‘bringing greater awareness of Fibromyalgia to the British Public’

change.org petition sign here

PLEASE NOTE: This petition was originally Published here on 2015/06/01. I have checked it’s status several times since, and again 29 / 10 / 2019 and it is still live, it has not been closed. Whether the petition organisers are still watching it is unknown to me, but if you wish to sign you can. I just can’t say if it will make a difference, or not. Many thanks ~ Carole

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!!

MANY THANKS in advance for your understanding –
from the administrator – fibrofly73 aka Carole

See our About Us pages  >>>

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