Blog Archives

Duchenne Croke Park Conference

Ensuring Irish Duchenne Patients have access to treatment conference will be held in Croke Park this October 6th. National and international experts include Proferror Michael Barry Dr Elin Haf Davies Professor Keith Foster Dr Declan O’Rourke Christopher Jones, (Mitchell’sJourney) We

Posted in Events, News

VHI Women’s Mini Marathon

VHI Women’s Mini Marathon

Posted in Events, News

SSE Airtricity -Dublin City Marathon Video

Good Morning. We hope you are well. We know you are busy. We know you have your own worries and problems. If you can spare a few moments please watch this video and share with your circle. It would help

Posted in News

World Duchenne Awareness Day

Celebrating World Duchenne Awareness Day September 7th 2017 in Roscommon Town This day marks the 4th International World Duchenne Awareness Day. On this day the International Duchenne Community stands united to raise awareness of this catastrophic disease. We use it

Posted in News

Young Hero – Archie Naughton

Archie was honoured to be chosen for their ‘ Young Hero Award 2017’. He is extremly grateful to every one who voted for him. He had a lovely day with his family and friends. Young Hero – Archie Naughton Archie

Posted in News

Join Our Boys Grant to Solid Bioscience

We are so happy to tell you that The Join Our Boys Trust recently awarded a €100,000 Grant to Solid Biosciences, in the hope it will help them accelerate part of their gene therapy programme. We are only able to

Posted in News

‘Our children were going to die and there was nothing we could do about it’

‘Our children were going to die and there was nothing we could do about it’ In November 2012, Paula and Padraic Naughton were told their three sons, Archie, George and Isaac, had Duchenne Muscular Dystrophy, a fatal disease The last

Posted in News

Mini Marathon 2017

We appreciate you are busy. We appreciate there are thousands of good causes that require support and funds. We also appreciate that so many of you understand our utter desperation and grief. This year we are aiming to ‘recruit’ 500

Posted in News

Access to Treatment Translarna

For the past year The Trust has been engaging with key stakeholders in relation ensuring that once treatments become available for children and adults with Duchenne they can be accessed immediately. Unfortunately at present this process is complex and frustratingly

Posted in News

Rare Disease Day

Today is Rare Disease Day, it takes place on the last day of February each year. The Join Our Boys Trust is committed to support this wonderful initiative. It is estimated that there are over 7000 Rare Diseases and the

Posted in News
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