allysallies.wordpress.com
Yes… I’m staring… at your feeding pump! | Ally's Allies
https://allysallies.wordpress.com/2008/02/25/yes-im-staring-at-your-feeding-pump
Yes… I’m staring… at your feeding pump! February 25, 2008. It was near the end of last summer when I took my girls to see a live Signing Time. Show at a local school theater. Having been long time fans of Rachel. And the amazing work she does for the hearing impaired, I made sure we got there early and got a front row seat… I was there with a friend and her two little girls as well. Although Rachel was a bit under the weather, the show was fantastic and the kids had a blast! No, I keep staring until that...
teamfaithfull.blogspot.com
Team FaithFULL: June 2010
http://teamfaithfull.blogspot.com/2010_06_01_archive.html
Spreading awareness, giving our family updates and helping to fund a cure for Cystic Fibrosis. Breathe Freely, Conner Man. My heart and eyes cry today for seven year old Conner who passed away Thursday, June 24, 2010. He battled cystic fibrosis and prune belly disease, which meant he essentially had no muscles to cough.and with CF, that's a terrible combination. It's evident that he was such a fighter and joyous child yet cystic fibrosis has taken another precious, innocent life. Faith had a fabulous tim...
teamfaithfull.blogspot.com
Team FaithFULL: February 2011
http://teamfaithfull.blogspot.com/2011_02_01_archive.html
Spreading awareness, giving our family updates and helping to fund a cure for Cystic Fibrosis. Although she gets a little nervous, Faith has been enjoying her art and science class on Fridays. Her 6th birthday is coming up next month! I am in awe each year that passes that Faith has yet to be put in the hospital for reasons related to cystic fibrosis. She is such a strong little fighter with a heart of gold. Subscribe to: Posts (Atom). View my complete profile. At GreatStrides May 1.
teamfaithfull.blogspot.com
Team FaithFULL: January 2010
http://teamfaithfull.blogspot.com/2010_01_01_archive.html
Spreading awareness, giving our family updates and helping to fund a cure for Cystic Fibrosis. We celebrated Brookie turning 3 by giving her an official party, finally. It was a great bash at the backroom of Strikes Bowling. Faith is loving dance class and Brooke is thinking about joining in soon. Faith's appointment went well this month.she gained about a pound since last month! Mid January we had this conversation:. Faith: "Mommy, if you have an eye in the back of your head, how does it see? As everyon...
breathe4tomorrow.wordpress.com
Parenting a Child with CF (Thank you Evan Burton) | Breathe 4 Tomorrow
https://breathe4tomorrow.wordpress.com/2008/11/11/parenting-a-child-with-cf-thank-you-evan-burton
Making life easier one breath at a time…. Parenting a Child with CF (Thank you Evan Burton). November 11, 2008 in CF. PARENTING A WARRIOR WITH CF. The Amazing Power of the Mind. 8211; Mahatma Gandhi. The Importance of Love above All Else. An Example to Learn From. Today I am 23 years old and I am experiencing great success in pursuing my dream of becoming a professional musician. My brother and I have toured the country with our band Indubious and began to spread our message to the world. Our fir...For m...
breathe4tomorrow.wordpress.com
A place for our CF community to chat… | Breathe 4 Tomorrow
https://breathe4tomorrow.wordpress.com/2008/11/20/a-place-for-our-cf-community-to-chat
Making life easier one breath at a time…. A place for our CF community to chat…. November 20, 2008 in Uncategorized. Http:/ breathe4tomorrow.chatango.com. We created this thought it would be a great way to interact between all of us! Let me know your feedback…. You can visit our website by clicking on the logo below. Thank you. Comments feed for this article. December 2, 2008 at 9:33 pm. Check out my blog! You have won an award =]. Leave a Reply Cancel reply. Enter your comment here.
breathe4tomorrow.wordpress.com
Cystic Fibrosis saved my life… | Breathe 4 Tomorrow
https://breathe4tomorrow.wordpress.com/2008/12/19/cystic-fibrosis-saved-my-life
Making life easier one breath at a time…. Cystic Fibrosis saved my life…. December 19, 2008 in CF. Last night I was having “one of those” nights… I am allowed those ever so often, so I am told… Anyways, whenever I feel that way, I like to think about the “good” that comes along with CF… and I was quickly reminded of a situation last year, that I would like to share with you…. The nurses kept telling me I needed relax, how could I? You can visit our website by clicking on the logo below. Thank you. I end ...
teamfaithfull.blogspot.com
Team FaithFULL: 2011 March 4
http://teamfaithfull.blogspot.com/2011/03/2011-march-4.html
Spreading awareness, giving our family updates and helping to fund a cure for Cystic Fibrosis. 6 years ago this morning I was honored to bring an amazing little girl into this world.allowed to snuggle and memorize her face for a few minutes before she was taken to NICU. Faith, you have taught me a love I never knew existed and you have touched many lives. You are beautiful through and through, strong, compassionate and ALWAYS see the glass half full. Subscribe to: Post Comments (Atom).