ESA and DLA

I appealed over 4 months ago for WRAG of ESA. I now have the suppport from the ME Association who are now dealing with my claim - as they have confirmed i should not be in the WRAG but the support Group due to my illness. I don't only have ME/CFS and Fibro - i have 3 other illnesses and she i have been on low mobility for 2 years nearly and was quite disgusted - as apparently i should be in the higher rate for both care and mobility. Lets hope this is the beginning and start of once and for all getting sorted out. Been along 2 years and finally hope there is a light in sight.

Dorset-angel wrote:

I appealed over 4 months ago for WRAG of ESA. I now have the suppport from the ME Association who are now dealing with my claim - as they have confirmed i should not be in the WRAG but the support Group due to my illness. I don't only have ME/CFS and Fibro - i have 3 other illnesses and she i have been on low mobility for 2 years nearly and was quite disgusted - as apparently i should be in the higher rate for both care and mobility. Lets hope this is the beginning and start of once and for all getting sorted out. Been along 2 years and finally hope there is a light in sight.

Hi,

Having the support and backing of an organisation relating to your illness should help immeasurably.

Good luck.

Pete

Wonderful News, Dorset Angel.
I also have ME and several other conditions, and didn't known that the ME Association would help and support those going through an appeal.
Is there anyone in the ME Association in particular you have to contact?
Cheers, Pen.