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02/24/2026

The average rare-disease patient waits years for a diagnosis, often seeing multiple specialists before receiving answers.

It’s time to change that. Join our Earn Your Stripes: Rare Disease CME Challenge with the National Organization for Rare Disorders, Inc. (NORD) to improve the early identification, diagnosis, and management of rare conditions.

Get started here: https://bit.ly/4kSv3ff

We are proud to launch the first Earn Your Stripes: Rare Disease CME Challenge exclusively in partnership with National ...
02/23/2026

We are proud to launch the first Earn Your Stripes: Rare Disease CME Challenge exclusively in partnership with National Organization for Rare Disorders, Inc. (NORD) improve the early identification, diagnosis, and management of rare conditions.

Complete a rare disease education program on Medlive through March 31 to earn CME credit and a sharable certificate acknowledging your commitment to improving rare disease outcomes.

Start earning your stripes now: https://bit.ly/40nnJi6

⚠️ If heart changes, nerve pain, or balance trouble keep showing up in your family, it could be more than coincidence. H...
02/11/2026

⚠️ If heart changes, nerve pain, or balance trouble keep showing up in your family, it could be more than coincidence. Hereditary ATTR amyloidosis disproportionately affects Black/African American families due to the V122I gene variant. Learn the signs and know your genetic history.

🔗 Register today to join the conversation: https://www.medlive.com/v/hATTRamyloidosisSocial

The Mended Hearts, Inc. BlackDoctor.org

👨🏾‍👩🏾‍👦🏾 Hereditary ATTR amyloidosis often goes unnoticed in Black/African American families where a particular genetic ...
02/06/2026

👨🏾‍👩🏾‍👦🏾 Hereditary ATTR amyloidosis often goes unnoticed in Black/African American families where a particular genetic variant appears more frequently. Learn the signs, how it may be passed down, and more.

👉 Don’t miss this insightful discussion - save your spot today! https://bit.ly/3ZZgdd3

The Mended Hearts, Inc. BlackDoctor.org

02/04/2026

Only ~20% of eligible patients receive CAR T therapy. Access shouldn’t depend on zip code. On , we’re highlighting what needs to change - from community-based care expansion to clearer clinical pathways.

Act now by watching the full CME program with our partners Association of American Cancer Institutes (AACI) & American Society for Transplantation and Cellular Therapy 👉 https://bit.ly/4jXNHSo

01/16/2026

✈️ Traveling with T2 conditions takes more than a packed bag. It takes planning.
In this video, Parker talks through practical considerations to help you feel more prepared and confident before you go.

For more tips and resources, visit 👉 https://bit.ly/4qvpsgU

01/15/2026

affects more than skin - it shapes everyday choices, confidence, and family life.

Amy shares how she supports her daughter Ella, making small changes that help manage flare ups while still allowing life to be lived fully 💛

Explore helpful resources here 👉 https://bit.ly/4qXvhU9

A lung cancer diagnosis can bring many questions about what’s next. 💙This short video features an expert who explains tr...
01/12/2026

A lung cancer diagnosis can bring many questions about what’s next. 💙

This short video features an expert who explains treatment options and ways to partner with your care team.
Get clear, helpful information to support your next steps.

Watch now to learn more ▶️ https://bit.ly/45KJD1Q

In partnership with: GO2 for Lung Cancer

A CIDP diagnosis can bring many questions, and support matters. Hear from people living with CIDP and infusion nurses as...
01/08/2026

A CIDP diagnosis can bring many questions, and support matters.

Hear from people living with CIDP and infusion nurses as they explain the condition and treatment options like IVIG and SCIG. 💬

Watch now: 👉 https://bit.ly/4jo2ci2

In partnership with: GBS-CIDP Foundation International

📣 Medlive and the National Organization for Rare Disorders, Inc. (NORD) have extended our exclusive CME partnership. Thi...
01/06/2026

📣 Medlive and the National Organization for Rare Disorders, Inc. (NORD) have extended our exclusive CME partnership.

This renewed commitment is a testament to what we’ve achieved, together, over six years of collaboration and nearly 125 outcomes-driven programs, reaching over 76,000 clinicians, patients, and caregivers.

Looking ahead, the expanded partnership will introduce innovative education models, integrate real-world data, and continue to empower the community.

📖 Read the full press release here: https://bit.ly/44Z6UNl

A diagnosis of BCC or cSCC can bring a lot of questions, and support matters. 💜Hear from a top dermatologist and a patie...
12/19/2025

A diagnosis of BCC or cSCC can bring a lot of questions, and support matters. 💜
Hear from a top dermatologist and a patient advocate as they break down treatment options, including immunotherapy, and help you feel more confident about next steps.

Watch now. 👉 https://bit.ly/3Y35Cgy

Proudly partnered with: GRACE - Global Resource for Advancing Cancer Education

Living with COPD can be tough, but you’re not alone. 💙 Learn from a lung doctor and a COPD Foundation expert about ways ...
12/17/2025

Living with COPD can be tough, but you’re not alone. 💙 Learn from a lung doctor and a COPD Foundation expert about ways to breathe easier and take control of your health.

Available to watch now. 👉 https://bit.ly/49eRNli

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