A great day

Last night was a much needed birthday celebration among my closest friends. Lou set it up so that Caryn, Dawn and James, Keri and Mike all surprised me at the restaurant.  I never would have planned that for myself because I would have been too hesitant to leave Ty like that, but it was the perfect way to bring me back to a more positive state of mind at a time when I was starting to feel kinda down.  We went out to dinner and I had such a great time.  Mr. Martini?... why hello, old friend!  Wine with dinner?... Yes, please! 

Ty had a wonderful birthday celebration.  It's very convenient that there was a parade in Long Beach.  He thought it was all for him :)  It helped even more when there was a bake sale for childhood cancer and they had a big, adorable picture of Ty on display.  He was so thrilled when he saw that.  Thanks to all of this supporters in Long Beach.  It was so nice to see our friends and neighbors, it's been too long!

His birthday party at Grandma's house was so much fun.  All of his cousins were there and he loved seeing them.  We decorated pumpkins…


We destroyed the "Dora the Explorer" piñata… (as an parent that is subjected to Nick Jr all day/all night, there's something especially gratifying about this photo).
 
We had Max and Ruby cake, as promised…
 
And, we saw SpiderMan (aka, cousin Richie - Ty was totally duped!). 
It was a great day for a great kid and he got some awesome presents.  His Harley Davidson scooter and Lightening McQueen car kinda scared Ty, though, so baby GaGa was more than happy to take them for a spin around town instead.
 
Thanks again to everyone who is following Ty on his fight for a cure.  We are so grateful for all of your prayers and positive energy. 

Comments

  1. Colleen RosenOctober 2, 2010 at 11:32 PM

    Good times! NIce going by Lou to set up your b-day dinner!

    I'm ready for the fight. Bring on the chemo. Let's do this. Let's fight and win.

    ReplyDelete

Post a Comment

Popular posts from this blog

Anything but cancer

Image
Cancer is not welcome here.  It can never, ever, ever, ever, ever come back.  As I mentioned yesterday, Ty has been showing some physical symptoms that we haven't seen in a long time.  Please, God, don't let it be cancer again.  Anything but cancer. I spoke to Ty's doctor first thing this morning and he believes the increased weakness we are seeing on Ty's left side is not related to new cancer growth - but that doesn't rule out the possibility.  He feels that Ty is suffering from spasticity, which is becoming more visible now only because Ty is getting stronger.  As Ty's muscles begin to regain mass and tone, the neurological weakness on his left side is becoming more noticeable.  This spasticity is likely permanent, but also treatable with continued therapy.  When I spoke to his physical therapist later today, she agreed that it would explain what she is seeing, and then she reassured me that walking again is still a highly...
Read more

Our baby is finally free. Rest in peace Ty Louis Campbell.

Image
Ty Louis Campbell is gone, but his story continues.  This is our promise to him.  His impact on the world around him gives his short but inspirational life such meaning.  His soaring spirit will continue to fuel a fire in our hearts, and strangers around the world will continue to fall in love with the little boy who fought so valiantly.  The little boy who hurt so much, but maintained a bigger, brighter smile than the healthiest of children.  Ty never did break his fever.  He never really woke up.  Not until he decided to leave this earth and fly freely among the clouds.  At that very moment, he was awake.  He had returned to Lou and I to say goodbye.  To say our hearts are broken would be like saying it tickles to have your stomach ripped open with a spoon.  I went to bed last night with so much worry on my mind, but I was able to fall asleep because I was calmed by the fact that in his semi-conscious s...
Read more

Our aching hearts

Image
My face is swollen.  My eyes are heavy.  I have been crying for what feels like an eternity.  But in between my tears, I have an overwhelming sense of freedom.  Today we were told that there are no more treatment options for Ty.  That his MRI Saturday night shows progressive lepto-meningial disease in three different areas.  Lou and I decided against surgery to fix Ty's shunt, and I am finally free from feeling responsible for whether or not he lives or dies.  Ty is in God's hands. No matter how many times I swore that I leave Ty in God's hands, I was always clinging onto him with every ounce of my being.  Researching.  Fighting.  Begging.  Doing anything in my power to find a way to save him.  Finally, I have exhausted my options and I am letting go.  I may be kicking and screaming, but I am still loosening my grip because I know that I have to.  We have tried so hard, for so long....
Read more