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Northwest
(11-4, 3-3)
vs.
Truman State
(3-12, 2-4)
Wednesday,
Jan 23
7:30 pm
Kirksville
 

 

 

 



Thank you so much for all of your prayers and support for Spencer and the rest of us during this adventure! We serve a mighty God and he is in control! Hopefully, we can use this to keep everyone informed of what is going on.


NEW ADDRESS
 Spencer/Cathy Barr
Target House II
1811 Poplar Avenue
Room 522
Memphis, TN 38104


PETITION


PHOTO GALLERY (New 7/15)

MARYVILLE DAILY FORUM ARTICLE #1

MARYVILLE DAILY FORUM ARTICLE #2

June 30 - 11:15 am

Well, Chayse and I are still in Memphis. We went to the airport yesterday afternoon, arriving over 2 hours early. With that, we volunteered to take a bump if they were overbooked. As we were boarding the plane, they decided they needed our seats. After rebooking on the 6:30 pm flight, Chayse said that he didn't have weight lifting or acceleration on the 3rd or 4th. With a call to the reservation desk of NW Airlines, we were able to change our flight to Monday afternoon. With the change, we are able to spend the weekend with Spencer and Cathy.

As for Spencer, he is feeling pretty good. He has had an MRI and CT scan this morning. Routine tests that have to be completed prior to the BMT. With two more apointments this afternoon, we will be off for the weekend.

June 29 - 10:00 am

Sorry for the lack of updates since Tuesday but we have been busy. Yesterday was a hectic day with several appointments for both Chayse and Spencer. It has been confirmed that Spencer is breathing and his heart is beating (not sure about the brain waves yet) :). We have moved into Target House II on Tuesday night. The room is setup a bit differently giving the appearance of more room. Since it looks out to the pavilion area, the bedrooms are much darker at night. Probably the highlight of the day yesterday for Spencer was going to watch Superman Returns.  Our little movie critic gives it four out of five stars. The highlight for Chayse was eating at Joe's Crab Shack. He recommends the Lobster Fondue. For Cathy and me, it was just spending the day together as a family. It doesn't get any easier getting ready to return to Maryville. Chayse and I will be departing for the airport at noon today and do not plan to return to Memphis until July 12, two days before the bone marrow transplant. It looks as if Spencer will finish up most of his testing the end of this week and will have a few days off before going inpatient on July 7.  

June 27 - 11:30 am

Chayse and I rolled into Memphis last night a little after 7:00 pm with Pagliai's pizza in hand. That might be the longest pizza delivery trips in history. It was great to see Spencer and Cathy after being apart for a week. We spent most of the evening catching up on the week's events and watching the College World Series. Following the game, Spencer and I had to face off in NCAA baseball on the PlayStation. After winning the first game, Spencer won the next two to capture the series.

This morning we met with the behavioral psychology staff. Spencer and Cathy will be participating in a research study looking at the effects of massage therapy and humor in the BMT process. They are believing that they will be in the group that receives massage therapy three times a week following the BMT. We have just found out that we will be moving from the Grizzly House to the Target House this afternoon at 2:00. From the previous trip to the Target House, we know it will take a couple of days to get Internet access there. After an afternoon of appointments for Spencer and Chayse, the plan is to take in some Memphis BBQ. Spencer is trying to get the lowdown on the best place in Memphis from one of the nurses in Assessment and Triage who claims to be an expert in BBQ.

June 26 - 12:30 pm

Well, we've already had a full morning of appointments and testing and are now waiting to see the eye doctor. We should have been done with the eye doctor by now, but it looks like they are running behind. We have an audiology appointment at 1:00pm, so hopefully we'll get called soon. This afternoon we will get a tour of 4th floor so Spencer will know what to expect when he gets the transplant.

We had a nice afternoon yesterday. We took the trolley downtown to the Peabody Place and ate lunch and took in the new X-Men movie which we both thought was really good. We ended up taking a horse drawn carriage most of the way back to the Grizzlies House since the trolley ends early on Sundays. Memphis really has a lot of things that are complimentary to St. Jude kids.

Rod and Chayse are currently on their way here after a later than expected start. Chayse has appointments the next three days. It will be so good to see them both again and spend some time with them.

June 24 - 6:45 pm

HAPPY BIRTHDAY, ROD!!!!  Spencer and I hope you had a great day and can't wait to see you and Chayse again Monday night. We love you and miss you!!

Spencer and I took a cab to the mall and window shopped for awhile today. We always love to check out the massage chairs at Brookstone (I think that's the name of the store). Right now I'm in the hospital lobby doing this update since we can't get wireless connection at the Grizzlies House. I just came from the cafeteria and have us all stocked up for snack and drinks until tomorrow. It looks like there are some good movies on TV tonight that I'll take in while Spencer plays his new PS2 game. I better get back so Spencer doesn't start wondering where I am. Have a great evening! Until tomorrow, good night and God bless.

June 23 - 12:00 noon

Not much happening this morning. We've been to assessment/triage to get Spencer's labs drawn and now we're waiting for the results to come back and see the nurse. We didn't get released from the hospital last night until 9pm. Like I've said before, nothing goes very fast when it comes to being discharged. After we get things finished up here at the hospital, we're going to find a way to get downtown to the Peabody Place and take in a movie and dinner. We still do not know what Spencer's schedule will be for next week, but we do know Chayse has appointments next Tuesday, Wednesday, and Thursday. As soon as we know, I'll get it posted so you all know what's going on.

June 22 - 6:15 pm

Whew! We had a bit of a scare earlier. After drawing some blood to check the chemo levels, they were really concerned the chemo was not flushing out as well as expected. In fact, the level came back at 270 which is extremely high, so they drew some more blood to recheck it and the results were right at a normal 65. We're not really sure what happened, but rejoice that the first reading was incorrect. Anyway, we're due to get out of here sometime tonight--hopefully not too much longer.

June 22 - 3:00 pm

Wow, you wouldn't believe who we just met. Emerson Drive, the country group who sings "I Should Be Sleeping" and "Fall Into Me". They all piled into our room and took lots of pictures with Spencer and me. They saw that Spencer had his Superman t-shirt on and they talked about the upcoming movie. Emerson Drive recently played in Trenton, MO and we talked about how close that was to Maryville and how I had just graduated from there. They were really cool and wished Spencer the best.

June 22 - 10:30 am

Good morning! It looks like another hot and humid day here in Memphis. From our hospital window we have a view of construction. Spencer had a good night and seemed to sleep rather well in spite of going to the bathroom every two hours. He is having some discomfort in his upper back by his right shoulder. I think he must have slept on it wrong. Right now he is playing MLB Baseball 2K6. We never did get to watch Mission Impossible II last night because something must be wrong with the movie reader in his PS2. It's no fun watching a movie with static and blue screens every now and then. Thank goodness he can still play his games!

June 21 - 8:30 pm

Good evening. We're doing fine, hanging out watching Mission Impossible II. The chemo was started at 5pm and will run for 24 hours. There was just a shift change and the new nurse said his pH level was looking good at 7.5. Spencer's dental appointment went fine with no cavities. He still has one more baby tooth to lose and it's holding on pretty tight. The x-rays look like it's a hat sitting right on top of the new tooth. The dentist wants him to wiggle it out within the next two weeks before radiation starts, either that or it will have to be pulled. Of course, Spencer thinks he can get it out on his own!

June 21 - 11:45 am

Greetings from Memphis! As I type, Spencer is undergoing IT therapy and should be done by 12:30pm. Hopefully that gives us enough time to catch a quick lunch before his dental visit at 1:00pm. After that, it's up to the second floor to be admitted for the final round of high dose chemo. Spencer's spirits are still high and he is feeling really good. He's been a great deal more talkative with the nurses and seems to really enjoy giving them a bad time. Imagine that! We had a quick visit with Amanda before going to procedures. She was the very first patient we met when we arrived here at St. Jude's and we became instant friends. There is a possibility she will need a BMT as well. We had a conversation about taking only one day at a time and not to get too far ahead of schedule. She too has felt like she got side swiped with the news of the possible BMT. I assured her God knew before we did and He is still in control and we must continue to trust Him for everything.

Rod and Chayse will drive down here next Monday as Chayse will undergo testing to be Spencer's bone marrow donor. He has appointments scheduled for Tuesday, Wednesday, and Thursday morning and then they will fly home Thursday afternoon. This way they can leave the van for Spencer and I to get around while we're here. I have not found out yet when we will get to move back into the Target House or exactly when Spencer will be admitted for the BMT. I imagine it will be around July 7, but still have not had that confirmed. Until then, we will stay at the Grizzlies House and have our meals here at the hospital. During this time, I will have to do the updates while at the hospital as we cannot get wireless Internet access at the Grizzlies House,  so hang in there with me and be patient!

We heard from so many of you who told us while we were home that you keep this page as one of your favorites and check it all the time. We cannot tell you how much that means to us knowing so many are keeping up on Spencer's progress and holding him up before the throne of God. Now that we're back here in Memphis for awhile, the updates will more frequently than when we were home. I feel there are five things God is having us pray against: Rejection (that Spencer's body would not reject Chayse's bone marrow), Infection, Side Effects, Set Backs, and Complications. We know the number five represents God's grace and it's His grace that will see us through this time. And, of course, we continue praying for a quick healing that would even astound the doctors!

I also want to take this time to again thank all of you who have sent cards, letters, games, books, money, and prayers. We are overwhelmed by the continuation of all of these things and cannot thank you enough for your generosity. We would love to be able to sit down and thank everyone of you personally, but that is not possible, so please know how much we love and appreciate you all!

 

June 15 - 12:15 pm

Time flies when you're having fun. First and foremost, Spencer is doing very, very well. It's hard to believe it has been a week since we last updated. Last Friday, I picked Cathy and Spencer up at the airport and headed to Joplin (with Minsky's pizza in hand) for my sisters wedding. Congratulations to Harry and Tiffany who were married Saturday afternoon. Following the wedding our family went out to eat with my mom and dad and then we caught the Pixar movie Cars. I think Cathy and I were more amused with the movie than Chayse and Spencer. After returning home on Sunday, we were able to watch Game 2 of the NBA playoffs (way to go Mavs). Spencer has spent most of his week hanging out with his friends. He was even able to go to St. Joe and watch a couple of Marcus' baseball game. Tuesday night, Spencer had Marcus and Tyler spend the night.  They pitched the tent and camped out (not sure how much sleep they got but they had a lot of fun). Wednesday, we received the good news that the MRD from the bone barrow aspiration drawn last week came back with 0 leukemia cells. Praise God! We also found out that the BMT will take place on the 14th of July rather than the 7th. One of the things Spencer requested before going back to Memphis was a trip to World's of Fun. On Thursday, our family as well as Marcus, Tyler and Whitney fulfilled Spencer's request. We had a great time! After a bit of coaxing Spencer, Tyler and I got up the nerve to ride the Patriot. Needless to say, we loved it especially Spence. He and I closed down the park riding it three straight times. It is the first big coaster that Spencer has ever been on but I am sure it won't be his last. We finished the night off with a trip to Minsky's and the trip home listening to Game 5 of the NBA Playoffs (not the best performance by the Mavs but we know they will bounce back). Spencer spent the night with Marcus and we hope to make connections with Chris Greisen later on today. Cathy and Spencer will return to Memphis on Tuesday. The next 3-4 days will probably be the last ones here for awhile for the two of them.

June 8 - 6:45 pm

We would have thought by now Spencer would have been released from the hospital, but not quite yet. I guess there was a mix up on submission of the discharge orders, so now we wait for the meds to be filled. Once again, practicing patience is being required of us. I think we are getting pretty good it! :o) ha ha We're hoping to get settled back in at the Grizzlies House in time for the Mavericks vs. Suns game tonight. Looks like tomorrow morning we'll have an appointment to check Spencer's levels to make sure the chemo is flushing out before they release us to go home. Rod will pick us up at the airport and then we'll drive to Joplin for Aunt Tiffany and Harry's wedding on Saturday.

June 8 - 11:30 am

Oh, what a fun day! After sleeping in and eating breakfast, we participated in Silly Field Day by ambushing our nurses with Silly String. It just so happens the nurse's station is right outside our room, and let's just say they were not expecting quiet and reserved Spencer to display such orneriness! They didn't know what hit them as he bombarded them with string! It was hilarious! They must have had a secret stash because it wasn't long before they retaliated. One of the doctors came to examine Spencer and was met at the door with a dousing of silly string. She was totally caught off guard and took it very well. She said she came to see how he was feeling and by the looks of things could see he was feeling great. We laughed and laughed! The only downfall was we ran out of Silly String way too soon!

June 7 - 3:45 pm

Spencer was admitted a little after 2pm and now we are waiting for the chemo to come, which should be anytime.

We should know more tomorrow, the end of the week, or first of next week, but tentatively it looks like the admit date for the bone marrow will be June 30. Before that date, Spencer will undergo several tests and radiation treatments before they harvest Chayse's bone marrow on July 7. Chayse will have to come a few days prior to that date to undergo tests as well. The nurse told us Spencer would be inpatient for 4-6 weeks.

We continue to pray and stand on the promises of God for Spencer's healing. We believe Spencer has a strong heart and that it beats with the rhythm of life. His blood flows to every cell of his body restoring life and health abundantly according to Proverbs 12:14 and 14:30.

June 6 - 5:30 pm

Spence and I arrived at the Grizzlies House just after 1pm and only had to wait a few minutes for our room to be ready. We didn't do much of anything but hang out and relax this afternoon. Right now we are at the hospital waiting for a nurse to take his labs and get him hooked up to fluids. Tonight starts the never ending trips to the bathroom! I believe our day will start at 9am tomorrow with clinics and procedures. They will do IT therapy as well as a bone marrow aspirate and then check him in as inpatient sometime tomorrow afternoon. Well, the nurse is here to take him to the room to draw labs. I will update again tomorrow. Until then, good night and God bless.

June 2

Another great day for Spencer. Yes, that is him riding bikes all over town with Marcus. Seems to be enjoying just hanging out. We hope to get to see several of you tomorrow night at the benefit!

June 1

Not much to report from the great town of Wilcox. Spencer is doing well. After spending a couple of days in Treynor, IA with grandparents, Spencer went to watch some of his friends play baseball last night. This morning he went for a scheduled visit to the hospital to get labs drawn. He is spending the afternoon with a friend. Kind of like normal.


May 1-31
April 1-30
March 28-31
March 27
March 26
March 25
March 24
March 23
March 22
March 21
March 20

March 19
March 18
March 17
March 16


Thank you to everyone who helped make the benefit a huge success! To everyone who have supported us spiritually, emotionally and financially, we say thanks! We have been so blessed by each and every one of you. It has been overwhelming but very much appreciated by our family.

Rod, Cathy,
Chayse & Spencer

 

 

eMail Spencer at

spencer@bearcatslam.com