A Remembrance Video of Mattie

Thank you for keeping Mattie's memory alive!

Dear Mattie Blog Readers,

It means a great deal to me that you take the time to write and to share your thoughts, feelings, and reflections on Mattie's battle and death. Your messages are very meaningful and help support me through very challenging times. I am forever grateful. As my readers know, I promised to write the blog for a year after Mattie's death, which would mean that I could technically have stopped writing on September 9, 2010. However, like my journey with grief there is so much that still needs to be processed and fortunately I have a willing support network still committed to reading. Therefore, the blog continues on. If I should find the need to stop writing, I assure you I will give you advanced notice. In the mean time, thank you for reading, thank you for having the courage to share this journey with me, and most importantly thank you for keeping Mattie's memory alive.


As Mattie would say, Ooga Booga (meaning, I LOVE YOU)! Vicki



November 13, 2008

Friday, November 14, 2008

Friday, November 14, 2008

Message of the day: My friend, Charlie wrote, "I know you’ve asked in the blog why people are willing to help and reach out to you and your family - today’s quote may help explain this."
Trouble is part of your life - if you don't share it, you don't give the person who loves you a chance to love you enough. ~ Dinah Shore


It has been quite an exhausting day and I will do my best to recap it. Mattie started to have a lot of pain at 11pm on thursday. At that point his pain medication was raised back up, since it was lowered during the day on thursday. The increase in medication seemed to help Mattie a lot until 5:45am. What happened at that hour? Well a surgerical resident came in, turned on all the lights, and started talking to us, and then waking up Mattie. Mattie did not know what hit him. The resident told us he was going to take out Mattie's drainage tubes. Basically each place Mattie has an incision from surgery, has a tube that sucks out excess blood and fluid. The resident decided Mattie no longer needed these tubes. Sounds good in theory, right? Well fortunately I saw Bob take out one of these tubes from the last surgery, so I knew it involved a dressing change at the very least. There was NO way Mattie could tolerate this after being awakened and without more pain medication. So in my stupor I asked the resident if he consulted with Bob before proceeding. The resident said he hadn't spoken to Bob, at which point then, I told him the drainage tubes weren't coming out. Peter and I then dismissed him from the room, and then at that early hour we left a message for our patient advocate, Julie Andrews. Julie is a special and elegant lady, who reminds us of the famous Julie Andrews and Mary Poppins all rolled up into one. Julie came to visit me at 8am and I told her what transpired with this resident. I don't question the fact that the resident has to do his job, what I do question was his level of insensitivity in performing his job.


Mattie had a day which consistented of periodic pain, almost every two hours, he needed additional Fentanol to help relieve his arm pain. Mattie's nurse, Jane, has been on top of Mattie's pain all day, and has helped mitigate what could have been an even more challenging day. In the midst of all of this, Mattie had 'Linda time' today. Linda was kind enough to sit with Mattie this morning while Peter and I had a meeting with Dr. Shad. Dr. Shad it the director of the pediatric oncology practice at Georgetown. While we were at the meeting, Mattie had a wonderful time with Linda, and then Jenny and Jessie also came to visit. I heard they blew bubbles, and my joke with Linda is, I love when she blows bubbles in the room, because it gets the floor all wet, and literally it cleans the floor beautifully. So Mattie had moments of happiness today!

Peter and I had a very productive meeting with Dr. Shad. Denise, our social worker, was also in attendance. Dr. Shad understood our need to consult others about Mattie's treatment options post-surgery. Peter and I are finding that qualified professionals are presenting us with different treatment options mainly because the research literature is conflicted and there just isn't enough information out there about the effectiveness of these chemo drugs. Overall there appears to be a dearth of research out there about pediatric osteosarcoma treatment, and then factor in Mattie's condition, multifocal osteosarcoma, and we are talking about something simply not examined for the most part in the literature. Dr. Shad has agreed to summarize Mattie's medical case, and send it off to our colleagues all over the country and in several international locations as well. She plans on giving us a list of everyone she contacts and she will be presenting what she finds from these consultations at a November 24th tumor board meeting at Georgetown. We have asked Dr. Shad if we could attend this meeting as observers. She is checking on this for us. Peter and I both feel that Mattie's case is so unique and because of the conflicting input we are receiving, that it merits the kind of inquiry Dr. Shad is making.

After the meeting, I went back to Mattie's room, and about 30 minutes later, we had three visitors. The visitors were surgerical techs and a nurse who were involved in Mattie's surgery with Bob on wednesday. They came up to check on Mattie and to say a prayer. They gave Mattie some books, and said they will keep us in their thoughts and prayers. I found that so touching, but then again I think Mattie has a way of growing on people. After they left, Maureen, a third year medical student came to visit with me. Maureen was present during both of Mattie's surgeries with Bob. Maureen wanted to check on us, and I sensed she was more personally interested in us, than just being part of her job. We had a delightful conversation, and we talked about what life is like in the OR. She had glowing things to say about Bob, and so I can safely say I found another person to add to the Bob Henshaw fan club. The club is growing in number. I later spoke to Ann, Bob's wife/our team Mattie coordinator, and told her she had to hear what a medical student had to say about her husband. It was so lovely, and I felt that Ann should know (though I know she knows this already!) how well respected Bob is at Georgetown.

Ellen came to visit with us today and brought Peter and I lunch. Thank you! We really enjoyed the food and we know Mattie will love the gifts you brought him. Any device right now that he can engage in without too much use of his hands is appreciated! Thank you Ellen for running around getting us coffee and tea today! I also want to thank Alison, who has coordinated lunches and other things for us this week and continues to check in. Ann and Alison are wonderful coordinators and tag team well together. Again, this is a difficult week for Ann, because her husband is Mattie's surgeon. She wants to support us, but yet respects how complicated all of our relationships are with each other. Though Peter and I are VERY absorbed with what is going on with Mattie, we don't want any of our readers for one minute to think we don't appreciate what you are doing for us. We are very grateful.

This afternoon, Mattie had a visit from Chris, the fellow from the Georgetown Chemistry Club. Several Club members came and made ice cream, right inside Mattie's room. It was very neat, and we are happy to report that Mattie ate 8 teaspoons of vanilla ice cream. His only food since surgery. Chris always plans something fun, and it isn't only Mattie that looks forward to his visits! You can see a picture of the students making ice cream right at the base of Mattie's bed. Chris is the fellow holding the liquid nitrogen tank!

I had the pleasure of bumping into Miki today. Miki is one of Mattie's HEM/ONC nurses. Miki and I spoke about Mattie's 1000 cranes that were made for him this week by Kazu's family. Miki told me how special a gift this is, and the significance of the cranes in her Japanese culture. Miki then continued on to tell me how impressed she is with Peter and I. She told me under such circumstances she has seen marriages and families fall apart. But instead of breaking down, Peter and I are a force to be reckoned with. Her comment has stuck with me all day today, mainly because I hadn't thought about it. But she is right, the stresses we are under could break someone and/or a relationship down.

At the moment, I am sitting with Mattie on his bed. Mattie received more pain medication at 4pm. With the increased pain medication I am noticing Mattie is having nightmares again. Mattie wakes up scared, thinking he is seeing things, and a couple of times I have witnessed him catching himself and waking himself up out of a nightmare. Mattie seems to find comfort out of me being around and right next to him, so you can imagine I don't venture far from the room .

I received three e-mails which I would like to share with you. The first e-mail comes from Phyllis. Phyllis lives in Los Angeles and is a family friend. Phyllis wrote the following on the day of Mattie's surgery, "I think today was a very good day indeed. I know that you've been able to see God's hand in the day's progression but I wanted to give you a real, tangible example that you could cling to in times where His hand is not so evident. I composed a prayer request letter that I sent to my entire acting company of Christian actors and to my friends that I consider true "prayer warriors." I did my best to describe Mattie's situation as it has unfolded and why today was so crucial that I was reaching out to them for help. I gave them a list of five specific points to pray for. I want you to see the list so you will know how awesome our God is that He literally answers prayers verbatim-- using the same words of pronouncement as I did in my request.

Please pray:
1. For success in today’s surgery with no surprises;
2. For effective pain management after surgery;
3. For strength for Mattie’s parents, Vicki and Peter Brown, who are exhausted and facing incredible trials that are not likely to end soon;
4. For both Mattie’s near-term healing from surgery and long-term healing from cancer;
5. For the incredible support system the Browns have in place; that they may be blessed exponentially for their efforts and that their faithfulness will not wane in what is sure to be a long haul.
I see #1 being answered quite literally: A successful surgery and NO SURPRISES! And the precious nurses you described in PACU seem to be most welcome additions to your ever-growing support system; maybe we should just call all your many helpers the "Heavenly Hosts" because they are definitely a Godsend.



Regarding the mysterious feeling you experienced waiting for Mattie to come out of surgery: I might have some insight on that and you can see if this jives for you. I'm not sure if you know this, but I am a two-time survivor of breast cancer. During the surgery for my first bout with the disease, I wish somebody had been taking pictures of the procedure for me. It might explain why I awoke from anesthesia with two ruptured disks in my neck. Too long of a story to go into detail here but let's just say that another major surgery 2 weeks later to fuse my disks, 6 weeks in a neck brace, radiation, chemo and a year of physical therapy on top of being just 5 weeks into a new marriage was a tad overwhelming. Despite being a woman of faith, I found it almost impossible to pray for my situation. I couldn't focus. And yet, in some way I was insulated, almost cocoon-like, in a peaceful knowledge that for this season it was okay if I wasn't able to pray through my ordeal. Others were doing it for me. This is what I came to term as "Floating on the prayers of the Saints." You cannot ever purchase this most priceless form of transportation through time; it comes only as a gracious and merciful answer to the many prayers sent up to heaven on your behalf. I truly believe that on Wednesday you experienced the ultimate "E Ticket" ride of "Floating on the prayers of the Saints." I completely agree with Phyllis. It is hard to pray at this time, even though we do turn to God for help and reassurance. But most definitely we are and continue to float on the prayers of the Saints.

The second e-mail I received was from my friend, Susan. Susan wrote, "What great news about the surgery! Mattie is quite a trooper and inspiration as well. I believe that God gives all of us gifts that we are to use to help others. It seems that Mattie is using his gift now to reach people. How young to have so much of an impact on so many people, particularly adults."

The third e-mail came from a colleague and friend of Peter's, Tom. Tom wrote, "By the way, I noticed in one of the pictures scrolling at the top of the blog Mattie in a superman costume...I think you've got it wrong. I think superman wears a Mattie costume!" Tom, I think you may be right!

Overall, Mattie is holding his own, and many of his reactions are expected post-surgery. Such as higher blood pressure, imbalanced electolytes, pain, and the need for oxygen. There is just so much to balance, and even more to worry about for saturday, as this will be Mattie's first day out of bed since surgery. As a mom, I worry about pain. Bob is trying to help me understand that some pain is good. But I guess none of us really like to see our child in pain. Bob will be doing a dressing change and removing drainage tubes on saturday morning.

Thank you for all your e-mails and messages of support through this challenging time. I did want to thank my lifelong friend, Karen in NY. She contacted Father McManus in Scarsdale, NY. Father McManus was the priest who confirmed me in the Catholic religion and even married Peter and I. Karen told Father McManus about Mattie and what our family is struggling with. It is nice to know that the congregation at Our Lady of Fatima, where I grew up, is also praying for Mattie. Father McManus called me tonight as well. Thanks Karen!

We want to thank the Kane family tonight for a great dinner. Thank you for supporting us through a challenging week! Tomorrow should prove to be an interesting day! I end tonight with two quotes I received today. Thanks Charlie and Susan!

"The greatest healing therapy is friendship and love." Hubert Humphrey

"Loving is half of believing." Victor Hugo

November 12, 2008

Thursday, November 13, 2008

Thurday, November 13, 2008

Quote of the day (Thanks Liza!): Where there is faith, there is hope and where there is hope, there is everything.

Before I begin today's posting, and I will try to make it a continuous posting like yesterday, I want to wish Peter a very Happy Birthday! Unfortunately we are in the hospital, and Peter also has to work today, but we are celebrating his special and milestone day! Bob gave us a wonderful gift (being disease free at the moment!) for Peter's birthday. With this disease, we are learning to appreciate whatever gifts come our way, and take things one day at a time. HAPPY BIRTHDAY PETER!

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8:30am: Last night Mattie experienced some pain and Dr. Natarajan (the PICU intensivist) was on top of things. She changed the pain orders a bit, and had Mattie go on a continuous drip of Fentanol. Mattie is very sleepy today, but is without pain. I understand the importance of the first 48 hours post surgery, and I attended the PICU rounds this morning and heard how Mattie's case would be managed today. Mattie right now looks very puffy, and he is retaining more fluid than he is putting out. So they are giving him a diuretic to manage this issue. In addition, they are monitoring his lungs and it is their hope that decreasing the level of fentanol (a narcotic), will help with his breathing. He is also experiencing a fever and high blood pressure, but I feel that Mattie is being monitored very well, and is comfortable.

I was remiss last night, because I want to thank the Phillips family for a lovely dinner. After Mattie was finally settled for the night, we realized that we needed to eat something. Thank you so much for the great food and for supporting us last night!

I received so many wonderful e-mails yesterday! I agree with many of you, Mattie and Bob make a good team! I wanted to share an e-mail with you from my friend, Grace, an RCC mom. I am so happy to hear from many of you that you enjoy reading what others write to me. I find the e-mails all of you send to me so comforting and I am happy that you feel these e-mails connect you to others in our caring community.

Grace wrote, "Vicki and Peter -I am thinking of you so much this morning; Mattie will be in my constant prayers today. I know those will be the longest eight hours of your life, but here are some positive things to think of during that time. Vicki, you mentioned that Mattie said that he was bored of you and wanted someone else to be his mommy. Believe it or not, this is a compliment. Most children in Mattie's shoes would be so consumed by their illness that their every thought would be about their illness and what was in store for them as a result of the surgeries, etc. But you have done such an amazing job with Mattie by distracting him from and informing him about the medical issues he faces, that his biggest complaint to you is about being bored. Most kids in Mattie's position would be so angry at their parents for hooking them up to machines and giving them medicines that make them feel bad and submitting them to surgery that disables them. But instead, Mattie isn't sad or angry at you, he's just bored like any other kid. And believe me, on any given day, my kids would gladly trade me in for our wonderful babysitter. Babysitters and art therapists have the luxury of doing fun things with your child with no responsibility to do the hard stuff that parents must implement and enforce. Who wouldn't want to be with the person that only does fun things with them? Mattie's a smart guy and wants to capitalize on the fun he's having--bring on more art therapists with all their goodies and fun projects! Again, this is a wonderful tribute to you and is another example of you being so effective in distracting Mattie. He's not spending his time worrying about what's happening to him. He just wants to have more fun! He's having fun! That's incredible.I imagine you're worried about how the lack of mobility will affect Mattie's mood, outlook and recovery. But just look at how well he's adjusted to being confined to hospital already; again, he's having fun! Kids are very resilient and malleable, and Mattie mirrors your positive, calm attitude which is so important in the recovery process. And remember, you have had a huge network of friends and family helping you out, and you know what? We're not going anywhere. We're here for the duration; we're going to overstay our welcome, and you'll have to push us out before we leave, and then we'll do so kicking and screaming. We are a force so united and dedicated to helping you and Mattie through this. We'll collectively figure out ways to keep him entertained with his new physical challenges. You and Team Mattie are yin and yang; we compliment each other and thrive on each other's energy. Your strength and determination feed us such a positive energy that has caused us to literally refocus our lives and stop and reevaluate what's important and cherish our loved ones. We hug our children a little closer, a little longer and don't get quite so mad when the silly hurdles of life get in our way. And we in turn, hopefully succeed in returning the energy you give to us by helping you and Mattie stay entertained, well and upbeat. Try to focus on how happy Mattie is now and know that he'll stay that way because the things that are making him happy aren't going to change. Despite his new physical challenges, he'll still have the most fabulous parents on the planet and family, friends, and wonderful hospital staff who will dedicate themselves to keeping Mattie happy and strong. Lastly, God works in mysterious ways. I firmly believe She :-) is out there watching over your family. When I saw that stunningly beautiful sun painting that Mattie had created, I thought..it's the Resurrection Sun! That sun symbolizes so much-- not only your "son" as you mentioned, but the Resurrection sun, the symbol of where you found a good place for Mattie to go to school and established life-long friendships. Everything is coming together; Barack Obama could take a page from your book to see how people from different nations can come together as one and unite for a great cause. And Mattie is one great and wonderful cause, and we will never stop fighting for him.

11:00am: Dr. Synder came to visit Mattie today, and she suggested that Mattie get repositioned since he was hunched over and his hips looked very uncomfortable. She called Anna (Mattie's PT) and within minutes, Anna, Kris (Mattie's PICU nurse), Linda, Dr. Synder, and I were helping get Mattie repositioned. After about 30 minutes, we finally found a comfortable position. While repositioning Mattie vomitted, probably because we are moving fluids around in his lungs, which is a good thing. Mattie is now resting comfortably. But as usual, though Dr. Synder is not on call this week on the PICU floor, she made a special visit to say hi and to see how she could help us. We are very fortunate to have an outstanding PICU nurse helping us, and Anna and I are now strategizing ways to help Mattie physically move after he has two days of bed rest.

4:00pm: Well my intention was to write throughout the day, but Mattie's left hand is bothering him and he wants me to continually massage it all day. I haven't been able to leave the room today because he wants me around. I guess there is nothing like having a mom around when you aren't feeling well! Alison came to visit, in the hopes of giving me a break from the room, but Mattie needed me around so I did not leave. Thanks Alison for the hot tea (which is helpful since I am keeping Mattie's room at a frigid 65 degrees because of his fever), and for our good chat. At around 12:30pm today, Bob requested that Mattie's perineural pain management system be shut off in his arm. Mattie is unable to feel his left arm or have feeling or movement in his left hand. I assumed it was because Mattie had a bone graft in the left wrist, so I wasn't too concerned about this, until others around me showed concern. However, after the perineural was shut off for an hour, Mattie began to experience pain in his left arm, and slightly moved a finger on his left side. Bob is coming to visit Mattie later today, so I we will get his assessment of the situation. In the mean time, the buzz of Peter's birthday is around the hospital. Jenny designed a beautiful Red Sox greeting card (see the picture) for Peter and everyone signed it. Linda brought Peter balloons and cupcakes from the Georgetown Cupcake store (see the picture). So despite not being at home, the hospital staff is trying to make this day special. It is our home away from home. Thanks Jenny and Linda!

5:15pm: We had a visit this evening from Bob. Bob examined Mattie's hand and explained why Mattie is unable to move his fingers or have sensation in his left hand (other than the obvious of which Mattie had major surgery on his left wrist). While performing surgery on Mattie's wrist, Bob had to move aside a particular nerve, a nerve that is involved with hand movement. Bob explained that in order to maximize pain management, he placed the perineural near this nerve in question. Which would explain the numbness and inability to use the fingers in the hand. Mattie continues to rest comfortably and we are now settling down for the evening and headed to enjoy a lovely turkey meal sent to us by the Smith family (a SSSAS family, who we don't know officially, but I am beginning to see we are all a part of this greater family). Thank you also for the special cupcakes. We are celebrating tonight! You can never have enough cupcakes.

8:20pm: Mattie is resting peacefully, and Peter and I are simply exhausted. So we plan on winding down now. Though we have come to understand that you really can't sleep in a hospital, well unless you are medicated. In any case, we wanted you to know that Mattie is comfortable, Peter and I are eating cupcakes, and planning for our visit with Dr. Shad, the chief of the oncology practice at Georgetown tomorrow. It has been a full day, but we couldn't sign off for the evening without thanking all of you for your e-mails and support. In Grace's e-mail above she says that Peter and I inspire Team Mattie and others, but this inspiration goes two ways. I can't tell you how blessed we feel to know that we have all of you behind us and are walking this journey with us each day. The fact that Mattie's story has touched your life in some way and you keep visiting the blog is a special gift during a very challenging time for us.

Wednesday, November 12, 2008

Wednesday, November 12, 2008


Message of the day (thanks Susan!): "Faith consists in believing when it is beyond the power of reason to believe." Voltaire

8:15am: Mattie finally fell asleep at midnight, but was up at 4am, rather upset. So I got up and jumped into his hospital bed with him, and we attempted to rest until 6am. At 6am, the lights went on and vitals were taken. It was quite a good morning wake up call. We are in room 1 of the PICU which is a total experience, filled with noise, and basically almost impossible to sleep. We tried to prep Mattie for this morning, but he was very groggy at 6am. Linda came in early and used a projector to display an amazing light show of stars for Mattie, which he found fascinating and was a great distraction. Mattie handled the transition from the room down to the OR like a champ. Totally incredible fellow. In the pre-op area, Mattie was greeted by several doctors and nurses, this number of people is almost overwhelming at 6 something in the morning. You can see a picture of Mattie before being wheeled off to the OR, with a beautiful smile on his face. Peter was in his "bunny suit" because he headed into the OR with Mattie until he was sleep. We will try to keep you updated throughout the day about Mattie's progress.

10:30am/12:15pm: Melissa, our surgerical liaison called me at 10:30am, to let me know Mattie was stable and the surgery got underway at 9:05am. At 12:15pm, we had the opportunity to meet with Melissa. She let us know that Mattie continues to be stable, doing fine, and his left humerus tumor is now removed, and they are working on Mattie's right femur (by the knee). Bob told me this morning that the goal is to remove all three tumors today, but based on Mattie's condition during surgery and potentially if anything else arises, that this could change the course of the surgery. Meaning that Mattie may not have all three sites operated on today. At the moment, things are looking like they are on target.

Thanks Charlie for the inspirational quotes for today!

Where hope grows, miracles blossom. - Elna Rae
No matter how steep the mountain - the Lord is going to climb it with you. - Helen Steiner Rice
Faith is a bird that feels dawn breaking and sings while it is still dark. -Scandinavian Saying

2:45pm: I just got a phone call from Melissa. She told me she had good news. The news is that Mattie's arm and leg have been operated on, and the incisions are now closed. Bob is working on the wrist now. I have no estimate of time of completion, but the fact that Mattie continues to be stable and Bob is able to work on the third tumor is a positive sign.

4:30pm: Melissa called with an update. Bob is continuing to work on Mattie's wrist bone graft. But Mattie is holding his own and is stable!

5:20pm: Jane, the PICU charge nurse just checked in with Peter and I. She called the OR and Bob reports that the surgery will continue for another hour! Just wanted to keep all of you in the loop. THANK YOU, THANK YOU for staying posted and for all your messages today! We feel like we are in a time warp or fog at the moment.

5:45pm: Bob just paid us a visit to Mattie's room. Mattie is still in the OR and being stitched up. Bob said there were NO surprises. In Bob's words, Mattie is now disease free. Wow! Bob removed 12cm of bone in the femur and 12 cm of bone in the left humerus. He also took out 5cm from the fibula (a bone not really needed for walking and movement) in the right leg and put that into the left radius for the bone graft. Additionally, Bob engineered a piece of the humerus as a bridge between the different sized radius and fibula. Mattie will most likely be in the recovery room for a hour or so. So we still wait, pace, and wonder when we will see Mattie. But it was such a blessing to see Bob and to hear his report. Bob said he took pictures during surgery and will send some to Mattie.

6:40pm: Mattie is now out of surgery and in the PACU (post anesthesia care unit). We are trying to to get down there to comfort Mattie within 30 minutes or so. Another bit of positive news is that Bob was able to preserve the left arm's nerve and muscle, so Mattie's prospects for functioning in that arm should be much better.

7pm: Peter and I spoke with Toby (the PICU nursing manager) at 7pm and asked if we could visit Mattie in the PACU. Toby called and advocated on our behalf. Within minutes, he spoke to the staff in the PACU, and then he escorted us down. When we entered the PACU, Mattie was surrounded by three nurses. One nurse was more lovely than the next. They were outstanding, competent, and compassionate. They couldn't do enough for Mattie or us. What an amazing experience that was. Peter and I spent the next hour in the PACU until Mattie was stable enough to come upstairs.

8:30pm: Mattie got back to his room and was in pain. They have been giving him fentenol to manage the pain, and Dr. Natarajan (the PICU intensivist) was on the scene to help us and to get the PCA pump for Mattie. It is 10:20pm, the PCA pump has just arrived.

10:20pm: Mattie has developed a fever (not unlike what happened during the last surgery), and has been vomiting. So he is now on Zolfran (an anti-emetic). The goal for the night is to make him comfortable and to rest.

I am not sure how I would describe today. It felt like I was frozen in time, or living life in slow motion. The ten hours Mattie was gone and in the OR seemed like an eternity! If I did not know he was with Bob, I probably would have really been besides myself. But I am at peace with Bob. I think Bob is the best and most capable surgeon to work with Mattie (and as you know Mattie's case is unique and challenging). Bob has guided us correctly every step of the way, and to have faith in a doctor makes all the difference in the world. Once again, Bob performed a miracle today. God works in mysterious ways, and all the prayers and good wishes that have been directed toward Mattie today, were answered. I believe God channels his powers through us on earth, and Bob is one of those people who has received God's special talents and skills. When Bob came up to Mattie's room this evening, after 10 hours of surgery, I asked how he was. Bob responded, "do not worry about me." I told him I always worry about him, because if Bob isn't okay neither is Mattie. Bob laughed at that. Bob stayed after the surgery and met us in the PACU. In the PACU Bob shared with us an x-ray they took of Mattie's wrist after the graft was put in place. We got to keep these x-ray copies, and I am sure Mattie will simply love them. When I looked at the graft, one thing was very apparent, this was not only a medical miracle to see, but an engineering feat. It almost looked like Bob built a beautiful trestle train bridge to strengthen Mattie's wrist. Of course, I feel Bob is too humble to really tell me about his work, but I have a feeling not everyone could have designed what he put together today.

I am now sitting watching Mattie, and I am in awe of what he survived today. Three major surgeries in 10 hours! All I can say is wow! I know the road ahead for Mattie won't be easy, but there is something to be said for surviving such major surgeries. He is a fighter! Before I sign off tonight, I want to THANK all of you for your prayers, wishes, e-mails, messages, and concern that you expressed to us today. You all have empowered us through this very difficult day, and your comments are so touching and meaningful. Thank you for your support and not just for today, but for your steadfast commitment to go the distance with us.

November 11, 2008

Tuesday, November 11, 2008

Tuesday, November 11, 2008

Message of the day (Thanks Charlie!): "Hope is some extraordinary spiritual grace that God gives us to control our fears, not to oust them." ~Vincent McNabb

Mattie woke up today and did not want to get out of his pajamas or leave the house. My parents came over toward the end of the morning and played with Mattie for a few hours. Mattie took everything out and by the time he was done it looked like there was an explosion of toys in his room. Fortunately Mattie was invited over for a playdate today with Charlotte, after school. That was a major motivator, and by 2:30pm, he complied with getting out of his PJs, washed up, and dressed. Thank goodness for friends!

Mattie had a wonderful playdate with Charlotte. They even walked to the upper school campus of SSSAS and ran around and built forts. Charlotte gave Mattie a wonderful Star Wars book and a solar powered keychain. While Ellen, Charlotte's mom, watched Mattie, I went out to lunch with my parents. While at lunch, Peter called me to let me know that Mattie's surgery had been bumped up to 7:30am, from the original 10:30am time schedule. So I immediately contacted Dr. Synder at Georgetown and asked her what we could do to get Mattie admitted to the hospital tonight. Dr. Synder made some phone calls and then she contacted me back and said we were all set.

When I picked Mattie up at Charlotte's, neither Mattie nor Charlotte wanted the playdate to end. Charlotte and Mattie were close buddies last year during kindergarten and it would be very natural and understandable if Charlotte moved on this year, and developed new friendships since Mattie no longer is at school. However, it is clear that Charlotte misses Mattie, and though she has other friends in her life, she hasn't forgotten about Mattie. They have a special connection, and as Mattie's mom, this warms my heart to know that Mattie in a way is irreplaceable in his friend's life. I know I feel this way about Mattie, but I am Mattie's mom. To see his friend feels this way is a special gift.

When we got back home tonight, I quickly packed things up for the hospital, and we had a lovely dinner thanks to the Goff-Glennon family! We loved all our Cheesecake Factory goodies! Thank you for a nice send off to the hospital. The chocolate cheesecake was the perfect medicine! When we arrived at the hospital, our room wasn't ready. It wasn't clean, nor was there a bed in it. So we carted all of our bags to the family lounge and hung out there for 90 minutes. While in the family room, I bumped into a woman I know from the Giant supermarket I go to near Mattie's school. She came up to talk with me, and let me know that her grandson was in the hospital. By the time she told me about her grandson, who is only 5, I felt like I had no problems what so ever. That should give you some understanding for the nature of her grandson's issues. He was born with no eyes, a half of a brain, unable to walk, respiratory issues, and I could go on, but I think you get the point. How a parent comes to deal with this, is beyond me. Here I am worrying about when will Mattie walk again, and in comparison to this family's issues, at least I know that Mattie will eventually be able to walk.

We finally got into Mattie's room tonight, and Melba, Mattie's HEM/ONC nurse delivered Mattie a special gift. The gift was dropped off by Kazu and his family. Kazu is a buddy of Mattie's from SSSAS. Kazu's mom and her family is from Japan. When we opened up the gift, it was simply amazing. It was 1000 origami cranes made with love by Kazu and his mom. Kazu's grandmother then put all the cranes together in a thread, one by one, praying for Mattie's strength and recovery. These cranes are truly beautiful! I have had the pleasure of trying to make an origami crane, and I know how hard it is, it is a labor of love! The fact that Kazu's family made Mattie 1000 cranes leaves me speechless. In Japan, these cranes signify a wish, and by giving Mattie these cranes Kazu's family is symbolically wishing for Mattie's successful surgery and recovery. Thank you so much for this very touching and symbolic gift. It will come with us on each hospital visit, and we hope its wish will come true! Below you will see pictures of these beautiful rainbow cranes, a gift never to be forgotten. Kazu's dad, Tad, wrote the following tonight about the cranes: "May these cranes take wing and reach those around the world who would join us in praying for Mattie."

I want to thank Team Mattie for having a planning meeting at Ann Henshaw's house last night. I hear the meeting was very successful, and I can not thank Ann enough for being our outstanding Team Coordinator. I hear the Team brainstormed some wonderful ways to help Mattie and it is incredible that through Mattie's illness so many talented individuals from our various lives (RCC, SSSAS, and GW) can be pulled together to create something so meaningful! Thank you for all your support, and thank you Carrie for hosting a bake sale at the upcoming Alexandria City Soccer Tournaments this weekend!

On the electronic front, we want to thank Susan, Linda, Kim, Cousin Donna, Cousin Rosalinda, Ms. Pollak, Karen, and Emily W. for all your wonderful e-cards and wishes for tomorrow. They are all appreciated! As we head into tomorrow, please say a prayer and keep Mattie in your thoughts. He heads into surgery at 7:30am and will be in the OR for at least 8 hours. As I did last time, I will try to do periodic updates on the blog throughout the day. Thank you for all your support, messages, and love. I end tonight with a quote sent to me by my friend Charlie: "Once you choose hope, anything's possible." ~ Christopher Reeve

November 10, 2008

Monday, November 10, 2008

Monday, November 10, 2008

The message of the day (Thanks Ann!): If God brings you to it, He will bring you through it. I hope so, I am counting on it!

Mattie slept through the night on sunday, and woke up in a good mood today. He sat through a central line dressing change this morning and was okay with the fact that he had a clinic appointment today. He always checks with me to find out if he is going in for just a check up or whether he is getting admitted to the hospital. When he arrived at the clinic, he was looking for Jenny and Jessie and found them and instantanously got them involved in a project. Jessie and Jenny have been accumulating boxes for Mattie. One of his favorite mediums to work with. He literally pulled out every cardboard box possible, and before I knew it he was creating. However, what he was creating today, in my book, was down right creepy. He created a huge life size model of a cockroach, and then designed a castle for this roach to live in. Don't ask me where he gets these ideas, but I think he loves to gross me out. Below you will see the roach and its house, I am sharing it with you because misery likes company.


Jenny downloaded a picture of a roach from the Internet, and then Mattie and Jenny designed the model magic roach!



The lovely model on top of Mattie's head!


Every roach deserves to live in a castle don't you think? Mattie's roach castle includes a staircase, and plush pillow accomodations!
Yuck!!!!!!!!!!!!!!!!




Mattie had a good clinic visit, and had his vitals taken, several blood tests completed (in preparation for his surgery on wednesday), and had an exam with Dr. Synder and a third year medical student. It is always fascinating to meet medical students and see how they deal with Mattie. Today Mattie turned to the student and said, "who on earth are you?" We all broke out in laughter and he put her through her paces. In addition, Dr. Toretsky came to visit us and I spoke with him about some of my concerns regarding Mattie's chemo treatment post surgery.

After our clinic visit, which mind you we were there from 11:30am until 2pm (because Mattie loves visiting with Jenny and Jessie), my parents and I decided to get something to eat. Mattie was starving by that point and said he could eat a "whole pig." Interesting! He ate very well at lunch and had fun chatting with us and coloring. When we arrived home, Mattie showed Grammie and Pop Pop his Christmas pooch that lights up. I described this new light as a Scooby Doo light yesterday, but in all reality this pooch looks more like JJ (naturally, no?). So we have renamed our new friend, "Christmas JJ." Below is a picture of Christmas JJ, who will be added to the Christmas light display this year.

Mattie also received a special package today from Susan DeLaurentis. Susan is Mattie's school counselor. In the large envelope Mattie found some great Thanksgiving joke cards from all the first graders in Mrs. Knowles' class! They were darling, thank you Mrs. Knowles' class. In addition, Susan included a wonderful turkey hat for Mattie to wear to get him in the holiday mood. I personally love Mattie as a turkey, how about you?


I don't know about you, but when you look at Mattie in these pictures, he looks like the picture of health to me. He looks happy and spirited, and from an outsider's point of view, you probably wouldn't guess the kind of torture he is living through. The beauty of his mind and spirit fascinate and impress me.
I would like to share two e-mails I received today with you. The first one is from Prof. Honey Nashman at GW. Honey is one of my supervisors. Honey wrote, "We wanted to let you know that STUDENTS in all of the Spring classes in our Human Services program are dedicating their service learning hours to "the spirit of healing and love for Mattie." Students who don't even need hours have offered to volunteer. Thank you Honey and the wonderful Human Services' students at GW! Your thoughtfulness means a great deal to us.
The second e-mail comes from Debbie Pollak. As many of you already know, Debbie is Mattie's art teacher at SSSAS and helped him create the beautiful sun painting on saturday. Debbie wrote, "About the painting......... I went to the Piazza (her studio) to put a coat of gloss medium on it last night. It was totally dark, peaceful, and silent as I put the keys in the door. I could sense that I would be overwhelmed when I saw the painting again. When I put the lights on, I could hear Mattie's squeals of delight as he was painting. I slowly put the medium on my brush and very carefully stroked it on the canvas. The tears rolled down my cheeks. I could not stop them. I did not try. His painting is a magnificent tribute to the strength, light, and joy that fills your little boy. I feel so privileged to have been the witness to this magical event. I was so happy assisting him, it was like I was floating with the angels, watching over him. It was the gift that keeps on giving. How can I thank you and Peter for sharing Mattie's time with me? This most precious time. As I sat in the silence of the night I just stared at the painting and decided it needs to be framed. I am taking it to my framer. When I put the lights out, I swear I could still see light coming from the painting. I walked down the stairs and felt blessed, incredibly blessed." I wanted to include, with Debbie's permission, a part of her e-mail to me today, because I want you to understand the depths of her compassion and love for Mattie, and she is committed to being a part of his recovery process. Thank you Debbie, the way you describe this painting glowing is almost spiritual in a way.
On the electronic front, we want to thank Brian Boru, Grammie, Kim, Susan, Coach Dave and Karen for your wonderful e-mails and e-cards! Also we want to acknowlege Michelle Idle (a former RCC mom) for sending us an adaptive homemade shirt that Mattie will be able to use post-surgery. Michelle has opened up a whole new world for me, because prior to my e-mail exchanges I was wondering what on earth to dress Mattie in. So tonight the count down begins. We have one more full day before heading back to the hospital for major limb savaging surgery. So some extent I understand that these surgeries have to happen, it is Mattie's only chance at survival, but on the other hand, it is so painful to see such a beautiful little body and skin all cut up. It is a harsh reality, and one I never thought I would have to face at this point in my life.

November 9, 2008

Sunday, November 9, 2008

Sunday, November 9, 2008

Mattie woke up before all of us today. In fact, he managed to slide out of bed without assistance, and came over to my side and tugged at me until I woke up. I did not understand why he was up so early. But after he woke Peter up as well, Peter clued me in that he promised to take Mattie Christmas light shopping at Target today. Apparently Mattie did not forget this promise from last night, and was VERY motivated to check out lights. In a way, it was a glorious feeling to have a quiet moment this morning while getting dressed without juggling 20 other things in the background. When Mattie came back from Target, he couldn't wait to show me his purchases. He picked out a Scooby Doo Christmas light, and felt that would be a good addition to the growing Christmas light display that Peter and Mattie assemble in our complex each Christmas. When I tell you that these guys light up our area with lights, that would be an understatement. If you ever watched the TV show, Home Improvement, then when I tell that Peter's display rivals Tim the Toolman Taylor's, I am not kidding. Mattie is very much looking forward to decorating this year. In addition to this Scooby Doo purchase, Mattie also bought me a gift. He knows how much I love lighthouses, and he bought me a beautiful Christmas lighthouse that actually lights up. I took two pictures of it, so you can grasp what it looks like. I love the picture I took of the lighthouse in the dark, because you can see Mattie's silhouette in the background staring at the glow. There is something magical about lights!

Later in the morning, Mattie had a playdate with his buddies Campbell and Livi. When Mattie got to Campbell's house, he started the playdate slowly and acted a little shy, but that did not last long, because Campbell proceeded to ask Mattie what he wanted to do, and the next thing I knew, all three kids were in the backyard playing with straw and leaves. Mattie LOVES leaves! Thank you Christine and James for taking care of Mattie for most of the afternoon, so that I could have some quiet time. While Mattie was having fun, eating pizza, and watching videos, Peter was home building a ramp onto our outside deck in preparation for Mattie coming home from the hospital in a wheelchair. Though this sounds like a chore, and it is, I know Peter enjoyed working outside in the fresh air, and building something. One of Peter's many great skills! I on the other hand spent these several hours by going out to lunch by myself. Prior to Mattie's illness this wouldn't be a way I would normally spend my free time, but spending time alone right now is a gift. Since I rarely have a minute by myself to just breathe. At lunch, I brought a stack of research articles I have been trying to read for the past two weeks. These articles relate to Mattie's chemotherapy options. Peter and I are tired of getting second hand information, so thanks to GW's databases, we have been searching and accumulating research articles as it relates to some of the major questions we are trying to answer. However, whenever I try to read them, I am too tired. Today was my moment, and I am pleased to say mission accomplished. However, while out eating and reading, I couldn't help but listen to other conversations around me. Not like I was trying to do this, it just happens. In any case, behind me were two women eating with each other and chatting about life. Their conversation caught my attention when one of them said to the other that she was okay if she had to die tomorrow. In fact, she said that she wasn't afraid to die, just of the process. Now I probably should tell you that both of these women were fine, not ill, and were having or attempting to have an existential dialogue. However, the conversation lost me when this woman continued on by saying that she hopes when she dies people will say that she was a special person, and that she made a difference in their lives. She went on to tell her friend about a recent funeral she attended where in the eulogy people were saying glowing remarks about the deceased. She said she hoped that this would happen for her as well. I don't know about you, but since I have now been forced to deal with the potential risk of losing my son, this whole conversation and the tone of the message truly irritated me. It irritated me because she is talking about life in such a matter of fact way. Is she really ready to die tomorrow? I think she can say this because she knows she is not, in addition, her reasoning for dying and what she would get out of it disturbed me even further. What could have been a meaningful dialogue between friends, became something self serving and insensitive.
When I arrived back at Campbell's house to pick Mattie up, he wasn't ready to leave. So Christine and I had tea together while the kids continued their play. I was so bothered by this conversation I over heard at the restaurant, that I shared it with Christine. Thanks Christine for a lovely afternoon, and for the opportunity to reconnect. I miss those after school moments!
My parents wanted to take all of us out to dinner tonight, but when Mattie got home he started to cry and he did not want to go out. What he really wanted to do was help Peter complete the building of the ramp. So Peter accomodated Mattie, and stayed home with him and they enjoyed the pizza JJ brought to them! Thanks JJ, we all need such a helpful puppy in our lives. My parents and I went out to dinner and by the time we got home the ramp was completed. Mattie was very proud of his accomplishment. It has been a weekend of building and creating for Mattie. Below is a picture of the ramp.




Also Mattie had an evening of building swings and car ramps out of plastic tinkertoys. I am happy Peter and Mattie had this time together to build and play.

















I received a lovely e-mail from my a former student of mine today. Thank you Mary. Mary wrote, "You mentioned generosity, Your generosity in letting us into your world, as you go through this life altering event, cannot be overestimated too. You are reminding us daily about what is really important. Thanks." Thank you Mary for this lovely message. One thing is for certain, when such an illness hits your life, you re-evaluate everything, and I have found I have become even more bold in my statements and feelings (if that is possible), because what on earth do I have to lose? Nothing else seems to matter at this point in time.
On the electronic front, we want to thank Brian Boru, Karen, Kim, Lorraine, and Susan for your lovely e-cards. They cheered up our day! As we head into monday, I can't help but feel a sense of nervousness about wednesday. It is hard to describe this feeling, but it seems like yesterday we were released from the hospital and now seconds later we are heading right back. I think we spend more time in the hospital than at home. Each time we head off to the hospital, I wonder what on earth gets Mattie to return there? For the most part he is compliant and doesn't question why he needs to keep going back. That to me alone is remarkable, because if I were his age I would be kicking and screaming all the way there! I could come up with several theories for this mature behavior, but I think having "his ladies" there is a great motivator!

November 7, 2008

Saturday, November 8, 2008

Saturday, November 8, 2008

Today's Message (thank you Carrie!): I believe in the Sun even when it is not shining; I believe in Love when feeling it not, and I believe in God even when he is silent. ~ Barb Flint Gifts of Many Cultures

Mattie had a very special day from start to finish. He started his morning with a visit and piano lesson from Caroline Eaton. Mattie enjoyed his time with Caroline and wanted to show her his new remote control car, he demonstrated it out for her, and even introduced Caroline to JP (our neighbor) and of course to our resident Jack Russell Terrier, JJ. JJ came with Dunkin Donut treats! JJ always knows how to put a smile on Mattie's face. Caroline was so thrilled to meet JJ, and she said she has read so much about JJ that she felt she already knew him. In a way, meeting JJ for the first time is a lot like meeting a Hollywood star, because both JJ and the stars get a lot of publicity and certainly JJ gets his share of blog publicity. I loved Caroline's analogy today, because she is right, in our world JJ is one of our stars. Caroline and Mattie played on the electronic keyboard today, and at several points it sounded like a jam session. Mattie was even getting his feet involved with playing. Normally I would have a big issue with this, but since he may be playing with his left leg for the next couple of weeks, I went with his clever idea. I tried to snap a picture of his new way of playing, but I wasn't successful at it. Every time he saw the camera, his foot would leave the piano. Below is a picture of Mattie with Caroline. Thank you Caroline for a lovely morning, and we are so happy to have the chance to get to know you better.
Peter spent the morning assessing all of our house plants to determine which ones we needed to either bring to his office or give to Larry Jenney (one of Mattie's Kindergarten teachers) to take care of over the winter. When we found out Mattie had cancer, all of our house plants were removed from the house and kept outside. There is the potential for molds to grow in house soil, and it is recommended that none be kept in the house this year. That may not seem like a big deal to most people, but to the "crazy plant lady," as Peter and Mattie affectionately call me, this is a major problem. I have had some plants for over 15 years, and I am very fond of them, some were given to me by family and friends, and these plants I hold dear, because I view them as an extension of our relationships. In any case because of the colder weather, several of our plants were relocated today to Peter's office, and the rest went to Larry's home today. Thank you Larry for opening your home to my green friends. While we were outside sorting through plants, I captured a photo of the newest Red Sox Nation Member (kidding of course, but I couldn't resist!). Got to love this grasshopper, who hopped onto Peter's hat.

After Mattie's piano lesson, we packed up into the car, and headed to Ms. Debbie Pollak's art studio in Alexandria. Debbie is Mattie's art teacher at SSSAS. Debbie worked hard to create a happy day for Mattie from start to finish. This day called for a lot of pre-planning and set up on Debbie's part. Debbie is very aware of the physical challenges that Mattie faces next week, and she thought if they created a painting together, this would inspire Mattie through his recovery process. He could look at the painting (which will hang in our living room), remember this special day, and this would hopefuly motivate him to work and rehabilitate his arms so that he could return to making more art work in the future. It was a lovely and heartfelt sentiment! In order for this day to go as smoothly as it did, Debbie purchased a large canvas and primed it with a background the day before. She invited Jennifer and Dylan Li (SSSAS students) to assist with creating the backdrop on the canvas. Debbie explained to Mattie that they were working with acrylic paints today, and that it was important to have the backdrop already done, because if not, they wouldn't be able to actually paint a scene today. It has to be done in stages. Fortunately Debbie thought ahead and worked on the first stage, so that Mattie could jump into the project today. In addition, Debbie planned both lunch and dinner for us, with the help of two lovely SSSAS parents. Thank you Luda for a fabulous lunch. We simply loved it! I became friends with Luda during SSSAS' weekly chapels. Luda was my chapel buddy, we sat next to each other each week. Debbie set a glorious table. She spoiled us with a silver tea pot, lovely china, and silver platters. It was like going to the Ritz for tea. Walking into Debbie's is an experience. She has transformed a car barn into an amazing Italian villa on the first floor, and a bright and airy art studio on the second floor. Each piece on the first floor was fascinating, and picked with love. I have come to see that Debbie is very sentimental and parts of her first floor reflect the special love she shares with important people in her life, such as her mom and dad. Being of the same sentimental persuasion, I truly appreciate this aspect of Debbie. Below is a picture of us enjoying our lunch with Debbie!




After lunch, Mattie and Debbie went upstairs to her incredible studio, and began working. I have included pictures below of the masterpiece from start to finish.









Mattie is dressed in Debbie's Hawaiian smock, and is standing in front of the canvas that was primed with a background color. So this is the pre-painting picture, before Mattie did anything to it.




The next phase of the "sun" painting.










This was the final product. It is hard to see the 3-D nature of this painting. Because the actual sun, is a separate piece of canvas that was hot glued onto the bigger canvas. In addition, we hot glued feathers onto the canvas, since Mattie learned a few weeks ago that Native Americans hold feathers while they pray... since birds fly high in the sky, it is believed that the birds carry prayers to God in heaven. So from my perspective, Mattie's sun is lighting the way for birds to carry our prayers to God in heaven.
Mattie even signed the painting himself with his left hand!





Mattie and Debbie! I love the expression I captured on Debbie's face, because she is a proud teacher happy with her student's accomplishment. Mattie was aglow with his sunshine. He said that looking at the painting made him happy!








Toward the end of the day, Dinny Li (a SSSAS mom) was very thoughtful and brought us a wonderful chinese food dinner. It was delicious and very generous of her family. Her children, Dylan and Jennifer (as seen in the picture), helped prime the canvas with Debbie yesterday, and came to see the finished product this afternoon. We thank the Li family for their support!

Debbie surprised Peter tonight with a birthday cake. Debbie and Mattie frosted this delicious and sinful chocolate cake earlier in the day. So Mattie felt very good about himself, that he was able to keep this a surprise from Peter. I really appreciate Debbie doing this, because normally Mattie and I would be baking a cake for Peter and frosting it, but since Mattie will be in the hospital during Peter's birthday, I just figured it wouldn't happen this year. Thank you Debbie for this special treat and surpise. I captured Peter and Mattie blowing the candles out. I don't need to ask, because I think I know exactly what Peter wished for!
Today was a very memorable day. I think Mattie's "Sun" creation is breathtaking, and I look forward to displaying this original piece in our living room. There is something special and healing about the sun. This painting is vibrant and alive, and I know it will help us through some difficult days ahead. This work of art is something that I will hold near and dear to me, because it isn't just a snap shot in time, it is something more meaningful. Through this art, it captures Mattie's brightness, vivaciousness, and personality. These bright colors fit him as a person. The sun provides purpose and direction to the time and place in our lives, and in essence Mattie is my sun (not just my son). This art piece will be part of our permanent collection. In a way, we created an important tangible piece of family history today. Thank you Debbie for this precious moment.

When we arrived home tonight, we received a lovely dinner from Davis Knox (a colleague of Peter's from the American Red Cross). Mattie thoroughly enjoyed the pasta as well as my parents. We look forward to eating your pumpkin bread (one of our favorites) tomorrow. Thank you so much for thinking of us and for your support.

I received a lovely e-mail from Carrie that I wanted to share with you. Carrie was commenting on all the emotions that Mattie is forced to deal with in any given day. She wrote, "I love the lamp Mattie made for you and he knows how special you are to him and he probably is trying to separate from you to be strong, so yes he may feel bored with you in essence (nurturer/mom)..... but I think that is to be expected considering what he is going through... I think I would have quite a bit of anger if I were in his place and he is dealing with all of this. He may have anger and then at the same time being with a nurturing person (mom) could be confusing. Like how can both of these things exist in my life at once? Hurt, pain, and then love? Do you know what I mean? Such a big lesson for such a young person. But mattie seems older (emotional maturity) than most people I know!" Carrie, I totally agree, it is hard for an adult to process all these emotions, much less a six year old.

On the electronic front, we want to thank Cousin Rosalinda, Karen, and Grammie for the great e-cards and videos! In addition, Mattie received a wonderful toy sports car from Leslie Williams (his Kindergarten teacher) today. Thank you Leslie, Mattie is busy playing with it tonight! He loves it. Also, we want to thank Patty Lease for the wonderful videos she is sharing with Mattie. Patty is Mattie's science teacher at SSSAS. These videos belonged to Patty's children, and we look forward to watching them together. It was very thoughtful of you to think of Mattie. I end tonight with a quote from Debbie Pollak's father: "If you can't do anything about your own problems, do something extraordinary for someone else. You will feel better." Thank you ALL for making us feel better each and every day.

Friday, November 7, 2008

Friday, November 7, 2008

Mattie's Methotrexate level cleared at midnight on thursday. So we knew that we would be discharged on friday morning. We are SO thrilled to be home! Each hospital stay seems to become harder and harder on all of us. At 7am, I started packing up Mattie's hospital room, while Peter jumped on several conference calls. It literally took me two hours to sort through the room, and pack in an organized fashion. We enter the hospital SO organized, and by the time we are discharged, things are all over the place. When Mattie woke up today, and said he did not want to come home. But as that thought of being released became a reality, his mood changed for the better. He hopped out of bed, got dressed, and was even helping me pack. I think Mattie and I were close before he developed cancer, but now we have a very tight bond, and though we may get upset with each other now and then, we both know it is out of frustration. Mattie was an excellent helper and had good insights about how to more efficiently pack our boxes with things. Peter and I packed up our car with Mattie's things, while Whitney and Lesley played with Mattie. Thank goodness for Childlife! We would have a real problem without these fine individuals. It made the move out process go much smoother today!

Mattie and I dropped Peter off at work, while we continued on home and met my parents in our parking garage. They helped us bring bags upstairs, and I slowly started to unpack. Unpacking is one of my LEAST favorite activities, after a long week at the hospital. While I was unpacking, my parents took Mattie for a walk, which was very good for him. On their walk, Mattie stopped by our local CVS and picked up a balloon and a remote control car. He was very animated about this purchase. Thanks Grammie and Pop Pop! See a picture of Pop Pop watching Mattie with his car below!


At 1pm today, Peter, myself, and Alison (our Team Mattie director of communications and public relations) had a conference call with Ted Kennedy, Jr. Thank you Brian and Danelle Fortune (RCC parents) for making this possible. Mr. Kennedy lost one of his legs to bone cancer in 1973 at the age of 12, and devotes much of his professional and personal energy to working as an advocate for the civil rights of people with disabilities. We spoke with Mr. Kennedy about his own battle with osteosarcoma, and then spoke about Mattie's current situation and treatment issues. Mr. Kennedy shared many valuable insights with us, and even mentioned his interest in learning more about MTP (the experimental drug at Sloan Kettering). At one point in the call, Mr. Kennedy basically said that Mattie was lucky to have parents who are devoting their time, energy, advocacy skills, and intelligence to help him. He commended us for doing the right thing, which is exploring all possible options for Mattie's treatment, so that by the time we make a choice about post surgery chemo options we will have no regrets. He also told us, never to be afraid to challenge a doctor, and that a good doctor should welcome such a challenge. We told Mr. Kennedy that we agreed with him 100% and challenging doctors is not a problem for us. Mr. Kennedy was very generous with his time and thoughtful in his responses. It is our hope that we will be able to keep him updated about Mattie's progress. Mr. Kennedy even told us that he has checked out Mattie's blog on occasion.

After our conference call, my parents and I took Mattie out to lunch. Mattie ate up a storm, as he cuddled up right next to me while eating. We fed some fish after lunch, in the pond outside the restaurant, and then we took Mattie to Toys R Us. He has been planning this toy store visit now for a week. It was so funny watching him in the store, because I could see him scanning the aisles, and I knew exactly where he was heading. He wanted a remote control airplane. He found exactly what he was looking at, and when we came home, we assembled it and though it was dark outside, we went out and flew it!

Thank you to the Ferris family for a "New England" feast. We loved the Lobster rolls and the fish soup from Kinkaid's. What a special treat, the chocolate dessert was demolished tonight as well! Much thanks! The food from Johnny Rockets for Mattie was a hit too! That was so thoughtful of you, we can't thank you enough for your support.

Mattie had the opportunity to open up some packages tonight. Thank you Grandma for the shirts. They are very appreciated and needed. Mattie loved the homemade halloween cards from his cousins, Nat, Sydney, and Will in Boston. Mattie also loved the scratch magic and story telling game. We also want to send a special thank you to the Morris family for enrolling Mattie in the Lego Brickmaster Club. Mattie was thrilled to get his first gift today, and is currently working on it. In addition, a former student of mine, Mary, was very generous with us, and sent us a Brookstone Sound Machine. While building legos, we have a peaceful sounding stream running in the background. I am loving it! It is a fantastic sensory experience for all of us. Thank you Mary!

On the electronic front, we want to thank Emily W., Brian Boru, Karen, and Grammie (great animal videos!) for the wonderful e-cards! As we head into the weekend, Mattie has a lot of wonderful things planned, and it is hard to imagine how in only a couple of days our world is going to change dramatically. Mattie will be truly disabled, and we will need to learn how to assist him as well as motivate him through this recovery process. In addition, our living room will be transformed next week into a hospital room, so that we can make Mattie comfortable when he returns home post surgery. I thank all of you for sending me links to adaptive children clothing links today! I appreciate all the thought you are putting into this and for those of you sewing and designing clothes for Mattie so he can be comfortable post-surgery. I end tonight with a quote from Leslie's hope book that she sent me. It seems so fitting for Peter and I.
"Even the strongest people must step back, take a deep breath, and summon their courage now and then."

November 6, 2008

Thursday, November 6, 2008

Thursday, November 6, 2008

Quote of the day (thanks Charlie!): "Hope sees the invisible, feels the intangible and achieves the impossible."

Wednesday night was so unusual. Mattie fell asleep at 8pm, and had a decent night of sleep (of course other than getting up to go to the bathroom from all the IV fluids, and having to do vital checks every four hours). I thought he was so tired last night mainly because yesterday was the first day post surgery without the bandage on his right arm. The arm is free now, and somewhat sitting in a sling. I say somewhat because we can't seem to find the right size sling for Mattie to support his arm. In any case, he is moving his arm very carefully.

We began our day with a visit from Anna, Mattie's physical therapist. Mattie and Anna continued their water gun battle, and then Mattie also worked on some additional exercises. He was mostly compliant with Anna's requests. During Anna's visit, Linda came in, and helped talk with us about Mattie's surgery next week. It is ironic, no matter how I think I have prepared Mattie, something always surprises me. Mattie thought he wasn't going to have another surgery until the first surgery site had healed. In addition, when he heard he was having surgery next week, he thought it was only going to be of one more part, not all three at one time. It was fascinating to see the wheels turning in his head, as he began to think about the consequences of three surgerical sites. So the questions started to roll, such as how will I be able to get dressed? What kind of pants will I wear? How will I be able to walk and get around? Why is Dr. Bob doing another surgery, since he isn't healed from the first surgery? All great questions, and we answered them one by one.

I found Mattie's questions so meaningful, that it reminded me of an e-mail I received from a friend, and former RCC parent, Michelle. Michelle wrote the following to me back in the end of October: "Vicki, I was reading your blog this morning before heading in to work yes, I'm addicted, even while on a work trip to Ohio!); reading about Mattie not wanting to leave the room with his back exposed gave me a thought. A friend of mine has a non-profit corporation called Sew Much Comfort (www.sewmuchcomfort.com) that makes adaptive clothing for wounded veterans. Long story short, when her son was battling cancer and needed multiple surgeries, she adapted his clothes - pants for Mike - by removing the seams and replacing them with velcro. This allowed Mike to wear "normal" clothes that he could get on and off, and the clothes could work around the various apparatus he had to deal with."
I think Michelle's idea is fantastic, and I spoke to Anna (Mattie's PT) about this today. I am trying to track down companies that make such adaptive clothes for children. I want to get this addressed ASAP, since Mattie will need such clothes in alittle more than a week from now.

After Anna's visit, Mattie and Linda went to the Childlife playroom. It was in that room, that Mattie worked on a birthday present for Peter. Mattie was going to give the present to Peter next week, but when Mattie saw Peter tonight, he was too excited and insisted on giving him the present. Mattie had help gift wrapping the present, but basically designed and wrote in his card with his left hand, and created a beautiful birthday cake out of model magic for Peter. Below is a picture!


Mattie had a visit today from Alison, who met all his food cravings, with a happy meal, a pizza, and a hot dog. He was all set. He slowly made his way through all the food throughout the day! Thank you Alison for a lovely lunch and the time to chat, and thank you Linda for this opportunity. When Alison and I got back from lunch, we found Mattie in his room with Linda. Mattie and Linda were playing the keyboard together, "Mary had a little lamb" to be exact! Caroline E., I think you would be proud! Then Mattie proceeded to tell me that he is bored with me as his mom, and he wished that Linda were his mom. Linda answered Mattie's request in a lovely way, saying that if Mattie spent as much time with her as he does with me, he would be bored of her too. At first, I was taken aback, but then I realized where his comments were coming from. It is so natural, he wants the opportunity to be able to be separate from me, and this circumstance doesn't lead to this kind of independence. Mattie continued with this line of reasoning and Alison sat down and talked with Mattie about his comments directed at me, and then she just started tickling him and redirecting his negative energy. By the time she was finished with him, he did not even remember what he was complaining about. It was wonderful!

Mattie then had a visit from Jessie (one of Mattie's art therapists). Jessie is a lovely person on the inside and out, and she is very creative in her approach to projects. She brought with her simple things like popsicle sticks, a box, a glue gun, and this interesting paper that transforms into a sponge when soaked in water. By the time Jessie and Mattie were finished, they transformed the box into a mouse's house, and designed a mouse out of model magic, created pieces of cheese for the mouse, and designed popsicle exterminators. Below you will see the whole creation! It was creative, and listening to Jessie play three different characters was a riot, I haven't laughed so hard. Thanks Jessie for a lovely afternoon, the play continued after your visit.




Tonight the mouse box game continued with my parents, as they played with Mattie and his mouse friend. However, toward the end of the evening Mattie was getting tired and crabby. He is eating up a storm this evening, watching Tom and Jerry, and is excited about the opportunity of going home tomorrow. We want to thank Alissa M. for a wonderful dinner tonight. Alissa is a former student of mine, and I so appreciate her support and kindness. I am blessed by having the best students.

On the electronic front, we want to thank Karen and Brian Boru for their lovely e-cards! We are ready to leave the hospital, as we try to prepare for the huge week ahead of us. At the moment both Peter and I are exhausted, but I guess 15 weeks of dealing with this can do this to a person. Unfortunately there is no end in sight, and frankly the near future looks daunting. We appreciate all the support that is being extended to us. It is a powerful force to know we are not alone.

November 5, 2008

Wednesday, November 5, 2008

Wednesday, November 5, 2008

Quote of the day: "Life is not tied with a bow, but it is still a gift."

I received the above quote of the day from my friend Charlie. I told Charlie, that it is hard to see life as a gift at the moment. Her response was, "As long as we are here, there is hope. Mattie and his spirit are a gift and an example for all of us, as you are." Thanks Charlie!

Mattie had a decent night of sleep on tuesday. Other than the usual awakenings to check his blood pressure, temperature, and bathroom runs. He woke up early this morning because he could hear Peter and I walking around the room, and trying to get ready. It is virtually impossible to tip toe around a 2x4 room. Mattie was hungry this morning, but refused his hospital breakfast. I think I should get a discount from Georgetown, since basically we really can't use their food service. Thankfully, Mattie had homemade pumpkin muffins (thanks Debbie) and banana bread (thanks Ann) to choose from. Mattie and I did some computer time together, learning to spell words, and while playing I was preparing him for the fact that I would be attending a hospital team meeting today, and he would be spending some time with Lesley.

The team meeting today was very helpful. If you thought there were a lot of people at the first team meeting, well then you would have loved today. It was standing room only at one point. There were people there that I did not even know. But of those I recognized in attendance were: Dr. Bob Henshaw (Mattie's surgeon), Bob's fellow from Washington Hospital Center, Dr. Kristin Synder (one of Mattie's oncologists), Dr. Houser (chief of the PICU), Dr. Ved (Pediatric chief of anesthesiology), Jeff Turner (nurse manager of the HEM/ONC team), Dr. Matt Biel (child psychiatrist), Denise Garner (Mattie's social worker), Kathy Myint-Hpu (Nurse Practitioner), Jenny Padden (Art Therapist), Jessie Masterson (Art Therapist), Anna Fragomeni (Physical Therapist), Nicole Droog (Pain Management), and of course Linda Kim (Child Life Specialist) and myself. The meeting accomplished two major objectives in my perspective, first of which was Mattie's coordination of care, and second, a discussion of Mattie's pain management after the next surgery. After a discussion, Mattie will have four different pain control options placed in his body: 1) an epidural (regional anesthesia placed in the spine), 2) a perineural (like he had with the surgery of the right arm), 3) sciactic nerve catheter, and 4) a PCA, which will pump a narcotic into his body on demand. I felt reassured to see all the team members talking with each other about Mattie's case, because the November 12 surgery will be an eight hour long ordeal.

After the meeting, Bob came back to Mattie's room to remove Mattie's splint and bandages. Mattie handled it well but was in some pain. However, Mattie's incision looked good and the blister by the incision had burst and healed (a natural by-product when using dissolvable stitches). Mattie was in some discomfort so he received some pain medication. Mattie refused oral pain meds for about 30 minutes (of which he was crying and uncomfortable), and thanks to Dr. Synder, she rescued us from a very unpleasant situation, by ordering for the pain meds to be administered through the central line. Thank God for small favors! This helped him fall asleep for a little while, and Linda, Dr. Biel, and I discussed Mattie's sleeplessness and how to prepare him for next week.

When Mattie woke up from his nap, he had a visit from Ellen. Ellen brought him a happy meal, and of course Mattie was thrilled by this, and loved the toy. Afterall it has a lot to do with the McDonald's toy, doesn't it?! Ellen also gave Mattie a Webkinz Gorilla, who Mattie named "Cutie." Now Mattie and Charlotte can play with their webkinz together on line. Thank you Ellen for your thoughtfulness and for playing with Mattie today while I got a chance to eat. I thoroughly enjoyed lunch and hearing you and Mattie playing 20 questions.

After Ellen's visit, Anna (Mattie's physical therapist) came for a visit and she was armed with animal shaped water guns. Mattie had a great time playing with Anna and also learning how to move his arm. In fact, I think all the activity today wore Mattie out. He fell asleep at 8pm and is still sleeping. It is a miracle! Below you will see a picture of Mattie squirting (or drenching) Anna with water. Anna was a good sport, and Mattie seemed motivated to learn how to move his arm using the technique Anna showed him.


Next Mattie headed down with myself, Linda, Whitney, and Lesley to the X-ray department to get some pre-op X-rays. He was with his ladies! How many other six year olds travel with four woman at one time? Fortunately we are becoming quite familiar with Theresa, the X-ray tech. She is very patient with Mattie, who was very protective of his unbandaged arm today, and was moving gingerly. You had to see all four of us helping Mattie onto the X-ray table. It was an absolute riot! While getting his X-rays, Mattie was visited by his "big brother," Jey. Jey also stopped by yesterday and gave Mattie a lovely American Flag for Election day. Jey is always looking out for Mattie, and stayed with us until the X-rays were completed. There are times I feel like I am living in a very surreal environment. An environment where people care about you, where you get a lot of attention, and where others seem to take the time to talk with you. After the X-rays were complete, Theresa printed out copies of the X-rays for Mattie on paper. He was fascinated to see his bones and where his tumors are. I of course don't know how to read films, but I have learned enough now (unfortunately) to spot where these tumors are. Theresa also gave Mattie a lovely dinosaur ring and lollypops for being such a great patient today.

As we head back upstairs to the PICU, Mattie decided he wanted to go to the playroom with Linda, Whitney, and Lesley. Linda gave me the time to go back to the room, and catch my breath. Which was VERY appreciated. While I was gone, Mattie told Linda he wanted to make me something. He said I am always with him, so he never has the opportunity to surprise me and make me something. I thought that was very special. When he came back from the childlife playroom, he surprised me with a beautiful painted lamp. See the picture below of Linda, Mattie, and Lesley and then a close up of the lamp!




Dr. Bob Henshaw spent the entire day working at Georgetown Hospital today, but before returning home, he paid a visit to check on Mattie. I updated him about Mattie's arm movement, and the fact that he had a busy and productive day. I know Bob realizes I am very apprehensive about surgery in general, but his calming demeanor is very contagious. He has a way of making me understand that this must be done, and done soon, so that Mattie can begin chemo and the recovery process. I truly believe Bob performed a miracle on Mattie three weeks ago, and though I have my own issues with surgery, I can't think of a more trusted person that I am turning my son over to for eight hours next week. What on earth are the chances that I would know the Henshaw's? You need to understand that Bob's skills are so unique that there may be only a handful of people in the world that can do what he does. Makes you believe in divine intervention!

Toward the end of the evening, Mattie had a visit from Jenny. Jenny showed Mattie how to make tissue paper flowers. Mattie wanted a flower on his IV pole, just like Brandon's (his big buddy). They had a good time with the tissue paper and talking with each other. Mattie even claimed one of Jenny's bracelets for his own since he liked them so much. Thank you Jenny! Below you will see a beautiful flower Mattie and Jenny created together. It is glorious and huge!



We want to thank the Katcher Family for a wonderful dinner tonight. We loved your shrimp, homemade applesauce (one of my favorites!), and of course your special applesauce cake! We appreciate your support.

On the electronic front, we want to thank Brian Boru and Karen for your lovely e-cards and constant support! I end tonight letting you know that Carrie and I have finalized Mattie's wristbands. Carrie let me know that the GW counseling honor society (CSI) plans on purchasing 500 wristbands to start the distribution process. I want to thank Carrie for all the work she is doing on make this wristband project a reality. I always felt Carrie was a talented doctoral student and TA, but now I am getting to know her as a person, and her depth, sensitivity, and compassion overwhelm me. Thank you Carrie and CSI!