Pinterest • The world’s catalogue of ideas
from Laura's pen

Why you shouldn’t judge a disability by its visibility

Don't judge a disability by its visibility: a blog inspired by Lauren Rowe's viral Facebook post

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ME Association Welcome to The ME Association, also registered as The ME Society. We provide information, support and practical advice for people, families and carers affected by M.E. (Myalgic Encephalopathy), Chronic Fatigue Syndrome (CFS) and Post Viral Fatigue Syndrome (PVFS). We also fund and support research, and offer education and training. We are the oldest established ME/CFS charity funding only biomedical research into the illness http://www.meassociation.org.uk/

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"M.E. / Chronic Fatigue Syndrome - Sleepydust Video" The video aims to help the friends and family of ME/CFS (including Myalgic Encephalomyelitis (M.E.), Chronic Fatigue Syndrome (CFS), and Post Viral Fatigue Syndrome) sufferers understand the illness and what their loved ones are going through. (9:00) I can't endorse the site that posted this video, or its free newsletter.

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How I recovered from Chronic Fatigue Syndrome -- Healing and recovery from Chronic Fatigue Syndrome, ME (myalgic encephalitis), Post viral fatigue syndrome

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from everydayhealth.com

Invisible Illness Awareness Week - Chronicling Chronic Pain

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