#MillionsMissing

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  • Опубликовано: 31 окт 2024

Комментарии • 6

  • @thegangov14
    @thegangov14 Год назад +3

    Thank you

  • @Mar-g8u
    @Mar-g8u 4 месяца назад +3

    It's truly a terrible disease. I've had CFS for a year. I've lost my future, my friends, and my education. I'm very sad and lying in bed. Even though I'm 20 years old, I feel very weak and can't do anything. This disease has destroyed my life. I beg the doctors to research this disease to quickly find a cure. I am very, very desperate. 😭

  • @Caketime2
    @Caketime2 2 месяца назад

    Also for those of us with fibro and other autoimmune diseases!

  • @mariacallaghan637
    @mariacallaghan637 Год назад +7

    I wish!! My partner has been ill since 2009/10? ME/CFS/ RLS..and much more! He had to have DWP update PIP assessment! 2hrs she took?? He was so exhausted he had to go to bed...he was ill for several days!!! And yes! she stopped his payments again! No surprise there..she claims he's good to go? As if this horrible illness isn't enough! The DWP has to degrade you as well.😢

    • @mdee860
      @mdee860 10 месяцев назад

      😡😡😡😡😡 This disease is so insidious.... and deadly. People truly just don't get it. It's a chosen ignorance - esp. in the medical community.

  • @jennycake8237
    @jennycake8237 Год назад +1

    Thank you again for having this event! And thank you again to @dannyjm of Always Tired NFTs for bringing this project to our community! It was amazing to be able to be part of this! #TiredAF #MECFS #millionsmissing #NFTcommunity