Written in a compelling and beautiful tone, the piece by foremost journalist, blogger and talk show host, Funmi Iyanda, is a narration about the vicissitudes of life – tragedies and triumphs, pitched around her gay friend – Akin Akintayo.
…on bravery, honesty and thriving.
I remember the first time l saw him at the cemetery.
I had been crying. I had not quite cried since leaving the hospital but when the flames of the incinerator swallowed Remi — in that beautiful coffin we had carefully selected -something gave in my chest. The unceremonious finality of cremation startled me. I ensured Remi got the sort of funeral she would approve of, but in all our many conversations l had never asked her preference. But then, I hadn’t expected her sudden death.
She was Buddhist, I suppose Buddhists automatically want cremation, but Remi liked the attention of those she loved. Would she not have preferred a burial so we can bring her flowers as she did her mother? White lilies, clean, neat, streamlined, as she liked things. Remi was a person who straddled contradictions effortlessly.
So l cried out of a sudden fear l had let my friend down. The deep dankness of grief would not hit until much later.
It was through those tears, on a cold November morning, that l saw Akin, he looked young but he looked old, he had a walking stick and dressed like he belonged in a 50’s swing musical; cravat, pocket square, hat and all. I didn’t think he’d dressed up for the funeral; there was casualness in his formality of dress.
When we were introduced. I said a warm hello, at least l think l did- and promptly forgot him.
Months after, a mutual friend tried to commit suicide so we both found ourselves by his side with two different approaches to wrestling life back from despair. Subsequently we got talking, infrequently but cheerily. I liked the immense amount of know “how-ness” and ribald sense of humor buried beneath his dapper exterior. He was a master of innuendoes and pointless trivia whose engineer’s mind solved and resolved tech problems.
I heard he was homeless but had recently got a tech contract job in Manchester, this must be true because he asked me for a small loan to rent an apartment whilst he waited for his first pay check.
I gave it to him without expectation of payback or much interest in his life, I used to be too busy to live. Soon enough l flew off to some job some where in the world l no longer remember.
But Akin paid me back as he said he would. He also started visiting me periodically from Manchester for long languid brunches where he’d ogle gingers and water his latest plant.
It started with a swelling in my foot after a reformer Pilates class, Akin laughed about repercussions of sexually suggestive inner things stretches. It was the last bit of exercise I’d do in the past two years. In those years the illness took almost everything l used to define myself by.
The early months were difficult, no less because of conflicting diagnosis and confusing doctors-but this is not that story.
What illness gave me is stillness and observation, l began to listen more and finally could hear the story he had told me many times.
You see, in 2009, Akin had been diagnosed with Kaposi Sarcoma; he got cancer at the height of his career and life. He lived in a penthouse by Amsterdam’s beautiful Ijhaven harbor from where he travelled widely and entertained often. He was an affluent Eurocentric Anglicized Nigerian, one of those shiny examples of diaspora success.
He had been HIV positive since 2002 but because he was simultaneously fatalistic and scared, he cloaked himself in invincibility. Soon after his cancer diagnosis, he also developed full-blown AIDS. Without any family in the Netherlands he spent weeks in hospital and months of chemotherapy on his own. He’s talks wryly about that time in hospital, watching others die and the pain of chemo. He talks of his faith in his ability to recover and a determination to live with the casualness the British talk about weather.
I have no idea how he took care of himself those years although he says his neighbors helped. I often ask why no one from his family came to stay with him but he’d say no one thought “it was that bad” because he kept blogging and lived as normally as he could. He was given 6 months off work post Chemotherapy but he took six weeks. He once wrote that his motto through life, cancer and AIDS was to thrive. In his words “I will never live as if I’m dying, l do not intend to start doing that now. I live to live well”.