Date

Cancer Schmancer…

You won't keep me down
Breast Cancer Ribbon

You’re one bad egg

posted by:
BlondGirl

Can I be 13 again?  I need to only worry about grades and friendship, how things that use to be so huge in my life seem so stupid and mundane!  I’m feeling so overwhelmed.  Found out that my eggs are bad today, something about vacuoles .  The doctor said it was most likely because of the cancer tests (all that radiation and such) and my stress level.  It is so weird to feel completely healthy and normal but have doctors tell you that you are not.  He said, “just worry about getting healthy again”.  I felt like screaming, but I AM!  Of course I am not, Chemo is just a week away.  It’s hard to wait for the dreaded poison to be inserted into me.  To prepare for when I’m actually sick.   I do plan ahead, tell people “oh sorry, I can’t go to your birthday or go out, I’m going to go through Chemo that week and I don’t know how I’ll feel”.

 

Cancer sucks.  I’m actually not even sure how much it does yet, but I’m prepared for the worse.  I have many books and shows lined up and G, I hope, is prepared for the monster to rear its ugly head. Chemo and Menopause.  If we can get through this, we can get through anything that is thrown our way.

 

I just only wish the odds were more (or not?) in my favour.  I seem to be always the small percent.  I kind of want the odds not to be on my side anymore, I don’t want to be the 1 out of 1000 odds but the rest of the 999.  I won the wrong lottery it seems, and I just want to be go back to normal before the ‘win’

I am OK.  I break a little at time, but I know I can rebuild myself.  I have all the pieces to do that around me, my friends and family.  I am lucky.  I keep telling myself I am, and one day it will sink in fully.  I know,  but now it’s hard.  I’m going through a lot,  I keep dodging missiles it seems, but soon I’ll have a gun which will blow everything to smithereens.  I want my bazooka now; I’m ready for it!

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Apricots and Oranges

posted by:
BlondGirl

For the past few days (this will be day 6 actually) I have been taking hormone injections and pills for IVF.  The injections have been going alright, a few minor mess ups such as dropping my $250 Puragon serum ( thank god it didn’t break),  forgetting to squeeze my stomach fat before and during the injection (big ouch!), and injecting the cat (just kidding). Tomorrow morning, I’ll be starting on a new injection (yay!) that will help release more eggs.  I had an ultrasound appointment today to make sure things are progressing.  The technician said that they will most likely not see any follicles, but alas they found 3!  She said this is a great start 🙂

My fertility doctor told me that my ovaries will grow to the size of large oranges by  next week.  Oranges!  They are normally the size of small apricots.  Goodness me!  She also said that I might feel slightly uncomfortable.  Slightly??? Are you kidding me, that is crazy!  After the appointment, I asked G if my ovaries can explode.  Kindly, with maybe a little eye-rolling, he reassured me that this cannot happen.  I understand this now, but I do worry that my ovaries (once the eggs are harvested) may not shrink back to normal size and they may be large, loose, flappy and floppy (like a deflated balloon).  G thinks I worry to much.  I talked to my mom about this and she thought that I thought that my eggs were going to be the size of oranges.  She must think me crazy!  I know that I’m not harvesting dinosaur eggs for goodness sake.  I just want to have my good looking, child sized ovaries back so I don’t have to get rid of my pink hummer 😉

 

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The power of dreams

posted by:
BlondGirl

This has been both the most amazingly wonderful year of my entire life as well as the toughest.  So much has happened, I finally met the man of my dreams, got breast cancer,  doing fertility treatments and now…. getting married!  I’ve dreampt about this moment my entire life, and I know without a doubt in my mind that G is the one I want to spend the rest of my life with.  Happily, he feels the same way (phew 😉 )!  I’ve always felt that it has been too easy with him, and well, too good to be true.  I actually, at times, thought that he could read my mind (still kind of do as he is so darn in tune to my feelings).  I never really believed it could be like this, I didn’t really believe it when people told me that they were totally in love with no doubts, until I met G.  I’m so happy that I let myself go with it, trust him (and us!)  and really…just love him.  He was worth the wait!

 

So…..my message to other people in relationships or single is that there is REAL love out there for everybody.  Personally, I don’t believe in ONE true love, I feel that we may have a few,  and that we can fall deeply in love with many people in our life time.  I feel that compatibility, trust and friendship makes the most difference in how things work out.  If I die, I would want G to be with someone else, and find a love that we had.  I know it would be hard for him cause I’m just so freakin’ awesome (lol) but I do want all the happiness for him and I know that he could find it.  Everybody can, if they let themselves.  I am just so, SO happy and amazed that I was lucky enough to meet him!

 

Don’t settle for just anybody and it shouldn’t be hard.  You shouldn’t have to really work on it.  I mean,  you have to show them that you care and do stuff together, but love should not be difficult.  It should feel right and be easy.  There will be fights, bickering, and such but you may feel stupid during it (or afterwords) and not at all worried that things will end.  Trust your heart, and your intuition and let your love grow ♥

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Living La Dolca Vita

posted by:
BlondGirl

A lot of things are brewing in the horizon but for now there are clear skies.

I’ve been the happiest ever these last two weeks, mostly because of fabulous family and friends. I’ve never really realized how important it is to have positive influences in my life, until now.

 

I have also realized that there are so many more good people than not. I’ve had trouble trusting people in the past, was weary of them and thought that some people meant more harm than good or that they were doing good things for selfish reasons. Wow, was I ever wrong and horribly judgmental. Our world is filled with amazing people. Loving people that will open their heart to you, if you only let them in. Now that I see people in a brighter light, I can understand human psychology better and I can grow into a much more enlightened human being.

I haven’t updated in a while, I’ve been trying to get a little bit of normality back into my life. Ignorance is bliss at times. I’ve decided to go ahead with the fertility treatments. With the support and advice from many specialists we will freeze embryos with the hope that some will survive the thaw and make us a baby when it is time. I will also be going into a early menopause (kind of like freezing my Uterus) so this may raise my chances of being fertile in the future. This is giving me hope, but I already feel stronger and understand that whatever happens, I am already better off.

I will start my hardy dose of Chemo Thursday, September 1st. I’m prepared for it, and already purchased some head scarves and wigs. I’ve read about some woman complaining that their families prefer them with their wigs rather than their actual hair. Can you imagine? I would hate for my family to say when my hair grows back if I could put my wig back on. But, I’m going to have fun with my baldness and treat every day like Halloween. Alright maybe not, but I am for sure getting a beehive hairdo like Marge Simpson. G thinks she’s one hot mama 😉

 

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At the edge of the woods…

posted by:
BlondGirl

I was listening to a song on YouTube and someone posted this:

“This song reminds me of walking on a crisp Fall day, grasping a piping hot Starbucks cameral brule in one hand. I watch stray foliage twirl to the ground, as my hair is gently tousled by a cool gust of wind. I’m wearing a fresh knit sweater and jeans. The smell of burnt lumber lingers in the air, someone has lit and stoked the seasons first fire. Everyone walks with an extra step, like they have somewhere to go. Not me, I soak it all in, it’s when I feel the most ‘real’.”

 

I felt like I could just inhale this imagery.  I sensed it, throughout my body, not just in my minds eye.  It made me think of October, walking the dog, and hiking in the woods.  It made me smile, and think of the love that surrounds me. Recently, I’ve been having trouble picturing the future.  I’ve thought about it, hoped for vacations down south, and made plans in my mind but Cancer kept getting in the way.  This small paragraph stopped me, and let me dream and crave.  I love the summer but can’t wait to put on a thick sweater, to feel and hear the leaves crunch under my feet, the cool wind on my face, and just breathing in that air.  It’s scary how I let myself get so down, how I could forget about the small pleasures in life…I forgot to really Imagine.  I need to try harder; I’ve lost my positive attitude for a bit but I’m fighting and itching for it back.

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Wish all was clear…

posted by:
BlondGirl

I am trying not to let the fire die down on me but some days it’s hard, like today for instance.  I have a whole bunch of emotions running through me, mostly sadness and fear.

I finally had a meeting with my Oncologist, Dr S.  I found out:

  • I am Stage 1 (she never really told me this though, she stated that stage wasn’t very important in my case – weird)
  • I am Grade 3 (the highest grade possible which means “cells look very different from normal cells. They grow quickly in disorganized, irregular patterns, with many dividing to make new cancer cells.)
  • I am HER2 positive, which means “HER2-positive breast cancer is a breast cancer that tests positive for a protein called human epidermal growth factor receptor 2 (HER2), which promotes the growth of cancer cells. In about 1 of every 5 breast cancers, the cancer cells make an excess of HER2 due to a gene mutation. HER2-positive breast cancers tend to be more aggressive than other types of breast cancer. They’re also less responsive to hormone treatment.”
  • I am ER Positive, which means “breast cancers that are estrogen-receptor-positive (ER-positive) are those that have estrogen receptors present on many of the cancer cells.”
  • My lympth nodes were clear
  • I have clear margins
  • My tumour was 1cm.
  • I will need 4 treatments of Chemotherapy every 3 weeks (Taxotere and Cyclophosphamide)
  • I will lose my hair (she said this was for sure 🙁 )
  • After the 2 treatments for Chemotherapy I will be started on Herceptin, 18 treatments every 3 weeks
  • I will have Radiation (I am not sure when, but will be meeting with this Oncologist June 29th)
  • I will have treatment for 1 and a 1/2 years and then start on hormone therapy for 5 years.
  •  A ‘Port-a-Cath’ will be inserted for the duration of my treatment.  Click here to read up about it http://www.huffingtonpost.com/hollye-harrington-jacobs/portacath-insertion_b_840429.html
  • I have a meeting with the Cardiologist tomorrow to check my heart because of abnormalities.

So, it has been a hard day.  I have so much to consider and take in, the most being my fertility.  I have missed my chance this month of harvesting eggs and will not be able to harvest until the end of August.  I can take a risk, start the fertility hormones and delay treatment but… being triple positive means that my cancer is estrogen based and with the HER2 status which increases the cancer, adding hormones and the small delay may not be a risk that I should take.  The doctor said I made her heart break a little because she couldn’t say or help more.  She couldn’t tell me more than that it is a risk, and I must make the final decision.

I really want a child, but I use to think more than anything.  I am not sure anymore.  It is so hard because I have to think about G’s feelings too and I’m so sad that if I don’t do the fertility that I might disappoint him (and me in the future). This is his life and his (future) child too.  We are just starting our life together, and I have so many health problems, I can’t help but feel like I’m damaged goods.  I feel bad for G.  I wish I could know more.  My Oncologist described my cancer as an garden, my cancer was a plant with roots, they can’t see if there are other seeds under the soil and Chemo will not help if those seeds root themselves down.  I wish that they could tell if I had tiny seeds of cancer still in me.  They can’t and wishing is useless.  I just have to make the most informed decision that will be the best outcome for the future.

I don’t have my answer yet.

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Zombies! EVERYWHERE!

posted by:
BlondGirl

All right, this is my bitchfest spew of the week. Before this entire cancer nightmare, G and I had hour-long deep conversations about our zombie society.  We talked about religion, life after death (or no life) and how almost everybody is asleep.  We talked about how people live each day in and day out without thinking, without dreaming, without happiness, without even really seeing.  I’ve seen so many people just wake up, go to work, have dinner, watch tv, and then sleep.  Talk about autopilot. There is no excitement, no challenge, no change.  Most people don’t even remember much of their years.  YEARS!   I’ve been there.  Completely, and some days I’m still there.  I know I have to shake myself sometimes.  I have to wake myself up, because there really is a beautiful world out there, an exciting and wonderful life all around us, just waiting for us to wake up, grab it and make it our own.

Take a walk.  Look around, NO I mean really look around you.  Talk to your friends, again I mean really talk to people, just don’t exist.  LIVE.   I am sick of people complaining about their mundane lives.  Do something about it people! If you don’t like your partner, job, lifestyle, or life – change it.  Change is hard but it is what is difficult that really wakes you up and you can’t get anything you want without first doing something about it.  You have the power to change it.  No one else will do if for you and it won’t change on it own.  What if this is it?  What if there is no heaven, no afterlife.  Nothing.  You die, and than you just don’t exist anymore.  No second chances.  This is what I thought about so much before the cancer.  What if!?  Would you do anything different?  If not, GREAT!  If so, DO IT NOW!  I’m not saying to do anything drastic like sell your house and move to Zimbabwe, but seriously if that is what you want to do, find a way to do it.  Look into it and plan.  Dream away, cause life is not going to wait for you and anything can happen that will change things.  One thing that it can’t change is your dreams.

Stop looking at what you don't have and SEE and be thankful what you do have!

Stop looking at what you don't have and SEE and be thankful what you do have!

Stop wasting time people, in my eyes that’s what this ‘zombie lifestyle’ is.   Also, appreciate what you have.  People take so much for granted.  I know I took my health for granted.  I always see people take their children, their friends and their partners for granted.  Don’t, cause really those are the only thing in life that matters.  Those are the things that TRULY should make you happy.  Everything else is just fluff.  Let yourself be happy.  Really, let go and just be happy.  We all have choices, and my choice right now (even going through all this) is to be happy.  Yes I could be sad.  I have every right to be.  But should I be?  Should I hold on to that anger, that fear?  I could, but it would do nothing for me.  It would only harm me.  So… I’m choosing to be happy.

I would do anything to have a child and I really HATE that I might not be able to bare one.  Will I let this stop me from dreaming?  Hell no, if I can’t have a child naturally, can you imagine what fun, how exciting (but nerve-wracking, and overwhelming I’m sure) will be ways to have getting one?  There are so many other options, just like in every obstacle of life and I guess it is how you look at it.  There are different roads and paths for everyone, all the time.  You just have to look for them.  Take the blinders off and LIVE.

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Knowledge is power

posted by:
BlondGirl

I am so itchy, I just want to scratch my stitches off but I can’t even get near them with these stupid bandages. Argh.  I found out two things, these past few days since my surgery.  I don’t do well with drugs and that G makes an amazing nurse.  He helped wash my hair and then changed my horribly disgusting bandages.  He watched over me when I was SO sick over the Oxycontin’s and he has fed me and comforted me.  Wow, he is so amazing!

My cat, BouBou keeps sleeping on me and sniffing me, which is kind of freaking me out but G says it’s because he smells the blood and senses my pain.  My other cat Hugo is still the same… wild and crazy.  He still stares at and tries to climb the walls, and attack imaginary objects or ghosts.  He runs around the house like he’s on fire and meows at the ceiling.  He wants my attention more when he sees BouBou getting love. But I love all my pets, well maybe not Jade the tarantula as much.  G says that I can cuddle with her too, but I always decline.  I wouldn’t want to smush her 😉

I’ve been thinking a lot lately about how and why I have (had) cancer.  I know now that I’m going to change a lot of things that I did before.  No more plastic water bottles that is for sure.  I’m looking to buy a glass or stainless steel water jug for my water cooler but finding one in or around Ottawa is nearly impossible.  This one is perfect, but it is only available in Toronto http://www.cedarspringswater.ca/glass.php Can anyone recommend where else closer I can find one?  I’ve also decided that no more processed food for me, will try to eat hormone and antibiotic free meats, and really read and research the ingredients of all packaged foods . G and I were also talking about cutting down (to 1 or 2 times a month) on red meat.  I’ve been reading a friends blog who’s been through the same thing, and love the changes she has made and feel like I should (and could) do the same.  Natural toxin free cleaners, cosmetics, and real food. Why does it take something like this to make healthy choices?

I’m unsure if this will change anything related to my cancer as no one really knows entirely what causes it but I do know that these changes will benefit my health as well as G’s.  He is worried that I will go overboard and become obsessed.  I’m not.  I will just become more knowledgeable and there is nothing more powerful than that.

 

 

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Smurfette

posted by:
BlondGirl

Yesterday was one of the longest and hardest days of my life.  G and I arrived at the hospital at 7am and l was released at 7pm.  12 hours, but I only remember 9 hours of it.

When we got there I was admitted almost immediately.  I was brought into the daycare unit (no, there were no toys or games sadly enough) and asked to take off my clothes, which were replaced with a beautiful evening gown aka hospital gown and overcoat.  G wanted me to steal it cause he thought it was incredibly sexy which I suppose means that I must go shopping for lingerie when this is all done.  That, or he likes the doctor/patient roll play games.  Anyways, I am getting sidetracked.  After changing, I was asked to make myself comfortable in the worlds most uncomfortable hospital bed, but they gave me heated blankets, which was a very thoughtful touch.  Around 8am I was wheeled (cause apparently patients walking around was forbidden) to get an ultrasound.  I thought the ultrasound was going to be easy and comfortable.  I thought wrong.  A very, very tall female doctor (they had to raise my bed up to full height and it was still not tall enough) numbed my breast, after marking out the tumor with a giant X, and inserted a long wire into it.  The freezing hurt a bit, but I could still feel the wire.  She apologized and said that sometimes that happens and froze me again.  This time was better, and I could only feel some pushing and pulling.  G asked me if I could keep the wire as a souvenir so he could make it into a ring, I was too embarrassed to ask for it, well that and too grossed out.  Can you imagine?  Someone saying what a beautiful ring you have, and me telling him or her it was homemade, and literally was close to my heart.   Grody.

 

With wire in tow, I was then brought to the x-ray station, where I had to do a mammogram.  Yes with the wire inside.  The technician was very kind, but we couldn’t get the right images so she had to retry a few times.  Good thing my breast was partly numb and that they didn’t squeeze it as much.  After this torture, I was brought to nuclear medicine.  I met with another technician who explained what was going to happen.  She was so nice!  G went down for coffee, and during that time I was brought into the radiative imaging room.  She asked me if I had wanted him to be there with me for the injection (of radioactive dye so that they could mark out my sentinel lymph nodes) and I said yes please.  She was so nice to wait on him for the procedure.   When he arrived back, she started the procedure, explaining everything as we went along.  The computers in the room looked like they were 20 years old, she admitted they were but they were no longer in use.  The imaging camera was from the 70’s (truly!) and she reassured us that it was only the case and that the guts were all replaced years ago with newer technology.  She told us that she likes the older ones better because they don’t break down as much and are made to last.  Just like old cars. G wanted to play on them but was told not to.  Good thing he had his iPad or we may have been kicked out!

After numbing my breast (a third time) she inserted some radioactive dye.  She told me that this might be very uncomfortable because they have to put in a lot.  It wasn’t at all as I hardly felt it.  I was then taken to the hallway to wait 30 minutes for the dye to travel to the nodes.  Usually they make you massage your breasts but with the wire in we had to just wait for it to do its job.  While we were waiting we watched “The IT Crowd” on the iPad through Netflicks.  It is such a funny show and kept my mind occupied.  I was than brought back to check if it had worked and it hadn’t so was asked to wait again.  No biggie J more TV for us!  45 minutes later I was brought in again but this time my nodes lit up like stars.  What an amazing image!  I asked if I can get a print out, and she told me it would be in my file.  It would make an amazing piece of artwork!  She used a homemade radioactive marker to trace the lymph nodes for the purpose of the biopsy (depth and area was needed) and she sent the file on its way.

 

The porter than took us back to the daycare unit.  I really felt like I should tip these guys, as they were so amazing at driving and so friendly.  Fortunately, or G would say unfortunately, we didn’t run over anyone or hit any walls.  I am not so good at work with the wheelchairs so I can’t even imagine how hard these are to maneuver. We arrived back around noon and the nurses asked if I needed anything.  I asked for Champagne but was turned down.  How rude 😉 I wasn’t even allowed water or anything else.  G jumped up on the bed and we watched more TV together and just relaxed.  I am so lucky he was with me.  He has been SO amazing through all this.  I am so very blessed!

 

My surgery was late; I was wheeled into the surgery unit around 2pm instead of 1:30pm.  The porter told G that he can’t come in but can give me 2 kisses, G snuck in 3 and the porter said that any more and he would have to give us a room.  He was sweet and funny and wished me luck.  I waited outside the operating room (my favourite number 11!) and soon met my handsome and young anesthesiologist who discussed the procedure and my medical history.  He told me his supervisor would soon be out to meet me, but he couldn’t remember her name!  A little scary, but I reassured him that everyone has brain farts sometimes.  He blushed, which was kind of cute but weird at the same time.  He told me that the IV would have to be put in my ankle, and all I could think of was ‘shoot I forgot to shave my legs, how embarrassing!”  His supervisor came out to meet me, but then said it will not go into my ankle cause I was only getting one breast done so they could use my left hand (phew).  They wheeled me into the OR room and I met with the nurses, said hi to Dr. MacGyver (my surgeon) and transferred to the OR bed.  The blushing Anesthesiologist looked at my hand and was bewildered about the size of my veins and seemed VERY worried about putting in the IV.  He tried putting one in but missed the vein (double ouch!) and was really nervous.  His supervisor eventually took over (thank God!) and talked to me about what I would be doing if I weren’t having the surgery.  I explained that I just moved out the day before and so most likely would be unpacking.  We talked about our pets and she told me she had a Miniature Schnauzer.  I was thinking how friendly and nice she was, and was so happy that she was trying to make me feel comfortable (but in retrospect she was just putting me to sleep) The last thing I remember saying was “Oh I love Miniature Sch…nau…zerss…..” and I fell asleep.

 

I woke up around 4pm to a nurse calling my name.  I had an oxygen mask over my face and there were people in beds all around me.  I was attached to a machine that measured my heart rate, blood pressure and oxygen level.  I guess my oxygen levels were low because the machine kept beeping and I was encouraged to take deep breaths.  Finally one of the nurses took the mask off, and I was able to breath on my own.  I obsessively watched the machine; I tried to keep my level above 93 but had a hard time at first.  The nurse explained that this was normal because of the meds and the anesthesia.  I was finally brought back to the Daycare unit around 5:30 where my vitals were monitored and I could finally have some water.  I went to the bathroom and noticed not only that my pee was BRIGHT blue but my breast was too.  I was feeling no pain and really relieved and so happy that the tumor was out.  I’m cancer free!  No more using the cancer card, ok well maybe not as I still have more treatment but at least hopefully no more cutting for now!  I asked if I was blue or green and the nurses said surprisingly no.  I knew G would be disappointed because he wanted a before and after picture.  M said she would make it her Facebook profile picture so I was relieved I wasn’t Smurf coloured.

I chatted with the nurses and relaxed until 6:30pm when I was asked if I wanted to change into my clothes and go home (did I ever!)   They wheeled me out, right up to my beautiful Caddie, and G greeted me with the most beautiful flowers: yellow roses and daises. my favourite!  Have I said how lucky I am?  He asked me how I was, if I was sore and such.  I told him I was feeling great, just tired.  We drove a bit and I asked him to pull over quickly, he did and I lost everything that I had drank.  Thank goodness it was only water.  I guess I wasn’t feeling so great after all.  I wasso  glad to get home, to be in my comfortable bed.  Days like this make you grateful for the little things, like pillows and water.

 

I am so grateful for all my friends and family, G’s family (who I feel so close to now) and just everybody!  I love the phone calls, the texts,  emails, notes and letters.  I love my Aunts for writing to me, C your words are so inspiring, loving and thoughtful.  I love you all so much!  Although I haven’t written back, as I have been so stressed, I just want everyone to know that I think about you all daily, and your support and love has helped me tremendously.  So, thank-you everybody!  You are all in my support circle.   In the books that I’m reading they recommend that you have a power circle and I feel that mine is the most powerful and dynamic of all.  xxx

 

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Just Breathe

posted by:
BlondGirl

These past couple days have been a whirlwind of emotions, both good and bad.  I had a pre-op at the hospital yesterday which lasted around 3 hours.  We talked with a nurse about what my surgery will be like (a very long day is seems) and I found out that I will have green urine for at least 7 – 10 days.  Oh the things to look forward to.  I also found out that post-surgery I will no longer be able to have blood drawn, give blood, or have my blood pressure taken from my right arm again.  That seriously sucks for me, and I almost cried because it hurts so bad out of my left arm.  The nurse said it was because of my previous break (in the elbow) and that there is nothing that they can do.  Oh well, c’est la vie.

Find the answers within.

When I arrived home I had a message from the surgeon waiting for me on the machine.  He told me that my bone scan, ultrasounds, and chest x-ray came back fine.  No other cancer!  I was so ecstatic! He also said that my hormone levels were positive, which he said was good news.  YAY again.  The HER2 test was not back, but he said he would call as soon as the results came back.

I woke up feeling good this morning, and excited to go into work to see my students and especially my coworkers.  They are seriously like a family, and I am so lucky to be a part of it.  My feeling turned when my surgeon called back.  He was very nonchalant on the phone, and blasé  He told me that he got the HER2 results back and my levels were high, which is unusual.  He also told me that my heart scan came back abnormal but was not very concerned about it.  He said that can happen, and the test can be altered by various reasons.  I wanted to know if I can start fertility treatment but he told me I had to wait to speak to the oncologists who should be calling soon.  I had no clue what HER2 receptor was (but have recently researched it) and am very concerned about my heart but I guess if the surgeon isn’t concerned I should breathe a little easier :s

able to jump to the worst conclusion in a single boundThe cancer center called soon after to book an appointment consult on July 12 with the oncologists for chemo and July 15 for radiation.  I wanted it sooner so I can start the fertility process but that was the earliest I can be seen.  I hate having no power over this.  While I was at work, the hospital called and switched my surgery to July 7 instead of the 19.  Crazy! That is next week!  I’ll be happy to have the tumor out but scared not knowing what my treatment will be and unsure if I can start with the fertility.  I’m hoping that this will get easier.

My  friend E (and coworker extraordinaire!) reminds me to BREATHE.  Inhale, exhale and repeat.  I must not forget.  I also must try to dance my worries out. To quote E “Don’t let life take your breath away”

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Can I be excused? I think my brain is full.

posted by:
BlondGirl

My right ovary was found!  Apparently it was never missing just really small, my left one is small too.  I suppose I just have child-sized ovaries; who would have thought?  G says I could compensate for my small ovaries with a faster,  more powerful car.

I went to get another abdominal ultrasound, but this time was to check my internal organs for cancer.  I really hate all these tests as I always worry that they will find more cancer (or other hidden diseases) I wish they would tell me after each test if things are alright but they always keep you in the dark.  I’m now hoping for no news, as it usually means good news (as the saying goes).  They had trouble finding my left kidney.  I asked if it was child sized, and received a sigh and a puzzled look.  The response, “Umm…it’s a normal adult size.”  I was relieved.  I was kind of worried that all my organs were child sized.  This cancer business is making me find all different things about my body.

So G and I are going to go ahead with this embryo making business.  I might have to delay Chemo for a bit to collect more eggs (if it’s safe) and start on hormones in two weeks.  This will be a wild and crazy summer!  G asked the doctor if the eggs can get freezer burnt.  There was no reply.  Not even a smirk.  I thought it was a little funny.  The doctor did mention, right after that there was a storing cost of $300 each year.  That put us in our place.

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Is that cancer I smell?

posted by:
BlondGirl

My best friend M just friended this Sheep on Facebook.  His name is Alfie, and he helped diagnose his owner with breast cancer.  Apparently he kept head-butting her in the chest repetitively one day and she developed a large bruise, which turned into a lump.  She (the owner, not the sheep) went in to get the lump examined and they found breast cancer.  To read more about the story, click here: My pet sheep saved my life

You can also friend or fan him on Facebook too, if you are so inclined (just search for Alfie Purl)

Well since most of us don’t have a cancer sniffing sheep, please remember to check yourself or better yet have someone you love check for you!

 

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The longest day!

posted by:
BlondGirl

Lost Overy!Happy summer solstice! As the longest day of the year, it was also the most exhausting.  Got a lot accomplished but didn’t realize before today that my right ovary was missing.  How does one lose one without knowing it?  Not to worry, the technician said my left one was in fine form and would do the business of two.  Hopefully she is right, as I don’t really want (or need) anything else to worry about.

 

I also finally got my bone scan, abdominal ultrasound (for fertility) and chest x-ray completed.  Phew, more tests down and only a few left to go (I hope!).   We went to the hospital for 8am.  G said now he will take over the driving, because in my rush to get there I drove over the curb and went through a yellow light.  I blame it on the cancer ;).

 

The bone scan was not as scary as I envisioned. It took about 40 minutes and the camera circled around my body capturing images in 3D. Pretty neat actually!

I got more radioactive traces injected into me but this time I hardly felt it and was sent on my way home.  Well not home yet as I had to get the chest x-ray done.  This was surprisingly fast, the only thing that was difficult was getting that stupid 3 holed hospital gown on(ok not really, but I did ask if I should have it opened in the front or back and she explained that it was a double thingy; silly moi!).

 

I finally received the paperwork from my doctor (it is recommended that you take home copies of all your own medical files to read and have on hand if needed for consultation or second opinions) I found out that I have Invasive Ductal Carinoma. (IDC) which is the most common type of breast cancer (80% of all breast cancers are this type)

 

I was surprised that it is invasive, which means that it has begun to spread to other surrounding tissues, but I’m keeping my fingers crossed it hasent yet invaded my lymph nodes.  My notes/report also stated that I will most likely need Chemotherapy, which I was hoping to avoid, but a friend has reassured me that she is fully fertile after treatment.  This is a big relief, I suppose I just have to wait this all out to know all the answers.

 

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The clapper

posted by:
BlondGirl

I finally took initiative and called by-law on my next-door neighbour.  Normally I’m not such a complainer but he has been driving me mad!  He hammers on his shed a certain number of times and then returns into the house.  When I say hammer, he pounds it like 10 times repetitively, and the sound echoes throughout all of the backyards.  He does this no matter what time of day it is.  So when he started again at 1am I had had enough.  I haven’t heard him do it at all today.  G’s plan was to engineer a clapper MacGyver’d to an air-horn so every time he banged the horn would sound, I’m not sure that would help matters but it would have been funny to see his expression the first time he hit it! 

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Life is a gift

posted by:
BlondGirl

Life is a gift so unwap it!Yesterday was a good day.  I hardly thought about the cancer.  I needed to get things done around the house and take care of things.  G and I are thinking of buying a house, our dream house.  It doesn’t look like it will work out but we have other plans.  We will make other plans. and dream other dreams.  We are happy and know that whatever we do,  we will do it together and things will work out.  It may not be as we planned but maybe that is better.  Sometimes it’s more fun to fly by the seat of your pants.  I spent the evening with my friends (my best friends) and it was wonderful to just relax and be stupid.  Friends are the most important part of life, well love actually is and I feel all full up.

Life is a gift and I’m just starting to unwrap it  🙂

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Father’s day message

posted by:
BlondGirl

A friend posted this article on Facebook.  I thought it was awesome and well said.

A father\’s day wish: Dads, wake the hell up!

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Another day, another test

posted by:
BlondGirl

It was a busy day yesterday.  G and I had a meeting at the fertility clinic first thing in the morning.  We had some questions answered and surprisingly started the process.  It looks like they will do embryo freezing but there is much to do to get this done.

The doctors took our blood and G is scheduled for an appointment for semen analysis on Monday.  His instructions made me laugh ” The specimen should be collected by masturbation after meticulously washing your hands.  Alternate methods may be discussed with your doctor but are not recommended.  DO NOT USE CONDOMS as these contain chemicals which may kill sperm and invalidate results.”

I wonder what the alternate methods are and really would someone really use a condom???  I also giggled on the meticulous washing bit!  It also said that it needs to be dropped off no later than 1 hour after collection.  G said that he may just do it in the parking lot or in the waiting room.  Hopefully there won’t be any arrests that day!  (joking!)

 

I also had a  MUGA Scan at the Ottawa Heart Institute.  They injected me with radioactive traces and then took pictures of my heart.  The IV really hurt this time, and I had to wait 40 minutes after they put it in.  It really sucked but these tests are needed and I know I have a lot more to do so I can’t be a big baby.  The scan was OK.  A little strange and something I hope I will never have to do again in my life time.  It took about 45 minutes and I was SO happy to get out of there and go home.  The worst part was being in the hospital and seeing everybody in the waiting room.  I wondered what they were there for and prayed that they would make it through this (whatever was happening with them)  There are so many sick people!  I hope they have the support and love that I do!

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Cancer Card

posted by:
BlondGirl

Yesterday I went to the pharmacy to pick up some muscle relaxants.  My body has not felt the same since the day of my ultrasound and mammogram over a week ago.   My body aches; my back and shoulder are sore and my chest is so tight.  I feel like my heart hurts and my lungs hurt.  I’m scared and worried that there is something else wrong but L and G assure me that it’s just the anxiety.  G reminds me that I already have 1 cancer that I can’t be selfish and claim another.

 

At Shoppers Drug Mart I asked the pharmacist about the muscle relaxants.   She inquired about my symptoms and I explained to her that I was just very sore. She asked why so I came right out with it.  I told her I just got diagnosed with breast cancer.  She was shocked but recovered quickly and explained which ones would be good and recommended a heating blanket.  She told me I shouldn’t take them more than a week.  I know this but bought the big bottle, just in-case.

Breast cancer card

It felt good to say it to a stranger.  I’m not going to play the cancer card very often but seriously if I have it I suppose it’s mine to use.   G say’s that is only in play for a limited time, bless him, so use it while I can.

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Centering

posted by:
BlondGirl

I woke up feeling a bit better.  Knowing that I had a full day to get use to this ‘cancer’ diagnosis and nothing really planned to do other than get my nails done.  I woke up at 6am, really tired, but not able to fall back to sleep because I wanted to write things down.  I worried about work.  Am I able to take time off?  Can I afford to take off the time I need to get the help I need?  I called human resources and the woman I talked to assured me that someone would call me back on Monday and gave me a sheet to give my doctor to fill out.  I looked at it but I don’t think that he can answer it fully yet because there is so much that is unknown.   I hate this.  I want the answers right away but have to wait and do all these tests.

 

freak out and break stuffSometimes I feel like I’m going to break.  I feel like I’m having a nervous breakdown. Hopefully I’ll just wake up from this terrible dream and everything will go back to the way it was before.  Pre cancer.  No such luck.  I know that I can always call my friend M and my sister L to talk to when I feel like this.  I’ve called them so much these past few days, laughing and crying (so much crying!) and they have always been my boulders.  I can’t imagine women going through this without support.  I have more than enough and I take comfort in this.  I guess I’m lucky after all!

 

The fertility clinic called me first thing to book an appointment.  I’m not sure if I actually have to pay for this consultant appointment but I’m sure it’s worth it.  I hope they don’t ask me too many questions because I’m not sure if I can answer anything as I’m still in the dark about what will truly happen.  I feel happy that I’m not dying but still overwhelmed and bewildered that I truly have cancer.  I am SO worried that this will take away my fertility.  I want to have children more than anything and can’t imagine that this small little lump can take it away from me. I want to be healed, cancer free but I want to keep my eggs.  I imagine little armies fighting in my breast, red coats for the cancer and white for the good cells.  I imagine the Lumpectomy being the allies but taking out everyone, with a nuclear bomb type thing.  This whole thing is happening in my boob.  G  says it’s much slower so maybe it’s happening in freeze time, or slow motion either way I hate war.

 

While I was at Wal-Mart, shopping for sports bras, the Ottawa Heart Institute called.  I’m not sure she knew my situation but I booked an appointed 2 hours after the fertility appointment.  I had to make a decision that was best for my health.  She told me Dr. L was pushing to get the results as soon as possible.  It was either that or wait to July, which would be impossible.  They need to know my heart is strong and healthy enough for Chemo.  I worried about the heart scan.  Am I going to have to run? I’ve always thought that I had a good heart but going in for tests makes me anxious and questions if everything will be all right.  I have so many what ifs.  What if the test results come back negative?  What will happen?  I’m so nervous and my heart is beating so much and fast, it actually hurts cause I’m so stressed, so what if the results are flawed.  Do they take that into affect?

 

I went out for dinner with friends.  When I got there I researched the MUGA scan because I was unsure if I can drink before this test.  Funny, I texted a friend that I was getting this scan done and it auto corrected to Muga Scam.  She wondered what the hell I was getting done.  I read that it will be an image or video of my heart (instead of an intense physical exercise regime) I always picture House episodes before each test and I’m happy that this is not the one with the person running on the treadmill.  It also said that I would need an IV again with a radioactive tracer.  I’m thinking that my veins will light up if I’m under black light.  I will glow through my clothes and you will just see my teeth and my blood flow.  Creepy.

 

radioactive tracer

 

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Day 1 (But seriously…feels like day 100)

posted by:
BlondGirl

Today I had my appointment with my surgeon Dr. L to find out if I had cancer.  When I got there, I noticed an older gentleman on the elevator up to the breast clinic.  I wondered if this could be my surgeon and scanned his demeanor and facial expressions.  When we walked in the receptionist greeted him “good morning Dr. L” and he walked on back.  The week long wait had been making me paranoid and when I checked in I studied the receptionist face as well as she looked at my file.  I was looking for signs, of pity or really just anything, I felt like I was going crazy with worry.

The week prior was the hardest week of my life.  Uncertainty mixed with anxiety did not help me and I had a really hard time centering and remaining positive. Friends and family were incredibly supportive but I knew that they were scared for me as well and possibly a little annoyed with my anxiety.   They would reassure me that things would turn out fine, that 8 out of ten biopsies turned out to be negative for cancer, that I was young and that the lump was small and in a place where my under-wire probably rubbed and caused a cyst or some thing similar.  I understood all this and tried to rationalize everything but my anxiety would take over and I would research more and make myself more crazy and paranoid.  My biggest fear was that it had spread to other parts of my body through my enlarged lymph nodes. I envisioned my body full of cancerous cells multiplying and attack other good cells.  I prepared myself (as much as I could) for the worst-case scenario.  I rolled played what was going to be said to me and tried to work out good ways to handle the news.  I also envisioned great news and thought about how happy I would be and how I should never take anything, especially my health for granted.

 

 

After being called into the office, my sister S, my boyfriend G and I sat down and talked with the nurse Kelly that I met earlier in the week.  She explained that they didn’t yet have the biopsy results but that I would still meet with the surgeon.  That went all right.  He seemed very nonchalant and explained the findings from the ultrasound and mammogram.  He told me that it cannot be diagnosed cancer without the biopsy results but again the growth was suspicious.  He proceeded to do a physical exam of the lump and of my lymph nodes.  I explained how nervous I was (which I was sure he could tell by the sweat pooled in my armpits, grody) and he left the room and told us to meet him back in the office.

 

He returned to the office and told us that he got the verbal results from the biopsy.  It was cancer.  I didn’t react much as I kind of expected this.   After this I was kind of numb.  I kind of walked through the rest in a kind of dream like state.  Like I was looking in on this, not really a part of it.  I am so fortunate that my sister S and boyfriend were there.  I was lucky to have them help me.  I felt so supported and taken care of at that moment and still to this day.  I don’t know if I thanked them for being with me, as I seriously couldn’t get by without them.  I think I would have crumpled; all I had really wanted to do was roll into a ball and go to sleep.  But they were there with me, and a HUGE help.

 

I asked if it was in the lymph nodes and he said no.  I was incredibly relieved.  He said that this was positive news but that sometimes the biopsy doesn’t get all the cells or nodes and that it still may contain cancer in the other nodes.  I felt a little more anxious but was happy to finally have some answers.

 

He went through some options but seemed a little unsure what the best treatment would be as it is unclear if I had the breast cancer gene.  He explained that they would normally do a lumpectomy since the cancer was small, remove some (if not all nodes) and treat with radiation but since I might have the gene he had mixed feeling about treating me with radiation as the chance of it recurring is higher.  Radiation should not be used on the same area more than once, they say, so they had to make sure to pick the best time.  He was also concerned about my age, having cancer at 33 is rare (1 in 1000) and I really want to have children, so he wants to do the least intrusive treatment for this.  We discussed freezing my eggs before treatment and were told that my hormone estrogen levels will have to be tested because my cancer may have been escalated or caused by an imbalance.  It is super complicated, this cancer.

 

I got home with an arm full of reading material.  My plan was to nap, as I was exhausted from not sleeping the night before and from the stress.  I wasn’t able to.  I called my work to book the next day off and was happy about how supportive they were.  I love my work, my students and especially my coworkers so I don’t want to take any unnecessary time off (I also know it will help keep my mind at bay as I’m prone to worry).

Can I feel it?

I told my friends and family, well S and G did (thank you!) People reacted differently; some were sad, some worried and some happy.  Not happy in the euphoric way but more in the relieved way that at least it wasn’t worse.  I heard that I was lucky a lot.  I don’t feel lucky, I mean I am VERY happy and relieved that I’m not dying but for goodness sake I have cancer. CANCER.  It is not something I ever wanted, not anything I wished for but I have it and do not feel lucky for it.  I hate that I have to go through this and I know that it could be so much worse.  A lot of people have it so much worse.  My friend is paralyzed; another friend’s coworker just got diagnosed with a brain tumor.  Those are so much worse.  I know this but can’t help but feel a little sorry for myself.  Why me?  Why now? What caused this?  Was it my antiperspirants, my love of tuna, or just a fluke? I don’t think I will find all the answers anytime soon.  I just need time to get use to this.  Yes it’s treatable but I still have a long road ahead with testing (staging, genetic and hormone), treatment (surgery and chemical) and than more future testing.  I’m worried that I won’t be able to have children after this.  I’m worried that it will come back more forcibly; hopefully this will not always be in the back of my mind but for now it is.  It is not everyday you get diagnosed with cancer.

During the week coming up to my diagnosis my boyfriend and I promised each other that we will make each day count, not live as zombies as so many of us are prone to do.  We will live well and strong and do everything that makes us happy.  Never take life for granted.

I was so scared that I was going to get a death sentence.  I didn’t want to die young not doing all that I wanted to do.  I’m happy to know that not going to die from this but I still am unhappy with the diagnosis.  One thing I do know for certain is that I am done being a zombie.  I am going to stop procrastinating; I’m going to live.  So thank you cancer, thank you for the wake up call.  I needed it!

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