Huge thank you to everyone that shows us their support it is truly appreciated. Please keep safe, remember to socially distance yourself even with a lessening of the lockdown pending we should be still keep prevention at the forefront of our minds.
Wishing you all wellness and less pain
Carole and the team
Includes other places around the #globe for #fibromyalgia #healthinformation and #resources
On this special day ‘International Fibromyalgia Awareness Day’, in 2014, FibroFlutters was born and today we celebrate our 6th Birthday, please help us to raise awareness.
Please support Fibromyalgia Action UK
Many thanks for supporting the work that the charity Fibromyalgia Action UK does towards raising awareness through educating people about what fibromyalgia is. Also, through the many support groups that the charity has throughout the UK that all support patients with fibromyalgia.
Fibromyalgia Action UK (FMA UK) is a registered charity in England and Wales (1042582). A company limited by guarantee (SC492045).
Registered address: 12 Seedhill Road, 3007 Mile End Mill, Paisley, Renfrewshire, PA1 1JS
FibroFlutters continuously supporting fmauk.org
#BecomeFibroAware #fibromyalgia #May12th #chronicillness #ChronicPain #fightfibro
Other places for fibromyalgia information and resources:
Got any to add from your country of residence please email me fibroflutters@gmail.com
Europe:
The European Network of Fibromyalgia Associations (ENFA)
Nordic Trial Alliance for Scandinavian links
Some resources can be found via this link:
Pakistan:
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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