by Maria McCarthy | 21 Apr, 2023 | #MeToo, Child sexual abuse, Death and grieving, Family and forgiveness, Memoir, Relationships, Trauma, Truth, Writing, Writing and wellbeing
I was 20,000 words into writing a memoir. It was a year since my mother had died, and the work was about my relationship with her; best described as difficult. Early in the process, I decided that I would only write about my relationships with the dead, with the living as incidental characters. The work was developing into a possible book about grief. Disenfranchised grief, to be precise; a phrase only recently learned from a writer friend, Victoria Field, when we met for coffee to talk about her published memoir, Baggage: a Book of Leavings, and my work-in-progress. It’s a complicated kind of grief, when you have been estranged from the deceased. You may feel, and others might feel, that you have no right to grieve. But the loss of a parent, no matter how difficult the relationship, is a big hit.
Another unresolved grief came up for me as I was writing. A close friend had died by taking her own life some 35 years before, the same week as my second daughter was born. I hadn’t grieved for Julie, the friend, at the time (the reason being closely tied to my mother, who had decided for me that I should not go to Julie’s funeral). I was pleased by the way in which the memoir was developing, and it was helping me through two complicated experiences of grief at the same time. But there was a snag, a fear. How would the living react to my work? Specifically my four siblings.
I spoke to several memoir writers I know about family reactions to their published work; the first being Victoria Field. I asked if anyone had objected to the memoir. She told me that a relative had said she didn’t want to read the book, as it might upset her. That was it really. The main figure in Baggage, Victoria’s ex-husband, had not raised any objections. She had disguised his identity, but not sought his permission. I wasn’t so sure about my own family’s reactions. I had included siblings in the work – as the middle of five children, I could hardly pretend I was an only child. Family dynamics played a part in the relationship I had with my mother. I had been sensitive, and had not used any names, but the terms ‘older brother’ or ‘younger sister’ were jarring.
I spoke to John O’Donoghue, the award-winning memoirist, author of Sectioned: A Life Interrupted. As an only child whose parents died when he was young, John had no experience of having to consider siblings as he wrote. He suggested writing to each of mine, telling them what I was working on, and asking their permission to use their names, or pseudonyms, if they preferred. He also said that I could offer to send them a section of my writing. My younger brother was fine with his name being used. ‘Anything that helps,’ he said. So far, so good. My sisters’ replies were identical. They did not wish to have their names used, or to be written about at all. They did not want to read anything I had written. One sister added that she found my writing ‘triggering’.
OK, not a dealbreaker, but a setback. Then John, my older brother, phoned me in a state. He told me that he hadn’t been able to leave the house, that he was suffering from anxiety since he heard from me, and that if I were to publish this work, he would have to move to another town, as he couldn’t face seeing anyone he knew. We had two long phone calls that day, and though I assured him that I had not let slip anyone else’s secrets, only my own, he was implacable. He did calm down to an extent, said that maybe I could publish it anonymously, once he better understood what I was about. We spoke a lot about grief, about Julie’s death as well as our mother’s. He shared that he, too, had lost a friend recently. However, seeing how distressed he was, I told him that I would discontinue work on the memoir. All was well between us once again.
The trouble was that I could not write for a year afterwards. John O’Donoghue advised that dark stories have a way of finding light, and that this would not be the last of it for me. But, he said, you can’t write with someone looking over your shoulder, and that’s how it felt every time I sat to write. What would John think? What would my other siblings think?
The second memoir I started was a year or so later. It was my story to tell, no-one else’s. I wrote with some fear, but not about what my siblings might think. The book-length work reached its first full draft within 3 months. It was about a police investigation after I reported a case of historical grooming and sexual assault – rape – by an older boyfriend I had when I was 15 and 16. The investigation was thorough on the part of the police, and the perpetrator was interviewed twice in connection with the offences. As I had predicted, they could go no further due to lack of evidence, but the man (whom I shall call Adam) was brought to account and faced with what he had done to me. It was a story that would help other women and girls, and the writing of it helped me process my experiences.
Only my younger brother knew that I was writing it; I didn’t tell my other siblings. I didn’t need their permission, nor did I need another reaction from John, my older brother. My suspicion was that he would be more concerned with what other people would think than I was. The book reached its third draft, after some feedback from John O’Donoghue, then I hit a snag. In my research, I found a photo on the internet of another man that had sexually assaulted me on a long train journey when I was 13. I couldn’t remember his name; only that he was in an Irish showband, and the name of the band. There was the face I had never forgotten; an obituary in connection with his musical career. Thank God the bastard was dead, but how many other young girls did he assault? I now knew the true meaning of being triggered.
That was 6 months ago. The work has been put aside, filed away, the various drafts in ring binders marked ‘Chalk Lane’ the working title of my memoir. Dark stories have a way of finding light… will I return to it, face my demons? Try for a publisher and get it out in the world? If I do, I will not fear the reactions of my siblings. John, my dear older brother, died a few months ago. I no longer need to worry about him. As for my other siblings, this is my story, and my choice to write it and let others read it. Like Victoria’s relative, they can choose not to read it.
Some other memoirs I would recommend: The Missing List, by Clare Best; First in the World Somewhere, by Penny Pepper; My Name is Why, by Lemn Sissay; To Throw Away Unopened, by Viv Albertine; Patricia Debney’s blog, which excerpts her as yet unpublished memoir, Learning to Survive; and my all time favourite, An Angel at my Table, by Janet Frame.
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by Maria McCarthy | 11 Apr, 2021 | Chronic illness, climbing trees, Death and grieving, Editing, Friendship, Memoir, Mental health, Relationships, Secrets, Trauma, Truth, Writing and wellbeing
I am part-way through the second draft of a long piece of writing. It’s book length, non-fiction, and that’s all I want to share. The fear has got hold of me, fear of if it’s any good, if anyone will want to read it, if I want anyone to read it. Perhaps I just needed to write it, and it doesn’t matter if no one reads it. Perhaps, once this second draft is complete, I’ll rest it, not look at it for a while, or never look at it again. I might just destroy it – a passing thought. I know I won’t do that.
I have written a paragraph to summarise the book, the kind of thing that might appear as a blurb, on the back cover. There I am, calling it a book, as if that might happen. Ha! I am drawn back to my MA class when Patricia, my tutor, would say, ‘What is it about?’ when we were discussing texts, or workshopping one another’s writing. And I find that the book is not just about what I set out to write. It’s also about loss, about grief, it’s about the toll that trauma takes on the body.
I wrote the first draft in two months, which is the fastest I have ever written anything of that length. I wrote a little every day, scared that if I missed a day, I wouldn’t return to it. Some days I wrote only two hundred words, others much more. I found that the gingerbread man timer I usually set to stop my wrists and back from hurting, if I type too long, had been ignored, and my wrists and back were indeed hurting when I stopped writing and noticed things other than the words on the screen, on the printed page.
Some things were hard to write, having held onto them in silence for so long, some for forty-five years. I felt better for speaking them, for writing them, but sometimes I don’t, and today is one of those times.
I didn’t plan this book before I wrote it, just wrote scenes and chapters as they occurred to me. I thought I could sort out the order later. And I find that they do make sense in the order in which they came. There is only one chapter that I might place elsewhere, or maybe cut it all together. I wrote it as light relief, as a positive story about that time, about myself. There are a few stories like that in the book. It’s good to remember those fun times as well as the trauma. Light relief for the reader as well as the writer. The reader! There it is again, the thought that someone might read it. Maybe they will, maybe it will go out into the world as a book. Maybe it will help others who have been through the same kind of things.
Early in the writing process, I wrote a dedication: For those that have not yet spoken, and for those that have. I must remember that, when the fear takes hold, why I wrote it. For myself and for others.
The ending is set on a day in March of this year, when I went in search of a tree to climb, in memory of my friend Karan, on the anniversary of her death. It’s a remembrance of loss, but also of hope, as the book will be. A memoir of grief, loss, hope, and understanding. Here is an extract, a reminder of facing the fear:
We slide down the muddy slope. It’s incline is one I would normally attempt, with a tree to hold onto on the first couple of steps down, then nothing to halt the slip and run towards the bottom. Bob goes first. He says, ‘Just go for it,’ and the rush of the last few steps is liberating, even though there is a risk of falling. How seldom we do this as older adults, just go for it, see what happens, risk falling on your face or your arse, and would that matter, after all?
I size up the horizontal branch. It takes a few attempts to pull myself onto it. I worry that I can’t do it. I just don’t have the upper body strength. Then I think of my granddaughter on a climbing frame at a playground a few weeks before. She tells herself that she can, when at first she thinks she can’t, when attempting scary climbs, or anything scary. I am doing this for Karan, to regain that childhood feeling, and I haul myself onto the branch, straddle it like a horse, and I am grinning, laughing. The seat of my jeans is damp and slimy where the mist has clung to the bark. My coat is splattered with mud. I am ten years old again.
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by Maria McCarthy | 15 Sep, 2020 | Chronic illness, Disability benefits, Truth, Uncategorized
Jane spoke without looking at me, without mentioning my name. ‘I think there is a personality disorder,’ she said. The meeting had been called to discuss the problems with the project I worked on, the clashing ideologies of the the national charity that employed me and the social services department where I was based. But mainly to address the concerns I had about how my volunteers were being treated, concerns that the volunteers had raised with me, which I had passed on to Jane, the social worker, her assistant Pat, and my manager at the national charity. Instead of discussing how these concerns might be addressed, I was being accused of causing trouble due to having ‘a personality disorder’.
My role was recruiting, placing and supporting young, full-time volunteers, in partnership with a scheme run by the social services department of a London borough. The scheme was based in a former children’s home. A couple of the rooms had been retained as bedrooms, as off-duty accommodation for the volunteers. While ‘on duty’, the volunteers lived in with a severely learning disabled person. There was supposed to be a paid carer at each project as well as a volunteer. The scheme was supposed to provide a positive experience for the volunteers as well as enable people with disabilities to live in their own homes, many having come from long stay residential care, at a time when Care in the Community was a new thing.
It soon became apparent to me that the volunteers were being exploited. Where there were insufficient paid carers and volunteers, sole volunteers were left at on duty for several days without relief. Also, the off-duty bedrooms were not exclusive to one person. Whichever bed was available was used, with no change of sheets, and there was nowhere for the volunteers to permanently keep their possessions. They were effectively living out of a suitcase. There was a volunteers’ house, too, given to the scheme by the council. It was ramshackle and tatty, and was infested with rats.
I thought that if I spoke the truth, if I tackled these problems directly with Jane and Pat, then they would be addressed. Instead, there was a kind of war against me, waged by Pat. Some of these skirmishes were direct – angry phone calls to my home on the days I wasn’t working. Others were sly, and difficult to deal with. Piles of jumble were left on my desk, paint pots and brushes piled behind my chair when the office I shared with Pat was being painted (she moved them there; they had been against a wall away from any desks). Pat complained that the name plates on our office door should be reversed in order: mine was above hers, purely because my surname came before hers in the alphabet. Instead of taking any responsibility for the volunteers’ poor living conditions, both Jane and Pat blamed these young people for being lazy and dirty. And I was blamed for not supplying the scheme with enough volunteers.
Whilst I was believed by my manager, who stated that she was very concerned about me working in those circumstances, and about the volunteers, nothing changed in that scheme. The charity did not withdraw from supplying volunteers (which I suspect was due to them not wanting to lose the funding), Jane and Pat did not make any improvements to the volunteers’ living conditions, and I continued to be targeted by Pat in her petty war. The only thing I could do, for my own wellbeing, was leave the job.
The reason for recounting this story is to show that telling the truth, speaking out, is not always received gratefully, or dealt with as it should be. It’s something I have been thinking of recently, of times where I have spoken out and told to keep quiet, incurred the wrath of others, or had my truth denied.
In the early days of my illness I was disbelieved by my GP. He put all my symptoms down to depression. This went on for two years, his blinkered view not open to the fact that the various symptoms I had might add up to other diagnoses. I was telling my truth and my truth was ignored, discounted. I felt I was going mad; not being believed makes you feel like that. Sure enough, when I changed GP I received a proper and full diagnosis.
Over the years, I have had skirmishes with the DWP over my disability benefits, and each of these has been due to me not being believed. This year, I was assessed for Personal Independence Payments (PIP), which is replacing Disability Living Allowance, a benefit I received for 20 years as an indefinite award. My husband and I filled in the form together, gathered evidence from professionals involved in my care and a friend who could account for how my disabilities affect me. My account and all the evidence were disregarded by the assessor. She spent less than an hour with me, and decided that most of what I said, what was written on the form, was not true. Because she said so.
It was not just the loss of benefit that affected me, it was not being believed. I did not exaggerate my difficulties, in fact it was really hard for me to put across how badly I function on most days, to address the truth of how limited my life has become. I contested the decision, asked the DWP to look again via a Mandatory Reconsideration. The letter that came (12 weeks later) ignored all my points, again ignored the supporting the evidence, and upheld the original decision. So I appealed to the independent tribunal service, expecting to wait a year until my case was heard. Imagine my surprise, a month later, when the DWP (not the tribunal service) wrote to say that they had reconsidered the original decision and the Mandatory Reconsideration. They were awarding me PIP at the highest rate. Although this is wonderful news, I have had trouble accepting it. First I was disbelieved, then disbelieved again, then all of a sudden believed! I am half-expecting another letter to say they are taking it away.
Truth -telling and how it is received … it is too big a subject for a short blog. Especially at a time when liars and deniers hold power in the White House and in Downing Street. Globally, truth and evidence are ignored in favour of what people choose to believe. Personally, individuals will always be ignored or vilified for speaking their truth, will be made to feel like they are going mad.
*Jane and Pat’s names have been changed.
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