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  • Опубликовано: 4 дек 2024

Комментарии • 30

  • @mavischadwick6445
    @mavischadwick6445 2 года назад

    Thanks so much Dr Alaho Olu on RUclips first of all for who you are as a person thank you for the wonderful work that you do for people in general no matter where you are I will always listen to your podcast and refer people to you because you care about people and the human body I listen to other people but you talk about the true disturbances disorders that means things that are out of order in the human system thanks 🙏 for curing my Amyotrophic lateral Sclerosis disease (ALS)…

  • @PrincessMeganElsaBoo
    @PrincessMeganElsaBoo 11 лет назад +1

    Aww this sad :((

  • @7777theguy
    @7777theguy 13 лет назад +2

    nice depressing music

  • @debbieandrade4482
    @debbieandrade4482 9 месяцев назад

    Why do I feel alone!!!!

  • @francesegan8344
    @francesegan8344 4 года назад +2

    my husband got it in 2017 its hell on earth for us all near the end now no cure they dont even look for 1 xxxxx

    • @francesegan8344
      @francesegan8344 4 года назад +1

      they tell you they are but they're not we have looked everywhere no cure how sad is that ??

  • @applejellypucci
    @applejellypucci 5 лет назад +3

    Ridiculous that there's only one drug on the market for ALS and that it only extends life by a few months, at best.

    • @francesegan8344
      @francesegan8344 4 года назад +1

      just awful

    • @fourshore502
      @fourshore502 4 года назад

      the slow rate of progress is extraordinary. theyve got alzheimers pretty much figured out, many cancers too. but als? decades of research and nothing. maybe 50 more years of research and they have at least figured out what causes it.

  • @SeriousSchitt
    @SeriousSchitt 5 лет назад +1

    This is published in 2010, it's 2019 now, is there a cure?

    • @johnpierce3511
      @johnpierce3511 5 лет назад +2

      No cure no cause no treatment. They never even decided if it's autoimmune or not. After all these years since discovery they basically haven t discovered anything. I have it and don't even go to neuro anymore. They don't care if they did research would be further along.

    • @francesegan8344
      @francesegan8344 4 года назад +1

      @@johnpierce3511 so sad x

    • @johnpierce3511
      @johnpierce3511 4 года назад +1

      @@francesegan8344 thank you for your concern

    • @DakgorimCountYeckley
      @DakgorimCountYeckley 4 года назад +2

      I had Carolyn exercise for two years before eventually becoming paralyzed in feet arms legs and arms, should she try and keep exercising?

    • @francesegan8344
      @francesegan8344 4 года назад +1

      @@johnpierce3511 my husband has it going on 3 years its just awful xxxxxx

  • @thegirlinaw26
    @thegirlinaw26 12 лет назад +1

    :'(

  • @mrDeKlos
    @mrDeKlos 11 лет назад

    I agree with Harlin Martin: too rosey. I have ALS myself. Find a cure!!

    • @SeriousSchitt
      @SeriousSchitt 5 лет назад +1

      mrDeKlos: How are you doing now, 5 years on, are you still with us?

    • @amandabaker98
      @amandabaker98 4 года назад

      Are you doing ok

  • @Stan-o9y
    @Stan-o9y 2 месяца назад

    Nothing happened in 13 years. Pathetic

  • @kristofferrasmussen8970
    @kristofferrasmussen8970 2 года назад

    This video is ridiculous. Take it down please.