I have CF and jeez I must say even though its a video this annoyed the hell out of me 😂

How are things going now?? 2023 . ..

Dear so pretty 😍 please spit that mucus which stuck in your lungs while you cough cough toy by taking a deep breath from your nose dear

I have CF too, for the last 2+ years now I've been a much healthier weight( debatably for the right reasons) but, now I have MASSIVE bloated, distension-esque stomach area. If I suck it in to attempt to look 'normal' I can barely breath.

What is her channel

The issue is when CFers don't have any medical ensurance issues. These ensurances pay for EVERYTHING for these people! A patient who is on a ventilator, and who has a trach, cant get vital stuff that they need because they have so many restrictions thanks to the CFers. A ventilator patient who has thick secretions and gets horrible mucous plugs can't get a vital medication that would actually help them. Why? Why do patients who have horrible mucous plugs and who has a tracheostomy can actually die from these plugs. They can't get a medication that would help thin the patient's mucous they cannot get this drug, because only the CFers get it. I get that CFers are sick. OK, I get it. But you don't see CFers with tracheostomy tubes, who are on a ventilator. These patients don't need a ventilator. Not only that, getting a VESt for a patient who is unable to cough well, who has a trach and a ventilator is nearly impossible. WHY??? Because it's restricted to the CFers!! I'm probably losing my vest which has helped me so much, because medicare and medicaid is refusing to pay for the thing, thanks to the restriction to YOU GUESSED IT!!! THE CFERS!!! Another thing? That vest has over 1000 hours, which prooves that I'm using it, however HILL-ROM is going to come and take my vest, because I don't have a diagnosis of CF. Another thing I notice? CFers are always griping and crying about how it's so hard. OK, Grow up and live with it. You have CF. You gotta do your treatments, and you gotta take your treatments. Be thankful that your ensurance is covering all that equipment. Cause they're probably taking my vest since I am not a CFer!!! Yet let's get thi straight. I have a trach, and am on a ventilator. What next Are they going to restrict ventilators to home patients and say that they'll only cover them for CFers? They do that? Us ventilator patients are DEAD!

I deliberately wanna love a girl with cystic fibrosis in America, if I could.

Don’t know if you know this, but you can also do a port in the inside of the arm. Not all doctors do it, it’s a bit less common, but a good option. The port itself is smaller than the one in the chest, and it’s more durable than a PICC.

I hate that people always ask "since when do u have it?" After I explain that you're born with it!!!!!

Thank you so much for this! I’ve been trying to find something to really work on my inner chest muscles. This was amazing. Loved following along!

I don't have CF I have CFTR dysfunction which is kinda similar. My friends always compliment me for being so slim but to be honest I'd rather be heavier...thanks for the tips ;)

Thank you so much!!!!♥️♥️♥️♥️♥️

So pretty much, I have a lot of symptoms of Cf, I would tell my mom but I'm scared she won't believe me, can you give me some tips please. Because, I don't want them to get worst, and I once even sneezed and out my mouth we, is yellow, thick, sticky mucus. That's the type of mucus CFers have. Once again, can you give me some tips please.

Your just faking it a persona said it to me and I’m like not to be rude but not all need tubes or have to stay at the hospital it hurt my feelings so I told them to maybe look it up more

Sorry, can't hear.

Same, there’s so many cases yet it’s rare to find other people with it. I’m 18 in 4 months and I’ve been diagnosed since I was born and my sisters 24 and she’s also been diagnosed since birth.

I'm struggling because I'm in a living situation where gaining weight isn't possible, even with my Gtube. I'm 82lbs and it scares me. And I know people in these comments probably don't care, but I don't have anyone to talk to about my CF problems.

I know this is a "what not to say to a cfer" but....i pissed off

Thank u so much for talking about the beginning bc that's the most important. We all wanna be big or huge but as we all know the road to it is very hard but we need to know that we can get there by just starting. Again thank u so much.

God I love new Orleans

What is this channel?? I have cf and just curious why there is someone new in each video

i always write that on get to know me papers!!!

i really love this channel😭 i am a 16 years old cf patient and it is very relatable and very helpful. thank you so much!!😭😭

One of the nice things about women with CF is they have lovely voices. Good luck with everything and thanks for the information regarding your diagnosis.

Hi Chelsea, my daughter and I just did some yoga with you, we sure would like to see more videos, maybe in front of the ocean 🏝🌅

Thanks guys for making this video, I had to recently explain the situation to my husband about why my stomach is so extended all the time why and why it looks like that you know he's not too sure everything about CF just yet we've been married for 7 years but I was only diagnosed at 15 years old so you know it's pretty hard but I had to show him this video so maybe you could understand it better because now I'm 30 years old in March 6th 2019 is when I will officially be 30 years old. So I hadn't watch this video to explain the cystic fibrosis got and what it's all about and why we haven't and it's just a thing we all have this is the fibrosis family has

yuygi

Thank you Miranda. You are so well spoken and openhearted and it is very helpful to listen to your videos. <3

good luck in your new adventures bro!

They tested me by a sweat test

I was also born in 89. I was diagnosed at 15

Same things i did too + Ginger tea 😉 xx

Do you have dysautonomia?

Yeah Tara I know the feeling of having a feeding tube as well but I had it Taken out about year ago, left another small hole, my second belly button. Lol

Wow, you are a very intelligent young woman , thank you for sharing with us.

For me those exact same things are working. No dairy, no meat, very little gluten, no processed foods and yoga. I would like to add drinking enough water every day to prevent DIOS. I am so happy that a lot of cfers are focusing on diet these days, I think it is essential to our wellbeing. We do not have to live with these issues, there are ways to improve the belly situation! Great video, lots of love from germany!

If you haven’t been able to get your lung function back. Try exercising while doing treatments. My lung function nearly doubled.

I had a blockage as well

Hi Chelsea yess I have the same belly issues effecting my lungs and gi.Im 29 nd have CF

When I drink Ensure it makes me hv gas, but I guess most milk does. Lol

I love this channel.

For me it’s pizza or anything with tomato sauce...And I def need extra enzymes with pizza and anything with a lot of cheese...What helps me is warm peppermint tea ☕️

It's very common I also have that issue

The enzymes brake down the fat and stop

CF hero. I'm on a trial as well

Congrats

I totally understand the GI issues, I'm the same way.

Great to find others with CF. I'm 29 years old diagnosed at 15 had it since birth.

Oh man! One of the most JERK things I have EVER said was to a very dear CF Friend of mine, asking her if she was pregnant (after YEARS of trying) only to have the response, "No, it's just CF belly." I seriously had a major 'I'm an A-Hole cry about it with my husband later... I think I cried like 3 times about how inconsiderate I was. Made me so sad. @sabrinawalker

Yo i totally agree with all of this. I think the degree on how sick you are at the moment has a lot to do with it. For me it also has to do with certain foods like diary products or things like soda, or certain fasts foods and such. Usually when im really bloated or just big in the belly, I like to drink some hot tea.