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#cysticfibrosis

Posts tagged as #cysticfibrosis on Instagram

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NEW POST up on my blog https://eloiselaughlearnnurse.home.blog/ . . Each Tuesday I intend to post about a different condition I come into contact with the most on the ward I work on. Just to give some information for those interested. . . "I never knew anyone with Cystic Fibrosis growing up, so I didn't know much about it until I starting my training. The ward I work on.. we see it a lot. It is something I have a real interest in at work and I feel is something that should have much more awareness out there than it does currently.  I'm sure most people have heard of it(I hope anyway) or some may even know someone who has it. Most people will know it to be to do with the lungs. But it's much more than that" . . For the rest of the post go at my blog 😁. . . For more posts follow ma insta 🤷‍♀️💁🏼‍♀️ . . For more info on CF visit @cftrustuk 💛. . . #nursingblog #nurselife #nurseblogger #childrens nurse #nurselife #bloglife #blogger #blog #newtothisblogthing #follow #cysticfibrosis #cf ,#,newblogpost
FIVE FEET APART EEEEEEEKKK I CRIED SO MANY TIMES IN THE MOVIE IT WAS SO GOOD AND SAD AHHHHHHH #fivefeetapart #colesprouse #haleyluhoo #stella #and #will #willandstella #justinbaldoni #cysticfibrosis #lungs #art #artistsoninstagram #procreate #fanart #digitalart
Wist je dat het #eiwit CFTR een kralenketting van 1480 kralen is? #taaislijmziekte #cysticfibrosis #lichaam #menselijklichaam #lijf #biologie
- Gemeinsam Mukoviszidose besiegen - Mukoviszidose ist derzeit unheilbar, aber Organisationen wie Mukoviszidose e.V. arbeiten immerzu daran, die Lebensqualitäten und die Lebensdauer der Leute zu verbessern. Durch Forschung, aber auch durch direkte Patientenhilfe. Alleine in Deutschland sind ca 8000 Menschen betroffen. Schon kleine Geldbeträge können den Patienten helfen und die Forschung vorantreiben.  Deswegen lasst uns spenden. Postet bis zum 01.06.2019 ein Foto von eurem Exemplar von "Solange wir atmen" (egal ob Ebook oder Taschenbuch) in eurem Feed. Verlinkt mich darauf oder nutzt den Hashtag #solangewiratmen und ich spende dafür 1€ an Mukoviszidose e.V. (Infos zu der Arbeit finder ihr auf www.muko.info) . . . #angelwingverlag #cf #mukoviszidose #bookstagram #instagram #spenden #krankheit #lasstunsspenden #instabook #jugendbuch #cysticfibrosis
When your cousin has a cold so you take extra precautions 😷😷 #twinning#cysticfibrosis#cousins#chroniclness#mask#infectioncontrol
CPT is done to mobilize secretions and to also help patients to better oxygenate and ventilate once the bronchi are clear of secretions.  #copdawareness #copd #nurse #nursepractitioner #rtschool #respiratory #rt #respiratoryboards #respiratorycare #respiratorystudent #respiratorytherapy #medicalstudent #mechanicalventilation #arterialbloodgas #cpt #cysticfibrosis #arterialbloodgases  #rtstudent #certifiedrespiratorytherapist  #registeredrespiratorytherapist #respiratorytherapist #رعاية_تنفسية #علاج_تنفسي
Registration is a mere 2 weeks away folks!! . Are you and your friends ready to show off you AMAZING lawn bowling skills?...Ready to have a great time while admitting you in fact have zero lawn bowling skills? Either way, we can't wait to see all level of skills, costumes and fundraising all to raise awareness and funding for Cystic Fibrosis Canada . - Registration *BAM* May 7th, 12PM - Event *BAM* Evenings of July 18th AND July 25 (Did you do the *BAM* sound effect?) . . . . . . #cysticfibrosisawareness #charity #aworldwithoutcf #cysticfibrosis #cysticfibrosissucks #cf #cfstinks #volunteer #volunteers #supercool #fundraiser #lawnsummer #lawsummernights #lsn #fun #friends #yycevents #yycnow #yyclife
👶🏻🔬 Infertility as per the American Society for Reproductive Medicine (ASRM) Tue, 23.April.2019 #medicine #doctor #ivf #pgd #fertility #infertility #pregnant #pregnancy #health #wellness #asrm #genetics #reproductivemedicine #cysticfibrosis #downsyndrome ------------------------------------------------------------------------------------------------------------- العقم (من موقع الجمعية الأمريكية لطب الإنجاب) 🔬 تعريف العقم: عدم القدرة على الحمل خلال سنة من المحاولة بدون إستخدام أي موانع.. أو عدم القدرة على الحمل خلال ٦ أشهر إذا كان عمر المرأة ٣٥ وأكثر 🔬 ١٠ لي ١٥% من الأزواج في العالم يعانون من العقم 🔬 ثلث مشاكل العقم بسبب الرجل، الثلث بسبب المرأة والثلث الآخر بسبب عوامل مشتركة 👩🏻👨🏻 🔬 أسباب العقم: العمر.. مشاكل في التبويض (بسبب أمراض مثل تكيس المبايض، الغدة الدرقية، الهرمونات).. تشوهات في قناة فالوب، الرحم.. العنصر الذكوري (تشوه/قلة/عدم تكون الحيوانات المنوية، السمنة، التدخين، السكري، التليف الكيسي cystic fibrosis، أدوية مثل الماريوانا).. طفرات جينية 🧬 🔬 من نراجع إذا عندنا مشاكل في الحمل/العقم؟ - للبنات: طبيب/طبيبة نساء وولادة (تخصص عقم) - للشباب: طبيب/طبيبة مسالك بولية (تخصص عقم) 🔬 هل ممكن يكون العقم بسبب طفرات في الجينات أو الكروموسومات؟ 🧬 إي ممكن.. مثال: 👨🏻‍⚕️ الشباب: متلازمة كلاينفلتر، متلازمة داون، طفرات جينية على الكروموسوم Y، عدم تكون
Another day, another peak. Stunning day for it, and only needed Hank for a small section of it. Feeling like things are proper improving again! #cysticfibrosis #invisibleillness #cfaware #cfnz #newzealand #mountains #hiking #campingwithdogs #destination_nz #ruffwear #icebreaker
He's also a husband, father, respiratory therapist, goofball, oh, and savvy #cysticfibrosis patient.
Did you know...? People with cystic fibrosis taste salty. CF affects epithelial cells in the skin's sweat glands. Kids with CF may have a salty "frosting" on their skin or taste "salty" when their parents kiss them. They also may lose abnormally large amounts of body salt when they sweat on hot days. #cfawareness #cysticfibrosisawareness #salt #salty #cysticfibrosis
Get ready for Saturday, April 27th! The villains are bringing back the 65 Roses show benefiting the @cf_foundation on behalf of @thegarbergforce! Since 2013, LHTG has earned over $20,000 to help the 70,000 individuals fighting this disease find a cure. LHHSGUILD.COM #curecf #65roses #cysticfibrosis #lhtgfamily
Haven’t play in a while , i was inspired by @claire.wineland Story about her life and having CF (CysticFibrosis) . I have to say to everyone with cystic fibrosis, you are the strongest people out there . You smile through it all . You will forever be heroes. #livelife #cysticfibrosis #endcf #fivefeetapart  #dontgiveuponme #clairewineland - Don’t give up on me by @andygrammer
Help promote CF Awareness and wear The Garberg Force or LHTG 65 Roses shirt on Thursday! Post your photo and tag us!  Take part in annual group photos too: LHHS: Meet at the tables by the theater right at break! UCLA: Meet in front of Royce Hall at 6:30 PM! OCSA: Check with OCSA team leaders, Larkin Ten Elshof and Landon Wouters. EDHS: Check with EDHS team leaders, Meghan Broadwater, Harrison & Kendall Bangert #cysticfibrosis #cysticfibrosisawareness #curecf
Smoothie bowl...yes please always🤗
Working out for the first time in 15 months. Why? Because with each of my babies, I have had crazy amounts of pain and issues with my back and hips that I wasn’t able to workout! It was SO hard each time. I always wanted to be the fit preggo momma but I never could! I was thinking today that truly just starting can sometimes be the hardest step. As I was finishing an audio book while running, something he said was “Future success is dependent on what you do today.” Those little, “insignificant” things today, DO make a difference! What is one thing you can do today to start?!?
So two years ago today I lost a brother/best friend. Everyone experiences passing of a loved one differently. I have been to many funerals the last couple years some older some younger and have watched how people go through with it. I may be different with passings an look at it differently. The person who passed definitely doesn't want to see people sad. So I look at it as an opportunity and as an experience. I wish nobody had to go through the death of someone but it’s life and sometimes life can be great and sometimes it gives you struggles. Either way look at it as the times you were able to have with that person sometimes good sometimes bad . Just remember they will always be looking after you, watching over you, and even though they aren't there physically they're there.  #cysticfibrosis#bestrong#grow#cfwarrior#findacure#bestfriend#brother#untilwemeetagain
I made a promise four years ago and saw it through today. I am proud to say that my beautiful mane raised $2000 for the Cystic Fibrosis Foundation and will soon be made into a wig by the Wigs for Kids foundation as well. The flow will return again one day. #sigep #cysticfibrosis #wigsforkids
Because I can’t remember the last time we took a picture together without the babies 💕 #husband #tiredparents #wecleanupwell #cfmama #cfparents #saltysquad #cfawareness #bestfriend #cysticfibrosis
BLAST OFF 🚀  Little Miss Janet rocked her Sinus and Chest CT Scan today!! #janetswish #cysticfibrosis #curecf #fucf #fuckcf #cfawareness #cfstrong #cfsucks
Guys/Gals we are down to 12 days until the walk. We are still in need of your help to beat our goal this year! Also if you are coming to the walk please register with our team. We need to know ASAP because we have to order the t-shirts!  Registration can be done by clicking join team at supportluke.com.  Please let us know your t-shirt size if you can make it and we will get you a shirt! #lukesskywalkers #greatstrides #greatstrides2019 #cfsucks #cysticfibrosis #cysticfibrosisfighter #cysticfibrosisawareness #cysticfibrosissucks #cysticfibrosiswarrior #cysticfibrosisfoundation #btfu #beardeddad #beardedvillains #givetomorrows #lakeland #lakelandflorida #munnparklakeland #munnparkhistoricdistrict #munnpark
Claire always "Lived Proudly". What is your intent? Head to www.myintent.org to choose your word and style, and receive a special 33% off your purchase with the promo code "CLAIRE". Our partnership with @myintent will donate back 33% of every purchase to Claires Place Foundation.
I have to #bereal with you all... . Ever since I announced I will shave all my hair off if my #andreasangels team raises $50,000 by the end of the year for the @cf_foundation I have been feeling quite terrified! . Yes, terrified of going bald because, let’s face it, I’m vain and I like how I look with hair! . Yet, I’m more terrified about not raising the $50k because I know me...I will feel like a failure! I know, I know, I’m not a failure but I’ll still feel like one. . However, I’m mostly terrified about not funding the science that has saved my daughter’s life and the lives of many CFers, plus the lives they will continue to save, plus provide ALL #cfers with wonder-drugs, and mostly until they find a cure for all #fibros and #cysters worldwide! . I NEED YOU!!!! . Join our fight. Register to raise funds on behalf of @_arider here: http://fightcf.cff.org/goto/andreasangels (link in bio) . Or make a donation clicking on the same link, then PLEASE ask family and friends to match your donation. . Thank you, thank you, thank you!!! . #cf #cysticfibrosis #cff #cysticfibrosisfoundation #cfirl
Super #happy to have you all #read about @kirataylorsings in the #may issue of #citytocountrymag Living with #cysticfibrosis Kira Taylor #advocates for others and works hard to bring awareness to #antibullying She’s a #singer #songwriter and #inspiration to many! Not your typical 19 year old. Subscribe to www.citytocountrymag.org 🔥🔥🙏🏼🙏🏼👍🏼😘 Writer: @suemcaughey
Five Feet Apart- 2 hrs 15 mins- Drama, Romance- 🧔🗣 He Said—> This his sort of your cliche teeny bopper love story that has been played time and time again but this one still tugs at your heart strings and was performed well by a relatively starless cast. This movie was funny, cute, sweet and very sad! I can honestly say I’m enjoyed this movie a lot and give this movie 3 1/2 Reels out of 5 Reels nd label it “Keeping it Reel” 👩‍🦰🗣 She Said—> This movie is sweet, touching and heart breaking. It does a great job illustrating the complexity of Cystic Fibrosis and teenage love. I really loved every single character in this film and loved how the different personalities were highlighted and they let them shine. This WILL make you cry, so be ready. Yes, the storyline may seem similar to other movies, but it was still a sweet watch. I give this film 4 reels out of 5 and call it the "Reel Deal". #fivefeetapart #movie #movies #lovestory #cysticfibrosis #cysticfibrosisawareness #sadmovies #film #couplesgoals #couple #movielover #movielovers #moviegeek #moviemagic #movieaddict #moviestarplanet #moviestar #filmreview #moviereview #hesaidshesaid #review #minnesota #critic #moviecritic #love #boxofficekingandqueen #boxoffice #cinema
i’m so exhausted.. i just had dance and it was so intense today but that’s good because we’re going to fierce at our last competition💗 ———————————————————————— [ #colesprouse #fivefeetapart #haleylurichardson #cysticfibrosis #riverdale #book #love #blue #willnewman #stellagrant #photooftheday #gainpost #lfl #f4f #wella #lilireinhart #camilamendes #kjapa #bughead #sprousehart ]
#yellowheartsquad it’s important to spend time around people who make you laugh, smile, and feel good overall. Today, I had lunch with my good friend @ziplu on the #disney backlot. It was so great to catch up over good food. I left feeling rejuvenated and inspired. Jamie and I have been friends for 15 years. She works with the group of people responsible for so much of the incredible work that Disney does in the world, including the support with my children’s book, “the Spider Who Never Gave Up!” In the moments that I feel lowest, it’s people like her that lift me back up and remind me why I’m fighting. #fightcf #cysticfibrosis #transplant #donatelife #gratitude #hope
CIAW( Canadian Infertility Awareness Week). 1-6 couples suffer from infertility. Briar is our success story❤️ it was a long road for her. It’s proving to be just as tough of a journey to a sibling.  It’s expensive, it’s mentally and physically draining and it’s just not something you can or want to talk about all the time. This week of this year  being in the thick of it again it’s a struggle to talk about it. We’re hopeful, we’re working on it, we have big decisions to make for our family. I want to leave this message though with something important. Coverage...want to know what we get to write off each year. Mileage. That’s it, that’s all. I hope that we can someday change that! #infertilityuncovered #ciaw #16 #infertilitysucks #infertilityawareness #ivfsupport #ivfjourney #siblingcycle #failedtransfer #rollercoaster #journeytooparenthood #herewegoagain #cysticfibrosis #65roses #beatinginfertility #everystorycounts
Sixty-Five Long Sleeve Shirt Cystic Fibrosis themed long sleeved shirt, part of the "Just Breathe" collection  Super soft Mens/Unisex Gildan 100% ringspun cotton.  For sizing guide visit site.(Link in Bio) $2 of every purchase will be donated to #cysticfibrosis until CF stands for #curefound . . . . . . . . . . .
Happy Earth Day!! 🌎🌏🌍 just a sample of the #cf medical type waste produced daily / weekly / monthly  I try to do my part and separate what I can put in the recycle bin...but who knows if that ever gets recycled?  This doesn't even account for: • 10 - 12 glucose test strips ------> EVERY DAY • lancets • insulin pump infusion sets • infusion set packaging • carbon footprint to get all this stuff delivered by courier  thank you #cysticfibrosis science, sorry #planetearth  #cfirl #cfrd
@chickfila Spirit Night for Ru’s Crew was SO fun. I can never get enough of this milkshake slurpin’ baby shark’s cuteness. Sweet Ru is smart, funny, and strong-willed—just as God created her to be. CF does NOT hold this girl back!!! • If you’d like to support Ru’s Crew and research on cures for Cystic Fibrosis, you can find several options on my website under the ‘Give Support’ under the ‘About’ menu. {Link in bio!☝🏻} • #chickfila #chickfilawesthills #knoxville #spiritnight #chickfilaspiritnight #untilitsdone #greatstrides2019 #cysticfibrosis #cf
Just a “little” trash generated from an infusion site change and a sensor change... #insulinpump #diabetes #diabetescfrd #cysticfibrosis
human touch. - - - 𝐚𝐜 mine! 𝐜𝐜 mine 𝐩𝐜 saddertutorials  𝐬𝐜 none  𝐟𝐜 1,140 𝐦𝐨𝐯𝐢𝐞 five feet apart (2019) #fivefeetapart #colesprouse #haleylurichardson #cysticfibrosis #explorepage #edits
I drew the beautiful @lilly_mei_knowles 💜 i tried my best to draw the hospital town but it was very hard. I love her, she is such an inspiration and her smile makes me feel happy and makes me smile too. Make sure to check out her IG! 💜💜 #cysticfibrosis #fivefeetapart #fivefeetapartart #lilymeiknowles #cf #cysticfibrosisawareness
In ✌️days, @fit4mom_smyrna_vinings is hosting #bringyourkidtoworkout day to raise money for Team James Alexander, benefiting the @cffgeorgiachapter. Join us on Wednesday, 4/24 at 9:15am at @cumberlandmall to make a difference in these kids’ lives - your donations are tax refundable and 90% funds #medical research that’s truly changing lives. #mondaymotivation: Pictured here is a member of our village, @alexia_sophia, her son James and her husband @samual916, with another family you can follow at @drivingmissdesi who also battle #cysticfibrosis. The kids are wearing purple shirts because this helps identify who has CF. Those battling this disease must stay 6ft apart from one another to avoid cross contamination. Meaning, if James is carrying a bacteria, and came less than 6ft from another person with CF, just by being within that proximity without a mask covering his face, hand gloves - precautions we need to take when we’re around each other, he could infect the other person with CF with bacteria they probably didn’t have. Through your donations, families like these hope to not only enjoy more days with their children and watch their children grow well into adulthood, but hopefully one day their children get to interact in-person with others battling the same disease without feeling so isolated. #untilitsdone #curecf #cfirl #giveback #socialgood #monday #mondaymood #hope #raredisease #momlife #dadlife #toddlerlife #parenthood #atlanta #smyrna #vinings #togetherforjames
While daddy umpired mommy and I explored. We found a pretty cool creek that I watched for a while until eventually it put me to sleep. #cysticfibrosis #cysticfibrosisbaby #baseballseason
. Ain’t no shame in my game 👏🏻🤣
Thankful to be out of the hospital so I can go for walks with my favorite human @kristin.b3ll and our amazing doggos @huskybell_yeah 🐺 • • •  #riseandgrind #cfwarrior #breathewithme #65roses #invisibleillness #cysticfibrosis #fucf #fistsup #chronicillness #cysticfibrosisawareness #breatheeasy #untilitsdone #watchmework
Often times babies’ eating patterns (and perhaps progress with baby led weaning) are disrupted during teething.  _ Though I am not a medical doctor and my posts on IG are never meant to replace medical advice, a common question I do get in clinic is “What natural remedies can I use to help my teething baby?” The following are some ideas, and I encourage you to consult your pediatrician about the proper dosage of medication if this is the route they see fit. . . . . . If you’re interested in getting more information on Baby Led Weaning, and want more easy solutions to problems like this one click the link in my bio for a copy of my new book! . . . . #dietitian #babyledweaningideas #guthealth #nutrition #nutritionist #pediatrics #doctor #medicine #baby #babies #teethingbaby #teething #blw #babyledweaning #cysticfibrosis #cf #food #kids #kiddos #mom #pregnant #momlife #newmom #boymom
Working hard to crank out these melts for you guys! Here are the limited scents now offered. Limited quantities available so snatch them while you can. Remember, 10% of your purchase from each collection gets donated to the following local charities: @seaturtlepatrol, @cf_foundation, and @sunanimalleague. • • • #candles #candlemaking #smallbusiness #handcrafted #soycandles #aromatherapy #floridacandles #madeinflorida #candlesofinstagram #shopsmall #supportsmallbusiness #shoplocal #etsy #etsystore #adoptdontshop #cysticfibrosis #waxmelts #workingmoms #essentialoils #vendor #florida #beach #homedecor #scentedcandles #candleshop #tbec #candleclub #donate #bosslady
slowing getting my energy back after my admission! Feeling so much better. I’m so thankful I could be out enjoying the warm weather and fresh air today with my horses!!☀️💜 #cysticfibrosis #cfawareness #cysticfibrosisawareness #terminal #chronic #spoonie #live #vogmask #justbreathe #fashion #different #admission #sickkidshospital #instagram #cf #toronto #vogger #cf #hospital #freshair #farm #cyster #equine
The growing success of this event requires an ever expanding army of supporters so PLEASE reach out to your network, share this post & spread the message — REGISTRATION ENDS MAY 1st — #x4ac
Why are people LOVING Briutcare? What's so special about it? ⠀ . ⠀ Our #intelligentmeshnebulizer can be used to battle many common #respiratorydiseases and symptoms in children and adults, such as asthma, chronic bronchitis, cystic fibrosis, cough, sore throat, common cold, and more. 😷😊 ⠀ . ⠀ It is VERY practical for those who need to take a few hours a day to do specific treatments or for people who are constantly on-the-go and need something that's portable and easy to handle. 🚗 ⠀ . ⠀ Thanks to modern mesh technology and Britucare's unique features, #inhalationtherapy has evolved in ways never imagined. 🌟 ⠀ Today you can experience: ⠀ >> Shorter inhalation times. ⠀ >> A silent treatment process. ⠀ >> An adjustable nebulization rate. ⠀ >> Advanced monitoring techniques. ⠀ >> and high portability. . ⠀ Briutcare's box contains: ⠀ 1 x Main device incl. medication container ⠀ 1 x Mouthpiece ⠀ 1 x Adult mask ⠀ 1 x Child mask ⠀ 1 x Instruction manual ⠀ 1 x Storage bag ⠀ . ⠀ Go to briutcare.com to get your hands on the latest technology that will make your life so much easier! 😉 ⠀ (hurry up before they're gone) ⠀ - ⠀ #asthma #asthmaproblems #nebulizer #cysticfibrosis #copd #portablenebulizer #medicine #modernmedicine  #nebulizing #steam  #chroniccough #cough #theflu #healthybaby #sickbaby #homecare #homehealth #newlungs #fight2breath #breathingissues #breathingproblems #dailystruggles
This is what I do 3/4 times a day, everyday. For about 20/40 minutes each session. Everyone with Cystic Fibrosis has a different routine and different machines, I still sometimes ask what other people use for there airway clearance! • • • I would show you how we have to get the mucus out of my lungs, but I don’t want you guys to see my tomato face!! And what’s inside the bowl later... • • • #cysticfibrosis #everyday #lifewithcysticfibrosis #cf #airwayclearence
TRAVESSIA CANASTRA 2019 -TURMA V  Gratidão por apoiar e incentivar as boas aventuras em prol da nossa causa !  Dias 19, 20 e 21/04/2019. 💪👊💚🤗 Turma super dedicada em divulgar a #fibrosecistica . . . . . #expedicao  #serradacanastra  #trilhas  #cysticfibrosisawareness  #rarosentrenos  #trekkingbrasil  #4x4  #cysticfibrosis  #fibrosecistica  #naaventurafibrosecistica #naaventurafc  #nafc #naaventurafctrilhas  #justbreathe  #liveyourlife #1salva8 #doeorgaosdoevida #quemdoavivemais #b2bcompanygifts
Happy Earth 🌎 Day! From the mountains to the ocean, what a beautiful world we live in. Get outside & enjoy it. Also, do what you can to protect it! Metal straws, don’t litter, recycle, etc. 💚
I am so overwhelmed by the amount of people who have donated to Raise Money for Cystic Fibrosis. I cant wait to see how much we can raise together. I will be getting the chop to my shoulders in only a week and a half (or so)! I'm so excited to help make a difference in the lives of people who suffer from CF. If you want to donate, I have the link in my bio - from 50 cents to $5 - you can help make a difference ❤ #cysticfibrosis #fundraiser #raisemoneyforcharity  #donate #donatinghair #helpmakeadifference

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