My disabled son drooled profusely too as a small child. It gave him rashes and would cause him to cough and choke at times, there was so much saliva. We used scopolamine patches which are meant for motion sickness but the side effect is dry mouth! So every 3 days a new patch behind the ear and it was very effective. At age 4 we decided that because the drooling was indefinite, he needed surgery. Two salivary glands were removed and two others redirected. He has never required a bib since and he’s 32 now 😊
Oh goodness!!! Maybe that would work for Griffin!!! I doubt if Will and Em have heard of this procedure!!! I HOPE that they see your comment!! It’s VERY important that they do, in case the other injections are causing his current problem!! I know the way their dealing with it now, is to check him into hospital every 6 mo.’s and put him under!! Not really good for Griffin, or Emily to leave other kids to do this, thus leaving Will to take off work to stay with other littles. I hope they will look into this!!!!
Griffen is such a sweet heart. Hoping he gets better soon. By the way you are one great mom. I don't blame you for feeling worried and frustrated. Glad you had a better team today thats helping.
Continuing to lift you, Griffin and your family up in prayer. Having any family in the hospital is exhausting but you and Will are doing the right thing / Hugs
I have spina bifida. That happened with me when I was little where everyone was saying different things and my parents ended up having to have a meeting with everyone to make sure everyone was on the same page. Don’t be afraid to do that.
My little girl had severe pediatric obstructed sleep apnea and it took 8 months from our first appointment to surgery day. (6 months after the sleep study) It's such a frustrating process but omg what a difference once those tonsils and adenoids were out its like a whole new kid. Sending lots of good thoughts your way!
I'm happy you are getting answers and the doctors "get it" finally. You and Will are great and Griffin is such a cutie. I love his smile. Hang in there, I'm always praying for your family.
I’m so pleased the staff had damn good beating and changed tune quickly! So pleased his tonsils are down ! Let’s hope they stay down! ☺️👏🏾👏🏾👏🏾👍🏾🙏🏾💪🏾🙌🏾🇬🇧❤️
You must be frazzled Emily - hospital atmospheres are so draining - information overload etc....but your doing such a great job for Griffin - you WILL get to the solution eventually - and he's such a sweet natured boy. Love from Scotland x
He's in such good spirits for not being able to eat normally. That's a plus at least. Ask them about giving him Pediasure if he still won't eat solid food. And I should ask about getting my arm wrapped up like that the next time I'm in the hospital. I always need to get my IV redone 3 or 4 times because it irritates me so much. Maybe if they wrapped it up I'd stop fussing with it. And this is coming from a 41-year-old woman. lol
Ugh I know that is so rough...you are so strong...my whole childhood I use to get tonsillitis and bronchitis atleast 10 times a year and I would always get them at the same time it was miserable...I'm praying for you all
He has such a beautiful smile. Bless him, Almighty God, with good health, tons of giggles, endless joy, and Your holy angels. In Jesus’ Name, Amen🙏🏻🙏🏻🙏🏻
Boy do I relate with all of this. At the hospital with my 2.5 year old who has mild cp and autism. He randomly started screaming and refusing to put any weight on his leg a few days ago. He’s typically so active and doesn’t feel pain because of cp so the fact that he won’t move and is screaming in pain is heartbreaking. Doctors office looked at him for five seconds and said he’s probably fine. Just wait a few days. Like ugh! We know our kids. How am I supposed to wait days of him screaming in pain without a known cause!! Sorry. Rant over. Praying for you guys, but it’s nice to to know I’m not the only momma constantly having to fight for my boy.
I’m sorry that you’re going through all of this! We’ve had our 6 year old dealing with a rare birth defect that has now caused her trauma around medical procedures, so she has to be sedated for everything! So getting anything done to help her takes forever and I feel like the doctors all contradict each other!! I feel your pain and frustration. Sending love!
So I've had to do 3 different swallow studies- 1 with food, 1 with only liquid, and 1 with an ng tube that measures pressure and how slowly the esophagus empties. That was the only study that showed something- mine empties slowly and causes me to choke/aspirate. I need muscle relaxants to eat/drink. It took forever to diagnose. I don't have tonsils- removal made no difference for me. You've got this!
@@crohniequeenab it's called an esophageal manometry test. Completely different than gastric emptying which has nothing to do with why you would be choking on foods.
Hope y'all are back home by now with some good answers to how to help Griffin. You and Will are such a good team, but I wish y'all had more support at home. Will having to take off work is surely a hardship. Since y'all became friends with The Landing Crew I've been praying their subscribers would discover your channel. It would be life changing if Will could stay home the way Lonnie is able to. Hang in there! Hugs from West Texas!
Yes- since Lonnie is home also, I was hoping Stephanie could help them out a bit!! Maybe sit with the other kids for a few hr.’s , a few times!! Nothing to much!!! Just a tiny bit of relief for Will and Em!!! But that little bit would help SO much!!!!
This may, or may not be of any help for you, but I just wanted to put it out there. I had a series of botox injections for TMJ. Not long after my second set of injections, I started having problems swallowing. I would choke if I drank anything. It seemed that I could swallow soft things that were thick...like potatoes or a smoothie. We had to start using a thickening agent for all of my drinks. Once the botox wore off, the issues stopped. Just something to think about.
Wonderful Vlog Emily....stay strong Momma!! To Will n kiddos I hope you are all doing ok! My ❤ it's with you all....everyday I think about you! ❤ From Minnesota P.s. are you going to have a PO Box for your Fans like in New York?
I did that swallow study and they said same thing about me . That nothing was wrong. But I still kept choking. So they did body cat scan and found I had a whole right at opening where food passes to the stomach and it was getting caught there and causing all my problems. I had to live with choking on everything meal for almost 13 years before they finally listened and found it. They still didn’t believe me until they followed my weight for a week and within about eight days I lost almost forty pounds. Then they did cat scan and found it. Need surgery to fix it still. But I had to start drinking whole chocolate milk about half gallon a day to put weight on. I’m praying your precious little boy don’t have this. Praying everything turns for the better from today on out for you.
@@christyb7455 yes that why I was put in hospital right away. Because they thought it could be cancer. But when you’re not getting anything down but your body is still using energy it takes it from your muscles, fat and water. First few days I was still going to bathroom. So that took some weight away. But was on I’v for almost 24 hours before they got anything from tubes to measure out puts. I had been going to doctors every couple days only way we knew now much weight I was losing. But I’m glad it wasn’t cancer.
I had my tonsils removed when I was three and they put me in this IV box where they put like ivy on your arm but you have to feel pain and and they put a mask on you before you go to sleep and they give you painkillers
I know it is hard for me for getting my tonsils out sometimes, It sounds like my words can mix up and that is stuttering and that makes my words backwards. So yeah, I am still healthy and lose weight a lot. Thanks Emily, your are still awesome and strong, and have a great day.
yay for the swallowing study, this will help rule out neuro-muscular issues that can affect swallowing/choking issues. They have to rule this out, I know the unknown is scarey and I'm sorry for the upset. Hopefully they'll recommend a level of diet that he can take (as in types of puree'd food etc... level 1, 2, 3, or 4 level diets for swallowing issues. I know you though it was just a tonsil issue, but feeding studies are essential for kids who have been diagnosed with Angelman and similar musco-skeletal disabilities. You'd hate to have his tonsils removed if there was something more serious going on.
I only hope Will isn’t having to take time off from work !! But I guess that has to be the only way one of them is with Griffin AND the other kids 24 seven!!!! Hopefully Will gets a LOT of sick leave !!!!!
I think (I have a medical background) that you need to find a doctor who will take Griffin's tonsils out. It certainly seems like his tonsils to me & this will keep happening periodically until they're removed. Griffin also needs the botox for his own dignity & while I don't believe the botox had anything to do with it, if the doctors don't want him to have it because of this, he needs his tonsils out for that too.
Will Griffin leave his hands off an NG tube??? How did the food go that you just spoke about? fries?????? I'm glad the doctors and staff finally got through to you, you seem a bit more reserved about the whole thing - a bit. Hang in there Em and Will. I hope you have some help at home also. You are both sooooooo wonderful! HUGS (and prayers) for all. P.S. how can they do a swallow study when they don't give him regular food, of course it'll be normal when he has squooshy food! What did they feed him to make the swallow study??
It’s got dye in it and it’s a liquid that can be pushed through NG tube down the nose or pt drinks it like contrasts for CT scan. It makes the GI tract glow and he’s put under imaging. It’s not solid food no way that would cause aspiration.
My disabled son drooled profusely too as a small child. It gave him rashes and would cause him to cough and choke at times, there was so much saliva.
We used scopolamine patches which are meant for motion sickness but the side effect is dry mouth! So every 3 days a new patch behind the ear and it was very effective.
At age 4 we decided that because the drooling was indefinite, he needed surgery. Two salivary glands were removed and two others redirected. He has never required a bib since and he’s 32 now 😊
Oh goodness!!! Maybe that would work for Griffin!!! I doubt if Will and Em have heard of this procedure!!! I HOPE that they see your comment!! It’s VERY important that they do, in case the other injections are causing his current problem!! I know the way their dealing with it now, is to check him into hospital every 6 mo.’s and put him under!! Not really good for Griffin, or Emily to leave other kids to do this, thus leaving Will to take off work to stay with other littles. I hope they will look into this!!!!
Griffen is such a sweet heart. Hoping he gets better soon. By the way you are one great mom. I don't blame you for feeling worried and frustrated. Glad you had a better team today thats helping.
Continuing to lift you, Griffin and your family up in prayer. Having any family in the hospital is exhausting but you and Will are doing the right thing / Hugs
Griffen is such a happy lil guy,his smile and excitement is the sweetest 💙
Praying for you and Will & the kids!
The best mom and dad ever!! ❤️
I have spina bifida. That happened with me when I was little where everyone was saying different things and my parents ended up having to have a meeting with everyone to make sure everyone was on the same page. Don’t be afraid to do that.
My little girl had severe pediatric obstructed sleep apnea and it took 8 months from our first appointment to surgery day. (6 months after the sleep study) It's such a frustrating process but omg what a difference once those tonsils and adenoids were out its like a whole new kid. Sending lots of good thoughts your way!
Thank You so much for the updates on the whole family. Keeping you in my prayers.
I'm happy you are getting answers and the doctors "get it" finally. You and Will are great and Griffin is such a cutie. I love his smile. Hang in there, I'm always praying for your family.
I’m so pleased the staff had damn good beating and changed tune quickly! So pleased his tonsils are down ! Let’s hope they stay down! ☺️👏🏾👏🏾👏🏾👍🏾🙏🏾💪🏾🙌🏾🇬🇧❤️
Your such a good momma ❤️
Sounds like answers are slowly, but finally coming! ♥️♥️
Bless his heart and yours and Will’s. Praying for precious Griffin.
Praying for you and your little guy!
Praying for you and your sweet boy!
Just hang in there! 💞
Griffin and your family are in my prayers!
You must be frazzled Emily - hospital atmospheres are so draining - information overload etc....but your doing such a great job for Griffin - you WILL get to the solution eventually - and he's such a sweet natured boy. Love from Scotland x
Hi hun yeah getting there but I am so pleased to hear you are well welcome to the shop today and commented on
He's in such good spirits for not being able to eat normally. That's a plus at least. Ask them about giving him Pediasure if he still won't eat solid food. And I should ask about getting my arm wrapped up like that the next time I'm in the hospital. I always need to get my IV redone 3 or 4 times because it irritates me so much. Maybe if they wrapped it up I'd stop fussing with it. And this is coming from a 41-year-old woman. lol
Sending prayers for Griffin and family
Great to hear Griffin fels a little bit better! FIngers crossed you find out what exactly it is tomorrow!!
Poor griffin prayers Emily 😢
Keep fighting don't give up
Am so glad things seem to be getting better. Take care of yourself. 💕 🙏🙋
Poor Griffen he is so brave ❤😢
Much love and prayers for Griffin! Hope you receive answers soon.
💕🙏💕🙏💕😘
You really went through so much!!!No wonder you had struggles.Soo glad you got through it and are out the other side!❤️❤️❤️❤️❤️❤️❤️❤️
You have a very good view from your sons hosptial room I love it I think your children have great parents
Ugh I know that is so rough...you are so strong...my whole childhood I use to get tonsillitis and bronchitis atleast 10 times a year and I would always get them at the same time it was miserable...I'm praying for you all
Sending prayers for all of you 🙏🏻 stay strong momma ❤️
Griffin is so cute. You hang in the Mama. You have to be his voice and you are doing a great job!
Praying for all of you ,I know this is so hard.Keep fighting for him,you know him better than any body.Love and prayers.💕🙏🙏🙏
Hang in there Momma you are sooo strong ! Keep fighting for Griffin don’t give up .
Bless you and your amazing family 🙏🙏
He has such a beautiful smile. Bless him, Almighty God, with good health, tons of giggles, endless joy, and Your holy angels. In Jesus’ Name, Amen🙏🏻🙏🏻🙏🏻
You’re doing a great job 👍
Don’t give up mothers intuition is always accurate .,
You’re a great mom 💕
I’m Praying for you Griffin and your family 🙏
Good luck little man.......so much for such a little man to endure. 🙏
He is so cute is smile is everything ❤
Love that smile 😊
Boy do I relate with all of this. At the hospital with my 2.5 year old who has mild cp and autism. He randomly started screaming and refusing to put any weight on his leg a few days ago. He’s typically so active and doesn’t feel pain because of cp so the fact that he won’t move and is screaming in pain is heartbreaking. Doctors office looked at him for five seconds and said he’s probably fine. Just wait a few days. Like ugh! We know our kids. How am I supposed to wait days of him screaming in pain without a known cause!! Sorry. Rant over. Praying for you guys, but it’s nice to to know I’m not the only momma constantly having to fight for my boy.
Praying for Griffen🙏🙏🙏
I’m sorry that you’re going through all of this! We’ve had our 6 year old dealing with a rare birth defect that has now caused her trauma around medical procedures, so she has to be sedated for everything! So getting anything done to help her takes forever and I feel like the doctors all contradict each other!! I feel your pain and frustration. Sending love!
I’m so happy 😁 and glad 😀 to hear 👂🏻 it from my heart ♥️
Prayers for you. 🙏🙏🙏
So I've had to do 3 different swallow studies- 1 with food, 1 with only liquid, and 1 with an ng tube that measures pressure and how slowly the esophagus empties. That was the only study that showed something- mine empties slowly and causes me to choke/aspirate. I need muscle relaxants to eat/drink. It took forever to diagnose. I don't have tonsils- removal made no difference for me. You've got this!
Yes that’s a gastric emptying study.
@@crohniequeenab no, it measures only the esophagus, how fast it empties, and the pressure of the esophagus, not your stomach.
@@crohniequeenab it's called an esophageal manometry test. Completely different than gastric emptying which has nothing to do with why you would be choking on foods.
@@crohniequeenab totally different. I've had the gastric emptying test and was diagnosed with gastroparesis. Not fun 😕
Hope y'all are back home by now with some good answers to how to help Griffin. You and Will are such a good team, but I wish y'all had more support at home. Will having to take off work is surely a hardship. Since y'all became friends with The Landing Crew I've been praying their subscribers would discover your channel. It would be life changing if Will could stay home the way Lonnie is able to. Hang in there! Hugs from West Texas!
Yes- since Lonnie is home also, I was hoping Stephanie could help them out a bit!! Maybe sit with the other kids for a few hr.’s , a few times!! Nothing to much!!! Just a tiny bit of relief for Will and Em!!! But that little bit would help SO much!!!!
Hope he gets better
Griffin is so cute! So glad his tonsils have gotten smaller.
This may, or may not be of any help for you, but I just wanted to put it out there. I had a series of botox injections for TMJ. Not long after my second set of injections, I started having problems swallowing. I would choke if I drank anything. It seemed that I could swallow soft things that were thick...like potatoes or a smoothie. We had to start using a thickening agent for all of my drinks. Once the botox wore off, the issues stopped. Just something to think about.
Your doing a great job but you already know that ! ❤️
Wonderful Vlog Emily....stay strong Momma!! To Will n kiddos I hope you are all doing ok! My ❤ it's with you all....everyday I think about you! ❤ From Minnesota
P.s. are you going to have a PO Box for your Fans like in New York?
🙏 Hang in there🙏
Sending my love xx
Praying for griffin
Prayers for Griffin
I did that swallow study and they said same thing about me . That nothing was wrong. But I still kept choking. So they did body cat scan and found I had a whole right at opening where food passes to the stomach and it was getting caught there and causing all my problems. I had to live with choking on everything meal for almost 13 years before they finally listened and found it. They still didn’t believe me until they followed my weight for a week and within about eight days I lost almost forty pounds. Then they did cat scan and found it. Need surgery to fix it still. But I had to start drinking whole chocolate milk about half gallon a day to put weight on. I’m praying your precious little boy don’t have this. Praying everything turns for the better from today on out for you.
40 lbs in 8 days??
@@christyb7455 yes that why I was put in hospital right away. Because they thought it could be cancer. But when you’re not getting anything down but your body is still using energy it takes it from your muscles, fat and water. First few days I was still going to bathroom. So that took some weight away. But was on I’v for almost 24 hours before they got anything from tubes to measure out puts. I had been going to doctors every couple days only way we knew now much weight I was losing. But I’m glad it wasn’t cancer.
@@karenselogic7742 Wow!! That had to be terrifying😥So glad it's not cancer too and I hope you're feeling much better❤
I had my tonsils removed when I was three and they put me in this IV box where they put like ivy on your arm but you have to feel pain and and they put a mask on you before you go to sleep and they give you painkillers
Hey mom 👋 😊 bill all write
Calm down it be happysome
Take care of him
Love GAynn God bless yàll❤❤
I know it is hard for me for getting my tonsils out sometimes, It sounds like my words can mix up and that is stuttering and that makes my words backwards. So yeah, I am still healthy and lose weight a lot. Thanks Emily, your are still awesome and strong, and have a great day.
I am praying so so so so so so so so so so so so hard for him and a 3 year old little girl on tick tock
yay for the swallowing study, this will help rule out neuro-muscular issues that can affect swallowing/choking issues. They have to rule this out, I know the unknown is scarey and I'm sorry for the upset. Hopefully they'll recommend a level of diet that he can take (as in types of puree'd food etc... level 1, 2, 3, or 4 level diets for swallowing issues. I know you though it was just a tonsil issue, but feeding studies are essential for kids who have been diagnosed with Angelman and similar musco-skeletal disabilities. You'd hate to have his tonsils removed if there was something more serious going on.
Are your in-laws helping out with your other kids? It’s a lot for you and Will to carry on your shoulders.❤️🙏
Her in-laws live in California
I only hope Will isn’t having to take time off from work !! But I guess that has to be the only way one of them is with Griffin AND the other kids 24 seven!!!! Hopefully Will gets a LOT of sick leave !!!!!
@@TitanTvMan7654 Oh, I thought they lived in Colorado.
Y are yall in the hospital?
I used to drool a lot thanks to cerebral palsy
They should running more tests on him.Also they over look things on him.
Next Wednesday is my birthday
HAPPY BIRTHDAY!!!!!!!! Hope u enjoy your day!!!
I think (I have a medical background) that you need to find a doctor who will take Griffin's tonsils out. It certainly seems like his tonsils to me & this will keep happening periodically until they're removed. Griffin also needs the botox for his own dignity & while I don't believe the botox had anything to do with it, if the doctors don't want him to have it because of this, he needs his tonsils out for that too.
Will Griffin leave his hands off an NG tube??? How did the food go that you just spoke about? fries?????? I'm glad the doctors and staff finally got through to you, you seem a bit more reserved about the whole thing - a bit. Hang in there Em and Will. I hope you have some help at home also. You are both sooooooo wonderful! HUGS (and prayers) for all. P.S. how can they do a swallow study when they don't give him regular food, of course it'll be normal when he has squooshy food! What did they feed him to make the swallow study??
It’s got dye in it and it’s a liquid that can be pushed through NG tube down the nose or pt drinks it like contrasts for CT scan. It makes the GI tract glow and he’s put under imaging. It’s not solid food no way that would cause aspiration.
@@crohniequeenab oh, ok, thank you!
but seems it doesn't show the point where it has to squeeze thru tonsil area
The Till
Are you still friends with our landing crew
Yes
❤😂😢😮
🙏💜🙏💜🙏💜🙏
Your son has the same disability that I have seizures
A777
Ask for a patient advocate and don't take no for an answer
She did watch past video
Just noticed your lisp today...