Saturday, October 10, 2009
Friday, September 4, 2009
I do ask, not to be rude or anything, that everyone hold the visits and the phone calls until Sunday atleast. Tucker will be out of his element, he is still pretty shaky and we have lots of settling back in to do...not to mention figuring out the medicine schedule for home and getting it all organized so as not to mess anything up.
We will be followed by Mercy very closely the rest of our recovery, with appointments each week for a while. But we are so glad to be coming back to KC.....
I'M LEAVING ON A JET PLANE, DONT KNOW WHEN I'LL BE BACK AGAIN!!! LEAVING...headed home.....not in BOSTON anymore.......Going back to KS with Toto.....Acting like a baby and heading out.........you know them all! -Mommy!
And Daddy is excited to have his family all together again.
This week has been quite a joy to me. Not only is Tucker and Karen coming home on Saturday, our son Brett returned home Wednesday from his Marine training. He broke his foot and had to stay an extra month, so it is a joyous time in the Bryant home.
I know we still have months of recovery at home, but I wanted to thank everyone for their support and donations to my family. We couldn't have done it without the thoughts and prayers of all our family and friends and newly found friends.
Thank you from the bottom of our hearts. We love you all!!!! -Daddy
Thursday, August 27, 2009
The day is filled with family fun activities including pony rides, crafts, inflatables and clowns,d food! Come out and support Tucker's Troupe and walk for Down Syndrome. Proceeds from this event go directly to individuals here in Kansas City.
Click Tucker's Troup badge to sign up. A $20.00 donation gives you a shirt and access to the walk on the 24th of October.
Last year we had a great turnout and we hope to see everyone there again this year!
Tuesday, August 25, 2009
OK, so tomorrow is the swallow study. WE NEED PRAYERS....we need good results, we need Tucker to fly through this...otherwise they are talking a Mic key button again. PLEASE ...man I don't want to go down that road again. I pray that it was a fluke and he flies through it, I pray that IF anything needs to be done it is to thicken liquids but eat regular. I thought we would go home with a tube down his nose until he got stronger if the results were that he was aspirating....Dr Lawson says that the tube down the nose will only mess up his swallow even more that he would suggest a belly tube placement...which means another surgery, another intibation, which means more time in Boston. Eating and no i.v meds are all we need to accomplish before going home....there are no more i.v meds now, as of today...and the eating was no issue until they thought he was aspirating....which they thought was happening because of the wet xray and the "junky" sound.. ALL of us know, Tucker always sounds junky, it is normal for him. Lawson said that they rely on the parents to know what is typical and what is not and he too thought maybe it was a singled out, tired boy being off the c-pap mask for so long, that caused the wet xray and not aspiration...again we will know tomorrow. Lots of good vibes this way tonight...PLEASE
I also asked about getting us home to Mercy...finishing our recovery there. He said that is something they do a lot of and it is definitely something he would bring up to our cardiologist..I got the impression, however, that is something that would take some arranging, not something that we could decide and do the next week....I may be wrong. It will be addressed again very soon. I want to be HOME...even if that means the hospital in KC!!
Tucker was mad at me when I first showed up in the room. He looked at me as if he didn't know me....I loved on him, kissed him lots and he finally broke it loose. He still loves me..THANK GOODNESS! He is resting now after fighting it for hours. We get to give him a tub bath tonight which will be nice. I would like to add that to his nightly regime so he knows it is about time to go down for the night. Just like being back home for those 2 weeks, I fell right back into it, as if I had never left.
So, we had our first night in the regular room. It wasn't too bad, just getting used to the new sounds and people in and out of our room at all times of the night. Tucker slept fine. He went to sleep around 9:30 or so. We finally have a TV that we can play his videos on and he seemed to really enjoy it. We were very luck and have a private room. I guess they figured we have spent hundred of thousands of dollars, we should at least get a private room. Thank goodness for insurance!!
Karen comes back today, she will be here around noon today and will hopefully only have to stay a couple of weeks. My goal while she was gone was to have Tucker in a regular room before she returned and we have met that goal so far. (Don't want to jinx anything, so that's all I have to say about that). I will be leaving tomorrow morning around 10 so I can be back home with Hunter, who starts high school today, and get back to work.
I didn't get a very good video of us leaving the ICU, but I have a little one of the nurses and assistants getting us settled into our new room, enjoy!! The other picture is of our nurse Katie. She went with us for our daily walk to the park.
Monday, August 24, 2009
Friday, August 21, 2009
After several doctors came by and did their routine stethoscope check, the decision was made to put him back on the mask for a little while. I must admit, this really busted my bubble. What I didn't realize was the plan was to put him back on anyway, just not this early. It was clear that he was just not ready to solo without the mask. Once the mask was back on, his saturation's returned to the high 90's and his color returned. The plan is to do the same as before, sprints off while he is awake and on while he is asleep. I was reassured several times by the staff that this was expected and we will still probably go to the floor early next week, so don't look at it as we are going backwards. It was hard for me as a parent to accept that, but like Karen and I have always said, we are on "Tucker Time"!!
After the mask was put back on, the decision was made to replace the NJ feeding tube so we can feed him without the worry of him aspirating liquid into his lungs causing them to get wet. As we know from the operations as a baby, until he gets stronger, sometime he swallows wrong and some of the liquid can go into his lungs. The plan is to have a swallow study done, of course it won't be until Monday, and Tucker can't have anything by mouth until after it is done.
After the mask was put back on, I felt as if my heart was broken. We were going so good and things were looking up, doctors talking about transferring us to the floor and now this!! I felt like the wind was knocked out of me. At about 8:30 pm, guess what, we took the mask off, put him into his stroller and strolled around the ICU again with just the oxygen in his nose. Saturation's were 100 percent!! That is just what I needed to put the wind back into my sails. That little boy just needed a little rest, he needed a little "Tucker Time"!! He amazes me each and every day. I used to wonder, when we found out he was Downs and had heart problems, what I did so bad for God to punish me with a child like Tucker, now I wonder what I have done for God to bless me with a child like him. If you have ever watched the movie "Radio", where Cuba Gooding JR., plays the handicapped kid that the football coach helps out, the coach has a great line, "If we treated each other half the time like Radio does all the time!!" That's the truth, what a wonderful world this would be. Tucker doesn't know a stranger, he shows love no matter who you are.