The seminar for tomorrow has been canceled.

As teen #socialmedia use grows, so do worries about #mentalhealth. In this video, our member Jane Harness DO discusses her research on what youth across the U.S. say about social media—from their habits to safety concerns to its effects on their well-being: youtube.com/watch?v=zfpu88…

The Sickle Cell Data Collection (SCDC) program leads efforts to improve access to care for people with sickle cell disease. SCDC's future is at risk after CDC Division of Blood Disorders and Public Health Genomics was eliminated. Sarah Reeves STAT bit.ly/statnews_SCDC

When families go on vacation, many parents hope to spend meaningful, quality time as a family, while teens may want space to do their own thing. Finding the right balance can be a challenge. Next week we look at how much independence parents give their teens when on vacation.

One in 5 parents (19%) say they have never allowed their teen to be away from them while on a vacation, higher for teens 13-15 years (24%) vs 16-18 years (12%). Latest #MottPoll report: mottpoll.org/reports/travel…

1 in 3 parents say they insist their teen interact with family members when on vacation; 64% prefer it but don’t force the issue, and 4% don’t care one way or the other. Latest #MottPoll report: mottpoll.org/reports/travel…

#Infographic: Leaving teens alone on vacation Latest #MottPoll report: mottpoll.org/reports/travel…

Though young adults in the US account for a disproportionate share of new HIV diagnoses, until this study from Nina Hill, MD, we didn't know much about trends in dispensing PrEP!! Free full text 👉 rdcu.be/em1X1

Dr. Reeves shares insights on Sickle Cell Disease care and the role of the MiSCDC Program in identifying service gaps and outcomes. Sarah Reeves U-M IHPI C.S. Mott Children's Mott Children's MD ihpi.umich.edu/news-events/ne…

🩸 It’s #WorldSickleCellDay2025 — a day to raise awareness about #sicklecell disease, an inherited blood disorder that affects ~100,000 people in the U.S., including ~4,000 Michiganders, most of whom are Black or Hispanic. 🧵

In a new Q&A, Sarah Reeves of CHEAR discusses the current landscape of #SickleCellDisease care and her team’s efforts to analyze data to inform policy and better support people with #SCD in Michigan: ihpi.umich.edu/news-events/ne…

Reeves highlights her work leading the Michigan Sickle Cell Data Collection (MiSCDC) Program, a population-based data system run CHEAR in partnership with Michigan HHS Dept to identify gaps in care and services for individuals with #sicklecell. 🎥: m.youtube.com/watch?v=FDRdys…

2 podium, 1 poster & 2 discussant presentations later, I wrapped up one of my busiest (& most fulfilling!) @ashecon meetings yet 💫My fav place to connect with brilliant colleagues, dear friends, and inspiring thought leaders. Already looking fwd to next year! #ASHEcon2025

📢We're Hiring! Join the Susan B. Meister Child Health Evaluation and Research Center University of Michigan as a Clinical Assistant Professor. Passionate about pediatric health services research? More information here: 🔗careers.umich.edu/job_detail/266…