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Gothic Gisborne
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Gothic Gisborne
@Goth_Gisborne
#actuallyautistic self-employed with #EDS #ME/CFS & #ADHD | MRes Psych student | former ODP | theatre graduate Them/They/Autistic/disabled/gamer
ye olde northworthy Katılım Şubat 2016
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@Goth_Gisborne @LeahFHardy Is you Dad able to answer a normal phone call?
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Accessibility includes respirator use and masking.
Khan 🧢 🌟@Khanstillday
Start a Problematic discourse??
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Thank you Professor Tamsin Ford- Chair of Psychiatry @Cambridge_Uni who, with a team of 32 experts state that there is no evidence ADHD is being over diagnosed. Calling out ‘Alarmist rhetoric’ by politicians. cam.ac.uk/research/news/… @DHSCgovuk @ION_Diversity @ADHDUKcharity

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@PlanetEarth_HD @elbecp I hadn't even considered this before but it makes so much sense to why my brain fog varies so much. The Fexofenadine is quite something! Just started a box by Zentiva which only looks like 2 e numbers thankfully
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Same old playbook. "Disabled people on benefits are being failed so I must kindly cut their benefits in half while pretending I'm actually investing in support".
BBC Breakfast@BBCBreakfast
'Too many children are being failed' Schools minister Georgia Gould told #BBCBreakfast the government will spend billions to make mainstream schools in England more inclusive for pupils with special educational needs and disabilities bbc.co.uk/news/live/c98q…
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@FndNope @Emma_h_mua @kirstymecfslife I went suspecting MS and she kept talking about FND. Asked about when my neurological symptoms started, she wasn't interested unless it was in the last year or so. Ive had symptoms for years that continue to be dismissed and rather than look at the bigger picture she didn't care
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@Emma_h_mua @kirstymecfslife Exactly how it went for us. The neurologist had already assumed Functional Neurological Disorder before even examining my wife , he literally started with his conclusion.
Many years later, she was diagnosed with Multiple Sclerosis.
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@Dan_Wyke Seems to be. Saw a neurologist yesterday for possible trigeminal neuralgia/MS. Left with a 'I think its FND, around half the people I see have it and its very common in people with CFS and Fibro'. Luckily, I am getting an MRI but yeah, frustrating
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@KShabby16334956 somehow that concept has got lost over recent years, and it's ended up replacing PIP and other forms of proof entirely. I think its because companies are worried about GDPR (seeing sensitive information), so they prefer a 3rd party do everything. Now it's just become ridiculous
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@KShabby16334956 So when the access card was first created, it was because people who'd been on DLA lost their awards when PIP was introduced. It was meant to ensure that disabled people, who had the evidence, still got reasonable adjustments if they didn't meet the new PIP criteria but 1/2
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So instead of just using the evidence youve alrwayd fought hard for (pip), you've had to justify it all again to Nimbus to get what you need.
That's against the Equality Act. They have no right inserting themselves as the mandatory middle man.
Jackie Wells@jacwyc
@Chuffin_ell My daughter has a Nimbus Access card and it works well for us. No need to constantly share information or justify your needs with different venues. It shows she needs a plus one, so free carers ticket bookable online without constantly needing to provide proof.
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