Wednesday, 22 January 2014

About M.E. | Telling friends and family

Whether you’ve been newly diagnosed or have been living with M.E. for some time now, telling friends, family and children you have the condition can seem like a daunting task. Many people have never heard of M.E. and are quick to dismiss it as laziness or something that’s all in the mind, but that simply isn’t the case.

Action for M.E. is here to help. Below you’ll find information that can be presented to friends and family in order to help them understand what you’re going through, along with several articles from our membership magazine InterAction focused on telling others about the condition.

Action for M.E. | About M.E. | Telling friends and family
Pamela is a former accountant, recovering journalist and international cat herder, disabled and chronically sick with Myalgic Encephalomyelitis, Fibromyalgia and Cervical spondylosis, fluent in three languages; English, Spanish and Rubbish. Mostly writes in the latter. She likes Genealogy, Model Railways and Cats.

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