News, Stories & Events from the Wren Project Steph Harland 19/01/2026 Steph Harland 19/01/2026 Ruth’s journey: Polymyositis with Scleroderma overlap and Raynaud’s. Read More Nicola Chantler 15/12/2025 Nicola Chantler 15/12/2025 ‘I try my best to hide my pain, anger and loneliness towards my diagnosis’ Read More Nicola Chantler 14/12/2025 Nicola Chantler 14/12/2025 ‘I was diagnosed with Crohn’s at 18…it hit me when doctors said I would have this forever’ Read More Nicola Chantler 04/12/2025 Nicola Chantler 04/12/2025 ‘I felt beaten up and for the first time wondered what my life was going to be like moving forward’ Read More Nicola Chantler 06/11/2025 Nicola Chantler 06/11/2025 ‘I was feeling the strongest I ever have… until I wasn’t’ Read More Nicola Chantler 16/10/2025 Nicola Chantler 16/10/2025 Impact of psychosocial support for people living with autoimmune disease lupus Read More Nicola Chantler 09/09/2025 Nicola Chantler 09/09/2025 Join the team: Communications Officer role Read More Nicola Chantler 02/09/2025 Nicola Chantler 02/09/2025 ‘My biggest concern was that I was going to pass lupus onto my kids’ Read More Nicola Chantler 07/08/2025 Nicola Chantler 07/08/2025 ‘I only had basic knowledge of autoimmune diseases before I volunteered… Now I understand how lonely and distressing it can be’ Read More Nicola Chantler 12/06/2025 Nicola Chantler 12/06/2025 ‘I was diagnosed with dermatomyositis at 18…this is a time when we are meant to be having fun’ Read More Nicola Chantler 09/06/2025 Nicola Chantler 09/06/2025 ‘I’ve lived with JIA since I was four… It’s taught me about strength and balance’ Read More Nicola Chantler 19/05/2025 Nicola Chantler 19/05/2025 The Wren Project to offer group listening sessions for people with autoimmune disease Read More Nicola Chantler 14/01/2025 Nicola Chantler 14/01/2025 Saucony 10k ticket: Race for the Wren Project this 2025 Read More Nicola Chantler 14/01/2025 Nicola Chantler 14/01/2025 ‘I spent most of my first year at university on steroids’ Read More Nicola Chantler 17/10/2024 Nicola Chantler 17/10/2024 Lupus Awareness Month: ‘I haven’t got to a place of acceptance… but that’s OK’ Read More Nicola Chantler 27/09/2024 Nicola Chantler 27/09/2024 ‘I have faced many challenges…one of the greatest was not being believed’ Read More Nicola Chantler 16/09/2024 Nicola Chantler 16/09/2024 Live in conversation: Kate Middleton on the impact of the Wren Project Read More Nicola Chantler 26/08/2024 Nicola Chantler 26/08/2024 The Wren Project announces ‘WrenGroups’ for Men living with lupus Read More Nicola Chantler 13/08/2024 Nicola Chantler 13/08/2024 Share your story in our ‘Wren Voices’ campaign Read More Nicola Chantler 06/08/2024 Nicola Chantler 06/08/2024 Join our team: Social Media Officer Read More Older Posts Get in Touch
Steph Harland 19/01/2026 Steph Harland 19/01/2026 Ruth’s journey: Polymyositis with Scleroderma overlap and Raynaud’s. Read More
Nicola Chantler 15/12/2025 Nicola Chantler 15/12/2025 ‘I try my best to hide my pain, anger and loneliness towards my diagnosis’ Read More
Nicola Chantler 14/12/2025 Nicola Chantler 14/12/2025 ‘I was diagnosed with Crohn’s at 18…it hit me when doctors said I would have this forever’ Read More
Nicola Chantler 04/12/2025 Nicola Chantler 04/12/2025 ‘I felt beaten up and for the first time wondered what my life was going to be like moving forward’ Read More
Nicola Chantler 06/11/2025 Nicola Chantler 06/11/2025 ‘I was feeling the strongest I ever have… until I wasn’t’ Read More
Nicola Chantler 16/10/2025 Nicola Chantler 16/10/2025 Impact of psychosocial support for people living with autoimmune disease lupus Read More
Nicola Chantler 09/09/2025 Nicola Chantler 09/09/2025 Join the team: Communications Officer role Read More
Nicola Chantler 02/09/2025 Nicola Chantler 02/09/2025 ‘My biggest concern was that I was going to pass lupus onto my kids’ Read More
Nicola Chantler 07/08/2025 Nicola Chantler 07/08/2025 ‘I only had basic knowledge of autoimmune diseases before I volunteered… Now I understand how lonely and distressing it can be’ Read More
Nicola Chantler 12/06/2025 Nicola Chantler 12/06/2025 ‘I was diagnosed with dermatomyositis at 18…this is a time when we are meant to be having fun’ Read More
Nicola Chantler 09/06/2025 Nicola Chantler 09/06/2025 ‘I’ve lived with JIA since I was four… It’s taught me about strength and balance’ Read More
Nicola Chantler 19/05/2025 Nicola Chantler 19/05/2025 The Wren Project to offer group listening sessions for people with autoimmune disease Read More
Nicola Chantler 14/01/2025 Nicola Chantler 14/01/2025 Saucony 10k ticket: Race for the Wren Project this 2025 Read More
Nicola Chantler 14/01/2025 Nicola Chantler 14/01/2025 ‘I spent most of my first year at university on steroids’ Read More
Nicola Chantler 17/10/2024 Nicola Chantler 17/10/2024 Lupus Awareness Month: ‘I haven’t got to a place of acceptance… but that’s OK’ Read More
Nicola Chantler 27/09/2024 Nicola Chantler 27/09/2024 ‘I have faced many challenges…one of the greatest was not being believed’ Read More
Nicola Chantler 16/09/2024 Nicola Chantler 16/09/2024 Live in conversation: Kate Middleton on the impact of the Wren Project Read More
Nicola Chantler 26/08/2024 Nicola Chantler 26/08/2024 The Wren Project announces ‘WrenGroups’ for Men living with lupus Read More
Nicola Chantler 13/08/2024 Nicola Chantler 13/08/2024 Share your story in our ‘Wren Voices’ campaign Read More
