Our History


Our history is one of perseverance, dedication and innovation. It demonstrates how rare disease patients and their relatives can be empowered to take control of their condition and actively drive forwards their own healthcare and treatment prospects, in partnership with medical experts.

Founded in 2003 by AKU patient, Bob Gregory, and biochemist, Prof. L. Ranganath, we were the first AKU Society in the world. At that time there was no effective treatment, specialist advice or support network for AKU patients, so when Nick Sireau’s two boys were born with AKU, he was determined to do everything he could to ensure it would not stop them from leading healthy lives. Joining Bob and Prof. Ranganath, Nick gave up his job, dedicating himself full time to finding a cure for AKU. The AKU Society formed to research potential treatments, connect AKU patients across the UK, and help patients and their relatives/carers live with the multiple and severe needs resulting from the disease. They could only dream of what was to happen next.

Nitisinone, a drug being used to treat a similar metabolic disease, was pinpointed as a promising option for treating AKU. It took 10 years of tireless campaigning, funding research projects, and building partnerships, before the AKU Society was ready to create the DevelopAKUre consortium and secure a six million Euro donation from the European Commission to begin a series of major international clinical trials  in 2012.

At the same time, the Department of Health agreed to fund a  National Alkaptonuria Centre (NAC) to be based at Royal Liverpool University Hospital, to provide AKU patients with expert care and advice from leading experts on the disease. NHS England and NHS Scotland also agreed that English and Scottish patients would be able to receive nitisinone off-label.

Today the scope of the Society’s work also involves providing support for patients in between their visits to the NAC or the clinical trial, in the form of patient visits, specialist workshops, online patient communities  and social media updates. Our reach has now spread internationally; we have helped to establish sister societies in 12 locations worldwide, including France, Italy, the Netherlands, Poland, the US, Canada, Slovakia, Jordan, Germany, Sweden, India, and Asia Pacific.

Our work has grown from strength to strength and our services are transforming the lives of AKU patients, now and in the future.

 
 



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Hannah Shepherd's Everest Story
15-Nov-2017

Here at the AKU Society we are very lucky to have so many talented and dedicated people working .. ...more

Introducing Reece: Admin and Communications Officer
07-Nov-2017

Last week we welcomed Reece to the AKU Society’s team in Cambridge. As Admin and Commu.. ...more

A Patient's Perspective: Best Practice 2017
03-Nov-2017

On 18th and 19th October, Lesley, our Patient Support Manager, and Carol, one of our AKU pat.. ...more

Meet Leanne Evans, the NAC's new Data Coordinator
25-Oct-2017

Last Month the National Alkaptonuria Centres' new data controller, Leanne joined the NAC team. H.. ...more

A Step for a Step…Everest Base Camp Climb!
12-Oct-2017

So, me (Hannah from the gait lab) and my friend Steven have decided to take on the .. ...more