Takeda

Being grounded in heritage shapes how we move forward. For Rosanna Sabia, Production Planning Manager, it shows up as a consistent commitment to doing what’s right for patients—carried through every role, team, and stage of her career.   That mindset has remained steady over time, even as the work continues to evolve. It brings clarity through change and connects long-standing values to how work gets done today. It’s also what has kept her building her career here for more than 15 years.   Learn more about how heritage shapes our people’s future: https://lnkd.in/eMZuJqpY   #TeamTakeda #MakeHistoryChangeFutures #BioPharmaHiring #LifeSciences 

The countdown is on for #SLEEP2026! We're looking forward to connecting with the sleep medicine community and contributing to scientific dialogue around #narcolepsy type 1 (NT1) and orexin science. Takeda will present clinical data from FirstLight and RadiantLight, two global Phase 3 studies that explored an investigational approach for NT1. NT1 isn't just a sleep disorder—it's a 24-hour disorder. Beyond excessive daytime sleepiness, people with NT1 face a cycle of symptoms that can impact many aspects of a person's life, from social interactions to everyday activities and responsibilities. At Takeda, we're committed to supporting scientific exchange and raising awareness of serious, often overlooked conditions like NT1. We'll see you at SLEEP 2026! [For healthcare professionals only]

For people living with #psoriasis, persistent itch, along with the appearance and location of plaques – especially in highly visible or sensitive areas – can significantly reduce quality of life. We recently sat down with dermatologist and clinical researcher Dr. Melinda Gooderham to discuss why understanding lived experience matters for people with psoriasis.

Even when people with #CeliacDisease follow a gluten-free diet, inadvertent gluten exposure can cause a range of unexpected symptoms and potentially lead to intestinal damage. "If I have a salad that a flake of crouton ended up on, or if a dusting of flour from the bakery ended up on my gluten-free pastry, that can make me very sick for multiple days.” Learn more about Bill’s story: https://lnkd.in/dS-mdwtK #CeliacAwarenessMonth

Living with eosinophilic esophagitis (#EoE) isn’t just about food. It’s about unpredictability, constant adjustments and learning how to navigate daily life amidst difficulty swallowing (dysphagia) symptoms. Some days, symptoms may be minimal. Other days, they can shape every decision. Understanding triggers, leaning on family and friends, and continuing to advocate for yourself can make a real difference. We’re sharing a patient story to bring awareness to the realities of living with this progressive immune-mediated inflammatory disease. https://lnkd.in/d2q6tVej

On World IBD Day (May 19), we honor the strength, resilience and lived experiences of people affected by inflammatory bowel disease (IBD)—and reaffirm the importance of working together to help improve care and outcomes for patients around the world. This year’s global theme, ‘IBD Has No Borders: Access to Care,’ is a powerful reminder that where someone lives should never determine the quality of care they receive. Yet too many people living with IBD still face barriers to timely diagnosis, specialist support, and ongoing care. Raising awareness is one important step toward greater understanding, equity and meaningful progress for the IBD community. Join the conversation. #WorldIBDDay2026 #IBDHasNoBorders #CrohnsDisease #UlcerativeColitis

Chronic inflammatory demyelinating polyneuropathy (CIDP), is a debilitating condition that damages nerves and causes progressive muscle weakness. In honor of CIDP Awareness Month, we’re raising awareness of the symptoms of CIDP. This knowledge empowers patients to get diagnosed more quickly and proactively manage their care sooner. Learn more about the symptoms of #CIDP below, talk with your doctor, and join us in continuing these important conversations year-round. #CIDPAwarenessMonth #CIDP

An early and accurate diagnosis can make a meaningful difference for individuals and families affected by mucopolysaccharidosis (MPS). This #MPSAwarenessDay, we stand with the community to underscore the profound impact these rare, inherited genetic conditions can have on patients’ lives. That’s why we are focused on advancing awareness, supporting screening initiatives and driving research alongside healthcare professionals to help improve the diagnostic journey for patients living with MPS II (also known as #HunterSyndrome). By working together with the MPS community, we aim to create a future where every patient receives the right diagnosis as early as possible. Check out Project Alive and National MPS Society to learn more and find ways to support this community.

#PsoriaticArthritis (PsA) doesn’t look or feel the same for everyone. In a survey of more than 2,200 individuals living with PsA, women reported experiencing a higher overall disease burden compared with men. Understanding these differences is key to improving outcomes for everyone. #PsAActionMonth

When a viral disease outbreak ravages a region, the ability to meet the immediate surge in vaccine demand has a tangible impact on people’s lives. Across our network, teams are working to shorten the time between manufacturing and batch release, helping make vaccines available where they’re needed most. Read more about our enterprise-wide “One Day Batch Release” initiative: https://lnkd.in/err9a-gs #InfectiousDisease #PredictiveBatchRelease #AIinPharma #OurStories