WORLDWIDE LAUNCH OF "LONG HAUL VOICES: LIVING WITH LONG COVID AND ME/CFS" RELEASED TODAY IN ...

WORLDWIDE LAUNCH OF LONG HAUL VOICES: LIVING WITH LONG COVID AND  ME/CFS RELEASED TODAY IN HONOR OF WORLD ME DAY 2022

"There is nothing more powerful than sharing authentic stories of individuals who are suffering from these often-debilitating diseases," added Amitay. We must continue to shine a light on the difficulties of living with complex, chronic conditions that have no FDA-approved treatments or cures."

The mini-series, created in partnership with Unfixed Media Productions, is directed by award-winning filmmaker Kimberly Warner and edited by Emmy award winner Michael Wolcott, both of whom live with chronic disease. Each featured member of the Long Haul Voices cast shares a connection to ME/CFS and/or Long Covid. Cast members include:

• Cynthia Adinig - Patient Advocate & Equity Policy Advisor (Long Covid, POTS, MCAS)
• Paul Burnside - Retired Banker & Organist (Long Covid, Vestibular Neuritis)
• Dr. Anthony Komaroff - Professor of Medicine Harvard Medical School
• Soh-Yeon Lee - Senior Program Analyst (ME/CFS)
• Lili Lim - Actor, Comedian (ME/CFS)
• Dr. Nina Muirhead - Dermatology Surgeon (ME/CFS)
• Dr. Amy Proal - Microbiologist & Viral Science Advisor
• Bilal Qizibash - CEO (Long Covid, Autism)
• Sarah Ramey - Author/Musician (ME/CFS, CRPS, POTS)
• Emily Taylor - VP Advocacy & Engagement at Solve M.E. (ME/CFS Patient Caregiver)

Complete episode guide here.

Before the pandemic, experts estimated there were up to 1 to 2.5 million cases of ME/CFS. Now, after two years of COVID-19, those same experts estimate between 5 and 9 million cases of ME/CFS. And a similar explosion of cases is happening with other post-viral conditions. Long Covid is estimated to affect 22 million U.S. adults – close to 7% of the population. Last month Solve M.E. released a whitepaper that provided a startling, in-depth look at the prevalence of Long Covid in the United States.

World ME Day falls in the middle of Solve M.E. 's annual Advocacy Month, a nationwide advocacy effort empowering people with ME/CFS, Long Covid, and other chronic illnesses; scientists; clinicians, and caregivers to share their unique stories with Congress.

About Solve ME/CFS Initiative (Solve M.E.)The Solve ME/CFS Initiative (Solve M.E.) is a non-profit organization that serves as a catalyst for critical research into diagnostics, treatments, and cures for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Long Covid, and other post-infection diseases. Our work with the scientific, medical, and pharmaceutical communities, advocacy with government agencies, and alliances with patient groups around the world are laying the foundation for breakthroughs that can improve the lives of millions who suffer from various "long haul" diseases.

About Unfixed MediaUnfixed is a media production company that shares and elevates stories of humans living with chronic illness and disability. The Unfixed portfolio of projects demonstrates that living well is not about eradicating our wounds and weaknesses but understanding how they complete our identities and equip us to help others. Current productions include the Unfixed docu-series, Unfixed Focus, Life Rebalanced Chronicles, MS Confidential, Long Haul Voices, the Unfixed podcast, and a feature documentary film Why We Matter.

To learn more about the Solve ME/CFS Initiative, visit www.solvmeecfs.org. Follow Solve M.E. on Facebook, Instagram, or Twitter.

MEDIA INQUIRIES ONLY CONTACTStephanie WorrellSedulo Communications on behalf of Solve M.E.Direct: 208.484.9470Email: [email protected]

SOURCE Solve M.E.