Showing posts with label chemo. Show all posts
Showing posts with label chemo. Show all posts

Thursday, December 1, 2016

Magic

My kids and I were in the car a couple weeks ago and we were pointing out Christmas decorations.  If you've met me, you know I LOVE Christmas and I get so excited that I just can't hide it.  If you've met my kids, you know they can't pass a Christmas tree or Christmas light without declaring it loudly.  This was the perfect time to happily turn on some festive tunes.  Toby, my son, asked me from the backseat, "Mommy, why do you love Christmas so much?".  First panic set in because my full answer would've taken the entire car ride home to explain and his attention span is only about 4 seconds.  So I decided on, "Because it's magical".  His response?  "There's no magic, Mommy.  Santa just puts all the toys on his sled and delivers them to the kids!".

Seriously.

Stop it.

I teared up and my heart smiled it's biggest smile.  Magical.

I had no idea how to start this blog post, so I chose my favorite recent kid story.  How I really wanted to start it was....I have cancer again.  (Seemed a bit harsh. It's the holidays.) For those of you keeping track, Santa has now given me the wrong gift 2 years in a row.  It's true.  It's back.  It's not in the same place, but it's in the same general area.  I won't go into detail because it involves the word vagina and that makes people uncomfortable.  There are typically 3 ways that cancer is fought: surgery, radiation, and chemo.  Unfortunately due to the location of the new tumor, surgery is not an option.  Radiation is not an option either, as you can't radiate the same area twice.  That leaves chemo.  My oncologist set me up to start chemo today.  One 8-hour round of a three drug cocktail every 21 days for 6 cycles.  The thing about the chemo is there's only a 20% chance it'll work.  20%.  Not great.

There's something I don't think I've shared on this little blog yet.  Which is surprising because I share pretty much everything.  The type of cancer I have is called Glassy Cell.  Why does that matter? With a quick google search, you'll see that Glassy Cell is no good.  The kind of cancer you don't want.  Not that you want any.  It's exceptionally rare and extremely aggressive.  Of all cervical cancer patients, less than 1% have this type.  It is also one of the types of cervical cancer not caused by HPV.  Yes, it's possible to get cervical cancer without having HPV.  Little known fact.  You're welcome.

I've know I've had Glassy Cell since day 1 which means I've known it was a possibility it was going to return at some point after I beat it.  Thanksgiving would've been my 6 month cancer free anniversary.  I expected it to wait a bit longer.

So in a turn of events, yesterday I was given an opportunity to go for a second opinion and I've decided to take it.  I did not start treatment today and have put it on hold so I can travel to Sloan-Kettering to see what they have to say.  I was nervous that my doctor wouldn't want me to delay treatment for a week because what we're looking at it is so serious. But I've been given the green light and I am incredibly grateful for this opportunity.

How did we get to this point?

After my last battle, I was set up on a 3-month plan.  Every 3 months I would get a check up at Roswell.  (I'm much better at making these appointments than I am at the oil change ones)  My last check up was in October.  They found something. At the time, in the office, it was hard to tell exactly what they found.  Could just be bad tissue from the radiation.  Could be cancer.  Could be nothing.  They did a quick biopsy there and that came back clear.  The doc sent me for a scan juuuuust in case.  Good thing.  You light up in scans when you have cancer.  I was lit.  Still, we needed to be sure.  This could be a false positive.  They sent me into the operating room and took "lots" of biopsies.  Now as I'm writing this I'm realizing I never asked how many they took and I'm curious.  These showed cancer.  That made it official.

Lots of emotions.  I haven't really cried a lot.  It's weird.  I'm an emotional person usually, but this doesn't do it for me.  I'm just annoyed.  Like stop it.  I want to live my happy little life without worrying if this is my last Christmas.  This also makes me feel super awkward.  I hate telling people that my cancer is back.  Unfortunately for most, I'm fairly blunt in my delivery of this news and people don't handle that very well.  Sorry.  I'm a realist, not a dreamer.  No puppies and rainbows here. I know what I'm up against.  This made telling family and friends way harder than the first time.  Most people I told found out via text.  And a lot of my friends are finding out right now.  Modern technology kind of made me an asshole and I apologize.  But it also is giving me this outlet and opportunity to share my story.  And that's amazing.  

Thank you, All.  Thank you for being with me on my adventures over the last year.  My support system is the best on the planet and I appreciate every single bit of support you've shared with my family and I.

Round 2.  
Ready.


Monday, January 25, 2016

Day 1 - One Down!

You know when you're pregnant for the first time and you subscribe to all those web sites that tell you what size fruit your baby is and what is happening to your body that particular week?  (If no, then just pretend you know what I'm talking about - or go ask a pregnant friend) Some people like to read ahead and see what size their baby will be and what their symptoms might be in the coming weeks.  I never liked to do this.  Why?  If it told me that the 3rd Tuesday of my second trimester, my left earlobe would itch at 4pm, I'd wonder if it really itched or of I just had it in my head because these crazy baby people told me it may happen. I'd rather just see what happened to me. Everyone is different. Life is an adventure!

Today I started chemo and radiation.  You know how many times the word nausea was brought up?  I could be nauseous all day every day.  I could not be nauseous at all.  As I sit here and write this, I feel completely fine....except for the impending doom of nausea.  Will I have to stop writing because I'll feel sick in 5 minutes?  Will I be sick tonight?  Will I feel ok? Will I wake up feeling like crap?  The possibilities are endless....and none are definite. While I appreciate the warning, part of me just wants to be surprised.  I know that's not a thing. Side effects are a thing.  But which ones will happen and when?!?  Life is an adventure.

Here is another issue.  I haven't had an appetite for months.  I normally like to eat.  Obviously.  It's one of my favorite hobbies. So this no appetite part sucks.  If the devil wore red Prada, I guess you could say I'm one battle with cancer away from my goal weight.  (Please find that funny.  It's funny.  I promise cancer wasn't in my original weight loss plan haha)  Aaaaanyway, today - on the last day I ever thought this would happen - my appetite mysteriously made a dramatic return.  And to celebrate, I ate enough to make up for my weeks of not eating.  Really.  I may be slightly embarrassed by the amount of food I consumed haha.  So here's the dilemma - if I get sick later....will it be because I had chemo today....or will it be because I stuffed my face like it was my last meal?  Smart move for Lesley? No, not really.  But I have stupid cancer and I get to do stupid things.  Life is an adventure. 

On another note, a shout out to a cool little dude named Ethan Franks.  His mommy was making us some meals for our freezer and he thought we needed some chocolate chip cookies.  Ethan is a super smart little boy :)