Christine Noke @christine_noke
Founder and CEO of the Middle East CF Association, MECFA. On a mission to help improve the lives of people born with CF in the MENA region. mecfa.org Izmir, Turkey Joined October 2019-
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Our founding clinicians paved the way for a brighter, healthier, and happier future of CF patients in MENA and Central Asia.
Did you know that the life expectancy of someone living in the Middle East with cystic fibrosis is roughly 50% of that reported in Western countries?
A decline in the health of cystic fibrosis patients in the Middle East can be attributed to a general lack of centers specializing in the diagnosis and care of patients with CF.
At MECFA, we believe that even small acts of generosity can create lasting change in CF patient's lives, their families, and their communities. Ultimately, transforming the future of patients in the region.
In this article, we share how MECFA works to improve the lives of #CFpatients in the Middle East through access to better healthcare. bit.ly/3kLxyTv
In this article, we explore MECFA’s #MissionStatement outlining our impact to-date.
MECFA thanks to doctors! shoutout.wix.com/so/19N5tmqDw
MECFA programs aid clinicians in the region who are committed to improving quality of life and life expectancy for CF patients in their countries.
MECFA's organizing principles are three-fold: 1️⃣ Early and Accurate Diagnosis 2️⃣ Training of Clinicians and Allied Health Professionals 3️⃣ Access to Essential Therapies
Did you know that most MECFA member countries do not have access to diagnostics, essential therapies or CF centers?
"I hope you can find some space for hope" - Kristin Entler shares what has been helping her cope with the unsettling stages of the covid pandemic. Read it all here: buff.ly/3s4h0cL #cysticfibrosisnewstoday #cysticfibrosis #livingwithCF #CFnews #CF #treatingCF
MECFA’S Impact To-Date: Donated… 👉10 Iontophoresis units, 👉10 sweat chloride analysers 👉supplies for 10,000 tests to hospitals in Egypt, Jordan, Sudan, Azerbaijan, and Ethiopia
In this article, we outline how MECFA works to improve the lives of #CFpatients in the Middle East through access to better health care. bit.ly/3kLxyTv
The high costs of effective #CysticFibrosis treatments make obtaining them a major challenge for CF patients in Africa, the Middle East & Central Asia
The MECFA mission is to improve the health outcomes of #CysticFibrosis patients in the Middle East, Northern Africa, and Central Asia.
ICYMI - Middle East Cf Association (Mecfa): Impact Overview.
ICYMI - Middle East Hospitals Gain Access to Much Needed Cystic Fibrosis Diagnosis and Treatment Resources
Katie Haswell 🇺�.. @KatieHaswell
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1 Followers 52 FollowingChristina Walker 💙 @Guatemalagirl
613 Followers 1K Following Mostly serious views on cystic fibrosis, health matters & drug pricing, with a bit of horticulture thrown in for good measureGayle Pledger @gayle_pledger
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364 Followers 4K Following all views expressed here are mine & do not represent my employer. writer, scientist, leftist, father to duncan. a better world is possible. he/him. 🌹✊🏼🕊Nicola Johnson @JohnsonMNicola
968 Followers 1K Following Director of People & Culture in a Multi-Academy Trust. School Governor. Mum, Step-mum, and raising awareness of Cystic Fibrosis when possible. #NoOneLeftBehindVertex Save Us @VertexSaveUs
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318 Followers 768 Following 2x CFF Impact Grant Winner • a new musical comedy about CF and transplant • we’re moving from script to stage! • DONATE! • based on a true story by @cystic4realCystic Fibrosis Resea.. @CFRI_CureCF
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66 Followers 662 Following i have #cysticfibrosis. i am post emergency life saving double lung transplant since 12.13.18! 🤘🏻😌 very very blessed. 👏🏻KA Associates @KaminkerLaw
1K Followers 4K Following Kaminker & Associates Immigration Law. Personal & Corporate Canadian immigration services. Technology companies are our specialty. Contact: 416 840 0525Ashleigh's Life Found.. @AshleighLife
82 Followers 522 Following Mission: To provide monetary Grant Awards to those who are at or near End Stage Cystic Fibrosis.ACPCF @acpcf
793 Followers 34 Following Association of Chartered Physiotherapists in Cystic Fibrosis - for all things relating to the physiotherapy management of CF, for professionals and familiesQuestion CF @questionCF
2K Followers 2K Following 2017 we found the 10 most important questions you thought should be answered by clinical trials in CF. We’re looking again.Anthony Thompson @bigbaddoctor
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38 Followers 143 Following #hocemotrikaftu #cistična_fibroza #cfsrbija #cfserbia #cysticfibrosis #wewanttrikafta #weneedtrikafta #fightcysticfibrosis #HocemoKaftrio #kaftrioTanya Koorts @TanyaKoorts
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178 Followers 342 Following chef, advocate, husband, dog parent, CF warrior @CFGetLoudSchenker Frédérik @SchenkerFrdrik2
787 Followers 5K Following Relations internationales Institutions & ONGs Associations & fondations Religions & spiritualité Musique Presse économique Presse politique Presse culturelleFall Risk the Musical @FallRiskMusical
318 Followers 768 Following 2x CFF Impact Grant Winner • a new musical comedy about CF and transplant • we’re moving from script to stage! • DONATE! • based on a true story by @cystic4realPatient Worthy @PatientWorthy
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39 Followers 97 Following Mother of daughter with cystic fibrosis. My dream is Trikafta..Gayle Pledger @gayle_pledger
530 Followers 597 Following CF mum fighting for all our CF warriors b/c lifesaving drugs should never cost lives. Founder @VertexSaveUs, ‘Right to Breathe’ campaign, working @JustTreatmentCystic Fibrosis Resea.. @CFRI_CureCF
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613 Followers 1K Following Mostly serious views on cystic fibrosis, health matters & drug pricing, with a bit of horticulture thrown in for good measureJacquelien Noordhoek @Jacqnoordhoek
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968 Followers 1K Following Director of People & Culture in a Multi-Academy Trust. School Governor. Mum, Step-mum, and raising awareness of Cystic Fibrosis when possible. #NoOneLeftBehindPeter Hodge @peter100percent
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3K Followers 3K Following Just a grandma standing before #X trying to make friends. I’m a speaker & author of 3 books. See my website for more ⬇️ Also, an advocate @CF_FoundationThe main barrier to #CysticFibrosis patients thriving in developing countries is access to essential CF drugs and equipment to manage the disease.
Chronic lung infections and breathing difficulties are common in people with #CysticFibrosis.
Kateryna's story is out. The CF Mom escaped from Ukraine with her daughter Anna. Her story on our Living with cystic fibrosis podcast: …vingwithcysticfibrosis.simplecast.com/episodes/ukrai…
Our founding clinicians paved the way for a brighter, healthier, and happier future of CF patients in MENA and Central Asia.
Did you know that the life expectancy of someone living in the Middle East with cystic fibrosis is roughly 50% of that reported in Western countries?
A decline in the health of cystic fibrosis patients in the Middle East can be attributed to a general lack of centers specializing in the diagnosis and care of patients with CF.
It’s a chilly day 🥶🥶🥶 Sporting my TEAM BOOMER gloves at coaching today. @cysticfibrosis
According to the 2020 Patient Registry Handout, between 2016 and 2020 the median predicted survival age was 50 years – reflecting the continued progress we’re making in the fight against cystic fibrosis. Explore more in the 2020 Patient Registry Handout: on.cff.org/2020-Patient-R…
While countries are getting the access to miracle medicines, #trikafta for Cystic Fibrosis we urge @MoHFW_INDIA to come forward for discussion with @VertexPharma for access to Indian patients. @OfficeOf_MM #Indiastandforcf @aiims_newdelhi
At MECFA, we believe that even small acts of generosity can create lasting change in CF patient's lives, their families, and their communities. Ultimately, transforming the future of patients in the region.
We’re working to empower the next generation of scientific leaders. Gilead's Research Scholars program supports emerging scientists who are exploring innovative basic and/or clinical research in areas of unmet medical needs. Share or apply today.
In this article, we share how MECFA works to improve the lives of #CFpatients in the Middle East through access to better healthcare. bit.ly/3kLxyTv
In this article, we explore MECFA’s #MissionStatement outlining our impact to-date.
MECFA thanks to doctors! shoutout.wix.com/so/19N5tmqDw
MECFA programs aid clinicians in the region who are committed to improving quality of life and life expectancy for CF patients in their countries.
Shocking statistic. Average life expectancy for those living with #cysticfibrosis in most MECFA member countries is BELOW 15. BELOW FIFTEEN 15 * 15 * 15 Below 15 years old #globalcfdrugs4all #globalcffamily #cfcantwait #breathe #cfgetloud #hope #MiddleEastCF #cfawareness
Would it shock you to learn that the average life expectancy for CF in most MECFA member countries is below 15?! Compared to the United States which is over 40!
MECFA's organizing principles are three-fold: 1️⃣ Early and Accurate Diagnosis 2️⃣ Training of Clinicians and Allied Health Professionals 3️⃣ Access to Essential Therapies
Did you know that most MECFA member countries do not have access to diagnostics, essential therapies or CF centers?