The Sad Reality Of Having Cystic Fibrosis (Bronch Surgery)
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- Опубліковано 2 жов 2024
- The sad reality of having Cystic Fibrosis. Just had bronch surgery. It's the most real I've been in a vlog. I really wanna show you all the hard parts of having a chronic illness, the bronch was done Friday & went well, just super junky lungs, but I am starting to improve a little, thank God! I hope you all enjoy this video. 💜💜😋
You’re being so unbelievably strong. You’re allowed to cry, grief and sadness are a part of chronic illness. But the fact that you’re so positive, loving and life-giving on a daily basis is inspirational and so damn commendable. You will get through this, we all believe in you ❤️❤️❤️
You are in my thoughts and prayers always! I hate this for you...your to young to be dealing with this horrible disease...I just can't imagine not being able to breathe...that must be so scary but you are handling it better than alot of people...you are such a trooper and definitely a little fighter and I'm proud of you for that! Just know I'm thinking about you and your family! Please don't say anything about giving up! I'm so sorry you have to endure all of this! There's so many people praying for you! I'm here for you...we all are! xo Hydie ❤🤗❤
I have asthma and terrible anxiety attacks and it’s not the same at allll but I know the feeling of not being able to get enough air and it’s terrifying and I’m so sorry but your attitude is amazing towards everything!
I had to undergo LFT testing last week which was not easy but i got an updated diagnosis with regards to my COPD.
It turns out that my COPD is severe but NOT at end stage according to my pulmonologist (i just love this guy btw) as he was quick to point out that i wouldn't have ever been able to make it to the office if i were in end stage emphysema. I'd be bedridden and on a Vent at that stage.
Next thing to do is get a sleep study done and get on CPAP again for my apnea. Hopefully mask technology has improved over the last decade because when I was on cpap a decade ago i went through several masks without much success. I swear i wish my ENT specialist was half as good as my pulmonologist because he still can't figure out why I have developed sudden hearing loss.
hey don't ever give up on anything you can fight through this and we are always here for you, you may be in a lot of pain now but later you will get better. but no matter what don't ever give up !!!!! always here for you xxxxx xo moya
KEEP FIGHTING GIRL
Girl you are the strongest person and will 100% be in my prayers regularly❤️ you are so genuine and real and you don’t deserve any of this.
i’m so sorry. i hope you feel better
When you were crying I did to your my inspiration
Birds Are life *to and *you’re. I’m terribly sorry. I do this to everyone.😬
Ohh its ok but I got to right and your (you’re)can be spelled ether way????but I got a good laugh out of it so I am good
ÅŸŁÅ .__. It’s all good
I have cf too I go to the same hospital keep fighting don’t give up
talia rawlins I am praying for you
Hunny dont u ever feel like u have to make excuses as to why u feel so bad. Just bcause ur lungs arent as bad as they cld b dont mean ur not sick. Any1 that's ever had a lung infection of any sort understands. Just bcause ur not as bad as u cld b dont mean u have it ez. No1 knows how u feel but u. I have a 13yr old daughter and I cldnt imagine her being in ur shoes. I am so sorry u feel so bad my heart is with u. I'm in indiana if I were closer I wld brng my little grl down to visit u I h8 u being alone thru this. I kno ppl gotta wrk I feel for ur mom having to leave u there. So happy u have ur peds nurses.. God bless and I've been binge watching ur vlogs for 2 days. Keep them up YOU ARE AMAZING xoxo
keep fighting and hope your doing good cf is hard but be strong
Girl keep fighting and know ilysm 💓💓💓💓
We’re all different and fighting our condition differently but you’ll get through it ! You’re strong , we’re all strong ! I also have Cystic Fibrosis, My usual hospital stay is 2weeks . #justbreath you should go check out my channel !
I am about as clueless as they get with make-up. You go girl
You are so strong an beautiful
An I love that! I wish you the best♡
Praying for you beautiful girl!
Don’t give up u are beautiful god challenges all of us a different way . You are strong and the devil tears u down. Don’t let him win give it to god.
Very pretty! Thank you for the makeup tutorial. Which Lancôme makeup did you use? I saw the compact. Maybe it was eyeshadow? Also, what is the name of the coconut water face spritz that you used? Be well, sweet girl!
Stay strong honey.
Your so beautiful ❤️❤️❤️
💜💜💜
Praying for you 🙏🏽
You are so strong
You look like Selena Gomez
Im praying for you hope you get better soon 🙏🏻
It's CF a where ness month make sure you wear you're purple.
I cried so hard you are so inspiring, in my opinion cf has made you who you are everyone in the world is blessed to have you with us. I know you hurt and we all send sympathy keep fighting lovley you are going to have a beautiful life. You don`t have to be ashamed of crying you don`t shed tears, but you shed light. I look at you and I am so happy to have you here. Everyone out there is fighting for something, I don`t have cf and I am not saying that it is anything like what your going through but I have been there trapped in hospitals so much. We love you keep fighting.
you are so amazing and strong
Keep fighting baby girl. We love you.😘
Thanks hunny your my inspiration
Keep fighting you are strong ✌😷.
Your really pretty without makeup
thanks hun!!
You’re so brave omg🥺💜💖
❤️
jeez, ur gorgeous!!
Be strong 💪💕
You are so cute
Hi haha I’m a new viewer, and you are so amazing hahah I was just wondering how old you are?? ❤️❤️❤️❤️❤️
18 she’s 18
Natalie Hamilton yea I kinda figured that out 🤷🏼♀️
do her parents have to pay everytime she goes to the hospital???
Yes, unless she has government insurance like Medicaid or Medicare. Most private insurance you still pay 20% plus deductibles , along with your monthly payment.
homero cortez my insurance covers it!