Epilepsy Society & Dr's: Have found both to... - Epilepsy Action

Epilepsy Action

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Epilepsy Society & Dr's

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Have found both to be a waste of space, Dr's in particular causing huge damage to my health, with respect to seizures. Anyone else found the same ?

Should the Dr treating a patient for epilepsy, onset 6yr's ago, speak to their patient at least once in 6yr's, having done the diagnosis via an ad - hoc phone call to an A & E unit ? And should such Dr's, or their designated Chemists, actually ensure the medication they've prescribed, is delivered/available, once the patient has become addicted to it ? And should such Dr's, when dealing with a patient with broken bones, due to the absolute failure of such authorities to even undertake such basics, basically be de-registered from, so that intelligent, educated individuals, with a comprehensive understanding and collated data relating to their condition, invest in private treatment and speak with friends/qualified Dr's, who can actually do something ?

Dr's and/or the NHS. Time serving waste of space

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