REMEMBER, IF YOU WANT THE CHANGES, THIS IS HOW WEVE GOT TO DO IT!!! IT HAS TO GO THROUGH PARLIAMENT TO CHANGE THE LAW!!

 

1. Its not just about getting fibro classed as a disability,( it needs to be moved from the impairments list to section / schedule one of the equality act for this to happen)

2. We're here to raise awareness of the condition and the other invisible illnesses and chronic diseases (me, cfs ) as part of our charities constitution

3. ITS NOT ABOUT BENEFITS OR MONETARY GAIN FOR OURSELVES

4. We want to get better treatment for others like ourselves

5. To educate the wider community and public

6. To banish the stigmas

7. To support others like ourselves through our page and our own community

8. get the help for fellow sufferers they deserve,

9. To help our charity who we are becoming trustees for, fibro flare awareness group (CHAIR Beth Urmston) do all of the above AND BELOW

10. To get our voices heard AS A UNITED COMMUNITY

11. WE ARE WILLING TO WORK WITH FELLOW FIBROMYALGIA GROUPS AND CHARITIES TO SPREAD THE AWARENESS AND ACHIEVE THESE GOALS

12, to hopefully assist in opening more treatment centres instead of just the main 2 (in London and Bath) we have in the Uk

Lots of hugs and spoons to all x