Catalyst
@CatalystForRare
We are committed to improving the lives of patients with rare diseases.
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Behind every advocacy organization is a story that drives the mission. Sofie's Journey was founded by Brad, Candy, and Sofie - a family who knows firsthand what it means to navigate life with epilepsy. For 13 years, they've been raising awareness and creating community for the…
Are you attending the @AANmember's Fall Meeting #AANFC? Team Catalyst is here at booth #708. Explore our work in the rare neuromuscular disease space, specifically focusing on Lambert-Eaton myasthenic syndrome (LEMS) and Duchenne muscular dystrophy (DMD), and learn more about our…
Want to learn about the latest in Duchenne muscular dystrophy (DMD) care, resources, and other crucial information? Catalyst is proud to once again partner with the @JettFoundation, an organization dedicated to empowering individuals and families affected by DMD. On November…
November is National Epilepsy Awareness Month — a time to honor the 3.4 million Americans living with epilepsy, including 470,000 children. Catalyst is proud to support families affected by this condition and will be joining the Epilepsy Awareness & Education Expo, presented…
Catalyst will be at the @Jefferies Global Healthcare Conference in London on November 17th. This event aims to bring together C-Suite executives from public and private organizations around the world, covering different fields in the healthcare industry. Our President & CEO, Rich…
Catalyst Pharmaceuticals reports benchmark Q3 financial results, exceeding the original forecast. Our results show another consecutive quarter of growth, driven by our product portfolio. This is supported by our commercial approach and our commitment to raising awareness of the…
Congratulations to @Santhera Pharmaceuticals on the completion of their 5-year GUARDIAN study. This historical data is helpful information for the Duchenne muscular dystrophy (DMD) community: santhera.com/assets/files/p…
Are you at the @AASAutonomic conference #AAS2025? Visit Team Catalyst's booth to learn more about the presentation of autonomic dysfunctions in a rare neurological muscle disorder, Lambert-Eaton myasthenic syndrome (LEMS).
Catalyst is excited to announce that we are named a @biospace "Best Place to Work" for 2026, an award chosen based on company qualities such as compensation, innovation, career growth opportunities, leadership, remote work, and more. We’re proud to nurture a workplace where…
"You may encounter us in a lot of different places." Whether it's the first time or tenth, social workers are there for you in your time of need. Dr. Maya Doyle, Professor of Social Work at Quinnipiac University, shares how social workers stand with families through both…
At @McKesson Accelerate conference today? Cancer-Associated Lambert-Eaton myasthenic syndrome (LEMS) is the most common condition of its type in people with small cell lung cancer (SCLC). Stop by Catalyst's booth #135 to learn more about the signs, symptoms, and diagnosis:…
At @AANEMorg today? Come watch Catalyst present DMD in Focus: Real Cases and Insights With a Novel Corticosteroid in the Grand Ballroom today, starting at 11:40 PT. Don't miss out on an insightful presentation as our speakers, Dr. Tesi Rocha and Dr. Katz, present real-life…
Team Catalyst is partnering with Muscular Dystrophy Association (@MDAorg) for their Muscle Walk of Dallas. Catalyst and MDA remain dedicated to empowering everyone living with a neuromuscular disease, so they can live longer, more independent lives. See how you can get involved:…
The Catalyst team had a great time at @JADPRO Live discussing the connection between small cell lung cancer (SCLC) and Lambert-Eaton myasthenic syndrome (LEMS). Our team spoke with many minds in the Oncology space and are thankful for the collaborative discussions focused on…
If you're at @AANEMorg, Catalyst is presenting on Friday, October 31st. Come listen for DMD in Focus: Real Cases and Insights With a Novel Corticosteroid, located in the Grand Ballroom. See you there: aanem.org/meetings/annua…. #AANEMinSanFran
At the @AANEMorg meeting starting today? Catalyst is exhibiting from October 29th-31st at booth #809. Visit us and learn about rare neuromuscular disorders, treatments, and more: aanem.org/meetings/annua…. #AANEMinSanFran
"One day at a time." That's her mantra. Emily, a young mom, faced significant changes to her daily life after receiving a diagnosis of Lambert-Eaton myasthenic syndrome (LEMS). Watch the story of her journey, detailing how she navigated the complexities of her diagnosis and…
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Mom With Lambert-Eaton Myasthenic Syndrome (LEMS): Emily’s Story
Team Catalyst is at @JADPRO Live! Did you know that 9 out of 10 cases of Cancer-Associated Lambert-Eaton myasthenic syndrome (LEMS) may not be diagnosed? Visit our booth #306 to learn more about the connection between small cell lung cancer (SCLC) and LEMS. #JADPROLive
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