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Cystic Fibrosis Blogroll

Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll!

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Cystic Fibrosis Blogroll | cfblogroll.blogspot.com Reviews
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Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll!
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1 cystic fibrosis blogroll
2 we're still here
3 cindy baldwin
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5 labels housekeeping
6 cf bloggers
7 parents and spouses
8 transplant talk
9 breathe easy
10 wwwbeingcindy com
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cystic fibrosis blogroll,we're still here,cindy baldwin,1 comment,labels housekeeping,cf bloggers,parents and spouses,transplant talk,breathe easy,wwwbeingcindy com,mypigeonpair com,theorganisedhousewife.com au,featured blogger,live*laugh*love*breathe
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Cystic Fibrosis Blogroll | cfblogroll.blogspot.com Reviews

https://cfblogroll.blogspot.com

Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll!

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cfblogroll.blogspot.com cfblogroll.blogspot.com
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Cystic Fibrosis Blogroll: We're still here!

http://cfblogroll.blogspot.com/2014/10/were-still-here.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 1, 2016. Friends of the CF blogroll,. I've had a few people ask me if I'm still adding blogs to the blogroll, and the answer is YES! I'm also always happy to feature any blogger from the blogroll who is interested. Send me an email or leave a comment here and I'll forward a copy of the interview questions! Hope to see YOUR blog here soon! Posted by cindy baldwin.

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Cystic Fibrosis Blogroll: Featured Blogger: Kayla of "One Breath at a Time"

http://cfblogroll.blogspot.com/2013/02/featured-blogger-kayla-of-one-breath-at.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, February 5, 2013. Kayla of "One Breath at a Time". If you'd like to be a Featured Blogger, leave a comment or e-mail beingcindybaldwin AT gmail DOT com, and we'd love to feature you! Today's Featured Blogger is Kayla of " One Breath At A Time. I "met" Kayla through the CF Blogroll and am excited to be able to feature her today! First, tell me a little bit about yourself!

3

Cystic Fibrosis Blogroll: Featured Blogger: Cheriz of "Life of Cheriz"

http://cfblogroll.blogspot.com/2013/01/featured-blogger-cheriz-of-life-of.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, January 22, 2013. Cheriz of "Life of Cheriz". If you'd like to be a Featured Blogger, leave a comment or e-mail beingcindybaldwin AT gmail DOT com, and we'd love to feature you! Today's Featured Blogger is Cheriz of " Life of Cheriz. I "met" Cheriz through the CF Blogroll and am excited to be able to feature her today! First, tell me a little bit about yourself! What kin...

4

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...

5

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...

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breathebravely.blogspot.com breathebravely.blogspot.com

Breathe Bravely: August 2014

https://breathebravely.blogspot.com/2014_08_01_archive.html

A blog about my beautiful life living with Cystic Fibrosis: to educate and help promote awareness and understanding associated with CF. Dedicated to sharing 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. Sunday, August 31, 2014. Enough clothes for a week's worth of all weather scenarios? Toothbrush, shampoo, hair brush? Contact case, solution, glasses? What am I forgetting? My su...

ontonewwindows.blogspot.com ontonewwindows.blogspot.com

On To New Windows: January 2015

http://ontonewwindows.blogspot.com/2015_01_01_archive.html

On To New Windows. My journey to new lungs. Every breath of the way! Tuesday, January 13, 2015. Its been awhile since my last post. Sorry about that. I have decided to stay home from school again this semester. Don't worry my health is good still! While I am home I am hoping to finally get a job! While I wait (and probably even while I am working) I have started an Etsy shop! Stop by and check out what I have for sale, also tell your friends! Check out my shop here. Subscribe to: Posts (Atom).

prettyclavicles.blogspot.com prettyclavicles.blogspot.com

Lena and Cystic Fibrosis: New clinic

http://prettyclavicles.blogspot.com/2015/03/new-clinic.html

Lena and Cystic Fibrosis. Friday, March 27, 2015. So, I  went to my new CF clinic this morning, my parents took me. It went shockingly well. I am going to miss my old CF team, but this team seems more suited to my individual needs. Anyways, I'm attaching an image of me doing my PFTs. I really don't think I have anything else to share, but, I'm sure there will be more in the future. Always is. Subscribe to: Post Comments (Atom). Lena and Cystic Fibrosis. Pennsylvania, United States.

cysticfibrosisblog.blogspot.com cysticfibrosisblog.blogspot.com

Cystic Fibrosis: Hope & Health: YOU are worth it

http://cysticfibrosisblog.blogspot.com/2014/09/you-are-worth-it.html

Cystic Fibrosis: Hope and Health. Tuesday, September 02, 2014. YOU are worth it. Watching the first episode of the red band society and the fault in our stars really helped cement in the truth I've known for so long. I wish everyone with a disease would know this and BELIEVE it. YOU are not your disease! YOU are worth loving! YOUR life isn't of less value because you're sick, in pain and need more help/assistance! Love is in sickness and health! Subscribe to: Post Comments (Atom). View my complete profile.

cysticfibrosisblog.blogspot.com cysticfibrosisblog.blogspot.com

Cystic Fibrosis: Hope & Health: Pregnancy, Birth & Postpartum Health Regimen

http://cysticfibrosisblog.blogspot.com/2014/04/pregnancy-birth-postpartum-health.html

Cystic Fibrosis: Hope and Health. Thursday, April 24, 2014. Pregnancy, Birth and Postpartum Health Regimen. New Chapter Perfect Prenatals Multivitamin. Pill a day (has a lot of vitamins and minerals but especially vitamin K to prevent too much blood loss). Pill a day (strengthen and prepare uterus for birth). 1 cup of mama's red raspberry brew tea a day*. 100 mg of b6. Postpartum peri bottle mix. New Chapter Perfect Prenatals Multivitamin 3 a day. 2 Alfalfa pills a day. 2 Red Raspberry pills a day. To pr...

lifeinabubbleoffun.blogspot.com lifeinabubbleoffun.blogspot.com

Life in a Bubble of Fun: April 2014

http://lifeinabubbleoffun.blogspot.com/2014_04_01_archive.html

Life in a Bubble of Fun. My journey and antics of my family, including dealing with a child with Cystic Fibrosis, and everything that crosses our paths. It's just a glimpse into our Life in a Bubble of Fun. I have put a lot of thought and consideration into my words for this blog. I pour out my heart and soul for you to read, learn and share about the ongoings in my families life. Thursday, 10 April 2014. Taking a Calculated Risk! We want the kids to have a "normal" as can be life and that means doing wh...

ontonewwindows.blogspot.com ontonewwindows.blogspot.com

On To New Windows: New Year at last!

http://ontonewwindows.blogspot.com/2014/12/new-year-at-last.html

On To New Windows. My journey to new lungs. Every breath of the way! Tuesday, December 30, 2014. New Year at last! As the new year approaches I am planning on making a few big changes! I'm finally getting back to school! Pepper and I will be ditching this chilly snow filled land for a more cactusy landscape! Things with her are going great. She has begun to alert me! Last night she even warned of an impending low early enough that I never had symptoms! I am very excited about this next year!

ontonewwindows.blogspot.com ontonewwindows.blogspot.com

On To New Windows: April 2015

http://ontonewwindows.blogspot.com/2015_04_01_archive.html

On To New Windows. My journey to new lungs. Every breath of the way! Wednesday, April 29, 2015. So Im sad to tell you that its been so long since I last posted that I actually forgot how to write a new blog post! I'll blame it on the chemo brain, how long does that last by the way? But as I mentioned before I am living a healthy productive, rich life and for that I am not sorry! It leeks from time to time but most of the time its nice and dry! The old me would have been miserable and constantly calculati...

ontonewwindows.blogspot.com ontonewwindows.blogspot.com

On To New Windows: November 2014

http://ontonewwindows.blogspot.com/2014_11_01_archive.html

On To New Windows. My journey to new lungs. Every breath of the way! Monday, November 24, 2014. It is a truly wonderful experience to feel so loved and connected to so many. It is a shame however, that such an amazing way to live only tends to happen when disaster strikes. It is time we stop having to face hard times to simply feel the love from fellow humans. We were made to love each other. Let's put an end to the isolation our culture has created. Fine good or fine just okay? Subscribe to: Posts (Atom).

ontonewwindows.blogspot.com ontonewwindows.blogspot.com

On To New Windows: A letter to my Stomach

http://ontonewwindows.blogspot.com/2014/07/a-letter-to-my-stomach.html

On To New Windows. My journey to new lungs. Every breath of the way! Wednesday, July 30, 2014. A letter to my Stomach. Dear Stomach, belly, Tummie or whatever else I may call you or you may prefer to be called,. Here is how it is going to work, I give you the food (I'll even be nice and leave out the rice.for now! And the enzymes, you get to work, share the task with the intestines (no you are not off the hook either kiddos! Love you (especially when you work! Subscribe to: Post Comments (Atom).

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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 1, 2016. Friends of the CF blogroll,. I've had a few people ask me if I'm still adding blogs to the blogroll, and the answer is YES! I'm also always happy to feature any blogger from the blogroll who is interested. Send me an email or leave a comment here and I'll forward a copy of the interview questions! Hope to see YOUR blog here soon! Posted by cindy baldwin.

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