Mitchell’s Story: Solving a Rare Undiagnosed Brain Disease

Sdílet
Vložit
  • čas přidán 8. 05. 2024
  • Mitchell Herndon lived a healthy life until he was twelve years old, when he began to develop devastating symptoms due to an undiagnosed brain disease now known as Mitchell Syndrome. In pursuit of answers, Mitchell and his family were connected to Dr. Hugo Bellen and his research team at the Duncan Neurological Research Institute (Duncan NRI). Through extensive research and genetic sequencing, Dr. Bellen was able to solve the root cause of Mitchell’s disease.
    There are so many children just like Mitchell who the Duncan NRI is honoring and remembering through our work. To support lifesaving research, please visit: www.texaschildrens.org/duncan....
  • Věda a technologie

Komentáře • 3

  • @odellwood2711
    @odellwood2711 Před 6 dny

    Much love to Mitchell n friends

  • @petersampson5202
    @petersampson5202 Před měsícem +2

    MRS. HERNDON, DR. BELLEN & EVERYONE AT TEXAS CHILDREN'S HOSPITAL,
    HAPPY NURSES WEEK.
    GOD BLESS YOU MY FRIENDS. I AM VERY PROUD OF YOU AND VERY HAPPY FOR YOU. I HOPE ALL OF YOUR DREAMS COME TRUE.
    I LOVE YOU SO VERY MUCH.
    I AM SO VERY SORRY ABOUT MITCHELL MRS. HERNDON. MY SINCERE CONDOLENCES TO YOU AND YOUR WONDERFUL FAMILY.
    I LOVE EVERYONE AT TEXAS CHILDREN'S HOSPITAL SO VERY MUCH.
    I LOVE TEXAS CHILDREN'S HOSPITAL SO VERY MUCH.
    SINCERELY PETER

  • @moshiar249
    @moshiar249 Před měsícem

    Ok Thanks