All applications are reviewed by the Joseph Patrick Trust Grants Panel. The Panel meets four times a year to make awards, and oversee the Trust’s budget and spending.
The Panel is made up of service users, parents and professionals from around the UK who volunteer their services.
If you can spare a few days a year and would like to serve on the panel, please contact us:
020 7803 4811
JPTgrants@musculardystrophyuk.org

 

David Jackson – Chairman

David says that he is both proud and privileged to have been associated with Muscular Dystrophy UK for over 50 years in particular the Joseph Patrick Trust serving in recent years as the Chairman of the Trusts Grants Making Panel. He was awarded the MBE in 2009 for services to Muscular Dystrophy.
David is always heartened each time that the Panel hears from the recipient of a grant and delighted that the Trust has been able to make such a difference to their lives and pleased that the effect that the trust extends to the much wider field of Parents, Carers, relatives and friends who benefit from the provision of various items of equipment such as electric beds, riser chairs, car adaptations and assistive technology equipment.
But David is far from complacent: “The number of grants to people with neuromuscular conditions continues to increase year by year thus reflecting the continual need for our work.”

 

Julian Pritchard

Julian is a former trustee of Muscular Dystrophy, serving on the Finance and General Purposes Committee. Julian has been on the JPT Committee since 2012 and is proud to be part of the Committee created in memory of his grandfather, Joseph Patrick.
Day to day life centres around commercial property, with Julian running two such businesses based in the Midlands. Julian is also actively involved with various other charitable organisations.

 

Kirsty Read

Kirsty has been a panel member since 2004. She has spinal muscular atrophy type 2 and so is very familiar with many of the challenges faced by children and adults who have muscle disease.

 

Jane Field

Jane joined the panel in 2005. She is the mother of Murray who has Duchenne muscular dystrophy, and Finella.
She qualified as an osteopath in 1980 and since 1981 has run her own practice in Worcestershire. Jane has worked with the British Olympic Junior Judo squad and lectured in diagnosis and clinical skills at the British School of Osteopathy. She is a professional classical soprano and has been a member of the Duo Dolcetini a pure soprano duo since 1990, using concerts to raise money for the charity.

 

Karen Duckmanton

Karen joined the panel in 2011. She is a manifesting carrier of Duchenne muscular dystrophy and has been a permanent wheelchair user for the past 13 years. Karen also has two nephews with Duchenne muscular dystrophy.
Karen has an OU LLB Law degree and, although, she has not been able to go into a legal profession, she works at her local Citizens Advice Bureau, both as a paid advice session supervisor and a voluntary advisor.
Knowing the struggles that people with neuromuscular conditions have to go through first hand, she joined the panel in the hopes she could make grants towards items of equipment that would help make the lives of other affected by these conditions a little easier.

 

Patricia Lock

Patricia joined the JPT panel in 2011.

 

Jane Freebody

Jane joined the JPT panel in 2016.

 

James Lee

James joined the JPT panel in 2017.

 

Robert Warner

Robbie joined the JPT panel in 2017.

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