UCB USA

UCB USA Official U.S. page for UCB Biopharma. Patients are at the heart of everything we do. Learn more at www.ucb-usa.com.

UCB is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology. We are unwavering in our purpose: delivering moments that matter for people impacted by severe diseases, now and into the future. People are at the heart of everything we do, inspiring us, driving our scientific discovery, and leading us to rethink the patient exp

erience. We work with stakeholders to address the unmet needs of patients and caregivers, helping them to achieve their goals and to live the lives they want. UCB is on a journey to be the patient-preferred biopharma leader by delivering medicines and solutions that improve lives while creating value for society.

07/08/2025

To help raise awareness of (MG), UCB proudly sponsored 4 special episodes of Tu Salud Tu Familia: a Spanish-language television show to gain a deeper understanding of rare diseases.

Each episode features:
🧬 MG awareness
💬 Real stories from patients + insights from medical experts
📘 Patient empowerment resources

Ready to learn more and watch the TV series? 🎥 Visit https://bit.ly/44leuCb

No one can pour from an empty cup. Caregivers are such strong pillars in the lives of their loved ones with rare epileps...
07/01/2025

No one can pour from an empty cup. Caregivers are such strong pillars in the lives of their loved ones with rare epilepsy and communities, but here are a few ways you can help ease the mental load:​

🫧 Offer to help clean or cook for the family home.​
📝 Acknowledge and praise the effort they put forth every day. Quick notes and texts are great reminders that you see them!​
👬 Encourage caregivers to join epilepsy networks and support groups to find emotional support, practical advice, and community connection​.​

Learn more about how to help caregivers at https://bit.ly/46iOOHt.

06/27/2025

Alexis has been living with Myasthenia Gravis (MG), a rare autoimmune neuromuscular disorder, for over half of his life. For him, symptoms often show up in his eyes, sometimes making an eye patch part of his routine.

While we can never truly understand what it's like to live with this rare disease, by listening to people like Alexis with we can learn how to be better friends and partners. Learn more about how we support people living with rare diseases like MG at https://bit.ly/4keecle. 💙🧠

06/25/2025

Movement looks different for everyone with myasthenia gravis, and that’s okay.
During , certified personal trainer Vanetta Fenton shares a few low-impact, seated exercises that can help with strength and flexibility on your own terms. Watch to learn exercises that meet you where you are.

06/23/2025

June is for Dravet. This International Dravet Awareness Day, explore resources and initiatives created to support families living with Dravet syndrome. For over five years, we’ve championed rare epilepsy communities, reaching 10,000+ patients worldwide. 🌍 Learn more at https://bit.ly/4e1ybCd

06/20/2025

Patient advocacy liaisons like Dr. Ericka Hylick are so essential in optimizing every part of our process, to continuously make sure people living with rare diseases like are heard and given the best care possible. Learn more about resources we offer for patients at https://bit.ly/3Hret6C

06/18/2025

In celebration of Sustainable Performance Week, a yearly event dedicated to UCB's commitment to meaningful sustainable impact, we asked some team members at our Atlanta HQ what their favorite eco-friendly thing is at work. 🌎 What should we ask our crew next? Learn more at https://bit.ly/4l0xf31

Today we announced the recipients of UCB’s inaugural U.S. Myasthenia Gravis Scholarship™ — a program created to support ...
06/17/2025

Today we announced the recipients of UCB’s inaugural U.S. Myasthenia Gravis Scholarship™ — a program created to support and empower students living with MG as they pursue their academic goals.
Congratulations to this inspiring group of scholars! 🎓👏 Learn more at https://bit.ly/4kNecK1

Big news: We’re investing to expand our U.S. manufacturing footprint with an economic impact of $5 billion! This new sta...
06/16/2025

Big news: We’re investing to expand our U.S. manufacturing footprint with an economic impact of $5 billion! This new state-of-the-art biologics facility will help us meet rising demand, deliver reliable access to our medicines, and fuel the next wave of innovation at UCB. It’s an investment in our future—for patients, our people, and long-term growth. Plus, we’re creating hundreds of skilled jobs and strengthening our U.S. presence. Learn more: https://bit.ly/3FR9bRq

06/15/2025

This Dravet Remembrance Day, we recognize the resilience of the Dravet syndrome community, a community that often experiences profound loss. Today and every day, we remain dedicated to providing meaningful support to the DS and broader epilepsy communities. 💜 Learn more at https://bit.ly/4e1ybCd

Jasmine Espy was just a teenager when she began navigating life with Hidradenitis Suppurativa (HS). Today, she’s using h...
06/13/2025

Jasmine Espy was just a teenager when she began navigating life with Hidradenitis Suppurativa (HS). Today, she’s using her voice to raise awareness, build community, and share her lived experience in hopes of supporting others on a similar journey.​
​
Read her story of living with HS, finding her voice and partnering with UCB to uplift the community in this new feature from BlackDoctor.Org: https://bit.ly/3FXvK6V

06/13/2025

We were honored to join The Association of Hidradenitis Suppurativa and Inflammatory Diseases "I Reclaim" Patient Summit, a powerful, patient-led event focused on education, advocacy, and support for the (HS) community. Together, with advocates like Socialcydd and other HS leaders, we’re proud to help patients feel seen and heard.

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