Who am I?

My name is Olivia Johnson and i'm living with Scleroderma for 20 years.

I decided to create this website to provide support for both people with scleroderma and their families. I knew that people with scleroderma often felt isolated and alone given the rarity of the condition, so I felt compelled to give some support and information about scleroderma to anyone affected.

In this website you will find important and useful information about the disease, which I collected from different sources, but mainly from my and other people's experience with Scleroderma.

If you want to share a problem, experience or just ask me some questions, please contact me on this e-mail: contact@sclerodermasociety.co.uk