Katie's Journey With Rare Kidney Disease:

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  • Опубліковано 7 вер 2024

КОМЕНТАРІ • 9

  • @lauren_WI
    @lauren_WI 17 днів тому +1

    Great collaboration!! I’m literally at UWHospital and am now scheduled for several appointments for LPHS to receive an auto transplant. 🤗 🤗 to those whose experience a chronic condition and who pain. Not a lot of videos that have this information, so thank you so much! Bless 😊you for sharing your story, you are a WARRIOR 👏

    • @diaryofakidneywarrior
      @diaryofakidneywarrior  15 днів тому +1

      Thank you for your kind words ❤️

    • @katienewell9605
      @katienewell9605 6 днів тому

      Thank you so so much for your kind words! Praying that your auto transplantation works wonders for you ❤

  • @kellymccomb8197
    @kellymccomb8197 4 дні тому

    It’s so great to see this topic covered! I’ve been recently diagnosed with LPHS and with it being so rare, it’s nice to know there are others out there who understand what we live through every day.

  • @rasuk2117
    @rasuk2117 Місяць тому +2

    Great Podcast, learn more about kidney disease every day 😢🙏

  • @michaelgray8841
    @michaelgray8841 Місяць тому +3

    Ive had 10 months of persistent kidney Stone pain & blood in my urine. This is excruciating! My nephrologist has concluded LPHS just today!
    Mrs Gray

    • @diaryofakidneywarrior
      @diaryofakidneywarrior  Місяць тому +1

      Sorry you’re going through this. I hope that getting your diagnosis means that you can now get the right treatment to help your condition.

    • @lauren_WI
      @lauren_WI 17 днів тому

      @michaelgray8841 I was diagnosed too! Are you considering ant medical interventions?
      I’m currently at UWMadison Hospital for a two day to meet the medical staff and get a procedure done.
      🤗 to you, I know that pain you feel. We are in a rare group that nobody wants to be in!