That moment when you puke your guts out... :) Thanks for watching, and don't forget to subscribe! ***WATCH YESTERDAY'S VLOG: • WELLNESS TEA & OLIVER ...
I'm coming to these videos from 2017, and I'm loving this family and can't help to comment on practically every one. You both have such lovely spirits. Thanks for taking us on the journey with you. I'm having a ball bingeing and getting to know you! Hope you don't mind comments on the older videos. ~cheers! Sherri
I have emetophobia (vomit phobia) and I'm currently sick with some upper respiratory crap (nose running, sore throat, caughing, fever etc NOT COVID tho haha) and I'm at the chocking from thick mucus stage... I watch your videos to get some courage to clean my lungs and not worry about puking
I think it is so inspiring what a positive attitude you have through all of your struggles. I just started watching your videos and your out look on life has made my day. I have to say that Peter you are an amazing person I don't think I would have the courage or patience to care for someone in the way that you do. I wish you too the best luck in your life you are so inspiring.
+Brittany Hi There! Thanks for watching and for your kind words! It means alot to know we have people cheering us on in this crazy journey called life!
My friend's little sister has cystic fibrosis also, and my friend told me that you are such an inspiration to her! You are one to me, also, as you taught me to live life like there is nothing wrong with it!! ❤❤
that castle was so beautiful in Scotland! I liked the "purple lights" around it. thanks for sharing Scotland with all of us vloggers! :-) you guys are the best! see you tomorrow!
I just discovered you guys and I am moved beyond believe at your wisdom! I don't know you but I think I love you. Wish you the best and am subscribing right now🌺🌞👍🏻
You are so much fun! I am a wheelchair user due to a rare genetic disorder and my son has classic autism. Sometimes it is hard to go out and fun, but I agree with you that it is worth it. We try to live life to the fullest and whatever happens, happens. Keep up the good work with your videos. Obviously it is intended to raise awareness of cf but you are so friendly and relatable to anyone, disabled or able bodied alike.
Hi, my name is Kat. My friends name is Kaylene. We're teenage girls who daily vlog our lives with chronic illness, vocational school, and being DJ's. I have fibromyalgia, and many other disorders/diseases and Kaylene has Basal Cell Carcinoma Nevus Syndrome. She's basically made up of tumors growing often and everywhere, and many other complicated health issues. I was wondering if you'd check out our channel? We're trying to build a community on our channel.
I didn't know emetophobia existed before I was 21 and I thought I was the only one in the entire world having a breakdown every time I get nauseous haha
+Nightcrawler NerdKing The hills in Edinburgh were too hard for my lungs to handle, so I used a wheelchair to be able to get out of the house and explore the city :)
+The Frey Life I saw that in some one else's comment but I didn't know what c.f. was but now I know it stands for cystic fibrosis but I still don't know what that is. My gf has cerebral palsy and I have Aspergers/ autism. I know life with a chronic illness is rough because if her. Her's affects only her body mine affects only my mind.
Nightcrawler NerdKing my son has classic autism and I love him to pieces. I am also a wheelchair user. if you don't mind me asking, is it easier to date someone who has a chronic illness? Does she understand you better?
Hi, my name is Kat. My friends name is Kaylene. We're teenage girls who daily vlog our lives with chronic illness, vocational school, and being DJ's. I have fibromyalgia, and many other disorders/diseases and Kaylene has Basal Cell Carcinoma Nevus Syndrome. She's basically made up of tumors growing often and everywhere, and many other complicated health issues. I was wondering if you'd check out our channel? We're trying to build a community on our channel.
Natalie W. Most people with Cystic Fibrosis live into their mid 50s these days, with medical advances. It also depends on if the person gets a lung transplant. People who have successful transplants can live even longer than that.
HliasXioNumber1 their vlog started as a way to update friends and family at home, sort of a diary of every day while living abroad. So that’s why. :-) cheers
Amber Mccaffrey When we were in Scotland, the city we lived in was built on very steep hills that were too hard for my lungs to walk up. So I had to use a wheelchair to get anywhere. Thankfully in the States, I don't usually need to use a wheelchair.
I'm coming to these videos from 2017, and I'm loving this family and can't help to comment on practically every one. You both have such lovely spirits. Thanks for taking us on the journey with you. I'm having a ball bingeing and getting to know you! Hope you don't mind comments on the older videos. ~cheers! Sherri
I just started watching you guys and I have been binge watching. You are so strong and I love your love for each other.
Kristen Adolph Thanks so much for watching and becoming a part of The Frey Life!
I have emetophobia (vomit phobia) and I'm currently sick with some upper respiratory crap (nose running, sore throat, caughing, fever etc NOT COVID tho haha) and I'm at the chocking from thick mucus stage... I watch your videos to get some courage to clean my lungs and not worry about puking
I have emetaphobia too. I’m sorry.
I think it is so inspiring what a positive attitude you have through all of your struggles. I just started watching your videos and your out look on life has made my day. I have to say that Peter you are an amazing person I don't think I would have the courage or patience to care for someone in the way that you do. I wish you too the best luck in your life you are so inspiring.
+Brittany Hi There! Thanks for watching and for your kind words! It means alot to know we have people cheering us on in this crazy journey called life!
I was just looking for a hyper pop song but this works too
My friend's little sister has cystic fibrosis also, and my friend told me that you are such an inspiration to her! You are one to me, also, as you taught me to live life like there is nothing wrong with it!! ❤❤
that castle was so beautiful in Scotland! I liked the "purple lights" around it. thanks for sharing Scotland with all of us vloggers! :-) you guys are the best! see you tomorrow!
I just discovered you guys and I am moved beyond believe at your wisdom! I don't know you but I think I love you. Wish you the best and am subscribing right now🌺🌞👍🏻
You are so much fun! I am a wheelchair user due to a rare genetic disorder and my son has classic autism. Sometimes it is hard to go out and fun, but I agree with you that it is worth it. We try to live life to the fullest and whatever happens, happens. Keep up the good work with your videos. Obviously it is intended to raise awareness of cf but you are so friendly and relatable to anyone, disabled or able bodied alike.
Hi, my name is Kat. My friends name is Kaylene. We're teenage girls who daily vlog our lives with chronic illness, vocational school, and being DJ's. I have fibromyalgia, and many other disorders/diseases and Kaylene has Basal Cell Carcinoma Nevus Syndrome. She's basically made up of tumors growing often and everywhere, and many other complicated health issues. I was wondering if you'd check out our channel? We're trying to build a community on our channel.
I have a phobia of vomit...!!!!!!!!!!!💋😍
I LOVE YOU GUYS..!!💋❤️😘
XxPaigeyLoverXx me too tho when it happens it rarely is as bad as i think it will be
Me three
Surprised Stephen King hasn’t written something on emetophobia. Personally, as long as I don’t have to smell it I’m fine.
Look at anneliese Michel 6 demons in rock on UA-cam
I didn't know emetophobia existed before I was 21 and I thought I was the only one in the entire world having a breakdown every time I get nauseous haha
Peter and his rippling biceps
Been there with puking my guts out. Worst feeling ever
I have a phobia of vomit and blood I throw up everytime I see blood or throw or I gagg
You got this buddy!!
I have cvs cyclic vomating syndrome and vomiting is my whol life
May I ask why you are in the wheel chair? I read about your lungs not being able to handle it. I just wondered.
+Nightcrawler NerdKing The hills in Edinburgh were too hard for my lungs to handle, so I used a wheelchair to be able to get out of the house and explore the city :)
+The Frey Life I saw that in some one else's comment but I didn't know what c.f. was but now I know it stands for cystic fibrosis but I still don't know what that is. My gf has cerebral palsy and I have Aspergers/ autism. I know life with a chronic illness is rough because if her. Her's affects only her body mine affects only my mind.
You can watch our Cystic Fibrosis Q and A to find out more
Nightcrawler NerdKing my son has classic autism and I love him to pieces. I am also a wheelchair user. if you don't mind me asking, is it easier to date someone who has a chronic illness? Does she understand you better?
@@thefreylife look at anneliese Michel 6 demons in rock on UA-cam
poor baby
I'm a nurse soon to be :)
Hi, my name is Kat. My friends name is Kaylene. We're teenage girls who daily vlog our lives with chronic illness, vocational school, and being DJ's. I have fibromyalgia, and many other disorders/diseases and Kaylene has Basal Cell Carcinoma Nevus Syndrome. She's basically made up of tumors growing often and everywhere, and many other complicated health issues. I was wondering if you'd check out our channel? We're trying to build a community on our channel.
i have cf as well it sucks
No you don't liar
how do you know? you are rude
how long does mary have left to live?
Natalie W. Most people with Cystic Fibrosis live into their mid 50s these days, with medical advances. It also depends on if the person gets a lung transplant. People who have successful transplants can live even longer than that.
I did look it up and I think that you can do this
Yes ok viod
How old are you two
Allison Whitlock 25 and 27...but I'm almost 26 :)
a
I just subscribed😍
why every vlog you are sick?
HliasXioNumber1 their vlog started as a way to update friends and family at home, sort of a diary of every day while living abroad. So that’s why. :-) cheers
you are adorable. :)
Why is she in a wheel chair??
Amber Mccaffrey When we were in Scotland, the city we lived in was built on very steep hills that were too hard for my lungs to walk up. So I had to use a wheelchair to get anywhere. Thankfully in the States, I don't usually need to use a wheelchair.
Oh ok The Frey Life