Versión en español • Versão em português By Eric Pyrrhus César Medina climbed mountains, lifted weights, and was an avid cyclist. He had a good job. He had a partner. But everything changed in November 2020, thanks to an infection with the novel coronavirus. Today he lives confined to his bed, abandoned by his partner, unemployed, and wearing special compression
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Part 3: The Missing Voices Speak Up in Mexico
In the last of a three-part series, people with neuroimmune diseases in Mexico speak up about the wide-ranging consequences of the disease on their life. If you haven’t already read the first part of this series, click here. Versión en español • Versão em português By Eric Pyrrhus “There’s so many mysterious or surprising variables in chronic illness,” comments 35-year-old
ContinuePart 2: The Challenge of Standing up for Patients in Mexico
In the second of a three-part series, people describe the challenges of pursuing fundamental rights for patients with neuroimmune diseases in Mexico. If you haven’t already read the first part of this series, click here. Versión en español • Versão em português By Eric Pyrrhus “I hope that in the future there will be some doctor, organization or someone who
ContinuePart 1: Millions Missing in Mexico
In the first of a three-part series, people describe the challenges of living with neuroimmune diseases in Mexico. The science of these diseases is also discussed, and we try to understand why the latest science is not informing proper medical treatment. Versión en español • Versão em português By Eric Pyrrhus “On days when the symptoms are manageable, I walk
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In Spain, patients with neuroimmune diseases such as fibromyalgia or myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS) have been disgusted at their government’s refusal to recognize them as seriously disabled human beings. This week brought news of a big step forward. By Eric Pyrrhus Versión en español • Version française • Deutsche Version In 2019 the Spanish government agency that oversees
ContinueExtracellular Vesicles and Micro-RNAs in ME/CFS
A conversation with Dr. Elisa Oltra and Dr. Jesus Castro By Eric Pyrrhus Versión en español In 2020, there were three different scientific publications about “extracellular vesicles” and four different scientific publications about “micro-RNAs” in myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS). What exactly are extracellular vesicles and micro-RNAs and why are they both such exciting fields of research? A vesicle
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