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

February 21, 2025

Friday, February 21, 2025

Friday, February 21, 2025

Tonight's picture was taken in January of 2006. That day I visited Mattie's preschool class with homemade gingerbread houses. The children got to use royal icing to attach candies onto the houses. This activity was very well received by all the children. So much so, that other classrooms came into Mattie's room to participate in decorating the houses. Pictured with me was of course Mattie, his best buddy Zachary and his friend Nancy. Zachary and Mattie were inseparable, starting on day one of preschool. I got to know Zachary so well, that he was almost like a second child to me. When Mattie was diagnosed with cancer, that did not stop their special bond. Instead, Zachary learned to accommodate to Mattie's needs and they found a new way forward. I learned a lot from these two friends. 


Quote of the day: There are only four kinds of people in the world: those who have been caregivers, those who are currently caregivers, those who will be caregivers and those who will need caregivers. ~ Rosalynn Carter


Today is National Caregivers Day, a time to recognize and honor caregivers and the important work that we do! The Providers Association for Home Health & Hospice Agencies, PAHHHA, established the third Friday in February as National Caregivers Day in 2015. They aimed to dedicate a day annually to recognize and appreciate caregivers everywhere. The first celebration of the holiday took place in 2016. 

If you know a family member or friend who provides care to a loved one, THANK them today! I would say that family caregivers are the unsung heroes in our world. We do tasks around the clock, without payment and without positive feedback. 

AARP put together this two minute video highlighting all that family caregivers do in any given day! I found it moving. 


To learn more about caregiving, check out: Caregiving in the U.S. 2020 - AARP Research Report). Some caregiving facts.....................

  • One in five Americans (21.3 percent) are caregivers, having provided care to an adult or child with special needs at some time in the past 12 months. This totals an estimated 53.0 million adults in the United States, up from the estimated 43.5 million caregivers in 2015.
  • 1 in 3 caregivers of someone age 65 or older reports the presence of Alzheimer's or dementia.
  • When a caregiver provides care to someone with a memory problem, they are more likely to help with getting in and out of beds and chairs, getting dressed, getting to and from the toilet, bathing or showering, feeding, dealing with incontinence, tasks more frequently rated "difficult" when caring for someone with memory loss.
  • Nearly one in five (19%) are providing unpaid care to an adult with health or functional needs.
  • More Americans (24%) are caring for more than one person up from 18% in 2015.
  • More family caregivers (26%) have difficulty coordinating care up from 19% in 2015.
  • More Americans (26%) are caring for someone with Alzheimer’s disease or dementia up from 22% in 2015.
  • More Americans (23%) say caregiving has made their own health worse up from 17% in 2015.

These four graphics from the AARP report caught my attention. I go about my everyday tasks and most of the time, I am not absorbing just what a face alone on any given day. Maybe because this isn't my only trauma and heartache I face. However, this bar graph shows me at the high end of caregiving, with over 41+ hours weekly! The average caregiver works (without pay) for about 23 hours a week, helping a loved one. 

Family caregivers (which are family members providing care) on average help a loved one with 1.7 activity of daily living tasks listed here. I do all six tasks daily! All for my dad and some for my mom.
With regards to instrumental activities of daily living, I manage ALL 7 for both parents. 
Given the hours I provide care and the intensity of tasks, I fall in the high intensity group of caregivers. 



This graphic is truly interesting and yet NOT surprising to me. When family caregivers are asked how many have outside support, only 31% report to have such help. The remaining 69% are like me. 


Caregiving is NOT a new role for me. I come from a long line of caregivers and I believe I learned the art from my maternal grandmother! I have a dear cousin who has devoted her life to being a caregiver and therefore if you think there is a genetic component to being a caregiver.... perhaps that is true! Caregiving is in my blood. If I see a person in need, my immediate reaction is to HELP! I have been like this since I was a kid! In high school, I never left school on time. Why? Because I was sitting and listening to friends and acquaintances. From an early age, people naturally felt comfortable talking to me. I take that as a high compliment and I can't think of a better role in life than helping other people. You never know what a smile or kind word can do to a person struggling or having a bad day. 

Is caregiving difficult? 100% YES! It requires putting your own needs, desires, and freedom on hold. When Mattie had cancer, I can't tell you how many people recommended that I take a break. That I care for myself and get rest! I did not listen! I did not want to live with any regrets. Mattie was my number one priority and I will always be at peace knowing that I made that choice. Once Mattie died, did I get sick? ABSOLUTELY! I was worn out, fragile, and constantly ill for months, if not years. So I am well aware of the toxic level of stress I am dealing with from both caregiving and the dissolution of my marriage. All I can say is I am cognizant of it and take it one day at a time. 

To all my fellow caregivers, my hat is off to you. I admire you greatly and may you always know the incredible difference you are making in the lives of those in your care.  

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