Whether someone with epilepsy is experiencing focal #seizures, seizure clusters, or a rare syndrome, their experience is unique. Read more from UCB’s Head of U.S. Neurology, Mike Davis, on how our treatments aim to address underlying causes and cure #epilepsy for all patients.

We are looking forward to exchanging ideas with the #epilepsy community at #AES2021. Find out more about how we’re addressing #healthequity for Hispanics living with epilepsy in the U.S.

Digital transformation provides the grounds for faster, greater and more sustainable advancements in #patient health. Hear about UCB’s evolving digital transformation, and how we’re working to improve patient care for those living with #epilepsy. #AES2021 bit.ly/3GalsLc

UCB is proud to support patients living with MG and their caregivers. We look forward to connecting at this year's mark hayhoe Patient Conference and all year long. Hear from Omar Sinno, M.D., UCB's Medical Lead, Rare Disease, on our commitment to the MG community. #myastheniagravis

We’re proud to support #SAPAW2022 and how critical it is to implement seizure action plans, including the knowledge of when to use rescue medications, so together, we can advance epilepsy care.

With Microsoft, we are exploring how to combine diverse #research data sets and uncover a deeper understanding of the biological causes of severe diseases. UCB’s Head of Research Analytics, Dr. Wang Yuan, shares how we're using data and AI to accelerate drug discovery:

This #InternationalWomensDay, UCB employees are joining together to #BreakTheBias by showing their support for gender equality. Together we can create a workplace culture that embraces diversity, equity, and inclusion now and into the future. #IWD2022

UCB’s Kim Moran brings her passion for digging deeper to see the connections in neurology in her new position as Head of U.S. Rare Diseases. Hear more from Kim on her commitment to bringing innovative solutions to patients living with #myastheniagravis.

Have you heard of #myastheniagravis? This autoimmune #neuromuscular disorder can create challenges in even the simplest of everyday tasks. This Myasthenia Gravis Month, learn more about UCB's commitment to helping those like Glenda enjoy the moments that matter most.

Not even an hour into our trip to the LGS Foundation family conference and she had a #seizure. #Epilepsy sucks. Traveling is hard. We are on the plane at least. #LennoxGastautSyndrome #RareDiseaseTruth #RareDisease

At UCB, we’re dedicated to helping people with severe diseases live their best lives. That’s why we’re excited to launch #MomentsThatMatter, a space to showcase the resilience of patients and caregivers and the everyday moments that matter to them. Watch now:

Leading up to #worldmitodiseaseweek, we stand united with United Mitochondrial Disease Foundation, MitoAction and the TK2d patient community to 'Take on #TK2d Tuesday.' Read more about this rare disease from Kim Moran, our U.S. Head of Rare Disease. #MomentsThatMatter

This #Rheumatic Disease Awareness Month, Trent shares how #PsoriaticArthritis hinders some of the everyday moments he enjoys, like holding hands with his wife. Watch Now. #RDAM #MomentsThatMatter

For those living with the challenges of disease, the #MomentsThatMatter may seem small, but they are the ones to cherish.

Everyday stories of people living with diseases like #epilepsy inspire and help us understand the moments that matter most to them. Read the latest from UCB’s Global Head of Epilepsy and Rare Syndromes, Mike Davis: #MomentsThatMatter #EpilepsyAwareness

We stand united with those who have lost a loved one to the sudden unexpected death in epilepsy (#SUDEP). ❤️ We are dedicated to raising awareness and furthering research related to this devastating risk. #TalkSUDEPNow #MomentsThatMatter

Lori's son lives with LGS. She wishes that he was just able to play - at the playground or on a sports team where he could score the winning goal. #LGSAwareness #EpilepsyAwarenessMonth #MomentsThatMatter

Thanks to everyone who stopped by during #STATOpenDoors to hear about how we’re innovating to accelerate drug discovery and support the next gen of scientists. STAT

This week, UCB lit up buildings at the Atlanta headquarters and in Illinois, joining buildings all over the globe illuminated in recognition and support of those living with a rare disease. #lightupforrare #rarediseaseweek

At UCB, we are driven by our commitment to people living with and caring for severe diseases. This #MentalHealthAwareness month and beyond, learn more about the impact disease has on their mental health, and our work to support these communities. #MomentsThatMatter