Thursday, October 30, 2008

OCTOBER 30, 2008


Really quick, since I still feel like crap. Made it through yet another round. Levi's still looking for a job, and has officially applied for unemployment. This round of chemo made me so sick that I actually had to ask for the bucket at the drs office. Thank goodness I didn't need it, but it came pretty close a couple of times. The nausea has been almost completely unbearable, and I can't imagine what it would be like going through this without my tanker full of anti-nausea drugs.

I am done, though. Neuropathy (the tingling and numbness from the chemo - not the cold sensitivity) was really bad this time. I am struggling to type today (if you see a typo, blame the chemo), and opening pill bottles is almost impossible. My fingers and toes are numb bu tso sensitive at the same time - it's an odd sensation that I can't explain. I mentioned it to the nurse today, and she set me up with an appt with Bill (my PA) on Wednesday.

Halloween is tomorrow - I am hoping that the nausea starts to go away. I tried another new anti med today - didn't do a thing.

As my mom said, the depression hasn't kicked in...yet. Maybe now's the time. I know I am fighting, and I know I have to, but I am so tired......here's hoping......

More tomorrow...if I can still type! :-)
Comments:
happy Halloween!

I am so praying that you are feeling better. We are also praying for Levi. 

we love you... 
remember - journaling is a great way to help with the down moments. just get it out by writing...
October 31, 2008 at 9:42 AM


Monday, October 27, 2008

OCTOBER 27, 2008


Wow - it's hard to believe it's been that long since I posted. It's been quite a week. Let's start with the big news - unfortunately, Levi lost his job last week. Last week was spent freaking out, wondering what in the world we are going to do. I got the call on last Tuesday morning, got confirmation on Tuesday evening, and spent the next day watching the planes (count them, FOUR layovers) that were bringing my husband home.

When he got here, I finally felt, well, whole again. One of my best friends mentioned to me that maybe the reason he is here is that whatever "Being" you believe in (I choose not to use this forum for my religious beliefs, so fill in "Being" with what you believe in) knew that I needed the support here, in Phoenix. So, I am hoping that that's the case, although if I end up in the hospital I will be pretty pissed off. :-)

So, we spent this weekend looking for jobs for him, and it feels like we applied him to a hundred positions. The waiting now begins. We are still searching for a telecommunications position, but ideally, we are looking to move him into another, more stable line of work. So, if you know of anyone in the Phoenix area looking for a decent, hard-working, reliable, mechanically-inclined, intelligent person with his own vehicle and that speaks English.....let me know. He's available YESTERDAY!!!!

Let's see - what else. I have to think about it. Um, I made it through the last round of chemo with some pretty rough side effects.....nausea being the worst of them. I am DREADING the nausea tomorrow, but I know it needs to happen. Again, it's the old "heart versus the head" conflict, and while I know that I need to go through this, I don't want to. Although, it will be nice to be at the end of this next week and to be able to say "I only have 2 more treatments..."

I did have a doctor's appointment with the PA last Friday. It went really well. My bloodwork looks fantastic, and all of the side effects that have gotten worse (nausea, neuropathy, and sensitivity to cold) are totally normal. Not fun, but normal. And, (this is a huge maybe) they might discontinue the Oxalipalantin (the nasty drug with the most horrific side effects) after this round, b/c of the neuropathy. There won't be any kind of negative effect on my prognosis at this point if we discontinue it, so here's hoping! (I know, there are people out there that will tell me to continue it.....we'll see what happens....)

What else? There is so much, but I have been SO busy this past week. We took the kids to a Hallweeen Bash in town this weekend, which was fun getting the kids dressed up. It was especially nice for me b/c I will only be a day out of chemo and thoroughly unable to enjoy Halloween on Friday.

Um, I think that's about it. As you can probably tell, I am still pretty depressed about the job thing, and I am struggling to maintain a positive attitude. But, I know that we will make it through this, and be better people on the other side. So, please, happy thoughts our way. It's going to be a rough(er) road than expected, but we are strong, and we will make it through.

Comments:

jnwhiteh said...
Of ALL of the places to find people spamming for World of Warcraft gold. For those of you that don't know, this is a black market that sells in-game goods for real money.

How bizarre! Michelle, if you can remove the comment, feel free.. this is just spam.
October 28, 2008 at 3:25 AM
Blogger Amanda: said...
Eek about the job loss - but I will say that I agree that it happened for a reason, and I'm sure that will be revealed in the future. But, on that same hand, I know how tough the "little things" can be during treatment, and this is a "big thing" regardless of everything else, so I will be sending positive thoughts your way. Here's hoping the side effects are minimal this time around(hey, it could happen!). Hang in there... you're getting closer and closer to the end of all this.
October 28, 2008 at 7:25 AM

Later:


You know how I am raising money for the Undy 5000? (If you don't , please click on "Support My Team Here" on the right-hand side of this blog!) Well, I am $50 away from my goal of $1,000. Can you imagine? I never thought I would make it to that, much less be able to blow that number out of the water. And, it looks like that's what's going to happen - maybe I shoudl raise my goal to $1,500?

Wow - I am blown away by people's generosity and support of me through this journey. I have had people donate to my cause that I don't know. I have had people donate to this that I never would have expected. And, I have had more people donate than I thought possible....

So, to all of you who have been SO generous with your contributions, thanks just isn't enough. Your contributions will be put to good use, to try to prevent and beat this horrible disease. Thank you a million times.

And, if you haven't had a chance yet to donate, the walk/run is less than a month away. November 15th is almost here. Please consider donating whatever you can spare - $5? $10? $25? Everything helps.

Again, thank you for your support - you are all my angels, and MY inspiration.

Friday, October 17, 2008

OCTOBER 17, 2008


I think the hardest part of chemo at this point isn't so much the physical demand it places on my body, but the emotional and mental drain it has on my spirit. I expect the physical demand - you have to. You are literally pumping chemicals into your body that are meant to seek and destroy cancer cells. Along the way, unfortunately, they also do the same to healthy, good cells, so there are losses on that front, but you have to take the good with the bad. And, knowing that going through this will get me through to the other side makes taking the pills, dealing with the pain, and handling the nausea a little easier.

However, the mental drain at this point is so hard. I feel like I can see the end. It's RIGHT there. And yet, with each treatment and cycle, it gets harder and harder to recover physically, which is so tough to take emotionally. You want to feel good - mentally, you feel like you should be able to conquer the world. But, your body says no way. Mentally, you know that you are capable of SO MUCH more. I know that I can take care of my kids. I know that I can take care of my husband. My house. Decorating for the holidays. Taking Julia to her carnival tonight. Playing with Kevin so he doesn't wake my dad up 6 times each night. But, I can't. I can't do those things right now. Because of the cancer.

I want so badly to live life again. And, I know that next week, I will start feeling better, I will start working again, and I will go back to living the "life inside cancer". When push comes to shove, I just want to live life without cancer again. I know that I will get there. I will always be a survivor (I think that's the first time I have used that term here!), but I can't wait to get to that point. I want to get to the point where cancer isn't the single most ruling figure in my life. I want to get to the point where I am the one making the decisions, not chemo, not doctors appointments, and certainly not the side-effects.

Please don't feel badly for me. I don't post these feelings to gain sympathy, or to have people feel sorry for me. Quite the contrary - I post these feelings b/c they are what I am feeling. I know that there are people reading this blog that aren't able to express their feelings, but that might be able to finally get a sense that someone else is having the same ideas, the same sadness, the same fleeting hopelessness. And, it is fleeting. If you go back through my blog, you will see that I typically get depressed on the Friday after chemo. In my mind, here's why.

I have made it through another round of chemotherapy. The pump has been removed, I got my shot, and I am recovering from the chemo. But, instead of feeling better on Friday, I feel worse. Yesterday, for example, I felt great in the morning. By afternoon, I was so nauseous, I thought I was going to be sick all over the house, and confined myself to the bedroom, so that I was never far from the bathroom. Meds helped, but only a bit. Today, I should be feeling better, and I do, but still not to the point where I feel good. It's 1pm, and I still haven't showered. (Heading there - honest, I am!) It is so frustrating to be here, confined to the house, knowing that life goes on outside of the house. Knowing that my kids are living their lives, and I can't be an active participant today. Knowing that my family is living their lives (except for my poor father, who is stuck here with me!), knowing that work goes on, school goes on, and the world still continues to turn. And, I can't take part. Yet.

I think the "yet" is my problem. I am kind of a "immediate gratification" person. If I pay for something, I don't want to have to wait to have it delivered. I want it now. If I ask for something, I want to know it's coming, now. As a kid, Christmas Eve was hard, b/c I knew Santa was coming *soon* and I would wait up for hours. I couldn't sleep, knowing that come daybreak, it would be a glorious day. I don't do well with waiting for things. And, this isn't helping. I am not doing well waiting for the last day of chemo to arrive. For the next PET scan, so that I can be declared "cancer-free!" I am not doing well waiting for the end of this ordeal. I want it done, now. And, it isn't. Yet.

But, there is hope is the word yet. It implies that the end is coming. It implies a solution to a problem. And, mine is here. Chemo is (God willing) the solution to this problem, for lack of a better term. I know - that's very simplistic. But, sometimes, that's what helps me get through. Simple things.

So, here's my list of simple things today. I am going to finish this post (right after I spell check it!). I am going to get my shower, then probably take a short nap. Then, I will wait while my Dad picks up my babies, and I will enjoy the time I have with them. I will call my husband (who is back in FL, in case anyone is counting!), and I will get to bed at a reasonable hour. And, I will make it to tomorrow, and hopefully feel better than I do today.

How's that for a simple to-do list?
Comments:
Happy said...
Hi Michelle,
Just wanted to tell you that I have thought of you every day since we have met. Know that you are in my heart and prayers. Who would of thought that Craigslist would bring me a person like you. My aunt just got her port put in yesterday and will begin chemo next week. Even though I know chemo is tough I also know this is the way to full recovery. Unlike my little friend (my neighbors daughter) who will soon finish her fight will cancer, my aunt caught it on time. My friend is now 78% cancer and isn't given much hope. (1-2 Weeks max) I'm sadden but at the same time glad to know that God will recieve her with open arms. I hope that you feel better and if you ever need anything, anything at all feel free to call me. (I'll e-mail you my number) I'm sure I won't be called on much, you seem to have a wonderful support group. God Bless You and your family,
Feliz Reyes
P.S. Seen you on the News!! You go Girl
October 18, 2008 at 10:13 PM
Blogger Amanda: said...
I promise it's not this hard forever. Some days, I kid you not, I would focus on making it through the next 15 minutes because I couldn't handle any more than that. But, 15 minutes at a time, we got through it. You will too. I wish I had more advice or support to offer you, but please know I think of you daily.
October 21, 2008 at 7:03 AM


Wednesday, October 15, 2008

OCTOBER 15, 2008


Well, if it's any indication to you, I am posting during chemo, so I suppose that tells you that I am having a pretty decent (relatively speaking) round of chemo. Yesterday sucked. I was nauseous more then I have been, ever, but I am pretty sure I can relate that back to the Burger King breakfast I ate (I haven't eaten at a place like that in MONTHS), and I can't imagine that grease was good for me. So, yesterday, I slept pretty much the entire day away, but today I am feeling better. Not great, but better.

I met this wonderful lady today at chemo that I am hoping I gave some hope to. She was diagnosed with (I think) uterine cancer earlier this year, had surgery, was told she was cured, and then last month was diagnosed with stage 4 cancer, meaning that her original cancer had metastasized into other organs. So sad. And, she was pretty depressed, but I hope that I provided her with some resources to help her out. Maureen, if you see this, know that I am thinking of you.

So, I won't post too much more, but thanks to all for your good wishes. The concert was a blast, and having the TV interview to share with others was a blessing, for me. What a chance. I thought it came off well, and that I looked pretty damn good for someone going through what I am going through! LOL! (Ego hasn't been affected, can you tell?)

Comments:

Maurmmreadmis said...
Hi Michelle, It was great meeting you at chemo. I have been thinking about you also and told my family about you. You gave me some very useful information that I will use. I hope I run into you again at chemo, the time went by fast chatting and you did give me some hope. Take care and hope to see you again.
Maureen
October 16, 2008 at 6:53 PM


Monday, October 13, 2008

OCTOBER 13, 2008


My mom has a friend, Shelley, who is good friends with the news director at the local Fox news station. In talking with her, Shelley mentioned my story and they became interested in it as a human interest story.


Well, with tonight being the New Kids concert (Woo!!!), they are doing a story on the concert, and thought that this would be a great tie-in for me! Oh my goodness. The lady is going to be here in about an hour and a half, and they are going to interview me at the house, then apparently we are going to meet back up at the concert and they are going to record video of Julia and I heading into the concert. 

It will be on the 9 and 10 o'clock news tonight. Channel 10. 

Do you think I might be able to ask for backstage passes?!?! It can't hurt, right? :-) 

I have to clean my house now. Um. Hmm. So much for relaxing. Anyways, I will post more when I have more information. And, if I am able to get pictures, I will TOTALLY post those as well. 

WOO! New Kids!



Later:


Now, I know that there are going to be people who don't care about these pictures. Tough - I also know ther are people who are going to want to see them. Please remember that I do not have a decent camera, and took what I could.



My boys....I had such great seats. Thanks to my company for providing them. It was truly a gift that I recieved them, and I am so grateful. And, I highly recommend the suite tickets if you can afford them - very nice!!!


Sigh - such a handsome (HOT!!!) group. When I was younger, I don't think I would have ever imagined taking my daughter to this concert. And, I can't imagine that I ever thought about what these guys would look like 15 years later. However, I wanted to buy a poster for MY wall - just hot! All of them - I have no favorites. Well, I do. Joey, always. Donnie - yum! :-)

Dancing on stage. They are such great performers.
 

This is the circular stage that they moved to halfway through the concert. It was almost at the opposite end of the arena, so it afforded everyone a different view. I don't think the people in the first rows were happy, but everyone else was.

Sigh - such a great concert. I wish that I could have stayed for the entire thing, but then again, I wish I didn't have cancer, so I guess you can't get everything you want. Oh well. :-)

Comments:

ahhh! this is great! great pics! did julia have a great time? What happened with Fox news? I am very tempted to stop at target on the way home and pick up their new cd... I am so glad that you had a great time. Take that energy with you this week going into ROUND NINE, baby! 

hugs from michigan

October 14, 2008 at 4:43 AM

Later:




Before you read this, you should really click on the above link and click "play" on the screen. Then, come back and read this....

Okay, assuming you have seen the TV program. Yes, that's Julia and I from tonight. As I said in my previous post, this came about because of the work of my mom's friend, and Shelley - thank you! I can't wait to meet you in person and give you a BIG hug!

Basically, the new station (Fox 10 in Phoenix) wanted to do a story on me as a human interest story, and thought the tie-in from tonight's concert was a perfect fit. While I wished that they had focused more on WHY I am such an advocate for colon cncer awareness, they did post a link to the Colon Cancer Alliance on their webpage, so that's something, I suppose. Anyways, I am pretty happy with how it turned out, how I looked, etc. :-) LOL! Of all the things to worry about...

Anywhoo, it was a great experience, and remided me that I can TOTALLY handle televisin interviews. It wasn't nearly as bad as thought, and they had a cute cameraman, which helped. (If you are familiar with country music at all, he looked like Blake Shelton.)

And, the concert. OH, the concert. I will say that I am bummed that I didn't feel as good as I would have liked to for this event. I noticed that I got tired so quickly, and wasn't able to scream quite as loud as I would have liked. (That's all right - Julia helped in that area!) But, the concert was wonderful. If you are a NKTB fan (even if you're not), you HAVE to check out their new CD. It's completely different from their previous music, and totally awesome. Very hip-hop, R&B feel. VERY sexy. No really, it is. They use some un-kid-friendly terms, and luckily, Julia didn't pick up on any of those.

The opening act (the one I recognized, anyways) was Natasha Bedingfield. GREAT voice, awesome performance. Then, on came the main act - whoo! Awesome. Just great. They played a mix of the old and the new, and it was just a great show. They started out on stage, then half-way through their show, moved to a small, circular stage with a piano that turned. Very cool. Julia and I had to leave early (someone - and it wasn't me - was tired and getting cranky, and the music was super loud, so her ears were bothering her....), but I am pretty sure it was towards the end of their performance, except for the encore. I am bummed that I didn't get to stay for the whole thing, but I am so glad that I went, and got to share this with Julia.

She did finid a favorite, much to my amusement and pride. After their first song, she sked me who the one in the pink shirt was. It was Joey McIntyre, who was my FAVORITE when I was younger. I am so proud. I bought her a poster, so she can put it up in her room. When she finally wakes up. LOL!

Overall, it was a pretty cool night. I will post pictures in the next post.


Comments:

THAT WAS SOOO COOL....man i wish i could have gone with you we could have stalked them after!!

You looked great on camera and i am so proud of you that you are being used in a good way even in your own trial. You are such a beautiful soul and I am blessed to know you.

October 14, 2008 at 7:34 AM
OpenID wyldirsh123 said...
OMG!!! You're interview was great and you look amazing! I love the short funky hairstyle on your Michelle! It kind of reminds me of my haircut! :-) Anyway, I'm so glad they interviewed you and you spoke so well... as you always do. You have such a knack for writing and speaking... so professional! And the concert looked amazing, as did your pictures. Wish I could've been there with you & Julia enjoying NKOTB. So great to see you in video, not just pics! Take care & talk to you soon! Murph
October 14, 2008 at 8:31 AM
Blogger Amanda: said...
Oh wow! You did SO great with the news people! Trust me - I KNOW how nerve-wracking that is :)


I'm so glad you had a good time - what an awesome thing for you!!!!!



Oh - in case I didn't mention it before, I LOVED Joey when I was a little girl - he was just so dreamy!!

October 14, 2008 at 9:03 AM

you are fabulous. 

you also made me cry!
what an incredible memory - and you have it all on tape. 
you are my inspiration... 
enough said...

October 14, 2008 at 5:19 PM

Sunday, October 5, 2008

OCTOBER 5, 2008


The thing about trying to be on virtual bed rest during the week of chemo and the few days after is that I tend to think about things. Sometimes, those things are silly and meaningless (like, um, I don't know - why haven't they brought back the Smurfs, but they brought back the Chipmunks?). Sometimes, the more serious things make me take a moment more and really re-evaluate what I am thinking about.

Example - today, I am feeling pretty good. I know I need to take it easy, but it's hard when there is so much I want to do and I am finally feeling up to it (sort of). And then it dawned on me - I think part of the reason that I am so antsy to DO something is that I can still see the end of this journey. Well, this chemo part of it. I can anticipate the time, in the not-so-distant future, when I will once again be able to live normally. I won't have to schedule life and it's details around my chemo schedule. I won't have to worry about whether I can schedule something, based on whether I have chemo that week or not. I will be able to breathe each morning without counting the pills I have to take, or worrying about the side effects that day, or worrying about my energy level. I can't wait to get back to that point.

I don't think that means that I will go back to the chaotic, unrelenting, super-busy schedule that I had before. On the contrary, this cancer has led me to look at life in a different way. I recently finished reading Randy Pausch'sbook, "The Last Lecture." I imagine that you have at least heard of this guy before. He was diagnosed with terminal cancer, and instead of living his life mourning the loss of the time he thought he had, he lived his life laughing, spending quality time with his family, and making sure that he taught everyone he came in contact with a lesson about life. If you haven't read this, I highly recommend it. It's a quick, easy read, but means SO MUCH! Anyways, part of the book is how Randy's diagnosis led him to look at life more fully. He took the time to stop and smell the roses, as they say. And, in doing so, he created a legacy that most can only hope to achieve. I want to be like that - I want to make sure that I take the time to read my kids bedtime stories, and run outside with them, and do their homework, and kiss and hug them each day. I want to make sure that I take the time to listen to what Levi has to say, and to make sure he knows how MUCH I love him. I want to make sure I take the time to make phone calls to family and friends, to make sure that I do my best to put a smile on their face. And, I want to make sure that I take the time to appreciate my life. To appreciate me. To remember that this is my second chance at life.

I know you probably get sick of me talking about these ideas I have, talking about my advocacy for the CCA and colon cancer awareness. I am sure that you scan through these posts, and while I might make you smile or (occasionally) roll your eyes, I hope that I, every once in a while, make you think about your life. What would YOU do if you had to deal with a cancer diagnosis? How would you change your life? Would it make you reprioritizethings a little bit? Would hearing the sentence "You have cancer" make you look at your email less? Allow you the freedom to let the phone go to voicemail, rather than jumping up to get it? Would it give you the permission to spend more time with your kids? Your family? Your friends?

Please, keep something in mind. You don't have to wait for a cancer diagnosis. I beg of you, don't wait for that moment. It might be too late. Instead, take the time, today, RIGHT NOW, to stop and think about your life. Think about the stresses you are going through. Are they going to be important in an hour? a day? a month? a year? Will those pending deadlines at work have any bearing on your life, long term? Will those emails, if they don't get answered today, make a hoot of difference in the long run? I bet they won't.

If you think about it, the biggest things we have to worry about is how we treat other people. How we treat ourselves. How they treat us. And, how we deal with those people. Your legacy isn't going to have any relation to the amount of money you make. It isn't going to have any bearing on the type of house you live in, the kind of purse you carry, the clothes you wear, or the "things" you have. The legacy you leave, when it's all over, is going to have a direct relationship to your relationship with people. How you treated them. How you raised your kids. How you handled family issues. And, how much you laughed. (I am a firm believer in this last one....).

So, take five minutes today. Think about how you can affect your legacy by spending time away from the computer, the TV, the Internet. And, take a moment to spend time with your family. Truly, you don't know how much time you have left. Savor what you have - and, let me know how that works out for you.

Comments:
So very well said, Michelle.
I needed that. thanks for keeping me "in the moment"
you pretty much summed it all up.
thank you...
lots of love from Michigan,
Jen & Kevin
October 5, 2008 at 10:53 AM
Mick ever since I got the chance to be blessed to feel the movements of my little man inside my tummy, to smell his sweet baby skin, to nurture him, to love him and to watch him grow I have embraced all that you commissioned us to do. Because God blessed me with him I realize what charge I have been given as a mother. So in order to BE that person I want him to be I have to live it, not talk about it, not think about it...BE IT. So thank you for your words of encouragement because my legacy while small in stature is growing up to be quite a man.
October 10, 2008 at 5:19 PM


Saturday, October 4, 2008

OCTOBER 4, 2008



(Imagine for a moment the Elton John song "SATURDAY.") So, for the last couple of treatments, I have felt like crap up until Saturday night. It's not like I suddenly feel up to partying on Sat night.....no, I just notice a change in my demeanor, my mood, and my body. It's like my body is breathing a sigh of relief - she's done abusing me for the week, and I can start to heal. 

So, I just had to share with you all, especially after my last post. I am feeling better today. In spite of my cold, thank you very much. Yes, as if to add more to my pile of issues, I now have what I believe to be the beginnings of an upper respiratory infection. Yikes. I called this morning, and I am now on antibiotics, on top of everything else coursing through my body. Fun, right? 

Yeah. That's it. :-)

Friday, October 3, 2008

OCTOBER 3, 2008


Well, the good news is that I made it through another round of chemo with few problems. The combo of Tylenol and Advil seems to have made a huge difference in my response to the chemo, along with the forced bed rest and regular meals (thanks, Daddy!). I was able to eat some semblance of breakfast, lunch and dinner on all three chemo days, and while I wasn't the prettiest girl at the fall festival (insert sarcasm here), I made it through. Take that, cancer! 

However, the bad news that pretty much ruined my day on Thursday was that this was Round 7 of chemo, not Round 8. Because of the issues I had back in August with the hospital stay and the following treatment issues with fever, they want me to repeat a cycle, which means 13 cycles instead of 12, and that means that this whole damn chemo schedule gets pushed out 'til December. That just pissed me off to no end, I can tell you that. 

I was pretty upset yesterday - I think it was only the third time since I was diagnosed that I have cried about this whole thing. It's like the end of the tunnel, the proverbial light, was right there, within reach, and WHAP! It was yanked out of my reach. It's still there, but a bit dimmer than it was on Wednesday, when I still thought I was in round 8.

I guess the thing to remember is that things change, and that we have to do whatever we have to do to make sure we kick this cancer's ass. However, having now been in chemo for over 3 or 4 months, this whole thing is getting old. The treatments are starting to wear on me mentally as well as physically. I am feeling like an old lady, unable to do much of anything without assistance. I can't get up and go when I want to, mainly b/c I don't have the energy. I can't just do things that I mentally know I am capable of, b/c my damn body won't allow me to. This is probably the single most frustrating time of my life, b/c so few people can truly understand what it's like to feel this way. 

My family has been so supportive, but it's hard to hear "This is for the best" or "We have to do this to win this battle" when I am the one on the front line. I know that this is what I have to do. I get that, in my brain, I really do. I understand logically what needs to happen, why we have to repeat the cycle, etc. But, that doesn't mean that my heart is following suit. I think this is something that cancer patients deal with - the difference in opinion between their heart and their brain. It's a tough battle to deal with internally - you want to live life to its fullest, especially knowing that you have just been dealt a serious blow that could potentially shorten your time here on Earth. But, to prolong that time, you have to deal with the sickness, the gross feelings, the exhaustion, the pain, the suffering. All that to try to get to the other side. It's not an easy battle, that's for damn sure. 

So, while I am upbeat about being able to make it through yet another round of chemo without ending up in the ER, I am pretty sick and tired of being sick and tired, esp knowing it's going to be prolonged. But, again, I have to do it. What other choice is there? Giving up? Not an option.

Comments:
You are right it's not an option... don't get ahead of yourself. You are more than 70% there. Focus on the successful treatments. Take it a day at a time. I know it has to be hard. But do what you have to do, one extra round of treatment may equal being cancer-free for the rest of your life. Don't focus on the numbers (funny how I can use that in this case when my doctors were telling me that while in treatment) focus on one day closer to being cancer free...
So we may have to push or vegas trip back a few weeks, big deal... We love you! (and I love seeing you on Facebook! Is it great?)
October 3, 2008 at 12:34 PM
Blogger Amanda: said...
I'm sorry you have to repeat a round. I KNOW how important "the date of the last treatment" is, and it SUCKS when that gets pushed back. Keep on trucking. One day this will all be a memory :)
October 3, 2008 at 1:37 PM