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Five Feet Apart - Official Trailer Reaction 

Finely Taylored
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2 авг 2024

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Комментарии : 35   
@ambergoff7908
@ambergoff7908 5 лет назад
I have Cystic Fibrosis. I'm 26 and was just approved for a double lung transplant by my transplant team. (We're just waiting for final insurance approval before I can be actively listed on the waitlist.) CF is a disease that affects us (people with CF) all pretty differently. None of us experience the EXACT same things, but we do experience a lot of the same things. Most of us struggle more/most with lung complications. A lot of us struggle a lot with digestive issue/pancreatic insufficiency. Some of us deal with developing diabetes as a direct result of having CF, as in wouldn't have it if we didn't have CF. (Not all CFers develop diabetes, but quite a few of us, including myself have it. And it generally develops in our teens and 20s as a result of damage to our pancreas.) Some of us deal with liver and kidney issues as a direct and indirect result, respectively, of having CF. Cystic Fibrosis is often thought of as just a lung disease; however, that is very far from reality. CF affects everything, from multiple major organs to bone density to joints (some people with CF develop CF-related arthritis because of chronic inflammation). And from person experience, one of the hardest parts about having CF is, in fact, that we are not supposed to be around other people with our same disease. We tend to make incredibly close bonds and friendships with each other via social media and it's so hard to not be "allowed" to hang out, in person, with some of our best friends because we could potentially pass infections between us and it's a very real possibility that it could kill one or both of us. Some CFers choose to take that risk, as some feel the benefits of the connection are greater than the potential risks. Cystic Fibrosis is genetic. In order to have CF you have to receive two defective genes, one from each parent. Everyone gets one set of genes from each parent. If you receive one "good" gene from mom and one defective gene from dad, you do NOT have CF, BUT you are a genetic carrier of CF, which means you can pass a defective gene to your children. If both parents are carriers of the defective gene there is statistically a 25% chance each child they have will have CF, a 50% chance of being a carrier, and a 25% chance of have two normal/healthy genes (so no CF and not a carrier). Genetic testing is available to find out if you are a carrier or not. CF is also tested for in newborn screening; however, only the most common mutations are tested for then (there are over 1700 different types of known mutations that can cause CF). It is most common among caucasians of European decent, but can affect all races. There are over 70,000 people with CF worldwide, with approx. 30,000 of them being in the United States. About 1 in 3000 caucasian newborns are born with CF. Approximately, 1 in 35 Americans are symptomless carriers of the defective CFTR gene. That was a lot of info. If you have any more questions, I'd be happy to answer them. :) Thank you for doing a reaction video for this movie. Its the first reaction video I've seen from someone who doesn't actually have CF or from someone who doesn't have someone close to them with it. This is also the first big film with CF so we're all hoping for it to portray CF accurately enough to show how severe CF really is and hoping for a lot of awareness! Awareness= fundraising= research= better drugs/treatments= someday a CURE!
@elizabetha5561
@elizabetha5561 5 лет назад
Amber Goff another cf-er just listed
@ambergoff7908
@ambergoff7908 5 лет назад
@@elizabetha5561 I was officially listed yesterday! :D I hope your call comes soon! And you have a smooth surgery and recovery!
@chakshudenod8107
@chakshudenod8107 5 лет назад
the world is unfair to so many people.. hope you get on to the mode- KICKASS soon... hugs
@sophiasleep8960
@sophiasleep8960 4 года назад
Wow u wrote alot
@kacp6485
@kacp6485 4 года назад
Keep fighting girl! You can beat it🥳
@avabacci4315
@avabacci4315 5 лет назад
I cried for an hour, my mom was worried
@WalmartJedi
@WalmartJedi 5 лет назад
It was such a tear jerker of a movie.
@arthurm.tellez275
@arthurm.tellez275 5 лет назад
that's because you have a lot of love to give and you express it by contact with others, i hope your boyfriend know how lucky he is. So Cry away and enjoy life.
@paolamachado4557
@paolamachado4557 5 лет назад
I watched the whole movie and I cried soooooo much
@bobbyriesco6420
@bobbyriesco6420 5 лет назад
So glad I put this suggestion on your page 😁
@JLamstudio
@JLamstudio 3 года назад
This movie takes on more relevance during Covid-19.
@OakGroveDolls
@OakGroveDolls 5 лет назад
You should totally read the book!! I'm also a crier, and the book made me bawl😂 It was absolutely amazing and it made me even more excited for the movie!
@kailynroyall4970
@kailynroyall4970 5 лет назад
maddie claire the book made me cry so much too
@emmie7254
@emmie7254 3 года назад
Ive watched this 12 times and i still cry
@cjboss4274
@cjboss4274 5 лет назад
ohhh looks goood !! 😊 very sad to go through that i think...Happy thanksgiving Taylor! 😀💖
@bosspayne9696
@bosspayne9696 4 года назад
I cried watching this movie
@RyansChannel0203
@RyansChannel0203 5 лет назад
You look beautiful, Taylor. Great reaction btw. Hope you have a great Thanksgiving. :)
@isabellad3980
@isabellad3980 4 года назад
I cry just because of the thought of this movie
@kacp6485
@kacp6485 4 года назад
Most of the reactions on this trailer are made by real CFers... Some of them said, that the fact the CF is mentioned here is way more important, that the fact that some two kids fall in love somewhere in the hospital.. I know exactly why did they say that, you know, CF is their life, but the romantic link is the only way, we, other people, can relate to it :-D I'm so glad you recorded this reaction, now i know i'm not the only one who focused on the lovestory part of the story💜😉 PD. you should know you're beautiful like an angel, girl😘
@manolialoumbardia4046
@manolialoumbardia4046 5 лет назад
I am excited for the movie and I just read the book and I cried in some parts while reading the book so I cant imagine watching the movie I will be balling my eyes out
@Camicazi
@Camicazi 5 лет назад
I really hope this movie doesn’t end like the fault in our stars or titanic were the guy dies in the end can we please have a happily ever after
@karlynch3356
@karlynch3356 5 лет назад
I'm really cry when I saw this
@amyrah8949
@amyrah8949 4 года назад
i just watched the movie, its cute
@karlynch3356
@karlynch3356 5 лет назад
I'm other language but I love this
@mayabaker6020
@mayabaker6020 5 лет назад
Your the only person who actually laughs st the same parts as me
@katiehindley2500
@katiehindley2500 5 лет назад
Hi I watched your video on the five feet apart trailer and u said u don't know what cystic fibrosis is well my little cousin had it and it's a genetic disease that affects the lungs liver intestines and other organs and what happens is your body produces too much thick mucus and it make it hard to breathe. If you catch another CF bacteria it can be fatal. If u catch a cold it can be fatal. My little cousin died last year in March at the age of 12 yrs. Old from cystic fibrosis.
@mikedurham3803
@mikedurham3803 2 года назад
The ending is sad
@sialalala2337
@sialalala2337 5 лет назад
💘💘💘
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