain. Perhaps it’s because the free swimming felt like a gift, an acknowledgement that caring for an autistic child is so difficult and here was somebody who wanted to help me in some way. Having to pay turns that into Tough. Get on with it. Perhaps I’ve just reached the end of my rope, can’t take any more knock backs. Perhaps it’s anger at how once again, the people at the bottom of the ladder miss out; if you’re struggling financially then exercise becomes a luxury. Realistically, even “free” activities require money; eg a decent pair of trainers if you’re taking up running, otherwise you’ll wreck your feet.

I’m left feeling like I can’t have nice things. That the Universe has some kind of personal grudge against me, that this has been a pattern for over 10 years now; any time that I find something that makes my life easier or happier, it’s taken off me again. Just a taste, just enough to get excited, then – poof! Gone. That I want to be happy, grateful and generous in this life – but events keep conspiring against me to a point where by rights anger and bitterness should surely be the default emotions. It’s so much work to try and reverse this negative spiral – yet it’s like pushing a washing machine up the helter skelter; crazy, difficult and the minute you try to rest for a minute, it’s going to slide back down and crush you.

A few days pass. I talk to Mum, who does her best to talk sense into me. “That’s only what you’d spend on coffee and cake in a cafe, and it would be doing you good,” she reminds me.

“Yeah, it’s just I’ve taken out gym memberships before and just wasted them, haven’t gone in.” Being surrounded by no-neck muscle-grunters and perky gym bunnies is not my idea of fun.

In the meantime, my blood results come back from the GP; surprisingly my thyroid is working just fine and for once I’m not anaemic – my constant tiredness is a medical mystery. However, I’m now officially in the pre-diabetic stage. If I don’t get my weight, blood sugar etc under control then I’ll likely develop Type 2 Diabetes within the next 5 years. I’ve been wanting to improve my general state of health – the blood results are the final kick in the pants that I need. It’s back to the 5:2 plan, to cutting my emotional dependency on sugar and comfort food and to getting back into shape. Perhaps the lesson that I need to learn is not that the Universe doesn’t want me to have good things, but that it’s time to start looking after myself properly, which means being willing to invest in my health . I call the Leisure Centre.

Hi. I want to take out membership.

A Year to Heal, Creating a life worth living, Home, parenting

The gift of an ordinary life

I think I might just have got the very thing I’ve been asking for for a long time; a week where nothing happened. Granted, it was preceded by a mental health crisis that I could have done without, but then there was definitely almost a week where there were no new problems to deal with. I cracked on with the garden, the housework, trying to catch up in general. It was bliss. This is what normal must feel like, I told myself. With the weather being so beautiful I’d persuaded the kids to catch the bus to and from school, which meant a much earlier start in the morning but resulted in so much more time and energy for me.

Of course, it couldn’t last. I made every effort to let the Universe know how much I appreciated the gift of a quiet, ordinary week in the hope that I would continue to be so fortunate, but no. Normality resumed. The quote for the shower came in around £500 more than expected. A phone call from school to let me know that other parents were expressing concern about Lily’s behaviour in class, given that she spent the whole time talking about being a vampire, seeing demons and being in possession of a Deathbook, all of which caused too much disruption in class to be tolerated. The CYPS crisis team had been contacted and were expressing concern that Lily’s epilepsy medicine might be behind what appeared to be some kind of delusional psychotic crisis, and the teacher urged me to contact them myself. Why? I found myself thinking. This is just normal for us. None of it is actually real, it’s more that Lily is now play-acting to an absolute extreme. A second call the next day to say that Lily had spent her IT lesson refusing to do any work, insisting instead that she needed to use the internet to help solve a murder in Utah. Thank God it was the last day of term, although the pastoral teacher didn’t think I was going to survive half term looking after Lily on my own and ordered me to make an appointment with the GP as soon as possible. All of this happened while I was in the middle of a meeting with a local charitable organisation in the hope that they could help me get back into work. Frankly, it did nothing but prove that a job would be impossible to handle right now.

The plan was to head up north to spend a few days with my family and celebrate my Dad’s birthday. We set out over an hour later than I’d hoped, because of course Lily had decided to get the late bus home from school so she could do her music, despite knowing we were heading out on a long drive. Similarly Ivy hadn’t bothered to pack the night before as requested, and the minutes slipped by later and later while I despaired of ever leaving, knowing how tired I was going to feel with a five hour drive ahead of me. Almost as soon as we set out though, the car started flashing up error messages; faulty brake light. Error; Anti pollution faulty. The car was struggling to get up to speed, feeling sluggish and juddery. I pulled into a garage to double check my air pressure, in the hope that this would magically transform the performance of the entire vehicle. No such luck. By the time we got onto the motorway, it was clear that the car wasn’t going to make it. Instead, we came off at the first junction and headed for home. This is after the car breaking down on the motorway in February, after paying to get through the MOT in January and after replacing the clutch last Autumn, plus repairs to the radiator. I did my best to get the car fixed on the following day, but the garage weren’t able to solve it in time before closing for the bank holiday, leaving me with a car that wasn’t behaving well enough to undertake any serious driving. Half term, bank holiday and we were stuck. The trip north was cancelled and neither could I risk any of our usual day trips.

Meanwhile Ivy has been falling apart over being placed in a new teaching group without any of her friends. She’s had such a hard time in the last couple of years that I’ve contacted school to ask if she can move classes – of course, all I’m getting back is the tired old we can’t make exceptions for one child or we’d have to do it for everyone. Oh really? So if she had hearing or sight difficulties they wouldn’t arrange for her to sit at the front of the class? Ivy has severe anxiety, probably ASD-related, and is still recovering from depression. I’m doing my best to explain to school that this grouping means putting her through further stress and anxiety, including IBS and nausea, so loss of appetite and skipping meals, insomnia and fear about going to bed, plus inability to concentrate in class, inability to raise her hand or answer questions, inability to contribute to group learning and projects, while struggling to control her breathing and fight off panic attacks. It’s taken so long to build up her confidence after all the trauma, and I’m tired of having her knocked down again by either Simon or school. But schools nowadays just close ranks; it’s all about conformity and saving face, there’s never an admission that they’ve made a mistake, there’s no compassion or flexibility. She spent most of today in tears and I’m tired of being fobbed off. So; yet another battle. And now Lily is intent on being “L” from Deathnote, at home, at the supermarket, at school… and now the Tax Credits form needs to be filled out, and so on and so on.

Please stop, I beg the Universe. Please, no more. Give me the gift of an ordinary life, just long enough for us all to recover. Outside, the roses are blooming; can’t we just stop for a while, long enough to smell them?

A Year to Heal, Garden, Self Care

Resilience

Advice on how to plant trees has changed in recent years; instead of being lashed to a stake that stands parallel to the trunk, it’s now thought best to put in a lower, diagonal stake that allows the growing tree to move with the wind. This way it will strengthen and gain more resilience, better able to withstand future storms.

I feel I have precious little resilience left. Looking at the storms I’ve had to weather in the past few years, some might say I’ve demonstrated incredible resilience – after all, I’m still standing. My answer is this: barely. In tree-speak, I’m like one of those wind-blasted thorn trees, gnarly and bent by Cornish winds, leaning at an alarming angle. Nothing is as it should be. Each setback seems to extract a higher and higher price on my mental health – and recently, the setbacks have been piling in on top of each other until breaking point has been well and truly passed. In truth, I don’t know how I’m still standing; my body seems to haul herself automatically through the days while my spirit remains curled up in the foetal position. Recent events brought me to a near-suicidal low after an argument with the children; apparently my attempts to get them into school on time and wearing the correct uniform make me unreasonable.

It was Ivy’s insistence that I was being ridiculous that somehow broke me, something she had no idea would trigger such a catastrophic state of mind. Of course, that was the word that Simon used almost non-stop during our disastrous mediation sessions, shouting me down with Ridiculous! Ridiculous! whenever I tried to speak the truth. I left that final session shaking and traumatised; the mediator should never have allowed it. Instead she seemed shocked that I had become upset and angry, that I wasn’t holding it together in the calm, rational manner that Simon was capable of, that so many abusers are capable of, smug in the knowledge that they are winning. There are so many aspects to domestic abuse that professionals need more awareness of, the subtle and insidious ways that abusers use to manipulate and control their victims. Simon’s ability to stay calm should never have been interpreted as proof that he was reasonable, nor that he was right – it’s only much later, with hindsight, that I can see the extent to which he was already lying, plotting and manipulating. You can’t win against someone who is willing to lie about absolutely everything, who will literally stop at nothing in order to get what they want (namely to destroy you) and all of the professionals involved were entirely taken in.

It wasn’t Ivy’s fault, she had no way of knowing the impact her words would have. To be triggered has become such an over-used buzzword, the millennial generation throwing it around for seemingly the slightest upset, the least bit of offence. To be triggered shouldn’t be equated to being over-sensitive, a special snowflake – realistically it means that you are unexpectedly floored by your reaction to what should be a non-event. It’s sudden, overwhelming panic, or shutdown or crisis. I should not have been upset by Ivy’s usage of one simple, inoffensive word, bad-mannered though it was. Instead, I spent the next few days feeling worthless, unable to carry on as normal in what seemed like an utterly pointless life. Feeling this low is exhausting and terrifying, and at times it’s only been the knowledge that I have kids to look after that’s carried me through it. None of this is a big red flag, a crisis call for help; I’ve gotten through it. Again. Resilience, I guess.

The garden is saving my life. Each time I go out there, I feel better. Gardening is a form of hope that the future will be better, we plant for the future. Having cleared the new flower bed for planting, I sorted through the plants I’d rescued from The House in the Sky to see what could go in along with the few new plants I’d bought. A lot of the old pots contained shrivelled up specimens of what used to be plants, or were overcrowded with weeds, and so I decided to take them down to the far end of the garden to get them out of the way. But as I picked up one pot and pulled out the weeds, I noticed a leaf. One single leaf poking through the dry soil that looked remarkably like a peony.

Back in the city years ago I’d tried to grow peonies without much success. They’re not keen on being moved and the plants I’d bought just wouldn’t settle in. When we moved to the House in the Sky though, there was a beautiful red peony near the front door, with gorgeous blowsy blooms. For seven years, I smiled at its flowers, not even wanting to pick them and bring them inside – they were too beautiful to cut. Once the decision to sell had been made, I had to agree to Simon sending in “gardeners” to tame the garden that we’d never fully taken control of, so overgrown was it by the time we bought the place from its elderly owners. Knowing that Astrid considered herself to be “good at gardening,” I had to specifically name her in the court agreement, that she was “not to attend the property” – otherwise Simon would bring her there each day so that they could get the house on the market as quickly as possible in order to buy their new home together. This woman who had been stalking me, spying on me, attacking me on social media, entering my home without permission, going through my belongings and papers – yes, Simon really was that tactless as to bring her to the house against my will. Even with the court agreement in place she still turned up at the house at least three times in the following week, at one point standing right outside the garden wall, shouting abuse at me in front of my children – You’re mad! You’re crazy! while Simon told the kids “Your mother is psychotic.” This because I objected to them breaking the court order, because I was upset and angry about being lied to and betrayed yet again, particularly as I had gritted my teeth and tried to be friendly towards Simon as he turned up at the house each day.

He hired “gardeners” to clear the garden, which they did using petrol-fuelled hedge-trimmers, slashing everything in sight. In desperation I tried to explain to them what should stay and what should go, otherwise they would literally have cut everything down to a stump, the old apple tree included. But they were Czech and barely spoke English, and my NO, don’t cut that was generally interpreted as No, I don’t want that. Meanwhile Yes, I want to keep this became Yes, please cut this down. I simply couldn’t win. I googled Czech phrases, we tied ribbons to the plants we wanted to keep and the kids hung signs on the apple tree, but it was too little too late. I sobbed indoors, hands around my head to block out the noise as they cut their way through the entire garden, then ran for my car and got the hell out of the destruction, unable to stop it, unable to cope with Simon strutting around the devastation like the Lord of the Manor, not even able to stop Astrid from constantly turning up. I stroked the leaves of my peony, trying to get them to understand, to save it. It was flowering, surely they could see how beautiful it was? When I came back, it was gone.

I’d dug up a few plants before the gardeners came, but wanted to rescue more plants to bring with me when I moved. I was too ill by then, bed-ridden with severe flu. Moving had become a disaster, Simon hadn’t even bothered to let the solicitor know that the money from the sale was supposed to fund my ongoing purchase. I could barely stand by that point, but was having to repeatedly haul myself off to the tip and charity shops. A last minute shout out to friends brought much needed help with clearing furniture that wasn’t going to fit into the much smaller new house. A friend offered to dig up any of the plants I wanted to bring – a few roses and a hazelnut were all I managed to remember; I didn’t even have the energy to make a proper list. But then, almost on the day of the move, I spotted something where the peony had once been. A small offshoot, a baby plant pushing through the soil where its parent had once sheltered it. A young seedling that probably would have been choked out by the dominance of the mother plant, if it had still been there. Carefully, I dug it out and into a pot. It was this same tiny peony that I found now, as I pulled the weeds out of its pot. One leaf poked up through the soil, so easily overlooked or thrown into the compost by mistake. I planted it in the new bed, whispered words of encouragement to it, watered it and crossed my fingers. Live. Please live.

Resilience.

Cat and resilient peony. I'm not sure how resilient it is to being sat on though.

A Year to Heal, Creating a life worth living, Garden

On Imperfection, Barrels and Buddha

May has brought a very unBritish heatwave, followed by its very own monsoon season, sometimes in the space of a single day and most usually when I’ve hung the washing out to dry. After over a week of scorching hot weather, the ground was too hard to dig and so I’ve shifted to other jobs; painting the fence and bench, revamping the patio area as well as trying to keep everything watered. Watering is tricky as there’s no tap at the back of the house and so watering cans have to be filled up in the kitchen or bathroom, carried dripping through the house and out into the garden. I’ve now managed to install a water butt, almost correctly, and so there’s some water available at the back, as well as a large barrel further down the garden, although this isn’t connected to any gutters and so only fills from rain falling directly in it. I’ve been setting out as many containers as I can to catch rainwater and manually refill the barrel – my garden looks like an episode of Bear Gryll’s The Island at times. It’s only when you don’t have water that you appreciate how sacred it really is. I will say nothing of the constant hiss of hosepipes in neighbouring gardens as I’m slogging down the path carrying watering cans of my recycled bath water. I’m so glad I mulched the new flower bed after planting, it’s done a lot to help my precious new plants to get through the hot weather.

Unable to make much more progress while the ground was so hard, I turned my attention to the patio. Oh dear. A large pile of thorny trimmings from the overgrown rosebush and trellis that needed shredding, bags of compost and mulch, plants awaiting a home, pots that once were plants and now were weeds, random bits of wood and pallets and much general debris. Not exactly a space that cried out to be sat in and enjoyed. After a good tidy up and sweep, the trellis repainted and the table and chairs reinstated, it’s now a lovely little patio where we can sit outside and chill, read on the bench, or have a meal. One of those jobs that feels overwhelming but doesn’t take all that long once you get down to it. It was all so much better… except for the barrel.

Yep. Not great. The barrel was left behind by previous occupants, and judging from the state of it, I imagine they inherited it from their predecessors. It was now a sad accumulation of weeds and building rubble, too heavy to even move. With the blazing hot weather still preventing me from digging elsewhere, it was time to tackle the barrel. Once I’d started digging out the soil, I discovered why it was so hard to move – the bottom of the barrel was full of bricks. I’m not sure if someone thought it needed bricks for drainage, or whether they just wanted to get rid of them or were hoping to use less compost, but it was as much brick as it was soil. It all came out, then fresh compost went in and I was ready to plant.

Back at The House in the Sky, I had bought half-barrel planters for Lily and Ivy, let them choose their own plants from the garden centre to create their own mini-gardens. It’s a lovely idea for kids, as it’s more manageable than a patch of ground and way cuter – the main issue is to make sure they get enough water. Lily chose a strawberry plant amongst others, and would proudly give Ivy the one, precious strawberry that it grew each year. There should have been others, I don’t know why it only generally managed one, probably slugs, snails and woodlice were to blame. But still, a moment of cuteness and generosity, a very rare thing to be treasured. By the time we moved, the barrels were falling apart and we left them behind along with so much else, so many hopes and dreams. All this was running through my mind as I planted, along with the interruption of a phone call from Ivy as the school bus had broken down yet again in the hot weather and could I come and pick them up?

I’m just in the middle of something, give me ten minutes and let’s see if they get a new bus out to you quickly.

Because sometimes you need to finish what you’ve started. The barrel was going to be something beautiful, a contemplative spot, somewhere for me to sit and enjoy. If I ran off now and left it unfinished, everything would likely sit there for several more days until I could get back to it, plants drying out in the heat, weed seeds blowing into the fresh compost, resolve dwindling in the face of new chores. So I planted, and put down a layer of cardboard between the plants and piled up cobbles and placed the centrepiece I’d haggled over in the garden centre…

Ta da! My new garden meditation spot. Not that I do any kind of proper meditation, but sometimes sitting peacefully outside is as Zen as it gets. My little Buddha is there to remind me to do just that, to take a moment and rest and breathe while enjoying the quiet, the birds, the flowers. To contemplate beauty and stillness, rather than the To Do list. The bus brought the kids home okay after all; Lily noticed the difference straight away and declared it to be our Japanese garden, while it took Ivy a week to notice, by which time the slugs were attacking the hostas with primordial vigour. No matter. My garden will never be perfect, neither will life be. I’m learning to try to make the most of it anyway.

A Year to Heal, Creating a life worth living, Self Care

What’s working now…

Pukka Lean Matcha Green Tea. I’ve long been suspicious of the bitter taste of a lot of green teas, but this one has a light, sweet taste that doesn’t go acrid if brewed too long, for people like me who tend to forget to take the teabag out. I’ve switched to a cup of this first thing instead of my usual builder’s tea and it feels like a cleaner, brighter start to the morning. Potentially a better source of caffeine than regular tea or coffee in my search to self-medicate for ADHD.

Sunshine. Good weather really makes a difference, especially in terms of getting out of bed for the school run. I try to compensate in the Winter with one of those alarm clocks that gradually starts to get light half an hour before you need to wake up. It helps. The weather has been uncharacteristically gorgeous in the past couple of weeks and so I’ve been trying to make the most of it.

Gardening. I always always feel better after working in the garden. It’s worth dashing outside even if it’s just to water the pots for five minutes. A decent session in the garden has a dramatic improvement on my mood, plus the bonus of being able to see my progress also lifts my spirits even if I’m just glancing out of the window.

Water. Drinking more of it, swimming in it (although I really hate public swimming baths), bathing in it, being next to it whether a little pond, a stream or the sea. Is it something to do with negative ions? I’ve decided my garden definitely needs a pond, plus it would be worth finding a little local spot where I can sit in relative privacy and enjoy the river.

Menu planning. At my worst I couldn’t think five minutes beyond my nose. I literally couldn’t manage to decide what we’d have for dinner a day in advance and so we ended up in the supermarket every single day after school, picking out a ready meal. A HelloFresh subscription got me cooking properly again, and made it easier for the kids to also help out with preparing meals – I’d definitely recommend them, although due to Ivy developing gluten and dairy intolerances, we’ve needed to switch back to our own meals. I’ve realised that even if I don’t have the brainpower to come up with a menu that covers the whole week, I can split the week into two (Mon-Thurs, Fri-Sun) and just make sure that the next 3-4 days are sorted. Cue better, healthier meals and a lower grocery bill. Current favourite cookbooks; The Happy Kitchen, and Jamie’s Five Ingredient Cookbook.

Magnesium Flakes. I’m not sure what peculiar sorcery is going on here, but a handful of these in my bath has transformed my skin from reptilian to baby soft. I’m hoping that the same magic is working somewhere on the inside too; magnesium is apparently an essential mineral for overall wellbeing. It’s apparently also good for plants, so I’m reusing the bath water in the garden whenever possible.

Massage. Wrongly seen as a luxury, this has been a lifesaver for both my physical and mental/emotional health. Stress leads to muscle tension which builds up into pain and headaches and ultimately looking like Quasimodo. Hot stone massage by a good therapist really helps to unwind me and keep me grounded; whenever I skip a few weeks because of budget or busyness, I end up regretting it.

Lifesum. A food tracker app, available on subscription. I used it for a while, then stopped when my comfort eating was getting out of control, but am now going back to it while I attempt the 5:2 plan. Lifesum has several different programmes you can follow with recipe suggestions, but mainly it makes it easy to record what you’re eating and keep an eye on the balance of carbs, protein, fats etc as well as counting calories. I’ve found that even just the act of recording what I eat means I make healthier decisions. I’ve not even been trying very hard, but week one and I’ve lost two pounds – not life-changing but the first time in four years that the scales have moved downwards.

Think Small. Book by Owain Service. A relatively short, easy read about goal-setting and making small, manageable tweaks to your daily routine in order to achieve the desired result. There’s plenty of stuff out there already, but this one really brought it home about how to schedule in new habits so that things actually happen.

The Durrells. Ivy and I have been watching since the first series, now Lily has finally joined in and discovered this essential Sunday evening drama series. Funny, heartwarming and touching without being saccharine, we’ve absolutely loved it; please make another series very soon as we’re already feeling bereft now it’s finished. I’m secretly looking forward to the second series of The Handmaid’s Tale – rather less gentle and not at all comedic but very gripping, one for me rather than the kids. In general there’s a need to be picky about what I watch, The News tips me over the edge into panicked, hopeless depression, and I can’t much cope with depressing documentaries at the moment, no matter how worthy. I’m wishing they’d show The Gilmore Girls again, heartwarming, cosy dramas are a must.

A Year to Heal, Creating a life worth living, Self Care

How will I know when I’m healed?

Reading Think Small has reminded me of the need to set achievable, measurable goals (SMART goals) that I can tick off as they’re completed. Although I try to do this with the daily To Do list and often add tasks that I’ve already completed just so I can tick them off, Think Small has helped me to see how big dreams need to be broken down into daily habits if they’re ever to be achieved. As I’ve designated this to be A Year to Heal, it got me thinking about what steps I can take in order to help myself heal – I can’t guarantee that at the end of the year I’ll be 100% better, but I’m keen to move forward rather than stagnate. First things first – how will I recognise that I’m healed, what are the main issues that are currently causing problems?

I think the main clue that I’ve healed will be when I no longer feel the desire to drive a pickaxe through Simon or Astrid’s skulls. I wish I was joking. Anger and injustice still burn through me on a daily basis whenever the details of what happened creep into the back of my mind. At first I questioned why I felt so bad, so unsafe, after all there are many women going through far far worse and I wasn’t facing physical violence. However, the Domestic Abuse recovery course explained to me that the way Simon and Astrid were spying on me and stalking meant a violation of my sense of physical safety. That’s fundamental in terms of Maslov’s Hierarchy of Needs, the need for shelter and safety. Which means we’re dealing with something primal; the need to protect yourself and your children. If an intruder entered your home, went through your possessions, took things, threw things out, and threatened your and your children’s right to feel safe in your home, you’d wind up pretty angry – if you caught them in the act, you would be permitted by law to defend yourself, which basically equates to physically attacking them. The fact that the intruder was my ex-husband and his girlfriend doesn’t make the situation any more bearable – in fact, the violation is deeper, more personal. I trusted him. He betrayed my trust again and again, and for that I basically want to hurt him; of course I would never act on my homicidal urges, but at times the intensity of my feelings makes it feel as if I will never heal. The anger has nowhere to go, other than creating havoc in my mind and body. I will know I’m healing when the incessant rage dissipates.

Fundamentally I don’t feel safe. I don’t feel safe in my own home despite having moved house, a hangover from the past few years of being afraid to go out, of worrying that Simon or Astrid were waiting to swoop in and invade my home yet again. When we’ve gone away for the weekend to visit family I still worry that they will try to break in to my new home, I won’t let Lily have a key for this very reason. When I’m out and about, I don’t feel safe either, other than in a very few limited places that I’m fairly sure Simon and Astrid don’t visit. Hyper-vigilance is ever present, scanning the horizon like a meerkat sentinel, ready to dart back underground at the first sight of anyone who might be them. My chest is always tight with anxiety, my heart fragile and fast to the point where I’m scared about my health. I will know I’m healing when I start to feel safe in the world again – although given current global politics, this may be heard to achieve. At least, I will know I’m healing when I no longer carry this constant burden of anxiety and fear, when I don’t have a panic attack every time I see someone who looks like either of them.

My mind constantly replays the abuse, trying to explain what’s happened, trying to reason with Simon, rage at Astrid, rehearsing what I should tell the judge if I’m dragged through court again, and what I should have said last time. I struggle to get to sleep at night, resorting to listening to meditations and sleep hypnosis videos on YouTube. I wake in the early hours and my mind immediately picks up where it left off. This is part recrimination against my failures to achieve justice in court, and part preparation in case it happens again, protecting myself. In counselling, we discussed how Simon essentially tried to destroy me with lies and accusations, and that this constant inner voice arguing against him is a survival mechanism determined not to give up. Silencing it means killing off that small part of myself that has endured, has fought back. I need to find it a healthier channel, switch from PTSD 24/7 to Peace of Mind. I will know I’m healing when my mind is no longer caught in this incessant loop of recrimination and replaying.

Physically, I’m a wreck. I’m overweight from comfort eating and horribly unfit – particularly after developing plantar fasciitis last year which made it hard to walk. I have insomnia and am still prone to anxiety and panic attacks. It’s not possible to be this stressed for this long without a serious impact to health. I’m permanently exhausted, a combination of said anxiety and insomnia, plus two demanding teenagers and perimenopause. Self care has fallen off the bottom of the To Do list – I feel fat, frumpy and tired. I will know I’m healing when I start feeling fitter and more energetic, and able to better take care of myself. This includes a healthier relationship to food and making sure I get some form of exercise.

The house move was impossibly hard, made far worse by being bedridden with severe flu for the best part of two months while having to downsize to a house that was about a third of the size of our existing home. The stress around the move was unbearable, but I told myself that this was the worst part, once I’d moved I could look forward to a fresh start and take my time putting things in order, there was no hurry. What should have then been a year of gently setting up home turned instead into a second year of having to fight my corner in court and being consumed by stress and anxiety. Overwhelm is not a helpful emotion when trying to set up home. It’s now time to create a home that nourishes us, to reclaim my environment. One of Simon’s accusations was that I was a hoarder, which has resulted in a year of obsessively watching the Hoarders TV show – I think I can safely say that I’m not a hoarder, but ADHD means that I struggle with organisation and tend to be somewhat messy and cluttered, it’s hard to make decisions about what should go where, what to keep and what to let go of (and don’t get me started on the donate/sell issue.) When the outward circumstances of your life are acute stress, anxiety and chaos, it’s no wonder that your home environment begins to reflect this. I will know I am healed when I’ve been able to deal with the remaining clutter and feel like I’m managing on the domestic front; when our home feels nurturing rather than a source of stress, when I can let go of the feelings of guilt and shame that Simon’s accusations engendered. Also Simon – given the amount of old crap in boxes that you’d stashed in the attic which I discovered two days before the move, you should maybe not be throwing around accusations.

Previously I used to have friends round for impromptu bring and share gatherings, food, wine, laughter and good times, but that’s not happened for a long time, it stopped even before I moved house. It’s not just that my house is now too small, it’s also that having people in my home makes me feel anxious and on edge. Inviting a friend over for an Easter dinner was a major achievement, and even then I found it hard not to watch the clock. Having a workman here to fix the boiler was unbearable, particularly when he had to go into all the rooms, including my bedroom. I will know I’m healed when I’m able to have friends round without feeling that I’d rather be undergoing major root canal surgery.

My career, tiny though it was, has been destroyed. A post-divorce name change didn’t help, it feels like starting over, plus several of my existing contacts have moved on to pastures new. Stress meant having to stop working, I couldn’t focus on writing. My previous blog was used against me, a story of mine was used as evidence in court and I had the joy of a potential client turning out to be Simon and Astrid using a fake alias to try and entrap me. Now, at the point where I could be returning to work, it feels like my brain is entirely addled. It’s hard to focus on anything, hard to stick at things, difficult to know where I should be putting my energies. My confidence is at a low ebb, particularly with Simon’s insistence that I was deluded about my abilities as a writer. It’s hard to reach out to former colleagues, never mind forge new contacts – no, not hard, impossible in my current state of mind. More than that, I’m scared of putting anything of myself out into the world again in case Simon finds new ways to use it against me. I will know I’m healed when I’m able to write again, consistently and professionally.

I will know that I’m healed when I start looking forward to the day ahead instead of dreading it. When I no longer have to fight hard to find reasons to go on living, beyond looking after the kids. Ultimately I will know I’m healed when I’m able to leave the past in the past rather than having the abuse creep into every aspect of my daily life with its poisonous, painful reminders. And right now, it’s the hope that one day I will be healed that’s keeping me going.

A Year to Heal, Creating a life worth living, Self Care

Quest for Fun

Fun. I puzzle the word over, chewing on it. There is precious little fun in my life and I’m trying to figure out why. Oftentimes during the marriage we’d set out to have fun, but somehow miss it – I’d always put this down to having to deal with Lily’s demands and outbursts, leaving us tetchy and exhausted. Now I wonder whether there was more going on, whether the dynamics of our relationship were skewed against any positive outcome. Certainly after the split my happiness quota went through the roof; suddenly I had friends, a social life, I held gatherings at The House in the Sky full of laughter, shared food, homemade wine and kids running amok in the lanes. My overriding feeling was of being me again, after years of losing touch with myself. But gradually Simon’s abuse began to curtail this newfound happiness; I was soon lost, confused, exhausted, fighting for my survival. I stopped having people over – I didn’t have the emotional energy to deal with others, there wasn’t enough of me left over to give out to anyone else. More than that, I’d raised the drawbridge. With Simon bringing Astrid into the home behind my back to spy on me, I no longer felt safe. I didn’t want to go out, nor did I want anyone else in my home. As soon as anyone arrived, I’d feel edgy and anxious until they’d gone again; sadly that’s still the case. If I went out, I’d worry that Simon or Astrid had snuck into my home again, were going through my papers – I took to storing all the divorce documents in the boot of my car. I felt like I was being watched wherever I went; Mum sent me Starbucks vouchers to go out for coffee, but I worried that someone was recording each bite of cake, that being able to afford a latte would be used in court as evidence that I had too much money to spend. In reality, it was a generous gift from my Mum, doing what she could from a distance to help with my increasing social anxiety. Paranoia began to take over – but is it really paranoia when you’re actually being stalked?

Abuse is isolating. It’s insidious, creeping up on you without you realising what’s happened – by the time you wake up and realise what’s going on, your confidence and wellbeing have already been deeply eroded. By the time you’re able to find the right labels for the confusing mess you’ve found yourself in, your life has already fallen apart. Stress – by which I mean full blown panic attacks, uncontrollable crying, insomnia, severe anxiety and palpitations – meant I had to sign off work. Although that was over two years ago, it’s only just this week that I’ve begun to realise the full implications. It’s not just the loss of my career, I’ve lost the social side that came with my particular line of work. Previously, most weeks I’d have some kind of event to attend – a reading of someone’s work, a workshop, a networking event. Now – nothing. I’ve lost touch with my former peers and colleagues, most people have no idea about what’s been going on. Before, I had something that was purely for myself, something that I was passionate about, something that bolstered my self esteem, that gave me purpose. Something that was ultimately fun, if at times demanding. To have all that systematically destroyed by Simon has been devastating. So; social life destroyed, career destroyed, confidence and self-esteem destroyed, home gone. It’s only now that I’m beginning to add up the full cost of Simon’s abuse and realising just how much I’ve lost; fun seems to be one of the many casualties. I’m no longer able to do a lot of the things that used to bring me joy, plus my now precarious mental health means it’s harder to find enjoyment in whatever I try.

Not much fun then. There are moments when the kids and I will be in hysterics over our own daft jokes, yet these are counterbalanced plenty by the number of arguments and conflict. I’m doing my best to appreciate the good moments, to count my blessings. Next minute I’m triggered and having to walk out of the Stress and Anxiety course session, breaking down in tears. Near constant conflict with Lily means that the good mood I’ve tried so hard to achieve is wiped out in seconds. The rest of it is the daily grind, the struggle to keep up with the endless round of chores and duties.

This is no good. The realisation of how much I’ve lost was a bitter blow, bringing further feelings of what’s the point? The feeling that I don’t have anything in my life that’s just for me. Wondering whether I will ever find happiness again, whether I can rescue my sense of fun. A Quest for Fun is in order, and so I’ve nominated Fridays as Fun Fridays – the one day of the week that I’m reclaiming for myself, with the sole purpose of doing something that I enjoy. As they say, if you always do what you’ve always done then you’ll always get what you’ve always got. If you want something to change – ie to enjoy life more – then you have to change something. It won’t happen on its own. So Fridays are now dedicated to rebuilding my long lost sense of fun, which actually requires some planning in order to make sure that this happens – at the moment I’m thinking I’ll attempt to visit some of the many gardens, stately homes etc that are in the area, as well as art exhibitions. Taking a camera is key – I don’t know much about photography, but I know that having to literally focus on taking a picture means that my mind isn’t focused on my problems but on something beautiful instead. One small shift at a time in the journey towards creating a life worth living, one small step towards self care: I matter, I have the right to take the steps necessary to heal, I have the right to a full life, I have the right to be happy.

A Year to Heal, Garden, Self Care

Beltane Moon

The kids have been dropped off at school. I’m supposed to be attempting the 5:2 intermittent fasting diet, but I stop off at the farm cafe on the way home, ostensibly to buy flowers for May Day – I’ll do my best to resist the almond croissants, even though I’m already hungry and it’s not quite 9am. The flowers here are usually beautiful, locally grown and artfully put together, but today they’re a little disappointing, the daffodils clearly having passed their best. Not worth the £9.95 price tag. I could point out their flaws and ask for a discount, but I’m not in the mood. They’re a gift for a friend who is going through chemo; she deserves more than flowers I’ve had to haggle over. The cafe used to be my favourite, but it’s since been taken over by the local gentry, the car park full of Range Rovers, posh people braying about their holiday plans. My god, but posh people talk loudly. They dominate the space, interrupt my thoughts, make it impossible for me to sit and quietly write.

May Day. The year is flying past already – is the world speeding up or is this the inevitable affect of age? Years seemed to creep by so slowly when I was a kid, and now I can’t keep up. “Have you got a busy day ahead?” the young man asks me as he hands me my tea – I’m proud to say I resisted the croissant. It’s a question I hate. My days seem pointless, full of chores but nothing I could point to and get excited about, nothing that seems worthwhile. I tell him that I was supposed to be taking my friend to chemo, but she’s not well enough and I’m waiting to hear what she feels up to doing. I don’t tell him that the flowers were crap this morning, clearly he’s on barista duty so it’s not his fault. I don’t tell him that my life feels pointless, that my mind is full of depression, anxiety and trauma, that I can’t seem to think clearly any more and I’m struggling to keep on top of the day to day tasks. That when I think about the days ahead, all I see is relentless treadmill of school runs, cooking, washing up and nagging the kids to get up, get ready, do homework, go to bed and occasionally take a bath. I used to be fun, I think. Nowadays I can’t remember what fun feels like, what on earth I’d do to feel that way again, how to get it back. I used to make sure we went out at the weekends, did an activity together, went to a museum or gallery or day out. Since Lily moved back full time, I’ve been too exhausted, have found myself trying to work out how to make a meal from chickpeas and slightly out of date bacon rather than having to drag myself to the shops.

Once I read a post by a young woman suffering from a debilitating condition that left her with chronic fatigue, trying to explain to a friend why she couldn’t always manage to meet up. The gist was that she only had 10 spoons worth of energy per day. Every single task required energy – getting out of bed, showering, getting dressed used up about 3. Even pleasant activities such as meeting a friend for lunch took up another couple of spoons, which meant that on some days she just couldn’t do it – and also showed how much she treasured her friend, in that she was willing to spend some of her spoons in order to spend time with her. I’ve never had a diagnosis to explain why my energy levels are so poor – there’s anaemia for sure, hormonal issues, post-viral fatigue, weird metabolism and blood sugar issues; I just know that certainly since puberty I’ve constantly struggled to have enough energy to get through the day. The difficulty comes when you wake up and have only 3 spoons to get you through the day, rather than the expected 10; or that the day ahead is a 20 spooner. Further difficulties arise when you’re surrounded by people who have never experienced what the doctors call TATT – Tired all the time, who judge you for being lazy. It’s not laziness; on the days when my energy levels are good, I prove this to myself by running around doing everything that needs to be done, knowing that I need to make the most of it. Waking up already exhausted rather than refreshed is hellish. I look down out of my window at the small area that I’ve cleared and planted, wanting to get out and mulch it, having to weigh up the energy cost against knowing I’ve still got to drive to pick the kids up, cook a meal, wash up, get them to bed. I don’t have enough spoons.

Depression worsens fatigue. Fatigue can cause depression. Bit of a vicious cycle, that one. My friend texts to say she fancies a walk across the hills followed by a coffee. I want to cry. Can’t we just have the coffee? The walk will mean I don’t have enough energy to garden today, or at least not to tackle the jobs I was hoping to do. She has cancer, dammit, and I’m the one moaning about energy levels. ADHD has an impact, having the equivalent of 105 tabs open in the brain at once all running together is tiring. Not getting enough sleep, not eating enough protein, developing an unhealthy reliance on sugar as an emergency fix; none of it is helping. Some would say I need to get more exercise, they might well be right, but how do you exercise when you’re already exhausted? Learning more about ADHD has led to experimentation with caffeine as a form of self-medication, to see if it helps settle my mind and help me focus; Pukka’s Lean Green Tea feels good, but switching from decaf tea to full strength tea and coffee seems to have mainly brought on severe headaches; caffeine fail. I’m left not knowing whether to take more naps, or take more walks, rest more or power on through. The phrase I need a break plays through my head like a mantra – I so desperately need a holiday that doesn’t involve camping or self-catering or struggling with Lily’s outbursts.

Gentle, I try and remind myself. Go gently. There’s no point in beating myself up over anything. When progress feels so frustratingly slow, it’s vital to raise flags over every tiny success, every step forward, so that there’s something to look back on, something to cheer you on. A Ta Da list as well as a To Do list. Sometimes you need to turn around and see how far you’ve come before you tackle the mountains ahead.

I catch a glimpse of the Moon as I stand up to go to bed – rising over the distant hill, almost full, twice her normal size, her halo rendering the clouds around her inky blue and copper. It’s a stunning sight that lifts my spirits, a reminder that there’s more to life than the endless rota of chores. A moment of beauty. Beauty. It’s something I need more of in my life – not the chauvinistic hectoring of the fashion magazines about what face cream I should be using, and keeping my eyebrows in shape, but true beauty, duende, being emotionally transformed by a work of art, or nature herself. I wish I could photograph her to capture this moment, but the end result looks like someone is shining a very small torch a very long way away. The beautiful moon is a reminder that life is more than this, more precious than what my life has become. The moon waxes and wanes and goes dark before shining again, the tiniest sliver of light in the night sky, far more mysterious than the sun. And as she rises, so can I; sometimes waxing, sometimes waning, sometimes hiding away but always ultimately shining.

A Year to Heal, Garden, Home, parenting

Breaking point

I’m painting the fence bit by bit, stopping before my body aches and demands a break. In general though a break would be good. Any kind of break, except for the ones involving bones or water pipes. A lucky break; the Lottery, please. A holiday break. But most of all a break from constant problems. Even just a week or so in between problems would be nice, but no, they keep on flying relentlessly towards me like oversized gnats with fangs and awful body odour. So, on the happy happy day that I got my new boiler, I also got a call from school to ask whether I was aware that Lily was self-harming and appeared to be having schizophrenic episodes?

Oh boy.

Please, just a week? One week without fresh trouble? One week in which to live as close to normal as is humanly possible?

No.

Lily insists she can see shadowy figures appearing in her bedroom, that someone is there, in the corner of her eye, taunting her. She’s using a shark’s tooth I gave her years ago to carve deep scratches in her arm and hands, says she enjoys it. Says she feels like she’s losing her mind and that most of her friends are too, and that the scratching makes it feel better.

None of this is good news. And if it was Ivy saying this, I’d be freaking out and rushing to the nearest child psychologist I could find (although frankly, referrals are rarer than unicorn eggs in our overstretched child mental health services.) But it’s Lily and therefore much more complicated. We’ve just come through a couple of months in which Lily has been lurking in the shadows, complaining that the sunlight hurts her skin – thankfully this was Winter, so there was precious little sunlight to deal with. Momentary concerns that this was due to a reaction to her epilepsy medication were pushed aside when Ivy explained that Lily has been writing her own manga comic about a Japanese vampire. She’s also been putting a considerable amount of effort into learning Japanese, and has mentioned a few times that she likes the taste of blood. So – no side effects, just Lily playing out being a Japanese vampire. She’s been asking for a parasol to keep the sun off her face – this has also been inspired by Abby, her favourite character in NCIS, who doesn’t seem to venture outside without a parasol and ear protectors. The inside of Lily’s mind must basically look like an acid trip, all neon colours, dancing squids and fantasy and reality blurring into one.

Lily has recently decided that she is now an Emo; all black clothes, Panic at the Disco, My Chemical Romance and such. Combine this with a bit of a wave of self-harm passing through school, a few friends with issues, and there we have it; Lily’s latest obsession, played out in all its glory. Hello Aspergers/ADHD. In the past it was cars and dinosaurs, now it’s Emo, madness and self harm. And although the scratches are disturbingly real enough, I suspect the madness is make believe. Except of course, it’s complicated – Lily then believes her own fabrications. What she invents then becomes real to her; she will swear blind that she really really did go to a parallel Universe and discover that she was actually dead in that reality. It really happened, and woe betide anyone who dares suggest that it didn’t. So how on earth anyone can start to unpick whether or not she’s really seeing people in the corner of her room, whether she really is losing her mind or whether she’s playing out an elaborate fantasy, I have no idea.

Another day, another call from school. Lily has been banging her head against the desk in an alarming and bewildering way. She’s threatened to cut someone’s throat. She’s been belligerent in class and answering back to staff. Her cuts are seeping through her school shirt – are they fresh scratches or has she been picking at the scabs?

I don’t know. I’ve run out of answers when it comes to Lily. Even though I suspect it’s make believe, I feel I’m in way over my head. The school nurse calls me in for yet another chat – there are probably some lucky parents who don’t even know that the school has a nurse. “I know it’s not my place to say this,” she tells me, “but I found I was questioning whether this real or not?”

I nod. “I don’t think it’s real,” I tell her. The trouble is, I don’t have a clue what to do about it. The scratches on her arm are too obvious, she’s been showing them off rather than hiding them. But still, they’re there, and it must have hurt.

“I always tell parents not to worry about it so much if you can see the marks,” the nurse reassures me. “It’s when they’re doing it more in secret that it’s a problem.” Although thinking about it, how would you know if they were doing it secretly?

Not real and yet all too real.

What do you do when your child is pretending to have schizophrenia? This is now just the latest problem, the new normal. Something has gone wrong with the kitchen light switch and none of the lights are working, I’ve rigged up a lamp so I can see to cook and wash up. The shower still isn’t fixed and I need to chase up the builders for a quote. The car is making a strange noise. Lily’s still not doing enough homework. There’s a damp patch in the hall. Ivy’s nervous tic has returned. A garbled message is left by the Child Maintenance Service, sending me into a panic that Simon’s found another way to pay less. One at a time, please.

I need a break from adulting. I’d like to resign, at least for a week or so, put my hand up and admit that I don’t know what the hell I’m doing. This is the reality of single parenting. I can’t go to Simon to discuss Lily’s problems; this is a man who has previously written to doctors to try to undermine Lily’s diagnoses when he thought her disabilities might get in the way of his plans to sell the family home. Instead, I worry that he will see her arm and call Social Services again; ammunition is more important to him than Lily’s wellbeing. It breaks my heart that it’s come to this, that the father of my children can’t be trusted to do right by them. That the responsibility for their wellbeing now rests entirely on my shoulders, the double whammy of hoping that I can do a good job of raising them while worrying that not only am I failing, or unable, but also that any mistakes will lead to further attacks from Simon. Parenting is hard enough without the other parent actively working against you.

Thankfully, a letter arrives from the local Young People’s Services offering us an initial appointment after a referral from school. Successful referrals are so rare that this is truly miraculous. The fantasy is that this will lead to Lily getting the help she needs. The reality is that it might go no further than this initial appointment. Fantasy, reality, normality. It’s not just Lily who feels she’s going mad, at times my head feels under so much pressure that I’m sure my skull is going to crack; the wrong kind of break. I’ve been at breaking point so many times in the past couple of years that broken feels normal.

Last Autumn the fence blew down. Ivy helped me to repair it, hammering new posts into the ground and patching up the broken, rotting fence as best we could. This past week I’ve been painting it, trying to make it look nicer while wondering whether I’m wasting my time, whether it will make it through another winter. Knowing I don’t really have a choice, I can’t afford to replace it – I’ve just got to make the most of what I’ve got. The pretty sea-green paint now reaches halfway down the garden, post by post, brushstroke by brushstroke, plodding on with it when I can. The broken fence was a problem; we dealt with it, and for now it’s holding. For now, I’m making the most of it while it lasts. For now, I’m being the best Mum I can manage to be. Maybe Lily really does have schizophrenia, or maybe this is the follow-up to the Japanese vampire phase. There’s no break from any of it; the challenge is learning to accept that and carry on regardless. That broken fence isn’t going to fix itself. No one else is going to paint it for me either. Just keep going. Paint while the sun shines, hang a lamp so you can see in the dark.

Garden, Home

Cultivating gentleness

I ebb and flow – the tides, the Moon, hormones, the weather. Whether or not I’ve managed to sleep, whether Lily has been in a cooperative mood. Anxiety levels rise and fall, energy, motivation. Sunshine helps, the returning light after the dark of Winter. Two weeks ago I could barely function, this week has been all go; the kind of go where you’re up at 6am baking brownies for a friend’s fundraising coffee morning, dashing from the school run to the supermarket to buy Lily’s ingredients for cookery and delivering them back to school, driving back for the coffee morning, then home for the boiler guy – the latest home visit in the Help to Heat saga – back to school to pick up Ivy and drive her to therapy, quickly head to the shops to buy food for dinner, back to collect Ivy, then back to the shop to collect Lily from the bus, home to cook dinner, wash up, and then remember to pay bills and renew library books online.

I’ve made it through to what seems to be the final round of the Boiler Lottery, another phone call and another engineer sent to the house to photograph radiators and pipes. The first guy could maybe have taken the same photos himself, rather than Guy 2 being paid to do the same thing, which might mean that there’s less of an admin cost in running the scheme and therefore more money available to pay for actual boilers, but what would I know? It will have been over a month without heating or hot water before I get the verdict, at which point either my boiler will be replaced, or I’ll have to get a quote to replace it myself. The not-knowing doesn’t help my anxiety, you can meet all the criteria yet still not necessarily get the grant. A mystical points scheme is in place. My fingers are crossed, and my Mum’s knitting group appear to be holding a candle-lit prayer vigil for my boiler rather than actually knitting. If I had money, I could have replaced it weeks ago. If I have to take out credit, it will cost an extra £1000 to the total amount payable, an additional 50% of the original price. Mum recalled working as a cleaner for a woman who obviously had more money than us, and who couldn’t understand why poor people didn’t take advantage of the deals at the shops, buying in bulk or the 3 for 2 offers. “I couldn’t afford to pay the extra,” Mum explained to her. When you don’t have money, you always end up paying more. Life is a lot less gentle without that financial cushion.

Anyhow, there were two major factors to Boiler Guy’s visit. One; there was no way that I was going to re-live the mortifying experience of Boiler Guy 1, in which I had made an effort to tidy up the kitchen largely by shoving everything into other rooms, only to discover that he needed to go into every room. Every. Single. Room. All of which were a total mess. I wanted to cry. It’s hard enough having someone else in the house, but for a complete stranger to come in and go through every single cluttered, messy room, including my own bedroom, was beyond hideous. So this time round there was much panicked tidying. Sunday = emergency tidying of Lily’s room, including mending her bed which she’d broken and not told me about, and trying not to scream because yet again she had completely trashed her space. That added a considerable workload to the panic clean, but it’s made so much of a difference; what seemed entirely overwhelming last week has been tackled in a couple of days. The house is far from done, but it has at least reached a state where I wouldn’t cry if someone else saw it.

One day later though and there is a pile of clean pants on the kitchen table, a stack of Lily’s loose recipes that should have been glued into her cookery book, and a fresh round of paperwork for me to deal with. I have to accept that my home will never look perfect, but then most people’s houses don’t look like a copy of Ideal Homes either.

Two, if you’re still counting, it was a beautiful sunny day on the Tuesday and I was desperate to get outside and garden. There simply wasn’t enough time, but the longing to be gardening felt positive, a recognition that this is what I need right now, body and soul. Another round of acceptance; it’s counterproductive to set myself artificial rules or deadlines – I must get out and garden every single day – as my life just doesn’t look like that. All or nothing tends to result more often in nothing, giving up. The process of making my garden needs to be as enjoyable as the final result; cultivating gentleness as much as seeds.