I have won my appeal but put in work related activity component that's better then nothing I think I'm so happy i won my cab didn't even do anything thankfully I had my sister with me.
Appeal : I have won my appeal but put... - Fibromyalgia Acti...
Appeal
well done
Good for you the battles we fight on our own and winn are even more precious than those for which we have have had help. I am so glad that your sister was there by your side as I am sure that was such a support to you.x
Having a representative (CAB) with you does actually make a difference. Them being there means things are done more how they should be done.
Great news.
Lu x
Great news shar .xx
I'm very pleased for you!
I am genuinely and sincerely delighted for you! Good luck
Glad to know you've been successful xx
Hi, I won my appeal too back in March & I was put in the work related activity group too. I was so happy when the appeal went my way but now I just feel I'm being pressured all the time by the job centre to do courses & learn new skills. This stresses me out as I havnt worked for 20 years because of my fibro. Now I'm just wishing the time away till I get reviewed again
great news
I have just been to my ESA tribunal and it was adjourned - so the medical evidence could be acquired and I could be given more than the 30mins I had been allocated, they said I needed an hour ?!
I had provided all of my hospital letters etc already and there were two bundles of papers, as well as a submission from a gentleman from the local Law Centre who had been assisting me.
I have also just been awarded PIP, at first time of asking, on 1st June, after a f2f and have Enhanced Daily Living and Standard Mobility ( I know this is not taken into account at the ESA tribunal, but the two assessments came so close together and had such widely differing results that I was told it was worth mentioning )
Has anyone else had any similar experience ? It is incredibly stressful and I suffer a variety of conditions, my primary one being RSD/CRPS which has disabled me for the past 23yrs. I can rarely leave the house now.
It's a never ending cycle, isn't it ? Proving how unwell you are ?