today we took both of the boys in to see the doctor (i might add levi and tytus have 2 of the best doctors i have ever been around they really know their stuff and are great with kids and always go above and beyond for us and our boys) so we took them [...]
Categories: Children, Cystic Fibrosis (CF), Levi, Tytus | 
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last night was great. i didnt hear levi coughing at all and i only hear tytus twice. ( i hope that is because they are getting better and not because im so exausted that i slept so hard and didnt hear them.) anyways last night went well. this morning the boys temps are in [...]
Categories: Blogging, Levi, Tytus | No Comments »
tytus has joined his brother in the not feeling well department. he had a 102 fever last night and was up coughing a few times but it is down to 100.5 this morning and he is his happy self. he has a not so good sounding cough(it sounds like it hurts him) but everything [...]
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it has been on and off with Levi. he had a rough night on saturday and then sunday was better and last night was tough again. it just breaks my heart when he can’t sleep because he is coughing so much. i have to say that i am so thankful that when [...]
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today the doctor called us and decided because we will be going out of town she wanted to start him on antibiotics. she also gave us a steroid to have on hand incase he starts wheezing. today he was pretty energetic but was coughing pretty hard on and off. we are doing [...]
Categories: Cystic Fibrosis (CF), Levi, Uncategorized | No Comments »
i’m bummed to report that i think levi is getting sick AGAIN! i’m thankful nothing has been too serious but it has been on and off for a few months now. he is coughing a ton again and had a fever earlier in the week. i’m praying it is nothing big again [...]
Categories: Blogging, Cystic Fibrosis (CF), God, Levi | No Comments »
here is our 2010 walk website check it out
Categories: Great Strides, Uncategorized | No Comments »
this is an amazing song with a powerful story. check it out! i cried and was inspired at the same time! you will see many posts in the near future about trying to raise money and awareness for Cystic Fibrosis. I’ll also post sometime soon about all the emotions that have been going [...]
Categories: Cystic Fibrosis (CF) | No Comments »
our little tytus is 9 months old. he is sitting up on his own and probably going to start crawling any day. i’m hoping he waits a while i know how that is once they mobil. levi and tytus are finally learning to play together now that tytus is able to interact and [...]
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a few weeks ago jason told me at 6 in the morning to pack my bags and that that day at noon we were going on a trip the boys were staying here with nana and papa and we were going on vacation. (yes i know so romantic and fun) needless to say i was [...]
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