Read more about the article Guest Feature from Fiona Lowenstein: Chronic Illness Communities on Vaccines

Guest Feature from Fiona Lowenstein: Chronic Illness Communities on Vaccines

The following essay is a guest feature from our friend, journalist Fiona Lowenstein. Fiona is the founder of Body Politic, a grassroots health justice organization for individuals with Long Covid. In... The post Guest Feature from Fiona Lowenstein: Chronic Illness Communities on Vaccines appeared first on Solve ME/CFS Initiative. Read More

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Read more about the article Ensuring the voice of the very severely affected ME/CFS patient is heard in research

Ensuring the voice of the very severely affected ME/CFS patient is heard in research

Ensuring the voice of the very severely affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patient is heard in research-a research model, by  Helen Baxter   Research article abstract: Most of the research about Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has focused on ambulant patients who are able to attend clinics. It is estimated…

Continue ReadingEnsuring the voice of the very severely affected ME/CFS patient is heard in research