Saturday, June 8, 2013

Dear Madeleine

I see your face, your big beautiful smile. I miss you so much!!! How God must have so much faith and love for me because I don't understand why this is our path. what I wouldn't give to go back and just be a regular family! and not have to worry about anything but loving you and takoing care of you.!! I miss you so much. I hate days like today. Started off on the wrong foot, whatever it is-it's all a mess. and all I want is YOU. nothing more, nothing less. and my heart weeps because you're gone. and I just want you here! I know it's not your job to save me. It's not your job to make me feel better. I'm the mommy, it's my job to just be your mommy and the best one I can be, to you and to sister. I didn't get that opportunity. I didn't get all the rewards from being a good mommy. Instead I got a broken heart!!! I just miss you so much. I don't want anyone or anything else, I just wish I could have you back, that you never left. Please God, take care of my baby/ Give her all my love!! I love you my Squishy, my Angel. My heart hurts every day for you. Today it's invading my face, my tears, my joy to be with family. It's so hard. I just miss you,

Friday, June 7, 2013

Amazing friends doing for others

I have amazing friends. Amazing, genuine, considerate people who have chosen to walk beside us and experience with us this truly life-altering, heartbreaking, faithful and blessed journey. This post is from my friend, China. She's amazing. Please support her heart's desire if you can. God Bless.

Hi everyone~
It's that time of year again for the Santa Cruz to Capitola Wharf-to-Wharf race on July 28th!  Last year, your support of my run raised over $1,000 for CASA and foster youth in Santa Cruz County- thank you!  This year, I am fundraising for a cause very dear to my heart, in honor of Madeleine Angela Vazquez, the beautiful baby girl of my childhood friend who lost her life this last January at only 15 months old to Atypical teratoid rhabdoid tumor (AT/RT), a rare tumor usually diagnosed in childhood that results in tumors (often multiple, recurring tumors) in the brain and central nervous system.  The malignancy rate for ATRT is a heartbreaking 11%. Although she only lived a short time, Madeleine's spirit not only changed my life, but the lives of so many.
·     Because of many of your kind donations towards the bake sale/silent auction I held at my work in January after Madeleine's passing, we raised nearly $1,700 for the family to help with Madeleine's funeral costs.  I am forever grateful for your support and honored to know so many giving souls, and hope you will continue that support at the macro level— to find a cure and support the children and families who suffer every day because of childhood cancer.
·        I am fundraising for the Jessie Rees NEGU (Never Ever Give Up) Foundation, which began in honor of Jessie Rees, who was diagnosed at 11 years old with an inoperable and incurable brain tumor called DIPG, from which she died at 12 years old.  Her story launched a global movement of compassion that her foundation continues with through the support of amazing corporations, athletes, charities, volunteers and people like you! 
* One of the attached pictures shows Madeleine with a “JoyJar” from the Jessie Rees Foundation – just one way they spread hope, joy and love to children fighting life altering medical illnesses.
http://www.negu.org/
 Our greatest gift in honoring Madeleine’s life is to live every day to the fullest.  I am running in honor of those who can't— the millions of children and families that suffer because of pediatric cancer, and yet keep striving and believing in a cure. Their strength has been particularly moving for me this year and serves as a reminder to keep trying no matter the obstacle.
I truly appreciate whatever level of support you can give.  Please visit my FirstGiving.com donation page for more information about the Jessie Rees NEGU Foundation and to donate: http://www.firstgiving.com/fundraiser/chinaburyn/chinaburynsfundraisingpage
In honor of Angel Madeleine ~

Thank you,
China

Tuesday, May 28, 2013

Changes

I haven't updated recently because I remember when we first began Madeleine's cancer Journey we were scanning the web looking for insight to this disease- anything that would give us hope that she could win her battle. And as you can imagine, there were very few happy sites- because all of these parents started out (for the most part) with hope and faith.... and all their children died. The blogs became a very somber place and completely overwhelming for us because we were trying to maintain our faith and focus that she would win, she could beat this, she has to be okay because we are faithful... and the sorrow I read about from these grieving parents would overtake me like an undercurrent wave in the ocean. I couldn't handle it. All I wanted was somewhere in the world to find another baby who had won their battle against ATRT and was now thriving in pre-school, elementary school, first communion, ANYTHING. 
So back to our updates:: I was doing GREAT for a while. We had gone to a grief camp in March, and while the weekend was completely exhausting, I left feeling lighter on my toes, as though God had taken some of this burden from me and I could actually begin to feel ok, dare I say pretty good, and I could begin to help other grieving mothers. In April- on April 17th exactly- a dear, sweet little girl close to my heart went home to heaven.
And I fell apart.
My tears were so strong and forceful I couldn't speak that morning; I quite literally couldn't get out of bed that day. I was reliving the every emotion and every moment of the day and night that Madeleine died. My own anguish over my daughter's death to such an awful disease led me to believe I understood the very thoughts of Sarah's mother. And now having been part of mothers' support groups, I know that I did that day, understand and was feeling everything she was going to feel, because she was still in shock. The shock phase of grieving is a lot like driving in thick fog- you can stay the course without much distraction but there is no real thought or feeling taking place because it just doesn't seem real.
So the 17th was a dreadful day. And 10 days later we got into our best dressed and stepped out, alone but as a unit, to celebrate and honor Madeleine at the NEGU Gala. The organization blessed us by highlighting our baby and our family as a means to demonstrate how a relationship is begun with a family through the first gift of a JoyJar. Her pictures, her big beautiful smile, flashed across a big screen and it took my breath away. It turned out to be a lovely evening, celebrating the children fighting and succeeding, and raising all this money to help more and more kids fighting for their lives. For us it was also very emotional and connecting to be with a family so publicly going through our same trials in bereavement, yet so privately holding their real daily anguish like us. We immediately felt like we had known them for years, felt like they were family, and I hope our time together brought them as much comfort as it did for Daddy and I.
Shortly after that, many other things took place in our life that actually helped distract us from the overwhelming sadness we had been feeling. We went from our family of four, back to three, and in some ways, back to four, since my 6yo nephew has been staying with us for the summer. Talk about a completely different household for all of us...
There is truly only ONE thing that is as it was September 30, 2011: our home. Other than that, NOTHING is the same. We don't recognize our old life. We are different people to the very core, we don't feel the same, we don't think the same. Even Annalise. We have all lost greatly.
Isaiah 61:3 ...to bestow on them a crown of beauty instead of ashes, the oil of joy instead of mourning, and a garment of praise instead of despair....
And as a result, how to do you settle back into an old life? It cannot be done. So eventually I began to look for what I thought would be cool [distracting] and convenient [close] to go back to work. I fell in love with a job at NFL network. I applied for some upper management position in the glamorous 90210. But nothing was coming through. Hmmm.... why not? I'm a very qualified individual. And then it occurred to me: I am not only qualified, but usually passionate. And with my heart ripped out of my body and shattered into a million pieces, there wasn't much passion to be had. I have always taken great pride in my career, choosing to focus there instead of my personal life for many years until I started a family. And I realized... I have passion. It's for cancer and grieving families. Children damaged but alive after a treacherous battle to claim their lives, and they prevailed- what inspiration, what courage! I want to help those children, those families, those organizations who offer support and genuine concern for these families. Because more than likely the people running these organizations started them out of the ashes of their own hearts.
I have a dear, sweet friend, a cancer mom whose daughter is recovering beautifully from a tumor in her leg, who wants to start a foundation because she is overwhelmed at the support she received during their family's time in the trenches of cancer treatment. God bless her and her tender heart. What I fail to mention is that she has not one, but three daughters. Her little surviving warrior is a twin. She's got her hands full with lots of flowing blonde hair and Barbies. And to her I say, you have done your due diligence... let me carry that burden for you. What I wouldn't give to be raising my daughters with their sister.... Let me give back for the both of us. Devote yourself to raising your daughters. And all the love and passion and grief I have for my Madeleine, Sunshine for all of us who love her, let me pour all of that back into these organizations with the talents God has given me. I love you Talli!!!
So that's what I'm doing. I'm planning to use every resource I have to bring more money to these organizations from all of the rich people, foundations, and grants that will fund programs and services for these children and families. Wish me luck.

Sunday, April 28, 2013

Dear Madeleine

 NEGU Gala
Dear Madeleine Baby, mommy couldn't wait to come see you today!! I was so proud last night, you were my Shining Star!! Seeing your pictures on the big screen at the Gala took my breath away. I gasped as I saw your sweet, smiling face, and with tears I snapped a quick picture before Daddy and I went to the stage and did a Pay It Forward to another family, selecting a magic #42 to bless another kid fighting cancer, to bring them joy and support, just like they did for us. I know God has put Jessie's family in our lives. Everything they do is for kids like you and Jessie. I'm so proud to be your Momma. Of course I'd give it all up to have you. Sometimes I think that's one reason you had to go; because I couldn't give as much or love as much if you were still here. You were my life!!!! I miss you terribly!!! God tries to remind me that you are safer and healthier than ever there with Him, not to worry because you're in paradise. I know, I know. It will never be enough though to take away the heartbreak I have because you had to go so soon. I miss you every minute of every day. I know we have to keep living, cause that's the only way I can get to you!!!


I miss you crazy bad Baby, but I know tomorrow will be better and we'll be together again. I love you!!!!



This week's flowers for you Baby