From ME Advocacy.
Advocating in the United States for the disease myalgic encephalomyelitis (ME) has reached a new challenge that threatens the very core of the recognition for the disease. While some advocacy organizations have diverged and taken the alarming path of partnering with the US Health and Human Services (HHS) in adopting, using and educating with the government constructed “systemic exertion intolerance disease” (SEID), which does not define a distinct disease – MEadvocacy remains focused on advocating for the specific acquired neuroimmune disease ME as defined by international ME experts. This blog covers the challenges ahead for patients who have ME as described in the International Consensus Criteria (ICC) getting proper care and treatments. It also details what ME advocates can do to ensure that the distinct disease ME per ICC gets adopted by HHS.
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