Lukas had his pic line removed from his arm today !! He was very nervous about removing it. It has become natural for him to have a line in his body and he also knows this means pokes when he goes to doctor appointments and scans. He knows way too much for a six year old. Anyway...he started screaming when the nurse asked him to lay down and didn't stop screaming until she was done. I kinda thought he would be tougher than that thinking of all the pain he has been through. Please pray God will comfort him and spare him from worry and pain as we near the time for the IV's he needs to get for his scans on April 19th, 27th and 28th.
On a brighter note... we went to the "MAKE-A-WISH" wishing place today!! They have a beautiful brand new place near arco arena. When we walked in past the fountain we saw one thousand hanging stars from the high ceiling. Luke will have his very own star up there, forever more. They gave him a special key to keep in his pocket and they spent some time getting to know him. He drew pictures of what his wishes might look like and then unlocked a big door with his key. He entered a glowing blue room (his favorite color). In the center was a wishing well. Luke thought carefully about his wish and dropped it into the well. Suddenly the lights started twinkling and flashing the music started playing and we all danced...
Luke's Journey
- Mike and Erica
- An information & update page about Luke and his family’s journey through discovery, and treatment of his tummy "bump". AKA abdominal mass.
Tuesday, March 23, 2010
Thursday, March 11, 2010
Everybody yell "OFF ISOLATION ! YAY !"
Thank you for your prayers. Our appointment with the transplant Dr. exceeded or expectations. The drive was nice, the weather was perfect and Luke's doctor said "he is now released from his six month isolation period !" The results are not in from his immune study yet, but Dr. Horn said judging from his last counts, he is good to go play with other kids and be outside without a mask on. Upon receiving results we will know how relaxed we can be. I'm not sure if we will ever be very relaxed about germs. Germ-a-phobia is pretty much part of our life now. We even have one of those hospital hand sanitizer machines at the front door! lol. Anyway...after Luke's appointment he wore his mask through the hospital out to the car and we headed over to a fancy bakery near the hospital where Mike's cousin Lynn works. We told Luke he could take his mask off to eat! He seemed little nervous (or maybe I was) but he quickly felt comfortable when Lynn brought him a big beautiful piece of quiche and a banana cream pie! We stuffed ourselves with yummy treats and headed over to have a tour at the "Mythbusters". Mike worked for the discovery channel show while they filmed in Ione last month and they invited us to stop by. We had a fun tour and got T-shirts !! A lovely day of celebration :) Thank you Jesus for your many blessings :)
Tuesday, March 9, 2010
Immune Study 3/10/2010
Hello to all !!
I just realized it has been 3 weeks since my last post. Sorry. Where did the time go? After many calls and a little frustration UCSF finally reviewed Luke's scans and compared them with all his other lung scans and they are still seeing some tiny 3mm nodules. They said it could be argued that it is scar tissue, since they cannot tell the difference (in a C.T. scan) between fungus and scar tissue . In the end, they felt it would be less risky to just continue his oral medication for another three months and scan again to make absolutely sure. Fungus can take a long time to kill completely.
We are headed to San Francisco Wednesday morning (8am appointment ! trying to get over the bridge before the traffic) for Luke's immune study. We are looking for the return of his T-cells and B-cells. I guess they are the last to regenerate after wiping out the bone marrow. The test takes a couple of weeks for results. So we are praying Luke's immune function is fully restored and he will able to play T-Ball soon. Grandpa got him a new glove, bat and ball and he has been practicing a lot.
I just realized it has been 3 weeks since my last post. Sorry. Where did the time go? After many calls and a little frustration UCSF finally reviewed Luke's scans and compared them with all his other lung scans and they are still seeing some tiny 3mm nodules. They said it could be argued that it is scar tissue, since they cannot tell the difference (in a C.T. scan) between fungus and scar tissue . In the end, they felt it would be less risky to just continue his oral medication for another three months and scan again to make absolutely sure. Fungus can take a long time to kill completely.
We are headed to San Francisco Wednesday morning (8am appointment ! trying to get over the bridge before the traffic) for Luke's immune study. We are looking for the return of his T-cells and B-cells. I guess they are the last to regenerate after wiping out the bone marrow. The test takes a couple of weeks for results. So we are praying Luke's immune function is fully restored and he will able to play T-Ball soon. Grandpa got him a new glove, bat and ball and he has been practicing a lot.
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