Wednesday, May 29, 2013

MAY 29, 2013


Well, after I posted on Friday, I took a pretty hard turn for the worse.  Saturday, I didn't get up.  I mean, I literally didn't get up out of bed.  I think I got up twice to use the restroom.  I was up for about 15 minutes in the morning to get breakfast (which I ended up not eating), and that was it.  I didn't eat.  I didn't drink.  I literally didn't move.

I couldn't.  I hadn't given my body what it needs to recover, and it couldn't.  Finally on Sunday, after getting a little food/drink into me, I asked Levi to take me up to CTCA for IV hydration.  And, it helped.  Not a lot, but anything at that point was an improvement.  Did the same thing on Monday, and yesterday, I was able to take care of myself and the kids.

Thankfully.

Today is even better, as I'm learning that my body needs immediate fueling every few hours, and it requires fluids to function.   I've found a drink that I can tolerate (actually like?) warm-ish, and that helps.  It has plenty of electrolytes and vitamins to boost my body up, and I see a difference almost immediately.

I'm still weak-ish, and when I get going and try to do too much, my body is quick to remind me that I can't.  So, I'm (once again) learning to listen to my body.  My head and my heart, however, aren't as agreeing, as they both think that there is just too damn much to do.  So, it's a constant struggle, but I'm trying to be patient with myself.

So, there you go.  This round was tough, but I made it through, and I still have two more weeks to recover before the next one.  I'm using that to my advantage, and trying to a) get things done, and b) rest.  Not necessarily in that order.  :)

The kids are off of school now, so they are home with me.  That helps, honestly, because they are both old enough to start taking care of themselves.  It makes me sad to think that they are growing up, but they are becoming such amazing people that you can't help but love watching the process.

Tomorrow is Kevin's birthday.  Through the graciousness and generosity of some amazing people (you all know who you are), we are going to be able to give the kids an amazing birthday.  I say kids, because Julia didn't get much from us at all.  She is still pretty bummed about it, so it will be fun to surprise her tomorrow.

I'm off to nuke yet another bottle of water and drink it down.  Hey - it's working, and I'll take it!

Comments:

 Joan Bardee said...
yeah for slowly feeling better and the party!
May 29, 2013 at 12:41 PM


Friday, May 24, 2013

MAY 24, 2013


Well, the pain was worth it.  My WBC was well up to within the normal (like, normal people, no cancer normal) range, and I was able to move forward with chemo yesterday.  Kind of a mixed blessing, if you know what I mean.  I didn't want to get chemo, but I also (more?) didn't want to get another booster shot.  So, it was like, chemo is the lesser of the two evils.  And, it means we are actively fighting this flipping cancer.  That's something, I suppose.

Yesterday was a long day, but I'm feeling okay today.  Mom, Dad and I headed up to infusion, and they started the pre-mneds.  That wasn't too bad.  Once they started the Oxalipantin, thought - yeah.  The nausea kicked in.  After making a call to my docs, they gave me a shot of Ativan (the nectar of the anti-nausea gods), and put me on a patch of Sancuso, which is the only anti-nausea patch that I know of.  So far, so good.

I was tired last night, but hungry, which is a good sign.  I woke up this morning, and was tired, but luckily the kids are fairly self-sufficient and can get ready for school mostly by themselves.  I took a quick nap this morning, and am feeling good right now.  Well, good is relative, I suppose.  I feel good for one day post-chemo.  :)

I noticed the cold sensitivity right away.  I can't eat or drink anything cold - honestly, even room temperature drinks seem to be too cold.  So, my current drink of choice is hot tea or chai latte.  Not exactly the best for you, but it's getting fluids into me, so that's super important.

I'm noticing some small tingles in my hands and feet, but nothing I can't handle right now.  I don't know if they are from cold or from neuropathy.  We'll see how things progress.  When I touch cold things (like, say, a carton of milk from the fridge)....oh yeah.  Sharp, stabbing pains.  When I walk on the cold tile....it almost feels like I am walking on needles, or like my feet have been asleep.

I'm justifying these things by saying that, if I'm feeling those, the chemo must be working.  For now...I'll take it.  I'm glad that the IV chemo is only once every three weeks.  I took my Xeloda last night and again this morning, and will be for the next 13 days.  If this is what I have to do to kill off this cancer, or at least, reign it back in....I will.

I'm sure this post doesn't make much sense - we'll blame it on chemo-brain.  Today is the kids' last day of school (hard to imagine), and I'm hoping to get my shower and still have enough energy to take them to lunch as a treat.  Then, I'm going in for hydration this afternoon, which will undoubtedly help.

Meantime, wishing you all a wonderful Friday, and a good start to the holiday weekend.  Don't forget the true reason for the holiday, and take some time to remember and thank service members for what they've done.

Comments:

God bless, Michelle. I've been thinking of you for the past few days and wondering how the first day of Oxaliplatin treated you. Glad it wasn't horrible like Erbitux. I remember reading what you were going through on that and it was a nightmare for you. Praying, praying and praying. Have a great weekend with your family.
May 24, 2013 at 4:53 PM
Blogger Martha Molen said...

Tingling and sharp pains. Oh yeah that is the drip. I used hot pads to touch cold things. Ironic? You can do it! I am inspired by your blog and your determination. Found you a year ago when I was diagnosed. Keep it up! As you know it is worth it! :)
May 25, 2013 at 5:14 PM

Thursday, May 23, 2013

MAY 23, 2013


5 years ago, I went into the colonoscopy room, thinking that the worst thing they would find would be a hemmerhoid.

5 years ago, I had no idea what a PET scan.  I didn't know what CEA meant.  I was not aware of the vast underfunding for cancer research, that the awareness of colon cancer was so fear-filled and sporadic, and that I would soon become a staunch, vocal advocate for awareness, prevention, and early detection.

5 years ago, my children were 6 and almost-2.  5 years ago, yesterday, my daughter graduated from kindergarten.  5 years ago next Friday, my son turned 2.

5 years ago, next week, I had surgery that changed the course of my life.

5 years ago, I had no idea how strong I could be when push came to shove.  I had no idea what battles I would face, what challenges I would overcome, and what kind of amazing people I would soon meet.

5 years ago, I was diagnosed with colon cancer.

I can't wait to see what the next 5 years (and 5 decades) will bring.
***************************************
Today starts, we hope, another round of chemotherapy.  We are in for yet another long, arduous battle against this unseen enemy.  It seems mildly ironic that I'm supposed to start chemo today.  Not so long ago, I  looked forward to May 23, 2013.  It would have marked 5 years since diagnosis, and me almost, almost reaching that amazing goal of "cured".

It seems like such a lost dream now.  There is no cure for me.  Stage 4 colon cancer patients, those of us that live past our statistical expiration date, tend to deal with our cancer like other people deal with diabetes or heart disease - it becomes a long-term, maintainable disease.

Here's hoping for many, many, MANY years of maintenance.

Comments:

Thandi said...
And may it be many many years of maintenance that doesn't leave you feeling terrible every day! Many years of smiles and laughter and loving on those precious children.
May 23, 2013 at 10:19 PM
Blogger Green Monkey said...
Hi Michelle,
First... this is NOT spam. Do you get a lot of spam? I sure do. I wanted to say hi. I'm just meeting you because I'm newly diagnosed with rectal cancer. I was diagnosed with breast cancer in 2011,, finished my last surgery on April 23, and then May 20th was my new diagnosis. I really want to live but I am fighting the idea of chemo and radiation. My breast cancer was found early and I didnt need it. anyway.... I am so glad you are out there. I wish you well and I hope to find comfort from your courage and dignity. Best, Shannon aka Monkey
June 5, 2013 at 5:36 AM

Wednesday, May 22, 2013

MAY 22, 2013


Well, yesterday was supposed to be day one of this first round of chemo.  Alas, as my life has been going, it wasn't to be.

My white blood counts were too low, so I instead was gifted with a Neupogen shot, which helps the body produce neutrophils (part of your white blood cells, and important to your body's ability to fight off infection).

Neupogen sucks - it hurts.  A lot.  Despite the reassurance from my doctor that it wouldn't hurt, it did.  I spent most of last night tossing and turning, moaning and groaning and cursing as my body struggled to build those numbers.  We go back in tomorrow to find out whether this worked, and if I'll be able to get chemo starting tomorrow.

The problem is that the chemo, we know for a fact, will lessen my body's ability to fight off infection.  If I go in and start chemo with an already depleted wbc (white blood cell count), I am leaving myself open to severe infection, which would (according to my doctor) land me in the hospital and, in his words, it wouldn't be pretty.

I don't know what I'm hoping for.  If the numbers aren't where they need to be, I'll get another shot of a different drug called Neulasta, which I've had before.  They basically do the same thing, except that Neupogen is a shorter lasting drug.  They both hurt - a lot - as they throw your bone marrow into overdrive production.  It's a pain that I'm not sure I can describe.  It's deep in your bones, and can be felt in your joints, back, pelvic area....pretty much everywhere. The general consensus is that taking a single dose of Aleve and Claritin-D daily while on the shots can help with the pain, but it definitely won't alleviate it completely.  After some begging and pleading out on some of the groups I'm part of on facebook, I learned that heating pads seem to help.  So, I'll try those again tonight and see what happens.  Today's pain has been much less than it was yesterday, but it's still there.

If the numbers are where the need to be, we are looking at starting chemo tomorrow.  This is good, because we'll be actively fighting the cancer.  This is bad because the chemo brings with it a whole other host of issues.  Nausea, diarrhea, lack of appetite, sensitivity to cold....yeah.  I don't know what I'm hoping for tomorrow.

That sounds so selfish - but, I'm so damned tired.  I just can't even begin to tell you how tired I am.  Physically.  Emotionally.  Mentally.  Just....drained.  I want to fight the cancer, because I want to live.  LIVE!!!  But, I don't want to *have* to fight the cancer.  Do you know what I mean?

I've had a pretty crappy week.  It started last week with finding out that the lung tumors are back, and that I'm going back on chemo.  The weekend wasn't too bad, just riddled with anxiety and emotions careening back and forth because of what was coming up.  Tuesday, we found out that the WBC is low, so onto that shot, which made yesterday and today fairly miserable.  And, then tonight, as we were going out for a dinner that we probably couldn't really afford (but needed to eat, because the thought of spending the energy to cook right now is completely, utterly, totally overwhelming, and we've already run through the generous gift cards that were sent to us), I hit a curb with my car.  In hindsight, I shouldn't have been driving, but it is what it is.  I hit the curb with my car, and we had to spend another $65 out of pocket to get the tire replaced.

*sigh*

What's that old saying?  When it rains, it pours.....

Man, I could seriously do with some sunshine.  Like, middle-of-the-summer in Phoenix sunshine.  Without the 120* temps.  :)
************************************
Tomorrow marks 5 years since I started on this journey.  It's also my mom's birthday.  I hate that the two are on the same day.  I'm so angry that she will be spending her birthday with me, at the hospital, hoping (I think) that my counts are high enough to warrant getting chemo.

I hate that I've been dealing with this for five long years.  I've learned so much about so many things since that day 1800+ days ago.  Things I never expected to learn, never hoped to need to know.  I hate that, for the majority of my children's lives, all they have known is sick Mommy.  I hate that my husband and I have had to adjust our marriage to let this mistress called cancer in.

That's kind of what it feels like - she's this horrific, awful, mean-spirited, heartless bitch who keeps trying to put up a wall between us.  She's almost succeeded a few times - tonight was another time when I just want to lay down, cry, and sleep away the emotions.  Sometimes, I almost want to let her win.   There are days when it seems like that would be the easiest way to go.

But, I'll keep fighting.  I'm hoping that somehow, someway, I can pull together money enough to cover what I did tonight ($65 is a LOT of money to us right now....I didn't really have it to spend on the damn car tire).  Kevin's birthday is next week, and I haven't bought that kid a thing.  Julia's still waiting for the shopping spree I promised her.  I don't have the money for that, either.  The money that we do have goes into basic necessities, like gas for the cars, food, and (apparently) dumb-ass mistakes that I make.  I'm hoping to take the kids bowling for Kevin's birthday next week.  Maybe some birthday fairy will drop some money our way.  I can hope, right?

Tomorrow is going to be a long day.  Regardless of what happens, it's going to be a long day.  I'll try to keep  you in the loop, but I can't make any guarantees.

Comments:

MsMarysKilla said...
I know you’re going through a lot and I want to help with a little extra spending money for you and your kiddos but I don’t know how to donate. Don’t hate me for asking, I just don’t know how to do it because I’m new to your blog. Do you have a site or a po box address to send gift cards or cash/checks to? I don’t have a ton to donate right now because I’m getting married on 6/15 and paying for some of the wedding on my own (my fiances’ parents are helping too), but I’d like to give something. Even if it’s just enough for your daughter and you to go shopping – lol. Please help me out and let me know thanks! J
May 23, 2013 at 11:28 AM
Blogger MsMarysKilla said...
whoops sorry, I wrote the other day too but it showed up under my *spam* email name hahah, hello my name is MARY. (:
May 23, 2013 at 11:29 AM
Blogger Joan Bardee said...
please contact me. I'd like to help. Don't know you but read your blog. Swear I'm a legitimate person!!! jabardee@gmail.com
May 23, 2013 at 7:12 PM

Friday, May 17, 2013

MAY 17, 2013


Warning - there may be a lot of cursing in this post.  If you don't like it, don't read any further.  This is going to likely be a very raw post, and very emotional.  Hence, the bad words.
********************************
The news yesterday, understandably, threw me for a loop.  Here I was, walking into the doctor's office, thinking that the worst thing I was going to have to deal with over the next few months was some radiation burns and maybe some more diarrhea.

Then, the bombshell.

I'm trying to be okay with it, but it's hard.  I have moments where I'm ready for the battle, in the mode to fight again, and ready to show this fucking cancer who's boss.

And then, almost immediately, I have this fear that grips my heart, messes with my head, and starts to put little niggles of doubt into my soul.  I start to get angry.

I haven't been angry much about what I've been going through.  I feel like it's just my battle to face, and I'm lucky to have the most amazing people all over the world supporting me.   But, it's hard not to get angry.

I want to be normal.  I would give my left arm to be normal.  Just to have a few years of calm, of the simple life, or a non-cancer life.  But, that doesn't appear to be my lot in life.

And it pisses me off.  I am so damn angry.  I shouldn't have to keep making phone calls that make my husband worry, that terrify my parents, that worry my brothers.  I shouldn't have to keep telling my children that Mommy has to go through yet another round of treatment because the cancer has come back.

I should have made more phone calls yesterday, to the people who have been by my side and have been essential to my family and me.  I didn't.  I couldn't.  I just couldn't bear the thought of going through my contact list, and trying to remember who I've called.  Telling people the same story over and over is mentally exhausting.  I feel like I chickened out, and that makes me angry.

I hate what I'm about to face.  I despise the IV chemo, and the way it makes me feel.  I hate walking into CTCA of my own accord, knowing full well that I'm walking in there to get poisoned.  I hate walking out of there, holding on to my caregiver (this next week, it will be my mom), because I can't stand up on my own.

But, I will.  I have to.

I don't know what the future holds for me.  I don't know how long I have, or how much time I have left here on this planet.  I don't know how the cancer is going to react to this chemo, and whether this will work.

Here's what I do know:

I have a birthday coming up next month.  I will not do chemo on my birthday; well, I will do my oral Xeloda, but no IV chemo.  I will, however, have a kick-ass celebration of the fact that I've made it another year.  My birthday's on June 21st - who's up for a rowdy celebration?  And, who wants to help me plan it?  I'm thinking it will be on June 22nd - y'all in?

Just because I have cancer and treatment doesn't mean I can't look good.  So, on that note, I went this morning and got my nails and toes done.  I did a wild orange-ish pink color on my toes.  I got some looks of condescension from some of the older ladies there.  I'm sure my tattooed, mohawked, bright colored self threw them for a loop.  Screw 'em - I'm just sorry they spend their energies in that manner.

I have started writing letters to my kids.  I figure that, if I start planning things, I won't need them for a while.  So, on that note, I'm also going to start revising out will and making sure that all of my important documents are in order.  I don't want to, but I have to.

I will remind myself to live each day to the fullest.  It's not about big, huge memories, but about the moments.  When I look back on my childhood, I remember some big events, but it's more the sense of home, of family, of security, of love. I want that for my children.  So, I'm going to make sure that's what I give them.  I won't plan elaborate things; I don't know if I'll be up for them.  But, I will make sure that I listen to what they have to say.  I will listen as they babble, trying to tell a story and searching frantically for the right word.  Each word they say is important, even if it doesn't make any sense.  I will use each day to make small moments with my husband; we've had a rough go of it lately (more on that in another post), and I can honestly say that I'm finally falling back in love with the man I adore.  Small moments with him are amazing, like when he holds my hand in bed at night as we fall asleep.  That is the kind of moment I will remember always, and I hope he does, too.

I still have too many things to do, so I'm going to try to get them done.  And, if I don't?  That's okay.  At least I tried.
**********************************
I am going to end here.  I had some things that needed to be said, and usually, putting them here in a posting that rambles and makes no sense helps my brain put it into place.  That's what this one did.  So, thanks for reading, and let's kick this cancer's ass again!

Comments:

Breaks my heart that you're still having to go through this. I want this cancer crap to be a distant memory in your mind that rarely, if ever, pops up!
May 17, 2013 at 4:33 PM
Blogger Una said...
Michelle, I found your blog through a friend fighting as well. I'm so sorry that you can't get a break from this demon. Keep fighting, you will win this battle. Know that there's another person pulling for you!
Una
May 18, 2013 at 4:05 PM
OpenID runningawayintn said...
I have no huge words of wisdom. And I know I rarely post a comment. And I realize you don't know me from Adam (or Eve). But know that I am thinking of you and giving you a big old cyber HUG....And I'm sending you every possible type of thought and vibe I have to help you wage this war.
May 20, 2013 at 7:13 AM
Blogger MsEpicAwesome said...
First of all, I don’t have cancer. You don’t know me. I came across your blog by accident because I was looking up the symptoms of what a “swollen uterus” could be since it’s not a pregnancy. I can’t get into my doctor until July 10th for a pap smear and full physical but my uterus, to me, appears swollen and of course I’m trying to talk myself out of things it could be – but every thing always comes back “cancer”. My aunt had bone cancer and now blood cancer but in the 80s she drank a ton of Tab, she has a poor diet, she smoked a lot – and she was notorious for taking “diet” pills – tons of them (she’s on my mom’s side). My uncle who worked as a railroad engineer (on my dad’s side of the family) had throat cancer from drinking/smoking. We don’t get cancer normally in our family. We die of Alzheimer’s or heart disease, usually the latter.
So I came across your blog and I thought, “Now I like this chick! She’s pretty awesome and I can read about her and just learn.” Well, honestly, I feel like I had to respond to this post even as a stranger.

You have every right to be angry. Use your anger! I take my anger and write poems. Then I self-publish books and print copies for loved ones. I think you could write whatever it is you want to write for your kids and self publish a book on lulu.com, no joke. It’s something your children will have *forever*, even if you don’t pass from cancer. Even if you live to be 80 years old and get hit by a flying scooter on your way to bingo – your kids will keep this book.

You can write poems, you can write short stories, you can write the same word over and over again and order copies. And it’s yours and your family’s forever. I’m actually working on a second batch of poetry (for a book) and my son has a copy of my first one and so do a few other close family members who wanted one.

I’m not sick that I know of, but I’ve had atrocities happen to me throughout my life and I use my anger constructively (sometimes let’s face it, destructively) – but over all I’m a better person for using what I’m given in this life to my advantage and not allowing it to pigeon hole me into a corner of fear, hate, despair, and all the negativity that comes with allowing too much anger in.
Anger is normal. I was angry my mom died when I was five. I was angry my dad was verbally abusive and an alcoholic. I’m angry that my dad died when I was nineteen.
I’m angry my first boyfriend/fiancé was physically abusive to me (I had a son with him). I’m angry he cheated on me. I’m angry my *next* fiancé cheated on me and treated me badly (no abuse though, I learned that lesson), and sometimes I feel sad for myself because I’m bipolar ii and I can’t change it. It’s part of who I am, how I think what I know – but it also makes me more sensitive, caring, and I try harder then most people to be a good friend, so in a way maybe it’s a blessing?

It’s hard not to feel sorry for yourself sometimes, that’s normal. I remember getting booster shots as a child and pouting and crying like a baby – because I thought it was just soooo unfair. And you know what, to a five year old – it was unfair! I’d been good that day, why do I have to get a shot?

I occasionally still obsess about what happens to us when we pass on. I went so far as to conducting electronic voice phenomenon recordings around the Midwest to prove you don’t just stop existing when you pass (and believe me, I can share my proof and you’d be surprised). This made me feel a little better – but really, where do we go? I wanted some sort of proof and in a weird way, I got it.

I don’t fear death now, which is good – but I do fear how I may die. I figure though focusing on it cancels out the time I have left here, the things I can do, the people I can help, who I can love/how I can love, and all the wonderful parts of life no one wants to miss.

I will never refuse to pass on feeling angry about something, because you need to. You need to have all emotions (jealousy, hatred, love, fear, etc) – because that’s how we live.
May 21, 2013 at 1:06 PM
Blogger MsEpicAwesome said...

Deathly Journey
I do not fear death.
I fear the flickering of tongues
not telling my story.
I fear my name being forgotten
among laughter and tears.

I fear my legacy being the faults
I gravitated toward.
I fear the sadness my loved ones
may not feel.
I fear the dark of uncertainty.

I fear the release in being free.
I fear the existence that I'm not so
sure continues to exist,
because it's an existence I cannot see.

I fear the pain in the end.
I fear the bravery and peace I may feel.
I fear the fact that I might be looking
forward to an end in sight,
and maybe living won't be such a big deal.

I fear gasping for breath,
and losing myself to my death.
I fear people wondering if my last wishes are honored,
or if they could do more.

I fear people looking at my empty body.
I fear being buried under dirt,
and suffocation if I weren't really dead.
I fear the fire touching my skin
and turning me into ashes instead.

I fear a list of plenty,
my dear sweet friend.
I pray I may one day let go,
as each journey must come to an end.
May 21, 2013 at 1:07 PM

Thursday, May 16, 2013

MAY 16, 2013


I am getting really, really tired of writing these types of posts.

I had an appointment with my med-onc, Dr. Kundranda, today.  I had no idea that the meeting was going to go the way it did; no one did.

Yesterday, I had bloodwork drawn.  Routine labs, nothing to be worried about.

But there is.  To confirm his suspicions, Dr. K. ran a CEA test.  My numbers are back up, from 6.6 to 10.1. This is not good.  Looking at that, plus the increase in my lung nodules....we are looking at the cancer rearing it's ugly head again.

Long story short, I will be starting chemotherapy again on Tuesday.  I will be on Oxalipalantin, Xeloda, and Avastin.  I was on the Ox back in 2008, and never, ever imagined that I'd be back on it again.  But, here we are.

The Xeoda has been pretty steady for a while, and we are looking at a potential increase in dosage, after this first treatment.  The Avastin will be used to kill off the blood supply to the tumors in my lungs.

Each cycle will be 21 days - Avastin and Ox (plus all the necessary pre-meds) on day one, and starting 14 days of Xeloda on this day.  Once I complete 14 days of Xeloda, I get a 7 day break until we start the next round.  We are looking at 3-4 rounds of this.  Dr. K. is going to test my CEA after the first round (movement 5 points one way or the other is acceptable; 50 points is not), then won't touch it again until we are done after round 3 or 4.

The hope is that we will be able to get this cancer back in check, and to use the Avastin and Xeloda as maintenance after 3 or 4 rounds of chemo.

I think he is planning to send out my tumor cells from the most recent surgery (in January) to a company that CTCA just partnered with, and this will give us more information on how we can treat this damn cancer in the future.

There was so much information thrown at me today, so I know I'm not reporting everything, and some information may be wrong.  My head is so full today; my heart is so damned heavy.  I'm just worn down, and need to give my brain (and my heart) time to accept and process what happened today.
****************************
On a fairly ironic note, right after this appointment today, I had a television interview with some local stations and with Grumpy Cat.  You may be familiar with Grumpy (aka, Tartar Sauce).  She's become an internet sensation, and is known for memes like some of my favorites, below.



Anywhoo, Grumpy came to CTCA today, and we (meaning me and ole' GC) were interviewed by local news stations.  I got to hold her (she's so damn tiny, and so much cuter in person that any meme could possibly show), and almost didn't give her back.  I honestly have NO idea what I said on camera today - I had literally just come out of the "Now you have to have more chemo" appointment, and had to pull it together for this.  I hope I didn't stumble over my words, or come off as a jackass.

Anyways, that's been my day.  Prayers, good mojo, positive vibes, and cancer ass-kicking thoughts all welcome.  Another battle....the war isn't over yet.

My army.....ENGAGE!!!

Comments:

Tina said...
Cancer sucks!!! So sorry you got bad news today. And the oxaliplatin...well we all know that sucks!
You are in my prayers, and you've got your army behind you!
May 16, 2013 at 5:52 PM
Blogger Mara said...
If you need anything, let me know! My heart is breaking for you and your family but you will kick cancers ass again!
May 16, 2013 at 5:57 PM
Blogger Carol Pack Urban said...
I am so thankful your doctor and you have s game plan to work with! I am praying!
May 16, 2013 at 9:17 PM
Blogger Tambre said...

You are one of the strongest people I know. Sending you tons of healing energy as you take these next steps. You are a fighter and a role model showing people to never give up. You and your family are being held in a circle of love by your community. It's an honor to know you.
Namaste,
Tambre
May 17, 2013 at 8:09 AM

Friday, May 10, 2013

MAY 10, 2013


Well, today was long and tiring.  But, apparently, well worth it.

My tests were quick, especially because they were able to have me drink the CT prep while I was getting ready for the MRI.  It made things go much quicker.

Anyways, after I got lunch (thanks, Dad!) and a quick nap at home, I got the phone call from Kia, my PA.  The MRI is normal and shows no spinal stenosis, no bulging discs, no herniated discs.  This is all good, but it still lends the question as to what the heck is causing my back pain.  I think I'm going to need to revisit the potential spinal block.

And, the CT scan showed everything as stable.  There are no new tumors that popped up, and there was minimal growth in the lungs, which they aren't worried about, because there are no new ones popping up.  Additionally, there was some shrinkage in the lymph node in my hip area (down to 8mm from 11mm), and the periaortic lymph nodes are stable, which means we will likely continue with the radiation next week.

All in all, good news!  Thanks for the good wishes!

Comments:

ALRIGHT!
May 10, 2013 at 8:17 PM
Blogger Lesley said...

I follow your blog avidly. So glad to hear the good news!
May 11, 2013 at 10:16 AM

Thursday, May 9, 2013

MAY 9, 2013


So, tomorrow brings with it no food or drink after I go to bed tonight, an IV (blech), an MRI where I will get knocked out, a CT scan where I have to drink the contrast and have it IV'd into me....

*sigh*

I'm having the CT scan, ordered by Dr. Chong, my rad onc.  I scheduled the MRI tomorrow (to try to figure out why I'm still having back pain) for the same time, trying to get it all done in one shot, since I'll need a driver/caregiver for both scans.  In hindsight, though, this may not have been the smartest plan I've ever had.

This is especially true because my body has decided that it will no longer accept any dairy, and will promptly and completely reject if, if I'm stupid enough to ingest it.  So, I've been super, ridiculously, obscenely tired today, since I had some ice cream last night.

*another sigh*

I will have a phone call from Dr. Kundranda's PA, Kia, tomorrow with the results of my CT and MRI, especially if something shows up.

So, yes....scanxiety is definitely rearing it's ugly head.  I'm anxious that they may find something.  I'm anxious that some rogue cancer will have decided to find a new place to tumorize (is that a word?), and this will change our gameplan.  That is, right now, my biggest fear.

Given that, it's probably best that I will be knocked out/in recovery for most of the day tomorrow.
**********************************
I returned to work this week, part-time.  It was exhausting (and, in hindsight, I shouldn't have gone in both Monday *and* Tuesday), and I probably (likely?) overdid it this week.  I was feeling so good, though.  It was so nice to be able to work a few hours, come home, cook my family dinner, clean up after the mess I made....and, yes, in typing that, I see the flawed thinking.

So, from here on out, I will be limiting myself to a maximum of ONE day per week in the office until I am able to go back full time.  And, that will be if and only if I'm feeling up to it.  If I'm not - that's what they made webcams and phones for.  :)
***********************************
Right now, my radiation simulation (where they figure out the dosing, machine, location, etc.) for my next phase of treatment is scheduled for this coming Wednesday.  Assuming all is well, and nothing odd shows up on the scans tomorrow.  I am in for 30 more rounds of radiation, with a weekly determination made on whether I continue with Xeloda.  Right now, we are going to hold off until my body is stronger and feeling better.  Thank God....
***********************************
This weekend, an old friend of mine, Jason, and his partner Jeff are coming into town.  I am super excited - the last time I saw them was back in 2008, when I was going through chemo the first time.  They are coming over on Saturday for a BBQ, then we are going to spend Sunday at my parents' house to celebrate Mother's Day!  I can't wait!  I'm hoping I'm feeling better by then....

And, with that, I'll post this and spend more time with my family.  I'm on the lookout for an on-line game that tests Julia (and Kevin) on the states, their locations in the union, and their capitals.  If you know of one, please let me know!

Comments:

Michelle...you are a lovely writer. And I shall be sending you those wickedly powerful great vibes in your direction tomorrow....
love to you,
erika
mayor: COLONTOWN
May 9, 2013 at 8:41 PM
Blogger Carol Pack Urban said...
Praying everything goes well tomorrow and that you sleep well tonight. You can sleep all day tomorrow, too. :)
May 9, 2013 at 9:31 PM
Blogger Amie said...
Your blogs are always so inspiring, vulnerable, and real. Keep strong and keep being you, Michelle. love you and will be thinking of you - xoxo
May 10, 2013 at 12:53 PM

Later:



I was asked to take part in a newspaper article about living with cancer - here's the link!  They got a few of the details wrong, so I updated my part of the story in the comments, but it's still a good article for those who are newly diagnosed.  Super excited!

http://www.azcentral.com/healthyliving/articles/20130502support-groups-classes-help-cancer.html

Sunday, May 5, 2013

MAY 5, 2013


Well, I saw both my med-onc and my rad-onc this week.  There is a small change in plans.  I didn't think we were going to do a CT scan until after this was all done.  Dr. Chong told me this past Friday that while he plans to proceed with the second phase of radiation, he wants to do a CT scan this week, just to see what's going on inside of this crazy body of mine.

This is a double-edged sward for me.  It's good that I get another week (maybe a bit more) of rest and will (hopefully) continue to get better.  It also means that I'm now fighting off scanxiety.

*sigh*

So, I'm trying to focus on (and not panic about) the fact that I return to work tomorrow.  It's part-time, and mostly from home, but still....I'm just hoping that I do okay.  I don't know why I'm nervous - Levi thinks I'm crazy.  He keeps reminding me that I've been doing this job for over 5 years.  It's just hard thinking about returning to work, after being through so much.  I'm trying to just remember to take care of me, and to not overdo it.

But, I desperately need to get back to doing something that has nothing whatsoever with cancer.  So, it's with excitement and anxiety and fear and hope that I go back tomorrow.

I will say that I am feeling better and better.  My body seems to be better handling a wider variety of foods (yeah!), and I'm feeling stronger and more aware each day.

Here's to a week filled with hope, good (amazing?) scans, and a fabulously easy and fun week back at work!

Comments:

Thandi said...
Hear hear!
May 5, 2013 at 11:44 PM
Blogger Lesley said...

Good luck with the scan!
May 6, 2013 at 11:50 AM