#ThisCushing

#ThisCushing is a global initiative developed by Recordati Rare Diseases in collaboration with award-winning photographer and internationally recognized experts in the field of pituitary endocrinological diseases.

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This is Cushing

We set out empower the Cushing’s community

#ThisCushing aims to inspire and empower the Cushing’s community and drive change in the way this disease is perceived. By elevating patients’ voices to raise awareness of the burden of disease we can help to reduce these burdens and ultimately improve quality of life.

About the photographer

Stefano Schirato is an award-winning photographer born in Bologna in 1974. He has been working as a freelance photographer with a keen focus on social themes for more than 20 years. He has led multiple projects in Russia, Eastern Europe, Africa and India, collaborating with several associations and NGOs such as Emergency and Caritas Internationals. 

His work has been published with The New York Times, CNN, Newsweek Japan, Al-Jazeera, and Le Figaro. He is ambassador of Leica and has been teaching photojournalism since 2014 in various institutions, including the prestigious Leica Akademie Italy.

Watch our campaign video

#ThisCushing is a global initiative developed by Recordati Rare Diseases aiming to inspire and empower the Cushing’s community and drive change in the way this disease is perceived. By elevating patients’ voices to raise awareness of the burden of disease we can help to reduce these burdens and ultimately improve quality of life.

"I may have Cushing, but Cushing does not have me. I am more than my illness, and I won't let it define me."– Patient

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Some of the stories

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Help your family and friends to better understand Cushing’s Syndrome by sharing this website and encouraging them to keep up with the conversation on social media by following #ThisCushing on Twitter and LinkedIn. 

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    This website is intended for users outside of the US and UK. The information provided on this website is intended for educational purposes and should not be used as substitute of a visit, consultation, or advice of doctor or other healthcare professional. This website is funded by Recordati Rare Diseases, and characters appearing are both real patients and healthcare professionals. No personal medical information is disclosed.

    All the photos taken by the photographer are sponsored by Recordati and exclusively licenced to Recordati by Stefano Schirato. Copyright © 2023 Recordati AG. All rights reserved. EMEA-LAC/CH/ENV/HCP-PAT/Feb-2023/39

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