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Jada ..

Our blog will update on Cystic Fibrosis...how it affects our family personally. Sometimes it is honest to the point of harshness. We live with CF everyday. Our 5 year old daughter, Zoe, has CF. Thank you for reading.....
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Positive thoughts and prayers needed! by Jada .. Posted in: Blog Posts in Cystic Fibrosis One of these days I'll be able to write good news in this blog! I'm positive it will happen! Zoe was re-admitted back into Wolfson Children's Hospital yesterda ... Read on »
Hospital again..... :-( by Jada .. Posted in: Blog Posts in Cystic Fibrosis After 4 xrays over the last month....persistent coughing while Zoe is sleeping...she's sooooo tired. She went to her CF Dr on Friday. They repeated another chest X-ray. ... Read on »
June 2013 by Jada .. Posted in: Blog Posts in Cystic Fibrosis The CFF Great Strides walk was a success! There were many supporters for our little Zoe. Bonefish Grill brought their Zoe for Life team...it's always so wonderful to ... Read on »
Great Strides time of year!!! by Jada .. Posted in: Blog Posts in Cystic Fibrosis I can't believe I haven't updated the blog since Christmas.....I'm so sorry! Zoe was admitted in January for IV antibiotics. She did 3 weeks of them...and was still co ... Read on »
Merry Christmas!!! by Jada .. Posted in: Blog Posts in Cystic Fibrosis I guess the old saying, "No news is good news" applies to my posting blogs.... I didn't mean for it to be over 3 months since posting....but it is actually because the sa ... Read on »
HAWAII !!!!!!! by Jada .. Posted in: Blog Posts in Cystic Fibrosis   Well we are in the final countdown... Only 3 days left until we leave for Hawaii on Zoe's dream trip!! Thanks to a wonderful organization in Jacksonville called Drea ... Read on »
Great clinic visit!! by Jada .. Posted in: Blog Posts in Cystic Fibrosis Two weeks ago we went to CF clinic because Zoe was so sick. She was coughing so much that she could not to her breathing test (PFT's)....the best number they could get out ... Read on »
Hospital Discharge day by Jada .. Posted in: Blog Posts in Cystic Fibrosis Today is discharge day!! They've already de-accessed her port and re-accessed it with a fresh Huber needle. She did cry a little when they put the new needle in...but w ... Read on »
End of year 2011 post.... by Jada .. Posted in: Blog Posts in Cystic Fibrosis It truly was a very nice year.....we all learned a lot about love, patience and endurance. God is awesome! Zoe was in the hospital only 3 times....that's a blessing to ou ... Read on »
Surgery, family and Great Strides!! by Jada .. Posted in: Blog Posts in Cystic Fibrosis Sorry it has been a while....things have been a little crazy around here. After Zoe went off of iv's, we went to her ENT Dr. to see how the CT scan of her sinuses was af ... Read on »
Off of Iv's by Jada .. Posted in: Blog Posts in Cystic Fibrosis Zoe finally is finished with her 3 weeks of iv antibiotics! Yay! She was very happy to be free of her picc line. The girls went back to gymnastics last night for the first ... Read on »
Zoe health update.... by Jada .. Posted in: Blog Posts in Cystic Fibrosis Thank you for all the good well wishes. Unfortunately, Zoe's pft's are even LOWER than before hospital.  Sooooo, one more week of iv's. 79!!! I was quite shocked. And sadde ... Read on »