after having my dla reduced to low rate even though my fibromyalgia is considerably worse. I have my appeal soon, so could anyone help with do dla accept that walking is better some days and bad others. also the symptoms are intermittently better and then worse. I am dreading it
help with dla appeal after over 1 yea... - Fibromyalgia Acti...
help with dla appeal after over 1 year waiting
Dear Chrissy,
If you would like the Benefits & Work Guides sent out for free , please email info@fibroaction.org and we can email them to you.
These may help advise you on how to proceed with the appeal
Best Wishes
Emma
Hi Chrissy,
I have been having trouble getting DLA at all for my conditions. I am now at the stage where I have an upper tribunal appeal going in. It has taken me just over a year and numerous paper appeals and the lower tribunal hearing to get to this stage.
Apparently, The Government plan to replace DLA with a new benefit. They are also trying to get people off DLA and ESA /income support.
I am on ESA and was examined by an assessor for that. I used the EMA proof in my appeal and the lower tribunal challenged the Drs opinion saying they assumed he thought I had a serious heart problem. I have cardiomegaly and am currently waiting to be seen by a heart specialist after suffering angina.They even challenged my own GP and told me I exaggerate my symptoms. I was so angry. They whole process has got me down.
I had help from the citizens advice to fill in my forms but even then they are challenging it.
I wish you well Chrissy and hope you manage to get your amount back.
debbie...
please both of you get the benefits & work info from admin as Emma [Mdaisy] suggests.
print out the sheets from pg 60, fill them in, make copies and give them to your gp's and consultants.
don't undersell yourself.
Ask them to write letters of support and to send them to you for your claim pack. copy these too.
good luck.
sandra.
They are making it so tough now for us to get anything and it angers me so much. I think the government are of the same opinion as Joe Bloggs, if you cannot see it it must not be there. I wish you well in your appeal xxxxx
I so agree with you. Because our disability is better someday than others people only tend to see me on better days because I don't or can't set foot out of my door on bad days so I don't have the excruciating pain they have heard about and I swear they are saying I am putting it on :’(
I know what you mean hun. But in my case it did not even matter to the judge that I also had an illness that at some point is going to kill me, especially if I do not get a handle on this smoking lark and quit. I have no idea how we are supposed to express how we feel without them thinking we are making it up, it really ticks me off. Plus I had been going to medicals on and off for over 20 years and each time I was declared unfit for work, even that was not taken into consideration. We as fibro sufferers are literally on a hiding to nothing and until the government sticks by what it has said, them saying they recognise fibro as a potentially disabling illness, then nothing will change xxxxx
I know babe we can't just concentrate on our wellbeing and feeling better because on top of this we also have to spend so much time on the stressful fight to get the financial help we are entitled to, to help make our illness so much more manageable and less stressful by taking away the financial pressure we are experiencing. Sorry for the rant I think I have woken up that way out this morning