🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

Each October 10th we celebrate Hereditary Factor X Deficiency Awareness Day. Spread the word as each day we countdown to 10/10 with a surprising fact about this often-undiagnosed, serious condition. Early detection can change lives #10/10 bleeding.org/bleeding-disor…

Each October 10th we celebrate Hereditary Factor X Deficiency Awareness Day. Spread the word as each day we countdown to 10/10 with a surprising fact about this often-undiagnosed, serious condition. Early detection can change lives #10/10 bleeding.org/bleeding-disor…

Each October 10th we celebrate Hereditary Factor X Deficiency Awareness Day. Spread the word as each day we countdown to 10/10 with a surprising fact about this often-undiagnosed, serious condition. Early detection can change lives #10/10 bleeding.org/bleeding-disor…

Each October 10th we celebrate Hereditary Factor X Deficiency Awareness Day. Spread the word as each day we countdown to 10/10 with a surprising fact about this often-undiagnosed, serious condition. Early detection can change lives #10/10 bleeding.org/bleeding-disor…

Each October 10th we celebrate Hereditary Factor X Deficiency Awareness Day. Spread the word as each day we countdown to 10/10 with a surprising fact about this often-undiagnosed, serious condition. Early detection can change lives #10/10 bleeding.org/bleeding-disor…

FDA Approves Kedrion's Bolognana Facility for Production of First and Only Treatment for PLGD-1, Ryplazim® - Kedrion us

From all of us to all of you, we wish you a Happy and Healthy Thanksgiving. As we gather together on this special holiday and reflect on the work that we do, the communities we serve, and the differences we make, we thank all of the employees for their dedication and commitment.

🌍 3️⃣0️⃣0️⃣ MILLION people worldwide live with a rare disease. Today, we recognize the strength and resilience of those affected by rare diseases. Each individual story is a testament to the power of hope, innovation, and community support. At Kedrion, delivering plasma derived

🌟 Did you know? 🌟 72% of rare diseases are genetic in origin, affecting millions of people worldwide. These conditions often start in childhood and can significantly impact the lives of patients and their families. Understanding the genetic basis of these diseases is crucial

🌍 Did you know there are over 6,000 known rare diseases? 🌍 Rare diseases affect millions of people worldwide, yet each condition impacts a relatively small number of individuals. This makes research, diagnosis, and treatment particularly challenging. 💡 Awareness and advocacy

🌍 Did you know? 🌍 5% of the world's population is affected by rare diseases, impacting approximately 300 million people globally. These conditions, though individually scarce, collectively represent a significant patient population. Raising awareness and supporting research

🦓 On this Rare Disease Day, do your part to raise awareness by showing your stripes. The zebra is the mascot of rare diseases due to a phrase in the medical community: "When you hear hoofbeats, think horses, not zebras." This phrase encourages medical professionals to consider

🚼 𝐑𝐚𝐢𝐬𝐢𝐧𝐠 𝐀𝐰𝐚𝐫𝐞𝐧𝐞𝐬𝐬 𝐨𝐧 𝐇𝐃𝐅𝐍: 𝐀 𝐂𝐚𝐥𝐥 𝐭𝐨 𝐀𝐜𝐭𝐢𝐨𝐧 🚼 March 12th is HDFN Awareness Day, highlighting Hemolytic Disease of the Fetus and Newborn (HDFN), where a mother's immune system attacks her baby's red blood cells, causing severe health issues.

Expanded access for rare disease medication becomes reality. prn.to/4bR71Nd

We've rebranded! At Kedrion we believe in the power of rare connections and our new brand brings that to life through movement, imagery and messaging. #ScienceAndCare #PowerOfRare #RareIsReal #Kedrion

✳️Bringing Awareness to Plasminogen Deficiency Type 1 (PLGD-1) on May 5th! ✳️ PLGD-1 is a rare genetic disorder that can be inherited and often goes unrecognized. It causes ligneous lesions to form in organs throughout the body and is frequently mistaken for other conditions.

👀 Chronic Conjunctivitis? It Could Be PLGD-1.👀 Kedrion Biopharma is recognizing Plasminogen Deficiency Awareness Day on May 5th. Plasminogen Deficiency Type 1 (PLGD-1) is a rare genetic disorder that causes ligneous lesions to form throughout the body. Ligneous conjunctivitis

🔎 PLGD-1: Rare, but Recognizable🔍 Kedrion Biopharma is recognizing Plasminogen Deficiency Awareness Day on May 5th. Plasminogen Deficiency Type 1 (PLGD-1) is a rare genetic disorder, affecting an estimated 500 people in the U.S. It causes ligneous lesions to form throughout