Dear Friends,
If you haven't had a chance I urge you to go to the CarePage for the Dunn Family. www.carepages.com under the search box you may look for them under JuliansNotes .
With our long journey ahead we are ready to start Meal Schedule for the family. The link below should get you to the right spot. If it doesn't let me know...technology is definitely not my gift but we will figure it out. I think that the link has to come from my computer but if you send me a email with your class names in the heading I think I can hit reply all and still send the link. Everything you need to provide a meal is located on this site. Thank you in advance for your loving care.
http://www.foodtidings.com/SignUp.aspx?ScheduleGuid=524f854d-cdfa-4884-a97b-474a0c8077b6
Of course, there are many ways to provide comfort for the family depending on your circumstances. We will be providing lunches for Nolan Dunn in 4-R. You may email our contact at Choice Lunch at lmcgill@choicelunch.com to move a credit or use your credit card to provide a lunch. Even a $5.00 donation for lunch is a huge help. If technology is not your gift either then you can give your donation to myself or Hannah Lee (mom in 4-R). We will have an envelope with us at all times. If we find money in our children's backpack we will assume that is a donation for Nolan's lunch. So lots of ways to help there.
Most of all your continued prayers for a miracle will bless this family in a powerful way.
Believing in The One who is able,
Carrie Olson
"Now to Him who is able to do immeasurably more than all we ask or imagine, according to his power that is at work within us, to Him be glory in the church and in Christ Jesus throughout all generations for ever and ever! Amen"
Ephesians 3 : 20 & 21
Friday, November 12, 2010
Friday, October 29, 2010
Message from Andrea - October 29, 2010
Not very good news
Posted 12 hours ago
Julian had his third MRI today since his treatment ended last January and we were anticipating another good report, however, they did see something suspicious on his lower spine that wasn't there before. It's a small spot, about the size of a rice kernel. So the plan is for him to have surgery on Nov. 5 plus a lumbar puncture to see if any cancer cells are floating around in the spinal fluid. They will analyze the growth and we'll know what it is. We will have a meeting with Dr. Shen next week to discuss treatment options in more detail. If it turns out that the growth is a return of the cancer, we're looking at chemo and radiation again and the cure rate drops pretty significantly. If, God willing, "all" he needs is surgery, he'll be able to return to school in about one week. We haven't said anything to either of the boys yet. Probably won't until later next week. We want to keep their routines as normal as possible. Julian has been so happy lately, enjoying school and the routine that he is in. Did not think we would be crossing this bridge so soon.
Posted 12 hours ago
Julian had his third MRI today since his treatment ended last January and we were anticipating another good report, however, they did see something suspicious on his lower spine that wasn't there before. It's a small spot, about the size of a rice kernel. So the plan is for him to have surgery on Nov. 5 plus a lumbar puncture to see if any cancer cells are floating around in the spinal fluid. They will analyze the growth and we'll know what it is. We will have a meeting with Dr. Shen next week to discuss treatment options in more detail. If it turns out that the growth is a return of the cancer, we're looking at chemo and radiation again and the cure rate drops pretty significantly. If, God willing, "all" he needs is surgery, he'll be able to return to school in about one week. We haven't said anything to either of the boys yet. Probably won't until later next week. We want to keep their routines as normal as possible. Julian has been so happy lately, enjoying school and the routine that he is in. Did not think we would be crossing this bridge so soon.
Monday, October 11, 2010
Back to School - A message from Andrea
Back to school, September 8.
I cannot believe it's been over two months since our last update. Well, these two photos sort of say it all: Julian celebrated his 7th birthday (and had a great time at his party!) and a few days later he started first grade at the same school as Nolan, Mariners Christian School. I think we were pinching ourselves the first few days of school; was this really happening? We sort of held our breath expecting a phone call at any time to come and pick him up, that he was too tired or that there may have been some other difficulty. But no such calls. How blessed we are that our son is able to return to school with his peers. And he is able to have the same first grade teacher as Nolan had three years ago, a wonderful, seasoned teacher who is supportive of his special needs. We know there are all kinds of 'late effects' of the treatment that may (or peprhaps, will) develop, but we're taking things one day/week/month at a time, and are so enjoying Julian and his new and better life now!
His next MRI is Oct. 28. We hope and pray that this one, just like the others since his treatment finished, will show no changes. Thank you for joining us in this prayer. Prayer is powerful!!!!
I cannot believe it's been over two months since our last update. Well, these two photos sort of say it all: Julian celebrated his 7th birthday (and had a great time at his party!) and a few days later he started first grade at the same school as Nolan, Mariners Christian School. I think we were pinching ourselves the first few days of school; was this really happening? We sort of held our breath expecting a phone call at any time to come and pick him up, that he was too tired or that there may have been some other difficulty. But no such calls. How blessed we are that our son is able to return to school with his peers. And he is able to have the same first grade teacher as Nolan had three years ago, a wonderful, seasoned teacher who is supportive of his special needs. We know there are all kinds of 'late effects' of the treatment that may (or peprhaps, will) develop, but we're taking things one day/week/month at a time, and are so enjoying Julian and his new and better life now!
His next MRI is Oct. 28. We hope and pray that this one, just like the others since his treatment finished, will show no changes. Thank you for joining us in this prayer. Prayer is powerful!!!!
Thursday, July 15, 2010
MRI IS CLEAR! A message from Rich and Andrea - July 14, 2010
MRI is clear!
Posted 14 hours ago
Praise God! Julian's most recent MRI looked great! Thank you for your prayers. He did well through the procedure and we are grateful to have received word today that the results were great. Every day is a gift in my book!
Posted 14 hours ago
Praise God! Julian's most recent MRI looked great! Thank you for your prayers. He did well through the procedure and we are grateful to have received word today that the results were great. Every day is a gift in my book!
Dear Friends - A Message from Andrea July 7, 2010
Dear Friends,
I can’t tell you how wonderful it is to live a ‘normal’ life again. There are moments when my mind goes back to the months not long ago when Julian was in the throes of chemotherapy and I remember how it would be for him at night, sleeping attached to a feeding tube and an IV, full of meds and often waking up during the night nauseated, and I look at him now, sleeping peacefully all night long. It is hard to comprehend that his life and quality of life were so radically different then. I think he has forgotten much of it, which is a great blessing to us all, and is now focused on just being a kid and doing what kids do: play.
He recently had his first haircut since his hair grew back and he looks very handsome. His hair has come back a slightly more wiry texture, and a little darker, but he usually wears a cap to keep the sun off or it would probably be blonder. While he doesn’t have all his energy or appetite back, he is enjoying many routine things: playing for hours with Legos (of course!), being silly with his brother, chasing birds, coloring, etc.
We just returned from something that wasn’t routine: our Make-a-Wish trip to Disneyland! Julian hadn’t been there since he was 9 months old so it was all new to him. They put us up for 5 nights at the Paradise Pier Hotel and we were so well-treated! Our trip included a special visit with Julian’s favorite characters Buzz and Woody, and the boys got to go behind the scenes to decorate cakes with the Disney pastry chef and staff. In addition to three days at Disneyland Resort, we went to Knott’s and Medieval Times. Equally as fun as the amusement parks were the late afternoons when we would come back to the hotel and jump in the pool! This was Julian’s first time in a pool in two years! He especially enjoyed the “shakoozi” and Nolan loved the water slide. Thank you to all the special people at Make-a-Wish and Disneyland Resort for creating an experience for us that we’ll never forget! We are still on Cloud 9 from it.
While we try and move on, there are unavoidable reminders of the past, like his next brain/spine MRI which is this Friday. Once again, he will have to be fully sedated because it would be too difficult for him to lay perfectly still for 90 minutes in a loud, hot tube. When he gets older, he may be able to do so, but he is still too young at this point. We would ask your prayers for that whole sedation process to go smoothly and that there would be no changes from the last MRI.
We also request prayers that he be independent enough for first grade. He still has a few skills to re-learn but is a little reluctant to do so. We also pray that he can handle a full, 6.25-hour day at school. Rich and I go back and forth on whether we think he is up to the task. But, we've enrolled him in a 1-week summer school class and a weeklong Vacation Bible School program so we'll see how he does in either of those.
Well, that is our quick update. If there is such a thing as “normal,” we are humbled and thankful to be able to report that things are still that way!
Blessings,
Andrea Dunn
I can’t tell you how wonderful it is to live a ‘normal’ life again. There are moments when my mind goes back to the months not long ago when Julian was in the throes of chemotherapy and I remember how it would be for him at night, sleeping attached to a feeding tube and an IV, full of meds and often waking up during the night nauseated, and I look at him now, sleeping peacefully all night long. It is hard to comprehend that his life and quality of life were so radically different then. I think he has forgotten much of it, which is a great blessing to us all, and is now focused on just being a kid and doing what kids do: play.
He recently had his first haircut since his hair grew back and he looks very handsome. His hair has come back a slightly more wiry texture, and a little darker, but he usually wears a cap to keep the sun off or it would probably be blonder. While he doesn’t have all his energy or appetite back, he is enjoying many routine things: playing for hours with Legos (of course!), being silly with his brother, chasing birds, coloring, etc.
We just returned from something that wasn’t routine: our Make-a-Wish trip to Disneyland! Julian hadn’t been there since he was 9 months old so it was all new to him. They put us up for 5 nights at the Paradise Pier Hotel and we were so well-treated! Our trip included a special visit with Julian’s favorite characters Buzz and Woody, and the boys got to go behind the scenes to decorate cakes with the Disney pastry chef and staff. In addition to three days at Disneyland Resort, we went to Knott’s and Medieval Times. Equally as fun as the amusement parks were the late afternoons when we would come back to the hotel and jump in the pool! This was Julian’s first time in a pool in two years! He especially enjoyed the “shakoozi” and Nolan loved the water slide. Thank you to all the special people at Make-a-Wish and Disneyland Resort for creating an experience for us that we’ll never forget! We are still on Cloud 9 from it.
While we try and move on, there are unavoidable reminders of the past, like his next brain/spine MRI which is this Friday. Once again, he will have to be fully sedated because it would be too difficult for him to lay perfectly still for 90 minutes in a loud, hot tube. When he gets older, he may be able to do so, but he is still too young at this point. We would ask your prayers for that whole sedation process to go smoothly and that there would be no changes from the last MRI.
We also request prayers that he be independent enough for first grade. He still has a few skills to re-learn but is a little reluctant to do so. We also pray that he can handle a full, 6.25-hour day at school. Rich and I go back and forth on whether we think he is up to the task. But, we've enrolled him in a 1-week summer school class and a weeklong Vacation Bible School program so we'll see how he does in either of those.
Well, that is our quick update. If there is such a thing as “normal,” we are humbled and thankful to be able to report that things are still that way!
Blessings,
Andrea Dunn
Thursday, May 20, 2010
Jammin' for Julian - A Message from Rich and Andrea
Jammin'
Dear Friends,Jammin' for Julian II last Sunday was wonderful! The young performers were just terrific and they inspired us all! Thank you to all the incredible singers and musicians who are using their talents in such a generous way. We raised $4,000 which will be divided among five non-profits to further assist families in the community. I have to tell you, it was pretty therapeutic to be able to focus our eyes on the needs of others, rather than our own! Julian enjoyed the concert and especially standing on stage with me. Nolan had great fun with his cousins (thanks Jordan for your awesome singing!) and friends sitting together from Little League (go Orion!). Our sweet neighbor, Lauren, and her parents, set up a beautiful lemonade stand -- complete with hot soup because the weather was quite chilly -- and together with a wonderful bake sale raised about $800 toward the total. Thanks to special volunteers and family helpers! Emcee Tom Johnson was awesome again. Thanks for jammin' with us!!! (P.S. The entire concert was filmed by Win Hodge and is uploaded on Ben Blackstone's website www.benblackstone.net. By the way, Ben is doubly talented: a terrific ballplayer and an amazing pianist. Thanks Blackstones!)
Dear Friends,Jammin' for Julian II last Sunday was wonderful! The young performers were just terrific and they inspired us all! Thank you to all the incredible singers and musicians who are using their talents in such a generous way. We raised $4,000 which will be divided among five non-profits to further assist families in the community. I have to tell you, it was pretty therapeutic to be able to focus our eyes on the needs of others, rather than our own! Julian enjoyed the concert and especially standing on stage with me. Nolan had great fun with his cousins (thanks Jordan for your awesome singing!) and friends sitting together from Little League (go Orion!). Our sweet neighbor, Lauren, and her parents, set up a beautiful lemonade stand -- complete with hot soup because the weather was quite chilly -- and together with a wonderful bake sale raised about $800 toward the total. Thanks to special volunteers and family helpers! Emcee Tom Johnson was awesome again. Thanks for jammin' with us!!! (P.S. The entire concert was filmed by Win Hodge and is uploaded on Ben Blackstone's website www.benblackstone.net. By the way, Ben is doubly talented: a terrific ballplayer and an amazing pianist. Thanks Blackstones!)
Thursday, April 15, 2010
MRI IS CLEAR! A message from Rich and Andrea - April 15, 2010
MRI is clear!
Posted 16 hours ago
So thankful. Julian's MRI from yesterday is clear! Dr. Shen said it was very good news because it was his first one since the chemo stopped and usually if they were going to see something they would see it now. We are very happy!!!
“Great is His faithfulness. His mercies are new every morning.” Lamentations 3:23.
Posted 16 hours ago
So thankful. Julian's MRI from yesterday is clear! Dr. Shen said it was very good news because it was his first one since the chemo stopped and usually if they were going to see something they would see it now. We are very happy!!!
“Great is His faithfulness. His mercies are new every morning.” Lamentations 3:23.
Tuesday, April 13, 2010
A Time for New Beginnings - A message from Rich and Andrea - April 13, 2010
Posted 16 hours ago
Dear Friends,
Spring is definitely a time of new beginnings. The flowers are blooming; the sun is warming things up; a pair of duckies has been visiting our front yard recently looking for bread scraps; and Easter was beautiful. It has truly been a time of rejuvenation for us. It all started two Fridays ago when Julian had his NG tube removed. We had been anticipating this for weeks and it finally happened. For the first time in 15 months, he has not been connected at night to a pump of one sort or another. No more alarms, beeps, bags and tubes! He is eating OK, preferring sweets to veggies, but he knows he needs to keep eating or that tube goes back in. Now he is asking when his other set of tubes, his central line, will be removed. He has started sleeping in his bunk bed again and Nolan is so happy to have his brother back. In more ways than ever, he is like a regular kid again. Tomorrow is his next MRI and in a few weeks a final infusion of antibiotic. Then his central line will be removed and our clinic visits will be reduced to monthly.
His hair is growing back, too, and his energy levels are increasing. He recently went to an Angel game with Rich (his first since March of 2008), and on Easter Sunday we went to church and had dinner with both sides of the family. That made up for last Easter when he woke up with a fever that put him in the hospital for about 9 days. We sure enjoyed spring break, too. We had lunch at Ruby’s Café at the end of the pier and saw a sea lion and a pod of dolphins nearby (I overheard someone at another table calling them a 'pod' so now I'm using that word). It was a cloudy, rainy day, and most people stayed away from the beach, but the sun broke out and it was gorgeous. The boys also got a close-up visit at a fire station (thanks Minda!) where the firefighters treated them like VIPs. And, Julian’s biggest wish was fulfilled last weekend: he has been aching to hold a baby chickie. We’ve seen them behind glass in incubators but we finally found some chicks at the Youth Expo that he could pet and hold. He was so happy. The boys also got to pet bunnies there and learned all about different rabbit breeds (for ‘future pet planning’). [Note to any of his nurses who might be reading this: I promise he washed his hands right afterwards followed by antibacterial gel!]
There is much more I can write but one thing I must include is that "Jammin’ for Julian II" is in the works. People have been asking us if we were going to do another one, so we’ve set 4 p.m. May 16 as the date and the location is going to be St. Mark’s Presbyterian in Newport Beach. The amazing young pianist, Umi Garrett, will be performing again (she will literally be stepping off an airplane that same day from an international performance)! This time, all the proceeds will benefit agencies that support families going through cancer (Miracles for Kids, Beckstrand Cancer Foundation, Kristies Foundation and Red Wagon Foundation). Updated info will soon be available on www.jamminforjulian.org.
Thank you for your continued prayers. His MRI is tomorrow and there will be many more to follow. Blessings to you!
Andrea, Rich & boys
Dear Friends,
Spring is definitely a time of new beginnings. The flowers are blooming; the sun is warming things up; a pair of duckies has been visiting our front yard recently looking for bread scraps; and Easter was beautiful. It has truly been a time of rejuvenation for us. It all started two Fridays ago when Julian had his NG tube removed. We had been anticipating this for weeks and it finally happened. For the first time in 15 months, he has not been connected at night to a pump of one sort or another. No more alarms, beeps, bags and tubes! He is eating OK, preferring sweets to veggies, but he knows he needs to keep eating or that tube goes back in. Now he is asking when his other set of tubes, his central line, will be removed. He has started sleeping in his bunk bed again and Nolan is so happy to have his brother back. In more ways than ever, he is like a regular kid again. Tomorrow is his next MRI and in a few weeks a final infusion of antibiotic. Then his central line will be removed and our clinic visits will be reduced to monthly.
His hair is growing back, too, and his energy levels are increasing. He recently went to an Angel game with Rich (his first since March of 2008), and on Easter Sunday we went to church and had dinner with both sides of the family. That made up for last Easter when he woke up with a fever that put him in the hospital for about 9 days. We sure enjoyed spring break, too. We had lunch at Ruby’s Café at the end of the pier and saw a sea lion and a pod of dolphins nearby (I overheard someone at another table calling them a 'pod' so now I'm using that word). It was a cloudy, rainy day, and most people stayed away from the beach, but the sun broke out and it was gorgeous. The boys also got a close-up visit at a fire station (thanks Minda!) where the firefighters treated them like VIPs. And, Julian’s biggest wish was fulfilled last weekend: he has been aching to hold a baby chickie. We’ve seen them behind glass in incubators but we finally found some chicks at the Youth Expo that he could pet and hold. He was so happy. The boys also got to pet bunnies there and learned all about different rabbit breeds (for ‘future pet planning’). [Note to any of his nurses who might be reading this: I promise he washed his hands right afterwards followed by antibacterial gel!]
There is much more I can write but one thing I must include is that "Jammin’ for Julian II" is in the works. People have been asking us if we were going to do another one, so we’ve set 4 p.m. May 16 as the date and the location is going to be St. Mark’s Presbyterian in Newport Beach. The amazing young pianist, Umi Garrett, will be performing again (she will literally be stepping off an airplane that same day from an international performance)! This time, all the proceeds will benefit agencies that support families going through cancer (Miracles for Kids, Beckstrand Cancer Foundation, Kristies Foundation and Red Wagon Foundation). Updated info will soon be available on www.jamminforjulian.org.
Thank you for your continued prayers. His MRI is tomorrow and there will be many more to follow. Blessings to you!
Andrea, Rich & boys
Monday, March 22, 2010
Message from Andrea - March 21, 2010
I would like to ask you to keep a young lady named Julia in your prayers. Julia is 15-years-old and has been battling craniopharyngioma since she was nine. She has gone through various surgeries, life-threatening infection, radiation and extensive rehabilitation and spent nearly 14 months during a 2-year period in the hospital or in rehabilitation. I've never met her, but many years ago her mother, Carla, spent a summer at our house back in 1977. Carla's mom and my mom were friends when they were school girls in Holland. I visited Carla and her family when I went back for a visit in the early '80s. Gradually, as the years passed, we lost touch, but we recently reconnected via Facebook. How great to catch up again. The internet has wiped away the many miles between California and Holland, and we can chat and catch up in an instant (fortunately, the Dutch speak and write very good English). But sad to hear that she has gone through such a long ordeal, and now to learn that Julia's condition has recently worsened. There is now a new cyst pressing on her brainstem. It's a dangerous situation and her doctors are going to determine her options on Tuesday next week. Please keep all of them, Carla, Julia, her other daughter Stephanie, and the doctors in your prayers. Thank you!
Thursday, March 11, 2010
Message from Andrea, Rich and the boys - March 11, 2010
It has been over a month since I’ve sent an update on Julian, so it’s high time! These past weeks have just flown by and part of the reason I haven’t put an update together is that it’s been nice simply not having to think about clinic appointments and medical “stuff” for a while. The number of visits we’ve made to CHOC lately has really dropped off and it’s been nice to just have time for some normalcy. I’ve actually caught myself having moments when I had forgotten Julian had cancer. Of course, those are usually followed by a deeper realization that my child has cancer and thoughts about what would happen if a future scan shows a recurrence, but then the stuff of life pushes those thoughts away again and we get busy doing the things we need to do. We’ve gone to the snow for a day (an absolutely perfect day), to a jazz concert, to a few of Nolan’s basketball games, to the park, to church, to the movies and to the store to pick up some decorations. (Julian loves to decorate the house for holidays and had fun with Valentine's Day. The house is now decorated for St. Paddy's day. You'd think we were Irish or something!) Our outings are short and we usually have to go home early, but it’s been great to get out as a family again.
Julian is now in his final week of his 6-week recovery period from his last chemo. His hair is just now beginning to grow back. His skin color is looking better and he has more energy. He is also starting to eat a bit more and joins us for a meal or two each day. His “meals” still consist of only a bite or two, but he is trying different foods and it is nice to have him at the table with us. It will be a few more weeks until we can justify having the NG tube removed since he still needs the calories he gets from the night-time formula feeds. When we go to places where there are other children, there usually is a child who will ask him what the tube is for. Maybe those questions will also motivate him to want it removed.
He still has his catheter port (aka “his tubies”) in his chest and will probably have it removed after his next MRI which is in April. After that, he’ll have to be poked when blood draws are required or if an IV needs to be started. That will be tough, but on the other hand, he’ll enjoy the freedom to go swimming this summer and not to have to protect his tummy likes he has to now. He still needs to have two more infusions of antibiotic, as well as blood draws every two weeks for now, so it’s very convenient and pain-free to have that port right now.
He has also received a set of hearing aids. He picked out a bright red color and seemed to perk up that first day he wore them; he certainly could hear better with them. But he’s been reluctant to wear them around the house since he can function quite well without them. His audiograms continue to show that there has been no further hearing damage since November. But when school starts in the fall, and when he’ll be in an environment with lots of competing sounds, it will be very good to have those hearing aids for him. Yes, we are planning to get him ready for first grade! I hope and pray that all will go well with that adjustment and that he’ll have exactly the kind of teacher he needs. Julian seems to be on track with Kindergarten reading and math. His challenge is using his right hand for writing and it will probably continue to be a challenge for him in the years to come. He compensates with his left hand, but doesn’t have the control with it since he is naturally right-handed. He gets a bit tired of the work, so his endurance levels will definitely need to increase to handle a full day of first grade. Right now he has a teacher who comes to the house three times a week about 90 minutes each visit.
The other thing we’re working on is helping him make some friends. All his peers go to school during the day and his close neighborhood friend just moved last week. Since he has more time on his hands now, we’re exploring some home school groups and will try and meet a group for a park play date this week so he’ll hopefully meet some new friends his age. Nolan’s been a great big brother to Julian and plays with him as much as possible, but Little League is starting and that is Nolan’s big love so he’ll be busy with that for a while.
And finally, we have been meeting with the Make a Wish Foundation and they are working on a wish for Julian. I don’t have all the details yet, but I’m excited about it!
I am thankful for these past weeks and for your prayers. Thank you so much for partnering with us in prayer through this journey.
With love,Andrea, Rich and boys
})
Julian is now in his final week of his 6-week recovery period from his last chemo. His hair is just now beginning to grow back. His skin color is looking better and he has more energy. He is also starting to eat a bit more and joins us for a meal or two each day. His “meals” still consist of only a bite or two, but he is trying different foods and it is nice to have him at the table with us. It will be a few more weeks until we can justify having the NG tube removed since he still needs the calories he gets from the night-time formula feeds. When we go to places where there are other children, there usually is a child who will ask him what the tube is for. Maybe those questions will also motivate him to want it removed.
He still has his catheter port (aka “his tubies”) in his chest and will probably have it removed after his next MRI which is in April. After that, he’ll have to be poked when blood draws are required or if an IV needs to be started. That will be tough, but on the other hand, he’ll enjoy the freedom to go swimming this summer and not to have to protect his tummy likes he has to now. He still needs to have two more infusions of antibiotic, as well as blood draws every two weeks for now, so it’s very convenient and pain-free to have that port right now.
He has also received a set of hearing aids. He picked out a bright red color and seemed to perk up that first day he wore them; he certainly could hear better with them. But he’s been reluctant to wear them around the house since he can function quite well without them. His audiograms continue to show that there has been no further hearing damage since November. But when school starts in the fall, and when he’ll be in an environment with lots of competing sounds, it will be very good to have those hearing aids for him. Yes, we are planning to get him ready for first grade! I hope and pray that all will go well with that adjustment and that he’ll have exactly the kind of teacher he needs. Julian seems to be on track with Kindergarten reading and math. His challenge is using his right hand for writing and it will probably continue to be a challenge for him in the years to come. He compensates with his left hand, but doesn’t have the control with it since he is naturally right-handed. He gets a bit tired of the work, so his endurance levels will definitely need to increase to handle a full day of first grade. Right now he has a teacher who comes to the house three times a week about 90 minutes each visit.
The other thing we’re working on is helping him make some friends. All his peers go to school during the day and his close neighborhood friend just moved last week. Since he has more time on his hands now, we’re exploring some home school groups and will try and meet a group for a park play date this week so he’ll hopefully meet some new friends his age. Nolan’s been a great big brother to Julian and plays with him as much as possible, but Little League is starting and that is Nolan’s big love so he’ll be busy with that for a while.
And finally, we have been meeting with the Make a Wish Foundation and they are working on a wish for Julian. I don’t have all the details yet, but I’m excited about it!
I am thankful for these past weeks and for your prayers. Thank you so much for partnering with us in prayer through this journey.
With love,Andrea, Rich and boys
})
Monday, February 1, 2010
Transitioning - Message from Andrea January 30, 2010
Posted Jan 30, 2010 1:18am
Today was Julian's final outpatient chemo push. No more chemo!! I remember thinking months ago, when Julian was eyeing Nolan's baseball trophies and he asked when he was ever going to get a trophy, I was determined to get him one for going through all the things he has had to go through. Every child going through cancer treatment deserves a trophy! Well, the nurses beat me to it and presented him with one today that has a big star and is inscribed with, "Congratulations! You Are Our Hero. Love, Your CHOC Oncology Team." I thought that was a very cool thing to do and it is proudly displayed in the center of our mantle. Thank you CHOC doctors, nurses and staff! They are all awesome and such tremendous partners in this process. We won't really have any time to miss them because Julian already has appointments on the books for clinic visits next week and for the weeks thereafter. In fact, he'll be monitored for 10 years. I tried to explain to him that, yes, chemo is done, but he will still be going to CHOC many more times, for a long time.
Up until now, he's had a central line and hasn't had an injection through his skin since Dec '08. Everything goes right into that port which goes directly into a main artery; convenient but always at-risk for infection. He'll have the central line removed in late February. After that, when blood draws are needed or if IV medicines are needed, he'll be poked and he'll probably wonder why we said he was "done." So, we've tried to downplay the end of chemo a bit because truthfully, while he's finished with one phase, he's entering a new phase and each new phase of this journey has its own set of challenges.
He will need brain/spine MRIs every 2-3 months and he had one done yesterday. Praise God, the results show there has been no change since the last one. The longer we can go without any changes, the better! Regarding eating, he still just nibbles about once a day (a few bites of pancakes this morning), but he often will want to try something new (today he said he wants to have some Cheetos; not sure if you would call Cheetos food, but it's something). Once he starts to feel better, we'll really be focusing on foods so he can get that tube out of his nose.
This morning, Rich was encouraging Julian and told him that he'll be doing great things when he grows up. Julian's reply: "Daddy, I'm already doing great things." How true!
God bless you for your prayers and please, please keep them coming! We have many prayer requests; always at the top of the list is that the chemo and radiation will have permanently wiped out the cancer cells and that there will be no secondary malignancy later. We are grateful for your encouragement; your messages are therapeutic and being able to update you is therapeutic. His journey is far from over and we will keep you posted in the weeks and months to come.
Today was Julian's final outpatient chemo push. No more chemo!! I remember thinking months ago, when Julian was eyeing Nolan's baseball trophies and he asked when he was ever going to get a trophy, I was determined to get him one for going through all the things he has had to go through. Every child going through cancer treatment deserves a trophy! Well, the nurses beat me to it and presented him with one today that has a big star and is inscribed with, "Congratulations! You Are Our Hero. Love, Your CHOC Oncology Team." I thought that was a very cool thing to do and it is proudly displayed in the center of our mantle. Thank you CHOC doctors, nurses and staff! They are all awesome and such tremendous partners in this process. We won't really have any time to miss them because Julian already has appointments on the books for clinic visits next week and for the weeks thereafter. In fact, he'll be monitored for 10 years. I tried to explain to him that, yes, chemo is done, but he will still be going to CHOC many more times, for a long time.
Up until now, he's had a central line and hasn't had an injection through his skin since Dec '08. Everything goes right into that port which goes directly into a main artery; convenient but always at-risk for infection. He'll have the central line removed in late February. After that, when blood draws are needed or if IV medicines are needed, he'll be poked and he'll probably wonder why we said he was "done." So, we've tried to downplay the end of chemo a bit because truthfully, while he's finished with one phase, he's entering a new phase and each new phase of this journey has its own set of challenges.
He will need brain/spine MRIs every 2-3 months and he had one done yesterday. Praise God, the results show there has been no change since the last one. The longer we can go without any changes, the better! Regarding eating, he still just nibbles about once a day (a few bites of pancakes this morning), but he often will want to try something new (today he said he wants to have some Cheetos; not sure if you would call Cheetos food, but it's something). Once he starts to feel better, we'll really be focusing on foods so he can get that tube out of his nose.
This morning, Rich was encouraging Julian and told him that he'll be doing great things when he grows up. Julian's reply: "Daddy, I'm already doing great things." How true!
God bless you for your prayers and please, please keep them coming! We have many prayer requests; always at the top of the list is that the chemo and radiation will have permanently wiped out the cancer cells and that there will be no secondary malignancy later. We are grateful for your encouragement; your messages are therapeutic and being able to update you is therapeutic. His journey is far from over and we will keep you posted in the weeks and months to come.
Friday, January 15, 2010
Almost Fnished
Almost finished!
Posted 14 hours ago
Julian goes in for his last round of chemo tomorrow! So happy that he is at the finish line and can't wait for him to feel better and get back to living life again. He has been such an amazing trooper through everything. It will take about six weeks to recover from this round and then his hair should start coming back again and he'll hopefully be feeling much better. We'll have to work on his eating so he can have the NG tube removed and he'll have lots of MRIs and follow-ups, but at least we're just about done with chemo!!!
This morning he had an audiogram done at Providence and, incredibly, there was no change since the last hearing test done in November and even a very slight improvement. The doctor said it could be that he was more focused on listening for the sounds this time, or maybe even due to the special medicine he was given before his last round of cisplatin. Probably we'll never know, but it is very encouraging. He'll be getting that medicine again to help protect against the effects of cisplatin tomorrow. We're so thankful that there are these options and that his hearing is stable right now. In a few weeks, he'll have another hearing test and then receive his hearing aids. He wasn't too thrilled about the idea of wearing hearing aids, but once he's in a classroom full of kids and sounds, he'll be glad he has them.
Well, gotta go and pack our bags!
P.S. Months ago, I asked for prayer for a boy named Noah. He passed away last October. His mother is amazing and just wrote a beautiful update. The name of the Carepage is NoahDowell.
Posted 14 hours ago
Julian goes in for his last round of chemo tomorrow! So happy that he is at the finish line and can't wait for him to feel better and get back to living life again. He has been such an amazing trooper through everything. It will take about six weeks to recover from this round and then his hair should start coming back again and he'll hopefully be feeling much better. We'll have to work on his eating so he can have the NG tube removed and he'll have lots of MRIs and follow-ups, but at least we're just about done with chemo!!!
This morning he had an audiogram done at Providence and, incredibly, there was no change since the last hearing test done in November and even a very slight improvement. The doctor said it could be that he was more focused on listening for the sounds this time, or maybe even due to the special medicine he was given before his last round of cisplatin. Probably we'll never know, but it is very encouraging. He'll be getting that medicine again to help protect against the effects of cisplatin tomorrow. We're so thankful that there are these options and that his hearing is stable right now. In a few weeks, he'll have another hearing test and then receive his hearing aids. He wasn't too thrilled about the idea of wearing hearing aids, but once he's in a classroom full of kids and sounds, he'll be glad he has them.
Well, gotta go and pack our bags!
P.S. Months ago, I asked for prayer for a boy named Noah. He passed away last October. His mother is amazing and just wrote a beautiful update. The name of the Carepage is NoahDowell.
Monday, January 4, 2010
Familiar Stomping Grounds - Message from Andrea 1/3/10
Posted 14 hours ago
Julian is sleeping soundly in room 321 at CHOC tonight and we expect to go home tomorrow. Kept the healthcare system fairly busy last week: two clinic visits, chemo push, NG tube replacement, home health visit, three days of special meds to boost his white blood cell production, a blood transfusion, ER visit and two nights at CHOC. In between he did have fun playing with his Christmas toys and going to the beach for a short while on New Year's Eve. But we were pretty worried yesterday afternoon when he said his shunt hurt and it looked fairly swollen and even appeared as if it had shifted downward. Bracing for news that he might need surgery to replace it. In the ER, they did an x-ray and a CT scan and, thankfully, the shunt is working just fine. (Earlier in the week, Julian had taken a tumble on the front lawn and said he had bumped his head, so these scans eased our concerns that his fall had caused any problems.) But because of the swelling and tenderness there could have been an infection, so the doctors wanted to watch him for a night or two and give him antibiotics. He also needed a blood transfusion because his red blood cell count was low again. So, we took care of business and spent the first couple of days of the new year at CHOC, but so glad he was in caring and capable hands and that he is feeling much better now. Want to wish you all a wonderful New Year and thank you for riding this roller coaster with us. Your prayers continue to help Julian through each dip and sudden turn on that ride. The events of this past week certainly confirm that! And thanks to Him for protecting Julian from injury and so much more (i.e. amazingly, he didn't catch my flu bug a few weeks ago!)
Julian is sleeping soundly in room 321 at CHOC tonight and we expect to go home tomorrow. Kept the healthcare system fairly busy last week: two clinic visits, chemo push, NG tube replacement, home health visit, three days of special meds to boost his white blood cell production, a blood transfusion, ER visit and two nights at CHOC. In between he did have fun playing with his Christmas toys and going to the beach for a short while on New Year's Eve. But we were pretty worried yesterday afternoon when he said his shunt hurt and it looked fairly swollen and even appeared as if it had shifted downward. Bracing for news that he might need surgery to replace it. In the ER, they did an x-ray and a CT scan and, thankfully, the shunt is working just fine. (Earlier in the week, Julian had taken a tumble on the front lawn and said he had bumped his head, so these scans eased our concerns that his fall had caused any problems.) But because of the swelling and tenderness there could have been an infection, so the doctors wanted to watch him for a night or two and give him antibiotics. He also needed a blood transfusion because his red blood cell count was low again. So, we took care of business and spent the first couple of days of the new year at CHOC, but so glad he was in caring and capable hands and that he is feeling much better now. Want to wish you all a wonderful New Year and thank you for riding this roller coaster with us. Your prayers continue to help Julian through each dip and sudden turn on that ride. The events of this past week certainly confirm that! And thanks to Him for protecting Julian from injury and so much more (i.e. amazingly, he didn't catch my flu bug a few weeks ago!)
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