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CF Happens | Sometimes in life CF (Cystic Fibrosis) happens…pun intendedSometimes in life CF (Cystic Fibrosis) happens...pun intended
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Sometimes in life CF (Cystic Fibrosis) happens...pun intended
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CF Happens | Sometimes in life CF (Cystic Fibrosis) happens…pun intended | cfhappens.com Reviews
https://cfhappens.com
Sometimes in life CF (Cystic Fibrosis) happens...pun intended
cfhappens.com
Health update | CF Happens
https://cfhappens.com/category/health-update
Sometimes in life CF (Cystic Fibrosis) happens…pun intended. My Life Story (Playing the Cards Life has Dealt). Cystic Fibrosis (CF) Facts. Category Archives: Health update. 3rd times a charm hopefully. Posted in Blog Life. Posted in Blog Life. SHANNONIGANS GEAR UPDATE: Lools like all gear has been delivered! Thank so much to everyone who purchased Shannonigan Strong gear. I want to put out a challenge to all business owners who follow my blog and Go Fund Me to donate to the Lung Fund! Posted in Blog Life.
asthma | CF Happens
https://cfhappens.com/tag/asthma
Sometimes in life CF (Cystic Fibrosis) happens…pun intended. My Life Story (Playing the Cards Life has Dealt). Cystic Fibrosis (CF) Facts. CF Clinic/Follow up from the hospital. Posted in Blog Life. Posted in Health update. Today is day 13 in lock up. I slept a lot of today since I sleep in spurts as it is at night. I had the parade of doctors as usual this morning. 2 pulmonary docs and an infectious disease doc. Continue reading →. October CF Clinic update. Posted in Health update. Posted in Blog Life.
Well hello, “Oscar,” we meet again | CF Happens
https://cfhappens.com/2015/05/21/well-hello-oscar-we-meet-again
Sometimes in life CF (Cystic Fibrosis) happens…pun intended. My Life Story (Playing the Cards Life has Dealt). Cystic Fibrosis (CF) Facts. Well hello, “Oscar,” we meet again. Posted in Health update. Until next time…. Holy lung spasms batman! Oscar and Oscar II have arrived ». Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. Pain Clinic follow up.
iv ball | CF Happens
https://cfhappens.com/tag/iv-ball
Sometimes in life CF (Cystic Fibrosis) happens…pun intended. My Life Story (Playing the Cards Life has Dealt). Cystic Fibrosis (CF) Facts. Tag Archives: iv ball. Well hello, “Oscar,” we meet again. Posted in Health update. 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. Consult your doctor for medical advice. Pain Clinic follow up. Depression; It’s real. 3rd times a charm hopefully. Follow Blog via Email.
Caringbridge | CF Happens
https://cfhappens.com/caringbridge
Sometimes in life CF (Cystic Fibrosis) happens…pun intended. My Life Story (Playing the Cards Life has Dealt). Cystic Fibrosis (CF) Facts. Get past health updates here www.caringbridge.org/visit/65rosescf. I started a caringbridge page July 26, 2006. So yes there is a lot to read on there if you are bored and have the time. Enjoy! Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). Notify me of new comments via email.
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Orkambi – Rejection, Appeal, and Life in Between | TheraPink
https://therapink.wordpress.com/2015/08/12/orkambi-rejection-appeal-and-life-in-between
The Pink Perspective on my life with Cystic Fibrosis. This blog represents only my opinions and my personal experiences, and in no way intended to provide medical advice. Please consult with your doctor before making any chances to your health care regimen. Follow Blog via Email. Enter your email address to follow this blog and receive notifications of new posts by email. Join 89 other followers. Alternative Medicine and Treatments. CF “School”. KIDS and CF Series. Lemons out of Lemonade. August 12, 2015.
TheraPink | The Pink Perspective on my life with Cystic Fibrosis | Page 2
https://therapink.wordpress.com/page/2
The Pink Perspective on my life with Cystic Fibrosis. This blog represents only my opinions and my personal experiences, and in no way intended to provide medical advice. Please consult with your doctor before making any chances to your health care regimen. Follow Blog via Email. Enter your email address to follow this blog and receive notifications of new posts by email. Join 89 other followers. Alternative Medicine and Treatments. CF “School”. KIDS and CF Series. Lemons out of Lemonade. June 22, 2016.
Cystic Fibrosis Blogroll: How To Get Your Blog Listed
http://cfblogroll.blogspot.com/p/how-to-get-your-blog-listed.html
Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. How To Get Your Blog Listed. If you have cystic fibrosis, or are the parent or spouse of a CFer, and you keep a blog—congratulations, you're eligible for membership on the CF Blogroll! The blogroll is a great way to drive new traffic to your blog and make new friends with CF in the process. Joining the blogroll is easy! Please help spread the word about the CF blogroll! If you're...
Cystic Fibrosis Blogroll: Featured Blogger: Kristy Of "Life in a Bubble of Fun"
http://cfblogroll.blogspot.com/2013/07/featured-blogger-kristy-of-life-in.html
Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. Tuesday, July 30, 2013. Featured Blogger: Kristy Of. Life in a Bubble of Fun". Today's Featured Blogger is Kristy from Life in a Bubble of Fun. First, tell me a little bit about yourself and your child with CF! My name is Kristy, I am a stay-at-home-Mum married with three children aged 6, 5 and 2. How old was your child when they were diagnosed with CF? The specialists at the Chi...
Cystic Fibrosis Blogroll: Featured Blogger: Melissa of "My Lung Transplant Journey"
http://cfblogroll.blogspot.com/2013/03/featured-blogger-melissa-of-my-lung.html
Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. Tuesday, March 19, 2013. Featured Blogger: Melissa of. My Lung Transplant Journey". Any member of the CF Blogroll is eligible to be a Featured Blogger! If you'd like to be have a little time in the spotlight and help bring more traffic to your blog, leave a comment or e-mail beingcindybaldwin AT gmail DOT com, and we'd love to feature you! Don't forget to pay her blog a visit.
Cystic Fibrosis Blogroll: Anything Is Possible: A CF Patient Interviews Her Parents About Life, Family, and Raising A Child With CF
http://cfblogroll.blogspot.com/2014/11/anything-is-possible-cf-patient.html
Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. Thursday, November 6, 2014. Anything Is Possible: A CF Patient Interviews Her Parents About Life, Family, and Raising A Child With CF. I was recently contacted by Erin Evans, a 31-year-old CF patient who works for the Cystic Fibrosis Lifestyle Foundation. Erin sent me a blog post that she'd written for the CFLF blog. See full interview here. Posted by cindy baldwin. One Breath at...
Cystic Fibrosis Blogroll: Organizing the CF Blogroll
http://cfblogroll.blogspot.com/2013/10/organizing-cf-blogroll.html
Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. Monday, October 28, 2013. Organizing the CF Blogroll. I never could have imagined when I began this blogroll just how much it would take off! We now have about a hundred bloggers who have been added to the CF Blogroll, with more requesting to join on a regular basis. I don't know about you, but I love the opportunity to have so many CF blogs in one place! Life With Cystic Fibrosis.
livinglifebreathlessly.blogspot.com
Living life breathlessly: August 2015
http://livinglifebreathlessly.blogspot.com/2015_08_01_archive.html
8220;Life is not measured by the number of breaths we take, but by the moments that take our breath away”. Monday, August 31, 2015. 31 on the 31st! Apparently this is called your Crown or your Golden birthday! Yay for being 31! Chris is taking me out for supper tonight, and I only worked half-day today, so it's been a great day. Tomorrow evening we're having supper with my parents so I don't need to think about what make for supper, which is awesome as it will be the first day of month-end at work. Anoth...
livinglifebreathlessly.blogspot.com
Living life breathlessly: August 2014
http://livinglifebreathlessly.blogspot.com/2014_08_01_archive.html
8220;Life is not measured by the number of breaths we take, but by the moments that take our breath away”. Tuesday, August 26, 2014. Last week in my 20's! 5 days to go till my birthday! Stressing a bit about the weather as there is (another) cold front due! Seems like the worst will be on Friday. but hoping it comes sooner so that it will be over sooner! Food is all organised now at least. and decor. Eeeekkkkkk! Barely getting time for gym! Had discus training again today, went pretty well. So yesterday ...
livinglifebreathlessly.blogspot.com
Living life breathlessly: June 2014
http://livinglifebreathlessly.blogspot.com/2014_06_01_archive.html
8220;Life is not measured by the number of breaths we take, but by the moments that take our breath away”. Friday, June 27, 2014. 53% again. yay. Lung function was stable yesterday at 53%. same as last time (although used a different machine). So that's good! Weight down a bit - need to eat more I guess, and blood pressure meds have been increased. I also did 6 min walk test (in boots. not best idea ever, shins sore today! Thursday, June 19, 2014. Was very surprised and it made my week! On a different no...
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CF Happens | Sometimes in life CF (Cystic Fibrosis) happens…pun intended
Sometimes in life CF (Cystic Fibrosis) happens…pun intended. My Life Story (Playing the Cards Life has Dealt). Cystic Fibrosis (CF) Facts. Posted in Blog Life. Posted in Blog Life. New CF Combo Therapy, Symdeko by Vertex, Approved by FDA for Certain Patients. Announced that the U.S. Food and Drug Administration (FDA) approved Symdeko. As a therapy for cystic fibrosis (CF) patients carrying two copies of the. Posted in Blog Life. Transplant Talk: Sinking in. Posted in Blog Life. Posted in Blog Life.
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