Who we are

JIA-at-NRAS is a part of the National Rheumatoid Arthritis Society (NRAS). We design, coordinate, fund and deliver a comprehensive and wide range of high quality products and services for all affected by RA and JIA.

Peter Foxton

Chief Executive

Stuart Munday

Chief Operating Officer

Ailsa Bosworth

NRAS National Patient Champion

Helen Ball

Finance Director

Meera Chauhan

Head of Data

Sadé Asker

Senior Policy Officer

Donagh Stenson

Innovation & Service Delivery Director

Maddy Roberts

Families and Young Peoples Service Manager

Nicola Goldstone

Volunteer Manager

Sarah Watford

Support Service Manager

Victoria Butler

Information Resource Manager

Emma Spicer

Trusts and Giving Manager

Emma Sanders

Individual Giving Officer

Helen Saich

Trusts and Company Giving Fundraiser

Charlotte Allum

Fundraising & Events Officer

Cathrine Mouttou

Salesforce Administrator

John Rogers

Salesforce Administrator

Eleanor Burfitt

Marketing Manager

Geoff West

Digital Marketing Manager

Aribah Rizvi

Digital Marketing Officer

Sam Grant-Riach

Office Manager

Amy Allen

Information and Support Coordinator

Rosie Evans

Information and Support Coordinator

Kate Lyall

Information & Support Coordinator

Kate Evans

Information & Support Coordinator

Sally Matthews

Research Coordinator

Tracy Dias

Services Administrator

Karen Farrington

Services Administrator

Juliet Young

Financial Accountant

Kim Watts

Executive Assistant to Peter Foxton

Cheryl Scowen

Receptionist and Administrator

Juvenile Idiopathic Arthritis at NRAS

JIA-at-NRAS is a service launched by the National Rheumatoid Arthritis Society.

From the Chief Executive

The National Rheumatoid Arthritis Society was founded in 2001 and is the only UK charity devoted specifically to offering support, information and advocacy for those living with Rheumatoid Arthritis and since 2014 those living with Juvenile Idiopathic Arthritis.

In 2012 NRAS conducted a review of JIA and JIA services across the UK with a view to being able to start to provide a much more comprehensive service for families and young people affected by JIA.

The first thing we did was to spend a year producing a major report, ‘A Focus on JIA’ by visiting rheumatology and paediatric rheumatology centres across the UK to find out what the state of JIA service provision was. We talked to many different clinicians and allied health professionals, parents, young people with JIA and NHS Managers and effectively mapped what service provision looked like. 

It is important to be clear to anyone affected by JIA who is reading this or interacting with our JIA-at-NRAS web area that JIA and RA are not the same while they are both inflammatory forms of arthritis they do differ in many ways.  Very importantly JIA does not ‘become’ RA after the age of 16. If you are diagnosed with JIA, then you continue to have JIA, unless your disease goes into remission, after the age of 16. Another important aspect of JIA is that it is not one disease, it has a number of different types and you can read about the different types here.

This website for those affected by JIA will provide you with the information about JIA and living with JIA which you are seeking,

With best wishes,

Peter Foxton
NRAS CEO

About Us

Our Core Values  

We approach our commitment and responsibilities to all with empathy, professionalism, passion and enthusiasm. We continually strive to achieve the best results and outcomes that we can for those we represent. These core values underpin the way we work. 

At all times, we act: 

Support our mission

Because of your generous donations JIA-at-NRAS will continue to be there for everyone affected by JIA.

NRAS in 2023

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