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Our history

Fight Bladder Cancer started from a very personal battle. Our founder Andrew was diagnosed with Stage 4 bladder cancer in June 2009. He had been experiencing symptoms for over 18 months but was misdiagnosed with an enlarged prostate. Faced with a poor prognosis and immediate life-changing surgery, Andrew and his wife T made contact with a fellow bladder cancer patient and his partner who had recently undergone the same treatment.

Just being able to talk to someone else who really understood what they were both going through helped them immensely. It was these snippets of real information that made a difference in those early days. Despite the fact that bladder cancer was so common, they were amazed to find out that most people knew nothing about it, and there wasn’t a dedicated bladder cancer patient charity in the UK.

Once Andrew was recovering from his surgery, they started the process of setting up what was to become Fight Bladder Cancer.

First beginnings

From its roots as a local bladder cancer support group in 2010, it soon became clear that the lack of available support for patients and their families was in fact a national problem, and needed to be tackled on a much wider scale. With a team of trustees on board, an online support forum for people the length and breadth of the country and a website were launched. These encouraged people to engage with others affected by bladder cancer honestly and openly. 

Following the success of the national support group, Fight Bladder Cancer then started to focus campaigning for better bladder cancer awareness. Fight Bladder Cancer officially became registered as an unincorporated charity on 8 July 2014. 

Andrew_BAUS

Building a team

In 2017, a new Board of Trustees was formed. They worked together to define a new strategy for Fight Bladder Cancer to ensure it was fit for the future moving forwards.

After 10 years of running the charity and being a voice for patients across Europe, in 2019 upon receiving a terminal bowel cancer diagnosis, Andrew asked his colleague and friend Dr Lydia Makaroff to step in as Chief Executive. 

At the time he said: "As I hand over the reins, I have great trust in the team I will leave to run the charity day-to-day. We want everyone affected by bladder cancer – patients, carers, family and friends – to have a place to come to for support, information and advice. They need to know that someone is speaking up for them when key decisions are made about policy, care, treatment and research." 

Andrew died on the last day of Bladder Cancer Awareness Month in 2019.  

Lydia continues to lead and grow the organisation. She has worked to implement Andrew's vision and to fill the gap he and T identified all those years ago so that bladder cancer patients and their families across the UK have a better experience and better outcomes. 

Our impact

Each year we support thousands of patients and their families through our helpline, support groups and website. Read more about our vision, mission and impact.

Get in touch

We’ve done everything we can to make all the information on this site as accurate as possible. Whilst we have had support from a small team of medical professionals advisors to review the general medical content of this site, please remember, that only YOUR medical team can give YOU specific advice about YOUR symptoms or illness. We encourage you to discuss any potential options with them.