Skin Rashes and Fibromyalgia Syndrome
By: Suzanne Elvidge BSc (hons), MSc – Updated: 23 Sep 2018 |
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The FibromyalgiaSyndrome website was designed and written to help support people with fibromyalgia, and their families, friends and colleagues. It provides an approachable and easy-to-read introduction to fibromyalgia syndrome, and gives no-nonsense information about living with this potentially long-term disorder.
http://www.fibromyalgiasyndrome.co.uk/
I like this because it explains quite well what skin is like for Fibromyalgia patients and think it ties nicely to this other article previously shared on this website fibroflutters.com –
Updated June 2017 / October 2019

FIBROFLUTTERS CHRONIC, INVISIBLE & RARE ILLNESS SUPPORT
Patient Advocacy Organisation & Online Community 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.
and if you have a problem we are always open to discussion, just e-mail Carole
PLEASE NOTE: We are not medical professionals, but as patients we are sharing news, articles, information and resources out to you as all stakeholders to help keep you up to date within the Medical healthcare industries and chronic illness health, rare disease and our advocacy work for patients, health, research and pharma, including digital and AI in medicine.
PLEASE NOTE: THAT THIS SITE USES GOOGLE ANALYTICS TO COLLECT DEMOGRAPHIC INFORMATION FOR INFORMATION AND CONTENT DECISION MAKING PURPOSES ONLY AND NOT TO SELL TO 3RD PARTIES.
MANY THANKS in advance for your understanding –
from the administrator – fibrofly73 aka Carole
And my profile on Synapse where you can read about the initiatives that I am involved with
https://synapse.pfmd.org/experts/O6wWb7Kd
FibroFlutters on Synapse where you can read about the initiatives that we are involved with
https://synapse.pfmd.org/organizations/fibroflutters
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