Last night Zoe started acting sick. Actually, to explain, Zoe hasn't caught many "colds". The last "cold" she had was probably about 2 years ago. Weird, I know. You see, when Zoe is sick, it is a lung bacterial infection. It takes us months and months of oral, inhaled and iv antibiotics to clear her up then. But, as far as the normal kid "colds" she just doesn't normally get them. Soooooo.....the big question now will be....will this "cold" turn into a lung issue???? I hope not. We are going to watch her for a few days and see what happens. Right now, it is an extremely stuffy nose, sneezing, watery eyes, occasional cough. MAYBE it will go away....
On another note, we met a wonderful gal tonight, talked to her about cf, the walk, etc....she told us that she and others will be on board to join our team, "Zoe for Life" for the Great Strides walk in April! It is always so wonderful to Scott and myself to meet people that seem to 'really' care.
Thank you all for your love and support...without you we would be NO-Where.
Have a great night!
Scott and Jada....and of course, Zoe
Zoe for Life.... Our journey with Cystic Fibrosis....
I hope this cold stays out of her lungs!
ReplyDeleteJust wanted you to know I bookmarked your new site. Thanks for letting us know about it in your other blog. :)
CowTown
You and Scott are such great "ambassadors" for CF! I love how you both are a "magnet" for support for Zoe--and for Great Strides! Good job with this site! Love it!
ReplyDeleteJust checked out your site. I love that pic of Zoe on the main page! That's adorable! And I really enjoyed your Montage, too - very well, done. I'll bookmark your site to keep up with what's happening...Aspiemom
ReplyDeleteHi, Jada,
ReplyDeleteI always am interested in reading your posts at cf.com. My little grandaughter has CF. She's 19 months old. I live in Bradenton Florida. She's in Virginia. I spend lots of time in Virginia, LOL.
I talk about her a lot on my blog, but not all the posts are about CF. Take a look at my little darling. She is such a joy to me...my only grandbaby.
I love the blog! Jada, you and Scott do so much to raise awareness and money for CF. I can't thank you enough.
ReplyDeleteStacey
Great job Jada! Thank you for sharing your family's story with the world. You are helping others understand why it is so important to cure CF and why we must continue to fight until we do!
ReplyDeleteIf anyone wants to get invovled with the Cystic Fibrosis Foundation and help to cure Zoe and others please feel free to contact me.