Scleroderma is a rare autoimmune disease. Here are all the most frequently asked questions about this condition.
Rute’un öyküsü
If you have a scleroderma diagnosis - you are not alone. In this collection of stories, real patients and carers share their experiences with scleroderma.
Teresa’nın öyküsü
This short film about Teresa and her life with systemic sclerosis brings hope and optimism for other people with the same conditions.
Michael’ın öyküsü
Listen how Michael's move to Mallorca and quality time spent with his wife and dogs is now considered by him as a new beginning.
Maria’nın öyküsü
Check out how Maria gains energy from her positive approach, spending time with her daughter and cat and not letting scleroderma to rule her world.
Jessica’nın öyküsü
Learn how Jessica remains fully independent and following her dreams after being diagnosed with systemic sclerosis at age 14.
Grazia’nın öyküsü
Listen to a brave story of Grazia, who managed to maintain a normal life with a husband, two sons and active systemic sclerosis.
Alex'in öyküsü
Follow Alex's journey from managing early systemic sclerosis symptoms to overcoming the mental health burden and enjoying life despite the disease.
sklerodermanın takibi
Skleroderma belirtileri zamanla değişebilir. Düzenli takibin hastalık kontrolündeki önemini keşfedin.
Skleroderma hastaları için ipuçları
Our hacks can provide you with practical tips to help you get on top of the cold, the cooking, childcare, holiday preparation and your mental health.