“Tell the Wolves I’m Home”, Carol Rifka Brunt

Book Reviews

Having just finished this novel, I’m full of questions and admiration for Brunt. Written in 2012, set in the 1980’s, it certainly addresses the taboos of society during this era surrounding AIDS, through the protagonist’s journey of realisation and love. June Elbus: the epitome of innocence interlinked with a newfound sense of rebellion. Her journey of learning to accept a wrong love is both poignantly naive and heartbreaking as she understands the ramifications of her unrealistic desires. What’s  additionally poignant is the fact that Brunt outlines the direction of the novel from the first page: we understand that we have to accept a loss before we turn to the second page.

I think the most interesting concept in this novel is we ultimately know what will happen in the end. There’s a foreboding death hinted throughout the second half of the novel, very subtly understated yet very prominent in the actions and decisions of the characters. In many ways, Toby’s death is just as painful as the loss of June’s innocence. We as readers grow to accept Toby for the actions he is accused of and what he has done, and our love for Toby is reflected through the endearing, innocent June and her love for Toby. We learn to admire Toby for who he is and everything he stands for, not for the supposed crime he has committed and what has happened to Finn.

Toby is everything Finn is not and that’s quite possibly what makes him so charming; he’s not an artist, he doesn’t have family in the country and he’s estranged from everyone and everything he knew. He’s learning to make his own way in this prejudiced world, alone and at a distinct disadvantage fundamentally due to his sexuality alienating him. His death hits the reader and June very deeply, almost unfairly snatched from us both as his true identity begins to unravel before us.

The topic of AIDS is so beautifully expressed in this text; Brunt confronts the issue with compassion and fragility, similar to the characteristics possessed by it’s victim, Finn. Times have changed with regards to AIDS and it’s treatments/cures which the reader will recognise whilst following the protagonists’ journeys, but we’re nevertheless transported into a time where AIDS was believed to be as  lethal as the plague and anyone in a close radius of a patient will consider themselves at risk of “catching” it.

I find the character of Greta most compelling, however. She is immediately and instantly dislikable with her cruel and cutting attitude towards her little sister; she’s calculating and malicious once she realises what her younger sibling is doing. Yet, we understand she’s coming of age and is fighting her own battles which torment her, too, thus making her a sympathetic figure by the end of the novel: we admire her and respect her, finally. Her fear of losing her younger sibling to another love she refused to offer results in her acting with cutting maliciousness through cold remarks and sarcastic rhetorical questions. Greta is quite possibly the smartest character in the novel and although she makes mistakes, they’re understandable and forgivable. Her brief snapshots of kindness and mature, older-sibling care are greatly appreciated by us, not so much by June as we understand before she does what exactly she’s going through; quite possibly some of the readers have experienced her internal conflict, too, and the evaporation of childhood towards the rush of entering adulthood.

We laugh with Finn and June as we follow their footsteps, internally grimacing and sympathising with June as she naively mistakes familiar compassion for romantic love and we cry with June as we lose someone we barely know, yet adore nevertheless. The embedded innocence in all of the characters is something conveyed so exceptionally by Brunt, connecting the reader to the character. The loss of two of the most beautiful souls is something the reader struggles to come to terms with, just as June and Greta do, yet we are comforted with the knowledge that they loved and were loved in return, in equal measure. And that’s fundamentally important for every living soul: to love and be loved.

A x

Dissipate

Mental Health Activism & Awareness

They’ll ask me: “what’s wrong?”

with the expectation of hearing “I’m fine”
to which they accept
and move on.
And so do I.
Inside, I’m far from fine;
I cry at everything
not knowing why.
I sleep a maximum of four hours a night.
“I’m fine.”
The offers for help are vacant.
“It’ll be okay” soon becomes
“maybe you’re overthinking things a little?”
You can help me with my maths homework
but you’ll never help me solve
the puzzles in my head.
One plus one doesn’t always equal two
up here.
You can’t help me get rid of the monsters under my bed.
“I’m here if you ever need a shoulder to cry on”-
fucking liar.
That offer is far too soon retracted.
I’m here for you if your boyfriend dumps you
but that’s all I can offer you.
My problems are not as shallow as that.
The depth of my problems compete with the ocean;
what will drown me first?
I guess I’ve learnt over the years
there’s only one hand that will reach down for you
into the abyss,
whilst you’re drowning and gasping for air.
Trying to gasp hold of the last fragments of sanity
as they dissipate between your fingertips.
That hand, my friend
is yours.

“Assisted Dying”, or “Assisted Killing?”

Current Affairs

I’m incredibly disappointed to learn that 330 MPs rejected the idea of allowing a terminally ill patient to end their lives with medical supervision, despite many doctors agreeing to administer the drugs and take part in it.

I understand the cons of the bill; the possibility of vulnerable patients being exploited by their families and pushed to end their lives. That patients may feel the need to end their own life to stop the misery and pain of their loved ones. I get that. However, I am of the opinion that those 330 MPs acted with complete selfishness and possible religious bias.

I am not terminally ill, so I cannot speak for those who are. I also strongly oppose the categorisation of people who qualify for the ‘right to die’ – those who only have 6 months to live. What about everyone else? What about those who have been suffering from constant pain for months and even years on end? What about those with absolutely no quality of life? According to the Guardian, “one in five people who travel to Switzerland for assisted-dying are from the United Kingdom.” Surely the statistics speak for themselves?

I’ve watched and read a fair few interviews with people who suffer from motor neurone disease and their biggest fears were living a life of complete paralysis, wheelchair bound and in pain without the ability to speak coherently and express their distress. For MPs to deny these people that right to me, is a complete failure of morality within the establishment of law-making.

Another obstacle in this debate is the concept of religion. In many religions such as my own, it is forbidden to take one’s own life. Full stop. There are no ifs, no buts; just no. I understand that life is precious and a gift; we only get one and we ought to do all we can to preserve it. But I will never understand the point in living if there’s nothing to live for because an illness or health condition is prohibiting you from doing so, and instead you’re sentenced to a life of pain and misery.

I sincerely hope this isn’t the end of the debate on assisted dying. We ought to give these people a chance to do as they please with their own lives, as they’re the ones living it. Not us. For authoritative figures to simply dismiss this chance in the name of “ethics” is simply incomprehensible and morally unacceptable.