In March I asked the Minister a very simple question: How many people were treated for an acquired brain injury last year? Today he confirmed the data collection on ABI is so inadequate, the Government do not know.
We need an ABI strategy now! United Kingdom Acquired Brain Injury Forum Headway - the brain injury association The Brain Charity
It's finally here! Good luck everyone running the Manchester Marathon today.I will be running for BANA Thanks also to Brain Tumour Support 💙 Brain Tumour Research The Brain Tumour Charity The Brain Charity for supporting people like me with a brain tumour. 👋👋👋 #manchestermarathon #ukrunchat #running
Chris Bryant United Kingdom Acquired Brain Injury Forum Headway - the brain injury association The Brain Charity I’ve asked if this is you and still no response.
It's free to join The Brain Charity's Neuro Gym!
#neurogym #gym rehab #health #exercise #exercise physiology #physiotherapy #wellbeing #sportsrehab #gym #gym therapy #resistancetrainer #personaltrainer #exercise forlife #exercise forseniors
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thebraincharity.org.uk/service/neuro-…
“Disabled, but not damaged” by Scott Whitney
medium.com/disability-and…
I remember this like it was yesterday
This is my greatest pain
Medium The Brain Charity Enable Magazine Policy@Manchester Scope
Chris Bryant United Kingdom Acquired Brain Injury Forum Headway - the brain injury association The Brain Charity If the best we can now hope for is a 'bridging document' from the current gov, let's pls at least have it. Sadly, all of us with #ABI are well aware we get put back into the 'too difficult box' across all services - a bridging doc is crumbs from the table, but something at least
Chris Bryant United Kingdom Acquired Brain Injury Forum Headway - the brain injury association The Brain Charity As a person who sustained a brain injury indeed we should know
.The Brain Charity
Have a letter with a 2 line diagnosis for cervical myelopathy from consultant, but zero help or info from NHS Leicester, Leicestershire and Rutland
Graduating paralysis, but writer of said 2 lines 'will see me in 8 months'
Is lack of medical care synonymous with cervical myelopathy diagnoses?
Chris Bryant Peter Marshall United Kingdom Acquired Brain Injury Forum Headway - the brain injury association The Brain Charity Having survived encephalitis and have lived with an ABI for 17 years now. I'm almost surprised the Government had even heard of ABI there is so little data collection. PS Thank you for all you do.
Chris Bryant United Kingdom Acquired Brain Injury Forum Headway - the brain injury association The Brain Charity Try asking that question to your beloved nhs they should know
🎭 Acting opportunity. 🎭
Claire Bleasdale Casting is currently searching for a young boy with #CerebralPalsy to play the role of Gabriel in a BFI short film called ‘Happy Snaps’.
For more info, email – [email protected].
cerebra.org.uk/latest-news/do…
#MEAction Network @invest_in_me (Invest in ME Research) 🇪🇺 Solve ME/CFS Initiative Open Medicine Foundation Bateman Horne Center Action for M.E. ME/CFS News UK/European Centre of Excellence for ME Smile For ME MEadvocacy.org Dr Sarah Myhill ME Research UK Workwell Foundation Disability Rights UK The Brain Charity If action isn’t taken for #SaveCarlasLife or #BringMillieHome then they will die and the hospitals WILL be responsible for not giving appropriate care according to NICE guidelines!
#dontletMEdie #ExposeMENow
#MEAction Network
@invest_in_me (Invest in ME Research) 🇪🇺
Solve ME/CFS Initiative Open Medicine Foundation Bateman Horne Center Action for M.E. ME/CFS News UK/European Centre of Excellence for ME Smile For ME MEadvocacy.org Dr Sarah Myhill ME Research UK Workwell Foundation Disability Rights UK
The Brain Charity
#𝐒𝐚𝐯𝐞𝐂𝐚𝐫𝐥𝐚𝐬𝐋𝐢𝐟𝐞