70 Best Cystic Fibrosis Blogs and Websites
Cystic Fibrosis Blogs
Here are 70 Best Cystic Fibrosis Blogs you should follow in 2024
1. Cystic Fibrosis News Today
Pensacola, Florida, US
Cystic Fibrosis News Today is a digital news publication dedicated to offering comprehensive daily news coverage of CF. Read the latest Cystic Fibrosi...s news and articles. Stay informed about approved therapies, new medications and developments to treat CF.more
cysticfibrosisnews..
RSS 22.7K 5.2K 9.1K 2 posts / day Apr 2014 51 Get Email Contact
2. CF Roundtable A Newsletter for Adults with Cystic Fibrosis
US
The purpose of USACFA is to provide a source of information for CF adults regarding the basis, nature and progression of the disease, as well as the l...atest treatments and research to fight it. It also offers a forum for CF adults to communicate with each other. Our many columnists provide insights on a wide variety of subjects related to CF.more
cfroundtable.com/b..
RSS 2.3K 971 1 post / month Mar 2011 28 Get Email Contact
3. The Frey Life
Boston, Massachusetts, US
We are daily vloggers on Youtube sharing this crazy journey called life with all of you. Laugh with us. Cry with us. See the world with us. Get a glim...pse of life with Cystic Fibrosis. Be encouraged as you watch our videos... we hope they make your smile and and bring joy to your day. Welcome to THE FREY LIFE!more
youtube.com/cha..
RSS 112.1K 7.1K 2 posts / quarter Mar 2014 Get Email Contact
4. Cystic Fibrosis Trust
UK
The Cystic Fibrosis Trust is the only UK-wide charity dedicated to fighting for a life unlimited by cystic fibrosis (CF) for everyone affected by the ...condition. Our mission is to create a world where being born with CF no longer carries a death sentence, when everyone living with the condition will be able to look forward to a long, healthy life. more
youtube.com/cha..
RSS 88.5K 27.8K 1 post / week Oct 2008 Get Email Contact
5. Cystic Fibrosis Canada
Toronto, Ontario, 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 lif...e-saving CF research and care than any other non-governmental agency in Canada.more
cysticfibrosis.ca/..
RSS 19.2K 6.4K 6.6K 10 posts / quarter Apr 2016 53 Get Email Contact
6. Journal of Cystic Fibrosis
The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and t...reatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. more
cysticfibrosisjour..
RSS 7 posts / month 35 Get Email Contact
7. Emily's Entourage Blog
Philadelphia, Pennsylvania, US
Emily's Entourage is a nonprofit organization that raises money and awareness to help find a cure for rare mutations of cystic fibrosis, a genetic dis...order that generally affects a person's lungs and digestive system. Our goal is to expedite life-saving treatments and a cure for those with nonsense mutations of CF who are waiting with bated and fading breath.more
emilysentourage.or..
RSS 9.4K 2K 7 posts / quarter 40 Get Email Contact
8. Cystic Fibrosis New Zealand | Creating Better Tomorrows
New Zealand
Cystic Fibrosis New Zealand is the only dedicated organisation caring for the social, emotional and financial needs of the 500 people in NZ who have t...he condition. CFANZ will optimise quality of life for people with cystic fibrosis and their families; striving for normal life expectancy.more
cfnz.org.nz
5.5K 1 post / week 33 Get Email Contact
9. Inspire; to breathe
Blog by Suzanne. Blogging about home, life, living with Cystic Fibrosis, gardening, general love for all things vintage, and reasons why those topics ...are more interesting than they sound.more
suzannebrandsen.wo..
RSS 588 1 post / month Jul 2010 16 Get Email Contact
10. Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
Bozeman, Montana, US
The Cody Dieruf Benefit Foundation was formed in March of 2006 in honor of Cody Dieruf who passed away from Cystic Fibrosis at 23 years old. Uniting c...ommunities and families living with Cystic Fibrosis by raising awareness, providing emotional and financial assistance, encouraging health management, and inspiring life experiences.more
breathinisbelievin..
RSS 2.1K 7 1 post / day 19 Get Email Contact
11. Tim Wotton | Counting up to 50
London, England, UK
Tim Wotton, a Cystic Fibrosis sufferer, has been defying the odds for over 43 years and is sharing his life lessons and experiences. After counting do...wn to the massive 40 milestone in 2011, he is now regularly sharing his trials and tribulations via this blog.more
timwotton.wordpres..
RSS 881 1 post / month Jan 2011 19 Get Email Contact
12. Living life breathlessly
Johannesburg, Gauteng, South Africa
Life is not measured by the number of breaths we take, but by the moments that take our breath away.
livinglifebreathle..
RSS 1 2 posts / quarter Dec 2007 18 Get Email Contact
13. CF Happens
Maryville, Tennessee, US
I am a military wife, bonus mom and happen to have Cystic Fibrosis (CF).I am not a medical expert and this is just my story.
cfhappens.com
RSS 32 2 posts / month Oct 2013 6 Get Email Contact
14. CF Stinks
US
Having CF Stinks, but that doesn't stop me! I'll share with you a little about myself, my life with Cystic Fibrosis and anything else that cr...osses my mind. more
cfstinks.com
RSS 210 1 post / week Dec 2010 5 Get Email Contact
15. TheraPink
US
I created this blog to raise awareness about CF through sharing my personal experiences and perspective. I hope to dispel some of the myths and provid...e a basic education on my experiences with Cystic Fibrosis. Blog by Therapink.more
therapink.wordpres..
RSS 1 1 post / month Jan 2013 16 Get Email Contact
16. Breathe Bravely
Sioux Falls, South Dakota, US
A blog about my beautiful life living with Cystic Fibrosis: to educate and help promote awareness and understanding associated with CF.Dedicated to sh...aring my experiences of the good, the bad, the ugly, and the funny, so that all who so eagerly support the fight against CF, will know how much their love and support truly means.more
breathebravely.blo..
RSS 234 1 post / quarter Apr 2014 18 Get Email Contact
17. Bright Hope
Strength for today and BRIGHT HOPE for tomorrow! I am a 39-year-old woman with cystic fibrosis. I am also a daugher, sister, wife, mother, teacher and... friend. Most importantly I'm God's child. This blog is about my life including the challenges and blessings of living with cystic fibrosis, my faith, my family, and more!more
bvbrighthope.wordp..
RSS 4 posts / year Apr 2014 4 Get Email Contact
18. Cystic Fibrosis community
Bethesda, Maryland, US
A worldwide Cystic Fibrosis community combining cultures, nationalities and age groups. The mission of the Cystic Fibrosis Foundation is to cure cysti...c fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.more
cysticfibrosis.com..
RSS 233.8K 31.4K 7 posts / year 34 Get Email Contact
19. Cystic Fibrosis Federation Australia
Sydney, New South Wales, Australia
Cystic Fibrosis (CF) is the most common, genetically acquired, life-shortening chronic illness affecting young Australians today. Understand the risks..., the effects and how to best live your life.more
cysticfibrosis.org.au
RSS 10.2K 45 Get Email Contact
20. Bennett Brinson Gamel: Fighting Cystic Fibrosis
Texas, US
Cystic fibrosis is a life-threatening genetic disease that causes mucus to build up and clog some of the organs in the body, particularly the lungs an...d pancreas. When mucus clogs the lungs, it can make breathing very difficult. The thick mucus also causes bacteria (or germs) to get stuck in the airways, which causes inflammation (or swelling) and infections that lead to lung damage.more
initforbennett.com
RSS 977 Jul 2008 17 Get Email Contact
21. Claire's Place Foundation
California, US
Claire Wineland is founder of Claire's Place Foundation, a 501c3 committed to helping others living with cystic fibrosis like herself. Our mission... is to heighten public awareness about Cystic Fibrosis and improve the quality of life for the families it affects by providing education, life skills, inspiration, and positive support.more
clairesplacefounda..
RSS 31.5K 21.5K 71.8K Jul 2011 48 Get Email Contact
22. Cystic Fibrosis Foundation | CF community Blog
Bethesda, Maryland, US
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling li...ves by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care. The CF Community Blog highlights voices from across the CF community, touching on all aspects of life with cystic fibrosis.more
cff.org/Blog
RSS 233.8K 31.4K 59.6K 66 Get Email Contact
23. Love to Breathe
US
Blog by Somer Love, I created Love To Breathe® to educate and raise awareness about Cystic Fibrosis and spread Love whenever I can. I want to change ...the world... Join my fight! more
lovetobreathe.blog..
RSS 10.2K 1.6K 13.3K Mar 2008 14 Get Email Contact
24. Past the Point of No Return
A place for me to record the highs and lows of life on the transplant list, and my new life beyond it. Cystic Fibrosis waited 4years for a double lung... transplant and finally recieved the gift of life 10.10.11! All views my own.more
tor-pastthepointof..
RSS 3.6K May 2005 20 Get Email Contact
25. Cystic Fibrosis Kids
Portsmouth, England, UK
CF Kids helps by providing equipment, such as nebulisers, which can be an essential part of a CF Kids daily routine at home, but may not be available ...because of the NHS budget. We also provide exercise equipment and lessons, plus have a number of other services we offer to families in the Portsmouth and Southampton areas. more
cfkids.org.uk
RSS 1.5K 257 29 Get Email Contact
26. Continent Chasers
Ireland
Continent Chasers Wife & Cystic Fibrosis Husband From Poland and Ireland travelling the world 84 countries. Mission is to Visit Each Country on the pl...anet and to highlight Cystic Fibrosis and to show that serious illness doesn't have to stop you following your dreams.more
continentchasers.c..
RSS 2K 1.8K 1.5K 11 Get Email Contact
27. 66 roses
Hershey, Pennsylvania, US
Blog by Erin Moore, I'm just a mom with 3 wonderful kids, two of which are twins, one of which has Cystic Fibrosis, and I want to share my thought...s. This blog, 66 Roses, is dedicated to finding the cure. more
66roses.blogspot.com
RSS 391 2.3K May 2010 21 Get Email Contact
28. The Sprog's Life
Cobham, England, UK
Blog by George. I started this blog back in January 2012. At first i didnt want this to be a public blog, just some where i could write my thoughts an...d feelings, sort of a diary and journey through my time getting on and waiting on the transplant list.more
thesprogslife.com
RSS 986 Jan 2012 11 Get Email Contact
29. The Living, Breathing Wendy
Wisconsin, US
A blog about living life to the fullest despite battling Cystic Fibrosis, a genetic lung disease.
thelivingbreathing..
RSS 423 317 Mar 2015 17 Get Email Contact
30. This is Eli
A blog about Eli. A blog about survival - and by that, I mean life! Eli, a boy living cystic fibrosis. We are all about living and ❤️ adventure. ...I write to shed light on life with CF - and mostly, that means writing about the game of survival called life. We do our best at wellness and nutrition to keep the tribe, and Eli, as healthy as possible. more
hithisiseli.com
RSS 415 15 Get Email Contact
31. The Unknown Cystic
US
Leaving a digital record for my family & virtual friends.
unknowncystic.com
RSS 1.1K Feb 2010 18 Get Email Contact
32. Stanley's Journey Get it off your chest CF
Leicester, England, UK
Stanley-Ray was diagnosed with cystic fibrosis at 20 days old, this facebook page is to keep people updated on his progress & to raise funds for CF tr...ust.more
getitoffyourchestc..
RSS 815 349 271 Sep 2016 7 Get Email Contact
33. IV Solutions blogs
US
IV Solutions is a full service cystic fibrosis pharmacy that provides home infusion treatments, respiratory inhalation therapies, and specialty CF med...ications. Since 1986, we've been there to help cystic fibrosis patients along with their families and healthcare providers. We're here to support you through individualized instruction, proactive refill reminders, on-going care coordination.more
ivsolutions.com/blog
RSS 1.8K 16 Dec 2015 20 Get Email Contact
34. Lucky CF Mom | Possibilities
Idaho, US
I have the most amazing good luck. 8 years ago, my world came crashing down when my newborn baby was diagnosed with the genetic disease cystic fibros...is. Today, we feel like the most fortunate family in the world because we have Kalydeco! Now my goal is to work toward more personalized research, to help bring the most effective treatment to each and every person living with CF!more
luckycfmom.blogspo..
RSS 439 Feb 2011 10 Get Email Contact
35. JAMIEBUG CF CEPACIA LUNG TRANSPLANT
Idaho Falls, Idaho, US
Jamiebug- I have Cystic Fibrosis with Cepacia...Despite being told by almost every hospital in the country that I was not a candidate for a lung trans...plant due to Cepacia- I didn't give up and I found the ONE place that took a chance on me! I am almost 3 years post transplant and I feel great! You will learn of her thoughts, feelings and how she got through each day. more
jamiebug.blogspot.com
RSS 96 38 Oct 2007 12 Get Email Contact
36. SaltySouthpaw.com
Why am I the Salty Southpaw? Why I'm Salty - Cystic Fibrosis is a genetic disease where my body has trouble transporting salt. This causes thick m...ucus in my lungs and body, and my sweat has more salt in it than yours. Southpaw - I am a left-handed baseball player! Baseball and pitching is my passion! Check out my journey with CF.more
saltysouthpaw.com
RSS 9 May 2005 12 Get Email Contact
37. The Race Marked Out For Me | Running with Purpose
I want to write about my cf journey for a bunch of reasons to Connect, Share, Spread awareness and educate, Importance of Exercise, Inspire and encour...age, Thankfulness. Embracing life's journey with cystic fibrosis.more
theracemarkedoutfo..
RSS Mar 2015 9 Get Email Contact
38. Behind the Smile of a Cystic
My personal spin with Cystic Fibrosis tips, tricks, positive outlooks. All while making my dreams come true! 'Always Smile. I want to encourage everyo...ne with CF young or old to reach for you dreams, no matter how big or small they can be. As long as you have the right attitude in life, your disease will not bring you down! more
behindthesmileofac..
RSS 191 Jan 2012 6 Get Email Contact
39. More Than DNA DNA doesn't define our family
Peoria, Illinois, US
Spreading Awareness about Cystic Fibrosis through sharing our experiences in life! AND finding a CURE for CF!
morethandna.org
RSS 1.1K 5 Get Email Contact
40. Cystic Fibrosis Guernsey
UK
Cystic Fibrosis Guernsey's aim is to give local families and carers friendly support and advice. Local families who suffer with the issues surroundin...g CF have little or no way of sharing there ups and downs, their problems, we should help each other.more
cysticfibrosis.org..
RSS 178 156 13 Get Email Contact
41. Two Salty Boys
Chicago, Illinois, US
Two Salty Boys discusses the ride of a lifetime, having two boys that both have CF. You will read about the rollercoaster of life issues on this blog.... more
twosaltyboys.blogs..
RSS Nov 2010 11 Get Email Contact
42. The Journey of Faith
US
Desiring to be more like Christ through the trials and joys of this life. On The Journey of Faith you will read about how a mom and family deal with ...the fact that they have a child with CF. You will read about the fun and happy times as well as trying times. more
heleadsus.wordpres..
RSS Feb 2010 10 Get Email Contact
43. But You Look So Well
Oxford, England, UK
Cystic Fibrosis blogger Helen Roper is waiting for a Double Lung Transplant. 'But You Look So Well' is the usual reply. She doesn't like writing a...bout herself in the third person! Capturing Helen Roper's journey through Cystic fibrosis whilst waiting for a double lung transplant in the UK with trademark dry humor.more
butyoulooksowell.com
RSS 1.6K 1 post / year May 2019 3 Get Email Contact
44. Every Breath Means Hope
Sanford, North Carolina, US
This is my life... Cystic Fibrosis. Friends. Family. Music. Animals. Love. Faith. God. Miracles. Dreams. Hope.
everybreathmeansho..
RSS 275 Sep 2012 5 Get Email Contact
45. Inhaling Hope
A blog about mothering despite Cystic Fibrosis.The owner of this blog discusses her journey through life as a wife and mother. However, she has one th...ing that increases her challenges to these things. She has CF.more
hopefulwithcf.blog..
RSS Mar 2011 10 Get Email Contact
46. Joyfully Breathing
Texas, US
A CFer's Joyous Journey Through Life. I hope you enjoy reading about how I live my life as CFer! My dream job is to work with other cystic fibros...is patients as a Registered Dietitian Nutritionist (RDN) to help them gain weight so that they can live a longer, healthier life. more
joyfullybreathing...
RSS Nov 2013 9 Get Email Contact
47. *Live*Laugh*Love*Breathe*
Colleen's blog is about how she tries to incorporate Live, Love, Laugh into her daily life with CF.
howilivelaughlovew..
RSS Jan 2011 9 Get Email Contact
48. Michael Goodwin Sailing
Hello, and welcome to my occasional blog about sailing adventures with friends. I aim to raise funds for the Cystic Fibrosis Trust through sponsorship..., so please consider making a donation to the trust via the link on this website to help us to beat this dreadful disease that limits the lives of so many young people. I do hope you enjoy reading my blog. more
michaelgoodwinsail..
RSS 16 12 Get Email Contact
49. I dream of Daisy
Former civil servant Donna Sim has joined the growing trend of parent bloggers. She takes you on a journery sharing inspirational moments, as well as... personal accounts written with a heavy heart about her life battling Cystic Fibrosis and her struggles to conceive her miracle baby Daisy.more
dream-of-daisy.blo..
RSS 217 59 146 Jun 2013 8 Get Email Contact
50. One Breath at a Time - Living with Cystic Fibrosis
A lot of people ask me what made me decide to start writing a blog. I first got the idea after finding out that I might need a transplant. This blog i...s to raise awareness too, and that has been the biggest blessing I could have asked for. I have people reading my blog and learning about what Cystic Fibrosis is. more
kayla-onebreath.bl..
RSS Jan 2011 10 Get Email Contact
51. The So What Life
US
A blog to inspire members of the CF community to live positively and embrace everything life has to offer. Thriving with a chronic illness, cystic fib...rosis.more
thesowhatlife.com/..
RSS 1.3K 11 Get Email Contact
52. Always Have Hope
Following my life with Cystic fibrosis.
hollyrosanna.blogs..
RSS Sep 2014 8 Get Email Contact
53. Illness Inspired Words
Oregon, US
The one thing that many don't realize about Cystic Fibrosis is how isolating it can be. We are discouraged to spend any quality time together unle...ss we abide by strict infection control protocols. With that being said, many CF'ers and their families have sort of decided to stay away for one another in a best practices effort to not cross contaminate. more
illnessinspiredwor..
RSS Jul 2009 8 Get Email Contact
54. Cat Boogies Dream | L Word
Raleigh, North Carolina, US
I like cats, iced coffee and the color purple. I like reading, writing, making soap and thinking about what's next. I am a double lung transplant ...patient with cystic fibrosis.more
catboogiesdream.bl..
RSS 3 posts / year Mar 2010 8 Get Email Contact
55. The Transplanted Dad
US
My life as a father and husband with Cystic Fibrosis and two donated lungs. Here I will share the story of my life with Cystic Fibrosis and the new di...rection it's headed in following my double lung transplantmore
transplanteddad.bl..
RSS 133 Apr 2015 8 Get Email Contact
56. Tales of Citrus and Salt
When Life Gives you Lemon is published by a mom of a little guy that has CF. You will read about her daily life as well as how to care for a child wit...h CF. more
teamddoes.blogspot..
RSS Aug 2013 6 Get Email Contact
57. With Every Breath: My Life with Cystic Fibrosis
US
Once you choose hope, anything's possible. it's also a good way for me to connect with others in the CF community. Others in my situation may find it... comforting to see they aren't alone. Blog by jordan.more
livewitheverybreat..
RSS Oct 2013 8 Get Email Contact
58. Blue-Eyed Breather
Blue Eyed Breather is a blog about a young lady who strives to live a normal life. Emily blogs about the good and the not so good in her life and abo...ut her walk with God.more
blue-eyedbreather...
RSS Jan 2012 4 Get Email Contact
59. CF Is Not Forever
Cystic Fibrosis is part of our family now on Earth, but we know that Cystic Fibrosis is not forever, but our family is!
cfisnotforever.blo..
RSS Mar 2015 3 Get Email Contact
60. The Salty Cyster
Life with Cystic Fibrosis and other random thoughts along the way.
thesaltycyster.blo..
RSS Apr 2015 4 Get Email Contact
61. Becoming Chayil
Chayil is a beautiful Hebrew word that translates to strength, courage, and virtue, especially in the face of adversity, borne of closeness to and dep...endence on our Heavenly Father. My story, found throughout the pages of this blog, is one of redemption, forgiveness, and our Father's incomprehensible, incredible love. My story is my own, but chances are if you're reading this now, it's yours too... Or you want it to be. And it can! I created She is Chayil not only for myself but in hopes of using my storms to uplift and encourage others who might be going through similar things.more
becomingchayil.com..
RSS Jan 2015 6 Get Email Contact
Cystic Fibrosis Bloggers
Blogger Name | Blog Link | Total Blog Posts | |
---|---|---|---|
Marisa Wexler | cysticfibrosisnewstoday.com | 32 | |
Margarida Maia | cysticfibrosisnewstoday.com | 20 | |
Lindsey Shapiro | cysticfibrosisnewstoday.com | 18 | |
Steve Bryson | cysticfibrosisnewstoday.com | 15 | |
Cystic Fibrosis Canada | cysticfibrosis.ca | 12 | |
Patricia Inácio | cysticfibrosisnewstoday.com | 12 | |
William Ryan | cysticfibrosisnewstoday.com | 12 | |
Lara Govendo | cysticfibrosisnewstoday.com | 11 | |
Andrea Lobo | cysticfibrosisnewstoday.com | 7 | |
Jennifer Chamberlain | cysticfibrosisnewstoday.com | 6 | |
Jennifer Bleecher | cysticfibrosisnewstoday.com | 4 | |
Mary Chapman | cysticfibrosisnewstoday.com | 3 | |
A. Downes | cysticfibrosisjournal.com | 3 | |
Brad Dell | cysticfibrosisnewstoday.com | 2 | |
Kristin Entler | cysticfibrosisnewstoday.com | 2 | |
DeShawn Woodards | emilysentourage.org | 2 | |
author1 | cysticfibrosis.ca | 1 | |
Tim Wotton | timwotton.wordpress.com | 1 | |
Betsy | bvbrighthope.wordpress.com | 1 | |
A. Anderson | cysticfibrosisjournal.com | 1 | |
A. Morales Tirado | cysticfibrosisjournal.com | 1 | |
A. Murabito | cysticfibrosisjournal.com | 1 | |
A. Serpico | cysticfibrosisjournal.com | 1 | |
A. Vukić Dugac | cysticfibrosisjournal.com | 1 | |
A. Williams | cysticfibrosisjournal.com | 1 | |
A.M. Murphy | cysticfibrosisjournal.com | 1 | |
A.P. Ergenekon | cysticfibrosisjournal.com | 1 | |
Alan Shi | cysticfibrosisjournal.com | 1 | |
Anand G. Iyer | cysticfibrosisjournal.com | 1 | |
Andrew T. Braun | cysticfibrosisjournal.com | 1 | |
Anna Bertolini | cysticfibrosisjournal.com | 1 | |
Anna Diana | cysticfibrosisjournal.com | 1 | |
Annalisa Orenti | cysticfibrosisjournal.com | 1 | |
AR Deschamp | cysticfibrosisjournal.com | 1 | |
B. Button | cysticfibrosisjournal.com | 1 | |
C. Crisan | cysticfibrosisjournal.com | 1 | |
C. Fevola | cysticfibrosisjournal.com | 1 | |
C. L’Hostis | cysticfibrosisjournal.com | 1 | |
C. McLaughlin | cysticfibrosisjournal.com | 1 | |
C. Rosazza | cysticfibrosisjournal.com | 1 | |
C. Short | cysticfibrosisjournal.com | 1 | |
C.M. Sloan | cysticfibrosisjournal.com | 1 | |
Callum M. Sloan | cysticfibrosisjournal.com | 1 | |
Carlo Castellani | cysticfibrosisjournal.com | 1 | |
Christina S. Thornton | cysticfibrosisjournal.com | 1 | |
Cian Greaney | cysticfibrosisjournal.com | 1 | |
Claire Kim | cysticfibrosisjournal.com | 1 | |
D. Li | cysticfibrosisjournal.com | 1 | |
D. Ravamehr-Lake | cysticfibrosisjournal.com | 1 | |
D. Sanders | cysticfibrosisjournal.com | 1 |