Kitty Fitton: “It’s vital that we keep our sense of humour, especially at times like this”
Author: Sophie BatesPublished: 2 April 2020
Prep: Cook: Serves:
Kitty Fitton, a blogger, comedian and business owner based in New Zealand, tells us how she struggled to find employment after her Parkinson’s diagnosis, her ‘accidental’ career in comedy – and why she thinks a sense of humour is “vital” during the coronavirus pandemic
Tell us about your career as a stand-up comedian.
I got involved very much by accident. I had complained that Parkinson’s magazines were full of old people looking happy on mobility scooters – I wanted to know where the people like me were. This led to an editor of a Parkinson’s magazine asking me to speak at a local seminar. I spent weeks writing my speech and although it felt odd talking about my condition, I received a standing ovation and knew I had to do more.
After that, the same editor suggested I try stand-up, which I resisted at first – but then I thought, why not? Since my Parkinson’s diagnosis four years ago, I have firmly believed in giving everything a go at least once. I made my stand-up debut and I’ve been hooked ever since.
I refer to myself as an observational comic. There is so much comedy in everyday life, so I talk about real things that have happened. Parkinson’s is a part of me, so naturally it seeps into my routines. If something strikes me as amusing or quirky, I’ll use it.
Why is humour important during a pandemic?
It’s vital that we keep our sense of humour, especially at times like this. The ability to laugh at oneself, and perhaps indulge in a little dark humour from time to time helps keep things in perspective.
It’s been a very strange time. Here in New Zealand we closed our borders and locked down movements of the public so quickly. In some ways I’ve never been so social – but it can also be rather lonely. We’re doing our best to stay positive.
Ultimately, let’s be honest. If we didn’t laugh, we’d all be sat crying.
How have you been tackling loneliness while self-isolating?
I have a number of friends who were quite lonely and a little worried about coronavirus, so we set up a video call on Zoom and chatted about our experiences of lockdown in different countries.
There were only a few of us, but next time there will be more people joining in. Now more than ever, it is so important to communicate – it’s easy to withdraw and see the world as a scary place. Talking helps us realise that we’re not alone, that others share the same worries, concerns, and hopes for the future. Communicating with others around the world absolutely cheers me up – and everyone is welcome to join our call!
What’s it like being your own boss while living with Parkinson’s?
Everything is more manageable when you work for yourself. I love the flexibility of being self-employed, but the hours are terrible and the money is inconsistent. I run my own business because despite being eminently qualified and competent, I really struggled to find anyone to employ me – which I truly believe is because I admitted I had Parkinson’s.
People advised to keep quiet about my condition to avoid being judged, but I’ve always been very pragmatic about it. I’ve been asked about my Parkinson’s in job interviews, and many people will understand the look of sympathy you get from some people. I don’t introduce myself as having Parkinson’s, but I don’t deny it either.
What are your top tips for navigating a career with Parkinson’s?
Don’t be ashamed. You didn’t want it, but there’s nothing to hide. Call people out that might make comments or are misinformed. You don’t have to be rude, just simply explain. Remember that you know best about this and don’t allow people to side-line you or ‘help’ you out because you’re ill.
Image credit: Joanna Piatek, Captured by Friday
Need to know: Kitty Fitton is originally from Leeds, UK, and was diagnosed with Parkinson’s in 2015 at the age of 41. She now lives in New Zealand with her husband four children. She runs a small business that offers digital marketing and website design – alongside public speaking about Parkinson’s, stand-up comedy and a little MC-ing.
For more information on Kitty Fitton or to contact her regarding her Zoom calls visit her website kittyfitton.com.
For more information on young onset Parkinson’s please visit the EPDA website.
Parkinson’s Life wins British Medical Association Patient Information Award 2016
Parkinson’s Life awarded ‘Highly Commended’ by the BMA
2 days ago
Scientists at MIT uncover new clues about Parkinson’s disease
Neuroscientists at Massachusetts Institute of Technology (MIT), US, have developed new tools that could improve understanding of Parkinson’s disease. As part of a study, published in Science Advances, the tools were used on animals to investigate the relationship between two types of signals that are disrupted in Parkinson’s – dopamine signalling and beta-band oscillations (coordinated waves of electrical activity in the brain). The scientists found that while the animals performed certain tasks, beta-band oscillations increased while dopamine signalling declined in particular parts of the brain. Factors including an animal’s past experience and the reward value of a task also impacted the relationship between the two signals. Helen Schwerdt, a research scientist at MIT, said: “Considering electrical signals side by side with chemical signals is really important to understand how the brain works.” Ann Graybiel, a professor at MIT, added: “As these methods in neuroscience become more and more precise and…
People with Parkinson’s disease have a higher risk of dying from Covid-19, study finds
A new database study of around 80,000 Covid-19 patients has found that those living with Parkinson’s disease have a 30% higher risk of dying from the virus than those without the condition. The study – conducted by researchers at the University of Iowa Health Care, US – identified that Covid-19 patients with Parkinson’s disease were generally older, more likely to be male and less likely to be African American. As these factors could also affect the risk of death from Covid-19, the researchers adjusted their statistical models to account for differences in sex, age and race and found a significantly higher risk of dying from Covid-19 in the group of patients with Parkinson’s disease. Lead researcher Dr Nandakumar Narayanan said: “We recognise the limitations of this study; it is retrospective data from a single database, but we are confident that these data show that Parkinson’s disease is [an] independent risk factor…
BIAL enters the US and acquires “promising” Parkinson’s disease programmes
Portugal-based pharmaceutical company BIAL has launched a new research centre, BIAL Biotech, in Massachusetts, US, which will focus on genetically defined Parkinson’s disease. BIAL has also announced that it has acquired the Parkinson’s disease research programmes of Lysosomal Therapeutics Inc, as well as its research and development team and clinical programme for LTI-291 – a therapy designed to treat a genetic form of the condition. António Portela, executive president of BIAL, said: “Our entry into the US with the creation of BIAL Biotech and the acquisition of the promising programmes from LTI, is a decisive step towards the fulfilment of our mission to contribute to improving the quality of life of people worldwide. “The development of this new research centre in the US, is a landmark of enormous relevance for us. We are investing in science and research, through our direct presence in one of the most important research hubs…