Fighting for breath: Diven’s story
Diven was shocked when he was diagnosed with interstitial lung disease. Through exercise, he’s learning how to live well with his lung condition and even ran the London Marathon this year! Here, he shares his story.
It’s ironic that I was probably the fittest I’d ever been when I first noticed the symptoms of my lung condition. I was climbing the stairs to the train platform on my way to work, but I was completely out of breath. I’d run a half marathon earlier that year – I knew this wasn’t right.
Waiting for a diagnosis
It took an incredibly long time to get a diagnosis, despite how debilitating my breathing problems became. My doctor sent me for tests to rule out asthma, but then I had to go private to get a CT scan. It took 18 months after I first noticed symptoms to diagnose interstitial lung disease with diffuse systemic sclerosis, which is an incurable autoimmune condition.
The news was a massive shock. I worried about how I could carry on living a life that I loved, and if my wife and I could start a family. There’s nothing worse than the unknown – having a speedier diagnosis would have taken away much of my worry.
No more sports?
Having to give up sports had a massive impact on me. I felt isolated, as sport was the focus of my social life. Going onto steroids and immunosuppressants stabilised my lung function and recently I’ve been able to return to the gym. I’ve got a personal trainer who understands my condition and I use an oxygen machine when I exercise.
My condition isn’t common, and it can be hard to know where to turn for support. Lung disease is a hidden disability – I look perfectly well until I struggle to breathe. People don’t understand the reality of lung conditions until it happens to a loved one.
An epic achievement
I ran the London Marathon this year. From the moment I knew I had a place, I didn’t know whether to feel frightened or excited. The training was hard and sorting out the oxygen machine logistics was difficult. The training day set up by Asthma + Lung UK really helped with my preparation, as did my colleagues and friends. Taking part in the actual marathon was surreal - the buzz, excitement and nerves all kicking in at once. It was an amazing day; other runners were coming up to me telling me how amazing I was doing and had so many words of encouragement. One person even said "Can I take a selfie with you to show my friend who has a lung condition to show her anything is possible?" Nothing will beat the feeling of crossing the finish line. My first thought was that I'm happy and proud of what I done and I've made everyone who supported me - family, friends and everyone who donated (some of who I don't even know) - proud.
A better future ahead
The biggest achievement in my journey has to be the amount of awareness I have raised through talking to people. I was featured in the Metro, the Evening Standard, The Insider and IG Global News which all went viral! I have also raised £20,000 for Asthma + Lung UK and my initial target was only £2,000, and encouraged others to participate in the London Marathon. Everyone has been asking me what’s next. Who knows? Time will tell but my work is not done. Losing control over your future is hard but I won’t let lung disease beat me.
At Asthma + Lung UK, we believe it is wrong that people lose years of their life battling with lung conditions when they could have been living well. Read our report to find out what we’re fighting for.
Could a little, or a lot, of exercise help you?
If you have a lung condition, being active can help to improve your quality of life and help you manage your condition.
Interested in the London Mararon?
Did you get a ballot place for the London Marathon? Use your place to help us fight for lung health!
Missed out on the ballot? Don’t worry, you can still apply for a charity place with Team Breathe!
We empower people with lung conditions to make changes that can be transformative.
Please donate now to help make sure people with lung conditions can live well this year.
Other Your Stories posts you may like:
Other posts you may like
Our amazing supporter, Gerard, sadly lost his wife Margaret to bronchiectasis in October 2023. This year he took on a special challenge to remember her and raise awareness of this condition. Here he tells us all about the challenge and what it meant to him.