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Episode 6! The Ladd Family - Our Journey with MPS 1 Hurler Syndrome - Ep. 6 

The Ladd Family
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**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
• A little about The Ken...
Episode 1-
• The Ladd Family - Our ...
Episode 2-
• Episode 2! The Ladd Fa...
Episode 3-
• Episode 3! The Ladd Fa...
Episode 4-
• Episode 4! The Ladd Fa...
Episode 5-
• Episode 5! The Ladd Fa...
Our New York Video
• The Ladd Family! New Y...
Kennedy and Lincoln have MPS 1 Hurler Syndrome. You can read more about Hurler Syndrome here.
mpssociety.org....
Kennedy and Lincoln received bone marrow transplants at a very young age (Kennedy 11mths and Lincoln 3mths) to slow down progression of the disease. There is no cure for MPS 1 Hurler Syndrome. When we were able to come home from Cincinnati (post transplant) with our daughter Kennedy, we started The Kennedy Ladd Foundation, Inc.
The Kennedy Ladd Foundation, Inc is a 501(c)3 non-profit to raise funds for research to find a cure for MPS 1 and to provide iPads to Hurler patients going into bone marrow transplant. You can also follow the foundation page here / @thekennedyladdfoundation and learn more on the website at www.KennedyLadd.org
Kids with MPS 1 have 3 options. 1-transplant before the age of 2 (in most cases after the age of 2 the disease has done too much damage) 2-Enzyme Replacement Therapy (an artificial enzyme infusion, done weekly, for life) 3-do nothing (Bodies will deteriorate and usually pass away by the age of 5-10).
The Ladd family will continue to fight and spread awareness to find a cure for MPS 1! We need your help! You can help by doing one or all of the following! Donate to The Kennedy Ladd Foundation, Inc., If you shop Amazon go to smile.amazon.com and setup The Kennedy Ladd Foundation as your charity, Donate to the MPS Society www.MPSSociety.org, Tell a friend about MPS 1, share our page, follow/share our Facebook Page @ Kennedy and Lincoln Ladds Prayer Group, follow/share our Instagram @ KennedyandLincolnLadd, subscribe to our channel, share our channel, and lastly but most important if you don't do anything else, we ask that you Pray for our babies and the rest of the families. We can't wait to share more with you!
www.KennedyLadd.Org
www.MPSSociety.org
The Kennedy Ladd Foundation Channel- / @thekennedyladdfoundation
Become a Donor- www.BeTheMatch.Org
Cord Blood Donation Info- www.parentsguidecordblood.org
Links To Gear We Use For Our Videos!
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#TheLaddFamily #MPS1 #HurlerSyndrome

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3 окт 2024

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Комментарии : 16   
@mellajoe
@mellajoe 2 года назад
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
@bocadogtraining1871
@bocadogtraining1871 3 месяца назад
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
@jonasschmitz506
@jonasschmitz506 Месяц назад
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 ❤
@sandip.7968
@sandip.7968 2 года назад
Never give up. When you kneel down to God, He stands up for you.
@TheLaddFamily
@TheLaddFamily 6 месяцев назад
Amen!
@susancoffey7843
@susancoffey7843 4 года назад
Allie & Ryan...you two are precious...so transparent and real! Keep on doing your videos just as you are. We became familiar with your story through Matt. He was our Hardscaping guy at Grande Vista Bay...and yes, I recall meeting Ryan at Los Primos...sitting at the bar with his brother🤣. Anyway, I’ve been incredibly touched by your testimonies...and your boldness in putting it all out there. I am retired but full of energy and would love to help you all in any events, etc. Please be in touch as I can help! Susan (and Jack) Coffey
@TheLaddFamily
@TheLaddFamily 4 года назад
@Susan Coffey Thank you for your kind words! We are trying our best to be an open book and put everything out there. Be careful what you ask for, we just may put you to work!🤪 thank you for reaching out! God bless you! ...you may find me sitting at that same bar, but at least it will be water this time! 😂
@tracyalley2728
@tracyalley2728 4 года назад
Definitely interested in a shirt and a vehicle sticker! 👍🏼
@TheLaddFamily
@TheLaddFamily 4 года назад
@Tracy Alley Thank you! We will get with you!
@harperladd7970
@harperladd7970 4 года назад
Love my awesome Aunt and uncle
@TheLaddFamily
@TheLaddFamily 4 года назад
We love you Harper!!!
@Orangeeyes83
@Orangeeyes83 2 года назад
Did you know that your other child could possibly have hurlers?
@kristin_peddicord
@kristin_peddicord 4 года назад
"pray and ask God to help!" Love that story!!!
@TheLaddFamily
@TheLaddFamily 4 года назад
Kristin Peddicord Thank You!!! Love seeing God work and perform Miracles!
@Orangeeyes83
@Orangeeyes83 2 года назад
So will all your children have hurlers?
@softbreezy6052
@softbreezy6052 2 года назад
Not necessarily, but there is always aa chance. I think its a 25% chance
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