Our July newsletter snapshot – The entire newsletter in a quick, easy to read format!
Too many people are left out of clinical trials – especially those from minority communities, people with disabilities, older adults, rural residents, and those with diverse gender identities – limiting our understanding of how diseases like MS affect them. The MS Minority Research Engagement Partnership Network is working to change that by making research more inclusive and accessible. Read more…
Why does diversity in research matter?
Improves accuracy Reflects all patient experiences
Fosters innovation Includes broad views to spark progress
Promotes equity Reduces unfair health gaps
Prevents mistakes Avoids biased or unsafe results
Builds trust Encourages community engagement
iConquerMS is dedicated to amplifying the patient voice in MS research. If you haven’t already, please consider joining today!
While the history of clinical research is marked by serious ethical failures, this has driven important reforms that now protect research participants. Stronger regulations, greater transparency, and ongoing community engagement efforts have laid the foundation for rebuilding trust. However, improving diversity in clinical trials remains an urgent priority. By learning from the past and committing to meaningful change, we can create a future where all communities are equally heard, respected, and empowered in clinical research. Read more…
