ME /fibro: Hi all Went to ME... - Fibromyalgia Acti...

Fibromyalgia Action UK

59,987 members67,154 posts

ME /fibro

mo1mo2 profile image
5 Replies

Hi all Went to ME/FIbromyglia conference on 23rd. Excellent as was run by the Patient and Client Council Had several MLAs there including the health minister who is interested in the condition. Varies professionals spoke and sufferers . What we want is a consultant and a clinic we can go to rather than all these pain management courses

Written by
mo1mo2 profile image
mo1mo2
To view profiles and participate in discussions please or .
5 Replies
rosewine profile image
rosewine

I bet it was extremely interesting. Yes that is what we want a centre of excellence where we can get the best treatment and advice. I would be more than willing to travel to anywhere where I felt I could get it.x

I

Reykua profile image
Reykua

Hi mo1mo2,

Thank you so very much for attending and giving us the feedback.

It sounds like it was really worth going - especially as the Health Minister attended as well. I'm wondering if that means the current government is keen to find out as much about the conditions as possible to support us or if they're trying to find a way around the conditions to ensure that they do not have to provide us with disability payments and force us into work.

Unfortunately, I'm a bit of a cynic - can you tell? I'm hoping against hope that they aren't intending to find a loophole or some stick they can beat us with so I shall be watching this space with bated breath.

If there's anything that was said that you think will indeed impact on Health or Government Policy, please do share with us.

Many thanks again and Well done.

Best wishes.

mo1mo2 profile image
mo1mo2 in reply toReykua

Hi know what you mean about sickness payment etc, am on DLA at moment but that could all change my doc told me to put down on forms all my other illnesses as they are not very sympathetic to fibro. Our ME facebook here posted articles from America where docs have proved ME is biological. What we want here is a proper consultant and a clinic and not more pain management clinics as they are just a fob off

Maureen

Gerry profile image
Gerry

Was this in Northern Ireland were I live if it was could you keep me posted would like to know more?.Thank you.

TheAuthor profile image
TheAuthor

Sounds brilliant.

Thanks for sharing

Ken

Not what you're looking for?

You may also like...

Fibro/ME/Lyme?

Fibromylagia or ME/ CFS? Hi, I've had ME symptoms for 8 years after getting lyme (rash and +ve nhs...
Frostielyme profile image

Fibro getting me so down!! :-(

Hi everyone just thought I would let you know how things are....and sadly they are not good! :-(...

Fibro friends

In post and replies the strength is found To cope with fibro fog our common ground Lifestyles lost...
littleeffie profile image

Professor fibro

Hello all you clever Professors of Fibro, and all people who know better than GPs and all The...

Mr Fibro

Deep in the shadows you hide the smile on your face is snide affecting all of my bones...

Moderation team

See all
Hazel_Angelstar profile image
Hazel_AngelstarAdministrator
Lynda_FMA_UK profile image
Lynda_FMA_UKModerator
Sarah_fmauk profile image
Sarah_fmaukModerator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.