BBC Breakfast (18.04.24) - National Epilepsy Week

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  • Опубликовано: 13 янв 2025

Комментарии • 9

  • @Bossman1959uk
    @Bossman1959uk 7 месяцев назад +2

    Interesting to see this. I have epilepsy myself and volunteer for Epilepsy Action. Good that efforts are being made to make the condition more visible to everyone and accepted. 😀

    • @Consistent_studying
      @Consistent_studying 7 месяцев назад +1

      Hi,
      I’m researching a potential approach for wearable seizure detection.
      Would you be open to do a 15 minutes interview?

    • @Bossman1959uk
      @Bossman1959uk 7 месяцев назад

      I am willing to do a 15 minute interview but most of my seizures are when waking up so it’s difficult to detect using a device as there isn’t a fall.

    • @fatemehasgarinejad
      @fatemehasgarinejad 7 месяцев назад

      @@Bossman1959uk I'm really sorry and thanks a lot for accepting. May I know if you are fine with an interview via Zoom?

  • @dav1dpri0r
    @dav1dpri0r 7 месяцев назад +4

    I have epilepsy and the video was sadly too relatable.

    • @lalehanm3984
      @lalehanm3984 7 месяцев назад

      Epilepsi ye candida mantarı sebep oluyor

    • @fatemehasgarinejad
      @fatemehasgarinejad 7 месяцев назад

      Hi,
      I'm working on an NSF I-CORPS project to develop an early seizure detector. I'd appreciate your time for a short meeting.
      Thank you for considering.

  • @Real-Name..Maqavoy
    @Real-Name..Maqavoy 7 месяцев назад +1

    Yet ppl never understand the difference between *Individual rights* and *Patient & Doctor*-Confiencidality.
    There's 5 diff *Seizures* but over 50 Versions of *Epilepsy*

  • @katiestephenson1442
    @katiestephenson1442 3 месяца назад

    Tonic colonic you never should stress them out or you make them do it as i have got and so much i hurt my self and lived my whole life with that Its lot of time it s neatly killed me . It make my hand s weak and never learnt at school . i cant do crowd If i need the toilet i need to go right away I dont like walking in massive places definitely how things are today . I now have PA and she said she understand that wen i get angry my brain cant function like everyone else's do and it sad like i mean if somebody is bossy someone could control it but it hard because i have it i think there taking or trying to take over me . i Never like to live with people because i have bean though bad issues and it cant control my seizure and it takes away a lot from me then what someone might not no . I do all the best when i live alone. so like i mean im eating what i need to help me with if i nead peace and quite iv got it , If my body need rest it there . When i lived in serported living staff use to bully me and it made it exstreamly worse , heat is a nother problem .