Summer 2011

Summer 2011
#teamtepperswag

Thursday, April 26, 2012

My Birthday Wish


I am participating in the American Cancer Society’s Relay For Life because I want to make a meaningful difference in the fight against cancer.

One in every three people will have to fight cancer during their lifetime. What kind of odds are those? Before I was diagnosed I thought that only the older generations got cancer. The older you were, the higher your risk would be.  It was the luck of the draw, and if you got it you fought it. If not you recognized that being able to watch your grandchildren play out in the grass was truly by the grace of God himself.

Today when I think about cancer I recognize the young lives that are compromised with such a difficult disease. My generation. My friends. Erin, Lauren, Cassandra. It's unreal; their strength, their determination, their perseverance.   They fight every day both physically and mentally, hoping that one day there will be a cure and they can resume a normal life. Until then these grandparents, mothers, fathers, aunts, uncles, sisters, brothers, babies… are working far more than a 9-5PM.

It’s invisible, this cancer stuff. There’s visible evidence - hair loss, gray skin, sickness – but no visible cancer. That’s true. But there’s something more obvious we should be all looking at: Cancer. CAN-cer. The very root of the word that gives us so much despair is filled with hope. It’s filled with strength, determination and perseverance.

We can conquer this illness together, simply by donating a few dollars to the American Cancer Society. This money not only goes towards treatment for current patients but also further research. I would love for everyone to be around and walk the track, but in donating, you’ve become part of the team – a team with goals, killing cancerous cells with every step. We walk to remember, to fight, and to celebrate. We walk to make a difference.

Please join my team or make a donation to help the American Cancer Society create a world with less cancer and more birthdays. Together, we can change the odds.

Every penny counts! Bless you all.

Monday, April 9, 2012

ACHOO "God, Bless that man!"

Dr. Weldon removed my NG tube today.  I have an NG tube after every surgery to drain out the contents of my tummy until it can wake up and do its job! I prepared myself; focused on my breathing while he removed the tape that held the end of tube to my cheek. Once he removes the tape I had to guesstimate of how much time I would have to inhale my last crucial breath. As he pulled out the tube I was not able to breathe in so I like to have a deep exhale prepared. He then slowly pulls the NG out of my stomach through my throat and nose. Of course I then have to blow some schnaz out of my schnoz, thinking “God bless that man.”  I am so much more comfortable now. (And I REALLY want a raspberry Popsicle or two!) I cannot wait until I can eat again!
The swelling I had in my hand is also just about gone and I now have not complete, but more normal function.  It was hard having a claw for a hand. I’ll admit I knocked over my fair share of water glasses trying to use it. Cats really seem to have the non-opposable thumb thing figured out - I’m a bit jealous. Good thing Happy and Polly aren’t here to watch me embarrass myself! Dr. Weldon confirmed that the numbness and swelling was caused by the positioning of my arms during surgery. I kept the left elevated which seemed to do the trick.
Yesterday I moved from my hospital bed to a chair for the first time since that oh so pleasant, planned surgery Friday morning. It’s really more of an “I just did that whole three feet move from bed to chair with my over-protective nurse and five more hovering around and holding me up thing today.”  It really makes a lot of sense to have 5 nurses practically carry you from the bed to a chair so you can get exercise.   Ha, ha, but I really do appreciate how protective they are with that initial change of position because it can really strike a nerve, whether it means passing out or getting sick. The nurses up here are great.
My whole family and Rachel’s boyfriend, Matt, visited yesterday afternoon on Easter. It was so exciting to see everyone and I wanted to talk about so many things, but it’s hard to keep the attention span of six people while a) nurses are walking in and out and b) you are horrible at telling stories. I let them go about their conversations (that I doubt were any more interesting than my fantastic stories!) while Rachel gave me a pedicure. We conversed, watched TV and hung out. I was struggling to keep my eyes open at the end of the day, but I didn’t want them to leave! I wish I had been a more awake hostess. Mmm Hostess Cupcakes…
I took my first walk today.  I needed two nurses and my dad to help with my pole and lines while I walked.  My balance wasn’t great.  I felt like I was walking with those silly drunk goggles on that they give you in the 5th grade D.A.R.E. program.  I was going too fast and my entourage was struggling to keep up with my pole and IV lines.  On my trip I ran into a nurse/friend Jamie.  She had seen me when I first came into the ER on Thursday and I was in pretty poor shape.   When she asked what was going on I filled her in.  One lap turned into two because I’m really bad at telling stories.  .
I’ve been flaunting the gifts that Nicole gave me to everyone who comes in my room and I know 3 or 4 of the nurses will be buying the ‘Baby Lips” chap stick.   I think I should be an official spokesperson.    My lips are now 77% more supple and 94% better moistened.    Jealous?!

Saturday, April 7, 2012

No Sleep for the Wicked

On Thursday at 1:00 PM I was driving myself to a weekly appointment when I began to feel severe abdominal pains.   They were so bad that I considered calling mom and dad to pick me up, but I finished my appointment and drove myself home.   By the time I got in the basement I was convulsing with pain and dragged myself up to my bedroom.   We thought it might be gas pains, but they didn't let up over the afternoon and by 4:00 PM I was throwing up more than I had in my entire chemo cycle this year.   By 7:30 PM I asked my dad to drive me into the ER at Childrens Hospital and we stayed there all night.   

They did blood work and took X-Rays, but didn't see the cause of my pain.  Luckily, my surgeon was on call that night and came to see me and requested a CTScan which showed a bowel obstruction as well as a cyst or mass near my ovaries the size of a softball.   Dr. Weldon told us that there were no other options, but to do surgery to resolve the obstruction and that they wanted to start right away.   By 5:00 AM they were putting me under with a raspberry-lemonade scented mask.  

The surgery took about 4 hours.   Dr. Weldon removed the obstruction, which was scar tissue from previous surgeries, and was also able to remove the cyst which he later told us was more cancer.    I woke up in the ICU to Alex, Nick and Rachel all trying to talk over each other in my tiny room.   Excited to see them I sat up and didn't realize I had a breathing tube that I was ripping out.  

I was in the ICU for one day and then they moved me to a recovery room for surgical patients on 10 South.   I have an epidoral for pain, a ng tube to drain my stomach and several iv lines.   Nothing new here.  Same as my other surgeries.  However, my left arm and hand are numb and not functioning 100% yet.   This happens sometimes because of how my arms were positioned during surgery.   I expect to be recovering for a week before I can go home.   

My anesthesiologist, Nicole, came in to visit me today and brought me a gift.  She's so nice!   She got me pink, purple and mint green nail polishes, nail polish remover and lip gloss.  We were talking about these things yesterday and she brought them today.  I'm really excited to use these with Rachel when she visits tomorrow. 

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