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

July 9, 2011

Saturday, July 9, 2011

Saturday, July 9, 2011

Tonight's picture was taken in June of 2007. Mattie was holding one of the jars we used each spring to place his tent moth caterpillars in. In this particular picture, you can see that the caterpillar had spun a cocoon and Mattie was awaiting for the miraculous transformation of it into a moth. I can't help but reflect on all the moths we released over the years on our deck, and I always wonder if the moths that visit us now are related to one of Mattie's. Even if they are not, I would like to imagine that they are. That something Mattie helped to feed and nurture is flying over us.

Quote of the day: We must not, in trying to think about how we can make a big difference, ignore the small daily differences we can make which, over time, add up to big differences that we often cannot foresee. ~ Marion Wright Edelman

I find this quote very powerful, because in all reality it is the small differences we make each day that have a very meaningful impact on us and others. Small differences like listening to someone's feelings and thoughts, and even sharing a smile. I have noticed lately, more than ever, that when I smile at someone it is very hard for them NOT to smile back. Even a complete stranger.

Peter and I worked together to get him ready and packed for his trip tonight to Nigeria. He flew to Frankfurt first, which is an 8 hour flight, and then from Frankfurt he flies to Nigeria, which is another 6 hour flight. With a three hour lay over in between. He is well on his way to Frankfurt now. 
I took two pictures of Patches today which capture her feelings about Peter leaving. This picture shows her calm and relaxed on our deck. She was out there with us while we were having lunch. This is the last of the calm and happy cat I will see until Peter returns!
As Peter was packing, the anxiety started! Patches jumped on Peter's luggage and if she could have prevented him from leaving, I think she really would have!
This evening I met up with Ann and her family and we visited Mary, her mom. Mary loved seeing all her grandchildren and hearing about their upcoming vacation plans. After the visit, I had dinner with Ann's family. I was explaining to Ann that this year more than last, it has become harder for me to connect with my friends and for my friends to connect with me. As more time lapses since Mattie's death, my role and activities as a mom become non-existent. I live very different lives from my friends who have children. Ann asked me whether I thought friends had to share such commonalities. My answer is YES. Certainly I think women who have children can be friends with women who do not have children. But here is the difference. I was a woman who had a child, and lost the child to cancer. My networks were built around the fact that I had Mattie and Mattie played with their children. So in my case, I definitely do believe that such a commonality is important to my friendships. In addition to that issue, I am trying to come to terms with my own feelings. I am very aware of the fact that hearing about the good times families are having with each other this summer bothers me. It bothers me so much that I don't want to hear about it and instead would prefer to isolate myself. From my perspective, I can't process what others are doing around me. I can't because this isn't a part of my life anymore and on a very deep level I HATE these differences and I am jealous that I can't have what other parents have, a live and healthy child. I could write more about this subject, but the anger, the feelings, and the resentments are all very real. Yet, to compound the problem, I also feel guilty for having these feelings.  

1 comment:

Anonymous said...

Oh, Vicki, How could you keep from having these feelings? I can definitely see how difficult it would be to try to process and interact with those who still inhabit that very different world that you used to share with them, that world that you can only long for, now....so conflicting.
I am going to meet with some of Keaton's friends for lunch today. They were in an honors camp involved with their school, on his actual birthday, which was Friday, but they all contacted me, and want to get together, and eat his favorite...sushi, and toast him with his quail eggs, like they did for his b-day last year, a few months after he left this earth.
I do love that they still remember and want to honor him...to keep his memory alive. But at the same time, just watching all of them happy and healthy, all their normal lives and activities going on all around me, can make me want to scream...to just run away and hide from the reality that he is not there with them, that he will never be a part of what he so desperately wanted and loved.And I, also, struggle to not be consumed by the anger at the unfairness of it all...the urge to just crush those dang quail eggs, and sweep the dishes off the table! At the same time, I long to hear every word from the boys, to know every detail about what is going on in their lives, every event that Keaton has missed, every plan that he will never be able to make....such conflicting emotions.
Well, I can already feel a headache coming on this morning....can't imagine why, with such a war going on in my head:) So, find my Excedrin, paste on my smile, try to focus on catching up with these boys(who I do love) lives....pretend my Keaton is with us....right in the middle of all the fun. My mom always used to call me the "Queen of make-believe". Guess I'll try to live up to that title.
Keeping you in my thoughts.

Karen, Mother of Keaton for Always
www.caringbridge.org/visit/keatonlee