Today I am wearing yellow in support of my Grandson and all those #CFwarriors that fight for their best lives daily. Cystic Fibrosis Foundation Cystic Fibrosis Trust cf/Aware cf/Aware
It’s #WearYellowDay for Cystic Fibrosis Trust and all the #cfwarriors out there!! So proud of our pal Brodie and his parents Rhona Taggart and Barry Taggart
Are you living with CF and interested in participating in our latest research study at the University of Portsmouth?
There is still time to be involved in this exciting study, investigating how individuals with cystic fibrosis respond to exercise in the heat! 🌞🧂🚴 #CFWarriors
Incredible night Field Museum supporting the CFF Chicago until #CF stands for #CureFound #CysticFibrosis #CF Warriors
📢CALLING PEOPLE WITH CYSTIC FIBROSIS📢
WE NEED YOU HELP, YOUR EXPERIENCES MATTER‼️
Share your experiences on essential topics like salt intake, hydration & heat illness🧂🥤
16+: portsmouth.onlinesurveys.ac.uk/salt-supplemen…
6 - 15 years: portsmouth.onlinesurveys.ac.uk/salt-supplemen…
#CFResearch #CFWarriors
Are you living with CF and interested in participating in our latest research study at the University of Portsmouth?
We are investigating how individuals with CF respond to exercise in the heat?
Please contact us for more information
#cysticfibrosis #research #CFWarriors
My first run in a very long time and it was a bit spicy for me 🌶️ #running #cysticfibrosis #cfwarriors
Check out Marc Cotterill's amazing challenge for CF! instagram.com/p/Cqf6HULjGfH/
Read more and donate here:
classy.org/fundraiser/418…
@cfaware #cfaware ness #cfaware #trikafta forall #kaftrio #trikafta #challenge #adventure #cysticfibrosis #breathe #epic #sharks #ocean
#cfwarriors
Another aspect of the #CFlife are the breathing treatments that need to be done on a daily basis!
Every. Single. Day.
#CFawareness #nodaysoff #fightuntilcurefound #aworldwithoutCF #CFwarriors #revengeofthefifth #invisibleillness #butyoudontlooksick
Gunnar Esiason Boomer Esiason Boomer Esiason Foundation Cystic Fibrosis Foundation #CFWarriors 💪
podcasts.apple.com/us/podcast/mad…
If you thought that #cysticfibrosis only affected the lungs... think again. #CF is a multi-organ, fatal disease that needs a cure or control found for all those #CF warriors that battle this disease every day!
#togetherinthefight #aworldwithoutCF #nodaysoff #notjustlungs #65roses
Probably my first CPET since the undergraduate (Sport&Exercise Science Uni of Bath) days...
I'm sure the results are very similar 🤥
Awesome to help out with UoP Clinical, Health & Rehabilitation Team (CHaRT)'s _laurenclayton_ PhD work funded by CF Warriors.
#Science #CFwarriors #CPET #Physiology #MoreOfAPowerAthlete
Winter is Here ❄️ Be prepared for seasonal respiratory Illnesses 🫁
#airwayclearance #lungheath #respiratory #lungs #copd #pneumonia #cysticfibrosis #cfwarriors #cffighter #bronchiectasis #chestpt #icu #respiratory care #pulmonologist
#pulmonology #respiratory therapist
#mucus
Starting the day with a hilly 4 miler and a bucketful of gratitude 🙌🏼 #running #cysticfibrosis #cfwarriors 🚀 #exercise #fitness
Free prescriptions for all cystic fibrosis (CF) patients
Please sign and ask others to sign💛 📷 petition.parliament.uk/petitions/6337…
#cysticfibrosis #cfwarrior #cfwarrior s #health
Children’s Community Nurses are worth their weight in gold. A quick visit if maybe 10-15mins and all our anxieties and stresses of Eli’s PEG are gone.
I’m sure these guys will become quite familiar.
#cysticfibrosis #CFWarriors
On Friday I will be wearing yellow to support Cystic Fibrosis Trust and all those courageous CFWarriors out there like my grandson who amazes me everyday and in his own words at only 2 years old tries very hard to be brave!! Cystic Fibrosis Foundation
