Solve Spearheads Call for New NIH Office for Infection-Associated Chronic Illness Research (IACIR)
This year, Solve is beginning one of our most ambitious advocacy projects to date — one which could alter the research landscape for ME/CFS, Long Covid, and other infection-associated chronic […]
The TREAT Long Covid Act is Back!
On May 11, as the Biden administration ended the Public Health Emergency for COVID-19, Congresswoman Ayanna Pressley (MA-07), alongside Representatives Don Beyer (VA-08) and Lisa Blunt Rochester (D-DE), reintroduced the […]
Solve Brings Army of Advocates to Capitol Hill, Presses Congress to Support the Care for Long Covid Act
Advocacy Week 2023 unites Long Covid, ME/CFS communities in an effort to educate congressional representatives, marking the first in-person gathering for the event since 2019. LOS ANGELES, CA – Today […]
Advocacy Week 2023
Advocacy Week 2023 will take place virtually and in person throughout the week of April 17th to April 22nd, 2023! Advocacy Week is a nationwide advocacy effort to connect people […]
Advocacy Cafe Chat
During Advocacy Month 2022, we premiered a new series spotlighting the voices of several standout members of our community as they inspired us with their stories, advocated for change, and […]
Solve Awarded Nearly $250k from Chan Zuckerberg Initiative to Fund Bold New Program
We’re thrilled to announce that the Chan Zuckerberg Initiative (CZI) has awarded Solve M.E. a significant grant in support of our Long Covid Patient Leader Advancement Network (LC-PLAN), a groundbreaking […]
Solve M.E. & Community Partners Denounce Misleading New York Magazine Article
The article published in NY Magazine on Nov 4, 2022, “Has Long COVID Always Existed? The pandemic might not have spawned a new chronic illness but rebranded an old one,” […]
RECOVER Study of Paxlovid to Treat Long Covid Begins January 2023, Has Implications for ME/CFS
The National Institutes of Health (NIH) announced that the use of Paxlovid to treat Long Covid will be the first treatment to be studied by its $1 billion RECOVER Initiative. […]
Ryan Prior On The Long Haul and How Patients Can Change the World
In his new book, The Long Haul: Solving the Puzzle of the Pandemic’s Long Haulers and How They Are Changing Healthcare Forever, CNN journalist and ME/CFS patient advocate Ryan Prior […]
World ME Alliance calls on WHO Director General to recognize ME/CFS alongside Long Covid
On Wednesday 12th October Dr. Tedros Ghebreyesus, Director General of the World Health Organization, wrote an op-ed in the Guardian. In it, he lays clear the devastation that Long Covid […]
Aila Health Presents Free Virtual Long Covid Summit
Our friends at Aila Health are hosting a free Long Covid Summit on Wednesday, September 21 8 AM – 3 PM PT to bring together specialists, longhaulers, caregivers, advocacy organizations, […]
Labor Lost: The Economic Impact of Post-Infection Disease
Each year in observance of Labor Day, we honor workers and their achievements. But the holiday is also an occasion to consider all of those who are robbed of the […]
