argenxglobal

argenxglobal argenx is a global immunology company developing potential therapies for people living with rare autoimmune diseases.

We see you, we hear you, we are here with you. Community Guidelines: https://www.argenx.com/community-guidelines

09/01/2026

Living with an autoimmune rheumatic disease can mean carrying more than meets the eye. ​

What’s happening inside the body isn’t always reflected by what others can see on the outside. This , we’re helping connect what’s happening beneath the surface with the realities of living with these conditions.​

Share this post to help others see beyond what’s visible.​

Thinking about joining a clinical trial? Swipe through to learn five important things we at argenx want you to know befo...
08/31/2026

Thinking about joining a clinical trial?

Swipe through to learn five important things we at argenx want you to know before deciding if participating in a clinical trial is right for you.

Learn more about clinical research: https://bit.ly/4y9HJUl

08/28/2026

Britt first experienced symptoms of chronic inflammatory demyelinating polyneuropathy (CIDP) when she was 35 weeks pregnant, like tingling of her hands and feet.

In this episode of the Untold Stories: Life with a Severe Autoimmune Condition podcast, she shares how she navigated a new diagnosis while preparing to welcome her first child. ​

Listen to the full episode to hear how Britt is adapting through life’s unexpected moments, and explore more stories from people navigating life with autoimmune conditions:​ https://bit.ly/4wVFDGC

08/26/2026

What happens after being diagnosed with an autoimmune disease? Others who’ve lived it understand the journey best.

We’re introducing a new series of short conversations bringing together real-life experiences and expert insights on navigating life with an autoimmune condition.

From receiving a diagnosis to adjusting to the changes that follow, the conversations explore the realities of living with an autoimmune disease and the lessons learned along the way.

Explore the conversations: https://bit.ly/4gwa3ZV

08/13/2026

Wellness is personal, and it’s not always what we expect.​

​After being diagnosed with myasthenia gravis (MG), Nicole’s perspective on wellness evolved in ways she hadn’t expected. This , her story reminds us that caring for ourselves and the people around us can take many forms.​

🎧 Explore Nicole's full story—and others—on the Untold Stories: Life with a Severe Autoimmune Condition podcast: https://bit.ly/4qjaUlh

08/05/2026

At argenx, our mission is simple: improve the lives of people living with severe autoimmune diseases.

Clinical research plays an important role in helping us better understand diseases and advance potential new treatments for the people who need them most.

Learn more about clinical research and explore argenx clinical trials: https://bit.ly/4buGgzb

08/03/2026

What happens when the nerve cells responsible for movement stop working as they should?

This , we’re exploring the science behind spinal muscular atrophy (SMA) to help build greater understanding of this complex disease. Whether you're living with SMA or supporting someone who is, greater understanding helps you better navigate what's happening in the body and what it
can mean in everyday life.

07/31/2026

Last month, more than 1,150 Argonauts came together by — a global initiative supporting patient advocacy organizations around the world.

Together, we:
✅ Logged 160,000 kilometers of movement
✅ Supported our partner patient organizations
✅ Shared countless moments of connection, community, and impact

From walks and runs to bike rides, yoga sessions, and team activities, it was inspiring to see Argonauts around the world rally around a shared purpose: supporting patients through movement and community.

Thank you to everyone who participated, shared their stories, and helped make this initiative such a meaningful success!

What does it take to turn scientific discoveries into new possibilities for people living with autoimmune diseases? In a...
07/30/2026

What does it take to turn scientific discoveries into new possibilities for people living with autoimmune diseases?

In a recent conversation with our partners at Scientific American Custom Media, our CEO Karen Massey shares how co-creation among scientists, healthcare providers, and patient communities is helping shape the future of autoimmune disease care, and what that could mean for patients and their loved ones.

🎧 Listen to the full conversation: https://bit.ly/4ftfNo5

07/20/2026

Different diagnoses. Similar experiences.

Mel lives with chronic inflammatory demyelinating polyneuropathy (CIDP). Lindsay lives with dermatomyositis.

From diagnosis delays to adapting to life with a rare disease, their conversation on the Untold Stories: Life with a Severe Autoimmune Condition podcast highlights how people living with different autoimmune diseases often face many of the same challenges.

Listen to the full episode to hear how Mel and Lindsay found common ground, and explore more stories from people navigating life with autoimmune conditions: https://bit.ly/44IR09l

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