The Ladd Family
The Ladd Family
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Kennedy's double hip, knee, ankle surgery. Gillette Children's St. Paul, MN - MPS 1 Hurler Syndrome
On November 16, 2023. Kennedy underwent double hip, double knee, and double ankle surgery. Kennedy suffers from a rare disease called MPS 1 hurler syndrome. This surgery was necessary to help decrease her pain while doing normal activities and to help keep out any arthritis in her joints. This is just a short video of our trip and her coming home!
Music Credit-
I Am a Man Who Will Fight for Your Honor by Chris Zabriskie is licensed under a Creative Commons Attribution 4.0 license. creativecommons.org/licenses/by/4.0/
Source: chriszabriskie.com/honor/
Artist: chriszabriskie.com/
Переглядів: 733

Відео

Episode 8! The Ladd Family- Our Journey With MPS 1 Hurler Syndrome - Cincinnati Childrens
Переглядів 2,5 тис.4 роки тому
E-mail Us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com Our Washington, DC Trip! ua-cam.com/video/HoIienLpZes/v-deo.html Social Media TikTok-www.tiktok.com/@TheLaddFamily Instagram- TheLaddFamily_MPS Twitter- TheLaddFamily_ Facebook- theladdfamilymps About the Kennedy Ladd Foundation ua-cam.com/video/zn...
Lincoln shows you how to workout and how to ride a balance bike! #WhatIsLincolnDoingToday
Переглядів 3504 роки тому
E-mail us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com Links to all the gear we use below! The Ladd Family In New York on the TODAY show! ua-cam.com/video/QYyqxKZe7X8/v-deo.html Follow us on Social Media! TikTok-TheLaddFamily Instagram-TheLaddFamily_MPS Twitter- TheLaddFamily_ Facebook-Kennedy and Lincoln Ladds Prayer Group About the Kenn...
The Ladd Family in Washington, DC for Rare Disease Week on Capitol Hill 2020! MPS 1 Hurler Syndrome
Переглядів 3144 роки тому
E-mail us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com The Ladd Family In New York on the TODAY show! ua-cam.com/video/QYyqxKZe7X8/v-deo.html The Ladd Family was one of the 900 Rare Disease Advocates for Rare Disease Week on Capitol Hill in Washington, D.C. 2020. Raising Awareness for MPS by meeting with legislatures to make a change. Ken...
Lincoln's First Trip to the Dentist!? Love it? Hate it? What Did He do!??! MPS 1 Hurler Syndrome
Переглядів 7564 роки тому
Our son Lincoln has MPS 1 Hurler Syndrome. He is very familiar with the doctors office and hospitals, but he has never went to the dentist. Here he is going for the first time! E-mail Us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com TikTok-TheLaddFamily Instagram-TheLaddFamily_MPS Twitter- TheLaddFamily_ Facebook-Kennedy and Lincoln Ladds ...
Lincoln with MPS 1 Hurler Syndrome has surgery to remove mediport at Cincinnati Children's Hospital
Переглядів 3,4 тис.4 роки тому
E-mail Us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com Lincoln has surgery to remove his port that he has had since he was 3 weeks old! We are so grateful and blessed that we get to remove this and be as normal as we can possibly be! Surgery is performed at Cincinnati Children's Hospital in Cincinnati, Ohio. TikTok-TheLaddFamily Instagram...
The Tooth Fairy Found Kennedy with MPS 1 Hurler Syndrome after her surgery at Cincinnati Children's!
Переглядів 2,1 тис.4 роки тому
Matthew 17:20 E-mail Us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com Kennedy has surgery at Cincinnati Childrens Hospital in Cincinnati, Ohio. She had to have a lot of dental work completed as well as tubes put in her ears. Thank you to all of our faithful prayer warriors for pulling us through! We love you all!!! God bless you! TikTok-Th...
A Free Way To Donate To The Kennedy Ladd Foundation and Save Money! Cure MPS1 Hurler Syndrome!
Переглядів 2374 роки тому
Give Josh Igou an opportunity to give you a quote and he will donate to The Kennedy Ladd Foundation, Inc.!!! Josh Igou State Farm Ins. 865-376-7672 E-mail Us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com TikTok-TheLaddFamily Instagram-TheLaddFamily_MPS Twitter- TheLaddFamily_ Facebook-Kennedy and Lincoln Ladds Prayer Group Kennedy and Linc...
Episode 7! The Ladd Family - Our Journey with MPS 1 Hurler Syndrome - Ep. 7
Переглядів 3,9 тис.4 роки тому
E-mail Us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com TikTok-TheLaddFamily Instagram-TheLaddFamily_MPS Twitter- TheLaddFamily_ Facebook-Kennedy and Lincoln Ladds Prayer Group About the Kennedy Ladd Foundation ua-cam.com/video/znyYgXIDDDQ/v-deo.html Episode 1- ua-cam.com/video/17su39LgDYs/v-deo.html Episode 2- ua-cam.com/video/_1Hur-GqBqA...
Episode 6! The Ladd Family - Our Journey with MPS 1 Hurler Syndrome - Ep. 6
Переглядів 3,4 тис.4 роки тому
E-mail Us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com Instagram-TheLaddFamily_MPS Twitter- TheLaddFamily_ Facebook-Kennedy and Lincoln Ladds Prayer Group About the Kennedy Ladd Foundation ua-cam.com/video/znyYgXIDDDQ/v-deo.html Episode 1- ua-cam.com/video/17su39LgDYs/v-deo.html Episode 2- ua-cam.com/video/_1Hur-GqBqA/v-deo.html Episode 3...
The Ladd Family! New York City! Today Show With Hoda & Jenna! Ambush Makeover! MPS 1 Hurler Syndrome
Переглядів 1,3 тис.4 роки тому
E-mail Us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com TikTok-TheLaddFamily Instagram-TheLaddFamily_MPS Twitter- TheLaddFamily_ Facebook-Kennedy and Lincoln Ladds Prayer Group About the Kennedy Ladd Foundation ua-cam.com/video/znyYgXIDDDQ/v-deo.html Episode 1- ua-cam.com/video/17su39LgDYs/v-deo.html Episode 2- ua-cam.com/video/_1Hur-GqBqA...
A little about The Kennedy Ladd Foundation, Inc.
Переглядів 8084 роки тому
The Kennedy Ladd Foundation, Inc. The Ladd Family is honored we got to start The Kennedy Ladd Foundation, Inc. in honor of our kids who have a terminal illness called MPS 1 Hurler Syndrome. The Kennedy Ladd Foundation, Inc. is an approved 501 (c)3 and provides an iPad, gift card, screen protector and case to Hurler kids going into Bone Marrow transplant. It also funds research to find a CURE fo...
Help us find a CURE for MPS 1- Hurler Syndrome
Переглядів 3434 роки тому
Help us Fight. Help us CURE. Help us Pray. Help us Share. Cure MPS1- Hurler Syndrome Our kids are rare. Our kids are terminal. We WILL find a CURE! Check out www.kennedyladd.org to find out when our next event will be. Music from filmmusic.io "At Rest" by Kevin MacLeod (incompetech.com) License: CC BY (creativecommons.org/licenses/by/4.0/) and "Eternal Hope" by Kevin MacLeod (incompetech.com) L...
Episode 5! The Ladd Family - Our Journey with MPS 1 Hurler Syndrome - Ep. 5
Переглядів 2,4 тис.4 роки тому
E-mail Us if your interested in Post Cards to hand out or for T-Shirt Orders TheKennedyLaddFoundation@gmail.com TikTok-TheLaddFamily Instagram-TheLaddFamily_MPS Twitter- TheLaddFamily_ Facebook-Kennedy and Lincoln Ladds Prayer Group Episode 1- ua-cam.com/video/17su39LgDYs/v-deo.html Episode 2- ua-cam.com/video/_1Hur-GqBqA/v-deo.html Episode 3- ua-cam.com/video/RiDd8ypvDFU/v-deo.html Episode 4- ...
Episode 4! The Ladd Family - Our Journey with MPS 1 Hurler Syndrome - Ep.4
Переглядів 2,3 тис.5 років тому
Episode 4! The Ladd Family - Our Journey with MPS 1 Hurler Syndrome - Ep.4
Episode 3! The Ladd Family-Our Journey with MPS 1 Hurler Syndrome - Ep. 3
Переглядів 8 тис.5 років тому
Episode 3! The Ladd Family-Our Journey with MPS 1 Hurler Syndrome - Ep. 3
Episode 2! The Ladd Family-Our Journey with MPS 1 Hurler Syndrome - Ep.2
Переглядів 4 тис.5 років тому
Episode 2! The Ladd Family-Our Journey with MPS 1 Hurler Syndrome - Ep.2
The Ladd Family - Our Journey with MPS 1 Hurler Syndrome- Ep.1
Переглядів 14 тис.5 років тому
The Ladd Family - Our Journey with MPS 1 Hurler Syndrome- Ep.1
SUPPORT MPS 1 HURLER SYNDROME AND THE KENNEDY LADD FOUNDATION FOR FREE WITH AMAZON SMILE!
Переглядів 1335 років тому
SUPPORT MPS 1 HURLER SYNDROME AND THE KENNEDY LADD FOUNDATION FOR FREE WITH AMAZON SMILE!
Happy Thanksgiving From The Ladd Family! A Family with MPS 1 Hurler Syndrome
Переглядів 3415 років тому
Happy Thanksgiving From The Ladd Family! A Family with MPS 1 Hurler Syndrome
Kennedy and Lincoln with MPS 1 Hurler Syndrome, play in the snow!
Переглядів 3255 років тому
Kennedy and Lincoln with MPS 1 Hurler Syndrome, play in the snow!
Kennedy with MPS 1 Hurler Syndrome Practices For Thanksgiving Play!!!
Переглядів 7915 років тому
Kennedy with MPS 1 Hurler Syndrome Practices For Thanksgiving Play!!!
The Ladd Family Channel Trailer
Переглядів 1,9 тис.5 років тому
The Ladd Family Channel Trailer
The Ladd Family Goes To Minnesota To Fight for a cure for MPS 1 Hurler Syndrome!
Переглядів 7855 років тому
The Ladd Family Goes To Minnesota To Fight for a cure for MPS 1 Hurler Syndrome!

КОМЕНТАРІ

  • @barbiebeeks8203
    @barbiebeeks8203 Місяць тому

    I happen to accidentally see your video and started watching all of them absolutely love your family

    • @TheLaddFamily
      @TheLaddFamily 7 днів тому

      Thank you so much! Please keep following, we will get back to posting videos.

  • @emeraldkimble7602
    @emeraldkimble7602 2 місяці тому

    How do you fiffer from hunter complex mos only biochemistry underdtandd

  • @joykendrick6156
    @joykendrick6156 2 місяці тому

    Merry Christmas, my grandma was Dollie Ladd.

  • @tegankate1
    @tegankate1 3 місяці тому

    I'm in New Zealand and my daughter has Hurler Syndrome. We are day +125 post transplant and she's doing really well and has just today come off all her meds and things are looking really positive. It's good to follow along on your journey of someone who is well ahead of us on their journey with Hurler as we honestly have no idea what to expect, but we know this is just part of our life now. Thank you for sharing your journey ❤❤

    • @TheLaddFamily
      @TheLaddFamily 7 днів тому

      Thank you so much for commenting! How are things going now!? Please reach out to us at kennedyladd.org

  • @chuckswizzy9597
    @chuckswizzy9597 4 місяці тому

    I want to donate

    • @TheLaddFamily
      @TheLaddFamily 7 днів тому

      Hey! I am so sorry we are just now seeing your comment. You can go to KennedyLadd.org and click donate. Thank you so much and God Bless!

  • @jojomiller1630
    @jojomiller1630 4 місяці тому

    Seriously I wanted to know what this disease was not your life story!

    • @TheLaddFamily
      @TheLaddFamily 7 днів тому

      You can go to KennedyLadd.org and learn all about MPS 1

  • @janroach1852
    @janroach1852 4 місяці тому

    These parents should be part of the Courageous Parents Network. God has blessed your two babies with wonderful parents who will make their lives happy and full no matter the lifespan. Those babies are adorable. There is time and I hope treatments and cures can be found. With two children with health problems, there is little time to post videos.

  • @EH-ww8pi
    @EH-ww8pi 4 місяці тому

    If we had universal healthcare in this country you wouldn’t have to raise money to pay for hospital bills. Wish your little girl the very best

  • @jonasschmitz506
    @jonasschmitz506 4 місяці тому

    My newborn the doctor said he has, now we waiting for the genetic test, my older maybe have autism, my grandpa is dying of cancer, and I was supposed to abandon my Lord and savior but it get more and more close to him, May God bless your Family ❤

    • @TheLaddFamily
      @TheLaddFamily 7 днів тому

      Please stay close to him, do not lead astray! He will help guide you and give you comfort. Any updates on your children?

    • @jonasschmitz506
      @jonasschmitz506 7 днів тому

      @@TheLaddFamily yes he have half of the gene (or whatever they say I don’t understand much) doctor said that he will be normal, he only has to be careful with who he will marry if have the other part of the gene

  • @mandyholmberg5106
    @mandyholmberg5106 5 місяців тому

    I am really! So very sorry for your loss 😢💔 even though it was a long time ago

  • @mandyholmberg5106
    @mandyholmberg5106 5 місяців тому

    I am sending out my thoughts and prayers and love to this whole family ❤

  • @NABaby41
    @NABaby41 6 місяців тому

    I have to tell you that this was the worst video you have done. The kids noise was impossible to hear you with! It was a very obnoxious and it drove me right of the video. Please try to make it more conducive to hearing for my old ears. I love you and pray for you, please keep us up to date.

    • @TheLaddFamily
      @TheLaddFamily 7 днів тому

      Thank you for the feedback and thank you for supporting us!

  • @bocadogtraining1871
    @bocadogtraining1871 6 місяців тому

    I think it would be good to meet you since I have a medical disabilities and think meeting you would be very helpful to help with my disability and starting a non-profit program for people with dofffersmt disorders and what they need

  • @donnareis6862
    @donnareis6862 7 місяців тому

    Love your familymily gGod bless!😊

  • @CWengrovius1420
    @CWengrovius1420 7 місяців тому

    She’s an amazing little girl even though she had this done four yrs ago! God bless your family always!

    • @TheLaddFamily
      @TheLaddFamily 7 днів тому

      We still fight all the struggles daily

  • @tamiwigginton7137
    @tamiwigginton7137 7 місяців тому

    Wow! what a journey!!!

  • @valisferle68
    @valisferle68 7 місяців тому

    God Bless you guys!

  • @ShareenLewis-ml4gk
    @ShareenLewis-ml4gk 8 місяців тому

    Put me in your belly June Sunday ok

  • @lorrainerussell6049
    @lorrainerussell6049 9 місяців тому

    ❤❤❤

  • @margaretcheshier8238
    @margaretcheshier8238 9 місяців тому

    We lost a grandson to hurlers syndrome about 30 years ago

    • @TheLaddFamily
      @TheLaddFamily 9 місяців тому

      I am so sorry to hear this. We have a place on our website @kennedyladd.org for families to tell their story. We love to hear stories of all hurler families. It truly helps the whole MPS community.

  • @lorapalmer3229
    @lorapalmer3229 9 місяців тому

    I love how raw and real you are. It is refreshing! Don’t edit! And you have a serious personality. I get it. God bless your sweet family!

    • @TheLaddFamily
      @TheLaddFamily 9 місяців тому

      Thank you so much for commenting!! We love your feedback!

  • @carrieland6945
    @carrieland6945 10 місяців тому

    Prayers for your precious babies and your family in Jesus name 🙏🏻🙏🏻🙏🏻

    • @TheLaddFamily
      @TheLaddFamily 9 місяців тому

      Thank you! God bless you for praying for us!

  • @bighush3481
    @bighush3481 10 місяців тому

    Praying very hard for a cure guys.

  • @kathythureen9341
    @kathythureen9341 10 місяців тому

    THE TRAGIC LIFE OF KATHY THUREEN

  • @KennedyLadd
    @KennedyLadd 11 місяців тому

    I hope your kids is are a little better

  • @KennedyLadd
    @KennedyLadd 11 місяців тому

    hey I really hope your kids get better

  • @kiranaziz1651
    @kiranaziz1651 Рік тому

    Hi-! Our Child Is Diagnosed With Hurler Syndrome… He Is 3 Years Old-! We Are Worry About Him -! Can You Please Do Us A Favour The Disease-!

  • @brookedepp300
    @brookedepp300 Рік тому

    A friend of mine has 2 kids with the same names!

  • @spiralrose
    @spiralrose Рік тому

    Why were the doctors worried about Kennedy’s ovaries if she wasn’t supposed to live past ten years?

    • @TheLaddFamily
      @TheLaddFamily 9 місяців тому

      The transplant would allow her to live a longer life, so that if in the future, if she was physically able to care for and give birth to a child, she would have the possibility of doing that.

  • @sarapeterson1271
    @sarapeterson1271 2 роки тому

    My granddaughter was just diagnosed with MPS-1. She was diagnosed at about a week old. I am just wondering what this process is going to be like any advice any help we would appreciate 🙏 thank you for sharing your journey.

    • @TheLaddFamily
      @TheLaddFamily 9 місяців тому

      I am so sorry we are just now replying to this. I hope that your child has received care and is doing great! Please reach out to our foundation @kennedyladd.org if we can help in any way.

  • @martinemikita9281
    @martinemikita9281 2 роки тому

    Ryan u seem so personable!! Nice to see that u can smile and get thru these conversations and maintain a sense of happiness.

    • @TheLaddFamily
      @TheLaddFamily 9 місяців тому

      Thank you! It’s truly a blessing no matter what! God has truly blessed us through it all!

  • @martinemikita9281
    @martinemikita9281 2 роки тому

    As I watched these videos I can help but see straight misery on Allies face. Ryan is VERY personable and he has an open welcoming voice.

  • @moniquewarren1433
    @moniquewarren1433 2 роки тому

    Just found your channel. Prayers for you all.

  • @sandip.7968
    @sandip.7968 2 роки тому

    Never give up. When you kneel down to God, He stands up for you.

  • @mellajoe
    @mellajoe 2 роки тому

    I I have a 7 year old with this diagnosis, I just had a baby 2weeks ago and they’re saying that he has this disorder at first I was heartbroken, but now I’m just waiting to see what the creato has in store

  • @kathy1138
    @kathy1138 2 роки тому

    Just found your channel and subscribed. I pray God's blessings for your family. He's always there when we need Him.

  • @Orangeeyes83
    @Orangeeyes83 2 роки тому

    So will all your children have hurlers?

    • @softbreezy6052
      @softbreezy6052 2 роки тому

      Not necessarily, but there is always aa chance. I think its a 25% chance

  • @Orangeeyes83
    @Orangeeyes83 2 роки тому

    Did you know that your other child could possibly have hurlers?

  • @maryannsomerville3505
    @maryannsomerville3505 2 роки тому

    Hello Folks !! 🙋🏻 Just found your vids today. My nieces baby boy has been diagnosed with Hurler’s. He’s 3 mos. old today & receiving his 3rd enzyme infusion. We’re all awaiting his transplant journey & ‘learning’ as much as we can. Thanks for your candid approach & courage to share your journey with Kennedy. I’m looking fwd. to watching more. btw - I love your advice about asking forgiveness rather than permission - it’s my standard rule of thumb!! 😁 🌸💜✨

  • @janleslie7163
    @janleslie7163 3 роки тому

    Praying for your family found you today and started following I don't know exactly where you live but I live in Livingston about 25 miles from cookeville bless you all

  • @pennyvoll1169
    @pennyvoll1169 4 роки тому

    Hey guys. Praying for you. We are neighbors. I'm in Jamestown.

  • @PrettySilly
    @PrettySilly 4 роки тому

    Not terminal u idiots

  • @PrettySilly
    @PrettySilly 4 роки тому

    My daughter had the bone marrow transplant. She's now a happy 9 year old.

  • @housewren2218
    @housewren2218 4 роки тому

    I am so grateful that you have faith in Jesus, you are so special and loved. I am so thankful you are a firefighter. So is my son-in-law and I pray that you can support him.

  • @housewren2218
    @housewren2218 4 роки тому

    Who ever gave this a thumbs down has no heart.

  • @housewren2218
    @housewren2218 4 роки тому

    I am sending you both love. These videos are so important. Thank you so much for taking the time to film this. Our grandson was being tested for Downs. How I wish it had been Downs. The MPS 1 Hurlers diagnosis has been the hardest thing we have had to face. Thank you so much again. You are so courageous!

  • @brendaweaver5652
    @brendaweaver5652 4 роки тому

    For the shirts,how about doing the shirts in Kennedy and Lincolns favorite colors.