Ambassadors of LUPUS UK
Alton Brown is an Olympic pathway athlete who lives in Great Britain. Holder of dual nationality, Alton is a representative of the Jamaican Olympic Association’s national karate team, where he represents Jamaica internationally at the highest levels within the sport.
Alton is currently ranked #1 for his division within Jamaica, #1 across the Caribbean, Central and South America, #14 in the world for the all-time ranking and #20 in the world on the Olympic ranking. He is a European Champion, multiple World Medalist, English Champion and British Champion.
Alton started karate at the age of 11 in a tiny church hall in East London’s Roman Road. The karate club was a place he truly felt at home and it taught him that he was 100% in control of what he could achieve in life. If he put in the work, nobody could stop him from achieving his dreams. He teaches the same life philosophy to his two beautiful daughters. He first competed for the English National Team when he was 17, where he was a member for almost 15 years.
But it’s not just about his personal success. Alton was Team Manager for British Universities & Colleges Sport, where he mentored and trained young athletes to success, and today continues to coach British athletes. Olympic athletes fund themselves, so he works for the Salusbury World Refugee Support charity, currently constructing an art heritage project from the oral histories of early refugees. He also works with young athletes around the world, such as in India with FairFight, a Dutch-based charity who use martial arts to empower extremely vulnerable young girls, teaching them self-confidence, self-defence and how to take charge of their bodies.
Alton has lupus. He was diagnosed in 2011 but had symptoms from 2009. As a competitive athlete, he cannot take steroids and is unused to taking regular medication. Alton says: ‘I take control of my pain and sport gives me a reason to be in pain that I cannot blame on lupus. In consultation with my rheumatologist I came off hydroxychloroquine and worked with my herbalist sister on a better diet. I have flare-ups once a month. Now that I understand (through attending a LUPUS UK event) that medication is to prevent inflammation, which has longer-term effects on the body, I am reconsidering. What kind of life do I want with my girls in the future and how best to achieve that?’