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') Update Read about our response to COVID-19. We use cookies to give you the best online experience. By using our website, you agree to our use of cookies in accordance with our cookie policy . Skip to Content Investors News & Media Contact Us Worldwide North America Latin America Europe & The Middle East Asia Pacific Canada United States Brazil Colombia Mexico Belgium Denmark France Germany Ireland Italy Netherlands Norway Spain Sweden Switzerland Turkey UAE United Kingdom Australia China Japan Partnerships In select countries, third-party companies manage our local commercial operations. Click for details Our Inspiration Living With Rare Diseases Real Stories aHUS gMG HPP LAL-D NMOSD PNH Support Services Albie, one of our guiding stars When Albie was born, his mom, Charlotte, said that he was “absolutely fine. Everything was fine for about two weeks.” Our Medicines Conditions We Treat aHUS gMG HPP LAL-D NMOSD PNH Medicines Our medicines help people like Donnan As a father of two young children, Donnan recalls being afraid of what the future would hold prior to his diagnosis. Our Research Research and Development Pipeline Research Partnerships Discovery Partnerships Externally Sponsored Research We innovate for Ruthie Married with a newborn son, Ruthie was scared to learn that PNH was a life-threatening illness that at the time had no approved treatment. Our Commitment Corporate Social Responsibility CSR-STAR in Action Charitable Foundation Global Access to Medicines COVID-19 We give back for families like Evie's At only three months old, Evie's parents were told that her case was severe and that there were no approved or effective treatment options. Our Company About Us Leadership History Business Partnerships Ethical Standards Quality Product Safety Roberta is our inspiration Despite having a constant struggle with symptoms, Roberta revisited her dreams and put herself through nursing school. Your Career Career Opportunities Working Here Benefits Culture Make a difference for families like Tristan's Tristan's parents experienced a whirlwind of emotions and fear after learning their 5-year-old son had such a rare and serious disease. Our Inspiration Living With Rare Diseases Real Stories aHUS gMG HPP LAL-D NMOSD PNH Support Services Our Medicines Conditions We Treat aHUS gMG HPP LAL-D NMOSD PNH Medicines Our Research Research and Development Pipeline Research Partnerships Discovery Partnerships Externally Sponsored Research Our Commitment Corporate Social Responsibility CSR-STAR in Action Charitable Foundation Global Access to Medicines COVID-19 Our Company About Us Leadership History Business Partnerships Ethical Standards Quality Product Safety Your Career Career Opportunities Working Here Benefits Culture Investors News & Media Contact Us Worldwide North America Canada United States Latin America Brazil Colombia Mexico Europe & The Middle East Belgium Denmark France Germany Ireland Italy Netherlands Norway Russia Spain Sweden Switzerland Turkey UAE United Kingdom Asia Pacific Australia China Japan Partnerships In select countries, third-party companies manage our local commercial operations. Click for details Inspired Every Day The work we do is guided by people living with rare and devastating diseases. We are driven to continuously innovate and create meaningful value in all we do to help patients and families fully live their best lives. SEE THEIR STORIES My hope for Tanner in the future is that he enters into adulthood. I kind of hope that he will be a doctor and maybe help kids like doctors have helped him.” RENE, MOM OF TANNER LIVING WITH HPP HEAR HIS STORY ABOUT HPP TANNER LIVING WITH HPP This experience has taught me to look at the small things that count. Now, I feel that I have something to look forward to and I am who I want to be.” ROBERTA LIVING WITH gMG HEAR HER STORY ABOUT gMG ROBERTA LIVING WITH GMG Now we knew what we were up against, we knew we could fight.” REBECCA, MOM OF TRENDY BROTHERS LIVING WITH LAL-D HEAR THEIR STORY ABOUT LAL-D THE TRENDY FAMILY LIVING WITH LAL-D I don't define myself as having a rare disease. It’s part of my life, but it’s certainly not who I am.” CHELSEY LIVING WITH NMOSD HEAR HER STORY ABOUT NMOSD CHELSEY LIVING WITH NMOSD I can chase my kids and play again. I think knowing what I have brings a peace to my life.” DONNAN LIVING WITH aHUS HEAR HIS STORY ABOUT aHUS DONNAN LIVING WITH aHUS Every day, those who live with rare diseases inspire us to push the boundaries of medicine, technology, and healthcare services. Our goal is to transform their reality for the better. 4 APPROVED MEDICINES 6 DEVASTATING RARE DISEASES 25+ OFFICES WORLDWIDE 3000+ TALENTED COLLEAGUES SEE HOW WE DO IT Everyday Stories FEATURED STORY During this global health crisis, we remain committed to serving the patients who rely on us. We are filled with gratitude for the work of those in our manufacturing facilities who come to work and ensure patients receive the life-saving medicines we provide. We asked employees in our College Park, Dublin, Ireland manufacturing location to share their thoughts on what motivates them to come to work during this challenging time. READ MORE FOLLOW US insta LATEST NEWS MORE NEWS I feel like tomorrow I can do something, whereas before, I didn’t feel like tomorrow was possible.” JESSE LIVING WITH gMG LEARN MORE ABOUT gMG × You are now leaving www.alexion.com, a website provided by Pharmaceuticals, Inc. This link will take you to a different site to which this Privacy Policy does not apply. CONFIRM CLOSE MEDICAL PROFESSIONALS Conditions We Treat Medicines Pipeline The rare disease community Real Stories Living With Rare Diseases Support Services INVESTORS News & Media Events & Presentations Annual Reports JOB SEEKERS Benefits Culture Working Here insta Contact Us Legal Statement Privacy Notice Terms of Use Do not sell my personal information -- This website is intended only for residents of the United States. © 2020 Pharmaceuticals, Inc....