Our UK MD, David Kelly, is running the inaugural Virgin London marathon next month for the MPS Society.   Hunters Syndrome (also known as MPS II) is an extremely rare degenerative enzyme disease affecting children and for which there is currently no cure. With only 39 live births in 10 years in the UK, awareness of this condition is very low, with little or no Government funding for research projects.  Every single penny that David can raise REALLY REALLY makes a difference. Any support you can give would be very deeply appreciated.

You can donate securely via his Just Giving webpage.   David is very passionate about this cause and won't let you down - his beloved 3 year old nephew and Godson Max in Dublin suffers from Hunters.   Thank you!