This is a story of a young boy who lost his life to a 14 month battle with childhood cancer, and the subsequent grief that his mom lives with since his death
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
Tuesday, October 10, 2023 -- Mattie died 732 weeks ago today.
Tonight's picture was taken in October of 2006. Mattie was four years old. I am sure I decided to snap this photo back then because of the eclectic nature of Mattie's clothes. He literally decided to put clothes on top of his pajamas. For no apparent reason, other than why not? There were many unexpected moments of laughter with Mattie. He had a mind of his own and I learned as his parent to embrace his strong will and appreciate the many gifts and challenges he added to our lives. I wish he were alive today, as I could use his strength, force, and loyalty.
Quote of the day: You can clutch the past so tightly to your chest that it leaves your arms too full to embrace the present. ~ Jan Gildwell
Tonight's quote may be exactly true, but given a choice, I much rather live in the past than contend with the present. Nothing makes sense to me, everything from my daily life to our world at a global level. The pain and destruction that people can cause to one another, is beyond what my heart and mind can actually absorb. Therefore, I much rather focus on the past, when I was an intact family of three, who had their whole lives ahead of them. This is my mood for today!
Tonight's picture was taken in October of 2006. Mattie was four years old. Mattie carved a pumpkin in preschool that day and was very proud of his creation. Which was why I snapped a photo of him with this orange cutie. From a very early age Mattie gravitated to the color orange. I have to admit, I was never an orange fan. But Mattie changed all of that for me and now it is one of my favorite colors.
Quote of the day: Given a choice between grief and nothing, I'd choose grief. ~ William Faulkner
This afternoon, after a full day of chores and managing my parents, I decided to leave the house and took Sunny with me. We went on a walk together. Poor fellow! Sunny has the spirit and desire, but physically he is very challenged walking. I don't push or drag him. We take our time together and what I have learned is by moving at his slower pace, it gives me more time to pause and notice the world around me. Typically when I walk, I am moving quickly. So quickly that I may not be observing what's around me in totality. In the world that we live in now, reconnecting with nature, beauty, and the value of life is more crucial than ever.
But here is it.... Sunny is helping me once again! Sunny came into my life in 2016. Life after Mattie's death has been impossible at time. But I would say Sunny is a consistent bright spot in my life. He is loyal, loving, and my companion. I certainly miss the walks we used to do in the past, where we could walk for 5-8 miles at a time. Those were the days, when we walked around the National Mall and explored the historic sites and beauty of the city. Life seemed simpler then, living with so much grief. But once again, when I am faced with great stress, sadness, and anxiety, I turn to walking. Walking with my buddy. Thank goodness for Sunny!
On our walk today, Sunny happens to love sniffing and exploring a bank of pine and oak trees. These were two of Mattie's favorites. I am not sure it is a coincidence that Sunny loves the same trees as Mattie. In any case, while Sunny was checking out the trees, I decided to collect acorns. Not unlike what Mattie used to do! I can't tell you how many acorns Mattie collected over the years. In fact, he would collect them and give them to special people in his life.... as gifts! I distinctly recall that Mattie's occupational therapist would receive an acorn in the fall each week! She must have had quite a collection going from us. Mattie may not be walking with me literally, but as I appreciate the acorns and pinecones, I remember my moments as a mom and feel that these gifts from nature continue to keep us connected.
Tonight's picture was taken in October of 2006. Mattie was four years old. This was what our October weekends used to look like! We would select a different fall festival each weekend to visit. As Mattie got older, he loved the slides and other fun adventures that these fairs provided. As you can see, we LOVED this giant pumpkin, and Peter snapped a photo of us in front of it. This is one of my favorite photos, and it sits in my office today.
Quote of the day: Tears are sometimes an inappropriate response to death. When a life has been lived completely honestly, completely successfully, or just completely, the correct response to death's perfect punctuation mark is a smile. ~ Julie Burchill
I am not sure where I sit regarding tonight's quote. But clearly if examining Mattie's life, he did not 'live completely' nor did he live 'completely successfully.' So in my case, there is NO perfect punctuation, and certainly NO SMILE!
I went on two walks today. The first one was with Sunny. Though Sunny is unable to do much walking, I am trying to take him out daily. I know how much he loves it and with each walk, I am trying to build up his stamina so I try to increase the distance with each walk. Sunny loves the cold weather months, so I have a feeling it will be easier to get him up and walking. All I know is he loves his time to explore and he also loves connecting with me. As I do with him! Since my parents moved in I have skipped Sunny's walks for months. Maybe for even a year. I think it was the combination of Sunny's decline on chemotherapy and my non-stop work helping my parents. But my commitment to myself is to get outside, absorb my green space, listen to music and walk. This is something I still love to do, and believe me my list of what I love to do has now dwindled.
This afternoon, I took my parents out to brunch. We visit this same restaurant every Sunday and I have come to love our server and know many of the managers at the restaurant. While dining, I heard two songs that stopped me in my tracks. There is nothing like music! It can transport me back in time, and I can recall the feelings each time I heard these songs for the FIRST TIME.
The first song I heard today, was introduced to me in 1986. I moved to Los Angeles with my parents in 1984. It was a very hard move, as I was about to enter high school. All the kids at my school already knew each other, and therefore, I was the odd one out! Around this same time, the movie, The Karate Kid came out in theaters. It was as if this movie was written for me! It was about a kid who moved from the East coast to Los Angeles. At school he got teased and didn't fit in, and of course longed to return home. As silly as this sounds, this movie got me through a very hard time adjusting to a new home, school, and state. To this day, whenever I hear any of the music from this movie, I am transported right back to the 1980s! Which was where today's song by Peter Cetera (the Glory of Love) comes in. When I heard it, it was like I was a teenager once again and could feel all the same emotions I had back in the 1980s and at the same time the happiness and comfort this song brought me for decades. In fact, whenever I would hear this song playing, I would say to myself..... something good or positive is going to happen! Funny, no? I did this for decades with this song.
The Glory of Love.............................
The second song that I heard today was Time of My Life. This song takes me back to my college days! This song was in the movie Dirty Dancing, which was released in 1987, my first year of college. Again another social adjustment. However, I was a lucky person, because in school, I found great like minded friends. One Friday night all my friends got together to go to the campus theatre, and what was playing was Dirty Dancing. I have always loved music and dance, so the fact that there was both in this movie, made it a winner for me. Needless to say, all of us were absolutely taken by the movie, and we loved it so much that we stayed for the second showing! So when Time of My Life played today, I was transported right back to Union College, surrounded by friends, and at a time when I thought I had my whole future ahead of me. Thankfully I had no idea what the future would actually hold for me, because it has been anything but a time of my life.
Tonight's picture was taken in October of 2004. Mattie was two years old. I will never forget this moment in time. That day his Montessori preschool went on a field trip to Butler's Orchard in Maryland. This is how I learned about this great farm! In any case, because Mattie was having difficulties with the director of this preschool and his classmates, I found my way to volunteer and serve as a class chaperone that day. Thankfully I did, because I would never have captured this adorable photo otherwise. The kids took a hayride out to the pumpkin patch, and Mattie picked this orange cutie to take home. I absolutely love the composition in this photo, with color, context, and Mattie's gaze into the camera.
Quote of the day: Words have the power to both destroy and heal. When words are both true and kind, they can change our world. ~ Buddhist quote
There are times within any given day where I say to myself...... can I really do this? Can I make it through another day living with such stress, chaos, and uncertainty? Of course what I am reminded of is the simple fact that I survived the worst stress possible in 2008 when Mattie was diagnosed with cancer. Though I did not undergo cancer treatment myself, I endured endless stress, anxiety, lack of sleep, and the chaos of living within a pediatric intensive care unit for 14 months. Now it is 14 years later, but the stress remains within me. Therefore, whenever I am faced with subsequent intense stress, I may not react like a "normal" person. Instead, I react in a very hyper-alert manor and in this mode, I truly can work non-stop, almost robotic like. Which means avoiding and absorbing true feelings, because there is no time to process them. Or if there where time and I did sit with these feelings, I wouldn't be able to function in my caregiving role. It is kind of a double edged sword. But a sword that is unfortunately very familiar to me.
I took my parents out to lunch today and my mom and I realize we can not talk about emotions or anything serious in front of my dad. It exacerbates his irritable bowel syndrome. So trying to keep things light and entertaining, is exhausting. On my drive home, which was about 40 minutes, I turned the radio on. The host was talking about dogs in the first hour and to make a long story short, we all were engaged listening to this show. It took our minds off our troubles and made a 40 minute ride, seem like 15 minutes.
I am happy to say that we finally finished the 1,000 piece puzzle of California. It took us WEEKS! But we did not give up. Initially I bought puzzles for my dad, but he has no interest in them and the activity only produced frustration. So instead, my mom and I are enjoying the activity and we work independently on it in whatever free moments we have in any given day. Tomorrow we start a puzzle of the world!
Tonight's picture was taken in October of 2004. Mattie was two years old. Each October weekend, we would take Mattie to a different fall festival. This particular one had a petting zoo for the children. Mattie was getting a close encounter with a sheep, and his open hand and the fingers moving, was my tell tale sign that Mattie was fascinated and taking it all in.
Quote of the day: Our grief is as individual as our lives. ~ Dr. Elisabeth Kubler-Ross
It was another difficult day. This afternoon, I picked up my dad from his memory care center, and then we all went out to lunch. While driving, my mom started in on me. I hear commentary day in and day out, and negative feedback constantly. Truly, I can take just so much. I tried to redirect my mom and also asked her to stop her lament directed at me. She wouldn't stop. So literally while driving, I was screaming at the top of my lungs. I explained to her that all this tension and stress is going to make me physically ill. If I become ill, the whole house of cards comes crumbling down.
Honestly there are times all this stress gets to me and I just don't know how I will take it one more day, much less one more minute. After we got back from lunch, it was literally evening. Dining with my parents is close to a four hour experience. In any case, I got my dad settled, my mom went upstairs to change, and Sunny and I went for a walk. Sunny can't walk more than a few blocks now because of his cancer, but nonetheless, I know I need to get out of the house, get fresh air, and see greenery. This is my form of therapy, which helps me manage stress.
Tonight's picture was taken in October of 2006. Mattie was four years old and that day we took him to Butler's Orchard in Maryland. They had a wonderful Fall pumpkin festival. We visited this farm practically every fall and spring. Mattie absolutely loved taking a hay ride out to the pumpkin patch to pick his own pumpkins. His love for all things ORANGE happened early in life, and we loved our fall festival adventures with Mattie. Prior to having Mattie, I literally never went to a fall festival before, so with Mattie there were many firsts.
Quote of the day: Life is not the way it is supposed to be. It is the way it is. The way you cope with it is what makes the difference. ~ Virginia Satir
This morning, after getting my parents settled, I went to meet my friend, Denise for tea/coffee. We have been friends a very long time and we met each other in graduate school. Denise has been part of Mattie's cancer journey and during that time, I met her daughter, Marisa. Marisa was in high school at the time, but she volunteered to visit Mattie when he was home between treatment from the hospital. Marisa engaged and played with Mattie, so that Peter and I could get out of our home and regroup. This was a challenging task for an adult, much less for a teenager. But Marisa rose to the occasion each time. Once Mattie died, it was Marisa's idea to create a bake sale at our annual Walks. Marisa ran our bake sale for ten years, until our Walk turned virtual because of COVID.
Denise and her husband, Dave, attended our psychosocial think tanks at national conferences in 2012 and 2013 and Dave helped us manage our exhibit booths. I mention all of this because you can see their entire family has been a part of our lives. Denise is a successful mental health provider, and when I used to teach my graduate level classes, I always had Denise come and guest lecture in my classes. Today, however, I had the opportunity to experience Denise's therapeutic gifts first hand. No she wasn't giving me therapy (as we are friends) but it was the way she was listening and responding to my issues and concerns that made me have insight into her wonderful skills. It is not like our coffee solved my problems, but it was a glorious feeling to be heard, supported, and valued. In my daily life I am balancing one problem, one heartache, one compliant after the other. Truthfully there is so much one person can take before cracking.
Denise surprised me with a box of assorted teas and look at these handcrafted chocolates! I absolutely love the fall theme. When Mattie was fighting for his life in the hospital, Team Mattie brought me tea and chocolates practically daily. So to me, receiving these specific gifts ironically reminds me that I am a mom. Not just any mom, but Mattie's mom.
Don't you know it while Denise and I were sitting at Starbuck's, ABBA's Dancing Queen played. Mind you I go to this Starbuck's all the time with my mom and have never heard Dancing Queen played. So the fact that it played today was not by coincidence. It was another sign that Mattie is with me, he is watching over me, and reminds me I am never alone. Having amazing members of Team Mattie, like Denise, who are involved in my life is proof that the spirit of Mattie is alive and well.
Tonight's picture was taken in September of 2005. Mattie was three years old. Mattie absolutely loved spending time in our bed. In fact, in the morning, once he was old enough to walk, he would jump out of his bed, come down the hallway, and then go to my side of the bed. He would tug on me and sometimes I was too exhausted to move, so he'd jump on top of the bed, looking for hugs. In any case, in this photo, it was the evening and we were reading books together and if you look closely, there was a toy truck along with us. Mattie did not travel anywhere without a toy car, truck, or train in hand! It was a telltale Mattie sign.
Quote of the day: People touch our lives if only for a moment, And yet we're not the same from that moment on, The time is not important, The moment is forever. ~ Fern Bork
My lifetime friend, Karen, sent me an hysterical message today about cats traveling in backpacks. She presented this content to her high school students today, asking them to dialogue about how the CAT FEELS TRAVELING IN A BACKPACK! Not how we feel, but from the cat's point of view!
The question is zany enough to get teenagers engaged, animated, and dialoguing. I love questions like this because in the process you learn a lot about another person's point of view.
To be honest, I have NEVER seen a cat in a back pack. I had no idea it was a rage right now. My neighbors in Washington, DC used to walk their cat on a leash, which I thought was hysterical enough, but a back pack??? I clearly have never owned a cat that I think could be calm enough to go into such a pack! All I know is both Patches and Indie would fight like no tomorrow, before being placed in a bag. Which is why I always disliked taking either to the vet, because you have to capture the cats first and put them in a traveling cage/bag.
I told Karen, I would to hear about her students answers to her question! Better yet, I would like to know if they have put their own cats in a back pack and how it went!!!
When I received the mail today, I found a beautiful and heartfelt card, along with this loving sunflower bracelet. My friend, Jean, sent this to me, just because. Jean and her family have been a part of Mattie's cancer journey from the beginning and Jean knows the importance of the sunflower to me.
When friends send me sunflower things, what this ultimately says to me is that Mattie's story and legacy are alive not just within me, but within them too! What an incredible gift to receive, a reminder of Mattie's beautiful legacy!
Tuesday, October 3, 2023 -- Mattie died 731 weeks ago today.
Tonight's picture was taken in September of 2005. Mattie was three years old. That day we took Mattie to a farm to pick peaches. As you can see, Mattie was having a great time. He was our little Farmer Brown. I can't tell you how many peaches I brought home that day. I was making everything from jams, to pies, and muffins. It was our first and last time peach picking as a family, but it was a moment in time I will never forget.
Quote of the day: Those things that hurt instruct. ~ Benjamin Franklin
Starting on September 23, life in my home has become so challenging. I go through moments when I feel fine, stable, and I can manage things, to then the exact opposite. Where I feel like I am going to crash and burn. Literally and figuratively.
It has been another nightmare of a day and the one positive was going out to lunch with my parents. Mainly because where we go is like my restaurant version of Cheers (the TV show). Where everyone working there knows me. I can't tell you what a gift this is, as all the staff comes over, gives me updates about their life, their struggles, and they appreciate the support and connection. This gratefulness goes both ways, as I can't tell you how wonderful it is to have dialogue with people who do not have dementia. It is refreshing and for that moment in time, it makes me feel like I am alive, I matter, and I am valued.
Tonight's picture was taken in September of 2005. Mattie was three years old and that day we took Mattie to a park to walk and explore. However, Mattie loved picnics! So as you can see, I made sandwiches, brought drinks, treats and towels. In so many ways, these were much simpler times in my life, and the funny part is I had NO IDEA!
Quote of the day: The fact that something has happened to a million other people diminishes neither grief nor joy. ~ Author Unkown
This morning, after dropping my dad off at his memory care center, I drove to Washington, DC. It literally took me about 40 minutes to get there. I had a dentist appointment, and though I live in the suburbs, I still use all my doctors from when I lived in the city. To me this dentist office is state of the art, and I am not leaving it.
In any case, I left my mom at home, and I had about two hours to myself. Who knew that going to a dentist could be respite. The waiting area in the office, has a beautiful picture window, soft music, and this TV screen showing this autumn scene. It is actually quite the screen, because leaves move in the wind, pages in the book flip over, and therefore it is relaxing while animated. It helps to set the tone for the visit.
When my hygienist came out to get me, she gave me a big hug. She knows I am a caregiver to two people with dementia. Her dad had dementia, so she knows what I am up against. My parents are also her patients. When we got back into the room where she did my cleaning, she lowered the lights and put on "rat pack" music. As she knows I like listening to these golden oldies. In any case, we got to talking and we shared a lot of personal issues with each other. It was almost therapeutic, as we found we have even more in common than we knew. Needless to say, we both go to the dentist office for RESPITE. As I always say, caregivers of all kinds, are attracted to each other. We just immediately understand the one another.
Tonight's picture was taken in September of 2006. That week, Peter took Mattie to Boston to visit with his parents. He did this, so I could have the time to focus on studying for my licensure exam. I really needed that time to review material and get myself prepped for the exam in October. I am not a good test taker, so I truly appreciated having this uninterrupted time. While Peter was visiting with his parents, they received this BIG box! Naturally all cardboard boxes were considered very useable by Mattie. Together they constructed a playhouse and Mattie colored and painted it! The beauty of Mattie.
Quote of the day: We must know the pain of loss; because if we never knew it, we would have no compassion for others, and we would become monsters of self-regard, creatures of unalloyed self-interest. The terrible pain of loss teaches humility to our prideful kind, has the power to soften uncaring hearts, to make a better person of a good one. ~ Dean Koontz
The highlight of my day is I took my parents out to brunch. Our server, who we have gotten to know well, showered us with Fall gifts. Last year she gave me the cute rectangular sign that says.... Autumn Leaves and Pumpkins Please.
Today she gave me this pumpkin with sunflower plate! I think it goes with Mattie's Mr. Sun perfectly!
She also gave us this lovely battery powered Fall votive!
Lastly I received this pumpkin and sunflower towel! It is very special on a such an emotionally dark week to receive just because gifts!
With heavy hearts, we said goodbye to our precious Mattie when he died on September 8, 2009 at 7:15am. He fought death for five hours, and he finally fell into a deep sleep. My hunch is he did not want to say good-bye to us, and it took massive amounts of drugs to ease his suffering.
Mattie in Summary
Diagnosis timetable: July 23, 2008 - tumor in the right humerus; August 1, 2008 - tumor in the left humerus; August 6, 2008 - tumors in the right femur and left radius. On August 6, Mattie was officially diagnosed with Multifocal Synchronous Osteosarcoma. Tumor Resection and Limb salvage surgeries (repiphysis): on October 20, 2008 and November 12, 2008. Percentage of Necrosis: 60% in right humerus; 80% in left humerus; 100% in left radius; 2% in right femur. Chemo began on August 8, 2008: High Dose Methotrexate, Cisplatin, Doxorubicin; Ifosfamide, and Etoposide were added to the treatment protocol on December 1, 2008; MTP-PE was added to the treatment protocol on January 12, 2009. Chest CT scans post surgery:December 5, 2008 – four 3mm lung lesions; January 8, 2009 – CT scans reveal no change in the lung lesions; March 19, 2009 - CT scans reveal slight changes in two of the lesions. With potential increases in size of up to 1-2 mm per lesion. On June 5, 2009, CT scans at 1.5mm cuts (so very refined cuts) revealed that Mattie's lung lesions doubled in size since January. The four lesions are now 8-9mm in size, indicating that Chemotherapy is not working. Median Sternotomy: June 15th, 2009, removed 9 lesions, four in the left lung and five in the right lung. We do know that two of the lesions had calcified indicating bone material was present. This confirms that the bone cancer has metastasized to the lungs and that Mattie's chemotherapy was not effective at fighting the cancer in his lungs. PET Scan: There appears to be a possible variant (i.e something abnormal) in the lower left femur, but as of now it is too small to determine what it really is. Normally, one would biopsy this, but the location is difficult as it involves the growth plate, and with lung surgery imminent, and Mattie just being off of chemo, the advice we're getting is to wait and watch, and to see what it looks like during the next scan. Echocardiogram: Mattie has a reduced LVEF (Left Ventricle Ejection Fraction), which in layman terms means that his heart is not pumping with its normal level of pressure. Although it is not at a dangerous level, the doctors do want to monitor it with a follow-up echo in a few months to determine if this is a temporary impairment or if long term damage has been done.
Washington Post Article on my Work
An article was published on July 24, 2010, in the Washington Post's Metro section.
Many thanks to Post Reporter Rick Rojas, for covering a great story! To read the article on the Post's website, click HERE
Washington Post Article on Reach the Day and Mattie's Blog
In the July 2nd, 2009 edition of the Washington Post, our story and our blog were briefly mentioned in an article regarding CureSearch's Reach The Day event, held June 22-23, 2009 on Capitol Hill.
Click HERE for a link to read the article on the Washington Post's web site.
Mattie's Channel 9 Story
To watch the YouTube version of Mattie's video, click Mattie's News Story
or
to Read the actual story on the 9NewsNow site, click HERE
Mattie's Situation
Mattie Had Bone Cancer Mattie had a bone cancer called Osteosarcoma. The diagnosis was: multi-focal, synchronous osteosarcoma. He had four tumors in his extremities: the upper portions of the right and left Humerus, which is the bone that connects the shoulder to the two lower arm bones (the radius and ulna), the lower (distal) left radius (right near the wrist) and the lower (distal) right femur (just above the knee joint). Although commonly found in adults, this type of bone cancer is very, very rare when found in six year old children.
Mattie started chemotherapy on Thursday, August 7, 2008, consisting of several five week cycles containing five types of drugs (Doxorubicin, Cisplatin, high dose Methotrexate, Ifosfamide and Etopicide). After the second cycle Mattie underwent a surgery (Oct. 20) to remove the tumor in his right humerus, and then a second surgery (Nov. 12) to remove the other three tumors. Mattie had three prostheses (both arms and the leg) that use the Repiphysis technology. We also tried an experimental drug called L-MTP-PE in the effort to give Mattie the best fighting chance of survival. It's a shame it wasn't enough.
All of our Family and Friends have done so many wonderful and amazing things for us to help Mattie. For that we are forever grateful. We want you all to know that we cannot thank you enough for these things and your selfless acts of kindness. We cannot adequately express how much your love, caring and devoted attention to Mattie meant to us. God Bless each and every one of you.
We made a deal from the beginning with Mattie to never lie to him about his situation, and we talked him through each step of the way. Mattie knew he had "some bad bugs" in some of his bones, and he knew that the drugs he was given were to kill the bugs, and the surgeries were meant to remove the bugs from his body. Mattie even requested from Dr. Bob Henshaw (who performed the surgery) "to let me keep a bone" once the procedures were over. Mattie did get several pictures of the procedures which he always thought were really neat.
This kind of statement only furthered our immense respect and astonishment that we had for Mattie and his emotional intellect, intelligence, and maturity. It was amazing that a six year-old could so quickly rationalize and embrace a situation and keep such a strong and positive attitude going, when his parents were a pair of emotional and physical trainwrecks. The irony is that Mattie gave us our strength to go on at a time when we should have been giving him his strength to fight.
Mattie's life during the 13 months of fighting cancer was not a normal one, even though we did whatever was humanly possible to make it as normal as possible. Fortunately, we have good friends who helped us get to the right doctors and to the program at the Lombardi Center in what everyone says was record-breaking time, who embraced us and helped us with what was unquestionably the greatest challenge of our lives. Of course, without our family and good friends, life would be a whole lot tougher than it is right now, so for those of you who are reading this, all we can say is Thank You and We Love You. God Bless.