Mattie Miracle Walk 2023 was a $131,249 success!

Mattie Miracle Cancer Foundation Promotional Video

Thank you for keeping Mattie's memory alive!

Dear Mattie Blog Readers,

It means a great deal to us that you take the time to write to us and to share your thoughts, feelings, and reflections on Mattie's battle and death. Your messages are very meaningful to us and help support us through very challenging times. To you we are 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 stop writing on September 9, 2010. However, at the moment, I feel like our journey with grief 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 us, and most importantly thank you for keeping Mattie's memory alive.


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



The Mattie Miracle Cancer Foundation celebrates its 7th anniversary!

The Mattie Miracle Cancer Foundation was created in the honor of Mattie.

We are a 501(c)(3) Public Charity. We are dedicated to increasing childhood cancer awareness, education, advocacy, research and psychosocial support services to children, their families and medical personnel. Children and their families will be supported throughout the cancer treatment journey, to ensure access to quality psychosocial and mental health care, and to enable children to cope with cancer so they can lead happy and productive lives. Please visit the website at: www.mattiemiracle.com and take some time to explore the site.

We have only gotten this far because of people like yourself, who have supported us through thick and thin. So thank you for your continued support and caring, and remember:

.... Let's Make the Miracle Happen and Stomp Out Childhood Cancer!

A Remembrance Video of Mattie

September 11, 2021

Saturday, September 11, 2021

Saturday, September 11, 2021

Tonight's picture was taken on April 9, 2002, five days after Mattie was born. In fact, that may have been Mattie's first day home from the hospital, since we were both hospitalized for five days after he was born. Between his emergency c-section and the fact that they removed a big lipoma from my bladder, I was physically a mess. From all the IV fluids they gave me, I was swollen. My legs were three times their usual size and everything below my waist wasn't functioning very well. Thankfully Peter stayed at the hospital with us to help care for Mattie and me. What I recall vividly was that NO hospital staff or personnel were there to truly care for me or Mattie. 


Quote of the day: Today's coronavirus update from Johns Hopkins.

  • Number of people diagnosed with the virus: 40,920,922
  • Number of people who died from the virus: 659,691


A day never to be forgotten! It is hard to believe that 20 years ago our country was attacked in such a traumatic and deeply disturbing manner. For most of us who were alive on September 11, 2001, we shall never forget the horrific visions we saw on TV, the stories that unfolded, and the level of fear and insecurity that engulfed our lives of months and years there after. For families who lost a loved one in these terrorist attacks, their lives were forever changed.

Though The lights, which were first installed as a month long tribute six months after the attacks, then lit up the sky on the second anniversary of September 11. They have been used as a tribute each year on the anniversary since 2003.




11 Facts that should never be forgotten:

  1. On September 11, 2001, nearly 3,000 people were killed, 400 were police officers and firefighters, in the terrorist attacks at the World Trade Center in NYC, at the Pentagon building in Washington, D.C., and in a plane crash near Shanksville, PA.
  2. 9/11 was not the first terrorist attack on the World Trade Center. A bombing in February of 1993 killed six people.
  3. On any given workday, up to 50,000 employees worked in the WTC twin towers, and an additional 40,000 passed through the complex.
  4. After the September 11th attacks on the World Trade Center, the rescue and recovery clean-up of the 1.8 million tons of wreckage from the WTC site took 9 months.
  5. Passengers aboard United Flight 93, heard about the previous airplane attacks and attempted to retake control of the plane from hijackers. As a result, the hijackers deliberately crashed the plane in a Pennsylvania field instead of at their unknown target.
  6. While video accounts of the WTC attack aired immediately, no video footage of the Pentagon attack was publicly released until 2006.
  7. Though both the police and fire departments of New York City had their own emergency response procedures, the two departments did not have a coordinated response plan to a major incident.
  8. The attack on the World Trade Center on 9/11 resulted in the largest loss of life by a foreign attack on American soil.
  9. 18 people were rescued alive from the rubble of the World Trade Center site.
  10. Cases of post-traumatic stress are common among 9/11 survivors and rescue workers. Respiratory problems, like asthma and lung inflammation, also developed at abnormal rates for those in and around the World Trade Center during and after the attacks.
  11. In 2019, the US Senate passed a bill ensuring that a fund to compensate victims of the September 11th attacks never runs out of money — and that first responders won't have to return to Congress to plead for more funding.


This is a video tribute to September 11. It has been classified as disturbing. However, the disturbing part is what it depicts actually happened and people's lives were lost and those who remain behind will never be the same. 

We have not forgotten!

September 10, 2021

Friday, September 10, 2021

Friday, September 10, 2021

Tonight's picture was taken in July of 2002. Mattie was three months old and that day we went over to visit Peter's brother, sister in law, and our nephews and niece. They all got a kick out of Mattie! Mattie loved taking in his world and absorbing everything around him.



Quote of the day: Today's coronavirus update from Johns Hopkins

  • Number of people diagnosed with the virus: 40,748,119
  • Number of people who died from the virus: 656,412


In 2003, I began my service on the DC Board of Professional Counseling. A licensing board is a government-regulated agency that sets the standards for the minimum qualifications needed to practice in a specific profession. In addition to writing and revising laws, the board also enforces them, so over the course of my 18 years of service I presided over countless ethical violation hearings. Some of these hearings went for 6-8 hours long, almost like a trial with a defense attorney, our government attorney, witnesses and so forth. I remember the first hearing I presided over, I was a nervous wreck. Of course with more familiarity and comfort working with the board's attorney, it got easier. Easier in terms of the mechanics of the hearing, never easier in terms of the issues and the dynamics among people in attendance. But understand that a board has the power to revoke a license, so overall it is a big responsibility. 

Since I have served in this role for 18 years, I know the history, how we have evolved, I know many of the public members who show up for the open sessions each month, and I bring to the table a vast experience working in an university training program for counselors as well as having many national leadership roles. In any case, today was the LAST board meeting I will ever attend. The Mayor selects board chairs and since I no longer live in the District of Columbia, I was in essence asked to step down. It is never easy leaving something that you like doing, that you find stimulating and rewarding, and respect the people you are serving with. The virtual meeting was four hours today and throughout the meeting, I heard many lovely comments and reflections on my service. In fact, one person who I serve with was crying that I was leaving. 

So for me it has been one thing after the other...... from packing our home in DC, donating items, going through Mattie's things again, moving to a house, dealing with the countless number of issues, repairs, workmen, the Thrivent contest last night, and today's board meeting. There is never a break, down time, time to relax and recharge, and of course today when I went out (after being cooped up for days at home) to go grocery shopping, the car had an issue. It was literally making a terrible grinding sound while I was driving it. I took my chances going shopping, but moved at a snail's pace because I was worried about the car. 

Peter returned home safely tonight from business travel for two days. He examined the car and found when it was serviced, and the catalytic converter was replaced, the dealership did not put back two bolts under the car. So another thing to have to do. I need a change of routine or a reality check. Worn out, exhausted, with no end in sight. 

September 9, 2021

Thursday, September 9, 2021

Thursday, September 9, 2021

Tonight's picture was taken in April of 2002. Mattie was a few weeks old and I snapped this photo because I was fascinated at watching him try to focus on this play toy in front of him. Look at those eyes! They seem to be telling us quite a story. 



Quote of the day: Today's coronavirus update from Johns Hopkins.

  • Number of people diagnosed with the virus: 40,480,607
  • Number of people who died from the virus: 652,993

THANK YOU TO ALL OUR SUPPORTERS WHO TUNED IN TONIGHT, WATCHED THE SHOW and VOTED FOR US!!! You make a difference in our lives. 


Mattie Miracle won second prize tonight, $7,500! We are so grateful to ALL our amazing supporters and the incredible chat messages you left me. I tried to photograph many of them after I presented. 


Here is the exciting new though, Daymond John, of shark tank said my presentation was the "perfect pitch." Peter captured some of what I said on video, as well as Daymond's comments. It is Daymond's comment that made me feel like I served Mattie proud tonight. Check out this video, click on the photos below.




Some of my comments caught on video:






Click on the photo to read some of the comments!
Click on the photo to read some of the comments!
Click on the photo to read some of the comments!
A supporter snapped a photo of her ballot!
Click on the photo to read some of the comments!
Click on the photo to read some of the comments!
Click on the photo to read some of the comments!
Click on the photo to read some of the comments!
Click on the photo to read some of the comments!













What I said tonight, or at least tried to in FOUR MINUTES:

Good evening and thank you for the wonderful introduction. As you just heard, I am Victoria Sardi-Brown and I am the co-founder and president of the Mattie Miracle Cancer Foundation, which is based in Arlington, VA. Mattie Miracle is honored to be selected as a Thrivent finalist, to share this virtual stage with four other amazing non-profits, and to have the opportunity to interact with the Thrivent network and Daymond John. 

On July 23, 2008, my life changed forever. On that day, I heard the four words NO PARENT ever wants or hopes to hear, and they are…. YOUR CHILD HAS CANCER. My son Mattie was only six years old when he was diagnosed with a rare form of bone cancer. After 14 months of aggressive treatments and surgeries, Mattie died in my arms on September 8, 2009. Yesterday was the 12th anniversary of his death. 

As you can imagine, after we lost our only child to cancer, we were devastated, lost, and hopeless. Yet Mattie’s death had to serve some sort of purpose. So, two months after he died, my husband and I created the Mattie Miracle Cancer Foundation. Mattie taught us two things that guide the work of the Foundation: 1) childhood cancer is a family disease and 2) childhood cancer is not just about the medicine. 

There are 16,000 children diagnosed every year with cancer. September is childhood cancer awareness month, and I am sure you have heard about the need for better cures and funding for medical research. However, what isn’t always highlighted, but is equally as important, are the devastating long term psychological, social, and emotional issues, that result from the medical treatment for both the child and the entire family. In fact, 60% of children with cancer are reported to have a diagnosable mental health issue because of treatment. Psychosocial support, provided to children and their families, has been shown to manage symptoms, alleviate pain and fatigue, and increase quality of life, but it is well documented that this support isn’t always adequately provided to address the concerns of patients, siblings, and parents. 

Mattie Miracle is the only national non-profit dedicated to psychosocial awareness, advocacy, support, and research of childhood cancer. To date we have raised $1M to support the cause. Annually, Mattie Miracle provides direct support to 1,500 children with cancer and 2,500 families, through our endowed child life programs, M&M family grants, and hospital snack and item carts. In addition to delivering locally based support, the Foundation had the vision and funded a three year long international project, with the help of an amazing team of health care professionals, to develop the very first evidence based Psychosocial Standards of Care. It is thanks to our advocacy that these Standards exist. The Standards are historic and were published in 2015, in a top tier medical journal. These Standards are designed to ensure that children with cancer and their families have access to optimal psychosocial care throughout their cancer journey at every treatment site in the country. 

Mattie Miracle is passionate about ensuring that psychosocial care is part of comprehensive cancer care and if we should win the $10,000 grand prize, this will enable us to start a new initiative, a psychosocial referral and resource program. This program would enable us to connect families coping with childhood cancer to qualified mental health providers in the Northern Virginia community and pay up to six therapy sessions per family. Such an initiative is vital because of four reasons:

  1. It doesn’t exist today. Hospitals treat only patients, all be it inconsistently, but that is insufficient as siblings, parents, and the entire family are all affected by a childhood cancer diagnosis. They have real mental health needs that arise, which many times go unaddressed. 
  2. Insurance coverage is all over the map or does not even include behavioral health coverage. 
  3. The mental health care and expertise for this population needs to be very tailored to address their unique needs and concerns and not every provider has experience working with this population. 
  4. Since there is no recognized referral and resource program currently available, families expend energy that they do not have trying to find mental health support and typically pay out of pocket to receive it. But this adds to the financial hardship families face during cancer treatment, and research shows that financial hardship impacts mental health and well-being of the family. 

So, in summary, even if we had an 100% medical cure rate for childhood cancer there would still be devastating long-term psychosocial issues for children and their families that AS OF TODAY go under or unaddressed. Mattie Miracle believes that our children deserve better, they are our future, and as Margaret Mead always said, never doubt that a small group of thoughtful, committed citizens (like yourselves) can change the world; indeed, it's the only thing that ever has. Thank you for tuning in tonight, please vote for Mattie Miracle, and help us address these important psychosocial needs of children with cancer and their families. 

September 8, 2021

Wednesday September 8, 2021

Wednesday, September 8, 2021 -- 12th anniversary of Mattie's death

Tonight's picture is the quintessential photo of Mattie! I remember taking this photo in the pumpkin field of Butler's Orchard in Maryland. Mattie loved going on their hayrides, out to the patch, to pick out his own pumpkin. It was a family tradition, and now I use this photo in many of our Mattie Miracle promotional material. 


Quote of the day: Today's coronavirus update from Johns Hopkins

  • Number of people diagnosed with the virus: 40,412,799
  • Number of people who died from the virus: 652,175


It is not too late to register for Take the Plunge! We need all our supporters and friends to sign up, watch the hour long event (tomorrow, September 9, 8-9pmEDT), and VOTE for Mattie Miracle. The more people who vote for us, the more likely we will win $10,000!

Register @

I started the day off with a prep call for the Take the Plunge Challenge tomorrow. I learned that 500 people in total have registered for the event so far. All five non-profits are working hard to get as many supporters watching and voting as possible. They tell us to have fun, but to me it is more nerve racking than anything else. No matter how I have tried, I can't get our message out in 4 minutes. 

Of course, Peter and I know all too well that today is the 12th anniversary of Mattie's death. Perhaps this Take the Plunge challenge is meant to be the day after Mattie's anniversary, I don't know! In any case, what I do know is that a day doesn't go by when we are not aware of our loss. Our loss defines us and the work that we do. It even influences how I decorate our home. That was true in DC, as it appears to be true in the house. Butterflies, sunflowers, Mattie Miracle colors, and of course Mattie art!

On every anniversary, I re-post the letter I wrote to Mattie for his celebration of life ceremony in 2019. The sentiments then are as meaningful and timely today.

---------------------------------------------

My Dearest Mattie,

It is said that parents love their children right from the moment they are born. However, in your case, our love for you began as soon as we learned we were going to have a baby. In fact, right after seeing your sonogram picture, we felt like proud parents. We posted those pictures everywhere. We shared these pictures with practically anyone who would listen or showed interest, and each September when I taught prenatal development in my undergraduate human development class, out would come your sonogram pictures to illustrate my points. Even my students got a sneak peek at our baby, a baby who would have a profound and meaningful impact on not just his parents but also every community he touched. Daddy and I did not only love you, we FELL IN LOVE with you, and that love grew stronger with each day. Your energy, spirit, love for life, intellectual challenges, sense of humor, and loyalty to your friends and family were only some of the wonderful traits we always admired in you.

This video is a tribute to you and your wonderful, yet short life. It seems fitting as we celebrate you, and say good-bye to your physical presence that I share the story about how you entered the world. The story of your birth had to be one of your most favorite stories to hear, and I found during times when you were reflective, overly tired, or in need of hugs and tenderness, the request for this story arose. In fact, I remember on August 5th, the day we found out that your cancer metastasized everywhere, you and I were sitting in the hospital’s rose garden, and you requested the story. It was almost as if you knew this was going to be a bad day, so in essence we might as well brace ourselves, cuddle, and prepare for this together.

Here is the story I always shared with you. A story Daddy and I will never forget. On April 2, 2002, at 11pm, I decided to head to bed. I was anxiously awaiting your birth, and as your due date approached, I couldn’t help but wonder, when will “the baby” be coming? I was restless and uncomfortable, so while in bed, I began to watch television. I was having trouble concentrating on what I was hearing, mainly because you were kicking up a storm inside of me. At which point, the kicking became so intense, that I literally felt something pop. You clearly wanted OUT, and you were going to kick your way into the world on your terms. Naturally after feeling this pop, I looked down at my tummy, and when I jumped out of bed, I realized my water had broken. This only happens to 25% of moms, and in retrospect, I should have guessed that this was just the beginning of how different our lives were going to be together. I immediately called the doctor and told her what happened. She asked if I was in pain, which I wasn’t, and she instead told me to get a good night’s rest, because my baby was going to be born the following day. Well I can assure you after hearing this news, sleeping was the farthest thing from our minds.

So on April 3, 2002, Daddy and I headed to the hospital and we were admitted to the maternity unit at 8am. The labor process began, but it was a VERY slow process for me, and at times as you moved inside my tummy, Daddy could see your head pushing against my backbone. Needless to say Dr. Mike, the anesthesiologist, became my favorite doctor that day. The hours kept rolling by, and still there was NO sign of our baby! I was getting weaker, I developed an 102 fever, and by 11pm I really had no energy to give birth to you. In addition, to how I was feeling, your oxygen supply was getting cut off, and your chin was positioned in such a way that would make the birthing process almost impossible. So it was at that point that the doctor recommended an emergency c-section. Things began to happen very quickly around me. I was signing paperwork for surgery and Daddy was being transformed by putting on a bunny suit so he could enter the operating room.

I had never been in an operating room before in my life, but I really wasn’t concerned at that point about myself. I was solely focused upon you. I was wide-awake for the c-section, but unable to see the process, which as you know, was probably a good thing. Daddy on the other hand found the whole thing very exciting, and began to videotape and take pictures of the surgery. Literally a team of people surrounded me and I will never forget Dr. Mike, the anesthesiologist who sat by my side, and talked with me and did whatever he could to keep me pain free.

When you have a c-section, your arms are strapped to the operating table, so I couldn’t move, and directly over my head was what appeared to be a rope with a clamp that was holding open my abdominal cavity. Normally by this point I would have passed out, but when it came to you, I developed strength I never knew I had. As the doctor began cutting, and finally got to you, the first thing she said was, “what is this?” That is NOT what you typically hope to hear when having a c-section. The doctor let me know that I had a grapefruit sized tumor on my bladder, and my immediate thought was, did this affect the baby? The next thing I knew, I felt her tugging, and I heard the loudest cry ever. Now here is the part of the story that I know was always your FAVORITE! I would always try to replicate the sound I heard coming from you that day, a sound that will always remain in a parent’s ear. It was a very large WAAHHH! WAAHHH! At which point the doctor told us two things: first, that you were one of the most beautiful babies she had ever seen, and second, that you had quite a set of lungs on you! I concurred with both statements.

The doctor then brought you over to me, and she felt that I needed to be the first person to touch you. So despite my arms strapped to the table, my right hand miraculously reached out and grabbed your tiny, soft, and cute foot. It was a moment I will always cherish, a moment in which I will never forget, and a moment I am so happy you too enjoyed hearing about. Each time I retold the story I felt as if it further bonded us together, and I always enjoyed hearing your comments, thoughts, and reactions to your story.

Seeing you made Daddy very happy! Though he was worried about me, since after the c-section, I had to have bladder surgery to remove the tumor, we both agreed that Daddy should stay with you and accompany you to the nursery. It is there that Daddy got to see you cleaned up, he learned that you weighed 6 pounds and 13 ounces, and that you had high Apgar scores of 8 and 9. Within an instant, Daddy became one of your fiercest protectors, and he cared for you for five days straight while we were in the hospital together. In fact, Daddy is the first person who changed your diaper, and though those were five very challenging days in the hospital, they were days that helped us form our strong family ties. Ties that were imperative and that we relied on for seven years of your life!

Your presence is so greatly missed. Nothing seems the same, is the same, looks, feels, or tastes the same without you in our lives. May you always know that Mommy and Daddy love you, cherish you, and that feeling will remain with us forever and always. Good-bye my Mooshi Moo angel and goodbye Daddy’s best buddy. With love from Una Moon and Daddy!

September 7, 2021

Tuesday, September 7, 2021

Tuesday, September 7, 2021 -- Mattie died 623 weeks ago today. 

Tonight's picture was taken in October of 2006. Mattie was four years old. Every fall weekend, we would take Mattie to a different Fall Festival. He loved them, particularly the pumpkin picking and the large slides. This happens to be one of my favorite photos that Peter took of us. In fact, it is framed and in my office. 


Quote of the day: Today's coronavirus update from Johns Hopkins.

  • Number of people diagnosed with the virus: 40,238,083
  • Number of people who died from the virus: 650,345


Are you ready to help us TAKE THE PLUNGE on September 9th? Register, Watch, and Vote.... It's that easy!

This link is to our e-communication that went out to all supporters this morning:

https://conta.cc/3zOFlEJ


Tomorrow marks the 12th anniversary of Mattie's death. It is hard to believe that Mattie has been gone longer than he was alive and part of our lives. This will be the first anniversary that Peter and I haven't been together. In the past, I had typically did the same things every September 8th.... I went to the hospital to visit his brick, I went to the church were Mattie's funeral was held, and visit the memorial brick his friends placed in the church's garden. 

This year, I am distracted and worn out from both the house and mentally preparing for this contest on September 9th. Any time I have to speak about Mattie, I get very worked up about it. In my mind, I have to get it right, I have to say the most meaningful thing possible, and yet in four minutes, it is hard to accomplish this. So I have to parse out my words and be succinct to get the message and need across to the audience. For me this is a challenge!

In any case, in the midst of my own internal stress, I have stress all around me today. I had the plumber for three hours and the electricians started at 10am and it is after 6pm, and they are STILL here. With power going on and off! It is a total show. If that wasn't bad enough, my neighbor, who is the street town crier walked up the driveway to find out what was going on at our house. He literally spoke to my electricians and helped himself to my backyard. I talked to him for 45 minutes, but WOW, how I kept it together was beyond me. 

For all of you who have registered for September 9th's event and are there to virtually support Mattie Miracle.... THANK YOU! 

September 6, 2021

Monday, September 6, 2021

Monday, September 6, 2021

Tonight's picture was taken in September of 2007. Mattie was five years old and that weekend, I joined the boys in a rowboat on the Potomac River. Mattie actually wanted me to come along to see what he was learning. Mattie loved being on the water and Peter was teaching Mattie the art of fishing.



Quote of the day: Today's coronavirus update from Johns Hopkins.

  • Number of people diagnosed with the virus: 40,007,253
  • Number of people who died from the virus: 648,957


Help us win $10,000 on September 9th (8-9pmEDT)! We have been selected to participate in Thrivent's Take the Plunge Challenge. It is easy.... just register, watch the hour long Zoom event (where you will hear us and four other non-profits present) and VOTE for Mattie Miracle. The non-profit with the most votes wins $10,000! These funds will help us start a psychosocial referral and resource program to support children with cancer and their families.




It was another busy day on the Farm. We are still unpacking and organizing. I know Peter feels great pressure as he is going on travel this week and wants to get some things done on the house before leaving. I decided to stop what I was doing today and take a walk with Sunny. I know how much Sunny loves his walks, even though he has free range of the backyard. Dogs apparently bond with their pet parents through walks, and because we have been so busy, our walks have been sporadic at best.

After we walked, I came back to the house and finished reassembling my desk area. Not only do I have to capture the essence of the Foundation in this on-line contest in four minutes, I need a space for my video background that represents the Foundation and doesn't look like I just moved in. Multiple challenges for sure. In any case, after organizing, I sat down at my desk for several hours composing what I wish to say on Thursday for the Take the Plunge challenge. It is hard to say it all in four minutes, plus describe a new initiative we wish to fund. Now that I have the words on paper, and for the next several days, I will work hard to become one with these words so that they flow naturally out of my mouth!

September 5, 2021

Sunday, September 5, 2021

Sunday, September 5, 2021

Tonight's picture was taken in April of 2002. Only days after Mattie was born. At that point, I think Mattie looked much more like Peter. His eyes were blue (like all babies) and his hair was much blonder as a baby. The one thing we learned about Mattie early on was that he was born ON. Sleep did not come naturally to him, and it took us months to teach him how to do it!


Quote of the day: Today's coronavirus update from Johns Hopkins

  • Number of people diagnosed with the virus: 39,936,101
  • Number of people who died from the virus:  648,436


We thank Thrivent for selecting Mattie Miracle to Take The Plunge on September 9th. We need the support of our Foundation friends. It is free and easy! Please register for the LIVE Zoom event held on September 9th from 8-9pmEDT. You will hear five short non-profit presentations and then you will VOTE on the spot. Your VOTE determines the winner as the non-profit with the most votes wins $10,000. We want to create a psychosocial referral and resource program to help families coping with childhood cancer find the mental health resources they need in the community. We will match families to providers and pay for up to six therapy sessions. 

Register Today @ bit.ly/TakeThePlunge-MMCF 


Another non-stop work day. I may be unpacking for weeks. The problem is I don't know where to put things. As strange at it sounds, I loved the closets in our townhouse. Here, I have no idea where to put Foundation items, memorabilia, and office supplies. I have even told Peter that we have to build out the closets and even create a new closet space altogether. For now, lots of things will remain in organized piles in the basement, until they have a home. Thankfully the basement is dry and in good shape. That is only because we worked for hours to remove every drop of water from the storms of Hurricane Ida. However, what I haven't reported is that half of the house continues to have electrical issues. The outlets aren't working. For now, we have extension chords from outlets that do work, to areas of the house in which we need electricity. It is a true show here. The electrician team (and we need a team here!) are coming back on Tuesday to figure this out!

Given that Peter is traveling on Mattie's anniversary, we went to visit is memorial tree today. Some of you may recall that we planted four trees at Mattie's school in his memory. The intention was to have ONLY one tree, but the first one planted in 2010 died altogether and then trees 2-3, had issues. So this is memorial tree #4, it is a very healthy white swamp oak. We put ribbons around the trees today and hung heart shaped ornaments for Mattie. 
A close up of some of the ornaments on the tree. 
Lots of butterfly ornaments!
The tree was filled with ladybugs today! I viewed that as a meaningful sign!
The acorns on the tree are beautiful! Their caps are much bigger than your typical oak, they are fringe like.  
This is memorial tree #3, a yellow wood tree. It stands not far from tree #4. This tree got hit in a storm and literally looked cut in two. Over time it has repaired itself. 
This is memorial tree #2, also a yellow wood tree. It stands on the site where the first oak tree was planted in 2010. I call this tree Charlie Brown, as it always looks somewhat fragile and about to fall apart. Nonetheless, I put ribbons on all of Mattie's trees, and I refer to this area on the lower school playground as Mattie's grove. 
Though tree #4 was planted in 2018, the original plaque from the tree planted in 2010, stands besides the new tree.