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Cancer Schmancer…

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Archive for the ‘Chemotherapy’ Category

In the beginning…

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Yesterday marked my 6 month anniversary of having breast cancer.  Well formally I should add. I’ve had a few people ask how I found it and realized that I’ve never written about the days before my diagnosis.  So here goes…

 

I never use to do daily breast exams, I would mostly check them every few days or once a week or just when I thought of it.  It would make me feel uncomfortable and nervous when I did them and I always thought that since my breasts (and I guess all breasts in general) are lumpy I would never be able to tell if I did find a lump.  Well, I was wrong.  I was in the shower when I found my lump.  I remember reading or hearing about that being the best place to do your exam, and so mostly would check when I soaped up.  So I felt something different, but it wasn’t huge and I couldn’t feel it if I pressed hard.  It felt like a small pea, just under my skin and near where my underwire (of my bra)  would be.  I was concerned, but was also concerned over a small bump near the bridge of my nose.  I showed G both, he had a hard time finding the lump on by breast, like I said you had to feel the skin very lightly and it was small.  But I could feel it, and it was different.  I had a bad feeling about it.

I made an appointment with my doctor right away and went it the next day.  He was not concerned.  He said it was most likely from my underwire and told me not to worry.  He was a little wary over the bump on my nose as he had no idea what it could be so he sent me in for x-rays.  He told me return in a month and he would check things again.  It was a hard month for me, I got more and more concerned over the lump but tried to reassure myself.  I went in for the x-ray and went back to the doctor.  The x-ray results were good but very weird.  I had jaw surgery over 10 years ago, and the bump I could feel was the screw from the surgery.  I was and still very grossed out by that.  I guess I’m sorta like Frankenstein!  Grody! We talked more about the lump, and I pressed him again to get it checked out, he reassured me (again) that it was most likely nothing as I was so young and that it was small but he went ahead and booked me a mammogram.

The day of the mammogram was one of the worst days of my life.  I went there for 8 (I had told work that I was going to  be a little late but should be there for 9am)  I was nervous, but surprisingly not very much and just kind of wanted to get it over and done with.  I reassured myself time and again that it was nothing so I was beginning to believe it. I even told G not to come with me, I was just going to be in and out.  Now, I know differently and I never want anybody to be alone in this situation so please bring someone with you if you find a lump.  I never want anybody to have to go through what I did alone.

So, I got changed and sat in this little waiting area with a handful of other nervous looking women and my named was called and I was brought in for an ultrasound first, they told me they usually do the mammogram first but there was a delay.  There were 2 ladies doing the ultrasound and I pointed out where the lump was and they began.  They saw the lump on the machine and started talking to one another “do you see that?”  “oh wow look at that Aura!”  I asked them if everything was alright, as they were talking amongst themselves and they looked at me kind of like remembering I was still there.  “ummm yes, we are just going to get someone else in here to help read this”.  So one lady left, and the other remained silent, and I just lay there worried.  Two other people returned, and introduced themselves, and they kept talking and ultrasounding.  I remember laughing nervously because there were so many people talking and looking, but no-one was talking with me and one lady looked down at me and asked if I was ticklish. I lied and said yes.  They continued pointing to the the screen and talking amongst themselves, and I started to cry.  One of the doctors, finally recognizing me, asked if I had any questions and I asked the first thing that came to my head and I felt was the most important “Am I going to die?” and she said “no, we are going to take care of you.” And that was that, they didn’t tell me anything else and whisked me off to get a mammogram.  Right after the mammogram they told me I had to stay, and put me in a small room.  They told me they needed to get a hold of the surgeon to book an appointment.  I remember I asked so many times if I had cancer and was told nothing other than ‘we found something suspicious and can’t tell you more’.  I was told I was to have a biopsy for the lump and my lymph nodes.   I waited over an hour by myself in that room.  I called work to say I wasn’t coming in, I called my sister to ask about my grandmother who had cancer and to find out if other relatives had cancer.  I filled out forms after forms but had no answers and was so confused, nervous and scared.  It was horrible.  They finally got a hold of Dr. L (the surgeon) and booked an appointment for June 15.  I remember asking why I needed an appointment with a surgeon if they didn’t know it was cancer and was just told it was a formality.  Now, I know they knew it was cancer from the beginning.  The nurse told me on  the 15th that they knew all along, but they needed it to be confirmed 100% before telling me.

My experiences post mammogram were great, everyone was polite and very professional.  I did complain to the manager of the Breast Clinic about how unprofessional the workers were and she reassured me she would have a meeting with them.  I hope for other patients sake, she did.

I know that this post is very long winded.  Thank you for reading, and making it this far!  I do actually have a point in writing all this but I needed to explain my situation before getting to the reason I’m writing about this.

The point is, we are the only advocate that will totally fight for what we personally need.  We know our bodies, we can feel if something is not right, if something feels different or out of place.  Call it intuition.  If I had taken my doctor to his word, not to worry about it than I might not have pushed to get a mammogram.  My prognosis would be very different.  I’ve heard many stories like this, and the stories have happy endings ONLY because the people involved pushed to get the tests they needed and saw many, many different doctors and therapists.  They did not drop the ball on themselves and are here only because they advocated for themselves.  Trust your body and trust yourself, it’s only your life to lose and that is the most important thing of all.

 

Hippos and laughter

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It’s been a while since my last post.  I wish I could say that I was gallivanting around the town, riding hippos and granting wishes but alas I was mostly house bound.  My last Chemo round really hit me hard, and I’ve been mostly recouping from that.  I had a few too many glasses of wine the other night (yes Mom I can have wine during Chemo, but usually only a glass 🙂 ) and during this intoxicated state had a long conversation with G.  I was worried that he found me lazy.  I’ve been mostly doing a lot of nothing and when I do do stuff, I get SO tired.  Most of my days are spent in a daze, kind of a sleepy, pillow over the head feeling.  I have so many plans, ‘I’m going to clean the house from top to bottom’ but have SO much trouble doing it.  I feel guilty because so many people going through this are throwing up all the time and my only issues are gastrointestinal and tiredness.  I’ve read about woman who are going through it and their houses are spotless.  Mine is far from it, but I did manage to get most of my Christmas decorations up!  Hooray for small accomplishments!

Oh yes, back to my drunken conversation with G.  So I cried and told him that I felt guilty.  He laughed.  Yes, what a bastard.  Just kidding, we all know he’s wonderful.  But while laughing he reassured me that the Chemo affects everyone differently.  He told me that I can blame my horrible laziness on the Chemo!  So nothing is getting done today, other than beat my score (and everyone elses’s) on Bejeweled and the horrible addictive bubble popping game Bubble Witch!  It’s a hard life 😉 Well, I’m actually feeling a lot better today, I feel less cloudy and will probably get a lot of work done that I’ve been putting off.  I need to start my jewelry making again, I had SO much trouble making the one bracelet (my hands were shaking so much) and after it was completed it broke.  Sadness.  So I haven’t tried again.  I haven’t really even wanted to.  Now I do!

I have a meeting this Friday coming up with my super cute, french from France,  Oncologist regarding radiation.  I’m unsure if I’m going to start right away in December or delay it ’till January because of the holidays.  I kind of want to get everything over with so I can start fresh in the New Year with only Herceptin and Tamoxifen to worry about.  I guess only time will tell!

Love and Support

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I’ve always had trouble with saying the right things to people when they are either sick, have family that is or had someone close to them pass away.  I usually say how sorry I am and hope that they get better soon and or something in those lines.  I always feel awkward and end up replaying what I have said over and over in my head hoping it was alright.  That being said, I understand that others don’t know what to say to me.

I’ve been getting a lot of how lucky I am.  I know I’ve written about this before, but I’m doing it again because I really want to stress how ‘unlucky’ I feel and how upset it makes me.  Lucky usually means something good, and there is nothing, NOTHING good about cancer.  The only thing that is remotely good about it is the ‘awaking’ part…but I’m sure not everybody who battles cancer reacts the same way that I have. I know I’m being quite bitchy, but I know that before I had it I would not know how to react or what to say to someone.  The biggest thing that has been happening a lot recently with new people is that they bring up people they know who have died from cancer.  I usually say “wow, that’s really sad” and move the conversation away from the topic.  It upsets me, I know that a lot of people die from cancer but that is also my fear and as much as I care I don’t really want to know that your sister has been battling breast cancer for 10 years and now is giving up and dying or that your great aunt died of breast cancer or your step mom had a terrible time of it and it ended up coming back in her lungs and she died.  Having said that, mostly everybody I meet and ALL my friends and family know exactly what to say and always say something that makes me feel better.

I’ve been feeling really rough lately, and a little depressed.  Next week is my last Chemo round and I’m feeling scared and anxious about it working.  I understand that this fear is not rational but I am just really very worried.  I am happy that this is my last Chemo round but I still have 17 more rounds of Herceptin every 3 weeks, and a full month of radiation everyday.  Herceptin scares me, the major side effect is cold and flu symptoms which I can definitely handle (hmmmm….maybe I don’t have a cold now and it’s just the side effects?)  but it also can hurt the heart which concerns me.  I get my heart checked every 3 months because of this which should help with my anxiety.

I know this experience has made me stronger.  It is defiantly a part of my life (hopefully a small part) that I will never forget.  I have talked to other ‘survivors’ and that is one question that I always ask.  Will I always be afraid? The answer is always the same.  Yes and No.  The fear will slowly diminish, but I will never take my health for granted.  I am SO thankful for all the support I’ve received and still so amazed with all the love that people have.  You are ALL so amazing and wonderful, I hope you all realize this because this is the absolute truth.  I think this is easier to forget (which is so very sad)  how important you are to someone, how just a little love and support goes so far.  Everybody deserves a huge pat on the back, a great meal and a giant hug!  I can’t say thank you enough!

Herceptin: 1 down 17 to go. Chemo: 3 down 1 to go!

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It’s been a hard week.  I had my usual, pre-chemo 3 week meeting with another oncologist this past Wednesday because my usual one was on rounds yet again.  As she was checking my body, mostly my glands and breasts she casually mentioned if I have thought having my ovaries removed.  I didn’t know what she meant, and told her that no one has yet mentioned this and asked her why would I have them removed.  She told me that since my estrogen levels were high, that it would mean I would most likely be put on Lupron (the menopause drug that lowers my estrogen) until I go naturally into menopause (I guess when I’m mid 50s?!).  We talked a little more about having children post Chemo and was told again that it is risky because it will increase my estrogen levels. She said that I can talk more about this later with my Dr. S (my actual Oncologist)

Argh.  I’m so frustrated and sad.  When I got home I researched the ovary removal and Lupron shots.  With the removal I will be fully menauposal, and it is not reversible.  So, I think I will be sticking with the Lupron.  I just HATE it when doctors drop this type of bomb, my last meeting, one doctor kept telling my that if she was me she would have the full double masectomy.  The other doctor basically told her to shut up (not in those terms) and said that we will discuss that at a later time.

Other than this, the treatment went well.  I was there from 8:15 to about 3:30pm.  It was my first Herceptin IV, and that took about 2 and a 1/2 hours because I had chest pains so the nurse turned it off for a bit, called Dr. S and gave me some drugs.  I felt better and we started again.  I’m happy that I have only 1 round left of Chemo, but sad that I have 17 more rounds of Herceptin and a month of radiation every day.  I’m feeling a bit depressed, and scared.  I’m worried about the cancer recurring, and I don’t want to be menopausal for 20 more years.  I hate these hot flashes and my mood swings!

I do understand that these drugs are saving my life, and this is much better than the alternative (death) but it is just so much to think about and it kind of freaks me out.  I guess I just need to take it one day at a time, and keep my chin up.  I have some side effects but I’m lucky compared to others that I have talked to.  I’m strong and will make it through this.  I just need more information to make the best decisions. 

My ‘what if’ curse

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I keep having ‘what if’ moments.  What if the Chemo doesn’t work?  What if I hadn’t found the cancer?  What if the cancer comes back?  What if I can’t have children?  What if, what if, what if…  I think I’m driving G mad.  I can’t stop thinking this though, and I’m sure everybody has many ‘what ifs’ in their life.  I like to plan and find solutions in my head for all of my what ifs.  I guess it helps brings the control somewhat back but I know I can really drive myself (and others) crazy with this.  I know that I can’t change anything, and I know I am doing my best and have done just about everything so that these ‘what ifs’ never happen but I still get scared and nervous.

I guess it just makes me appreciate the present.  I want to do stuff now.  Man, I wish I could go on vacation.  I want to go zip lining, I went before and it was a great time.  I want to go snorkeling again.  I will.  I might go zip lining next week.  Anybody want to come?  I’ve had a wonderful past; I’ve met and been with the greatest people.  I don’t have any regrets, isn’t that the most amazing thing to say?  Everything that has happened to me, the people that were once in my life were all there for a reason, and I have made some fabulous memories.  I want people to think back of times they laughed like crazy, and when they cried, and remember whom they were with and what they were feeling.  Isn’t it great to reminisce?  Doesn’t it feel good to know that you have lived?  Things can get tough, but no one can take away those good feelings, those memories, and well…. that living.  You make your present and YOU can alter your future.  YOU are in charge of your memories.  Isn’t that amazing to realize?   I understand now that I have the power to change how my day is.  Some days I just wake up and say, “this is a great day” and I do everything to make it be positive.  Most of the time it’s not hard, it’s actually quite easy and I find that it usually gets better and better.  When I’m happy, my day is happy and the people around are happy.  I love that I have the power to shape my day.  Now I’m working on having amazing memories to empower my future!

Round 2….over!!!

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It’s official.  I’m an ebay junkie, an addict to the ‘buy now’ button.  I can’t stop buying wigs, hats and now beads.  I’m going stir crazy, so I’m making bracelets, necklaces and bookmarks.  I also bought a crotchet book and yarn to make my own hats.  I’m not so good at teaching myself though, and my hands shake so it might take me awhile to make stuff but at least I’m having fun at it!

This chemo round has been a little rougher on me than the last one.  I’m thinking it is because my immunity is down.  I started with my white blood count at 10 and now it’s 5.5 (normal is 4.5 to 10.5), so it’s not really low but kind of low to start again.  Good think I got my Neulasta shot.  It’s crazy expensive, but it helps make more cells in my bone marrow which is very painful.  I feel like an arthritic 90 year old!  I’m also getting major hot flashes, stomach pains, and migrains. Poor G, I feel like I’m crazy at times, very emotional, bitchy, sore and just stupid.  I get SO distracted and have a hard time focusing.  Chemo brain I have, hopefully I’ll be back to normal after this is all done.  My friends/family might think that I’ve always been a bit brain dead, kind of true,  but now I’m worse!  Yippee!  🙂

Ok enough of my complaining.  Things are great otherwise and I’m starting a new cooking blog soon! I’ll begin by making copycat recipes from different restaurants and write about how each tastes.  I’m pretty excited over this as there are so many wonderful and tasty recipes to choose from!  Too bad my taste buds are off but G will be my Guinea Pig; hopefully, he’ll be fine with eating all my creations!  🙂

Planes and Documentaries

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It’s only been a few days of being bald, but I must say that is all it took for me to adapt.  I was very sad the first night and day after.  Very sad.  But than it hit me, it really is just hair!  It is a small price to pay for my life.  And really, losing my hair means that the Chemo is working!  It is doing its job, and I really should be concentrating on that.

I like my wigs.  I also love this weather, which is PERFECT for hats over wigs cause I  am still not completely confident about my hair line.   This weather is amazing!  I love the cold breeze, and fresh air.  G is flying his remote control plane a lot and now has a following.  About 6 boys always run to the park and talk with us and are always just so excited to see G fly.  It is so cute, they have recently been bringing their own wooden and paper planes to fly with him.  G will make a great father one day!

G and I are watching a lot of documentaries recently, mostly from a series called ‘50 Documentaries to See Before You Die“.  There are 5 episodes that summarize the top 50.  I really recommend watching this series, and than choosing some docs to watch!  Some really open your eyes to what is happening, new information, and what life is all about.

Mohawks and Hubcaps

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G shaved all my hair off yesterday after a great day of sporting a Mohawk.  I can’t tell you I felt ‘liberated’ or happy for taking action into my hands or even relieved.  It felt terrible.  And sad.  I’ve never felt like a cancer patient patient until the moment my head was shaved bald.

I’m having trouble looking at myself; I finally put a hat on (to sleep) because I didn’t want to wake up drowsy and scare myself, G or the animals.  G says I’ll get use to it, that maybe even one day I’ll be happy to show off my bald look but right now I can’t.  This through me for a loop, I guess I never really took my cancer that seriously until now.  I don’t want to take it seriously, I don’t want to feel like a ‘cancer patient’.

I’m going to try to find ways to cope.  I’m not happy with the bald look so I’m going to hide it with my amazing wigs, scarves and hats.

Hopefully they will stay on my head, and won’t go flying off and hit people like when I got my winter tires put on and the stupid garage mechanic didn’t screw in my hubcaps.  I drove away and one by one they flew off my car and hit pedestrians walking down the sidewalk.   I think it may be safer with the wigs, and well, much funnier.

Listen to the mustn’t, child,
listen to the don’ts,
listen to the shouldn’ts,
the impossibles, the won’ts,
listen to the never haves,
then listen close to me –
anything can happen, child.
Anything can be.

– Shel Silverstein

Hair today, gone tomorrow.

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I’ve never really been a ‘hair’ girl.  I mean, I’ve always liked my hair but I’ve never obsessed over it, until now.  The past few days, it’s been falling out, but a few strands at a time.  Normal like.
Well, until today.  Today I would run my hands through it and come out with handfuls of hair.  Totally gross, and every-time I would show it to G.  “G, look at this!  Shoot, it’s coming out”.  He eventually told me I didn’t have to show him all the time, that he believed me. I might have grossed him out too.

It’s hard.  I never thought I was shallow but losing my freaking hair is not easy.  I’m happy though.  My life is good and  I bought wigs, and tons of hats.  My head will never be cold.

G cut my hair tonight.  The first of a few hair cuts.  He did such a great job, I might even get him to be my special stylist après Chemo.  If anybody wants a hair cut, and  a few drinks come on over! G is super sexy, fun, and has a great pair of scissors!    🙂

To be honest, this Chemo experience has not been terrible.  It has been manageable so far, and has made me comprehend even more how much life is so important and so fun.  It makes me want to go out and live, love lots and experience everything that I can possible can/do.  We take so much for granted, complain so much, expect so much, want so much.  This makes me settle down, look back and just be satisfied with what I have.  I want more, of course I do, I think everyone does (and should!) but I’m satisfied with what I have.  I have big dreams. I want to love more, I want to experience more.  I want to live more.  And, I will.

Thank you Cancer for opening my eyes to what I have and what I can have and will have.  I have my whole life to shape.  I’m just getting started 🙂

Before

After!

Round 1… done!!!

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Yesterday was a long day.  Was at the dingy old cancer center at the Civic at 7am for my port-a-cath insertion.  The nurses and surgean were all very kind and funny.  My nurse was able to insert the IV in my arm on the first try!  That was a huge accomplishment because it usually takes over 4 times.  Phew!  Super nurse extraordinaire!

The surgery went well, they had trouble putting the port under my skin, so they had to make a few incisions in a few different places (I got my bandages changed today, so I was able to see the gory results).   I’m feeling a bit of pain today.  They also had to leave the needle and stupid tubes in for a week.  I feel and look bad enough with thick bandages and stitch-marks and now I also have many tubes hanging from my collar bone as well! Sorry if I grossing people out, maybe TMI?

My Chemo was scheduled for 12:30pm at the new beautiful Cancer Center at the General and I was seated around 1pm.  I had a little crying fit break down, walking to my bed.  The nurse was really friendly and G asked if I could have a sedative.  She said that wasn’t a problem, but I declined.  I told her I would get it together.  I pictured Orderly’s running over with a giant needle and a straight jacket, but luckily I was able to calm myself.  I was talked over each step, and was hooked up to a saline IV at first.  Next came my Taxotere and my cold (ice) mitts and slippers  I had to also put nail polish on and hand cream on.  These steps are to help decrease the chance of me losing all my nails, I really hope it works.  The mitts and slippers were SO cold and quite uncomfortable and stayed on for over and hour.  I had to change them twice when they warmed up.  After that was done, I was onto my my next cocktail (I wish it was a Cosmo) but alas, it was Cyclophosphamide.  I can’t even pronounce it.  The nurse warned me that if my nose started to run or if I got sinus pressure she would slow the drip down.  That happened but with only 3 minutes left, so they gave me two Benadryl when I was leaving.  I felt perfectly fine otherwise, no nauseousness just a little drowsy. The nurse recommended that G take me to the car in a wheelchair but I told her I was fine to walk.  She looked doubtfull, I guess I must have looked like crap!

Today, I’ve been feeling good.  No headaches and no nausea.  I feel quite a bit of pain from my port, and water tastes like chalk which I must say is not something that is yummy but it has all been doable.  I’m in great spirits, and am so thankful for all the love and well-wishes from everybody.  I am constantly amazed with all this support.  I can’t tell you all enough how much it means to me!  Thank-you so much, I love and appreciate you all 🙂