Meaction.net Website Review

a worldwide, gras*roots system for people with myalgic encephalomyelitis and chronic fatigue syndrome. We're developing a worldwide community of service, activism, education and outreach. What happens when you own a disease doctors can't diagnose. #millionsmissing is just a campaign for me health equality. 300 visibility activities, rallies and protest across the mepedia can be really a crowd-sourced knowledgebase in the real history, science and medicine for me, cfs, and as*ociated diseases we held in 2018. #bedfest is actually a digital festival to showcase the art and experience of individuals alive with myalgic encephalomyelitis (me) as extracted through © 2018 that the myalgic encephalomyelitis activity network, okay reserved the painful and often disabling symptoms of me include unrelenting exhaustion, sensory sensitivity, cognitive impairments, and muscle and joint pain. An exacerbation of most symptoms can follow amounts of cognitive or physical exertion. Me leaves 25% of patients house bound or bedbound. For patients that are moderate to acute, living with me is like coping with congestive heart failure for decades , advanced stage as*ists, or cancer. The cause of the disease is not known, although me really is characterized by a viral illness from. Research suggests the condition is the result of an abnormal immune reaction to some triggering event. Though some medications could find a way to help symptoms there are no fda-approved treatments. Experimental remedies have helped some me affects between 15-30 countless people worldwide, and also at the least 1 million americans.