Hunter's Hope - Hope through Newborn Screening

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  • เผยแพร่เมื่อ 10 ก.ย. 2024
  • Families affected by Leukodystrophies share the hope that newborn screening offers...
    www.huntershope.org

ความคิดเห็น • 44

  • @SomethingAboutBeautee
    @SomethingAboutBeautee ปีที่แล้ว +15

    I know all of us have different beliefs BUT one thing that should be mandatory is early testing even if there’s no symptoms showing because the symptoms don’t show until it’s too late for the most part. We should ALL want that kind of health security for our children. ❤

  • @danettehartsock6366
    @danettehartsock6366 2 ปีที่แล้ว +14

    God bless you all for working so hard to help babies!

  • @krystalbaker-clark
    @krystalbaker-clark 2 ปีที่แล้ว +16

    At a time when someone might question their faith; they embraced it. You will be reunited with your child again!

  • @user-sr9gx9ms5q
    @user-sr9gx9ms5q 4 ปีที่แล้ว +9

    I'm a Syrian mother of a Mld child and I've been through all this pain which these mothers had and now my son is 9 years old and I couldn't do anything to help him I really hope that we find any hope and science would find a solution for these poor angels ❤ my prayers for all of them

  • @cynthiablandford6213
    @cynthiablandford6213 2 ปีที่แล้ว +8

    Always,always be grateful for your health.😔❤

  • @eatymceatison97
    @eatymceatison97 4 ปีที่แล้ว +18

    My heart goes out to these parents. I hope new-born screening will be available soon.

  • @molliedevenbaugh1986
    @molliedevenbaugh1986 5 ปีที่แล้ว +35

    I just want to thank you for pushing for nb screening. My youngest son is 2 weeks old and is undergoing more testing due to finding 2 Krabbe markers. I’m so thankful we live in MO now, because I never knew this could be an issue in any of my boys due to the oldest 2 being born in MI. I’m beside myself with worry for my boys, but I’m so thankful for nb screening.

    • @HuntersHope
      @HuntersHope  5 ปีที่แล้ว +6

      Hi Mollie - we would love to answer any questions you have... Please email us at hope@huntershope.org

    • @molliedevenbaugh1986
      @molliedevenbaugh1986 5 ปีที่แล้ว +7

      Hunter's Hope Thank you! I actually emailed you last night.

    • @shananalexander9789
      @shananalexander9789 4 ปีที่แล้ว +7

      Mollie Devenbaugh Mollie I just prayed for you.

  • @DippyHippie
    @DippyHippie 2 ปีที่แล้ว +5

    These parents are hero’s!

  • @aburgess9886
    @aburgess9886 4 ปีที่แล้ว +18

    My sweet boy suffers from Krabbe disease. My heart is broken💔

  • @AfallinAngel
    @AfallinAngel 6 ปีที่แล้ว +16

    You are wonderful parents. So brave and caring. God knew he could trust you with these angels.

  • @kristy802
    @kristy802 4 ปีที่แล้ว +7

    It says my state tests for ALD as of may 2019. Im in Vermont you guys are encouraging change I thank you just had a baby in December!

  • @tulipvalley111
    @tulipvalley111 4 ปีที่แล้ว +6

    Shared!! Save these sweet babies

  • @np100
    @np100 2 ปีที่แล้ว +5

    Can parents be tested before they get pregnant?

  • @melissashanfield1028
    @melissashanfield1028 2 ปีที่แล้ว +5

    Also those planning to have a kid can get genetics testing to see if you are a carrier for anything.

    • @elliesouza717
      @elliesouza717 4 หลายเดือนก่อน

      And doesn't mean your child will have difficulties

  • @teresahardin5241
    @teresahardin5241 4 ปีที่แล้ว +5

    Didn't like that the sick baby boy had to hear he's dying. God please help these families.

    • @catherinespark
      @catherinespark 4 ปีที่แล้ว +5

      Yes, I had queries about this too. Most of the time Krabbe affects the body but not the mind, though dementia can occur. I am certain that his mother had thought of this though. It may be that he has received help in making peace with this already - these children have to learn a lot in a short time at a young age. He may have been talked to about heaven and getting healed there, which is how a lot of children find peace with illnesses like these. In which case, hearing that would not have been news to him. His mother knows him better than anybody else, and is the best person to know what is and isn't appropriate to say in front of him at the time of filming.

  • @shananalexander9789
    @shananalexander9789 4 ปีที่แล้ว +6

    What do we do to get this done? Who do we talk to and who do we beg to make this a normal routine of testing for this disease?

  • @AudinJeffries
    @AudinJeffries ปีที่แล้ว +2

    ❤❤

  • @annisjohnson844
    @annisjohnson844 2 ปีที่แล้ว +2

    can thèse tests Bérard used To diagnose Tay Sachs disease in time to treat it?

  • @marymosqueda5224
    @marymosqueda5224 4 ปีที่แล้ว +7

    Is Krabbe only affecting male children?

    • @HuntersHope
      @HuntersHope  4 ปีที่แล้ว +2

      Krabbe affects both male and female children...

    • @briannec2016
      @briannec2016 4 ปีที่แล้ว +2

      My mother and Dad had a little girl, Holly, who had it. She died October '78, they were five months pregnant with me, I was born March '79. They almost didn't have me because they didn't want to watch another baby die.

    • @shananalexander9789
      @shananalexander9789 4 ปีที่แล้ว

      I just watched Tori’s story. Both genders can get this.

  • @stepht7508
    @stepht7508 2 ปีที่แล้ว +3

    I didn't realize that if diagnosed early enough there was treatment available for these children.My God,why aren't all newborns tested?This makes no sense 🤬

    • @HuntersHope
      @HuntersHope  2 ปีที่แล้ว +3

      We agree! We will fight until every child is screened for Krabbe at birth... You can learn more on the NBS section of our website.

  • @JackieD3924
    @JackieD3924 ปีที่แล้ว +3

    Is this disease a result of vaccine injury? No disrespect intended. We just watched a documentary which addressed vaccine injuries becoming more prevalent beginning in 1989, predominantly in boys.

    • @HuntersHope
      @HuntersHope  ปีที่แล้ว +2

      Hi Jacqueline! It is not. You can learn more about leukodystrophy on our website here: www.huntershope.org/family-care/leukodystrophies/ Thank you!

    • @jrpacer6355
      @jrpacer6355 ปีที่แล้ว +2

      Its genetic disorder

    • @elliesouza717
      @elliesouza717 4 หลายเดือนก่อน

      That's ridiculous

  • @jeannieves6275
    @jeannieves6275 11 หลายเดือนก่อน

    🙏🏽

  • @myahbattley1291
    @myahbattley1291 ปีที่แล้ว +3

    Aswe Jamal Adams county Ohio health and we can go out and Alaska t

  • @myahbattley1291
    @myahbattley1291 ปีที่แล้ว +2

    2015

  • @TrinketStarz
    @TrinketStarz 3 ปีที่แล้ว +2

    Can Lorenzo's oil help?
    Did you know about Lorenzo's oil at the time? Grand misdiagnosis is a time waster. My son suffered for years before they finally pinned it down.

    • @astrinymris9953
      @astrinymris9953 2 ปีที่แล้ว +4

      My understanding is that Lorenzo's Oil only helps half of the children who are started on it before symptoms manifest, meaning that you still need newborn screening. The bone marrow transplant seems like a more effective treatment.
      Either way, newborn screening is the key.

  • @franny5295
    @franny5295 2 ปีที่แล้ว +1

    Dang, that's sad...

  • @ramosjanish738
    @ramosjanish738 ปีที่แล้ว +2

    😭

  • @caporfact6205
    @caporfact6205 2 ปีที่แล้ว +1

    I know a another TH-cam er that that looks like your son that you just showed us on video it's called Sunshine baby

  • @myahbattley1291
    @myahbattley1291 ปีที่แล้ว +2

    😂😂😂😂😂😂😂😂😂😂😂😂😂❤❤😂😂😂😢😢😢😢😢😢😢😢😢

  • @aprilrobinson3379
    @aprilrobinson3379 2 ปีที่แล้ว +1

    Hi