Reviewing & Updating the statutory direction for education regarding the treatment of disability at all levels , in every Medical Schools

En attente d'une révision interne par Éducation, Jeunesse, Sport et Culture a propos de leur gestion de la demande.

Dear Education and Culture (EAC),

Under the right of access to documents in the EU treaties, as developed in Regulation 1049/2001, I am requesting documents which contain the following information regarding who oversees that Education regarding the treatment of disability in early stages in every Medical Schools & that it is made statuatory & regularly reviewed & updated in that there is objective patient orientated research at every level.

Yours faithfully,

Julie Shrive

EC ARES NOREPLY, Éducation, Jeunesse, Sport et Culture

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From what you said regarding my address suspect you are trying to deliberately delay in order to refuse request because education on disability at all levels is NOT happening .
I know because being passed from pillar to post at primary level when had specific research to allow for more appropriate treatment with Doctors allowing NHS to have it as Low Priority Policy therefore no tertiary treatment & objective research happening . The GPs told me this before Thatchers Cuts when referring to hospitals ,As a result suffered cardiac arrest[dying 3x] with no monitoring appts ,now not happening again with admin staff using Choose & Book to send to those who are totally inappropriate.As a result requesting internal review to make statuatory , with Dept Health to help those in particular being ignored by the Low Priority Policy when should be at tertiary level .

Yours sincerely,

Julie Shrive

Julie Shrive a laissé une remarque ()

Autodfill not working & signature with address.

[postal address]

Julie Shrive a laissé une remarque ()

This relates to what the average GP & Specialist learns in Medical Schools regarding the treatment of disability & rare chronic untreatable conditions & objective research.
I was told in 1980s in UK that was referred to hospitals as they were not taught how to treat, to Specialists who were also not trained this was then cut back .This also includes the mental & any rare condition that could not be treated in 10 minute - 20 min appts it appears if you have rare conditions eg: lipoedema sepsis & the chronic you are treated like a fraud by the UK system reducing your life span as a result.
This is called the Low Priority Policy & is used not to allow amputees wheelchairs or social care for anyone in discretionary area needing research.Many foreign Doctors have told me don't test as "hands are tied".This could be reason the hippocratic oath is no longer taken & many Doctors not fully trained or able to do objective research ?!