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Health education for patients, caregivers and HCPs. Join our growing community! Education.

08/26/2025

This session brings together a top neurologist and a person living with gMG to help you understand current and emerging treatment option. You'll learn how to talk to your care team to get the best care!

08/22/2025

If you have RA, what you eat and how often you exercise can improve your quality of life. Listen to this video for more information!

👉 Watch more RA videos & resources now on Medlive: https://bit.ly/3JMMCib

Partner: AiArthritis

08/13/2025

🌟 We’re going LIVE today at 11 AM ET! 🌟

Living with a rare disease like can feel overwhelming but you are not alone.

Join our Medlive Patient Education Session to:
💡 Learn what C3G is and how it’s diagnosed & managed
🩺 Hear from experts who understand your journey
📚 Access practical tools and resources designed for you

📅 Today at 11:00 AM ET
🎥 Access here: https://bit.ly/412YxhT

Let’s navigate this together. 💙

In collaboration with NephCure , National Organization for Rare Disorders, Inc. (NORD) & KDIGO

08/01/2025

🩺 Building Your Multidisciplinary Care Team for paroxysmal nocturnal hemoglobinuria (PNH).

Kathryn, a nurse practitioner at the Moffit Cancer Center explains why it's important to have a team that understands your unique needs. From PNH specialists to primary caregivers, and other experts like gastroenterologists and social workers, each plays a crucial role in managing your health.

Learn why connecting with a PNH specialist regularly, even if you have a local hematologist, is vital for your care: https://bit.ly/3IVkskY

Partnered with National Organization for Rare Disorders, Inc. (NORD)

07/18/2025

Your rheumatoid arthritis (RA) care team goal is to achieve remission, which means you feel no or very few symptoms. The good news is that there are 3 types of treatments that relieve symptoms and slow RA down. 👉 Access more RA information on Medlive: https://bit.ly/4m1R8as

07/15/2025

🩸 July is Cord Blood Awareness Month!

Did you know your baby's umbilical cord could save lives? Cord blood is a rich source of stem cells that can help treat over 80 diseases including leukemia, lymphoma, and sickle cell disease.

Choosing to preserve or donate cord blood is a powerful decision that could make a life-changing difference for someone in need. Whether you're expecting or just learning about it, now’s the time to explore your options.

🔗 Additional information and resources:
NMDP 👉 https://bit.ly/46seBxh
Cord Blood Association 👉 https://bit.ly/3IrgqAk
Parent's Guide to Cord Blood Foundation 👉 https://bit.ly/4nNqFix

07/10/2025

Happening TODAY at 4:30pm ET!

Join us for a free, live online session created specifically for patients and caregivers. You'll gain a clearer understanding of , explore current treatment options, and hear directly from medical experts in simple, patient-friendly language.

Don't miss out: https://bit.ly/4kvmFk2

07/02/2025

☀️ It’s UV Awareness Month!

Did you know that 1 in 5 Americans will develop skin cancer by age 70? The good news is that most skin cancers are highly preventable with the right precautions.

Here’s how you can protect yourself and your loved ones:
🧴 Wear sunscreen every day - yes, even on cloudy days.
👒 Cover up with hats, sunglasses, and protective clothing.
🌤️ Stay in the shade between 10 a.m. and 4 p.m. when the sun is strongest.
🔍 Check your skin regularly for any new or changing spots, and talk to your doctor if you notice anything suspicious.

Early detection saves lives. Let this month be your reminder to take care of your skin!

Get more resources here: https://bit.ly/4knkj6G

07/01/2025

🌍 Living with a rare disease can feel lonely, but you’re not alone. Medlive Rare gives you expert advice, trusted information, and the help you need to understand and manage the condition for yourself or someone you love.

👉 Follow Medlive and empower yourself with Medlive Rare - https://bit.ly/4dHr8yc

06/27/2025

🎥 Now Available On-Demand: Free Educational Session on IgA Nephropathy ( )

If you or someone you care about is living with IgA nephropathy, don't miss this opportunity to gain valuable insights from leading experts!

💡 What You'll Learn:
-The latest advancements in IgAN treatment options
-Current recommendations for managing IgAN effectively
-Strategies for collaborating with your healthcare provider to make informed decisions

🔗 Watch now: https://bit.ly/4lnsQaA

Proudly partnered with: National Organization for Rare Disorders, Inc. (NORD) , KDIGO & IgA Nephropathy Foundation

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