Worldwide protest of patients with ME against social exclusion After being ignored for years and being excluded from participation in society, ME patients have had more than enough of it. With a virtual march on social media and demonstrations from America to Australia patients call for recognition of their disease and demand care and research.
INTRODUCTION The Centers for Disease Control (CDC) is revising and creating new educational materials for its Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) educational program. The hope is that this fourth try at producing ME/CFS educational materials will result in equality of care for ME/CFS patients and they will, for the first time, experience appropriate care throughout
FROM THE FRONT LINES OF #MILLIONSMISSING ROUND 2: SPEECHES BY TASHA AND HER DAUGHTER ZARA (AT NYC PROTEST)
MEDIA ADVISORY FOR: Tuesday, September 27, 2016CONTACT: Anna Zuccaro | [email protected] 4PM: DC Residents Protest Lack of Support for Patients Suffering with Myalgic Encephalomyelitis / Chronic Fatigue SyndromeThousands Worldwide Join an International Day of Action Urging Public Health Officials to Ramp Up Funding for ME/CFS Research, Clinical Trials and EducationMyalgic Encephalomyelitis is a Neuroimmune Disease That
MEDIA ADVISORY FOR: Tuesday, September 27, 2016 CONTACT: Anna Zuccaro | +1-914-523-9145 | [email protected] TUESDAY 12PM: Seattle Residents Protest Lack of Support for Patients Suffering with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome Thousands Worldwide Join an International Day of Action Urging Public Health Officials to Ramp Up Funding for ME/CFS Research, Clinical Trials and Education
MEDIA ADVISORY FOR: Tuesday, September 27, 2016 CONTACT: Anna Zuccaro | +1-914-523-9145 | [email protected] TUESDAY 11AM: Bay Area Residents Rally Demanding Support for Patients Suffering with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome Thousands Worldwide Join an International Day of Action Urging Public Health Officials to Ramp Up Funding for ME/CFS Research, Clinical Trials and Education
MEDIA ADVISORY FOR: Tuesday, September 27, 2016 CONTACT: Anna Zuccaro | +1-914-523-9145 | [email protected] TUESDAY 11AM: Pittsburgh Residents Rally Demanding Support for Patients Suffering with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome Thousands Worldwide Join an International Day of Action Urging Public Health Officials to Ramp Up Funding for ME/CFS Research, Clinical Trials and Education Myalgic
MEDIA ADVISORY FOR: Tuesday, September 27, 2016 CONTACT: Madison Donzis | [email protected] | (210) 488-6220 TUESDAY 4:30PM: NYC Activists Protest Lack of Support for Patients Battling with Myalgic Encephalomyelitis Thousands Worldwide Join In Protests Urging Public Health Officials to Ramp Up Funding for ME/CFS Research, Clinical Trials and Education Myalgic Encephalomyelitis is a Neuroimmune Disease
MEDIA ADVISORY FOR: Tuesday, September 27, 2016 CONTACT: Madison Donzis | [email protected] | (210) 488-6220 TUESDAY 12PM: Michigan Residents Protest Lack of Support for Patients Suffering with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome Thousands Worldwide Join an International Day of Action Urging Public Health Officials to Ramp Up Funding for ME/CFS Research, Clinical Trials and
MEDIA ADVISORY FOR: Tuesday, September 27, 2016 CONTACT: Madison Donzis | [email protected] | (210) 488-6220 TUESDAY 12PM: Dallas Residents Voice Lack of Support for Patients Suffering with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome Thousands Worldwide Join an International Day of Action Urging Public Health Officials to Ramp Up Funding for ME/CFS Research, Clinical Trials and
