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

06/09/2026

Myasthenia gravis (MG) symptoms aren’t always easy to recognize, and they can change throughout the day.

This , we’re shining a light on the different ways MG may affect everyday life. 💙

Symptoms can include:
🔹 Muscle weakness
🔹 Drooping eyelids or blurred vision
🔹 Difficulty speaking or swallowing
🔹 Fatigue during everyday activities

Greater awareness and understanding helps people living with MG feel more seen, supported, and understood, while also helping encourage earlier diagnosis and continued research.

05/29/2026

200,000 miles, one shared purpose. 🏃

brings argenx colleagues together in support of people living with myasthenia gravis (MG) and chronic inflammatory demyelinating polyneuropathy (CIDP) around the world.

Over the next two weeks, every mile logged helps unlock donations supporting patient advocacy organizations globally, turning everyday movement into meaningful impact for patients.

05/28/2026

Have you struggled to find resources that are accessible and fit your needs?

Patient training resources can often be complex and difficult to access – especially when time is limited and content isn’t available in your language.

That’s why we collaborated with The Synergist and several patient advocacy groups to co-create the Patient Engagement and Capability Accelerator (PECA), a training program shaped by patient insights to make learning more flexible and accessible.

With short video modules, multiple language options, and practical, real-life examples, PECA is designed to fit into everyday life.

Start exploring the training modules: https://bit.ly/42Mo935

CIDP doesn’t always follow a predictable path - and that’s okay, especially if you know what to look for. 💙 Symptoms of ...
05/27/2026

CIDP doesn’t always follow a predictable path - and that’s okay, especially if you know what to look for. 💙

Symptoms of chronic inflammatory demyelinating polyneuropathy (CIDP) can shift over time and affect different things, like balance, movement, and everyday activities in ways others may not see.

Building awareness of these shifting effects is key so people better recognize CIDP and feel more supported throughout their care journey.

05/14/2026

CIDP doesn't always look the same, with varying symptoms that often overlap with other conditions. So, it can be hard to recognize and diagnose.

Chronic inflammatory demyelinating polyneuropathy, or CIDP, is a rare autoimmune disease affecting strength, sensation, and mobility, making everyday activities more challenging.

This , we’re raising awareness of the signs of CIDP, especially those similar to other diseases, because early recognition is critical for accurate diagnosis.

Learn more about CIDP: https://bit.ly/4eGA1uA

05/12/2026

Helping patients navigate the complexities of care takes more than expertise. It takes…

✅ Empathy
✅ Persistence
✅ A deep commitment to making a difference

Introducing Andrea Monroe, a Nurse Case Manager who is passionate about helping patients get access to the care they need. To put it simply, she helps make a complex process more manageable by partnering closely with each patient every step of the way.

This , we’re celebrating Andrea and nurses everywhere dedicated to supporting patients when they need it most.

Thank the nurses you know for everything they do!

People living with autoimmune diseases deserve long-term solutions that go beyond managing symptoms and support better o...
05/04/2026

People living with autoimmune diseases deserve long-term solutions that go beyond managing symptoms and support better outcomes over time.

As our understanding of autoimmune diseases continues to evolve, so does the conversation around what long-term care can look like and how innovative solutions can translate to better outcomes for patients.

🔗 We explore why innovation is needed and what it could mean for those living with autoimmune diseases here: https://bit.ly/4tLf5ah

Too many people living with rare neuromuscular diseases continue to face unmet needs. Our entrepreneurial approach to s...
04/28/2026

Too many people living with rare neuromuscular diseases continue to face unmet needs.

Our entrepreneurial approach to science means asking bolder questions, challenging assumptions, and keeping our focus on what matters most: expanding impact for patient communities worldwide.

04/22/2026

The impact of living with Sjogren’s disease isn’t always seen.

For many, diagnosis comes after years of delayed recognition, invisible symptoms, and daily challenges that extend far beyond dryness.

This , we’re highlighting what it really means to live with this condition - including the experiences that often go unseen.

04/21/2026

Every person living with a rare neuromuscular disease has a different experience with unique challenges.

By digging deeper into the underlying causes of these conditions, we’re working to better understand what drives them and where more solutions are needed. Because meaningful progress begins with understanding.

Learn more about we keep patients at the center of our research: https://bit.ly/4tIvk8l

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