Photos and pictures of cysticfibrosis

Here is what we found on #cysticfibrosis from instagram. 226 550 posts total.

#cysticfibrosis analytics

Posting speed: 20

20 posts per hour.

Posting speed of hashtag cysticfibrosis shows you how many media is posted with tag per hour. If this value more than 500 hashtag is very popular, but your post will go down in the list soon.

If you looking for hashtags that will give you likes, comments and followers you should use hashtags with higher engagement rate and posting speed between 5 and 10.

Latest #cysticfibrosis media


Madi hosted a paint party for CF! What are some of your fundraising ideas?⠀ ⠀ #cysticfibrosis #aworldwithoutCF #spoonie #chronicillness #fundraise #paintparty
My late husband had Cystic Fibrosis so the Boy Wonder and I are wearing yellow today to support the CF trust during CF week. Have you signed up to the organ donation register? It's really quick and easy. ⠀ 👉 http://buff.ly/2sGzVtW ⠀ 💝 💝 💝 💝 ⠀ #CFTrust #CysticFibrosis #OrganDonation #CFYelfie #TheUltimateGift #TheGiftOfLife #65Roses #CysticFibrosisTrust #CFAwareness #CFWeek #CureCF #JustBreathe #sixtyfiveroses
So I got some pretty cool news! I received a phone call yesterday from the Cystic Fibrosis Foundation and was asked if I'd be interested in doing some public speaking. This involves going to different events and talking about my life and personal experiences with Cystic Fibrosis. I had to jump all over that opportunity and of course I said I was interested! Anytime I have the chance to teach people about CF and raise awareness you bet I'll do it! I don't care if I have to speak in front of thousands of people! That's thousands of more people who are know educated on CF! So big thumbs up to that right there! 👍😀🤙 #cf #cysticfibrosis #cfwarrior #cysticfibrosiswarrior #cfawareness #lungdisease #thumbsup
. Thank you to @kineticasports for coming along on my journey back to Personal Training and helping with my nutrition. . People with Cystic Fibrosis don't absorb their food and nutrients properly. We also need roughly 50% extra calories just to keep our weight stable. . With having Kinetica Sport on board I am looking to build back that 15-20kg I lost because of the PTLD. Having a good nutrient intake will help with this and help my body recover better. . LET'S DO THIS👊 Stay beautiful people 😘 #transplant2trainer #cysticfibrosis #lungtransplant #transplant #fitnessjourney #personaltrainer #fitfam #irishfitfam #fitfamireland #instafit #bulking #nutrition #weighttraining #resistancetraining #workout #bodybuilding #buildthemlungs #bodyunderconstruction #transformation #fitnessfriday #bulking #EvoShave #MadeToMove #heretocreate #fueledbykinetica #adidas #underamour #gymshark #firstneverfollows #IWILL #impossibleisnothing
Today is Wear Yellow Day as part of Cystic Fibrosis Week so it's prime time to support me and @elliedunstall with our skydive for @cftrustuk . We have received so much support and generosity so far and we couldn't be more grateful 😊 Els has just finished 2 weeks of IV's which takes about 3 hours per day, alongside working 2 jobs and studying British Sign Language. I honestly can't comprehend how she does it all and still keeps a smile on her face! Please support us in raising money via our skydive by donating online at www.justgiving.com/sixty-five-roses OR text CFET65 with your amount to 70700. Even the smallest amount can help find a cure and help find a #LifeUnlimited #cfyelfie #cysticfibrosis #sixtyfiveroses
Tonight I will mostly be baking a rainbow cake ready for @emmslouisex charity fundraiser tomorrow... all for a good cause raising money for Heartlands Cystic Fibrosis Centre ❤ If you would like to donate and support the cause you can use the link below 😊 https://www.justgiving.com/fundraising/forcysticfibrosis #cake #rainbow #colours #cakemix #charity #fundraiser #cysticfibrosis #heartlands #baking #cakemaking #friday
176/365: Texts between my college roomie, @sierra_m_pierce, usually end up like this. When you both have illnesses that are very different but are still super annoying and effect everything you do, you have to have a sense of humor. Well, we do, or we'll lose our minds!! 😂 . #cyster #cysticfibrosis #cfawareness #cff #cysticfibrosisfoundation #cysticfibrosisawareness #antifungal #hospitalization #ivantibiotics #collegeroomies
wear yellow day for our gorgeous Osk and @cftrustuk #cysticfibrosis #cftrust #wearyellowday 💛💛💛💛 #CFYelfie
Please go vote for @emilysentourage! #share #Repost @emilysentourage ( @get_repost) ・・・ Have YOU voted yet? Emily's Entourage is SO close to getting a $50K grant... but it's up to us. So let's mobilize, people!!!! 1. Go to https://www.thewawafoundation.org/hero-award/ and submit your vote for EE [LINK in profile] 2. Share this post on your own page to spread the word. Voting is open until June 29 and limited to once per email address and device. #Wawa #CureCF #BeatCF #CysticFibrosis #CFAwareness #CFAware #EmilysEntourage #Breethe #TeamEE
Shout out to @andyelliott82 for organising the Cystic Fibrosis Charity Event at work today 💛🍋🌞 #cfyelfie #cysticfibrosis #wearyellow
Have YOU voted yet? Emily's Entourage is SO close to getting a $50K grant... but it's up to us. So let's mobilize, people!!!! 1. Go to https://www.thewawafoundation.org/hero-award/ and submit your vote for EE [LINK in profile] 2. Share this post on your own page to spread the word. Voting is open until June 29 and limited to once per email address and device. #Wawa #CureCF #BeatCF #CysticFibrosis #CFAwareness #CFAware #EmilysEntourage #Breethe #TeamEE
This guy tho 💛🌞 raising his awareness for #cysticfibrosis #CFweek and his lemon crunch pudding went down a storm today!!!!! #lemoncrunch #cfbakeoff
Gym gear #yelfie #bfitgym #cysticfibrosis 💛💛💛
Proud to be part of a great cause for a kid in need. Be glad for every breathe you take and appreciate every day. #cysticfibrosis #teeshirtlife #teeshirt
Welcome to our tribe Brooks!!! This guy has hockey in his blood and here he is with his proud dad Rod! We were thrilled to connect with the organizers of the Annual Rod Brind'Amour Cystic Fibrosis Golf Classic. And listen to this - this tournament held in the small town of Campbell River (British Columbia 🇨🇦) just raised $120-thousand dollars!!! So amazing and it sounds like it was an incredible event! We love partnering with great causes and so happy to have you join our tribe Brooks! . . . #littleicetribe #littleicetribemember #causecollab #hockey #hockeyfamily #giveback #cysticfibrosis #campbellriver
We think @James_Dunmore has made excellent use of our #CFYelfie filters. Top chap! @Regrann from @james_dunmore - 💛💛💛💛💛💛💛💛💛💛Today is national Cystic Fibrosis wear yellow selfie day! I soon discovered I don't own any yellow so I had to get creative. Please text "yellow" to 70500 and donate toward the Cystic Fibrosis Trust to show your support, raise awareness and improve the lives of those living with CF in the UK. #CFyelfie #cysticfibrosis - #regrann
Waiting on some lab work! Bubba does NOT like this fasting thing! #cflife #cysticfibrosis
Join us TODAY for Caring Cranes! You can pick up one of these handmade origami cranes for a donation of $10 or get a special event tattoo, with proceeds benefiting the Long Beach Ronald McDonald House, the Peter Mayhew Foundation, and the Cystic Fibrosis Foundation. We'll see you at the shop! 💖 . . . . . . . . . . . . #origami #origamicrane #cranes #petermayhewfoundation #cysticfibrosis #cysticfibrosisawareness #cysticfibrosisfoundation #ronaldmcdonaldhouse #longbeach #longbeachlocals #supportlocal #donate #donations #charity #specialevent #flashtattoo #giveback #tattooshop #tattooartists #localartists #handmade #community #art #floral #papercranestudio
Meet Patient Alissa Gabriel. She was diagnosed at 5 days old with #CysticFibrosis. She wants the world to know that #CannabisHeals and #Marijuana is her #Medication.
Another day another trip to another kaiser 🙈🙈 Cystic Fibrosis yearly blood work and x-rays. Best big sister Dani sat with Aubrey while I sat with Broc. Such a great helper ❤️❤️ And of course even with so much blood taken, my little heroes were so brave 💜 #teamaubreyandbroc #cysticfibrosis #cfclinic
My #CFyelfie for the @cftrustuk wear yellow day as part of #CFweek! Ft. Hospital gown, bandana and IV pole! Who else did one? #CF #CysticFibrosis #DonateMate #OrganDonation
Celebrating that I got my Creon filled for the first time since December 2015 with ICE CREAM! No more avoiding fat because I'm trying to conserve enzymes. I'm gonna eat EVERYTHING!!!! Woooo!!!!! #cfirl #cysticfibrosis #creon
Be sure to stop by Steel Cactus in Shadyside during the Jam on Walnut tomorrow! $4 Miller Lite, $5 Henry's, Leinenkugel, and Reds! #jamonwalnut #shadyside #pittsburgh #cysticfibrosis
So with Cf not being a well known condition. CF awarness week happy Cf day. The daily struggles we all go through and the judgement. #happy #instadaily #instagood #outofhospital #nomakeup #cf #cysticfibrosis #awareness #65roses #girl #cute #smiles #notinpjs #photooftheday #OOTD #follow4follow #butterfly #like4like #cfday #blogging #blogger
Flying Scholarships for Disabled People is charity which provides a 'once in a lifetime' challenge for disabled people, to help them realise their abilities through the medium of flight and 'reach for the sky'. We would appreciate some likes, follows & hashtag suggestions! #reachforthesky #fsdp #disabled #disability #support #wings #aviation #aviators #caa #deaf #ms #amputee #spoonie #arthritis #ehlersdanlossyndrone #paraplegic #paraplegia #wheelchair #spinabifida #cysticfibrosis #cerebralpalsy #multiplesclerosis #HereditarySpasticParaplegia #HSP #rheumatoidarthritis #poliomyelitis #hemophilia #learntofly #pilot #POTS
Did you all know about CF snap chat filters?!? You have to unlock them with a card from abbvie. A new filter at the beginning of each month until November! #quinntessentialcure #cysticfibrosis #cfwarrior #cfthroughthickandthin #snapchat
You are my Sunshine! We are rocking summer yellow today with our bright baby clothes bouquets. Supporting #wearyellowday for #cysticfibrosis #CFYelfie #summerbaby #yellow #sunshine #babybouquets #babygifts
The Spinnaker Tower in Portsmouth will be turning yellow tonight to raise awareness of #cysticfibrosis Text Yellow to 70500 to donate £5 to @cftrust #cfyelfie #CFWeek
Pouty McPouterson 😂 even after getting my lips done I can't pout properly 🤣 #fridayfeeling #weekendfeels #weekendvibes #roses #crown #selfie #cf #cysticfibrosis #feelinggood
💛💛💛💛💛💛💛💛💛💛Today is national Cystic Fibrosis wear yellow selfie day! I soon discovered I don't own any yellow so I had to get creative. Please text "yellow" to 70500 and donate toward the Cystic Fibrosis Trust to show your support, raise awareness and improve the lives of those living with CF in the UK. #CFyelfie #cysticfibrosis
It's Friday everyone. So set your timer to 8pm and go to ibnxradio.com/atlantanx for "No Filters Fridays" with these three lovely, funny and cool sisters. Get the drop on everything that's hot and not. Plus some great music. Respect Winning HTTPS://WWW.SOUNDCLOUD.COM/CAMEEN/FRIDAYS HTTPS://WWW.CAMEEN.COM @nofilterfridaysibnx @drsAtl1 #CameenMusic #fridays #nofilterfridays #AtlantaRadio #beautifulWomen #professionalwomen #talk #ibnxradio #Cameen #FamilyFriends #Business #Charity #Stjude #Shriners #CysticFibrosis #Autism #Diabetes #AllCancer #DViolence #Hiv #CameenSupports #Hardwork #WinningAttitudey
Watch the full-length version of "Sink or Swim" directed by Michael Cameneti by clicking on the link in bio. . . . . . . . . . . . . #endpain #weareendpain #documentary #shortfilm #cysticfibrosis #cf #sinkorswim #chronicillness #inspiring #shortdoc #filmoftheweek #cysticfibrosisawareness #awareness #invisibleillness #illness #love
CF week, Day 5: I am far from being a quitter (I'm way too stubborn for such things!) but even I have days that are genuinely a bit of a struggle, simply because life can be exhausting. And I don't just mean for me, I mean everyone. We all have days where we could quite happily throw in the towel, crawl back under the duvet and hibernate for a few days. Sometimes it can feel like it's a constant uphill struggle - CF patients put in so much time and effort just to get through the day, have so many treatments and meds just to keep things from crashing, and at times it can feel like I'm taking 2 steps forward then another one back. However, I am very lucky, because when I have my bad days when I'm just tired and fed up, I have so much in my life to give me a boost. So many reasons to want to stay as well as possible, so many reasons to continue smiling. These people are my reasons to keep fighting, because they bring so much happiness to my life, in the good times and the bad. I mean come on, only my friends @j12hln_sw & @angel01laura would turn up to see me in hospital only to end up throwing sherbert all around the room and have me laugh so hard that we can be heard at the other end of the ward!!! Honestly, I don't have time to give up fighting, because there is so much more fun to be had and so many more memories to be made with this insane bunch of people!!! 😍😂 What more reason could a girl need?! 💜Laura xx #cysterwhofightsuk #cysticfibrosis #cftrust #cfweek2017 #cfwarrior #laurasarmy #myreasontofight #keepfighting
💛💜CF WEEK 💛💜 Unfortunately, I do not have any yellow items of clothing 😣 but I do have something yellow and that represents CF! At my Grandparents house, when relatives or friends come and visit, they have this little CF fundraising box. Most people know I have CF, but are not even aware that there is a @cftrust !!! This little box helps explain the cf trust to people and the amazing work they accomplish! If people want to give donations, we happily let them and let them realise what an amazing cause they are supporting. I encourage you to donate to the @cftrustuk - whether its £1, £5, or £10 - your donation really will make a difference! Please help more people with CF have the opportunity to experience new treatments, have an even better quality of life and to THRIVE 😊💛💜. Please help remove the stigma and help raise awareness 💛 Many thanks, Nu x #cftrust #cysticfibrosis #cfawareness #cfweek #cysticfibrosistrust #blog #post #miniblog #blogger #educate #unpredictable #cfaware #pwCF #happiness #diabetes #blogging #happiness #share #love #determination #message #talk #yelfie #fundraising #awareness
#whataday... #feelingsad... Mark had a heartbreaking phone call off a friend last night... He's suffered with #cysticfibrosis all his life and has been in and out of hospital for as long as we've known him but he's taken a very bad turn this time...his body is failing him and the stark and brutal reality is that he might not see the outside world again... Hooked up to machines literally 24/7, unable to breathe properly unaided, unable to benture far from his hospital room because the sheer amount of equipment needed to help keep him alive is too weighty...facing the very real possibility that he's near the end of his life and yet he's still thinking about other people... He gave #river this beautiful box of wooden animals ♡ It damn nearly broke my heart...Puts a lot of things into #perspective... #cf #cysticfybrosissucks #lungtransplant #organdonation #chronicillnesswarrior #trooper
It's as easy as that! Text "YELLOW" to 70500 & support @cftrustuk #Donate #cysticfibrosis
Bendiciones para mi familia del @luzsmo, gracias por su cariño y oraciones - - - - - - - - - - - - @Regrann from @luzsmo - El Servicio Médico Odontológico de La Universidad del Zulia solicita a nuestra comunidad universitaria un aporte económico para Luis Eduardo. Un príncipe de 3 años de edad, hijo de la compañera Paulimar Ledezma, adscrita a la Facultad de Odontología quién padece la enfermedad FIBROSISQUISTICA DE PULMON Y PANCREAS. En estos momentos necesita nuestro apoyo para costear los gastos de traslado a otro país ya que en venezuela no hay tratamiento disponible para su patología. Confiamos en los corazones de nuestra familia universitaria que a pesar de la situación actual, siempre está dispuesta a ayudar a quien más lo necesita. #sosvenezuela #fibrosisquistica - #regrann - - - - - - - - - ------------------------ 🌟 Luis Eduardo, 3 años 🌟 Fibrosis Quística de Pulmón y Páncreas. 😷 📍Maracaibo - Venezuela Conoce mi historia y colabora! Donaciones: BOD CUENTA CORRIENTE # 0116 0113 83 0010803602 A nombre de mi mami: Paulimar Ledezma C. I. 15.938.853 unrespiroparaluis @gmail.com +58 414 683 06 03 #unrespiroparaluis #luiseduardoFQ #maracaibo #venezuela #fibrosisquistica #FQ #vivirconFQ #ayuda #cysticfibrosis #CF #lifewhithCF #help
The Peachtree Society is seeking leaders for the 2017 class! #linkinbio If you know a rising young professional looking to expand their network while challenging themselves to raise funds for a great cause, we encourage you to make a nomination for the Peachtree Society. The Peachtree Society is comprised of Metro Atlanta's finest individuals who exhibit success in community leadership, philanthropy, and industry. Candidates who are selected to be a part of the 2017 class will spend 3 months attending monthly CFF sponsored networking events while raising vital funds to support the mission of the Cystic Fibrosis Foundation. The program will conclude on November 2nd with an induction ceremony into the Society followed by the Battle for a Cure - a tasting event of Atlanta's hottest restaurants. Upon completion of the program, candidates become members of Peachtree Society, a network of accomplished young professionals who remain engaged with the Cystic Fibrosis Foundation. Membership in the Peachtree Society offers a number of member-only privileges such as networking opportunities and introductions into other CF Foundation events. Questions? Contact Ginny Conrad at vconrad @cff.org or 404-325-6973. Nominations are due by July 7th. #atlyoungprofessionals #atlanta #cysticfibrosis
Here's my #CFyelfie! Today is wear anything yellow for CF day! The only yellow thing I own is this long dress, not sure I can get away with wearing it all day though 🤔💛 Text YELLOW to 70500 to donate a fiver to the @cftrustuk
Forgive the snapchat filter but after being in hospital for a week, you need a filter or two! Today is CF's Yellow Friday to raise awareness of #cysticfibrosis #cf #yelfie #selfie #yellowselfie #raiseawareness #awareness #yellow #yellowfriday #friday #snapchatfilters #snapchat #hospital #hospitalroom #hospitalstay #piccline #redhair #blueeyes #smile #instasmile #instaselfie
Amor con amor se paga, agradecido por el apoyo de mi amiguita Sami. Que la luz que tus ojitos necesitan se encienda pronto. En mis oraciones y la de mi familia. ----------------- @Regrann from @unaluzparasami - Buenos dias feliz inicio de semana a pocos dias para el viaje a Bogota esta pautada para la primera semana de Julio sami necesita de tu apoyo ...aca un poco de mi historia compartan..👇 Hola mi nombre es Samantha Hernandes naci el 30/03/2016 fui diagnosticada desde mi nacimiento con glaucoma congenito luego me detectaron la distrofea corneal todo esto sumado a la "Anomalia de Peters" diagnostico recientemente recibido...he sido intervenida 6 veces para controlar mi glaucoma pero lamentablemente he rechazado dos veces la valvula de admeh en mi ojo izquierdo que fue implantado desde el mes de Enero del presente año...estamos en busqueda de nuevas opciones quirurgicas!!! las mas modernas se desarrollan en colombia y necesitamos de tu ayuda para trasladar a la princesa, con tu apoyo podemos lograrlo...para cualquier donativo pueden hacerlo a traves de la cuenta bod ahorro # 01160245270203528972 a nombre de mi abuelita yeny moran CI.13610288 telf:04246692617 muchas gracias Dios los bendiga! - #regrann ------------------------ 🌟 Luis Eduardo, 3 años 🌟 Fibrosis Quística de Pulmón y Páncreas. 😷 📍Maracaibo - Venezuela Conoce mi historia y colabora! Donaciones: BOD CUENTA CORRIENTE # 0116 0113 83 0010803602 A nombre de mi mami: Paulimar Ledezma C. I. 15.938.853 unrespiroparaluis @gmail.com +58 414 683 06 03 #unrespiroparaluis #luiseduardoFQ #maracaibo #venezuela #fibrosisquistica #FQ #vivirconFQ #ayuda #cysticfibrosis #CF #lifewhithCF #help
Me and my ex squad 🔪... I'm thankful for the machines and devices that helped keep me alive🙌🏼. But now I have no more need for them. We have gone our separate ways✌🏼. These were the things that I was attached to 24/7, relying on them to breathe, always a constant noise of air. I was always surrounded by the noise of slight rushing air, never a silent moment while wearing oxygen. My sense of smell was also affected, barely being able to smell food which also in turn affected how things tasted. Now post transplant I can smell 👃🏼 and hear 👂🏼everything, and it's awesome!! Not being attached to anything I feel so free! I can just zip around without carrying a backpack outside the house. I don't have tubing trailing behind me at home. Laima would always know where I was, no way to sneak 🙈🙊up on her! But now... I am a silent ninja! The reason I still have all my O2 supplies is because the doctors want to wait a bit before I have the o2 company pick it all up just in case I may need it for some reason or another. For now, they will be sitting silently unused in the corner and basement. I hope to never have to hang out with that squad (o2) again! 🙅🏻✌🏼 peace out Girl Scout! ✌🏼💨blog post up! Last one about the transplant and being in the hospital. Link in bio! ⬆️💜♻️ #lungstoryshort #cysticfibrosis #cfawareness #65roses #curecf #newlungs #doublelungtransplant #transplant #organdonation #donatelife #unos #recycleyourself #cffoundation #posttransplant #o2 #oxygen #oxygentank #liquidoxygen #concentrator #squad #byeeeee #peaceoutgirlscout
Great vibe in our salon today, for a great cause. Last hour to buy your raffle tickets for our yellow hamper #cysticfibrosis #turnknutsfordyellow #fundraising #knutsford #cheshire #toniandguy
It's Cystic Fibrosis week!! And I'm so glad to call this little warrior my nephew. He has been so healthy and we are so very thankful for that! #cysticfibrosis #65roses #cfawareness @easttncff 🌹💜
I'm on holiday but it's more like boot camp , I'm walking twice a day to get in 10 miles which is what I need to do for my China Charity walk in October . Still spell bound that Ed sent me the wonderful video message👌 #valbakesedsings #edsheeran #nspcc #cysticfibrosis #teamvalgreatwallof China walk
💛Love this #leelozano - Split for D.L who likes Yellow - @thaddaeusropac #thaddaeusropac #london #juliapeytonjones new global director . . . . . . . . 💛💛 #yellow #cfyelfie #cysticfibrosis #awareness #cftrust 💛💛www.organdonation.nhs.uk/register-to-donate/register-your-details/
Happy Cf Day! Although been ill all day, still smiling. #CfAware #CfYelfie #CfLife #CysticFibrosis
It's Wear Yellow day today to raise awareness for Cystic Fibrosis and the @cftrustuk 💛 This is Zoe's friend (both Emily and her brother have Cystic Fibrosis). Emily's mummy is now a good friend of mine and watching them all deal with this condition has been inspirational. 💛 Let's Fight this fight together 💛 TEXT Yellow to 70500 to donate £5 to the trust. If you want to get involved wear something yellow take a snap and share it with the tag #CFYelfie 💛 #cysticfibrosis #yellowday #cfawareness #cf #charity
As we kick off summer, we wanted to introduce you to our newest CF Foundation Board Members in Minnesota. Alison and Elana joined the board in January 2017. CF has been a part of Alison’s life for as long as she can remember. When Alison was five years old her best friend, and now her personal hero, was diagnosed with #cysticfibrosis. Alison’s family has been involved with the CF Foundation by participating in a variety of events over the last 25 years (across Minnesota, Wisconsin and Illinois) and even worked with Dr. Warwick in getting the first vest approved for children. Alison remembers doing her first stair climb when she was in junior high and has participated in the climb and organized a team every year since then. Elana became involved with the Foundation in 2009 when her cousin was diagnosed with #cysticfibrosis as a newborn. It was a large surprise for her family and as a pharmacist she took an interest in learning more about the disease and treatment options. Elana shared that “I have watched my cousin blossom and grow into an amazing young girl.” Both Elana and Alison have participated in numerous events over the years and are really proud to be a #CFBoardMember with the CF Foundation. Welcome these two women to their new role - finding a cure for cystic fibrosis.
Raising awareness for our warriors #CFYelfie #cfyelfie #cfawareness #cftrust #cysticfibrosis
#CysticFibrosis is a #geneticdisease that causes problems with the ability of different organs in the body to work properly. The buildup of mucus inside the lungs, pancreas, and other organs can lead to frequent bacterial lung infections, reduced lung function, and chronic gastrointestinal (digestive) problems. While symptoms can vary among individuals, CF is a life threatening disease. Improvements in treatment have led to an increase in life expectancy and quality of life. There are about 30,000 people in the United States and an estimated 21,000 adults in Europe and Canada living with cystic fibrosis. Learn more about this condition at ThinkGenetic.com and @cf_foundation #knowcf #cfliving @cftrustuk #cftrustuk
Get on the greens with green pants. Register via the link in our bio and help us raise funds for @cfcanada nationwide. #yeg #lawnsummer #lawnsummernights #lawnsummeryeg #cfstinks #cysticfibrosis #aworldwithoutcf #yegevents #edmonton #yeglife
Tomorrow's fun adventure! Nothing like running 13.1 miles at 8000-10,000 ft. If I can do stupid hard things like this, you can certainly forgo that $10 Starbucks and help me out in raising $$$ for Cystic Fibrosis 😜 No donation is too small! Seriously. click or copy and past to go to my fundraising page http://fightcf.cff.org/site/TR/Hike/22_Colorado_Denver?px=3633584&pg=personal&fr_id=6395
A hard, fast run tonight, along Lancaster canal and then back along The Lune. A personal record for the fastest mile! And to pass the time, got a vital message whilst coping with the zombie apocalypse! #zombiesrun #halfmarathontraining #halfmarathon #lancaster #TheGreatNorthRun #run #running #cysticfibrosis #cysticfibrosistrust #sponsorme justgiving.com/Holly-Kiyani
Beer, Tacos & Good Karma @baffinbrewingco tomorrow all day raising money for Team Boomer to fight cystic fibrosis! If you're in town... stop by. Can't make it? No worries... click the link in my bio to donate! #beer #tacos #cysticfibrosis #newyork #marathontraining #marathon
Its been a long week. Ive learned many new things about my body and its a little overwhelming, but thats kinda how life can be sometimes. Full of weird little surprises. #camelpose #yoga #cysticfibrosis #cysticfibrosisawareness #breathe #backbends #cf #strength #yogi
Alessandro was diagnosed with a chronic kidney disease. His Wish for a fishing trip came true in March! His mom, Mireille, said, "Watching Alessandro fish all day and catch some big mouth bass was so amazing! It was a very emotional trip especially for Tony and I because we know how much Alessandro goes through and how much is yet to come. Thank you is not enough to say for what you have done for our family. The memories from this trip will last us for a lifetime - priceless memories that we will forever be grateful for." #wishes #childrenswish #cwf #charity #donations #ab #alberta #calgary #yyc #edmonton #yeg #fundraising #fundraiser #illness #cancer #disease #disneyworld #disneyland #cerebralpalsy #cysticfibrosis #cancer #heart #hospital #children
#Repost @erikcoleman ・・・ Chatting with #GunnerEsiason @esiason17g last night about #cysticfibrosis and the impact the @boomeresiasonfoundation has made in raising money & awareness for #cysticfibrosis At the Foundation's 22nd Annual "Empire Challenge" High School All-Star game between NYC's 5 boroughs and #LongIsland. @cbssports #blessed @boomeresiasonfoundation @team_boomer_usa @drimington @wfansportsradio @cbssports @nflalumni @nflalumninynj @wsucougars_com @wsucougarfootball @sabricoleman @jetsarmytv @gothamcitycrew
Seen here is my 2 year old trying very hard to give herself one of her pills. She won't swallow them whole so she tries to open the tiny capsule with her uncoordinated hands, and dump the contents in her mouth. She has about a 10% success rate but it makes me so proud to see her try. (I let her practice with her lower dose creon leftover from months ago, so not to waste any medication.)
We love our Cystic Fibrosis Pendant! What a great gift this would make! 💙💚 #Karlande #jewellerythatconnects #cf #cysticfibrosis #cysticfibrosisawaresness
My best friend has Cystic Fibrosis, and let me tell you, CF is no fckin joke. CF means you can't go away for a night for your birthday without ending up in the ER the next day. CF is an inability to go anywhere or make any last minute plans without your mountain of medicine. CF won't let you have a good week without reminding you at the end that you are completely at the mercy of your lungs. It is explaining to your boss why you have to call in sick again, even though you look okay on the outside. But CF is also hilarious jokes about death and weird looks from the nurses. Getting to know the entire staff of nurses on the floor and becoming best friends with some of them. CF is a whole different outlook on life that those of us who are fortunate enough not to suffer from it will never understand. CF is gratitude for every breath that doesn't hurt. It's sneaking out of the hospital for a night to go on a drive in the city. It's grabbing life by the horns and doing it, because the time we have is here and all we have is now. I'm grateful for you, @misskrys65 and for your beautiful perspective that I have been lucky enough to borrow pieces of. It has been an absolutely wild year so far, I'm glad we have each other to get through it with. #fuckcf #lifeunlimited #cysticfibrosis #cf #redefininglifecf #ogdenartists #Ogden #historic25thstreet #breathe #61roses #dirtypour #painting #etsy #artbombogden #dailydoodle #finished #artistsofogden #artistsofslc #slc #Ogden #historic25thstreet #contemporarypainting #lightpainting #newmediaart #moxi #artfusion #artoftheday
Wear yellow! Show your support this week & every other week in fact 💛 Cystic Fibrosis Week 🙏🏼 * cystic fibrosis is a genetic condition affecting more than 10,800 people in the UK. You are born with Cystic Fibrosis and cannot catch it later in life, but one in 25 of us carries the faulty gene that causes, usually without even knowing. The gene affected by CF controls the movement of salt and water in and out of cells. People with Cystic Fibrosis experience a build up of thick sticky mucus in the lungs, digestive system and other organs, causing a wide range of challenging symptoms affecting the entire body* please see cysticfibrosis.ork.uk for more information 🙏🏼 #wearyellow #weareone #cysticfibrosis #cf #cfweek #love #cute #positive #viral #closetomyheart #support #gmrclothing #cfyelfie
Heard about our poker run? Find a flyer in your local store today! Or stop by the website #cysticfibrosis #motorcycles #personalinjuryattorney
So seeing as it is Cystic Fibrosis Awareness week and today is wear it yellow! Here is my #cfyelfie 👙🏝☀️A lot of people think Cystic Fibrosis is just to do with our lungs and a shorter life expectancy, but with it comes so many other issues such as CF related diabetes, hypoglycaemia, depression, pancreatic issues and early onset of osteoporosis. Many of which I am affected by. I am so lucky to have the support from my loved ones, friends and healthcare specialists. Hopefully in the near future we can find a way to cure Cystic Fibrosis or at least a way to prolong our lives comfortably! Here's to at least another 26 years 🎉🍾💃🏻💪🏻 #cysticfibrosis #cfwarrior #cysticfibrosisawareness #lucky #alifeunlimited #justbreathe #family #saltygirl
Thanks to @repkathleenrice, @repjoecrowley, Representative Dan Donovan, and @reppeteking for meeting with our teens from the @cf_foundation Greater NY Chapter yesterday to discuss the issues important to the CF community!
We wear yellow on Friday 23rd, carry on the support and create your outfit with a bit of yellow in today for cystic fibrosis! #cfweek Available here at GMR Clothing 💛 Please do not hesitate to comment or DM for orders and queries 📲⌨️‼️ #cf #cysticfibrosis #cfweek #cfyelfie #positive #support #closetomyheart #viral #love #wearyellow
Day #23 / 9 . Wearing something yellow for #cysticfibrosis 💛 Here is my selfie dear Val Fairbrother and Laura Tyler xxx . Had a great time in my local gym, made new friends and feeling happy 😊 . #30daystohealthylivingandbeyond #gym #siłownia #fitwomen #fitnessinspiration #lovesupporting #motivation #motivate #womeninbusiness #yellowisnewblack #blackandyellow #beforenightshift #entrepreneur #loveit #gopro
Today my two gorgeous girls wore yellow to support #cysticfibrosis trust❤️❤️ these have been through every thing but over come them❤️ love u my two little brave warriors💝💝💝
•6.23.13• 4 years ago today, Dr. Abbas Ardehali walked into Maddie's Room at @ucla to nearly 100 people clapping. He arrived to tell us that @jaket_123's double lung transplant was a huge success. We are forever grateful for this day and have never forgotten the love, support, & prayers we received throughout that tumultuous time. Happy (2nd) Birthday, bud 💜 #teamjake . . . . #doublelungtransplant #cf #ucla #latergram #family #love #fbf #flashbackfriday #cysticfibrosis #donatelife #miracle #flashback | cc: @mamabiggs, @tjbigley14, @lbigsize, @cf_foundation
If you have a child with #cysticfibrosis and you are not instilling in them, BY EXAMPLE, a love for physical exercise, you are robbing them of a component as important as their breathing treatments. At this age they want to be you, so live like you want them too! #cf #noexcuses #exercise #crossfit #calisthenics #livebyexample #betterparenting #likefatherlikeson
I am happy to be keeping up with the gym. Almost 2 months now. I have got to the point that I crave going and want to go more each week but have to take those stupud rest days lol #cysticfibrosis #cysticfibrosisawareness #cfwarrior #cfsucks #cystersandfibros #gym #disabilitywontstopme #workingout #feelinggood #workhard #nofilter
Today is International Women in Engineering Day. We are extremely proud of our scholar Bethany Colburn who started as an apprentice engineer at the RAF Museum and now works for QinetiQ - she is still only 23! http://www.fsdp.co.uk/scholar-stories/bethany-colburn/ #internationalwomeninengineeringday #reachforthesky #disabled #disability #support #wings #aviation #aviators #caa #deaf #ms #amputee #spoonie #arthritis #ehlersdanlossyndrone #paraplegic #paraplegia #wheelchair #spinabifida #cysticfibrosis #cerebralpalsy #multiplesclerosis #HereditarySpasticParaplegia #HSP #rheumatoidarthritis #poliomyelitis #hemophilia #learntofly #pilot #POTS
#CFweek day 5! Check out #SV’s team photo in support of #CFtrust! #WearYellowDay #CysticFibrosis #CFweek
Yellow bandanas for cf awareness week with bae #cfyelfie #cysticfibrosis
After 4 days in hospital starting Orkambi I can finally go home with no side effects! #orkambi #cflife #cf #cysticfibrosis #cfwarrior
Raising awareness for cystic fibrosis today at school .💛 #cfyelfie #cysticfibrosis
Cystic Fibrosis awareness #cfyelfie #cysticfibrosis #yellow #charity
Part of the new Lucosky Brookman Foundation and CF Bane campaign! CF Bane and his Army run for those who can't. CF Bane wants YOU to join his Army and help raise awareness for Cystic Fibrosis. Connect with us on Facebook and Instagram or visit www.thelbf.org to learn more about how you can help fight for a cure! @lucbrofoundation #thelbf #cfbane #cfbanesarmy #cysticfibrosis #awareness #curecf
Yellow goodies in my branch today, raising money and awareness for @cftrustuk @teacheractive #teacheractive #cysticfibrosis #cfyelfie #cftryst #yellow #newcastle #quayside
Update on jaelynn: I have a doctors appointment today. I am kind of nervous. But my best friend is coming to the doctors appointment so I think I will be okay. Like I have said in a pervious post I think I have gained weight. I wounded what my pfts (pulmonary function test) I'd going to look like🤔👀I will tell you guys how it went later. #cysticfibrosis #cf #cysticfibrosisproblems #CF
So, I was writing this morning and wanted to reference how many miles I have ran in the month of June alone and realized after today's run I will be over the century mark for June! My recent P.R. for the month was 40 miles. Showing up and just giving your best is key guys. I love you all, and thanks for all the support. I also come to realize the beauty is my training to the 50k finishing the race will be rewarding, but training for it is just as rewarding if not more so. . . #running #runner #cysticfibrosis #cysticfibrosisrunner #cysticfibrosisawareness #ultramarathontraining #lovelife #determination
Lazy Fridays are the best! Ok it isn't really lazy we are racing around doing laundry and cleaning. But we are home and happy! . . . . #toddlermom #boymom #onlychild #cysticfibrosis #cfmom #toddlermeals #highfat #momblog #momblogger #workingmom #advocate #iowamom #2yearold #glutenfree #celiacdisease #fitmom #coffeeaddict
DAY 15, 16 & 17 (Monday to Wednesday) . Day 15 Monday Road to #Banff Bear creek falls trail Emerald Lake : stunning!! 👌 Kicking Horse Pass National Historic Site 🚂 . Day 16 Tuesday Went up Sulfure mountain in the gondola, did the hike down. O2 sat was 👌 for an altitude of 2300m. . Day 17 Wednesday LAKES DAY 📍Louise 📍Mirror 📍Agnes 📍Moraine We did the Lake Louise to Agnes Lake Tea House hike. A great trail of 8km (3h) return. We had snow at the top and it was freaking cold!!! . #fibrosekystique #cysticfibrosis #11moispostgreffepulmonaire #11monthspostlungstransplant #donatemate #fight2breathe #mydonormyhero #justbreathe  #aworldwithoutcf #unmondesansfk #Canadiantransplantassociation #lungstransplant #transplant #travel #Alberta #BanffNationalPark #CascadeMountain #SulphurMountain #LakeLouise #MoraineLake #MirrorLake #AgnesLake #BritishColumbia #YohoNationalPark #Lake #Revelstoke #EmeraldLake #Tea #House
The @cftrustuk has also released a filter on their website! Please help and show your support like my favourite Queen and post your #cfyelfie to make social media turn into a bright and yellow place in honour of Cystic Fibrosis Awareness. Love and miss my Chez Hole💛 #cysticfibrosis #curecf #wearyellowday #sixtyfiveroses @cftrustuk
Tune in for tonight's vlog later.. it's really informative... #insta #instavideo #CFAware #CFirl #cysticfibrosis #vlog #vlogger #CFWeek
@Regrann from @unrespiroparaluis - Hoy nos levantamos confiados en que nuevos aires nos esperan 🙏 Agradecidos por el apoyo y compañía de tanta gente que aún sin conocernos nos ha tendido la mano. Dios tiene el control. ------------------------ 🌟 Luis Eduardo, 3 años 🌟 Fibrosis Quística de Pulmón y Páncreas. 😷 📍Maracaibo - Venezuela Conoce mi historia y colabora! Donaciones: BOD CUENTA CORRIENTE # 0116 0113 83 0010803602 A nombre de mi mami: Paulimar Ledezma C. I. 15.938.853 unrespiroparaluis @gmail.com +58 414 683 06 03 #unrespiroparaluis #luiseduardoFQ #maracaibo #venezuela #fibrosisquistica #FQ #vivirconFQ #ayuda #cysticfibrosis #CF #lifewhithCF #help
Hoy nos levantamos confiados en que nuevos aires nos esperan 🙏 Agradecidos por el apoyo y compañía de tanta gente que aún sin conocernos nos ha tendido la mano. Dios tiene el control. ------------------------ 🌟 Luis Eduardo, 3 años 🌟 Fibrosis Quística de Pulmón y Páncreas. 😷 📍Maracaibo - Venezuela Conoce mi historia y colabora! Donaciones: BOD CUENTA CORRIENTE # 0116 0113 83 0010803602 A nombre de mi mami: Paulimar Ledezma C. I. 15.938.853 unrespiroparaluis @gmail.com +58 414 683 06 03 #unrespiroparaluis #luiseduardoFQ #maracaibo #venezuela #fibrosisquistica #FQ #vivirconFQ #ayuda #cysticfibrosis #CF #lifewhithCF #help
We're wearing it yellow for the Cystic Fibrosis Trust! #cfyelfie #cysticfibrosis
Wearing yellow to support my best friend and everyone else who suffers with #cysticfibrosis. Help to spread the awareness of #cf by wearing yellow today and take a #cfyelfie 💛
As per I don't have any thing yellow to wear apart from my yellow hair bands on my wrist ! So all my minions are showing their support with me again! #CFYelfie #pleasedonateifyoucan #wearyellowday #minionmadness #cysticfibrosis #cf
Fridays have us like 🙌. It's the most wonderful day of the week - #FundraiserFriday! Today in the fundraising spotlight we have @lawnsummeryvr team Rainbowl Magic who have managed to raise $1,905.00 for LSN. We reached out to them to see how they were fundraising and here's what they had to say: . "We are a new team and so have yet to organize anything special to raise money. Our team is made up of the kind of people who help out in their communities and support others, so all we have to do is ask for a little support back, and we're pretty successful! Friends, family, and co-workers are our biggest supporters. Plus, having more people on your team means a greater reach for fundraising opportunities. We'll certainly be back in years to come with more innovative fundraising ideas". . A big shoutout to this team for their amazing fundraising efforts, and supporting #lawnsummer! . . . . #lawnsummer #yvr #vancouver #vancouvereats #cfcanada #cf #cysticfibrosis #vancity #lululemon #lsn #onthegreens #Canada150 #CanadianCollective
Next page