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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AKU Blog

Duncan's Decade on Nitisinone
15-Aug-2018

The newly published results of a study held at the National Alkaptonuria Centre (http://www... ...more

Stand Up for AKU 2018
08-Aug-2018

We’re really excited about our third Stand Up for AKU Comedy Night on 3rd October. Thi.. ...more

New Research Shows Nitisinone Treats AKU
31-Jul-2018

New research has proven for the first time that a drug called nitisinone treats AKU in peopl.. ...more

SOFIA-Paediatric: New Research Study
25-Jul-2018

We have some exciting news. The AKU Society has just been awarded a £60,000 grant .. ...more

Vacancy: Fundraising Officer
18-Jul-2018

We are looking for a Fundraising Officer. The vacancy is up online (http://www.akusociety.org/vac.. ...more