WhatTheCF
@WhatTheCF
The only way to live with Cystic Fibrosis is with no fear, good health insurance, and a vile sense of humor. 🤘💩🖕🤣 My name is Jenn and I have CF.
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Yeah it does! So do it every day even if it's horrible and ESPECIALLY if it's hard. . . . #musicislife #breathingislife #cfislife #CFaware #cysticfibrosis #justbreathe instagram.com/p/BwIwhDNHRx5/…
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What The CF (@whatthecf) • Instagram photo
What The CF (@whatthecf) • Instagram photo
Yo CF is kicking my ASS this month! Anyone else? . . . #cysticfibrosissucks #cflife #cysticfibrosis instagram.com/p/BtzaUnunYj6/…
How do you stay so thin??? So much fun! #cflife #cysticfibrosis #cysticfibrosismemes #CFfun #WhatTheCF #cysticfibrosisfun #poophumor #cysticfibrosislife #CFproblems
"Guilt doesn't only flare up on the bad days; it spills over into the good ones, too. People often think in binaries; you're either sick or you're not. But with this disease, you're sick and you're not." on.cff.org/2GjpzJk
Tobi Podhaler is the shiz. #tobipodhaler #tobramycin #breakingbad #jessepinkmanbitch #CFlife #cysticfibrosis #cysticfibrosismemes
Womp womp instagram.com/p/BtLpE8in8zM/…
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What The CF (@whatthecf) • Instagram photo
What The CF (@whatthecf) • Instagram photo
Never really 100% sure if I'm telling someone "I love you", "rock n roll" or "hang ten" but at least it's all positive vibes, right? 🤟🤘🤙#isitjustme #noncfpost #iloveyou #rocknroll #hangten #totallytubular #WednesdayWisdom
Yup. Excellent read by @thejenn link.medium.com/YdmkuOCqtT
link.medium.com
I Have Cystic Fibrosis and This is What I Have to Say About Five Feet Apart
Hi. I’m Jenn. I have cystic fibrosis (CF) and yesterday I learned about Five Feet Apart.
2 months late, but YES! 1000% yes. My exact reaction when I found out about this BS movie. #cysticfibrosis #FiveFeetApart #idontneedyourpity google.com/podcasts?feed=…
A very handy skill to have when representing a person with #CF. While I haven't seen #FiveFeetApart the movie (obvs), I did read the book and that super fun aspect of #cysticfibrosis was pretty much a non-issue. Kills the romance I guess ... #CFlife
Fantastic! @G17Esiason Been stuck in the "related posts" vortex for about an hour now. gunnaresiason.com/dont-say-that-…
We're on #Instagram and #Facebook too. Come find us at @whatthecf. facebook.com/whatthecf instagram.com/whatthecf
If you got out of bed today, you did your meds, and you gave it your all even though you felt like 110% shit, you're doing okay. And if you didn't do any of that, tomorrow is another day. #onedayatatime #fakeittillyoumakeit #hereslookingatyoukid #positivevibes #cysticfibrosis
When your significant other asks mid- meal if you've already taken your enzymes. Cause that's true love. Also, I swallow enzymes like a ninja. #truelove #cflove #itsthelittlethings #CFlife #cysticfibrosis #anythingispossible #cfawareness
My immediate gut check reaction to finding out there's a movie coming out about teens with #cysticfibrosis? People better not start looking at me all "poor fucking you." Ain't nobody got time for that. #fivefeetapart #therealCFlife
@achdandme thought you might find this interesting. I really hope the film #fivefeetapart doesnt make the general public feel sorry for those with CF but shows those with the illness living happy, mostly normal life's! Realistic awareness is always best teenvogue.com/story/what-you…
teenvogue.com
What It's Really Like to Live With Cystic Fibrosis
"Not all awareness is good awareness."
As someone who has #CF and a strong desire to live life to the fullest, it's very difficult to be around people who DON'T want to grab life by the horns. #JustDoIt #CysticFibrosis #youonlygetonelife #noregrets Here's to grabbing 2019 by the balls! #NewYearsEve2018
Loving this blog by @thevftos. For example: theviewfromtheotherside.com/history-behind… Incidentally, "salty tasting skin" is one of the symptoms of #CF that I find most humorous. Because, you know, the safest way to identify a sick person is by licking them. #WhatTheCF #CFsymptoms #SaltyAF
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