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Hi first time on your channel did the doctor have those shoes in the office?? They r so cute!! Love how they zipped like that!!!

What cause this to happen with both of her feet

Have you ever thought about giving Elizabeth one of those sticker books where you put the stickers in different places or those dolls that you dress up with sticky clothes

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I love how Elisabeth got excited to go get Michel to show him his homeschool stuff. So cute.

I am on ASD high functioning and am deaf 🧏‍♀️

I’m on the autism spectrum myself and I’m 19 in my final year of high school hope ever thing goes well with him in the future

I have autism I am 28 now and I said my first word at 4 and couldn’t speak full sentences until I was 9ish my mum had my brother who also had ASD effects him completely different to me and then my sister with cerbal palsy, when I was younger I would definitely bite myself and would head but walls and floors I eventually got a helmet that I had to wear just in case i did start banging my head I have a lot of symptoms but when I was growing up I was diagnosed with ADHD but now it’s ASD I’m moderate to high functioning autism

I just have regular autism, when I born I had autism since then, Jacob seems like a nice kid and I wish him the best of luck in the future

He is at mi scll

It seems close to cerebral palsy on the mobility and stuff as my sister had the braces Northern Ireland we call them splints so I’m assuming it is a more severe form of that I am in the middle of moderate to high functioning autism I didn’t walk till I was 5 and didn’t speak full sentences till I was 8 I have a form of spina bifida and hip dysplasia as long with other conditions like restless leg syndrome and narcolepsy, osteoarthritis and other conditions that they are getting checked I could be MS and also I know I have hydrocephalus that comes with the spinea bifada

Thank you to both of you for sharing Elizabeth’s journey. I was thinking that she had cerebral palsy. what nystagmus is is uncontrollable movement in the eyes. They move back and forth on their own. You both are doing an amazing job with all three of the kids. It shows through and through. I know that god is in control of the hole situation. Keep on the great journey and continue to show the step that are being made with your great family. See you soon.

Hi, my daughter Shea is in the group. I’m glad someone is getting this information out to the public. I hope Elizabeth continues to grow and improve!!! It’s hard having this diagnosis. You feel alone because there’s not many of us out there. We grow in strength while in the valleys. Prayers

how old is Elizabeth?

Hi I'm a newer subscriber I fallow your Brother Jeremey and the rest of the J house vlog fam. I got a recommend video of your channel after watching JHouse. I like learning about different disabilities I have a rare disability just like Elisabeth mine is Called 18p- or Chromosome 18p Deletion and had a few of the similarities of Elisabeth I have Hypotonia and had trouble gaining weight as a baby too.

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It can be difficult but when Kendra saw their cousin Caleb having one that was when they went for the EEG testing and when they got the results back from it that was when they found out that he has the epilepsy And I started my RUclips channel Lea's Army because at 12yrs old I was diagnosed with my smith magenis syndrome and 1 in 3 percent can get my syndrome and with it being a rare genetic condition it was hard the standard testing can't even find it we had to go through with the exome testing and when we got the results from it from my genecist Dr picker with Boston children's and I was diagnosed with my scoliosis the year prior and June 23rd 2020 was when we found out that it was a symptom of the Smith magenis syndrome

Ashley and Travis, I’m sorry Jacob’s G.I tests came up with nothing, but am glad there wasn’t something serious going on. If worse comes to worst, there’s always the ‘elimination diet’. Elisabeth is doing well with just the feet inserts. Michael, I’m impressed with how patient you are! I would’ve been pacing if I didn’t bring a book or an iPad.

I am praying for you elissibirth

It makes me feel bad 👎 😞 😔 😕 😢 😪

I am here for comfort ✨️ 💕 💖 ❤️ 💓

And I am scared 😱

I am going to have surgery tomorrow aswell

I had a similar issue to Jacob when I was little and thankfully I grew out of it but unfortunately they never found out what caused it. I was put on a dairy free diet but I still got the pain occasionally. I hope you get to the bottom of it❤❤❤

It could be Jake’s gul bladder

What an amazing big brother Michael is.

are the inserts what you were aiming for for her? I've only ever had braces and cables so not sure what others' goals are lol

They couldn't,t find eny think wrong with my stomach but my mum google U can get stomach Migraines so I take medication for stomach Migraines bec for I got put on medication I had really bad stomach pains I even got a camera check too nothink was found I hope it gets worked out what is wrong with him .I have no stomach pains ever since I got put on medication ❤😊

You could log everything he eats then log the symptoms and what she ate around the symptoms. This could tell you something about it. It may help been in your shoes

Just thinking does he have trouble swallowing and does it hurt when he swallows cuz I have a GI issue that is called achalasia that only 1 in 100,000 people have I need a feeding tube cuz of it just asking and trying to help

Could Jacob be allergic to gluten

Congratulations it's awesome to see them feel better

Doctor done yet

I know that their cousin Caleb had the endoscopy done and that was how they found out that he has the Celiac disease

She's cute, hope the new shoes help in her medical condition.

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Hope the shoes work out as planned, she seems real great at adapting to new things. Also hope Jocobs issue is just a passing issue. And Michael, he needs a big brother award for being so patient, I'm sure you do your best, hope he feels just as special. I still tip my hat to Mom and Dad for sacrificing for the family. I'm just a random stranger, but still have a lot of respect for you guys. Wishing you all the best possible.

I love and watch all your videos and think you’re a great family. Just wondering why do you home school Elizabeth and Michael but not Jacob ?

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And try a weekly planner

Pink one for aac

New iPad for play

When she adult she will always get device if needs at points

Can eibsbeth talk

Why do people do that to help them talk better

He is so amazing to his siblings !

My bro does band I use to do mini cheer

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