Let's talk medical research

C3G kidney disease is a rare condition, and this blog takes a look at how it is diagnosed and treated.

Becoming a medical studies participant is a great way to have a major impact on the research and future treatments of a condition.

It’s difficult for patients to discover how to participate in clinical trials, which is why creating a patient-centric user experience is so important.

Mitral valve regurgitation is a common type of heart disease, and it is important for patients to be informed about the support available to them.

Alexis Smith had eczema as an infant, but had lived a mostly itch-free childhood until hitting puberty at 12. That's when her symptoms came back.

In this Talk of the Towne podcast episode, we sat down with Tonya Winders from Allergy & Asthma Network to learn the latest on allergy, asthma, and atopic disease research initiatives.

Learn the key symptoms of peripheral artery disease and find community support.

We spoke with BrightFocus Foundation about their new live-streaming talk show, “Brain Info Live.”

We share three tips for people who want to participate in a clinical trial.

We share four things you should know about the disease, including key symptoms and a few valuable resources.

Here’s how to treat your primary biliary cholangitis and where to find support.

Here’s what you need to know when reading a clinical trial listing using Antidote’s matching tool.

We break down the basics of Duchenne muscular dystrophy and where to find support.

There are many ways to connect with others living with lupus. We share three great places to start.

We spoke with Sara Gorman, a writer, lupus community advocate, and the owner of a company called Sara Gorman's Pillbags.