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Tough Questions | Cystic Fibrosis Canada
Fight for answers to the tough questions that still surround cystic fibrosis.
CFSource - Cystic Fibrosis en CFTR: van leren tot leven Met meer kennis over Cystic Fibrosis (CF) en 'Cystic Fibrosis transmembrane conducta
Cystic Fibrosis en CFTR: van leren tot leven Met meer kennis over Cystic Fibrosis (CF) en 'Cystic Fibrosis transmembrane conductance regulator' (CFTR) kunt u meer doen: voor uzelf, uw familie en in uw dagelijks leven
Cystic Fibrosis Queensland | Australia
Cystic Fibrosis Queensland is the peak community not for profit charity working with and for the increasing number of people living with cystic fibrosis who attend a Queensland Health clinic for treatment. We advocate for the entire cystic fibrosis community and seek to raise much needed awareness.
Cystic Fibrosis Canada
Cystic Fibrosis Canada is a national charitable not-for-profit corporation committed to finding a cure for cystic fibrosis (CF). We invest more in life-saving CF research and care than any other non-governmental agency in Canada.
Run as 1 for Cystic Fibrosis | Mackay | Cystic Fibrosis fun run |
5km fun run and 1.5km dog walk to raise funds for Cystic Fibrosis research
Cystic Fibrosis South Australia - cfsa
We are fighters and advocates for our community. We support people and families impacted by cystic fibrosis in South Australia.
MukoDiagnosis - Cystic Fibrosis
Knowledge about cystic fibrosis (Cystic Fibrosos, CF). The website provides an overview of the main problems related to the diagnosis, symptoms, diagnostic tests, treatment centers, disease progression.
CFQ-R - Cystic Fibrosis Questionnaire-Revised Application
Cystic Fibrosis Questionnaire-Revised Application
cysticfibrosis.com - Your Cystic Fibrosis community
We offer the Cystic Fibrosis community an active forum, blogs and medical articles, and a wealth of other resources: Connecting the Cystic Fibrosis community Forums Our forums continue to be an excellent way for the community to connect, and a searchable source of information – 1 million threads! Join in, ...
Respiralia Foundation against Cystic Fibrosis
This is the Home site of the Respiralia Foundation and Cystic Fibrosis Balearic Association. We
What is Cystic Fibrosis - Medic Vision
Cystic Fibrosis is the most common chronic illness affecting young Australians, learn more today with Medic Vision.
CFDB - Cystic Fibrosis DataBase
A free access tool to evaluate the current evidences about clinical effectiveness of interventions in cystic fibrosis.
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Benefiting Cystic Fibrosis Patients
Home - Johns Hopkins Cystic Fibrosis Center
Working together with patients and their families to stay healthy with cystic fibrosis.
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Find cystic fibrosis resources and support for patients and caregivers from AbbVie here.
Run, Sickboy, Run - Cystic Fibrosis and Exercise
This blog follows one man with Cystic Fibrosis trying to run one whole mile.
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Cystic Fibrosis Foundation | CF Foundation
Cystic Fibrosis Foundation: We will not rest until we find a cure for all people with CF.
Cystic Fibrosis (CF) - Lung and Airway Disorders
Cystic Fibrosis, Lung and Airway Disorders, disease of the mucus and sweat glands
Bambini Travel – Adventures with Twins, Cystic Fibrosis + a Food Allergy
Adventures with Twins, Cystic Fibrosis + a Food Allergy
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The Big Roast | Helping cure cystic fibrosis one roast at a time.
FINDING A CURE FOR CYSTIC FIBROSIS ONE ROAST AT A TIME By hosting a roast this July, you could join thousands of people across Australia as
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**** Percussion Therapy for Cystic Fibrosis Patients
CPT specializes inaggressive **** percussion therapy (CPT)for patients suffering from chronic respiratory ailments such as Cystic Fibrosis. Our purpose is to slow down the progression of the disease. We educate the families about a more effective way to achieve Bronchial hygiene in Cystic Fibrosis patients.
Checking for Cystic Fibrosis – Thefreo Doctor
Thefreo Doctor provides various testing services and can provide your practice or patient with an accurate Cystic Fibrosis testing. Click here for more info.
Cystic Fibrosis | After Hours ACT
According to After Hours ACT, genetic screening tests to identify the risk of conditions like Cystic Fibrosis are essential for doctors. Click here for more.
Cystic Fibrosis Treatment Option | Pulmozyme® (dornase alfa)
Pulmozyme® (dornase alfa) is a nebulized cystic fibrosis (CF) treatment option to help manage CF symptoms. See full safety for more information.
Cystic Fibrosis (CF) Information and Resources | CFSource
Learn about cystic fibrosis, including the causes and potential treatment options, as well as resources that can offer additional support for you or a loved one.
CF Source - Daily Life with Cystic Fibrosis
CF Source is dedicated to providing information for people living with Cystic Fibrosis (CF). With greater knowledge of CF, you can go from learning to living.
South African Cystic Fibrosis Association (SACFA)
Cystic Fibrosis (CF), is an inherited genetic disease that affects a number of organs in the body, primarily the lungs and pancreas by clogging them with thick and sticky mucus.
Float For A Cure - Cystic Fibrosis Charity Event
Float for a cure is a donation event held in Stillwater, Minnesota. Enjoy a paddle boat ride along with live entertainment to help those suffering from cystic fibrosis. Donate today. Get your tickets before October 4th, 2019.
Cystic Fibrosis Research Institute - Research - Education - Advocacy - Support
Nonprofit organization funding innovative research and offering education, advocacy and psychosocial support to the cystic fibrosis community.
- Cystic Fibrosis - Home - Blog - Leef je leven - Adem in, adem uit
Ik neem je mee in mijn leven met Cystic Fibrosis. Dagelijkse beslommeringen met als motto: wacht niet tot de storm voorbij is, maar leer dansen in de regen.
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OC Chapter, Dana Point - Cystic Fibrosis Foundation
Nearly every CF **** was made possible by the Cystic Fibrosis Foundation and because of funds raised from Great Strides. Join me at Great Strides!
Cystic Fibrosis (CF) Information and Resources | CFSource
Learn how cystic fibrosis (CF) progresses over time, take a quiz to separate CF fact from fiction, and power up your CF knowledge with guides, resources, and video content.
Your Source for Cystic Fibrosis (CF) Lifestyle Content | Everyday CF
Cystic fibrosis (CF) can pose many challenges for patients, caregivers, and family members. View our Everyday CF content for support navigating life events, tips on physical and mental well-being, recipes, and helpful resources for managing your day-to-day.
The Stanley Richard Foundation | Living With Cystic Fibrosis in NJ
MAKE A DIFFERENCE MAKE A DIFFERENCE WELCOME TO THE STANLEY RICHARD FOUNDATION | A NON-PROFIT 501C ORGANIZATION Our Mission The mission of the Stanley Richard Foundation is to enhance the quality of life and empower those affected by Cystic Fibrosis, through generating
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Kin Canada -Cystic Fibrosis Canada Partnership - Lethbridge Kinsmen
National Service Project – The Kin – Cystic Fibrosis Canada Partnership From a relationship that began on a barstool in 1963, a 43-year friendship has grown into a committed partnership. Over the years, Kinsmen and Kinettes have devoted their efforts Read More ...
The Ride For The Breath Of Life
The Ride for the Breath of Life is an annual motorcycle fundraiser in support of Cystic Fibrosis Canada. Riders from all different backgrounds band together each year to help make a difference in the lives of those battling cystic fibrosis.
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Relay For Life events are life-changing cancer fundraising events that help communities across the globe fight back against cancer. Get involved today!
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Information Join us for an exciting day of golf and help raise $25,000 for the Cystic Fibrosis Foundation of Canada, an Advocis/GAMA charity. 120 of 144 registrations have already been sold; only 6 foursome opportunities remain. Don’t be disappointed, register TODAY! All inclusive: * 18 holes championship golf and cart * Great food- BBQ lunch and deluxe buffet dinner * Complimentary beverages * Quality vintage wines with dinner * Prize for every golfer Click here for more information.
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Rise n' Grind
On 28 May make your morning coffee pack a punch for cystic fibrosis! Rise n' Grind is a fundraising event designed exclusively for cafes and coffee lovers across NSW in which participating cafes offer complementary coffee to raise money for cystic fibrosis.
Author: Cystic Fibrosis Community Care
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