NS Pharma, Inc.

Our extended team recently got together at the Muscular Dystrophy Association 2024 conference and it was a reminder that we are fortunate to work with so many intelligent, compassionate people! We are grateful for this opportunity to gather and help individuals with #RareDiseases and their loved ones.

We’re excited to congratulate our outstanding Patient Services team on its recent award at #asembia24 from Two Labs ! As category winners, our team delivers compassionate and effective #patientservices in the field of #neurology. Pictured are Associate Director Judy Cohen, MBA and Senior Director Jonathan Cabral. Please join us in acknowledging our whole team's hard work and dedication to our patients. #raredisease #patientsmatter

Our team was pleased to attend the Parent Project Muscular Dystrophy Cardiac Meeting in Baltimore, MD and connect with #healthcare professionals to explore the current issues and latest advances in cardiac care for patients with #Duchenne muscular dystrophy. Pictured are our Regional Customer Engagement Lead Ty Morgan, Medical Science Liaison Mary Fayazi, PhD, MPT, Associate Director, Medical Affairs Michelle Previtera, and Regional Business Director Jennifer Tamberino. #pediatriccardiology #cardiology #raredisease

It was such a pleasure – as always! – catching up with our colleagues from the Jett Foundation at its Family Workshop in Charlotte, NC on May 4. Our team was on hand to provide information and support to patients and caregivers. Pictured are Jett Foundation team members Emily Hubert, Julie LeClair, Jessica Campbell and Alexa Tinsley with our Associate Director, Patient Experience Rob Jacobs. #Duchenne #raredisease

We were honored to sponsor the April 27 Family Workshop in Spanish by The Akari Foundation! Pictured are our Medical Affairs Liaison Laura Torrente, PhD, Akari Foundation founder Luisa Leal, and our Patient Engagement Liaison Julz L. The event was very well attended, providing much-needed outreach and support to Spanish-speaking families in Puerto Rico. #Duchenne #raredisease #patientadvocacy

We’re visiting Charlotte, NC this weekend for the Jett Foundation Family Workshop, featuring guest speakers with expertise in #pediatriccardiology and #neurology. Thank you for hosting this information-rich event for patients with #Duchenne muscular dystrophy and their families. #raredisease

We had gorgeous weather – to match the amazing smiles on people's faces – at the Muscular Dystrophy Association Day event at Valley Children's Healthcare April 27th, which we were honored to sponsor! Events like this make it possible for patient families to connect with resources and information in their area. Pictured: Laura Flores and Angela Romero-Waterman, with our Patient Engagement Liaison Cindy Cruz.

President John F. Kennedy once said, “Children are the world’s most valuable resource and its best hope for the future.” We agree, and that’s why we were overjoyed to host our employees’ kiddos on Bring Your Kid to Work Day. Twenty amazing children, ages six to 17, visited our office for learning, arts & crafts, pizza and a little bit of Mad Science. We’re already planning ahead for next year!

We are grateful to be joining leading healthcare practitioners and pharmaceutical professionals this weekend at the 20th Asembia Specialty Pharmacy Summit. We look forward to connecting with everyone over the next few days. #Asembia24

Our team had a fulfilling month connecting with families living with #RareDiseases all over the country! Over the course of the next two days, we will be partaking in the 17th Annual Pediatric Neurology Symposium with Le Bonheur Children's Hospital. We look forward to engaging in meaningful discussions on how to improve diagnoses and enhance treatment plans in #Duchenne and other nervous system disorders.