Scroll down Support for living with JIA JIA-at-NRAS is a part of the National Rheumatoid Arthritis Society (NRAS). We provide information and support services for those affected by juvenile idiopathic arthritis (JIA), their families, friends, carers, and health professionals. About us Donate to help What's Happening News, 05 Aug Coronavirus and JIA We understand that many people with RA or JIA and their families may be concerned at the Coronavirus pandemic described by the World Health Organisation as ‘a global public health emergency’. News, 18 Jun Our new JIA medicines booklet We are pleased to announce the launch of our new JIA booklet ‘Medicines in JIA’. The focus of this booklet is on the medicines that are used to treat JIA, but it also contains information about what parents and young people with JIA can expect at every stage from diagnosis onwards, showing that medicines are […] Event, on 14 Jun 2021 #WearPurpleForJIA #WearPurpleForJIA is an annual campaign dedicated to raising awareness and funds for the benefit of those living with JIA. Get all the latest news and events straight to your inbox with our quarterly email. Don't worry, we won’t send you spam! Sign up About Juvenile Idiopathic Arthritis All our information on Juvenile idiopathic arthritis, what it is, how it’s managed and living with the condition. What is JIA? → JIA means there is inflammation in a child’s joints that isn’t caused by any other condition. Symptoms of JIA → JIA is more than just painful joints. There are a number of symptoms that may be experienced and age is a big factor in this. JIA Diagnosis → There are a number of different investigations used in diagnoses, including blood tests and scans, along with a discussion about symptoms. JIA Medication → JIA is an auto-immune condition, so the main drugs used to control it are drugs called ‘immunosuppressants’. Search for resources Try searching our resource hub to find the articles, videos, tools and publications most helpful for you. I am… Child Health Professional Parent TeacherSelect topic… Diagnosis Diet and Exercise Healthcare professionals JIA-at-NRAS News Medication Mental Health Other Conditions Research School Symptoms TransitionSelect resource type… Article Publication Video Clear All Video Facebook Live: #WearPurpleForJIA Week: Children’s Q&A with Health Care professionals Facebook Live: #WearPurpleForJIA Week: Children’s Q&A with Health Care professionals 17/06/2021 Video Facebook Live: #WearPurpleForJIA Week Specialist nurses Facebook Live: #WearPurpleForJIA Week Specialist nurses 14/06/2021 Publication Medicines in Juvenile Idiopathic Arthritis Video Facebook Live: An update on our JIA services Facebook Live: An update on our JIA services 27/05/21 Debbie (JIA Young Persons Project Co-ordinator) and Nadine (Support Services Manager) talk about our new JIA membership, new online groups, #WearPurpleForJIA and other exciting developments. Article Research and drug trials Treating children | Some of the issues Juvenile Idiopathic Arthritis (JIA) refers to a group of seven different conditions with chronic ongoing arthritis as a common factor. Symptoms can range between mild to severe and the different types of JIA may require different types of management and treatment. Traditionally, treatments (medicines, injections, physiotherapy) and investigations […] Load more ↓ Get Involved There are many ways in which you can get involved to support JIA-at-NRAS, from holding a tea party to joining in with our campaigns. Help by donating Donate today to change the lives of those with juvenile idiopathic arthritis. Help by fundraising We need your help to continue our work and there’s lots of ways to do so! Help by campaigning Find out about what we do and help us to campaign for the change we need. Products View JIA Wristband £2.50 inc. VAT View JIA-at-NRAS T-Shirt (Child) £5.00 inc. VAT View JIA-at-NRAS T-Shirt (Adult) £6.00 inc. VAT Your Stories Summer’s story – a mother’s perspective of life with JIA Summer was 7 when she first complained of aches and pains in her legs. I put it down to growing pains which I remember having myself as a child. These pains went on for weeks and progressively became worse, so I made an appointment with our local GP who suggested she had a blood test. Lucien’s Story When I look at a photograph of my boy just before his 3rd birthday, he’s like a live wire, bursting with energy. That’s the way we see young kids. Yet my kid has what’s called Systemic Onset Juvenile Idiopathic Arthritis which is the rarest form of JIA and can have the greatest impact. Yes, kids can get it too I’m going to be honest, I’m awful at writing about myself. I find it awkward and I’m never sure if I’m too whiny, or if it comes across that I’m trying too hard to be light-hearted and just ends up sounding absolutely miserable as a result. I am a worrier by nature, so I of course panicked when I was told that I had developed a disease. Bella’s story At 18 months old, Isabella-May woke up feeling poorly with a high temperature and sickness – nothing overly concerning. By the next day she was limping and still poorly so we took her to the GP who decided she had an ear infection. A week passed and she still wasn’t right. She was barely moving and limping when she did. Click to close video modal Close Help support others Because of your generous donations JIA-at-NRAS will continue to be there for everyone affected by JIA. MonthlySinglePay in Funds £5£8£15Other £10£25£50Other £50£100£200Other Donate now! NRAS in 2020 £ 0 raised through #WearPurpleForJIA 2020 0 Calls answered 0 Publications sent out 0 People reached
What's Happening News, 05 Aug Coronavirus and JIA We understand that many people with RA or JIA and their families may be concerned at the Coronavirus pandemic described by the World Health Organisation as ‘a global public health emergency’. News, 18 Jun Our new JIA medicines booklet We are pleased to announce the launch of our new JIA booklet ‘Medicines in JIA’. The focus of this booklet is on the medicines that are used to treat JIA, but it also contains information about what parents and young people with JIA can expect at every stage from diagnosis onwards, showing that medicines are […] Event, on 14 Jun 2021 #WearPurpleForJIA #WearPurpleForJIA is an annual campaign dedicated to raising awareness and funds for the benefit of those living with JIA. Get all the latest news and events straight to your inbox with our quarterly email. Don't worry, we won’t send you spam! Sign up
News, 05 Aug Coronavirus and JIA We understand that many people with RA or JIA and their families may be concerned at the Coronavirus pandemic described by the World Health Organisation as ‘a global public health emergency’.
News, 18 Jun Our new JIA medicines booklet We are pleased to announce the launch of our new JIA booklet ‘Medicines in JIA’. The focus of this booklet is on the medicines that are used to treat JIA, but it also contains information about what parents and young people with JIA can expect at every stage from diagnosis onwards, showing that medicines are […]
Event, on 14 Jun 2021 #WearPurpleForJIA #WearPurpleForJIA is an annual campaign dedicated to raising awareness and funds for the benefit of those living with JIA.
About Juvenile Idiopathic Arthritis All our information on Juvenile idiopathic arthritis, what it is, how it’s managed and living with the condition. What is JIA? → JIA means there is inflammation in a child’s joints that isn’t caused by any other condition. Symptoms of JIA → JIA is more than just painful joints. There are a number of symptoms that may be experienced and age is a big factor in this. JIA Diagnosis → There are a number of different investigations used in diagnoses, including blood tests and scans, along with a discussion about symptoms. JIA Medication → JIA is an auto-immune condition, so the main drugs used to control it are drugs called ‘immunosuppressants’.
Search for resources Try searching our resource hub to find the articles, videos, tools and publications most helpful for you. I am… Child Health Professional Parent TeacherSelect topic… Diagnosis Diet and Exercise Healthcare professionals JIA-at-NRAS News Medication Mental Health Other Conditions Research School Symptoms TransitionSelect resource type… Article Publication Video Clear All Video Facebook Live: #WearPurpleForJIA Week: Children’s Q&A with Health Care professionals Facebook Live: #WearPurpleForJIA Week: Children’s Q&A with Health Care professionals 17/06/2021 Video Facebook Live: #WearPurpleForJIA Week Specialist nurses Facebook Live: #WearPurpleForJIA Week Specialist nurses 14/06/2021 Publication Medicines in Juvenile Idiopathic Arthritis Video Facebook Live: An update on our JIA services Facebook Live: An update on our JIA services 27/05/21 Debbie (JIA Young Persons Project Co-ordinator) and Nadine (Support Services Manager) talk about our new JIA membership, new online groups, #WearPurpleForJIA and other exciting developments. Article Research and drug trials Treating children | Some of the issues Juvenile Idiopathic Arthritis (JIA) refers to a group of seven different conditions with chronic ongoing arthritis as a common factor. Symptoms can range between mild to severe and the different types of JIA may require different types of management and treatment. Traditionally, treatments (medicines, injections, physiotherapy) and investigations […] Load more ↓
Video Facebook Live: #WearPurpleForJIA Week: Children’s Q&A with Health Care professionals Facebook Live: #WearPurpleForJIA Week: Children’s Q&A with Health Care professionals 17/06/2021
Video Facebook Live: #WearPurpleForJIA Week Specialist nurses Facebook Live: #WearPurpleForJIA Week Specialist nurses 14/06/2021
Video Facebook Live: An update on our JIA services Facebook Live: An update on our JIA services 27/05/21 Debbie (JIA Young Persons Project Co-ordinator) and Nadine (Support Services Manager) talk about our new JIA membership, new online groups, #WearPurpleForJIA and other exciting developments.
Article Research and drug trials Treating children | Some of the issues Juvenile Idiopathic Arthritis (JIA) refers to a group of seven different conditions with chronic ongoing arthritis as a common factor. Symptoms can range between mild to severe and the different types of JIA may require different types of management and treatment. Traditionally, treatments (medicines, injections, physiotherapy) and investigations […]
Get Involved There are many ways in which you can get involved to support JIA-at-NRAS, from holding a tea party to joining in with our campaigns. Help by donating Donate today to change the lives of those with juvenile idiopathic arthritis. Help by fundraising We need your help to continue our work and there’s lots of ways to do so! Help by campaigning Find out about what we do and help us to campaign for the change we need.
Your Stories Summer’s story – a mother’s perspective of life with JIA Summer was 7 when she first complained of aches and pains in her legs. I put it down to growing pains which I remember having myself as a child. These pains went on for weeks and progressively became worse, so I made an appointment with our local GP who suggested she had a blood test. Lucien’s Story When I look at a photograph of my boy just before his 3rd birthday, he’s like a live wire, bursting with energy. That’s the way we see young kids. Yet my kid has what’s called Systemic Onset Juvenile Idiopathic Arthritis which is the rarest form of JIA and can have the greatest impact. Yes, kids can get it too I’m going to be honest, I’m awful at writing about myself. I find it awkward and I’m never sure if I’m too whiny, or if it comes across that I’m trying too hard to be light-hearted and just ends up sounding absolutely miserable as a result. I am a worrier by nature, so I of course panicked when I was told that I had developed a disease. Bella’s story At 18 months old, Isabella-May woke up feeling poorly with a high temperature and sickness – nothing overly concerning. By the next day she was limping and still poorly so we took her to the GP who decided she had an ear infection. A week passed and she still wasn’t right. She was barely moving and limping when she did.
Summer’s story – a mother’s perspective of life with JIA Summer was 7 when she first complained of aches and pains in her legs. I put it down to growing pains which I remember having myself as a child. These pains went on for weeks and progressively became worse, so I made an appointment with our local GP who suggested she had a blood test.
Lucien’s Story When I look at a photograph of my boy just before his 3rd birthday, he’s like a live wire, bursting with energy. That’s the way we see young kids. Yet my kid has what’s called Systemic Onset Juvenile Idiopathic Arthritis which is the rarest form of JIA and can have the greatest impact.
Yes, kids can get it too I’m going to be honest, I’m awful at writing about myself. I find it awkward and I’m never sure if I’m too whiny, or if it comes across that I’m trying too hard to be light-hearted and just ends up sounding absolutely miserable as a result. I am a worrier by nature, so I of course panicked when I was told that I had developed a disease.
Bella’s story At 18 months old, Isabella-May woke up feeling poorly with a high temperature and sickness – nothing overly concerning. By the next day she was limping and still poorly so we took her to the GP who decided she had an ear infection. A week passed and she still wasn’t right. She was barely moving and limping when she did.
Help support others Because of your generous donations JIA-at-NRAS will continue to be there for everyone affected by JIA. MonthlySinglePay in Funds £5£8£15Other £10£25£50Other £50£100£200Other Donate now!
NRAS in 2020 £ 0 raised through #WearPurpleForJIA 2020 0 Calls answered 0 Publications sent out 0 People reached