This is Jake's Story...

Jake is a 20-year-old twin who has been diagnosed with stage 4 Rhabdomyosarcoma, a very rare form of cancer. Going through a vigorous daily radiation treatment and weekly Chemo treatments make him extremely tired, weak and sometimes nauseous.

Jake is otherwise a normal teenage kid. He likes playing computer games, paintball, swimming and golfing. He loves hanging out with his four brothers, 4 wheeling, camping, and ruining his mom's laundry baskets while making home videos. He hopes to someday become a computer programmer.

This blog was started to keep his family and friends updated on his status.

Addendum: Jake became cured of cancer, free of pain and everything this world brings on September 29, 2010. He continues his journey in Heaven. He is doing awesome! Hope you're doing the same!

His family thanks you for your generosity in donations, love and service. God has shown us many tender mercies!
Thanks for being one of them!





Friday, October 29, 2010

Chemo: Round 16

Please keep your hands and feet inside the ride at all times!

 
 
 The CT Scan showed the candy in his pocket.

You'll have to click on this picture to see the full effect.  To the right of the capital building is LDS Hospital where 4 of my boys were born.  Occasionally we get a nice view from Jake's hospital room.  Last time, we had a nice view of the parking garage!  See the storm rolling in? I had to drive home in a huge snow storm!

Ever since Jake found out he had cancer he has been wearing two different shoes because one of the shoes rubbed on his toe wrong and gave him an infection.  He ended up having his toenail removed.  I finally asked him if he wanted a new pair of shoes (I thought he was making a fashion statement).  He said, "yes, that would help!"  Hmmmm, all this time I thought he liked wearing his shoes like this!
 

Here's Jake with some of his Conkerr Cancer pillow cases.  They let him pick some colorful pillow cases when he is admitted, to brighten up the drab white colors of the hospital.  The tubes connected to him (which are actually connected to line up by his heart) are where they give him saline to make sure he is hydrated enough so the chemo doesn't fry his insides (too much).  When he is hydrated enough, they push the chemo through this IV that goes directly into his arteries.  I hate to think what it is doing to his heart!


He often brings his own blanket from home.  I have to wash everything when I get it home because it is toxic from his sweat.  He is smiling...for me.  He gets hardly any sleep because he has to go to the bathroom every hour.  The best part of the hospital stay is coming home.

Besides losing his hair and his appetite, he is losing a lot of strength and feeling in his fingers and toes.  I have to open toothpaste and water bottles for him.  He is down to 125 lbs.  It's getting harder and harder to find a place to give him his shots.  I have to make him double up and pinch the skin together to fabricate fat.

Love you Jake!  Hang in there, bud!








5 comments:

  1. Dang chemo!! It had better cure the cancer, that's all I'm sayin'.

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  2. I'm your newest follower from Kellie's blog. Sending prayers and love. I have a 19 year old. Can't imagine what you are going through as a mom. Stay strong. Be brave. Know you are loved by many who haven't even met you. Do you mind if I post about you on my blog to send you some more supporters?

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  3. I found your blog through my cousin Kellie Hendricks blog. I am grateful for your thoughts and will keep Jake and your family in my prayers!

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  4. I am your newest follower through Kellie's blog. :)
    Jake you are in my prayers!

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  5. Thanks for the words of encouragement and prayers! You are welcome to share Jake's story with anyone who is interested (thus the blog!).
    We're all getting tired of the treatments, but...what can you do?! We will be so grateful when this part is over!

    ReplyDelete