Global PNH Awareness Campaign

Join our Global PNH Awareness Campaign taking place September 6th to October 12th 2024

Paroxysmal nocturnal haemoglobinuria (PNH) is a rare acquired genetic disease, so it cannot be inherited and can’t be passed down to children. It occurs in both men and women at different ages, and patients are usually diagnosed in young adulthood.

View the video below to learn more about this rare disease!

Arabic

الترجمة العربية

Bulgarian

български субтитри

Chinese

中文字幕 Zhōngwén zìmù

Dutch

Nederlandse titels

French

Soustitres en français

German

Deutsche Untertitel

Hindi

हिंदी उपशीर्षक Hindī upśīrṣak

Italian

Sottotitoli in italiano

Japanese

日本語字幕

Lithuanian

Lietuviški subtitrai

Persian

زیرنویس فارسی

Polish

Polskie
napisy

Portuguese

Sob títulos portugueses

Romanian

Sub titluri română

Russian

с русскими названиями

Serbian

Српски
титлови

Spanish

Subtítulos castellanos

Swahili

Manukuu ya Kiswahili

Turkish

Türkçe
altyazılı

Ukrainian

Українські субтитри

Subtítulos castellanos – Spanish subtitles

Deutschen Untertiteln – German subtitles

Sottotitoli in italiano – Italian subtitles

Soustitres en français – French subtitles

Sob títulos portugueses – Portugese subtitles

Nederlandse titels – Dutch subtitles

Türkçe altyazılı – Turkish subtitles

с русскими названиями – Russian subtitles

Polskie napisy – Polish subtitles

Subtitrări în limba română – Romanian subtitles

Српски титлови – Serbian subtitles

Українські субтитри – Ukrainian subtitles

中文字幕 – Zhōngwén zìmù – Chinese subtitles

हिंदी उपशीर्षक – Hindī upśīrṣak – Hindi subtitles

الترجمة العربية – Arabic subtitles

български субтитри – Bulgarian subtitles

日本語字幕 – Japanese subtitles

زیرنویس فارسی – Persian subtitles

Manukuu ya Kiswahili – Swahili subtitles

Lietuviški subtitrai – Lithuanian subtitles