Kicking Cancer's Butt

Look at this incredible video of Ty kicking the seat in front of him in my car.  This is from yesterday afternoon.  He is finally feeling better and making some great progress!  This afternoon I convinced him to come in the pool with me again, and he was moving his arms and legs so much.  I saw a lot of his stomach muscles working hard, too.  I am so proud. 

CLICK HERE TO SEE HIM IN ACTION

September is Childhood Cancer Awareness month.  You'll be hearing a lot from me starting Saturday.  Please help us to spread awareness. 

Photo Credit: People Against Childhood Cancer

Comments

  1. AnonymousAugust 28, 2012 at 7:37 PM

    Yes Ty and family you are kicking cancers butt!!! This is a miracle thanks to the Campbell family!

    ReplyDelete
  2. AnonymousAugust 28, 2012 at 7:53 PM

    That leg moving is the most beautiful thing In the world!

    ReplyDelete
  3. AnonymousAugust 29, 2012 at 8:49 AM

    Awwwwwwwwwww!

    ReplyDelete
  4. DeenaAugust 29, 2012 at 11:58 AM

    Incredible. You go Ty!

    ReplyDelete
  5. AnonymousAugust 29, 2012 at 6:31 PM

    I cried! I am so excited for him. Keep up the great work Ty,and you too Mom!... Billyjean

    ReplyDelete
  6. Leslie SmithAugust 29, 2012 at 7:21 PM

    AMAZING, AMAZING, FANTASTIC!!! Ty is shaking the ground cancer dares to creep on!!!! I just love that little man, I have goose bumps after that video...he always rises over the prognosis!!!!!! YiPEEE!!!!!! GO TY, GO TY!!!!

    ReplyDelete
  7. AnonymousAugust 29, 2012 at 9:49 PM

    His smile is priceless. Good job Ty!!

    ReplyDelete
  8. laurenAugust 29, 2012 at 11:25 PM

    WOW!!! His progress is amazing!! He has come so far since I met him. I LOVE LOVE LOVE this video!

    ReplyDelete
  9. UnknownAugust 30, 2012 at 9:13 AM

    The video is amazing!

    ReplyDelete
  10. AnonymousAugust 30, 2012 at 7:39 PM

    that is such great progress, cindy ! YOu didn't tell me he was already doing that ! that is AMAZING !!!! ~marilyn

    ReplyDelete

Post a Comment

Popular posts from this blog

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 state, Ty seemed so incredibly peaceful and comfortable.  I laid down next
Read more

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 attainable goal for Ty.  And "
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.  Ty's doctors and nurses, they are so special.  They have given us beautiful. prec
Read more