www.fibroduckfoundation.com

The Fibroduck Foundation is a registered charity committed to funding bio medical research for Fibromyalgia

On our FaceBook Fans Page we ask our members daily questions.

These are designed to help show people what it's like to live with Fibromyalgia. The questions (and replies generated) became so well received that we have started a dedicated blog to archive them.

If you are newly diagnosed with Fibromyalgia, you may find this blog very helpful. By reading our archives, we hope you'll also feel less isolated and alone.

Please visit our website's and join the 'One million ducks campaign' Fibroduck.com and The Fibroduck Foundation

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Saturday 1 May 2010

Medics Aware Gallery

Don't forget to take duck to your next medical appointment - we want a photo of your doctor/nurse/consultant holding Fibroduck, we'll put them in our new medics aware gallery, which I'm working on right now, lets honour those medics who are FM/ME/CFS aware.

*What is ME? I know what FM/CFS is, but not sure what ME is.

*ME is just like chronic fatigue syndrome except "Where the one essential characteristic of M.E. is acquired CNS [central nervous system] dysfunction, that of CFS is primarily chronic fatigue."
Apparently.

*Same as CFS virtually. It's just was us Brit's call it.

*but more severe.

*I need to find a doc in Aberdeen who believes in Fibro!

*I'd like to launch the new Medics aware gallery as part of our awareness day events on May 12th. At present we have seven medics aware :)

*I'll have to send my mum a duck for her next rheumy appointment (we share the same doctor.

*Thanks for the info. I have a loved one with CFS.

*Gave my fibro duck card to my OT

*My GP asked what the fibroduck keyring was.

*I don't do Doctors no more, more mess ups with them then with out them. Not just me I had a buddy have his leg taking off, for NO reason. I'm sure the money was good, then gave him a by pass. that he did need! Can't sue in Canada.

*HI all, Where do you get the ducks from?

*What a cool idea!

*The section is built and ready to go next month, I just have to publish the page on the day. More photos would be great, not just any old Medic though, they must be FM aware/friendly to go on this gallery :)

*Cool idea, IF my Dr knew much about FM/CFS. I was handed off to this one by the Dr that left 2 yrs ago, not once has he sat down & talked with me. Just writes my scripts, which I appreciate, but come on. To find a Dr, I would have to pay for visit with each one, I don't want all my meds messed with, I just want some one that actually knows how to pronounce fibromyalgia!

*But I think the time has come where my money has to be spent on specialist doctors, I'm sick of being messed around :(

*Can't wait to press the 'publish' button come awareness day!
It's all ready to go with 7 medics up there at present although we welcome more please! They must be FM/CFS/ME/MS aware-friendly

*Does Eastern and Central Oregon, USA count??? My two guys are the best in the States! They deserve recognition.

*Yup they can be from anywhere cos it's a worldwide project.

*Ok will do. Hope I have the time!