Adenrele Adebisi MD’s Post

Maverex supports Rare Disease Day. We understand the unique challenges in gaining market access for rare disease interventions. Speak to a member of our market access team to discuss how we can support your rare disease market access needs and help bring innovative interventions to patients worldwide #rarediseaseday #rarediseaseday2024 #marketaccess

Last week we had good company at our last strategic meeting of the year. In total six meetings with a focus on ultra rare disease. Gave us lots of information and insights. Let’s continue next year! #orangebrain #orangebrainhealthcarematters #strategicmeeting #advisoryboardmeeting #rarediseases #ultrararediseases.

🗓️In observance of World Liver Day today, it’s becoming clearer that #liverhealth is a prevalent issue that must be prioritized in 🌐 health agendas! Looking forward to joint the upcoming Innovations in SLD think-tank in 2 weeks! For more info look below ⬇️ # steatoticliverdisease #worldliverday

Today, on Rare Disease Day, we stand with our client Target ALS in their commitment to advancing research for all people living with ALS, including those with the rarest forms of the disease. To learn more about their critical work, visit targetals.org. #RareDiseaseDay #ALSResearch #ScientificAdvancements #EndALS #RareDisease

A disease is rare when it affects less than 1 in 2000 people, but that doesn't make it less important to research and treat. Rare Disease Day 2024 is February 29. Rare Disease Day raises awareness for the 6000+ rare diseases (90% are without an FDA-approved treatment!) that affect over 300 million people worldwide.  We are proud to support clients dedicated to advancing science and education for these patients.  Find out more about rare diseases and what can be done to improve awareness at https://lnkd.in/e76yAESx Graphics and Facts c/o RareDiseaeDay.org #RareDisease #RareDiseaseDay #HealthcareAwarenes

Today is the Rare Disease Awareness Day. It is a day to raise awareness and generate change for the 300 million people worldwide living with a rare disease, their families and carers. Rare diseases are conditions that affect less than 200,000 people in the United States, and they often pose significant challenges for diagnosis, treatment and quality of life. However, there is also hope and innovation in the field of rare disease research. Let’s come together to spread the word and offer our support! #RareDiseaseDay #ShowYourStripes #RareDiseaseResearch #RareDiseaseAwareness

Have you heard of bronchiectasis (BE)? It’s a chronic, progressive, inflammatory lung disease that may cause permanent lung damage. This #WorldBronchiectasisDay and every day, Insmed is committed to advocating for and empowering the BE community through patient education and support. Be informed about BE – learn more about how to raise awareness and get involved: https://bit.ly/3L3V4r2

May is #LymeDisease Awareness Month, and at T2 Biosystems, we're dedicated to shedding light on this prevalent but often misunderstood illness. Lyme disease affects millions worldwide, yet diagnosis can be challenging due to nonspecific symptoms and unreliable tests. Join us in raising awareness this month and learn how the #T2Lyme Panel has the potential to make a difference in the fight against Lyme disease. #HealthInnovation https://ow.ly/fbpM50RikUE

It's Cushing's Awareness Month! As a patient of the disease, I was able to share a snippet of my story with Recordati. It is featured about half way through this short video and here is the webpage link: https://lnkd.in/gMwfZDTg

We want to empower you to know more about rare disease. 💙     Read the journeys of people who live every day with a rare disease, and learn about the new research and researchers working to create a better future.    Start learning at knowrare.com    -    #raredisease #rarediseases #rarediseaseawareness #rarediseasewarrior #rarediseaseadvocacy #rarediseasesupport #clinicaltrials #clinicalresearch #clinicalstudies #KnowRare