Wisconsin rare disease community: We need your voice today! Lani of the Wisconsin Rare Disease Alliance, a rare mom, shares why this matters. If you’re a Wisconsin resident, contact your state senators and ask them to support and co-sponsor SB 203. Every call and email counts! #RareDiseases #LivingRareWI | National Organization for Rare Disorders, Inc. (NORD)

That’s a wrap on this year’s NORD Rare Diseases and Orphan Products Breakthrough Summit—two incredible days of connection, collaboration and commitment to shaping the future of rare disease research, treatment, and policy. As our CEO Pam Gavin said, “We are living in challenging times, but the rare disease community continues to show what unity looks like. Together, we’re going to keep pushing to support the 10,000-plus rare diseases that need treatments and cures.” The rare disease community is