Courtney Wulf spoke to us about what a strong support system, COVID-19, mental health, research, and advocacy means for the lupus community.

Knowing the right things to say (or not say) and do can help you have more empathetic and thoughtful conversations with loved ones who have IBD.

People who live with IBD can find comfort in the wide array of resources available, from support groups and advocacy group chapters to local events, online message boards, and helplines.

We took a look at some of the latest research news in IBD: sugar consumption and increased risk of IBD, sun exposure and decreased risk for IBD, and a new, noninvasive test for IBD.

We take a look at the drugs, surgeries, and changes in diet that may be effective in managing ulcerative colitis

We spoke with Tina Aswani Omprakash, a Crohn’s disease patient and advocate, about her IBD story.

These five essential guidelines for clinical trial patient recruitment help sponsors save time while creating a positive experience for patients.

We share a snapshot of how clinical trial patient recruitment companies work on behalf of sponsors to find the right patients for trials and support enrollment.

Consider using one or several of these services to support your next clinical trial patient recruitment campaign.

We share three strategies you can use to make your clinical trial recruitment materials patient-centric.

We outline how clinical trial matching software works and how to use it for your research portfolio.

Our infographic sums up seven strengths and three weaknesses of decentralized trials.