Alexion (@alexionpharma) 's Twitter Profile
Alexion

@alexionpharma

Alexion, AstraZeneca Rare Disease was created following the 2021 acquisition of Alexion Pharmaceuticals, Inc.

GL/NP/0116
GL/NP/0095

ID: 246664765

linkhttps://alexion.com/Documents/Alexion-Community-Guidelines calendar_today03-02-2011 06:37:18

1,1K Tweet

12,12K Followers

331 Following

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Generalised #MyastheniaGravis (gMG) can be challenging to diagnose because its symptoms often mimic other conditions. Continued research and awareness are critical to help patients receive an earlier diagnosis. #MGAwarenessMonth

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Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune disease characterised by unpredictable relapses. Learn why relapse prevention is critical for patients.

Alexion (@alexionpharma) 's Twitter Profile Photo

It was a privilege to meet with experts at the EAN Congress as we work toward our shared goal of improving patient outcomes for rare neurological diseases.

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What is a rare disease? It’s defined as a condition that affects a small population of people, but the definition can vary by region. Swipe to learn how the definition of “rare disease” differs in various countries across the globe.

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The complement system is a strong and powerful tool that protects the body against harmful invaders – but when thrown out of balance, its proteins can trigger a dangerous, uncontrolled cascade of reactions that attack cells and tissues. Watch the video to learn more.

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At Alexion, we’re fueled by one purpose: to transform the lives of people living with #RareDiseases. Does this sound like you? Apply today: spr.ly/6010geW1M

At Alexion, we’re fueled by one purpose: to transform the lives of people living with #RareDiseases. Does this sound like you? Apply today: spr.ly/6010geW1M
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We spoke with Seng Cheng, Head of Research and Product Development about what creativity, serial innovation and passion looks like in rare disease R&D. Watch the video to learn more.

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For those living with #RareDiseases, the path to diagnosis can feel like an endless odyssey, marked by countless challenges. Millions navigate a maze of misdiagnoses, unanswered questions, and relentless uncertainty. We’re hoping to change that through education and awareness.

For those living with #RareDiseases, the path to diagnosis can feel like an endless odyssey, marked by countless challenges. Millions navigate a maze of misdiagnoses, unanswered questions, and relentless uncertainty. We’re hoping to change that through education and awareness.
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Today, AstraZeneca completed the acquisition of Amolyt Pharma. This acquisition bolsters the Alexion, AstraZeneca Rare Disease pipeline and expands on its bone metabolism franchise as we work to serve more #RareDisease patients around the world.

Today, <a href="/AstraZeneca/">AstraZeneca</a> completed the acquisition of <a href="/AmolytPharma/">Amolyt Pharma</a>. This acquisition bolsters the Alexion, AstraZeneca Rare Disease pipeline and expands on its bone metabolism franchise as we work to serve more #RareDisease patients around the world.
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Living with a #RareDisease like neuromyelitis optica spectrum disorder (#NMOSD) can be challenging, and patients often feel alone on their journey. Hear from Alex, who shares the importance of connection and community.

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At Alexion, every team member plays a crucial role in advancing our mission to serve patients in need. Are you driven by purpose and ready to make a difference for the #RareDisease community? Explore our job openings and join our team today: spr.ly/6018im3rq

At Alexion, every team member plays a crucial role in advancing our mission to serve patients in need. Are you driven by purpose and ready to make a difference for the #RareDisease community? Explore our job openings and join our team today: spr.ly/6018im3rq
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Raj joined Alexion because he was inspired by the mission to find solutions for devastating conditions that have few or no available treatment options. Watch to hear more about the challenges that motivate Raj to follow the science every day. #LifeAtAlexion

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We're proud to partner with EFNA and other global stakeholders to develop The Rare Neurology Charter. Sign the Call to Action today to support the development of action plans aiding EU policy change for rare neurological diseases: spr.ly/6015codUR

We're proud to partner with <a href="/EUneurology/">EFNA</a> and other global stakeholders to develop The Rare Neurology Charter. Sign the Call to Action today to support the development of action plans aiding EU policy change for rare neurological diseases: spr.ly/6015codUR
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We’re committed to raising visibility of #NMOSD by amplifying the stories of people living with this rare neurological disease. Learn more from Marie about her experience in our “Rare Connections in NMOSD” short film.

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#RareDiseases affect more children than you might think. In fact, 50% of those diagnosed with a rare disease are children. Share this post to drive awareness and education for children impacted by a rare disorder.

#RareDiseases affect more children than you might think. In fact, 50% of those diagnosed with a rare disease are children. Share this post to drive awareness and education for children impacted by a rare disorder.
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Curious about #LifeAtAlexion? Our Director of Global Medical Sciences Katherine Garlo shares how our commitment to bringing together diverse perspectives creates a positive and thriving workplace.

Alexion (@alexionpharma) 's Twitter Profile Photo

Having navigated neuromyelitis optica spectrum disorder (#NMOSD) for nearly 8 years, Craig has many lessons from living with this #RareDisease. Hear from him on the importance of speaking up and advocating for yourself.

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Patient centricity isn’t a buzzword for us — it’s embedded in our DNA. Learn from several of our colleagues as they discuss how we act with a sense of urgency and intention to help address patient barriers. #LifeAtAlexion

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We’re seeking talented individuals who are driven to push the boundaries of scientific discovery and bring life-changing therapies to those in need. If you’re ready to be part of a dynamic team that committed to making a difference, apply now: spr.ly/6016Yu2qg

We’re seeking talented individuals who are driven to push the boundaries of scientific discovery and bring life-changing therapies to those in need. If you’re ready to be part of a dynamic team that committed to making a difference, apply now:  spr.ly/6016Yu2qg
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We’re excited to share that an accessible version of our “Rare Connections in NMOSD” short film is now available with audio description. Our hope is that those who are visually impaired can experience the film in a new, meaningful way: spr.ly/6013mXLq3