We talk to filmmaker Kit Vincent, whose deeply moving documentary Red Herring explores his life with a terminal brain tumour.
At 24, my biggest concern was to graduate university and to survive another shift at a rowdy football pub just off of Baker Street Station. For Kit Vincent, it was to come to terms with a life changing diagnosis.
Kit was diagnosed with a terminal illness in 2018 and given between four and eight years to live. A few months after his diagnosis, he picked up a camera and began recording his life, exploring his relationships with those around him through the lens.
The result is Red Herring, a warm and thoughtful documentary about Kit’s life. The project started life as a film about Kit’s father, Lawrence, coming to terms with his son’s illness, but quickly developed into something more.
The film sees him point a camera at his family and himself while undergoing scans, endless phone calls with doctors and asking his loved ones the questions no one is comfortable talking about. Yet Red Herring isn’t a film about death, but one that celebrates life and family.
Here we chat to Kit about making the film and what prompted him explore such a difficult subject.
Congratulations on the film. Can we start with just the very basic question of how did it all begin? How did it go from like an idea to an actual project?
It was very intuitive and natural. I was working at a production company when I was diagnosed. We had a camera in the house and I had to have surgery and go home and recover at my dadās house and I thought āOh, God, Iām going to be so boredā. It wasnāt really an idea, it was just like, maybe this is something worth filming. This is the craziest thing that has happened to me and I was in a state of my life where I wanted to make a film, so maybe this is worth filming. Who knows? I took the camera with me and then, when I was at home, I just started filming stuff, conversations, my dad.
When I showed some of the footage to Dea (Gjinovci), one of the co-producers and one of my very good, old friends, she was like [your dad] is perfect. So I would cut together like a little, two, three minute teaser with the help of Hattie (Brooks-Ward) who became the editor for the whole thing, sheād also never made a feature before. We just went from there, it was very natural. The responses to my dad are really what initiated the project, that was the genesis of the project. People were like I want to see more footage of your dad being him.
You point your camera at your family, and you do talk about some really difficult things. Like you say we donāt really talk about death which is ridiculous, because itās coming for all of us. What was their first reaction of being filmed and talking about all these difficult things that we donāt want to talk about?
Initially, I was only filming with my dad, I only wanted to make a film with my dadās just because I didnāt want to go there with my mum. I knew it would be more difficult. [The film] was a distraction at the beginning for me, just like a lot of things that my dad was doing at a time were distraction for him.
Of course, he didnāt want to talk about it. I donāt know if you can tell from the film, but Iām quite a tenacious person. I donāt really give up easily and also, me and my dadās relationship is such that I can say what I want to him, and heās not gonna get offended, upset or angry. Heāll just take it and if he does get angry or offended, heāll be fine five minutes later.
And also, they are your family. They canāt really say no, either.
That’s what the joy of this film was and this is the problem Iām having with making my next film. I made [Red Herring] with my family, they couldnāt say no but other people can say no to me! I donāt know how to deal with that.
What was the timeframe like from you getting diagnosed, to making the film, to now?
I was diagnosed in 2018, in May, then I had surgery in October, which is roughly when I started making the film. The film premiered in March last year andā¦ weāre at now, itās going into cinemas!
Read more: Red Herring review | A thoughtful, devastating documentary
I was such a child at 24 years old, so the whole idea of someone telling you that you have a terminal illnessā¦ What does the word terminal even mean to you at that point?
Oh, it still doesnāt really mean anything to me, right now. Terminal is such aā¦ Itās like if something doesnāt kill you first, this will kill you. I think that sounds ominous for people but for me, I take a kind of confidence in that. [The doctors] have no idea how long itās going to be, they can keep an eye on [the tumour] and see whether itās growing or not growing.
At the time when I first got diagnosed, when theyād done one scan and they werenāt sure how close it was to a very sensitive part of my brain, they said if we canāt operate, you might have under two years to live. And I think thatās what gave my dad the heart attack, what keeled him over because obviously that wouldā¦ But now itās more vague, it kind of varies. I try not to attach too much emotion to the word terminal. I let it wash over me.
When you get a diagnosis like that and a prognosis like that, do you start counting or keeping track of how many years or months you have left?
No. Your relationship to everything changes. Your relationship to time changes so dramatically, your understanding of time. Your relationship to your relationships changes and whatās important changes and all the things that you used to think are central in your life suddenly start fading away. You realise that the simple things in your life become so much more important, like maintaining good relationships with the people that you love and not stressing about really mundane stuff.
I think we could all do with a bit more of that in all fairness. You have seizures as well, donāt you? How do they present?
At the beginning, I had grand mal seizures for the first year or so and after my surgery. Then the medication helped but I was still having them quite regularly, like leading up to scans, theyād get worse. Then after radiotherapy, they got a bit better. It still just depends on factors like tiredness and stress and anxiety, those kinds of things. I still have them but now theyāre more local seizures, absence seizures. Like if I was in a conversation, I wasnāt the centre of attention, which is quite rare, but if that was the case, people wouldnāt know that I was having one. I could just be doing my own thing and you wouldnāt necessarily know whatās going on.
I only found out recently that what Iāve been having for years are actually seizures and like you said, there are so many elements that affect the frequency. When I do have one, people tend to freak out around me. I find that frustrating because, even though Iāve now got medication, itās not going to go away.
Yeah, that doesnāt change. [When] my dad sees me having a seizure, itās like the worst thing possible for him. Thereās a [scene] in the film where Iām like, I have these all the time, itās fine, I can cope with them. I think for him, if you see your child going through any kind of pain or dealing with anything like this, it must be heartbreaking. Also, seizures are just a very visceral thing that people donāt understand and theyāre so individual that I think itās quite hard to comprehend.
The scenes with your mum were particularly affecting. When you do point a camera at your family, do you think it changed anything? Does the presence of the camera somehow alter the conversation?
Massively. I think the camera is such a fascinating tool. It allows people to open up in a way that they would never be able to without a camera. It gives people so much space to interrogate their own emotions because they have a reason to. Weāre not given the space a lot of the time to go into those places without prompt. When thereās a camera and somebodyās asking you these questions, thereās a real reason to do it. You think of it in the kind of, āokay, we are doing this, weāre talking about thisā way and that has a huge impact on the outcome of those conversations and the way those conversations happen.
With my mum, I found it really useful. I would never have had those conversations with her if I wasnāt using a camera to do it. And for me as a filmmaker, it gives me something to kind of hide behind, something that I can use as an excuse to ask those questions.
But at the same time, rather than making a fictional film where you can do 30 takes of a scene, here you donāt really get another take. So when you are there and youāre having those conversations, do you go in with a need to get something specific out of them?
No. With my mum, I knew what I wanted to talk about with her and with my dad as well. I knew what I wanted the general topic of the conversation to be but I never wanted to guide them or to get them to say things. I never did what some documentary filmmakers do where they ask, ācan you just say it like thisā.
It also became way more apparent to me throughout the process that the filmmaking process was a part of the film, like a character in the film and I wanted to include it in the film. It became super helpful having my editor watching all of the footage as we were going, because she would tell me like āoh, this is a really interesting journey that weāre going on with your dad, maybe you could ask him some more about thisā.
I assume your family has seen the film by now?
My dad has seen it in almost every screening, all around the world. Like two weeks ago, he went to a film festival in Zürich without me because I couldnāt go and he was there instead of me.
Heās the star of the film!
He loves it. He did say to me though, heās kind of done now. I was like, āI was done with it a year ago and youāre still watching it”, like itās normal to not want to keep watching the same film over and over again, especially when youāre in it.
What was the first time like when you watched it with them? You said in your director statement that you wanted it to be a light experience, thereās a lot of laughter [in the film] and itās not a depressing film in any way but it must have been quite hard for them still.
I gave a copy to my dad, him and my stepmom watched it. Then my mom and her partner watched it. I let them tell me what they thought, had some feedback from them and I listened. The opening scene is because of my stepmom! We were really struggling with what to do with the opening scene and it wasnāt the same in the version I sent. Then she gave us a great idea and we were like, āwow, that might really workā. We tried it and we were like, āthis is perfectā and it ended up being the opening scene. I think it was much harder for my mom.
We did a screening for my mom, my dad and my whole family, my sisters. I actually didnāt go to that one. I was a real coward. I was like I canāt be in the room whilst all of them watch it together, so I didnāt go. In hindsight, I should have been there. Before [the screening], I was happy to have discussions about it but after that, I was like this is the version that the world is gonna see, I donāt want to answer questions. If you donāt like it, sorry! You have to be like that at a certain point.
You just let it go and you let it have its own life. Have you done a lot of interviews like this about the film? Do people like me treat you differently at all during them, considering the filmās subject matter?
I donāt think so. Thatās really interesting because that was such a big fear of mine. Iām now going to do this process where Iām trying to separate myself from myself as the guy with brain cancer. Iām trying to become myself again and itās a super difficult process, because Iāve made a film entirely about that. Itās embalmed in time, audiences see that and thatās what they think of me as so itās quite difficult for me to pull myself apart from that.
Obviously, I know when I do these interviews, the only experience that person has of me is from that film. Itās hard because Iām instantly pulled back into that reality when Iām trying to go on my own journey now, trying to figure out who I am, that isnāt that person.
Red Herring is in select cinemas and on demand from the 3rd May 2024.