“Life in Lockdown: What Matters When All Is Lost”
Thoughtful post by Naomi Whittingham who reflects on living through
the lockdown as someone who has effectively had to live through their
own lockdown due to severe ME for decades
Similar Posts
Health Care Responsibility and Compassion-Visiting the Housebound Patient Severely Affected by ME/CFS
Many people with severe Myalgic Encephalopathy/Chronic Fatigue Syndrome (ME/CFS) commonly receive no care from healthcare professionals, while some…
Call for people to take part in a ME research study
Call for people to take part in a ME research study The ME Association is funding a study…
ME/CFS and anaesthesia (myalgic encephalomyelitis or encephalopathy/chronic fatigue syndrome)
This resource aims to provide people with ME/CFS who need to have an anaesthetic or sedation with information…
People with ME often have difficulty carrying on a two-way conversation
People with ME often have difficulty carrying on a two-way conversation not because of disinterest or anxiety, but…