Mattie Miracle 15th Anniversary Video

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

April 7, 2020

Tuesday, April 6, 2020

Tuesday, April 6, 2020 -- Mattie died 549 weeks ago today.

Tonight's picture was taken in April of 2007. Mattie's fifth birthday party was held at the National Zoo. It was quite the day with intense rain. I really thought Mattie's party was going to be a disaster. But it turned out as a real adventure. The kids loved touring the zoo in the rain and every animal was out and about for the kids to enjoy. In fact, given the torrential rain, I would say that we had the zoo to ourselves that day. It made for a very special and memorable day. 

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

  • number of people diagnosed with the virus: 387,547
  • number of people who have died from the virus: 12,291



Peter dropped Sunny off at the surgical center this morning at 7:30am. It is now 7pm, and poor Sunny just got into the operating room. He has been waiting ALL DAY, given the number of emergencies that came into the center today. Under normal circumstances, I would be livid. But given that we are dealing with the virus, most surgical centers closed down, and multiple dog fight victims that came in, we really have no other choice but to be patient. Sunny absolutely needs this surgery and we are lucky that this orthopedic surgeon is willing to fit Sunny into her schedule. 

This morning I received an email from Adina, our child life specialist at Children's Hospital at Sinai (Baltimore, MD). She wanted to share a few photos and to also let me know that our ipad wheeled stands arrived. Not only have they arrived but they are already making a difference at the Hospital during the pandemic. 

Adina shared this story with me, and I think it truly illustrates how vital her role is and the incredible difference she is making in the lives of children with cancer and their families..................................................

When a mom came to the emergency department over the weekend because she was experiencing COVID-19 symptoms, she did not anticipate the turn of events that would separate her from her children.


She was admitted for respiratory support and her three children remained in the Pediatric Emergency Department over the weekend until a plan could be made for where they would go while their mother was being treated. When they were ultimately moved to the Pediatric inpatient unit, the child life team arranged comfort items in their room, including a variety of snacks and treats from the Mattie Miracle Snack & Item Cart.


Thankfully, their mother is doing better. Utilizing the iPad stands from the Mattie Miracle Cancer Foundation that just arrived today (and were ordered just last week), the child life team was able to coordinate for the children a video chat with their mother and they were reassured to see she was doing better. The iPad was wheeled into their room so Adina could introduce herself and child life services via the iPad and explain how they could use the iPad to video chat with their mother on the other side of the hospital.


The collaboration to normalize the hospital for these children was the combined effort of child life, nursing, doctors, and social work- the multidisciplinary team uniting during these difficult times.







Many times children and families get admitted to the hospital and do not have an ipad or laptop with them. This is a problem, because without these devices it gets harder to remain in communication with family and friends. The hospital has access to ipads, and they allow families to borrow them. But now with the wheeled stands, it is easier to bring these devices into patient rooms and secure the ipads so that they do not get misplaced or taken off campus. Now ipads can remain in patient rooms and when not in use, they can be cleaned and directed to another patient room in need of this technology. We know more than ever how crucial the internet and technology are during this pandemic. These devices keep us connected and sane. 

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