Category Archives: Treatments

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Radiation Therapy Journal – Day 28 – Friday December 7, 2012

Treatment Notes:

– Today is my last day of “regular” radiation therapy, and next Monday begins my “boost” radiation therapy.  Up until now the radiation has been spread over my whole boob, which actual tissue is farther and wider than one might think (the delineated soon-to-be radiation “no fly zone” stretches – measured laying on my back with both arms bent back up over my head – from the center of my sternum all the way around to the center of the left side of my body, and from a point along the outside edge of my boob level with the top of my sternum down to an inch and a half under my inframammary fold.).  Starting Monday, the 1.8 Gy fractionation per treatment spread across the whole boob becomes a 2.0 Gy fractionation per treatment concentrated in the tumor bed only.  Where the whole boob deal was administered from above-and-down-from-the-bottom-right (the machine emitting the radiation was positioned basically above my stomach and pointed just “south” of my armpit) and from below-and-from-the-top-left (the machine is slightly below me angled up from just “south” of my armpit pointing basically toward my stomach) (both of which angles if the depth were miscalculated would harmlessly shoot away from my body into the open air, the boost part will be straight down into my body from above (I’m imaging from somewhere above the left side of my body angled some top-to-bottom, left-to-right way entirely through my body front to back – I’ll know more on Monday when it actually happens), carefully (I sure fucking hope!) calculated to hit the bottom of the tumor bed, but no farther down into my body.

– Oddly enough, with the first blast of down-from-above today, I got some pain where the my ribs connect to the top of my sternum.  Also, as I’m wearing a bra today for the first time in more than a couple days (since the increased pain lately made me wonder if I should be dealing with gravity more deliberately), but I’m finding it generally uncomfortable, slighty cutting into me on the side where I’m more swollen, and then there’s the rubbing on the nipple.  Welcome back to damned-if-I-do, damned-if-I-don’t.

Side Effects:

– Fatigue/lightheadedness – Seems to be a regular deal these days having this hit me while I’m walking from treatment out into the parking lot to go to work.  I’m not sure if it’s one or the other, or both.  I can’t always necessarily separate them (not that I’m trying so hard to do so.)  Thankfully, when I sit down in the car to drive to work, my mind is all there and I’ve not felt like I would be a danger to myself or anyone else (or I’d not drive until I was safe).

– Just plain fatigue – yeah, I’m typing this and it’s only 12:35pm.  Seriously?  That’s it?  Time’s now going backwards, right?

– When I got home and got ready to do my evening gooping, I stopped at the exposing the boob part, since mine had (guess I wasn’t going to get away without it after all) gone full red – like lobster colored.  Fabulous, my last mother-fucking day of full-boob radiation.  Plus…

– more numbness (means more swelling, or more concentrated swelling is now interfering with nerve conduction) and more overt swelling/pain in my axilla

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Radiation Therapy Journal – Day 27 – Thursday December 6, 2012

Treatment Notes:

– Okay, today I got a real zotz when the treatment first started, straight through my nipple, then it went away and didn’t hurt anymore.

[Right, sorry, “zotz.”  Okay, so I tried to find the definition of this word I always thought was Yiddish, but I’m not so much finding an actual definition in a casual web search.  So I’ll define it for you as I’ve always used it and known it to be used, so you know what the hell I’m trying to say.

A “zotz” is a sharp, stabbing or burning pain that comes on instantly and is gone almost before you actually realize it’s there, but leaves an echo behind for a bit.]

Side Effects:

– Tired (come on, you’d wonder what was going on if I didn’t feel the fatigue anymore).

[But of course that’s also not surprising given my 11:00pm actual bedtime last night.  No, 7 hours isn’t enough sleep for me when I’m Not in primary cancer treatment – it’s Definitely not enough now.]

– more pain than I’ve been having the last few days.  Not entirely surprising – I’m extra tired today and that always makes things hurt more, and I got manhandled pretty good yesterday (which was necessary, but still made me hurt more).  So early to bed and maybe tomorrow will better.  At least tomorrow will be Friday, which is Always a good thing!

Copyright Ridingthebcrollercoaster.com 2012 All Rights Reserved.

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Radiation Therapy Journal – Day 26 – Wednesday December 5, 2012

Treatment Notes:

– Again, really nothing to feel during treatment, although once they got me into the position they wanted me in, I felt kinda tweaked.  But we can do anything for 5-10 minutes, right?

Physical Therapy:

– today kinda hurt – I’m having some increased swelling, including some into my arm, but certainly into my axilla and down the side of my body.  She also got rid of some adhesions underneath my nipple scar – breath in, breath out, she’ll stop in a minute.

– PTher is also going to start the process of getting me a sleeve.  You see, one of the fun things about this cancer and its treatments is the risk of lymphedema in the affected arm (for me, that’s left) . . . in hot weather, when ramping up exercise, just being at altitude, or plane travel . . . For The Rest Of My Life.  Woohoo!   So they have these spandex or lycra or something sleeves to add some compression to help the lymph system drain more normally.  Though I haven’t had lymphedema in the arm, I could start, at any time.  Of course, sometimes if I need to wear the sleeve, it’s possible that fluid can get stuck down in my hand and cause my hand to swell – more fun – so I’ll have to be prepared with a glove too.  Dontcha wish you could be me?

– On the plus side, however, when I first started getting PTher, she said a lot of people like to do it at the end of the day, then go home and relax.  It turns out that the lymphatic system is very shallow under the skin.  Therefore, very little pressure is needed to move the lymph fluid through the system.  The result of this information is that lymph drainage feels like a very light swedish massage (over the affected parts of the lymph system) and is very relaxing.  Unfortunately for me, because they start early, their “last appt of the day” is nowhere near late enough to be after I’m done with work.  But today, I’m not going to work (same with two weeks from now), so I can enjoy the relaxation of my PTher (after the pain) and go home to nap (after breffast/brunch of course – see my schedule for this week).

Side Effects:

– Tired (yes, I’m getting as bored typing it as you are reading it) – this time it hit me on my way to the car.

– More pain today, though not entirely unexpected after I’ve been (necessarily and as gently as she can) manhandled.  Of course I don’t want adhesions under my scars, of course I want to minimize the tissue damage my treatments necessarily cause.  So I went home (eventually – after brunch & a quick apple-acquisition stop) and lay down – that always helps the pain.

Copyright Ridingthebcrollercoaster.com 2012 All Rights Reserved.

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Radiation Therapy Journal – Day 25 – Tuesday December 4, 2012

Treatment Notes:

– Same old, same old now (if it’s not films/doctor day).  Marina was kind enough to bring me a warm blanket today without me having to ask – she seems to know which days are cold enough to be automatic-blanket days and which days to ask if I want one.  That girl’s gonna do fine (she’s doing her internship with my regularly-scheduled/licensed guys).

Side Effects:

– tired, again (still?) – I keep throttling back on what I’m doing (on wise advice of Dad, trying Very Hard Not to Overdo when I feel okay), and yet it only takes one long day to really wipe me out at this point – the fatigue slammed me midday when I headed out to pick up lunch.

– some nipple pain today, and me with my lidocaine gel down in the car – the good news is the pain’s not bad enough I hafta run down there ‘n’ fetch the gel.

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Radiation Therapy Journal – Day 24 – Monday December 3, 2012

Treatment Notes:

– They needed to do new films today, and have the doctor come in while I’m positioned on the table because I was swollen and she needed to confirm application of cell-destroying radiation – um, okay.  So my guys could see that on the films (that I was swollen from the treatment – if you’ve been reading me you know it actually happened Treatment Day 1 or 2), and I’m imagining the CT scans taken last week to plan the boost Did Not exactly match the CT scans taken a week before I started treatment because treatment made me swell damn near immediately!  But could she have believed me when I told her this 4 weeks ago?!  Apparently Not – she must be a fan of Dr. House (who gets the reference – 1st section?)!  But other than it taking a bit longer than normal – nothing much to see here, move along.

Doctor’s Visit:

– I’m inclined to believe that my ROnc actually did talk to my RSurg last week as she claims she did, for two reasons:

1) Mom pointed out that she said she did in my medical records and she couldn’t/wouldn’t do that if it weren’t true ‘cuz of this little thing called Medical Ethics.  Count on Mom for reminding me of the logical side of things.  But even more than that, I believe they talked because . . .

2) ROnc did Not try to push me into what she thinks I should do.  She walked into the room with printouts (as I had asked her to do) of the boost plan.  She explained them to me.  She then hands me and explains to me several study abstracts backing up her claim of the benefit the boost will provide to me And shows me the fairly good cosmetic results also covered in the studies.

She then tells me that she’ll do her visit notes with me and when we’re both happy, Then (electronically) sign them and print me a copy (to avoid having to void and reissue the notes as I had her do last week regarding my use of painkillers to get through the pain caused by the swelling (that she actually now believes exists) caused by the treatment itself.

She reads the notes right up until the last sentence, which I happen to see as she’s printing and closing that screen: “Patient will be given discharge instruction on last day of treatment.”  I repeat this to her and ask her to get them to me earlier (I don’t need things like that to be last minute in case I end up having questions, but she says they basically say “Call me if you have any questions or problems.”) and then she says she’ll have them printed and I need to bring them back to her, signed, on Friday, which will be my last day of treatment if I decide not to have the boost.

No further pressure – just giving me the information and letting it be my decision.  This is actually why I quit smoking (98 days CFT, BTW!) – because my RSurg Did NOT tell me to quit – she just told me what would happen to my body if I didn’t and I decided all by myself, just like a big girl who doesn’t have to be told, that my boobs and what I was going through to keep them, were more important to me than smoking.  I have to come around to things in my own time.  Forcing me there does not get me there sooner, it Delays Me Getting There.  Christ Almighty, she could have saved me so much angst if she had figured this out sooner!

Side Effects:

– lightheadedness, again – intermittently throughout the day

– So, interestingly totally normal blood pressure (107/62) this morning during my morning activities & the weekly installment of putting my doctor in her place.  Okay, so I seemed all calm this morning.  I figured I’d go with it.  Then midday I get nauseous and start to hurt, badly.  It’s actually my back that hurts, but I know it’s coming from stomach upset – this is a fairly familiar GERD pain pattern.  So maybe my Monday Morning Stuff manifested this way instead of as higher than normal blood pressure.  Okay, so I take a Zofran for the nausea.  30 minutes later the nausea was gone.  The pain wasn’t.  Took a pain pill.  45 minutes later no nausea And no pain!  Yay!  Time for lunch – soup, just to be on the safe side.  All’s well with the tummy for the rest of the day.

Copyright Ridingthebcrollercoaster.com 2012 All Rights Reserved.

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Schedule: Week of November 26-30, 2012

Monday [Radiation Therapy – Day 19]:

7:10am-7:55am Drive from Home to RTher
8:00am-810am RTher
8:15am-9:00am Appointment with ROnc
9:00am-9:30am Waiting for requested med records to be printed
9:30am-9:45am Making additional acupuncture appointments

[Going from only on non-support-group weeks to weekly, for now, at least while I’m still in radiation therapy, and while Mo is in her clinical rotation (before she graduates and the next class comes in).]

9:45am-10:00am Walked over to lab building across the street (Please see “Seriously, this Woman Knows Her Way Around a Vein – I’m Naming Names Again“) to get my lab results that should have been faxed to me last week.  Yep.
10:00am-10:15am Drive from Disney Family Cancer Center to Work

[With a drive through McDonalds

for junk 740 calorie breakfast (eggs, sausage, hashbrowns, biscuit) – really, there’s only so much one can shoehorn into a morning and still get anywhere near a full-day’s work done.]

10:15am-1:30pm Work
1:30pm-2:00pm Lunch
2:00pm-5:30pm Work
5:30pm-5:45pmpm Drive from Work to Acupuncture
6:00pm-7:00pm Acupuncture
7:00pm-7:55pm Drive from Acupuncture to Home

Tuesday [Radiation Therapy – Day 20]:

7:15am-8:00am Drive from Home to RTher
8:00am-8:20am Wait for RTher
8:20am-8:25am RTher
8:25am-8:35am Slather boob goop/visit with “Dana”

[I had invited “Dana” to join me at Support Group, which is tonight, and then go to breffast tomorrow before going home to rest after we do our crazy crack-of-dawn cancer business, but…

… it seems her blood work yesterday is such that they didn’t do her chemo, and she’s been feeling like something’s going in her body just now, so she’s not really supposed to be around people until her blood counts recover – this all means that her immune system is compromised to a point where she needs to be Extra-Careful ’til things turn back around.

She told me she was disappointed and I am too.  Of course, timing may not have worked out tomorrow anyway with my new CT films, but I hadn’t had a chance to tell her about that.  She said she’d call and I reminded her that we both have the rest of our lives to get to know each other if we want, and we’d keep trying to just find some quiet time for us to hang together some.

Throw up a little prayer for my new friend, if ya feel like it?  Thanks.]

8:35am-9:00am Drive from RTher to Work

[With 1 stop to put gas in the car and buy lottery tickets.  Damn, if there was any time I could go for winning a lottery that would allow me to quit my job, if even just for a while, it’s now!]

9:00am-1:30pm Work
1:30pm-2:00pm Lunch

[Seems I’m back to shorties to make up work time missed for medical appts.]

2:00pm-5:30pm Work
5:30pm-6:30pm Drive from Work to Support Group
7:00pm-8:30pm Support Group
8:30pm-9:15pm Drive from Support Group to Home

[Yeah, sorry, you only get two days of this week.  Even with taking Wed off – this week was my first of 4 consecutive Wednesdays off – I’m getting  pretty tired.

It’s weird, the treatment really doesn’t feel like much – you can’t see it, smell it, or taste it – and yet it can lay you low.]

Additional Tasks Accomplished This Week:

– blogged
– wrote check for housecleaner who came the Monday after Thanksgiving instead of her regularly-scheduled day which landed on the day after Thanksgiving last week
– made it working Monday, Tuesday, Thursday and Friday
– bought lottery tickets for the first time in weeks (months?)

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Radiation Therapy Journal – Day 19 – Monday November 26, 2012

Treatment Notes:

– really nothing to report, except for slipping by one of my guys at the front of the suite on my way back to the machine – being Perfectly on time and having him scramble to catch up with me today – hehehe (well, I’d take credit, but I think we’re maybe headed into that amorphous time of half-holiday-light traffic as we gear up for schools to start letting out for Christmas Break (yeah, I’m Jewish, I celebrate Chanukah, I’ve been known to have a Christmas tree, not a Chanukah Bush, get over the ultra-political-correctness already, will ya?)

Doctor’s Visit:

– Yeah, long story short:

She said she called my RSurg, had a discussion with her, and that my RSurg was okay with a “regular boost,” but was concerned that I was getting a “super boost,” and therefore was comfortable with the boost plan in place for me

. . . which claims, all of them, will be checked out by me, hopefully telephonically, with my RSurg, since I trust her, but do Not trust my ROnc to have the Whole Me in her best interest.  I wish I did, but I don’t.  Oh well.

. . . which boost plan has not been drawn up – What?  Yes, the boost plan (the last week or so of treatment where they take the daily amount of radiation currently spread over the whole boob, and concentrate that amount of radiation in the tumor bed only) has Not Yet been planned.

As I was writing the last sentence, my ROnc called me – she wants to get new CT readings (since I’m having some swelling – or she finally believes I am – she never got to see me before I started rad therapy and I swelled almost immediately) but using my existing tattoos – to make sure the boost plan is completely accurate (since my body has changed with the swelling since beginning this treatment, the CT scans done a week before I began treatment may not be accurate to my anatomy today).  Then she will take Thursday and Friday to do the boost plan.  She will print it out for me (like I asked her to do today with the regular plan) so we can discuss it next Monday at our visit.

Then I’ll have all of next week, still on the original and unchanged first part of the plan to decide if I want to do the boost or not (which, if I do it, will start the following Monday) without getting me into a situation where I don’t have enough time to consider boost or no boost before we’re forced to consider an unintended break in treatment.

So, that’s the plan for the moment, so to speak.]

Side Effects:

– Um, other than blood pressure of 140/75 this morning (WAY high for me – I’m usually – well, BC as in Before Cancer anyways – around 110/60 normally), but since I was planning to follow my “new normal” Monday schedule of 1) get my radiation treatment, 2) put my doctor in her place, 3) go to work – I was okay with that reading (this too shall pass) – the good old “white-coat syndrome” magnified and all that.

Update: This early evening before acupuncture, Mo took my blood pressure again – 110/70.  Not surprising at all.  I was having the Pavlovian relaxation reaction just being there knowing what we were about to do was going to make me feel better, immediately and for days to come.

In fact, when I left I shared the elevator down with another cancer patient I had met at acupuncture and we both had that ever so slightly sleepy, very relaxed ‘I just had acupuncture’ look on both our faces and shared that moment together in the elevator on the way downstairs.

– less pain today.  I’m inside the week that my acupuncture treatment effects seem to last (I managed to get another appt with Mo tonight – yay!), and the past 4 days of not having to wear a bra, and being able to rest and/or sleep Whenever I Want have helped too – a much needed break indeed.

Copyright Ridingthebcrollercoaster.com 2012 All Rights Reserved.

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Schedule: Week of November 19-21, 2012

Monday [Radiation Therapy – Day 16]:

7:10am-8:05am Drive from Home to RTher
8:05am-8:15am Waiting for RTher
8:15am-8:25am RTher
8:25am-8:40am Waiting for appointment with ROnc
8:40am-9:00am Appointment with ROnc
9:00am-10:00am PTher
10:00am-10:10am Post RTher-ablutions [in other words spreading boob goop]

[Yes, you are reading correctly – I had radiation therapy, a doctor’s visit And physical therapy, All Before going to work. :)]

10:10am-10:25am Drive from RTher to Work
10:30am-1:15pm Work
1:15pm-2:15pm Lunch

[I’m pretty sad about this Hostess thing – not only because I’m tired of upper management in companies being greedy, bankrupting their companies in the first place, And Then blaming it on the workers who put all that stolen money in their pockets!  And Then of course, a world without Twinkies and Ding Dongs would make me sad.  Are they healthy to eat?  No.  Is it okay to eat them once in a while?  Yes, I think it is.  Are they a reminder of my childhood I would be sorry to see disappear from the earth?  Yes again.

It has been said (most likely correctly) that another company will buy up the assets of the company (the brands and their accompanying product recipes – at least where the Hostess brand is concerned), so that these bad-for-you but occasionally good-for-your-nostalgic-soul-and-sweet-tooth cakes may indeed survive their original maker’s demise.  Just in case they Don’t get sold and survive, I was going on a hunt for ’em in my local neighborhood – namely my closest (within 5 miles or so of work) Hostess Outlet.

Long unnecessary story shorter than it could be – I came away with two bags of powdered sugar Donettes, but there were no Twinkies or Ding Dongs to be had at all in the outlet (good thing I have a box of each coming from Amazon – let’s not talk price – we definitely achieved the ‘silly’ level, but Did manage to stop short of ‘crazy,’ ‘ridiculous,’ and my personal favorite ‘batshit insane.’)  I’m low on time and energy in general these days (and interest too – a touch of depression anyone?  Yeah, I’m being treated for that – it’s cool.), but I’m thinking that was a lunch hour well-spent.]

2:15pm-5:30pm Work
5:30pm-5:45pm Drive from Work to Acupuncture
5:50pm-6:05pm Get blood drawn for lab work

[Please see “Seriously, this Woman Knows Her Way Around a Vein – I’m Naming Names Again.”]

6:05pm-7:00pm Acupuncture
7:00pm-7:45pm Drive from Acupuncture to Home

[Including a quick drive-through of a pharmacy to drop off the Rx for pain meds I was grudgingly given this morning.]

Tuesday [Radiation Therapy – Day 17]:

Hm, I completely did Not (obviously) keep track of this day, and since this is actually being posted Monday November 26, 2012, I’m gonna let this one go…

Wednesday [Radiation Therapy – Day 18]:

[Otherwise known as (effectively) Friday this week, with Thursday and Friday off from work.  :)]

7:05am-8:00am Drive from Home to RTher
8:05am-8:15am RTher
8:15am-8:20am Post-RTher ablutions
8:20am-8:35am Chatting with “Georgia” at the main lobby reception desk at the RTher facility
8:35am-8:45am Driving from RTher to Work
8:45am-1:00pm Work
1:00pm-1:30pm Lunch

[On days before holiday weekends, my company intends to close early.  To that end we’re asked to take short lunches.]

1:30pm-3:00pm Work

[Yup, we did close.  Yay!  (You see, I work in a fairly small shop, and the policy is ‘we all go or we all stay,’ so work that has be done by any one of a handful of us can scuttle an early day for all of us.  I’ve been both the scuttler and a victim of someone else’s scuttling in the past – but not today!)]

3:00pm-4:15pm Drive from Work to Home

Additional Tasks Accomplished This Week:

– blogged
– RSVP’d to two Thanksgiving Dinner invitations – one yes and one no
– indulged my returning knitting habit by buying more yarn for the stash (yeah, I know but it’s a thing with us crafters)
– that’s about it – it was a short week, ya know?

Copyright Ridingthebcrollercoaster.com 2012 All Rights Reserved.

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Seriously, this Woman Knows Her Way Around a Vein – I’m Naming Names Again

So Monday [See “Radiation Treatment Journal – Day 16 – Monday November 19, 2012.”] I talked to my doctor about bruises I don’t remember getting.  While it is unlikely that I would get Thrombocytopenia from radiation therapy alone (without also having or having had, chemotherapy), it is not out of the realm of possibility, plus I’m on two other drugs that contribute to this condition.

So, in order to humor me (which is generally Not okay with me – I do not like to be “managed” as anyone who knows me offline will tell you – but in this case is okay, because a test that tells me there’s nothing wrong will set my mind at ease and allow me to let go of it), she ordered some blood tests.

Of course, Thanksgiving is tomorrow, so I wanted to get this done and get results before the world all crawls into the Thanksgiving hole this year.

Therefore, I tried to shoehorn getting blood drawn into my day Monday (See “Schedule: Week of November 19-23, 2012” to be published later this week).

[Hm, do I put Thursday and Friday of this week in the week’s schedule or the weekend’s schedule?  Dunno yet.]

In order to try to be less of a bull in a china shop, while at work I called the lab in the building across the compound (for lack of a better word right now) from the Disney Family Cancer Center to make an appointment.  No, they don’t take appointments.  And of course, the time just after work is busy because everybody Else who works and needs labs done wants to come when I do – between leaving work at 5:30pm and having my acupuncture at 6:00pm (or in their case whatever else they have planned for after work).

I will admit at this juncture, that my tolerance for other people’s scheduling issues is realistically, well, nil.  If you’ve been reading my schedule posts, that might make more sense to you, because when I say I don’t have time for this shit, I Literally Do Not Have Time for this shit.  In fact, I think I’ll make a new Rule for this – Rule #3: I Do Not Have Time For This Shit.  You may still think my looking at things that way is not fair or not okay.  And I’m not saying it is right or fair of me to think that way.  I am, however, accepting of the fact that at this point in my life, it is my reality.

So, no appointment made (because they don’t do such a thing there), I walk into the lab lobby to find it completely empty!  Seriously, this holiday light stuff is finally working for me!  I signed in and headed down the hall to the actual lab as directed by a receptionist in that office’s lobby.

And I walk in, admittedly, like a bull in a china shop – because I needed my vein tapped, taped and me across the way in 10 minutes to make my acupuncture appointment on time.

Okay, so I was there 12 minutes instead of 10.  In that time Nick (dude, you rock!) managed to take my bad attitude and turn it around so that I was smiling and thanking (them both) on the way out.  For you being able to do that alone, thank you.  Yes, you talk the talk “[his] job is to help patients, not to be an additional burden to them,” and you walk that walk, seriously.  🙂

And then there’s Prudencia.  I’m here to tell you, if you ever need to get blood drawn for labs anywhere close enough to Burbank that it makes sense to go to 201 S. Buena Vista, Suite 125, Burbank, CA – make the trip and ask for Prudencia.  This woman took hold of the butterfly dealie they use, I felt one tiny stick, looked down to see no blood in the micro tube connecting the needle to the catch-tube-container (yeah, not very medically precise, but you know what I’m getting at, and if not, check out the pic at the top of this post), and watched her connect a tube at the collecting end and it sucked my blood right down there with no further pain at all!  Two tubes later, she removes the needle, covers the microhole she made with a gauze pad, attaches the red self-adherent gauze I provided to her (See “I’ll Take Red Please“), and I was on my way to acupuncture.  Since then I’ve had no pain there at all, and the next morning I had a tiny little red mark beside what may be a tiny little bruise – about the size of a pea or so.  Today, no bruise at all.

I mean on the one hand, with what-all this cancer shit is putting me through, so what if one needle stick turns out to be an (Capital-E) Event?  That would pale beside some of the other things I’m getting to experience (yup, that was my tongue in my cheek, you aren’t wrong).

On the other hand, with what-all this cancer shit is putting me through, does a simple blood draw need to be an (Capital-E) Event?  Because really, with all that other stuff do I need something More to be bigger than it has to be?

Thanks to two great people, last night mine Wasn’t.  🙂

I thanked you guys Monday night before I left, but if you ever land on this page, thanks again for helping me shoehorn that into my schedule and even though I came in the door snarling, for sending me back out of it smiling.

And yes, I now believe this cancer journey is maybe making me just the tiniest bit crazy – I just wrote almost a thousand words about getting my blood drawn <facepalm>.

Well, if you’re still here, Happy Thanksgiving to all – please be present with thankfulness about something in your life (even if what your thankful for doesn’t make any sense to anybody else), and tongues explicitly permitted in cheeks during this exercise.

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Schedule: Week of November 12-16, 2012

Monday [Radiation Therapy – Day 11]:

7:00am-8:00am Drive from Home to RTher

[With 1 stop @ Starbucks because it’s Veteran’s Day (which I don’t get off from work), so traffic is holiday-light, so I got nearly to RTher by 7:40am and stopped to get myself a treat (yeah, I know, quit counting, k?) on the way for no other reason than I had time.]

8:05am-8:15am RTher
8:15am-8:30am Appointment with ROnc
8:30am-9:05am PTher
9:10am-9:25am Drive from PTher to Work
9:30am-1:30pm Work
1:30pm-2:30pm Lunch
2:30pm-5:30pm Work
5:30pm-6:35pm Drive from Work to Home

Tuesday [Radiation Therapy – Day 12]:

7:08am-8:15am Drive from Home to RTher
8:25am-8:35am RTher
8:40am-9:05am Post-RTher ablutions

[Walked back into the female changing room after RTher and found one of the private rooms open, with my new friend “Dana” doing her post-RTher ablutions, so I slipped into the room with her (so we could share the mirror) and proceeded to chat and do our stuff together – sharing with each other what we’re each using and having a lovely time actually.  As wonderful as my entire support system is (And They Are!), there is something incredibly freeing and relaxing about being around someone (even if, to other people, they would seem a stranger) who is going through what you are – there is an instant intimacy and community like no other.  So we slathered boob goop on ourselves and chatted, I shared this blog and my contact details with her.  She said she’d read my blog and gimme a call to give me her contact info.  I hope she does – I had to get to work and she had to get upstairs for something so we couldn’t talk for but a few minutes – but I really like her.  So “Dana,” if you’re reading this like you said you were gonna, gimme a call.  :)]

9:10am-9:25am Drive from RTher to Work

[With 1 stop to put gas in the car]

9:30am-1:30pm Work
1:30pm-2:45pm Lunch

[No good deed goes unpunished.  I had 3 sweaters I had bought and after getting them home decided they didn’t fit well enough to keep.  Every year my company finds a family who doesn’t have all of what they need and helps them out.  One of the things this year’s family asked for was food.  I figured I’d take the sweaters back and use that money to buy food for this year’s family.  I can do that in an hour, right?  Wrong.

So after daring to take a few minutes this morning to talk to someone who, more than almost anybody else in My world right now, knows Exactly what I’m going through, I’m all of a sudden (with yesterday’s PTher) an hour down on work time this week.  And now after doing my good deed (despite giving myself an out not to do Anything for Anyone this year – oh, and I’m sticking by that for my own family – won’t they be surprised?), I’m an hour and 15 minutes down on work time.

So much for a foot massage Friday at lunch, eh?]

2:45pm-5:30pm Work
5:30pm-6:30pm Drive from Work to Support Group
7:00-8:35pm Support Group
8:35pm-9:15pm Drive from Support Group to Home

Wednesday [Radiation Therapy – Day 13]:

7:05am-8:20am Drive from Home to RTher
8:30am-8:45am Drive from RTher to Work

[Wait, aren’t we missing an entry in there?  Yes, yes we are.  As it turns out the entire computer system for the hospital, and by extension, the Cancer Center went down at 4:30am this morning.  It still wasn’t up when I walked in for RTher this morning, and of course since the medical records are all electronic, they couldn’t even call me to save me driving an hour an 15 minutes for nothing.

And if the system comes up, it takes at least 45 minutes for the machine to warm up, Then they have to go through their daily calibration (or whatever they call it), so who knows if I’m getting my treatment today or not.  So I was originally going to have my last treatment on December 12th, but since my facility is closed on Thanksgiving and the day after, we’re now taking two days on the end of my treatment.  And if I don’t get treatment today, then we’ll add this day onto the end of my treatment.  And then if I (yes, I, not my doctors, it’s not there body – I’m going to get two of their opinions and then make the decision myself) decide not to have the Boost at the end, then that adds another 7 treatments or so on the end, so I’ll be lucky to be done with this by Christmas.

And I have no idea when they’ll be able to treat me today, which means as much energy as I’ve put into making this as easy on my employer as possible, I now have to tell them I need to wait by the phone and bail on them immediately if it rings.  They’ll understand, but it pisses me off.  I simply Do Not have time in my day for it to get rearranged like this.  Please see Rule #3.

Happy Hump Day!]

 8:45am-1:00pm Work

[Got a call at 9:15am from one of my guys.  Apparently the machine is back up and he wants to know if I want to come in for my treatment today.  I ask him when.  He says he has 1:15pm, 1:30pm . . . I take the 1:15 spot, since that actually does Not need an announcement at work – I’ll just take my usual lunch hour and use it to go get treatment instead of…

…what I was going to do was make a deposit to my HSA account to get the tax breaks of maxing out my HSA deposit for this year and be able to pay some of the medical providers who’ve been sending me bills.  But now that will have to wait for another day.  Doesn’t sound like a big deal, I know.  My life feels so full right now, tho, that getting rearranged is more of a big deal than it might be for, well, you.

And I’m doing things on my lunch hour sort of because I am so tired these days, in that A) there’s no way I’m doing it on the way home, I’m completely done by the end of my work day,  so this way Some of it gets done, and B) I’m afraid that if I stopped and rested at lunch I may not get going again for the afternoon, so this way I have something to keep me going while I plow through my day in one fell swoop, as they say.]

1:00pm-1:20pm Drive from Work to RTher
1:20pm-1:30pm RTher
1:30pm-1:35pm Post-RTher ablutions
1:35pm-1:45pm Drive from RTher to Work
1:45pm-5:30pm Work
5:30pm-6:30pm Drive from Work to Home

Thursday [Radiation Therapy – Day 14]:

7:05am-8:05am Drive from Home to RTher
8:05am-8:15am RTher
8:15am-8:20am Post-RTher ablutions
8:20am-8:30am Drive from RTher to Work
8:30am-1:00pm Work
1:00pm-2:00pm Lunch

[Doing today what I wanted to do yesterday at lunch – depositing some money into a couple of accounts so bills can be paid – and they can leave me the hell alone already!  :)]

2:00pm-5:30pm Work
5:30pm-6:30pm Drive from Work to Home

Friday [Radiation Therapy – Day 15]:

Additional Tasks Accomplished This Week:

– blogged
– took a hat I had knitted for myself and gave it to one of the supervisors at my office to send to her sister, who has finished chemo and radiation, but whose home got slammed in Sandy – at least last week she was wearing a hat (‘cuz her hair hasn’t grown back yet from chemo), under multiple blankets and eating chips for dinner ‘cuz she had no power or heat – ‘cuz I do have hair, power and heat at home, and the means to cook a hot dinner.
– managed Not to run out of gas in the car (it was a pretty close call one day)
– emailed with my cousin on whether I will or will not be coming to her Thanksgiving shindig next week.  It makes me sad that I had to decline, but with Hubby maybe having to work over TG weekend (yeah, crappy, but oh well), and me literally not knowing how I’m going to feel day-to-day right now, since she needs to know for sure by Tuesday noon to plan her party, I had to decline as I honestly can’t guarantee knowing by then if either Hubby or me will be able to/up to doing Thursday.  So Hubby and me are on our own for Turkey Day, but it’s not the first time (prolly won’t be the last) and we’re okay with that.  We’ll either find somewhere else to go, do our own little thing just the two of us, or just hang out together and have peanut butter & jelly sandwiches.

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