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 CHRONIC*INVISIBLE*RARE ILLNESS SUPPORT

Patient * Health * Research * Pharma * Advocacy


Locally we’re a Support Group for people with Fibromyalgia, Chronic Pain, EDS/Hypermobility, Mental health, Chronic fatigue/Me, Rare & others offering friendship, support & advice in Sunderland, NE UK … 
… but we also offer online support, advice and advocacy via our social media network , chronic illness portal, across the globe.


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!!




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!!





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