She forgot half the northern hemispheres supply of trammies…..
She forgot half the northern hemispheres supply of trammies…..Disability rant. Apologies in advance.
Is there any actual proof she has arthritis? She posted a LONG thread on all the things she’s tried for the AGONY… but none of them were arthritis medications other than possibly steroids which isn’t the best or even the primary treatment for RA.
Sunbeds are NOT a treatment for RA at all by the way. She’s confusing the ultraviolet rays of sunbeds which burn and prematurely age your skin (even using factor 50.. ) with the soothing warmth of infrared lamps (as sold in Boots etc). They’re a totally different thing.
View attachment 1887753
She seems to misunderstand arthritis- it’s not an ‘achy shoulder’ or a bad back etc it is an autoimmune disorder- one of my friends has it and the poor guy is sick a lot as he has to take an immunosuppressant and when he catches a virus it can take months for it to burn out.
For chronic RA with flare ups so bad she can’t walk up stairs her doctor would absolutely try her on methotrexate or similar. And she’d be able to claim non means tested PIP as she’d be classed as disabled if it’s lasted over 12 months or is reasonably expected to. (And get a parking permit etc).
She did add on (almost like she forgot which is odd as she calls it lovely so why ask for recommendations but moving on)
View attachment 1887822
This is strange to me because I’m also on Naproxen and it’s ok (doesn’t touch my bad days but I know each medication affects people differently) and you are diagnosed Omeprazole with it as it causes issues with your stomach / gives you awful reflux if taken alone. Also, if you took that with tramadol (or 40 tramadol…) you’d be incredibly poorly.
I have been ‘disability shamed’ loads of times - literally people standing in disabled parking spaces as I drive an arguably nice car and therefore I clearly am not disabled, a few weeks ago even I had an older man try and break into the disabled loo I was using and when I opened the door to scream at him shouted at me I wasn't entitled to use the loo as I was too young to be disabled (I was out of my chair for a change and on my stick). I am 39 by the way so maybe it’s a complimentI used to be so embarrassed and get upset but now I shout and shame them right back.
And I really REALLY don’t want to be that person. But knowing this particular person and her distant relationship with the truth and her addiction to attention I struggle to believe it when she plays the disability card because I equally struggle to understand why ANYONE would suffer for years yet never take the help both medical and financial they would be fully entitled to.
The comparison is stark Nadiya is a delight to watch and every inch the professional while remaining current, interesting and you just know the food is delicious. Which makes you know who thoroughly unprofessional, constantly recycling previous slops that you 100% know will taste awful.I'm watching Nadiya. She is excellent on TV -'s her food looks lovely.
I also rarely see her wishing her 'pals' a good day on twitter and listing off her many ailments.
Makes you think.
So it's the equivalent of Jack being able to speak Italian.Stickers on the keys are the equivalent of having an English/French translation book in your pocket and thinking you know how to speak French because you can look it up.
Gall stone pooYummo, love the taste of a good bollock.
View attachment 1887892
Big Dave’s WWII artillery is all proper and above board, it’s not actually his he’s just involved in the upkeep/engagement. It doesn’t fire and even if it did Big Dave would be the last person to break the law by firing it, I’m certain!Coming from the past so apologies if already said but military adjacent friend says Big Dave’s gun will have been decommissioned. If it’s able to fire blanks it’s still able to fire live ammo so says she’s talking bullshit. Quelle surprise.
Imagine this defence to the small courts claim.Yes, and uncannily convenient when the squigs are threatening her with small claims courts. So vulnerable she can’t press a button and pay. Bless.
Hopefully stopping Jack from trying to attack the KingIf he did that for the joobs I wonder what he’s got in store for the ‘nation in May? Driving a tank through the streets of Thorpe Bay and terrorising the patrons of the local dog cafe?
It’s not just the medical and financial help - it’s also the fact that PIP is a gateway to other types of non-financial but more practical support. I’ve helped friends with the claim forms (which can be tricksy if you’re not answering the specific question in specific ways) and appeals, and they’ve won their PIP awards. And that means they also get things like a blue badge (for the person who drives you around, if you can’t drive yourself), access to a Motability lease if that’s what you want to spend the mobility component on, a disabled railcard entitling you and your companion (not uncommon to need a companion to travel if you’re autistic) to cut-price tickets, or reduced rate tickets with special seating at certain types of events. PIP can also be a gateway to home adaptation grants and council tax reductions.Disability rant. Apologies in advance.
Is there any actual proof she has arthritis? She posted a LONG thread on all the things she’s tried for the AGONY… but none of them were arthritis medications other than possibly steroids which isn’t the best or even the primary treatment for RA.
Sunbeds are NOT a treatment for RA at all by the way. She’s confusing the ultraviolet rays of sunbeds which burn and prematurely age your skin (even using factor 50.. ) with the soothing warmth of infrared lamps (as sold in Boots etc). They’re a totally different thing.
View attachment 1887753
She seems to misunderstand arthritis- it’s not an ‘achy shoulder’ or a bad back etc it is an autoimmune disorder- one of my friends has it and the poor guy is sick a lot as he has to take an immunosuppressant and when he catches a virus it can take months for it to burn out.
For chronic RA with flare ups so bad she can’t walk up stairs her doctor would absolutely try her on methotrexate or similar. And she’d be able to claim non means tested PIP as she’d be classed as disabled if it’s lasted over 12 months or is reasonably expected to. (And get a parking permit etc).
She did add on (almost like she forgot which is odd as she calls it lovely so why ask for recommendations but moving on)
View attachment 1887822
This is strange to me because I’m also on Naproxen and it’s ok (doesn’t touch my bad days but I know each medication affects people differently) and you are diagnosed Omeprazole with it as it causes issues with your stomach / gives you awful reflux if taken alone. Also, if you took that with tramadol (or 40 tramadol…) you’d be incredibly poorly.
I have been ‘disability shamed’ loads of times - literally people standing in disabled parking spaces as I drive an arguably nice car and therefore I clearly am not disabled, a few weeks ago even I had an older man try and break into the disabled loo I was using and when I opened the door to scream at him shouted at me I wasn't entitled to use the loo as I was too young to be disabled (I was out of my chair for a change and on my stick). I am 39 by the way so maybe it’s a complimentI used to be so embarrassed and get upset but now I shout and shame them right back.
And I really REALLY don’t want to be that person. But knowing this particular person and her distant relationship with the truth and her addiction to attention I struggle to believe it when she plays the disability card because I equally struggle to understand why ANYONE would suffer for years yet never take the help both medical and financial they would be fully entitled to.
Need a decent set of drain rods to dislodge something like this.Yummo, love the taste of a good bollock.
View attachment 1887892
Oh my lovely... I have been living with arthritis for the last 30+ years (diagnosed shockingly early in life). I've worked full time all the way through, dealing with disabling bad back while running a business, taking codeine every 4 hours when it was really bad. Running a multi million pound business while in serious pain, never used it for a poor me give me a break situation.Disability rant. Apologies in advance.
Is there any actual proof she has arthritis? She posted a LONG thread on all the things she’s tried for the AGONY… but none of them were arthritis medications other than possibly steroids which isn’t the best or even the primary treatment for RA.
Sunbeds are NOT a treatment for RA at all by the way. She’s confusing the ultraviolet rays of sunbeds which burn and prematurely age your skin (even using factor 50.. ) with the soothing warmth of infrared lamps (as sold in Boots etc). They’re a totally different thing.
View attachment 1887753
She seems to misunderstand arthritis- it’s not an ‘achy shoulder’ or a bad back etc it is an autoimmune disorder- one of my friends has it and the poor guy is sick a lot as he has to take an immunosuppressant and when he catches a virus it can take months for it to burn out.
For chronic RA with flare ups so bad she can’t walk up stairs her doctor would absolutely try her on methotrexate or similar. And she’d be able to claim non means tested PIP as she’d be classed as disabled if it’s lasted over 12 months or is reasonably expected to. (And get a parking permit etc).
She did add on (almost like she forgot which is odd as she calls it lovely so why ask for recommendations but moving on)
View attachment 1887822
This is strange to me because I’m also on Naproxen and it’s ok (doesn’t touch my bad days but I know each medication affects people differently) and you are diagnosed Omeprazole with it as it causes issues with your stomach / gives you awful reflux if taken alone. Also, if you took that with tramadol (or 40 tramadol…) you’d be incredibly poorly.
I have been ‘disability shamed’ loads of times - literally people standing in disabled parking spaces as I drive an arguably nice car and therefore I clearly am not disabled, a few weeks ago even I had an older man try and break into the disabled loo I was using and when I opened the door to scream at him shouted at me I wasn't entitled to use the loo as I was too young to be disabled (I was out of my chair for a change and on my stick). I am 39 by the way so maybe it’s a complimentI used to be so embarrassed and get upset but now I shout and shame them right back.
And I really REALLY don’t want to be that person. But knowing this particular person and her distant relationship with the truth and her addiction to attention I struggle to believe it when she plays the disability card because I equally struggle to understand why ANYONE would suffer for years yet never take the help both medical and financial they would be fully entitled to.
I'm sorry about your daughterThis boils me. My daughter was diagnosed (after 9 months of agony) with juvenile form of RA aged 17. While her peers were learning to drive, going out meeting friends, she was having me to ties her laces and fasten her bra. Taking methotrexate every week and trying not to vomit after it ( a well known side effect).Jack just self medicated with plenty of booze and tramadol . She hasn't a f'ing clue. If she's having a flare up why not get help from professionals.
She really has the Unholy Trinity of an account that's boring, unpleasant and pointless.I wonder how it makes Jack feel seeing her follower numbers rapidly tumble every time she Tweets now.
We'll be down to 560 k by the weekend(still 560k too many, mind).
Ooooh the VBI anniversary….let’s all party on Saturday.Looks like the anniversary is this Saturday:
(ss from @Flash123 on thread 243)
Although she might actually have stolen it from a squig a year earlier:
(ss from @Silver Linings on thread 126)
She also has the most beautiful hands!I'm watching Nadiya. She is excellent on TV -'s her food looks lovely.
Huge numbers of people living with crippling mental or physical issues and often the most affected never complain, just adjust their lives as best they can to suit their needs. The most affected people I know, one is first class in their field despite a really serious physical disability. They must have pain and nerve pain and they certainly have difficulties getting around (visible) but never tell you. If I couldn't see them I'd never know there was anything unusual about them. They value everything they get out of life and work harder than most other people I know. Even to do the same as everyone else they'd need to work harder, but they are actually better at it too.Oh my lovely... I have been living with arthritis for the last 30+ years (diagnosed shockingly early in life). I've worked full time all the way through, dealing with disabling bad back while running a business, taking codeine every 4 hours when it was really bad. Running a multi million pound business while in serious pain, never used it for a poor me give me a break situation.
We are all *different*, we all react to pain and stuff in a different way and that's ok - I would never, ever judge because I am me, and cannot speak for anybody else.
However - Jack can go to the absolute fuck. If she's truly disabled, fair enough. Apply for the relevant help and SHUT.THE.FUCK.UP about how ouchy you are. Don't use it as an excuse, mate, it doesn't wash. There are plenty more people out there in real situations that need help, and try to get on the best they can.
Sorry, but this truly makes me see red. Cheating, lying, tricksy, false, grifting, despicable tosser.
Pterry would have never, ever let her use his work. Would have seen through her straight away.Looks like the anniversary is this Saturday:
(ss from @Flash123 on thread 243)
Although she might actually have stolen it from a squig a year earlier:
(ss from @Silver Linings on thread 126)
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