Welcome friends- we’re the Ransome Fam (Billy, Tayler and Sully).
On this channel you’ll find content about: - our family (vlogs, traditions, days in our life) - kidney disease/medically complex parenting as we walk through a season of dialysis and transplant with our son - motherhood/fatherhood/parenting content - our faith
We hope the content you find here brings a smile to your face, points you to Jesus and encourages you that in tough circumstances there is still beauty to be found!
Interested in working with us? You can reach us at theransomefam@gmail.com for collaboration opportunities.
Sullys parents are the picture of devotion!!!! You are definitely shining your Light brightly!!!!!! May Jesus keep you all safe through this journey!!!!
@@RachaelCarri for sure-basically dialysis majorly dehydrates the body, and so there’s nothing helping the poop move through. If he gets backed up dialysis is painful, and he throws up a lot. We basically are just working hard to ensure things keep moving, so the term “laxative” is used for things like stool softeners and other things that help him go!
Sounds like a lot but you guys are such amazing parents you make it look so easy and it’s easy to tell he’s well loved! 🫶🏼 Praying for your adorable family
I know it's really hard for some ppl to understand...but God does not make mistakes and he is intentional. I dare someone to watch that video and not smile or chuckle. I sure did!
You can do it Im different to and my mum was poorly me and my dad had to do my stuff and we did it and it's nowhere near as hard as your son hugs my granddad used to help me out when I was poorly also thank the lord for my family ❤
I personally think you are wonderful parents. Everything you do is for your son . I don't see any of this being an issue for sweet Sully . You are raising him to be open and honest about his medical needs . Your videos are very informative, and we all appreciate you taking us on this journey with you . I have learned so much . Continued prayers for sweet Sully and his awesome parents. 🙏🏻🤍
Your son shouldn’t have his medical info, name, and face shared online. Please reconsider exploiting him, and keep his personal information off of the Internet. If he is going to wear diapers as an adolescent imagine just how embarrassing it could be for that fact to be broadcasted to the world.
the futures we hope for and the futures we get... poor baby, poor parents. good on those parents for not only doing right by their kid but for also having the energy to make this video and share with others
😂😂😂 Yeah you aren’t a parent, nanny, or babysitter if you haven’t had another human’s feces on you. Lol. What would you do later in life when he grows out of diapers? If he leaks, there has got to be a solution that accommodates it without wearing a diaper or incontinence underwear.
@@Gremlin_rh I wouldn’t call it a poor kid situation as it isn’t a bad thing to need incontinence underwear. I am just curious what the solution would be.
It’s interesting to learn about but I suggest taking this (and any other videos you may have like this down), covering his face and not saying his name. You’re already choosing to tell the world you two have a son with this medical issue, which means neighbors could stumble upon this years later and learn. But you’re making sure his likeness is attached to this. He will likely get comfortable with his medical concerns and even learn to be okay with them, like I have with mine. But as I was born in 1990, my mom wasn’t posting all about my invisible disability. I already had a very hard time with it in my teens and I’d known of it for years. So… yeah. I say share, since this is helpful to share if other families have questions. But please let him choose who knows what health issues he has and at what point. By all means encourage him to talk about it if he’s comfortable, but in a few years you don’t know if he will be.
This yes. Awareness of conditions like this for both parents and individuals is great, but children deserve privacy 🙏 I hope it becomes more normalized NOT to share videos of kids / their names before they're old enough to give consent.
Maybe spend time learning about his condition instead of criticizing the video, I grew up with a very sick sibling and by some miracle he is still here to talk about it, with a 05% chance to live. If you spend a little time you would learn he is waiting for a kidney, his parents are amazing and personally educating others on medical conditions helps others have an understanding and maybe consider being a donor. I look forward to the day his family says his kidney transplant was a success! Remember be kind and this family hasn’t had it easy. ❤
🙏🏻🙏🏻🙏🏻🙏🏻 for Sully - that a kidney becomes available ASAP and he can have the surgery with no complications and be able to live a more normal life as a toddler and ultimately live a full, long, healthy and productive life.🙏🏻🙏🏻🙏🏻🙏🏻
God does things in his own way. Sounds like this person's health discovery was fairly serious. Don't you worry. He knows what he's doing. His timing is perfect. But somehow I think you already know this. May God continue to bless your family with peace and patience.
Oh no,back to square one again.😒 At least Sully still has a chance he could get a kidney if the hospital puts him on a pediatric kidney transplant list if a random adult with the right blood type and perfect picture of health where to die in an accident or be taken off life support from an accident tomorrow or next week.
Dear Lord, please find sweet Sully the kidney he needs so he can live a happy, healthy life . And please watch over Billy and Taylor, his beautiful precious parents . Amen 🙏🏻🤍
So thankful he is big enough now!! I hope your family is led to the path God has for you!! Have you ever googled kidney failure and heavy metals? I would love to share some info with you that helped my uncle and our friend.
You’re both amazing parents! Don’t feel guilty if part of why you’re hoping to get Sully a transplant makes your life easier. Doing dialysis must be very difficult- for both of you and for Sully. Praying you find a donor soon ❤
@@lindan1122 thank you for being so kind ❤️ mostly we just want him to feel so much better too! Hard to wait when you know so many good things are on the other side of a transplant for him ❤️
When my daughters were in the nicu for 77 days, I held on to the phrase “right on time”. God gives us what we need right on time. Even when it doesn’t seem that way.. God knows when and it will be perfect 🤍
