Guest Post: The Mask of Invisible Illness and Fibromyalgia – Hope In Pain | My Fibro Team


One lady’s account of her battle with Invisible illness – chronic fibro pain & fatigue


She says:
“What nobody sees is the struggle it takes me to get out of bed each morning”


This post was written by Elizabeth of Hope in Pain in Australia, and has been living with chronic pain for 22 years.

Posted on July 14, 2016 on My Fibro Team


“MyFibroTeam is the social network for those living with fibromyalgia. Get the emotional support you need from others like you, and gain practical advice and insights on managing treatment or therapies for fibromyalgia.”

https://www.myfibroteam.com/





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FibroFlutters patient, health, clinical research, medical, pharma, digital health & AI advocacy.
Support and advice for people with chronic illnesses and rare disorders. Including, Pigmented Villondular Synovitis (PVNS), Ehlers-Danlos Syndrome (EDS), Hypermobility Spectrum Disorders (HSD’s), Fibromyalgia, Chronic pain disorders, Musculoskeletal conditions, Chronic Fatigue Syndromes / ME, and Mental Health.

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FibroFlutters ~ CHRONIC, INVISIBLE AND RARE ILLNESS SUPPORT / ADVICE / ADVOCACY| Disclaimer | Privacy Notes | 8 May 2018


FibroFlutters continuously

Advocating for a Multi-Disciplinary approach to all aspects of medical healthcare. With a model approach using all the ‘stakeholders’ I’m using a patient’s perspective of what patient-centred care, patient-included, patient-involved, patient-centric should look like and involve, that’s everyone by the way!  

You all need to pitch in and be socially responsible for each other!!