



We made it to the pumpkin patch twice this year and met up with the Allreds on our second trip! We had so much fun and I loved seeing both kids run around together and have a great time. Last year, Teagan had just had her Glenn and was struggling a bit- needing her NG and not feeling great. This year she was all over the place trying to keep up with Gavin!

Gavin and Cade- best buddies!



Waiting for our appt. and enjoying fruit smoothies- yum!
After the dr. cut off her cast she started to cry and tried to put it back on! Eventually she thought it was funny to be able to put it on either hand and was pretty entertaining. We went over to x-ray next and they came back showing that she wasn't completely healed- so the dr. re-casted her! 
Here she is getting her pre-cast padding on. I don't have any pics of the finished product but we went with a much lower key purple this time.
After two more weeks we took her back in (this last tuesday) and had it taken off for good!A few days after Teag was re-casted we attended the Harvest Ball fundraiser benefitting Seattle Childrens Hospital. Teagan was the 'feature patient' this year and I was so bummed that she still had her cast on! I have so many pictures from the night that I'll have to write a new post soon!
Last week Teagan had a cardiologist appt. for the first time since July. She had an ekg, echo and all the other usual stuff and everything went great! I was nervous about how she would handle her echo since it had been 6 months since her last, but she laid there and watched cartoons like nothing was happening!
Right now her heart function looks good (for her anatomy) and we're scheduled for a SAT check/follow up in Jan. Dr. Herndon didn't up any of her meds, and discontinued her ranitadine (for reflux). So she's only on her aspirin, Captopril (2mls- 3x's/day) and furosemide (lasix) (.6mls-2x's/day). We decided that she no longer needed her reflux med (ranitadine) and so far she's done fine without it. I think she's actually eating more now that its stopped! She's still not on the growth chart- weighing in at 20lbs 3 oz at 19 months- but no one is too concerned. We've really been pushing the pediasure and Boost Kid essentials in between meals and she's slowly gaining weight... Her sats were 87! Which is a little higher than last time (her usual is around 83). I asked if it was normal for her sats to be going up instead of dropping and Dr. H said, "hey, we'll take it!" ha...
I'm working on another post about the Harvest Ball and also have some exciting news to share soon!
Teagan broke her arm this week! I still can't believe that it happened, but I'm reminded every time I see that flash of neon pink running around... We were out at the store on Saturday and she fell pretty hard on the tile floor. She seemed ok, and I was able to calm her down within a few minutes so we headed home. But that evening and all day Sunday she seemed a little 'off' and would complain when we dressed her or touched her left arm. So on Monday we took her in for an x-ray and sure enough she fractured both bones in her left forearm! The Dr. said it looked like a 'Torus' fracture and told us its pretty common in little kids and heals fast. But that it would be good to cast her because its hard to tell an 18 month old to 'be careful'. Funny, I tell her that all the time! She only has to wear it for 3 weeks but I can't imagine how it will look by then. Its already brown and has bits of food in the cracks... mealtime is interesting for sure! I've been using lots of purell on her cast hand and trying to find clothes that fit over her arm which has been challenging. Teagan doesn't seemed phased at all by her new accessory and thinks its funny to bang it on every surface she can to see what noise she can make. She's also learned that its quite the weapon when playing with Gav!

Not slowing her down in the sandbox!

