Sunday, 28 March 2021

Life living with Epliespy working round Epliespy and treatment.

I can only go round how my life was when I was facing seizures but I will try to put on this links on how they advise you to live with Epilepsy these days but also some of the old ways maybe still going as well.

How your life could be is to how, mild, major, types, a dose of medication, treatment, etc, and those in your life who may be your employer, teacher, etc for your safety and by law will need to work around that.  

People will need to accept it when you need to see you check GP, have check-ups at the hospital, etc for the sake of your health.

  https://patient.info/brain-nerves/epilepsy-and-seizures/treatments-for-epilepsy

This also, may or may not depend if this is the first time have faced epilepsy, or you have always faced it or if you have been having certain amounts of times without seizures, whether it's days, weeks, months years, etc. 

This may also depend if you are facing other problems as well or not such as disabilities, mental health, and other problem, which can happen any time before birth, during, and after birth. There may be a difference in how others need to support you etc, which could depend on what is facing and when. If it's something that keeps on coming and going, unknown it's going to or come back or not, your rights, support, etc shouldn't change just because something may come and gone, etc because if it's unknown it's beyond your control, and everyone's control as long as you make them aware of it, even though they may not change it but to know your safety and rights, etc are still in consideration and also may depend on how well or not well people who you may be working for, who may be teaching you, etc knows you. They have a responsibility to work around your safety, needs, etc so you can enjoy whatever you enjoy doing as much as possible. This also may depend on what you are doing which therefore you most likely won't have to stop necessary but some changes may or may not need to be made. Even if you do have to stop something may be similar if not the same but safer possibilities may be put in place if not where are but maybe elsewhere.  https://epilepsysociety.org.uk/living-epilepsy/wellbeing/safety-and-risk/risks-epilepsy

https://www.betterhealth.vic.gov.au/health/ConditionsAndTreatments/epilepsy-first-aid-and-safety

https://www.epilepsy.com/living-epilepsy/seizure-first-aid-and-safety/staying-safe

https://www.epilepsy.com/living-epilepsy/seizure-first-aid-and-safety/staying-safe/safety-work


No comments: