Meet the Black Down Syndrome Association
by guest contributor, Crystal Lotterberry, co-founder of the Black Down Syndrome Association About the Black…
Kate O’NeillJuly 7, 2023
LuMind IDSC joins Advocacy Day on Capitol Hill
In April, leaders from LuMind IDSC joined with 350 self-advocates, caregivers, and professionals to meet…
Hope and Action for Down syndrome Alzheimer’s research on WDSD 2023
Each year, the Down syndrome community and our supporters – family, friends, businesses, organizations and…
Kate O’NeillMarch 21, 2023
An athlete’s heart and a charmer’s smile: meet Armond Maillard
March 21st is “Down Syndrome Awareness Day,” a day designated by the United Nations to…
Kate O’NeillMarch 17, 2023
Beyond Down Syndrome: The Friedman family turns experience into guidance
Parent, advocate, and published author, Steve Friedman has used his family's recent experiences to help…
Kate O’NeillMarch 15, 2023
New Year Greetings from Hampus Hillerstrom
Dear Friend of LuMind IDSC, Recently, I spoke with a family whose newborn baby had…
CapetivateJanuary 18, 2023
Statement on accelerated approval of Leqembi to treat mild-stage Alzheimer’s disease in the general population
On Friday, January 6, the U.S. Food & Drug Administration (FDA) granted accelerated approval for…
Kate O’NeillJanuary 10, 2023
Our Impact Report 2022 highlights our accomplishments as an organization during a remarkable year. 2022 saw Down syndrome research receive unprecedented attention from policymakers, the media, and the pharmaceutical and life sciences industries. Click here to read our full report!
https://lumindidsc.org/wp-content/uploads/2023/01/Impact_Report_2022_FINAL_Digital.pdf
Random Acts of Kindness During Down Syndrome Awareness Month
Nowadays people with Down syndrome live healthier, longer, and more fulfilling lives than the generations…
Kate O’NeillOctober 6, 2022
Why is Down syndrome research important?
Learn more about Down syndrome research Learn more about resources for families Learn more about…
Kate O’NeillOctober 3, 2022
