But we don't stop there. Our commitment extends beyond providing treatments; we strive to offer comprehensive support and resources to help patients navigate their unique journeys.
We actively support initiatives that go beyond just providing products, ensuring patients receive the care they need.
We work closely with patient associations, to strive to make healthcare more accessible.
Everyone has a different journey to diagnosis. These videos present you a selection of stories from people living with Cushing's syndrome from the UK, Norway and France. We are extremely grateful to Sammy, Ida and Lily for sharing their stories and we hope that you find them helpful.
Sammy, Ida and Lily have been diagnosed with Cushing's syndrome – listen to their stories.
Sammy's video takes you through the story of a typical patient with Cushing's syndrome.
Changes to her health worsened over many years without doctors being able to discover what was wrong. When a diagnosis was finally made and Sammy was treated for Cushing's syndrome, she was able to live a more normal life, with valued support from the Pituitary Foundation.
Ida is a woman with Cushing's syndrome.
Living in a remote village in Norway, Ida had to wait 14 years before the doctors found the correct diagnosis. Having now been diagnosed and treated, Ida feels she can do all the things she wants in life.
Lily is a Cushing's syndrome patient from France.
She struggled with her symptoms for 5 years before a physician was able to confirm a diagnosis of her disease.
Benelux 
France 
Germany 
Italy 
Portugal 
Spain 
Spain (CAT) 
UK