I just received an email from Georgie Allan Max Clifford, whilst Mr Clifford cant help us, he is willing to give us celeb agents contact details to help us. I for some reason cant copy email but if I could send it to anyone can you please pm me your email address and perhaps you can show it on here
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Pm'd you my email addy.
x
Just sent it to you, foggy brain today just couldnt copy it,Ive also sent her a link about dla tribunals
I've written to her lally, did you want me to copy her email to you onto here ?
yes we can do Hele. If we stick together hopefully we canget something done, my foggy brains struggling today, legs ache like hell, we might need to see who will join us and set up a working group to fight this
There you go . I've left off your private details such as name and personal e-mail address and just copied the reply you received .
Not sure if I'm allowed to put his contact details on here but if anyone wants them, pm me.
Thank you very much for your email, however I am very sorry but this is not something that we are able to assist you with in this instance. It would be best for you to go directly to a newspaper with you story.
I hope you can understand that whilst Max would like to be able to help everyone who contacts him, sadly because of the sheer volume of correspondence he receives, this is not always possible.
Are there any celebrities in particular you would like to contact. I would be happy to try and look up their agents contact details for you.
Wishing you the very best for the future,
Kind regards,
Georgie.
cool well done lally & helen xxxdottiedog
It your stories and struggles have inspired me not just to sit and take what this government throws at us. we need this illness recognised, we need the correct medicine, we need help with our mobility, and care, what we dont need is the dwp putting us through hell to get a few £ for us to have any life,
Me too, Im behind you all the way.Lets do it, we have to make a stand. GO FOR IT GIRLS!! Good luck.x
Do we know of any celebs with fibro or that have relatives with it? They mite be the best bet to try & contact 1st....sorry, not seen a previous post about contacting Max, but anything I can do to help just let me know....love & gentle hugs, Janey xx
Hi I am more than willing to help here. I believe we are over looked, we have to fight to get a diagnosis and then treatment. My GP wont refer me to a pain clinic as I have found out it cost the practice money!
People don't understand the illness so we need to raise awareness in a big way and a celebrity would help.
Sinead O'Connor has FMS
how about starting an E petition to get some one to take notice.
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Fibro, family, friends & well everyone you may know! Part 1A wish on Crowdwish website to raise funds for FibroAction needs your support. Please can we have your vote?Can you picture this? Thunderclap campaign for UK Fibro Awareness week
in memory of my MaxCongratulations to all here at HealthUnlocked -FibroAction....
