March 26th and Green Paper Mega Discussion (ITV leaks, etc)
Comments
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They probably think you can treat fibro with pain killers as they don't understand chronic pain & like @secretsquirrel1 said no idea what its like to start your day at less then zero before you get out of bed.
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If only pip was easy to claim. That was so stressful, my assesor lied and wrote the opposite of what i said so at first I didn't get any points but when I did the MR I got full pip after my letter. They should be forced to go through it and see how stressful it is and that it is not easy to claim. I don't know where this came from that pip is easy to claim. It has never been easy and UN have even said the process is horrible
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That is for starters. The thing is Starmer was a carer himself as he looked after his now late mum.and brother. You wonder **** why he wants to punished other disabled people. If you want further information google it as it is not as common as Starmer tried to keep it secret.
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First assesment i had in person at home said i couldn't do more then 50m, next assessment over the phone said i could do more. I soon rang and wrote asking them how that could be possible. Dont know for definate it worked but got my award the same as the in person. Do another assessment next year filled with dread now
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when I first applied for pip my assessor also lied , ignored my GP letter and misquoted my specialist letter. Zero points . Tribunal bullied me , worst was the disabled member of panel . All to look good for the dwp represensitive . They even tried removing points I got at MR. I went to upper tribunal and won . Took two years and left me bed bound but I fought for everyone not just me .
Glad you won in the end , good for you
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Fingers crossed their back benchers revolt . Hopefully they’ve gone too far this time
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hi @Kimmy87
I don’t think we’ve ever talked directly but I know that you seem to spare some of your time answering members questions and are pretty knowledgeable on workings of the gov and dwp (I don’t know if you’ve spent many an hr reading up on things)
I don’t know your personal opinion if some of these rumours/leaks get confirmed (if you want to concentrate on helping others by answering questions or if you are thinking along the lines of some overs of being more proactive if certain things get official confirmation) - but you’re smart, have a lot of respect within the scope forum and if the number in your user name is your birth year than we are similar in age (it’s sometimes easier to speak to others of the same generation)
I was wondering if it would be okay to chat via pm at some point in the next week. It would be great to bounce a few thoughts and ideas off someone like yourself
thank you in advance
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every time I go Drs for different complaints caused by fibromyalgia or ME they can only prescribe more medication. I feel sorry for my Dr really as what can she do ? There’s no cure , treatment for ME is useless and I think found to be unethical. Different painkillers for different types of pain . Who would employ someone in all that medication anyway .
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I know WHY so many Labour MPs aren't happy as they know IF they support then it be them LOSING their seats...
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mines up next year too but I’m going to record it . Last time dwp wrote my assessment was to be over phone and recorded due my stress. Dwp always been nice to me . He had knowledge of my conditions. On the morning of assessment they called me 30 mins before start to say they can’t record it . This time I’ll record it myself. Buy a recording device and tell them you’re recording, they can’t lie then
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100%. I wouldn’t be surprised if they oust Starmer at some point as they don’t stand a chance of reelection with him as leader
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Last time i spoke to a Dr about my fibro pain i was offered a knew type of painkiller but i am unable to swallow tablets so it was a no go. What i was on my body got used to it so ended up 4 hrs side effects zero pain relief. Now i just sleep if it gets to bad.
Ive got m.e too i was advised to work out baseline & slowly build it up if i could. Baseline is zero i get tired going out on my mobility scooter. Also got F.N.D, 3 things that cause fatigue & brain fog, i forget so much all the time
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Also last daft question of the day, would it not be against the law to target hidden disabilities?
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I’m surprised that no one has posted this today
I personally think backbenchers will be too scared/want to keep the image of a Labour Party in solidarity at this early point of a labour first term
I don’t think there’s much chance of a significant public backbencher rebellion imo - if something happens it will be mps quietly putting pressure on starmer/reeves behind the scenes.
I’ll be watching with interest which labour mps endorse the green paper publicly and which speak out and prehaps most intriguingly whom stays quiet and avoids the subject2 -
I had my one recorded by them, apart from the distance i don't think they twisted anything else. Just remember been asked the same question multiple times if different ways to catch you out
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On front page of the Telegraph about Labour MP's not being happy :
Though I am confused as it says - There is no need to vote on the cuts as they do not require any new legislation.
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Before you read what I wrote below please know that I am in NO way undermining anyone’s condition.
I’m a full time carer for my wife with Fibromyalgia as well as a host of other illnesses.
The problem is with things like mental health, ME and Fibromyalgia etc… they are usually invisible illnesses and as such they are easier to fake. Which as we know some people do.A lot of people have cottoned on to the Fibromyalgia thing and have used it to claim when they shouldn’t.
Our GP herself said that sometimes if they can’t find a diagnosis it gets put in the Fybro category.The government know this and are using this green paper to flush these people out.
At the expense of those who are genuinely suffering.It’s easy pickings for them.
Like I said though, I know lots of genuine people are suffering g with Fibromyalgia and other invisible conditions.But Labour don’t care.
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I wonder if thats about the freezing of pip increase as surely the other parts would right?
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By then pip won't exist most likely
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I’d imagine it would be discrimination to target any particular condition or disability really. Plus of course pip criteria isn’t about which condition you gave but how it affects you . But these idiots probably don’t know that
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