Friday, July 29, 2016

I know I said the next post would be after surgery unless I felt like bitching about something or an event happened.  Well an event happened.

I just returned from a great vacation with my sister and her family in Florida, that's the good news.  I ate seafood for the first time in 7 months, saw my pelican friends, played in the ocean like a little kid, rode on the motorcycle, and drank a little too much.  Basically I enjoyed life the way we all are supposed to be doing.  My young nephew even put a smile on my face before we left for Florida by making this for me:


He knows me well!  It was a great trip!

I'm glad I took a break from most all social medias while I was gone because today when getting back and checking on my friends at various boards it came to my attention that one of the very first ladies that reached out to me, who was diagnosed the same as me, passed away.

We only knew each other by nicknames, like most on the boards do.  She was an inspiration to me because she was always quick to respond and almost always with enthusiasm and support.  When I left I knew she wasn't feeling well, but fully expected to see her back on the board chatting away with us all.  What I also didn't realize was the outpouring and sadness on one Facebook group for the real named woman, was the same nicknamed woman who reached out to me.  It wasn't until the two were connected today that it hit me.  I am heartbroken, and realize how many lives she touched now that the connection has been made.  Her name was Julie, but to me she was PurpleMinion.  She wanted so desperately to see her daughter graduate from high school.  She didn't make it, and that also breaks my heart.  Her daughter is 16.  She was a mom, a vet, a soul mate, a friend.

Her passing makes things real.  Even though things have been very, very positive for me, it lets some of reality and worry seep in.  It reminds me that I'm having major surgery next week that has me scared shitless.  It reminds me that this disease is ferocious.  It reminds me that I am in a fight for my life, and it's not over.

Which leads me back to my vacation.  Julie's last communication to a woman in my group was to enjoy life, all of it, and to the fullest.  We never know when our time will come, any of us.  That's what I did this past week, and what I try to do every day.  Some days living life to the fullest is The Price is Right in my PJs and not worrying about the laundry, sometimes it's riding on the motorcycle around town with my husband, vacationing with family or friends, or talking (or texting) to my daughters.  Sometimes it's sitting alone on my deck watching the birds and listening to the kids play in their yards.

Since my diagnosis my mantra is "What are you waiting for?"  I believe this fits in my life very well now, and I say it to friends as often as necessary.   My husband has wanted a big, used truck for as long as I can remember.  We always look at them, test drive them, talk to our salesman, study them, then walk away.  I finally said to my husband exactly that, "What are you waiting for?"  We bought the last one, and it's worth every penny to see the look on his face when he drives it.

I once remember reading somewhere.......Use the good China.  Agreed.  If you don't it will sit in the dark, collect dust, and never be appreciated.  And that thought leads me to something written many years ago by one of my favorite smartasses:

If I had my life to live over...

Someone asked me the other day if I had my life to live over would I change anything.

My answer was no, but then I thought about it and changed my mind.

If I had my life to live over again I would have waxed less and listened more.

Instead of wishing away nine months of pregnancy and complaining about the shadow over my feet, I'd have cherished every minute of it and realized that the wonderment growing inside me was to be my only chance in life to assist God in a miracle.

I would never have insisted the car windows be rolled up on a summer day because my hair had just been teased and sprayed.

I would have invited friends over to dinner even if the carpet was stained and the sofa faded.

I would have eaten popcorn in the "good" living room and worried less about the dirt when you lit the fireplace.

I would have taken the time to listen to my grandfather ramble about his youth.

I would have burnt the pink candle that was sculptured like a rose before it melted while being stored.

I would have sat cross-legged on the lawn with my children and never worried about grass stains.

I would have cried and laughed less while watching television ... and more while watching real life.

I would have shared more of the responsibility carried by my husband which I took for granted.

I would have eaten less cottage cheese and more ice cream.

I would have gone to bed when I was sick, instead of pretending the Earth would go into a holding pattern if I weren't there for a day.

I would never have bought ANYTHING just because it was practical/wouldn't show soil/ guaranteed to last a lifetime.

When my child kissed me impetuously, I would never have said, "Later. Now, go get washed up for dinner."

There would have been more I love yous ... more I'm sorrys ... more I'm listenings ... but mostly, given another shot at life, I would seize every minute of it ... look at it and really see it ... try it on ... live it ... exhaust it ... and never give that minute back until there was nothing left of it.”


― Erma BombeckEat Less Cottage Cheese and More Ice Cream: Thoughts on Life from Erma Bombeck

I started this post very, very sad.  I feel a little better now.  Thanks for listening.

Now off to Germanfest, where I will visit with friends, revisit memories from high school in Kaiserslautern and raise a mug to my friend Julie.

Prost! 🍻

Ruhe in Frieden, mein freund. 🙏👼




Friday, July 15, 2016


Well Hello!!  

I hope everyone is enjoying their summer.  Mine has been a busy one so far.  Since I last blogged, many things have happened.  I took an intentional break so as not to bore you with daily occurrences as I'm sure you all are busy with your own lives :)

Thanks to these ladies for everything
The ride put together by my co-worker was a success and fun was had by all, maybe a little too much ;)  Thank you to everyone that contributed in your presence, your donations, and your friendship.  Bob and I truly appreciate all the support we have gotten from everyone.

So where to begin......when I last reported I had three chemo sessions left.  I'm happy to report I'M DONE!!!!  4 Red Devils (AC), three Carboplatins, and twelve Taxols.  Finished.  Chemo sucked, but it worked.  I can't thank my main nurse Julie, and my scheduler Mary at Moorland Froedert enough for their support through it all.  Really to everyone involved at Froedert, they have been so supportive and fantastic.

                                           
                                                  Mary
Julie

                                   
This is a comparison of the first MRI and the newest.  If you look close in the second picture you can see that the skin is less thick, the node is gone, and the mass has shrunk.  Yeah!



My oncologist and surgeon are very happy with the outcome.  I will not get my hopes up too much yet.  Once pathology comes back from surgery clean, then I will get excited.  I will shout from the rooftop if it's clean!

June 24th I had an appointment with a oncology gynocologist.  It was decided that since no reconstruction will be done during surgery (ie no long surgery time) they would remove my ovaries and fallopian tubes.  These are removed because A)  I don't need them anymore; and B) it helps to prevent estrogen from fueling my Cancer and hence a reoccurence.   Can you say Hello instant menopause.........😈🔥👊

June 28th a meeting with the oncology surgeon.  A very different meeting than the first time.  She took plenty of time to explain what she would be doing and prepare me for what I will look like.   She even sat and socialized a bit after.  Phew.  Much better than "get your affairs in order".  She was very pleased with the MRI results, enough to say they will also be taking my port out during surgery.  Hallelujah!  Didn't expect that for awhile, but she says "I don't need it anymore"!!!  Surgery time should be about 4 hours total, with a luxury stay in the hospital (Froedert) for anywhere between 2 to 4 days.  Joy :/

Now that chemo is done I've had a chance to have a little fun and enjoyed Summerfest by seeing two concerts.  Chris Stapleton with Alabama Shakes, excellent both, and Tesla/REO Speedwagon/Def Leppard.  Great show!!  Guess who was my favorite ;)


Me and the boys 😉

After that it was the annual Kuspa Christmas Mountain Dells trip.  So happy to be able to participate in this.  If chemo had stayed on track, I most likely would have had surgery and been homebound.  Instead we all had a great time.




Had a visitor by the pool. Wonder who?




Lola spent the time at Doggie Dorms.  Needless to say, she's glad to be home.





So two weeks after the last chemo and I can say it sucked, really, really sucked.  But its over and it worked.  Its parting shots to me?.......I lost my voice (going on three weeks now) and shingles.  Ugh.  My lost voice is frustrating since nobody can hear me.  So I just sit, mostly quiet....probably a relief to a few 😆  Shingles are terribly painful.  Thought it may have been a reaction to the sun, no such luck.  Had to take a prescription for 10 days, but it didn't stop the pain.  That just takes time.  For those that have never seen shingles before, this is what it looks like.  They also typically are on one side of the body or other, not both.  Mine started in the middle and spread right.


I also have mild neuropathy in my left foot, this is a tingling and numbness.  At times there is enough of an issue that the leg goes up, and I'm forced to sit down.  I'm told this can go away after awhile, fingers crossed.  And last parting shot, my armpit is numb on the cancer side, and gets mild shooting pains on my underarm.  It will be real numb after surgery, so at least I will be use to it.  I am unsure why this happened, or if it will go away.  Time will tell.  Gotta love the side effects.

On July 7 just before vacation, I had a CT scan to compare some liver spots in a before and after chemo.  Thankfully on July 11 the results showed everything is the same and nothing new popped up.  What a relief.  I have to admit, this occupied my mind for several days, especially since my voice was gone.  I worried there may have been a spread to the throat or lungs.  Guess that will be a common thing from now on.

Scheduling has been coordinated with the two surgeons and as long as my pretesting comes out well, I'm scheduled to say goodbye to the girls on August 4th.  Two more appointments on July 19th for a physical and a meeting to show how to take care of the post surgery breast area and drains.  Sounds like fun huh?


Once we are all edjumacated on how to take care of me post surgery we are off to Florida one more time.  This time we are taking my sister and her family who have never been to our place.  I'm super excited and happy to have a chance to visit my pelican friends and enjoy Florida one more time before the Fall and dreaded Winter.

 The Bye Bye Boobie party is scheduled for July 30, no location yet.  Then off they come, sassy things.


Enjoy the Summer people.  Before you know it, it's back to school and bye, bye Summer.

Next up on the blog, probably post surgery.....unless I get a bug up my butt and want to bitch about something.  ;)   .........Or something interesting or significant happens.........

And before I forget.,...I HAVE HAIR!!!!  White with sprinkles of dark, but hair!


......still no eyebrows to speak of...........