Dan Coffin shared with Bowling Green Daily News in Kentucky the importance of the SOAR (Supplemental Oxygen Access Reform) Act […]
Read More… from How my Alpha-1 Diagnosis Led Me to SOAR Act Advocacy by Dan Coffin
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From July 8-13, 2026, the Alpha-1 Foundation (A1F) participated in Asociación Latinoamericana de Tórax (ALAT) 19th Congress in Cartagena, Colombia. The ALAT Congress is the […]
Read More… from Asociación Latinoamericana de Tórax (ALAT) 19th Congress
Dan Coffin shared with Bowling Green Daily News in Kentucky the importance of the SOAR (Supplemental Oxygen Access Reform) Act […]
Read More… from How my Alpha-1 Diagnosis Led Me to SOAR Act Advocacy by Dan Coffin
April 25, 2026 marks the ninth annual European Alpha-1 Awareness Day led by the Alpha-1 Europe Alliance, a date in which those afflicted with […]
A1F Board Chair Jon Hagstrom shares with the Critical Path Institute (C-Path) how his Alpha-1 journey is informing research and […]
Every February, the rare disease community comes together with a shared purpose: to raise awareness, inspire action, and amplify the […]
Read More… from Rare Disease Day 2026: Advocacy & Awareness | Alpha-1 Foundation
The second Latin American Alfa-1 Meeting titled “Consolidando avances, ampliando horizontes”, (“Consolidating Advances, Expanding Horizons”) was held on December 10, 2025, in Buenos Aires, Argentina. Organized by Alfa1 Argentina and supported by […]
The 30-day Alpha-1 Awareness Month campaign has been a tremendous success! This year celebrated the Alpha-1 Foundation’s (A1F) 30th anniversary, honoring […]
This week showcased the heart, dedication, and spirit of the Alpha-1 community as everyone raised awareness; teams and supporters walked, […]
A1F’s role as the global leader among the world’s Alpha-1 community was highlighted recently at an Alpha-1 Awareness Month Recognition […]
Week 3 brought heartfelt stories, new beginnings, and meaningful moments from teams and walkers across the United States. Each walk and […]
November continues to raise awareness and funds for Alpha-1. This week focuses on the theme of INNOVATION. A1F is known […]
The annual American Association for the Study of Liver Diseases (AASLD) The Liver Meeting took place from November 7-11, 2025 […]
Read More… from A1F raises awareness at AASLD: The Liver Meeting
November 2025 kicked off with incredible energy and creativity from the Alpha-1 community coast to coast! Teams walked, paraded, and […]
November is Alpha-1 Awareness Month, a 30-day initiative that encourages the Alpha-1 community to share stories and resources while raising […]
The sun was shining over beautiful Dunedin, Florida, as the Alpha-1 Foundation (A1F) once again joined forces with the American Lung Association (ALA) for […]
Read More… from 3rd Annual Alpha-1 Gulf Coast Ride in Dunedin, FL
The 28th Gordon L. Snider (GLS) Critical Issues Workshop entitled, “AAT Polymers: Disease Pathogenesis, Detection, and Therapeutic Targeting” took place […]
Read More… from A1F 28th Gordon L. Snider Critical Issues Workshop
Mark Your Calendars! Medicare Open Enrollment happens from October 15th – December 7th and is the time each year when […]
Read More… from 2026 Medicare Open Enrollment Webinar For Alphas
The Alpha-1 Foundation’s (A1F) 30th anniversary was nothing short of inspirational at the American Lung Association’s (ALA) Escape to The […]
It is important for Alphas to be up-to-date on their seasonal vaccines. AlphaNet has provided a chart to keep you […]
Read More… from Guidance for Alphas on Adult Seasonal Respiratory Vaccines
Below is the official letter addressed to key leaders in the U.S. Senate and House of Representatives urging support for […]
Read More… from A1F Joins Advocacy Groups in Signing Congressional Letter on Rare Pediatric Program
On September 1, the wheels start turning across the nation as hundreds of riders, families, and supporters join together for […]
The Alpha-1 Foundation had the pleasure of meeting Richie Ramirez at the Alpha-1 National Conference, where his passion and story left a […]
Read More… from Richie Ramirez’s Alpha Story Featured on CBS Mornings
At just two years old, Richard “Richie” Ramirez was diagnosed with Alpha-1 Antitrypsin Deficiency (Alpha-1), a rare genetic condition that […]
Read More… from Richie’s Ice Cream for Alpha-1 Raises Over $2,100
Natasha Durant, Alpha Mom and Co-Leader of the Oregon Alpha-1 Foundation (A1F) Support Group, is helping lead the charge in […]
Read More… from Community Parade in Oregon Drives Awareness for Alpha-1