Good and Bad, Happy and Sad                                                         (TW suicidal ideation & planning, self-harm)

I’ve had a few reasonable days recently, and also some very weary days. I had a (mostly) lovely weekend, but I then basically slept from early Sunday evening until lunchtime Tuesday. Even lovely days wear me out, although to be fair, Saturday was a lovely but emotional day. A young couple in our church got married. It was a wonderful mix of traditional, up-to-the-minute modern, with touches of off the wall! It summed them up perfectly, young and vibrant, but with traditional Christian values at heart. It was a truly beautiful day.

To be fair, I did have a migraine, which is always very draining in its own right, but I managed to dose myself up enough to get to the evening reception where my son had been asked to take photos. Although I left a little early, having arranged for him to be brought home later, I had got through the day with only one anxiety wobble and no inconsolable sobbing.

Yes, I understand it’s permissable to cry at weddings, but since being widowed I have been known to start bawling and then be unable to stop. Slightly embarrassing to say the least! Considering how very low I was only 2-3 weeks ago, I think I did ok.

I’m not sure where the low came from. As so often in Bipolar, it just seemed to descend on me and engulf me. Added to that I noticed one of my little gerbils was unwell, and I forced myself to get a wash and put some clean clothes on so I could take him to the vet. I admit I am the crazy gerbil lady, but agreed to paying out £100 for him to have surgery to remove a lump from his tummy, which he came through well, only to pass away two days (and more cash) later. I was gutted. I held him as he slipped away, and I thought how I had already administered more end-of-life care than one person should in a lifetime. Not that I begrudge any of those I have nursed, human or animal, patient or family, and as hard as the thought is now, I will no doubt do it again. It was just a particularly bitter pill to swallow when I was already feeling so wretched. RIP little Phillip.

The following week my mood was worse still, and vague thoughts of suicide developed into ideation, planning, all the time becoming clearer, more detailed, more achievable, more desirable. I decided upon the perfect place from which to hang myself, chose a strong leather belt with which to do the deed and at one point I stood in front of the mirror with the belt pulled tight around my neck just to see what that would feel like, how much it would hurt. I guess something at that moment clicked in my head, because I undid the belt and put it out of sight.

When my CPN said he was too busy to see me that week I thought I would lose the plot. I cried solidly for over two hours after I put the phone down on him, and spent the next couple of days back in my pit, just surviving, wondering how on earth I would get through. By the end of that week though, my mood was improving again, and I took the positive action of contacting the local Mind wellbeing centre to see what was involved in accessing their services. In particular, I want to do their self-esteem course, as so many of my problems seem to be laid at the feet of my shockingly low self-regard, esteem and confidence.

My referral for Mind has now been done and I am awaiting an initial assessment date from them. I have received a date for my assessment appointment with RASAC at the beginning of September, and whilst that fills me with dread, I am proud of myself for even getting this far, and am focusing on my holiday next week to take my mind off it for the time being. And talking of my holiday, in conversation yesterday with my son’s social worker, she casually asked if it was possible for him to join my dad and I for a couple of nights of the break (we’d been previously told this wouldn’t be possible). So me, being me said three nights would be better, and given our last couple of weekend contacts have gone so well she has agreed to it. I am seriously not sure who is more excited, me or him! Have contacted the holiday company this morning and everything is set! Yay! 

My final positive at the moment; I haven’t self-harmed now for six months. Half a year I’ve been clean, 26 weeks. I wish I had some strategies to pass on, but I don’t. It’s been painfully hard at times, and just my sheer bloody mindedness that made me not want to let myself, and others down. I do use a Koosh ball to take my aggression out on, digging my nails into it as hard as I can (as I once would have done to my own skin). I still carry a small pocket knife with me as I feel more secure knowing it is there, which seems to make me less likely to want to use it. If it hadn’t been for the support of my CPN I know I wouldn’t have got this far, but he seems to have the knack of getting through to me when no-one else can. I know, in comparison to many, I am extremely lucky in this respect; I have a care coordinator I utterly trust with my craziest and darkest thoughts and feelings and his no nonsense, say-it-as-it-is approach suits me well. He knows I hate feeling patronised, he knows I won’t take any bull, so he doesn’t pull any punches. The therapeutic relationship just seems to work. Even the therapist I saw from the CMHT commented on the effectiveness of it, despite the inability to put his finger on exactly why!

I am aware I am using some of the DBT skills I have learned on courses I have done in the last year and a half. That and the few sessions I had with the therapist (he is currently unable to see me because of temporary increased job commitments) seem to be helping me make small but significant steps forward. I am hoping he will be able to work with me again in the future, but aside from that, when he said he was not able to continue our sessions at present, I was disappointed, a little tearful, but not the sobbing hysterical person I would once have been, unable to cope with the smallest of changes or losses.  

So I guess what I am trying to say is, I’m still up and down, having both good days and bad and very much riding the bipolarcoaster, but I can see pockets of progress and achievement. To even be able to admit that is a positive step for me. I still hope a tweak of my medication may offer me further stability of mood, because the prospect of this being as good as it gets is rather a depressing thought, but generally I am working hard to hold on to the hope that I can and will get through this. Again.

Thanks for reading.

Angel 👼🏼

The Therapy Shuffle (TW: Child Sexual Abuse)

It has been a few weeks since I started sessions with my new therapist from the CMHT. After starting off on a decidedly precarious footing, the therapeutic relationship is taking shape, and although I have moments where I feel unsettled or suspicious of his motives, essentially, from my point of view, it is going well. I can talk very openly to him, which is obviously key to the success of any work he does with me. There is a point of crossover seeing two members of the mental health team, and as they share information sometimes I can’t work out or remember who knows what! But I do feel, for the first time in a good while that I am able to address some of the issues that keep me ill instead of just trying to keep them and the associated emotions suppressed. This is a totally different kettle of fish to managing my symptoms; this is bringing stuff to the fore that makes me more vulnerable, more emotional and subsequently more prone to extreme swings of mood. Dealing with my past is neither easy nor pretty but if I am going to achieve a life of any future stability I know it is necessary.

Therapy has been intense, because I’m aware I need to make the most of the sessions and the intervention that has taken so long to access. It has been my community psych nurse who has been picking up the pieces. When the emotions become just too intense, he’s the one I reach out to. It has become fairly obvious both to him and myself that essentially the work that is being undertaken still centres primarily around my low self esteem, self hatred, even, that is tied in with having been sexually abused as a child. As much as I wanted to believe that having had counselling previously I was ‘over it’, it is still massively affecting my life. Because when losses and changes came in recent years, new memories, responses and emotions surfaced that needed coming to terms with all over again.

I have been able to identify positives in the process though. Small cautious shuffling steps forward, as if feeling my way in the dark. In sessions my thinking has been challenged. “Where is the evidence for that belief?” I am asked. I reframe things, try to wriggle out of having hard evidence, but calmly and gently I have the truth repeated to me, “It wasn’t your fault. It doesn’t make you bad / dirty / shameful or any of the derogatory names you choose to call yourself.” As I roll my eyes and look out the window, I know in my head he is right. It’s just getting that message through to my heart (or wherever deep held beliefs about oneself reside).

On reflection again with my nurse, I know what I require is open-ended intensive counselling, much longer and more specialist than he can access for me via the NHS. The local Rape And Sexual Abuse Counselling were first recommended to me well over a year ago, following my last inpatient stay, but it has been something I have, if I’m honest, been in denial about. Since his earliest involvement in my care last September it has been brought up numerous times. When I replied this week maybe I would consider it when my mood was a bit more stabilised, my nurse reminded me I had said that six months ago. And if I had put myself on the waiting list then, I would possibly be starting to see someone around now. It was a harsh reality to hear, but I think I needed it.

The truth is, it terrifies me. I can’t even say the word RASAC out loud. Although I acknowledge I was abused as a child and a teen, I don’t associate myself, in my mind as being someone who requires their services. It’s so…….so blatant. I guess there’s a part of me that still wants to hide the shameful truth that somehow (I allowed that) it happened to me.

Much of the work I do with my current therapist is CBT / DBT based. We look a lot at my emotional responses and how I can manage them, what has worked in the past etc. I have actually been able to identify recently how I am managing my moods better. I joked with my nurse about one difficult evening I had had in the last week, how I had coped by ‘taking it out on the stress ball’. I added “M (therapist) would be proud of me!” His response threw me. This is the ultimate grumpy Yorkshireman who shares my dark and slightly cynical sense of humour. He said, “I’m proud of you.” I wasn’t expecting that. And hard as it is for me to hear positives, because I trust him implicitly it hit me deep.

As I pondered therapy on Wednesday and seeing my nurse Thursday, and the small shuffling steps I have been taking forwards recently, I knew what I had to do. Not to make my nurse or therapist proud, but because I owe it to myself, and in fact to my son, to aim for that increased stability I know only specialist counselling will be able to offer me. So I could feel proud of what I have achieved. So far, I have yet to speak to an actual person, but I left a message at RASAC yesterday. I was shaking and hyperventilating, but I did it. Let’s see what the next shuffling step will bring.

Thanks for reading 👼🏼

No More Secrets

Those of you who read my blogs on a regular basis will have realised that I tend not to hold back. I say what I feel, I say what I see, albeit primarily from my perspective, though I do try to be as objective as I can, but being painfully honest is, essentially what my writing is about. It was always intended in the first instance to be a therapeutic exercise, particularly during a period of time when I was unable to access more specialist therapy than my community psych nurse could offer on a rushed weekly visit, when so many other things; my mood, meds, benefits, interaction with the team caring for my son and so on also ate into that precious hour a week. If I couldn’t be honest with myself in my writing, it would, frankly have been pointless. It has in the past also proved a useful tool in sharing more sensitive information with my CPN, as I have directed him to my writing rather than having to verbalise the painful details of certain life events.

However recently, at the suggestion of my CPN, I have started some more therapeutic psychological work with a new member of the CMHT; but rather than my writing becoming defunct, I evisage it evolving into a way of processing and mulling over the issues discussed, as well as continuing to document my past and present struggles around my mental health, widowhood, historical abuse and in fact the whole dysfunctional package that is my life!

Today I attended my third session with the new therapist. In a very short period of time I have felt able to be very open with him, albeit in a slightly detached manner, but already something shifted today. The session was extremely emotionally intense and I was aware I was allowing myself to actually feel what I was expressing, for the first time. I have a very real awareness of how long I have waited for therapy, and also that funding is not unlimited, so I need to crack on with the most problematic of issues whilst I have the opportunity.

If you have read some of my previous blogs, in particular the one entitled When Love Hurts you will be aware that my late husband was emotionally and verbally abusive to me. It was while discussing this with my therapist today that I blew my own dirty little secret – I cheated on my husband. 

There, I said it. I’m not proud of it, and if I have shattered anyone’s illusions of sweet church-going little Angel, I apologise.

At the lowest point in our marriage, 

When my husband was being particularly cruel, 

When I had recently been discharged from psychiatric hospital 

When I was being ‘preyed upon’ by an unscrupulous male colleague who showered me with attention, 

When my Bipolar Disorder took me into the most extreme of hypomanic phases I have experienced to date,

The unfortunate outcome was that I had sex with said male colleague.

Who promptly dropped me like a stone when I had served my purpose.

My husband had been accusing me of cheating for as long as I could remember, and calling me every name imaginable to that end, and at some point I just snapped, fuelled by hypomania, and decided if I was going to treated as I if I was doing the crime, I may as well at least reap the bounty. One of my husband’s ways of exerting power over me was to withhold affection and intimacy in the relationship, and ironically when I angrily admitted to him that, yes, I had been with someone else, after calling me every derogatory name he could think of, he admitted that it was his actions that were responsible for pushing me into the arms, and bed of another man.

I was forgiven, but I made it clear that things had to change. He promised to change and we were together a further 12 years until his death. My ‘indiscretion’ was never mentioned again in all that time, and things improved in some areas of the relationship, while some things I just learnt to live with and exercised some Radical Acceptance.

I have always stated that both my husband and I made mistakes and behaved badly in the relationship at times. I hope this blog redresses the balance to some degree, as I feel until now I have given a one-sided view of how I was the wronged party. In conversation with my nurse recently, in clarifying he said, “So your husband withheld intimacy because you had cheated on him?”

I replied, “No, there just was no intimacy, right from the start, and there’s a limit to how many times you can be called a cheat and a slut before you start believing it.”

Thanks for reading 

Angel 👼🏼

Not Counting my Chickens

The end of May is not generally a good time for me. My late husband’s birthday and our wedding anniversary fall within 8 days of each other, so emotional memories flow abundantly. Last year I was in a psych ward for those dates, and although my friend came and ‘celebrated’ hubby’s birthday with me, and we released a balloon, I was essentially too unwell and too medicated to really feel the impact. This year however, feelings were exceptionally raw. Having realised in the last 12 months the extent of the effect on my mental health of my husband’s controlling and bullying behaviour during our marriage, has left me with such varied emotions. Firstly I still love him. We were together 20 years, and 6 years into our marriage, when I could have left, I acknowledged that although it was a far from perfect relationship, I still wanted to be with him. And after this point, when I made clear that some things needed to change, mostly it was better. I was prepared to compromise a lot because essentially he was not a bad person, he was just as insecure as I was, and had had a controlling, bullying father as a role model. Hence I also feel some sympathy, pity even for him, despite how he treated me at times. However in contrast to that, I at times feel intense anger towards him for mistreating and disrespecting the one person who stuck by him through his terminal illness, fought his corner against know-it-all junior doctors and was there at his bedside in ITU the night he took his final breath.

So I was very low, what would have been the day before our silver wedding anniversary. I am exceptionally poor at asking others for help, but on this rare occasion, even I could sense the danger of being at home alone as distressed as I was. I called a dear friend who dropped everything to come and help me pack a few things and take me back to hers. She looked after me when I couldn’t look after myself. I really wasn’t well. I begged her to shave my head for me, which she duly did, despite not understanding my urgent insistence. She fed me and listened to me and held my hand and supplied endless cups of tea.

After a couple of days of being intensively looked after, I was craving my own space and independence again. The first night back home, I struggled and once more needed to ask for help. I can not stress how hard that is, or how much of a failure or a burden I feel doing it. But a friend stayed with me until I was calmer and so exhausted I was ready to fall asleep. I had a couple more really difficult days, but since then (2 weeks ago) I have gradually been feeling better.

For the first week I barely acknowledged to anyone that I seemed to be doing ok. Both my nurse and my therapist were on leave. I really wanted to be able to survive that week without putting in calls to CMHT or Out of Hours. I felt so determined not to fall apart in their absence, but I still had a niggling doubt; was I ok, or was I going slightly high? I had been rapid cycling for so many months it seemed like I had completely forgotten what normal felt like. Every time I had thought I was doing ok recently it turned out I was just midway on an upward journey into hypomania. So when my nurse returned this week I called him up, still very cautious that although I mostly felt ‘just ok’, every now and then something would alarm me that perhaps I was ‘going a bit batshit’.

He came out to visit me towards the end of the week, and I was still feeling ok. Kind of normal (for me anyway!) The ‘batshit’ moments had lessened too. As we talked I shared some of the ways I had been trying to track my moods and act accordingly to prevent extremes. I explained how I had been jotting down observations about myself, what works for me, what doesn’t and what affects my mood. I added that this felt a bit self-obsessed, but I have become aware that unless I find patterns of what helps I am not going to be able to make positive changes to enable me to look after myself. I noticed the huge grin on his face as he told me how good it was to hear me talking positively about putting my own self care first, and how long it had taken me to get to this point. I found myself grinning too. 

I told him how feeling positive and optimistic like this makes me feel nervous. He asked if I felt guilty for enjoying myself. I said not guilty, no, just anxious that something would go wrong or my mood would just randomly crash, because I don’t really expect my life to go well. Then I laughed at how ridiculous that sounded.

So, I’m definitely not counting my chickens before they hatch, but I noticed when told at my choir today that I look better, my auto-response was, “I feel better”. And I do.

Spectra, Labels and Diagnoses

It is three weeks now since my psychiatrist, when pushed, broke it to me that she is treating me for Bipolar II. Although I felt like I kind of knew this already, it still shocked me. The mood stabiliser I had started the month before was increased to a therapeutic dose, and off I trundled, pretty bewildered by what had just happened.
At first I seemed to be in shock, I had heard the diagnosis, but had yet to absorb the information. Then I wanted to tell everyone, and had to rein myself in until I had had the opportunity to discuss it with my son’s social worker and ultimately discuss it with my son and my dad.
Next I made a very frank announcement on my Facebook timeline and began to tell friends in real life. Most people’s response seemed to go along the same lines; “Oh well that’s good because now you are on the right treatment you’ll be fine.”
This (I assume) well meaning statement really did little to reassure me. Especially following conversations with others who have Bipolar, who essentially told me to expect a period of perhaps up to two to three years of experimentation with various medicines and mood journals etc, before any kind of stability may be expected.
And then of course, there are those who struggle to maintain any true periods of stability at all, despite their best efforts and those of their support networks.
I wanted to believe my well meaning friends, but in contrast the majority of those with lived experience of Bipolar were painting me a rather different picture. And not only that, but a bleak prognosis of long-term care under the NHS to boot.
And then there were the statistics I discovered while doing my own research. One in ten people with Bipolar Disorder take their own lives. One in ten children with a Bipolar parent go on to develop the illness too. This diagnosis is not only casting a long shadow over my future, but potentially over my son’s as well. That alone makes me want to weep.
One friend in particular said how unhelpful she felt it was that I had been labeled Bipolar. I said what I found unhelpful was well meaning individuals who loved to quote the spectrum of mental health at me. Telling me that everyone has mental health (I do get that) and that we all just fall on different places along a spectrum, in my opinion, completely belittles my current experience and my pain. I plainly told her that until she had been unable to work, look after her own child, or even have the energy to get out of bed due to her position on the spectrum, I didn’t find her thoughts on the subject terribly valid. At least at the moment. I did share with her though, that having been labeled (or diagnosed as I prefer to call it) Bipolar, on the contrary, had not been unhelpful for me, but despite my concerns for the future had actually offered me a sense of relief. Suddenly my history fell into place. The times I had acted erratically and wildly out of character actually made sense for the first time. Not that I wish to just make excuses for my behaviour at those times, but I realise now I wasn’t a bad person, I was hypomanic. I was ill. I can trace severe mood shifts back at least until my teens, if not before. I felt a lot like a jigsaw, all my varied pieces coming together to make the complete picture of my life so far. It helped me identify with something. I wouldn’t have chosen to be Bipolar, but actually it is what I am, and I can kick against it in vain, or work with it to try and make the best of the rest of my life.
I admit I have struggled since the diagnosis. My mood has been getting lower since the increase in the mood-stabilising medication and my anxiety symptoms are the worst they have ever been. My CPN admits he doesn’t really know how to support me. I guess to be honest, his just listening, as I try to make sense of everything right now helps as much as anything. At least he is honest and doesn’t quote sickening platitudes at me.
I noticed another thing; I feel like everything has changed, and yet everything is the same. I’ll explain. As I mentioned I feel kind of like a complete jigsaw now. I’m exactly the same person I have always been, except now I make more sense (at least to myself). However my world and my future feels like it has been utterly turned upside down. I am terrified to make plans, for a short break away (something I would regularly do easily pre-diagnosis) or even a night out, as my moods have been rapid cycling so severely for the last six months or so and currently my very low mood and high anxiety have caused me to lose any shred of confidence I may have had left. I actually can’t trust how I will feel at any given time, even a short while ahead.
People have commented I have been quiet recently. I think that’s understandable given what I have been, and am still trying to get my head around. I will bounce back, I’m sure, it just may take a little longer yet as I get used to my new ‘normal’.

Surprisinging Myself

A month ago I excelled myself. What I have discovered though, is that blogging about my positive experiences is considerably harder than writing about the more difficult times. To be fair, that is probably a reflection of my life in general. As a person who constantly battles with low self-esteem, poor self confidence and depression, seeing the worst in myself, and in general, seems to come much more easily. I naturally feel awkward if praised or paid a compliment, it doesn’t feel right or comfortable. So although I set myself tasks to challenge me beyond my current comfort zone, I still tend to feel somewhat awkward if others notice, and comment upon my successes. And hence this blog has been a work in progress for so long now.

Anyway, going back to the end of February. I attended a training course to become a future tutor with an inspiring organisation called Tempo Wellbeing Ltd. Even the act of applying had been a massive challenge for me. As my mood went up and down, so did the confidence in my ability to attend the course, let alone imagining myself taking on the role of a tutor within the organisation. Ever! I had dithered and deliberated over the forms for weeks, mainly uncomfortable with the need for two references. Having been out of work due to my health for so long, I just couldn’t think who to ask. It was only one evening when I mentioned it to my choir leader in the pub after practice, and she kindly and enthusiastically offered to be a referee for me, that things started to fall into place. That, coupled with some wonderfully encouraging emails from the team at Tempo, urging me to take that leap of faith, whilst assuring me that they would be there to catch me, were enough of an incentive to motivate me to finally apply.

Tempo Wellbeing first became known to me last summer when I had recently been discharged from an acute inpatient stay. I saw a psychologist from the HTT, and I mentioned to her I was thinking of joining a local community choir, as I felt it would be good for my mental health and wellbeing. She asked if I was aware that the health trust had just started running Recovery Choir Workshops at their inpatient units, and would I be interested in going back as an outpatient to attend? It was a no-brainier for me, in my world you don’t pass up free singing workshops! So my relationship with Tempo began.

After the first Tempo session I attended, I went back to the psychologist, totally sold out. My words to her were these, “They are so amazing and inspiring! I want to be a part of that, I feel so passionately about what they do. Even if I make the tea for those guys, I just want to be a part of it!” I had no inkling how that was ever going to happen, but when having signed up for their email updates, I saw they were looking for partners, I felt in my heart I would at some point be involved.

I continued attending Tempo workshops, and was fortunate enough to be able to spend part of World Mental Health Day with the team last October ‘on tour’. It was around this time they announced they intended to run training workshops in the future, so I registered my interest.

During my ‘shall I? / shan’t I?’ period of filling in the application forms then binning them again, I was approached by the guys at Tempo to ask if I would consider speaking at the training weekend, highlighting the positive effects of the workshops on my mental health from a service user’s point of view. I agreed, although I knew speaking to a group of strangers was way out of my comfort zone at the time. I felt it was important to push myself to do it, whether or not I attended the training myself, and if I approached it as an academic exercise rather than a personal goal, it may help detach some of the emotion around it.

I busied myself preparing a presentation for the training event, but my health was poor, with severe mood swings sending me flying high one day, then crashing down the next. The weekend before the Tempo Training, with my presentation still far from finished, my mood dipped so badly I could see no option but to take my own life. I gulped down a handful of Chlorpromazine tablets with a can of beer and pulled the duvet over myself. I had however, left a message for the Out of Hours team earlier, and it was at this point they decided to call back. In the end, when I managed to get a word in, I admitted what I had done, and after their consulting with A&E, an ambulance was sent. I had various tests, including a couple of ECGs, was put on a drip to bring my blood pressure up, given ‘the talk’ and sent home. I essentially slept from Sunday evening to Tuesday teatime, and all the while my presentation for the Tempo training weekend wasn’t getting finished.

In the end, when awake enough, I emailed the Tempo team and confessed that the presentation was unfinished, I had been in crisis and had taken an overdose, and that I had little idea how I was going to be, whether I would complete the presentation, be able to give it, be able to get there even. I felt awful letting them down, and was adamant that if I could possibly find a way to do this thing, I would do it to the best of my ability.

I was still finishing off the Harvard Referencing when I got the email to let me know that my time was about up, and the PowerPoint needed submitting for checking and Tempo-ifying. I tied up the loose ends, emailed it off, and waited anxiously for some sort of feedback. Was it what they wanted? Had I lost the plot completely and sent off utter drivel? Apparently not. I think the phrase ‘exceeded expectations’ was used. I sighed a huge sigh of relief. Then promptly started panicking about actually standing up in front of a room full of strange people and speaking it out!

I had booked myself into the hotel where the training was being held. I wanted to make everything as easy as possible for myself to give my full attention to the training and giving my presentation; so no unnecessary travelling, (even though it was quite local to home), no cooking or washing up, even my clothes were pre-selected. I knew the experience would most likely be emotional and tiring, due to my depression, so wanted to give myself the best chance of success.

It was a lovely weekend! The team of four who head up Tempo are such kind and genuine people, and the delegates (or future tutors as we were known), although from a diversity of backgrounds were wonderfully united in Tempo’s desire to improve mental wellbeing through singing. We just seemed to instantly gel, it was wonderful.

We spent the Saturday learning lots of theory, about acute mental illness, Dementia, safeguarding, how our voices work, and so on. After lunch I came to do my talk. I was so nervous. I had asked Kim from the Tempo team if she would come and help me with hitting the button to move on the PowerPoint. I discovered afterwards this was like asking the blind to lead the blind, but we muddled through somehow! My talk included my background, how I had come to be unwell currently, how I first discovered Tempo, how it had helped me, and a bit about how singing benefits healthgenerally, particularly mental health.

It was a little bit of a blur to be honest; I was so caught up in my nerves and emotions, but I sensed it had gone ok, if a bit longer than planned, and when I asked at the end if there were any questions, I was completely stunned when people started raising their hands not to question me, but to praise me for my honesty, courage, openness etc. in fact I was pretty overcome!

I chatted with another of the future tutors later when we had our break. Despite the positive feedback, I still had doubts about how appropriate some of the content was, and did I go on too long? She reminded me that in some ways it didn’t matter, that I had engaged with a room full of people, unknown to me before today, connected with them, kept them captivated and that that is a gift; content can be changed or not if needed.

At the end of the first day, I retired to the bar with my laptop and a small Guinness to do my homework, had a wonderful meal in the hotel restaurant, then retired to my room for a Lush bath, Casualty in my PJ’s and a box of Matchmakers. It was bliss.

The second day of the course was much more workshop based, and again, took me well out my comfort zone! Academic learning comes naturally to me, getting out my seat and actually having to do something is slightly terrifying! But with lots of laughs and encouragement from Team Tempo and the other future tutors, it was mostly ok, and even fun. I was aware how much I had to push myself, but that just made me feel more proud about achieving. Overcoming my fears, doubts and inhibitions just demonstrated how strong I could be. I was still emotionally exhausted at the end of the weekend, and was so relieved I had put precautions in place to minimise my stress, but I was, essentially grinning like a Cheshire Cat, because I had done it!

And to return to where I started; I felt proud. Although a little uncomfortably, I had accepted praise, and was able to acknowledge my accomplishments. And that felt good. Team Tempo have already asked me to speak again at their next training weekend (whenever that may turn out to be). That to me was the highest praise. Being asked back must be the ultimate compliment that what I did was what was required? I will allow myself to revel in that for a while……

The Invisible Line

TW Suicide, Overdose, Self Harm

At some point on Sunday night, somebody (can’t remember now if it was a paramedic, doctor or nurse) asked me if I made a habit of ‘doing this’ (taking an overdose). I said I didn’t. We established it was my first time. I guess as someone who has quite a lengthy psychiatric history, the look of surprise was justified. Why it should make any difference, I fail to see, surely anyone in such a desperate situation deserves the same compassion, but I seemed to have passed the ‘frequent flyer’ test and was regarded with suitable kindness.
When I had lined up Phases 1, 2 and 3 of my planned overdose, I had intended to complete the job, end my life. However when I finally built up the nerve to down Phase 1 (14 Chlorpromazine tablets and a can of Murphys) I realised if I could just sleep through this unbearable phase, that would be good enough. I still planned to move onto Phase 2 if sleep wasn’t forthcoming. However the Out of Hours nurse, who I had left a message for, happened to ring back just then. She talked a lot, didn’t let me say much. In the end, I just blurted out, “I’ve taken too many tablets!” She actually stopped talking at me, and began talking to me. She said she would need to contact the duty doctor to see if I needed to go to A&E. She said she would ring back in five minutes and let me know the outcome.
In my mind I had decided to move onto Phase 2 if it took any longer than that. I just wanted the pain to end.
But then the phone was ringing……sending an ambulance…….
I couldn’t keep my eyes open. I was awake but my eyelids were so heavy. I spoke to the paramedic with my eyes tightly closed. I remember them pricking my finger to test my blood sugars, and I remember them saying my blood pressure was very low. They argued about whether I could walk to the ambulance or whether I needed a wheelchair, in the end I walked and had to open my eyes.
I recall lots of different people asked me during the course of the night, what had been the trigger to taking an overdose. I replied to them all that I didn’t know, I couldn’t think of anything, my mood had just plummeted.
I was put on a drip, I think to get my BP back up, and was left, freezing cold, to myself, half asleep, half awake, in a miserable no mans land.
The MH liaison nurse arrived, who I had spoken to on the Out of Hours line earlier. She seemed kinder in real life. She asked how I was feeling. I was just tired, I said, I wanted to go home to bed.
She asked if I could keep myself safe if I went home. I replied, genuinely, “I think I have learnt my lesson.” I already felt like a complete idiot for what I had done. And I felt ashamed.
I can’t even begin to process the events of the last days. It makes no sense at all. I feel utterly detached from it. I haven’t spoken to any family or ‘in real life’ friends about it. I just want to forget it ever happened. Yet I feel as though I have crossed an invisible line. I have been to a place I had never visited before, and never want to go to again, and yet, I know, having crossed that invisible line, it will be so much harder next time I feel so awful, not to go there again.

Thank you for reading.
Angel x

When Love Hurts

Trigger Warning: Domestic Abuse, Child abuse, Bereavement, Sexual Content.

I have been pondering with interest recently DVUK’s wristband appeal, Love Doesn’t Hurt http://domesticviolenceuk.org
I not only find it incredible that I have found myself even looking at a domestic violence support website, but have found myself readily sharing their advice and links on my Twitter feed, purchasing and wearing their merchandise (with pride, no less) and generally empathising with the cause. So why does someone who was apparently happily married for eighteen and a half years until their husband died, suddenly have such affinity with women (and men) who have suffered so brutally at the hands of an abusive partner? And why has the release of the Fifty Shades of Grey movie left me feeling so rattled? I confess I never read the book. I guess it kind of passed me by as ‘just not my sort of thing’ but it is only recently, having seen excerpts of some of the text, that alarm bells have started ringing. What a couple consent to, behind closed doors, frankly is their business, but if coercion is used, that is not consent. I have become familiar via various media sources of a portion of text where Ana is begging Christian to stop what he is doing, and trying to kick him off. His response is to threaten to bind her feet and gag her if she doesn’t comply. Hey, hang on a minute! Doesn’t sound much like consent to me. Sounds a lot like assault. If a woman’s says no, at any point, that is rape. End of.
Anyhow, I digress. Love Doesn’t Hurt. When my husband died in 2008, I thought it impossible to feel any more broken. We had stuck together through some really trying times, his ongoing disability and illness, my first breakdown, and all the usual ups and downs that happen when two people from very different backgrounds decide to make a life together ‘for better or for worse’. And some. We both made big mistakes along the way. But we met at the youth group of our church, were married, in our church, and attended church together, well you get the picture. And in church the pressure was on to stick together, pray about any difficulties in the relationship, trusting God to intervene and to remain faithful to each other ‘until death us do part’. It was a wonderful ideal. It was a shame our marriage rarely lived up to the ideal.
Take me, at 17, when I met Andrew. Attending sixth form, studying for A Levels, and hoping to train to become a teacher at a local Catholic college. I’m not Catholic, but had fallen in love with the wonderful spiritual atmosphere of the place and the breathtaking architecture. Not to mention it ran the course I wanted to do, primary teaching with French, and, get this, it was on my Dad’s way to work. Perfect.
I was quite new to the Christian faith, had lots of quirky throwbacks to my very troubled early teen years, dressed almost exclusively in black, argued with anybody, was incredibly feisty and sometimes outspoken and was very definitely anti-men. I was fiercely independent and determined, yet inwardly, about as screwed up as a girl could be.
Andrew appeared confident and super cool on the outside. Three years older than me, he would zoom up to the church in his sporty little hatchback, park on a double-yellow, pop up his orange badge and saunter, leisurely-like into the building. Often sporting a smart suit and shades, he had an air of self-assurance about him. Anti-men or not, he certainly caught my eye. Twenty-seven years on, I can tell you about a very different side to the man I married.
But to cut a long story, slightly shorter, we fell in love, were engaged within months, and had our wedding planned for two years after we started dating. We wanted it that way, because at the time I asked Andrew out, he had just suffered a major health relapse, narrowly escaped death and had been given a prognosis of 6 months – 2 years. Aged 17, discovering not only that you are properly in love for the first time, but that the person you are in love with is terminally ill is a bit of a bitch.
We, being the young devout Christian people that we were, made the decision not to sleep together until we were married. With hindsight, that makes me chuckle a little. I was always the one saying, “But if we’re going to get married and be together anyway, does it really matter?”. Andrew always took a slightly superior attitude at this point, but the truth was, we were so crazily into each other at that point, although we hadn’t actually had full sex by the time we were married, there was not much besides that we hadn’t discovered!
There was a part of me that wanted to wait, anyway. The whole beautiful picture again, of sex being God’s wedding present to us, to unwrap and enjoy as a married couple together, it had such a lovely old-fashioned romance about it. And besides, older, wiser folk in the church told us how it was worth the wait (usually with a wink!)
So imagine my dismay, having waited those two years, to find the fiancé who had been so into me, turned into the husband who wasn’t, on our wedding night. Bitterly disappointed and utterly rejected, I tried to accept his reason, but I soon learnt not to question it. I learnt there was no point. Whatever the reason, or lack of one, Andrew would not discuss our sexual relationship, and that was it. He would angrily close down on me, as I questioned myself over and over as to what the hell was wrong with me. Before marriage he wanted me, now we were together it was as if he stopped making any effort whatsoever. I can only guess that he assumed now I ‘was his’ he could do want he wanted, even if that meant neglecting his bewildered young bride.
I should have taken the hint and run for the hills that first night. Or at least the next morning when the only thing on his mind was breakfast. But still the hopeful optimist back then, I just presumed that once all the excitement of the wedding had died down and we settled into a routine together, that things were bound to improve. They didn’t. On the odd occasion that he would finally give in to my requests for intimacy it was certainly not the fairytale wedding present I’d dreamt of. It was as if he didn’t really want to be there. He would refuse to take the lead and just lay there, waiting for me to do what I did, so long as it was something he approved of, and the moment he was done, he would skulk off to the bathroom to ‘deal with the mess’. I would curl up alone in the darkness berating myself for causing his disapproval again, and questioning how God could repay me for waiting, with, well, this.
Was it all my fault? With hindsight, I understand it probably wasn’t, but as Andrew kept reminding me, I was the one who had come to the marriage with the history of abuse. So it must be my fault, right? I was just too screwed up to have a relationship, obviously. The fact that I had just completed eighteen months of intensive psychodynamic counselling to get my head sorted before our marriage didn’t count for a thing when the chips were down.
It wasn’t just in the bedroom things were going downhill either. He wouldn’t permit me to share the sofa with him in the lounge. Before marriage, we had cuddled up together in front of the TV at his parents’ house, or mine, night after night, but the minute we were married he didn’t even want me to sit near him. Again I soon learnt not to question.
My going to work made him happy, my doing the cooking or the cleaning made him happy (I remember once suggesting that we should make love and his response was, “I can’t be doing with that, the housework needs doing.”) I laughed. I couldn’t help it. I didn’t even know that men existed who preferred housework to sex. I learnt then that it was no laughing matter.
My refusal to wear ‘pretty, flowery dresses’ displeased him. I really wasn’t a pretty, flowery dress sort of girl. But I even gave that a go for a while to see if it made him happier, made him want me. I gave up again and went back to clothes I liked. I grew my hair to please him. I hated it. I still never met with his approval. Nothing I did was ever right. He knew I wanted to get my ears pierced, he said he wouldn’t permit it. Aged 26 I did it anyway. He sulked and refused to speak to me. He lost the plot any time I mentioned changing from my natural hair colour. It seemed such trivial little things. He despised me trying to lose weight, even though I was way bigger than was healthy. Many of these things came down to just one of his big insecurities, “Who are you doing that for?” Whether it was a smart outfit for an occasion, sexy undies, a touch of subtle make up, new perfume, you name it, in his mind it was because I was trying to impress another man. Couldn’t get it through his head that it was him I wanted, and maybe, if I even knew he still wouldn’t want me, doing those things made me feel good about myself.
I became used to being talked down to, to being ordered around, being controlled. Over the course of first few years of our marriage it just seemed to become normal. He would put me down in front of others, but in an apparently humorous way, yell at me in public, and give me the cold shoulder behind closed doors. But in front of the people who mattered he was the perfect gentleman.
Before I was sent home from my nursing training because I was depressed, I had made the mistake of confiding in the acting charge nurse on the ward where I was working. He had spotted I was unhappy weeks before, and wore me down with shoulder massages, cups of tea, a listening ear and offers of cigarettes and cheese! In the end I admitted to him how unhappy I was in my marriage.
Then when a meeting was arranged to send me home to get well, he and Andrew did a right job on me. Andrew needed me in work, because we needed the income. He also wanted to be seen as the concerned husband. So he phoned the A/CN and asked if he should come with me to the meeting. The A/CN said no. Then when I arrived alone, before the Head of Nursing turned up, the A/CN laid into me, basically calling me a liar for saying my husband wasn’t bothered about me. He also accused me of leading him on. I didn’t even care what anyone thought anymore. What was the point? My nursing career ended that day.
Andrew always denied that he wasn’t attracted to me. He always claimed that he loved only me. But in honesty, I don’t think that he even began to know what it was to love a woman. Not as a friend, a mother, a sister or housekeeper, but as his wife, his lover, his soulmate. I believe in his own way that he did love me, or at the very least, he thought that it was love, but love doesn’t hurt. Or at least it shouldn’t.
I really loved him. But we were always more like best friends than a couple. We enjoyed each other’s company and laughed long and hard together. After a serious dose of radical acceptance on my part, we were amazing parents together. We just weren’t sexually compatible, mainly due to his insecurities and fed by mine. I nursed him until his death.
It took me five years after his death to realise that Andrew had been emotionally and verbally abusive to me. It took me a further year to admit that, verbally, to another person.
That’s how I found myself sporting a Love Doesn’t Hurt T-shirt and supporting the work of DVUK. Don’t suffer alone. Love doesn’t hurt.

Angel x

Thanks for reading.

Events of 2013 (or Prologue to Depression Part 2)

TW: Dementia, End of Life Care, Death, Bereavement, Depression, Generalised Anxiety, Separation Anxiety, Panic Attacks, Suicidal Thoughts, OCD, Intrusive Thoughts (violent/sexual), Sectioning under MHA.

It’s a long one!

Recovery from my first long depressive episode came about in 1998, at which point I was discharged from the psychiatrist and CMHT, and was followed up for a period of a further year under the close scrutiny of my GP to reduce my anti-depressants. In October of 1999 I became med-free, for the first time in nearly 6 years.

It wasn’t until the Autumn of 2013 that I conceded defeat (in my mind at least) and admitted that I was depressed again and that I needed to be medicated once more. I can now see that accepting tablets was not a sign of weakness, but an essential step in proactively helping myself. It was my own impossibly high standards that caused me to feel I had failed.

Back in that recovery period of the late nineties, I had vowed I would never let myself get into a depressive state again, and in fact for many of the subsequent years, I did actually believe that I had sufficiently learnt more effective coping strategies and self-care principles that would sustain my mental health come-what-may. And to be fair, my track record, over 14 years had been pretty good. It certainly wasn’t an absence of stress that caused me to remain well, so it did appear that I was coping better. It is only recently when I have meticulously scrutinised that seemingly illness-free period, that a few doubts have began to niggle at me, but that will, I believe, become a whole other blog at some point. On the whole, I coped during that time with parenting, caring, working, volunteering, studying, physical disability and a hugely significant bereavement. However, that ‘bit in between depressions’ will also become another blog in its own right at some point, if not several!

In the Spring of 2013, I was approaching the final semester of my Foundation Degree. I had applied and been accepted for the following year’s BA Top-up course. I had been volunteering in a pre-school for over two years previously, which appeared unlikely ever to evolve into a paid position, so when a fellow-student at uni suggested I apply for a vacancy at her nursery, I decided to give it a go. It would mean working all year round, rather than just term times, but the post was only actually contracted for one day a week, the rest would be made up of casual hours (which I was under no obligation to accept in school holidays unless I wanted to). I had chatted with my son, and he was confident that being home alone one day a week was manageable, so I went ahead and applied, very much impressed my friend and the other manager at interview, and I believe the expression used was, “Blew the other candidates out of the water!”

I was feeling like life was going pretty well for me. My biggest concern was my mother’s health. She had been diagnosed with Dementia, and my dad was caring for her full time at home. I had encouraged him to contact Adult Services to see if they were able to offer him any respite care, at least when he did his shopping each week, as he had been asking me to sit with mum, which was becoming increasingly difficult when I was trying to get my final Fd(A) assignments completed. He seemed to be coping ok though, most of the time, and I helped out when and where I could between parenting, work and uni.

As the summer holidays approached, and my assignments were handed in, life suddenly decided to bowl me a curveball. My son, just turned 13, had an unexpected return of the anxiety symptoms he had suffered from periodically since age 8. There didn’t appear to be an apparent reason, he was happy at school and doing well there, wasn’t being bullied or feeling worried about anything in particular, he was just anxious. Especially where being separated from me was concerned. This didn’t bode too well for the imminent long summer break where I was going to be working one day a week. I determined not to panic, and hoped that once the holidays started and we would be able to spend lots of days together, plus our week’s break away, that things would begin to improve. I even managed to work my one contracted day on the first week of the holidays, and although my son wasn’t too happy about it, the following week we would be together at the seaside, nicely chilled, enjoying some quality mum/son time in the sunshine. Surely a lovely relaxing holiday would put the world to rights?

Well, sadly not, it appeared. Despite it being a very familiar, and safe environment, my boy’s separation anxiety was only getting worse. The more time he spent with me, the less able he seemed to do anything without me. He also appeared to be experiencing a sudden, massive influx of growing-up hormones, which he found unsettling, distressing even, however much I reassured him that it was very normal for a lad his age, and that even finding it daunting was not an unusual response. His anxiety was just spiralling more and more out of control.

We returned from our holiday mid-morning on a Monday. I telephoned my dad, as I always do after a journey to let him know that we were home. He sounded distracted and cross, which is not how my dad usually reacts to hearing from me. He was obviously not in the mood for a chat, so I took the bull by the horns and asked him what was upsetting him. I wasn’t really prepared for the onslaught that followed, which although not directed specifically at me came like a bolt out of the blue. “I’ve got a social worker coming this afternoon. I can’t cope with your mum anymore, she won’t take her tablets, thinks I’m trying to poison her, that I have her imprisoned here, and she is so nasty to me and keeps lashing out!” Somewhat taken aback, and slightly overwhelmed as I surveyed the mountains of luggage, just in from the car, but yet to be unpacked, my reply came without hesitation, “What time is the social worker coming? I’ll be there.”

Even given this conversation the scene that met my eyes that afternoon was worse than I could have imagined. At one point I had to physically put myself between them to stop my mum attacking my dad. In front of the social worker. Every time dad tried to speak to myself or the social worker, my mum would screech over the top of him, “Don’t listen to him, he’s telling the most wicked lies about me!” And she actually believed it. The haunted look in her eyes gave her away. Dad just looked broken, exhausted and so, so sad. He’d been her carer for a good while, but he’d never looked so old and worn out. It was just horrible.
The social worker was vague to say the least. I pointed out to her that my dad needed an emergency respite break, clearly they couldn’t continue as things were. The longer mum went without her medication the more paranoid she was becoming. Yet still the social worker left without giving any firm assurances that dad would get the break he desperately needed. They promised they would be in contact.
Tuesday came and went and dad heard nothing. When he still didn’t hear anything by Wednesday afternoon I called them for him. Still they were fobbing us off, and still mum was getting worse. Come Thursday, I told my son I couldn’t take the day off work, it wasn’t fair on my colleagues and that I had arranged for him to go to the house of a family friend. He wasn’t best pleased, but with a lot of my attention having been directed towards my parents in the previous days, he accepted that the friend, who always stopped what she was doing when my son visited so she could devote her day to him, was at least second-best to having me at home.
I loved my new job. The children I worked with in the pre-school room were truly delightful and I adored their chatter, their imaginings, their honesty, their wonder. It was a magical place to work and the staff had accepted me readily and wholeheartedly. At the end of the day, I drove home to get changed and freshened up before going to collect my boy.
Back home I noticed the phone’s little light was flashing to indicate someone had called, but there was no message. I scrolled up to see the call list – my parents’ number. I rang them immediately, but there was no reply.
My mind was racing, but deep down I had a feeling that my mum had been taken into the dementia ward so she could be assessed and stabilised and my dad could have a rest. I assumed he was still settling her in. When I finally got a call from my dad later, yes, that was the general gist of what had happened, but in the version in my mind I hadn’t really thought through the necessity for an ambulance, paramedics, GP, police officer and social workers because mum had point-blank refused to go to hospital voluntarily and had been sectioned under the Mental Health Act. My dad was clearly traumatised by the whole experience, but I did my best to assure him that it was absolutely in both their best interests in the long run, and that mum would be well looked after in hospital.
When I collected my son, he was distraught to hear about the plight of his beloved grandparents, and once more his anxiety went through the roof. He realised, as I did, that my dad was going to need a huge amount of support from me in dealing with the hospital staff and social workers in the coming days.
Balancing the needs of my elderly parents with those of an anxious teen was never going to be a walk in the park. Already I was beginning to notice how tired and stressed I was becoming. Our holiday felt a lifetime ago. I wasn’t sleeping terribly well and was getting irritable. I knew what I had to do. I made an urgent appointment with my GP and told him I was stressed, exhausted and needed a sick note for the time-being. He didn’t argue. I think at that point he asked whether I thought I was becoming depressed, but I was pretty confident that without having to worry about work for a while, and with mum now safely in hospital, hopefully things would settle down a bit and I would have an opportunity to rest up before the sandwich making and school runs recommenced.
It was a nice thought. My dad found it hard to relinquish his caring responsibilities and it wasn’t long before I was accosted by the ward sister one afternoon when visiting mum. She was very concerned that my dad was still planning to have mum home with support from visiting carers, when their observations on the ward led them to believe she now needed 24 hour residential care. And could I have a chat with him? See if I could get him to see it their way?
In the meantime my son’s anxiety continued, gradually worsening as the beginning of the new school year approached.
I can’t remember the exact point in the Autumn I returned to my GP and said I had tried my self-care measures as best I could under the circumstances, but I was still feeling low and increasingly anxious. The anxiety had come to a head when I had to take a sick note into my managers at the nursery. As soon as I approached the gate I could feel my heart racing, chest tightening and tummy churning, and by the time I reached the front door I was having a full-on panic attack, hyperventilating, shaking and sobbing uncontrollably. It was my lovely manager (not the one I had studied with) who gently suggested perhaps now was the time to accept medication. I knew she was right.
I never went back to work at the nursery. I did manage to complete the first semester of my BA Top-up course, but the events of that Autumn term comprehensively sealed my fate.
My dad was utterly devastated that the ward sister was recommending residential care for mum, but when he asked what my opinion was, and I had to confess that I thought the sister was right, he just trusted me. He concluded, “Well you had better have the final decision on a care home, as you know about that sort of thing.” Thanks.
Actually it was the first care home we looked at that social services suggested may have a vacancy for mum that we were totally sold on. A friend who works in community nursing couldn’t recommend the place highly enough, and several other friends had positive experiences to share too, so we were decided. Except in the meantime mum had started to deteriorate due to the staff finding it increasingly difficult to get her to take her tablets, even covertly, as she wasn’t eating. May have had something to do with her mislaid dentures, but I am saying nothing. I have experienced working in dementia care and property does get misplaced. We also *nearly lost her engagement ring, too. I found that though, eventually, unlike her teeth. They never did surface.
It took a huge amount of time and energy to get my son back to school in the September, often I would have to physically walk him into the school office and wait for a trusted teacher or member of the pastoral team to receive him from me and take him to registration. I always did everything in my power to get him into school, and had a good open line of communication with his head of year. I worked with school and they worked with me to help my son cope with his anxieties. I think by the October half term he was a little less unsettled than previously.
The hospital persisted with mum, but she was very unwell. The place at the lovely care home couldn’t be held for her any longer, and it was suggested that due to her deterioration we would now have to find a nursing home, rather than just residential care. It was my intention to work on this after half term when the boy was back at school.
We spent the first weekend of the school holiday at Center Parcs in Nottingham with many friends old and new from WAY – Widowed and Young. It was the first time we’d participated in their annual pilgrimage to Sherwood Forest, and I was really excited. Sadly my son didn’t share my enthusiasm, at first at least, and not long after arriving I was being consoled by friends while he was given a bit of a talking to! Thankfully it did the trick, and a little longer into the weekend he was begging me to book for the following year!
While we were there, a violent storm was forecast for the Sunday night into Monday. We were due to be driving back to Hampshire on the Monday morning, and I panicked a bit. In fact I was so reluctant to attempt the journey home, that I went online and booked a budget hotel nearby for the Monday night. I called my dad early Monday morning to let him know we’d decided to stay another day, and was surprised when he said, “I was just about to ring you!” Immediately curious I asked why. He went on to tell me that mum had had a fall in the early hours, had broken her hip, been transferred to the general hospital, and was booked for a hip replacement op in a couple of hours. I was stunned. Again my mouth went into autopilot, and the words, “I’ll be home as soon as I can” tumbled out.
It wasn’t a pleasant journey. I was worried sick that mum, being as frail as she was, may not even survive the surgery. And although the worst of the storm appeared to have passed, it was still very wet and windy, the roads were littered with debris, and some were closed completely – including the main A34, the final leg of our trip home. The first alternative the sat nav gave us was also blocked, and we ended up on a not-so-magical mystery tour of the country lanes of Oxfordshire and Berkshire. With a near empty fuel tank!
Eventually we made it safely back to Winchester and caught the tail-end of visiting hours at the hospital. Although obviously sleepy, mum seemed fairly perky for someone who had just had a general anaesthetic. She also recognised us and was pleased to see us (both of which were often hit and miss). I left feeling cautiously encouraged.
My caution, however turned out to be justified. Mum refused her tablets, even pain relief, refused food and drink and definitely refused to attempt her physio. By Wednesday she was attached to a drip when we arrived, and by Thursday morning we got the ‘come to her bedside’ call. I took my son in to see her for the last time. She had rallied a little since the nurse had made the call, and vaguely woke briefly when he spoke to her. There was a flicker of light in her eyes as she registered her grandson. I arranged for our church minister to come and collect my son shortly after that, as dad and I settled ourselves for mum’s final hours.
I had telephoned my brother as soon as we had ‘the call’ and he’d said he would get to the hospital within the hour. As the day progressed, mum was weak, but stable, but still there was no sign of my brother. At about 6pm, having sat by the bedside all day with only the odd warm drink and a couple of biscuits, dad and I spoke to the nurse. It was decided we would go and get a meal, and pop home and pack a bag so we could continue the vigil overnight. Apparently soon after we left my brother appeared, but according to the nurses ‘didn’t stay long’.
We spent most of the night popping mum’s oxygen mask back on, as she repeatedly pulled it off again. When left off, her breathing became so laboured and distressed. A number of times during the night she was peaceful, and I watched as her breathing became more and more shallow, wondering if that was the last time I would see her chest rise. I admit I silently prayed to God to release her at those times. Yet each time, I thought, “This is it” she would suddenly start, as if waking from a nightmare, rip off her oxygen, and so the process would begin all over again.
In the morning the doctor came in to review her. When he saw us struggling to keep her oxygen mask on mum, he told us to leave it off. I protested, but did as he said, and within moments she was noisily gasping for breath. Doctor said he would give her something for her distress. I knew exactly what that meant.
It was at this point my dad decided he needed to go home. I asked the nurse if this was advisable, but she promised to call us if things changed, so I drove dad home. No sooner had I got back to mine, than we got the call to go back. Except dad wasn’t ready and wasn’t going to be rushed. By the time we got back to the hospital mum had gone. It was 1st November 2013. Two weeks before her 80th birthday.
My dad leaned on me heavily to arrange her funeral (“Well, you’ve done it before”) and deal with all the other administration. I would battle the boy into school of a morning, go to dad’s, stay with him during the day sorting paperwork etc until school ended then I would rush back to collect my son, and spend the rest of the day making sure he was feeling as safe and secure as possible. He was really struggling to sleep at night though, which was tiring us both out.
Somehow everything came together in time for the funeral, and I survived in a bubble of disassociation and busyness. I continued the rounds of school runs, admin, late nights settling the boy, oh and going to uni on a Tuesday.
A couple of weeks after the funeral, I had an essay deadline and presentation to give on the Tuesday afternoon. Just as I was getting ready to leave home, I got a call from my son at school on a friend’s mobile. He was really distressed and was desperate for me to go and collect him. I inwardly panicked, yet tried to reassure him as best I could. My mind was racing. Even if I collected him I still needed to get to uni, I couldn’t fail two assignments after all the work I had put in, even in the worst of circumstances. Children were not permitted on the uni campus. I told him to go and see the school nurse, who was very good with him, and to stay with her if necessary, and that I would see him at home after school, the minute I had finished giving my presentation. I am still unsure as to whether I made the right decision, but at that point in time, failing the assignments was unthinkable.
I handed in my essay and tried hard to keep my mind on the job in hand, which was introducing a new way of working, as if in a staff meeting to a group of early years colleagues. Giving presentations was always my least favorite form of assessment, as I struggled with my nerves. But I did my best, gave it my all, and got the heck out of there as quick as humanly possible to get home to my boy.
I was pretty shocked to see the state of him. He was utterly distraught. By all accounts it seemed he had suffered some sort of breakdown in school. I got him the next possible appointment with our GP and just sat soothing and reassuring him for the rest of the day.
I didn’t even attempt to get him back to school in the short term. Our GP concluded my boy was depressed, and had he been an adult he would be writing him a sick note, and that he would be happy to write a letter to school to that effect. He prescribed benzos to reduce his night time anxiety and help him relax and also made him a referral to CAMHS.
I was floored at how I had failed to notice how unwell my darling boy had been getting. I felt like the worst parent ever. I handed in my notice at the nursery, and determined to put his needs first from now on. I didn’t have to work out my notice as I was still signed off with depression myself.
Even without the pressures of school, and with me at home, by son’s health was still continuing to deteriorate. He became unable to sleep in his own room unless I sat in there with him until he was soundly asleep, which was often not before 3 or 4am. I was beyond exhausted myself, and in utter frustration and experiencing such horrendous sleep deprivation I started allowing him to sleep in my room, in the hope we may both get some rest.
All the while I was chasing up the CAMHS referral as well as hounding Children’s Services for support, given we were both suffering with our mental health. It felt a bit like climbing Everest given my own depression. My GP had referred me to italk, but after my first long assessment call, it was concluded I required more support than they could offer.
My son finally got an initial assessment appointment from CAMHS through. In communication with school, as the Autumn term was drawing to a close, it was decided we should forget attempting to get him back before Christmas, but start afresh in January.
Before the appointment with CAMHS, things worsened again though. My son began experiencing distressing thoughts of a violent and sexual nature about people he saw. He was absolutely horrified, as he was such a gentle soul and nowhere near as worldly-wise as his peers. It was highlighted particularly because we had arranged to exchange Christmas presents with family, and his thoughts became focused on his younger girl-cousin.
He was in such a state and I was useless explain to him what was happening. Because the thoughts were causing him to feel suicidal, I was advised to call an ambulance. We were taken to A&E. I remember we knew the nurse who received him from the paramedic. The sheer relief to see a friendly face was overwhelming. She also brought me a mug of tea and biscuits, bless her. After chatting with various A&E personnel, the duty child / adolescent psychiatrist was contacted. She wasn’t able to come to the ED but she spoke at length first with the casualty consultant, then with me. She told me that my son was suffering with OCD Intrusive Thoughts. I was amazed that his distressing symptoms actually had a name and were a recognised ailment. She even reassured me that it seemed to be the case that it affected those least likely to act on the thoughts, and it didn’t mean he would grow up to be a murderer or sex offender. He had already expressed such fears, so I was massively relieved to be able to reassure him. She prescribed Fluoxetine, stating it would help his mood as well as his obsessions.
At the subsequent CAMHS appointment we were seen by the Systemic and Family Psychotherapist. It was agreed he would start sessions with my son after Christmas. Finally, as 2013 was drawing to an end, it seemed he was being heard. Next was to get help for me!