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- CFS/ME - Appeal Tribunal on Thursday - feel scared
CFS/ME - Appeal Tribunal on Thursday - feel scared
- Crow
- Topic Author
Firstly, thank you all for your kind words of support.....they mean even more now that I have just received a letter to say that, due to industrial action, my Tribunal has been postponed. They will write to me with a new date. I've been waiting for the Tribunal for 6 months, and fighting this appeal since the end of August last year - what's another few weeks/months?!? I am so upset and angry at this.
Rest of post deleted, see [url=http://www.benefitsandwork.co.uk/faq/forum-faq#deleted]FAQ[/url
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- Andy
I have heard that as ME/CFS is a fluctuating condition I will not be entitled to anything..
Hi, Crow
It's NOT TRUE that you are not entitled to anything because you have a fluctuating condition. The tribunal will be interested in how your condition affects you overall. So it's fine to explain that the are day-to-day variations but make sure they understand what a 'bad' day is like and how often you have them.
Good luck.
Andy.
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- Basher
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- Jim Allison BSc, Inst LE, MBIM; MA (Consumer Protection & Social Welfare Law)
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Crow I saw on TV last night that there is a public sector strike on Thursday and this included courts and am wondering if your appeal will still be heard.
Can any of the mods let us know if Tribunerals will also be affected on Thurs?
I hope the strike does not affect your appeal Crow.
My partner has his joint appeal this afternoon.
Tribunal Members are part of the judiciary, so they cannot go on strike.
However, the Tribunal has to have a clerk in attendance to deal with administrative matters. My advice would be to ring the office dealing with your appeal and ask if it's going ahead.
Good luck.
Jim
PLEASE READ THE SPOTLIGHTS AREA OF THE FORUM REGULARLY, OTHERWISE YOU MAY MISS OUT ON IMPORTANT INFORMATION. Nothing on this board constitutes legal advice - always consult a professional about specific problems
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- Andy
My wife came with me as moral support... I was pleasantly surprised that the panel asked her to provide her point of view, which was very helpful to me.
Thanks for that info, Basher.
I, too, have ME. I've been puzzling how on earth to get things across to the tribunal given I'm not on any medication and not seeing a specialist, just trying to cope (grudgingly!) with living within the limits the ME imposes. My wife is the only person who actually has first-hand knowledge of how the illness affects me. She's willing to come with me, obviously, but we'd assumed she might be seen as "biased" and not expected/allowed to give evidence. So what you say is very encouraging.
Thanks again.
Andy.
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- Crow
- Topic Author
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