Search results for #cysticfibrosis
Pulmonary ionocytes, a rare airway cell type with high levels of CFTR, the protein defective in CF, regulate the acidity of airway liquid. buff.ly/49UUwh7 #cysticfibrosis #cfwarrior #curecf #cysticfibrosislife
#PIP #CysticFibrosis stopthetories.vote #TacticalVoting #VoteTactically #Benefits #PintSizedLoser #RishiSunak #LocalElections2024 #MentalHealth #Homelessness #ToryBrokenBritain #Carers 🦽 #SicknoteCulture #GP #NHS #DWP #Disabilities #ESA #HMRC #GTTO #GeneralElectionNow
Because of an amazing lady told her loved ones she wanted to #donate her organs, my daughter is alive today. #OrganDonation #GiftOfLife @share_wishes @LiveLifeGiveLife #liver #kidney #cysticfibrosis
💬"CF is a #multisystem disease and requires a #multidisciplinary approach, and the care of patients has been #team-based for many years," Mark Selleck, MD, PhD, at @ChildrensLA, told Healio. #cysticfibrosis Read more⬇️ healio.com/news/pulmonolo…
Most (missing Veronica!) of our committee at our CF GI study day today. Representing adults and peads CF dietetics across the U.K. follow us here and on Instagram -bda_cysticfibrosis #BDACF #CFdietitians #CF #cysticfibrosis @SnowballJoanna @laurakinseyRD
As her 5-year-old daughter begins to struggle with CF treatment compliance, columnist Jennifer Chamberlain seeks answers. buff.ly/3WgEriz #cysticfibrosis #cfwarrior #curecf #cysticfibrosislife
Completely agree! @UKParliament #Government @RishiSunak please do not penalise people living with #cysticfibrosis and other lifelong chronic conditions. You will be undoing all of the good work & progress made by the #clinicians & advances in #research #treatments
Completely agree! @UKParliament #Government @RishiSunak please do not penalise people living with #cysticfibrosis and other lifelong chronic conditions. You will be undoing all of the good work & progress made by the #clinicians & advances in #research #treatments
Get ready to #CrossOutCF with us this May! As #CysticFibrosis Awareness Month near, we're gearing up for a month of inspo, unity & hope. Join us as we envision a future *beyond* #CF—where we can all #DareToDream boundlessly & free ✨ More soon! #CFAwarenessMonth #DareToDream
#Lupus #Lyme #MCS #EDS #Fibro #Celiac #Stroke #CysticFibrosis Here is a list of all of May's daily holidays and monthly health awareness's. itstimefortheholidays.blogspot.com/p/may.html
Event Reminder: Tonight's Evenings with Genetics will be at 7:15 on Zoom and the topic will be "The Genetics of Cystic Fibrosis". Register online: bit.ly/3W1MgbI #Genetics #CysticFibrosis
Event Reminder: Tonight's Evenings with Genetics will be at 7:15 on Zoom and the topic will be "The Genetics of Cystic Fibrosis". Register online: bit.ly/3W1MgbI #Genetics #CysticFibrosis
My son has type 1 #diabetes & #cysticfibrosis every day he's kept alive & well by #NHS meds & care. We're hugely appreciative but terrified at what we've witnessed has been done to the service & workforce. We must all fight for it before it's destroyed
My son has type 1 #diabetes & #cysticfibrosis every day he's kept alive & well by #NHS meds & care. We're hugely appreciative but terrified at what we've witnessed has been done to the service & workforce. We must all fight for it before it's destroyed
EU expands #cysticfibrosis treatment for infants with #KALYDECO ca.investing.com/news/company-n…
Tomorrow kicks off #cysticfibrosis awareness month! Before Bradley’s diagnosis I honestly didn’t know anything about #CF. Through the month of May #BradleysBattleBuddies will try to share info about this horrible disease to help educate & raise awareness as we fight for a cure 🫁
Fun for everyone - walk, run, hop (?!) @TheLeanneFund 5/ 10km Run on the 1st of June in Point. Rainbow attire optional, guaranteed fun! Visit entrycentral.com/TLF5K10K2024 to register! #hebrides #funrun #isleoflewis #westernisles #cysticfibrosis #stornoway #leannefund
Wishing everyone in the #cysticfibrosis community a great week ahead!
(2) From working with people with #CysticFibrosis I know what an ordeal it can be when up against panels lacking proper understanding and knowledge, not all genuine #disabilities are obvious/visible & many get turned down requiring tribunals @cftrust @Autism
(2) From working with people with #CysticFibrosis I know what an ordeal it can be when up against panels lacking proper understanding and knowledge, not all genuine #disabilities are obvious/visible & many get turned down requiring tribunals @cftrust @Autism
💯 spot on! There should be ways of understanding a genuine claim & not. Panels need to be manned by genuine experts in order to do this. Working on behalf of people with #CysticFibrosis I know what an ordeal it can be when up against panels lacking knowledge @cftrust
💯 spot on! There should be ways of understanding a genuine claim & not. Panels need to be manned by genuine experts in order to do this. Working on behalf of people with #CysticFibrosis I know what an ordeal it can be when up against panels lacking knowledge @cftrust
The European Commission has approved Kalydeco (ivacaftor) for CF infants as young as a month with at least one CFTR gating mutation. buff.ly/4b7JMgs #cysticfibrosis #cfwarrior #curecf #cysticfibrosislife