Sunday

Well, my first colonoscopy is now - so to speak - behind me, as well as my second (non)-biopsy.  More on the latter in a minute.  I was told my colon is "perfect" - I doubt that, but it is comforting to know that the combination of good genes and no-red-meat diet for many years has somehow resulted in no polyps or other issues.  I didn't ask, but I believe I won't need another colonoscopy for 5 or 10 years.

As far as the biopsy, I was told - on waking up - that once Dr. M got in/up there, there was nothing to biopsy; everything was normal.  Okay with me.  I told him of our move to Maine.  I will miss him.  Seeing him always gives me confidence in my own well-being.  He said my next check-up should be in 6 months - for a CT scan and follow up visit with him.  I think I may try to return to CT for that scan and visit with him.  I will probably also set up a relationship with the doctor to whom Dr. M referred me in Portland, but if it can be arranged (and is covered by my insurance), I would still like to come back to see Dr. M for follow ups, at least for the next couple years.  Maybe until I reach my 5 year NED milestone (I'm half way there already!).

The worst part of the whole experience was the "bowel prep" which involves - for those of you too young, too lucky or too anxious to have had to deal with this - typically I believe and at least in my own case, taking 4 laxative tablets (4 x the "normal" dose) AND an entire 8 oz bottle of something like Miramax mixed in 64 ounces of Gatorade, lemonade or the like (typically I believe you mix a tablespoon or so with an 8 oz glass of water, etc.).  The idea is to clean you out, and I do mean clean you out.


I've done this a few times now, and this was the hardest time for me.  I ended up getting nauseous - which I guess is fairly common - and then throwing up (not that there was anything to throw up since for the day before the procedure you can't eat solid food, only clear liquids, Jello, bouillon, etc.).  But I made it and it's now over.

Hurricane Isaac ... Haiti ...

Keeping all of Haiti in my thoughts tonight as Hurricane Isaac bears down.

Peace.

Update and a little bitty rant

First, update: saw Dr. R today; all is well. I told her about our relocation plans. She was happy for me. She did say she thought I was due for a CT scan in October, but my memory is that Dr. M said I was now on a yearly CT scan schedule rather than every 6 months. Dr. R said she would defer to him, and she tended to be conservative, but she thought 6 months was a good idea. That was a bit of a bummer. I'll talk to Dr. M about it when I go through the BP&VP (butt poke and vagina pull), but I'm thinking a year is soon enough. I've read some disturbing things about the amount of radiation from CT scans; it would be pretty ironic to GET cancer from CT scans whose purpose is to look for cancer recurrence.

Second, little bitty rant: I was thinking it might be appropriate to see how Todd Akin liked a little legitimate - or even illegitimate - bop upside his bitty brain. Of course, the Democrats may end up owing him a debt of gratitude. I hear Paul Ryan proposed legislation in 2011 that said essentially the same thing Akin is now being torn limb-from-limb over. Be nice if some of Akin's tar could run off onto Ryan's arrogant feathers. Enough.

As Rodney King - may he rest in peace - would ask, "Can't we all just get along?" Tonight I would answer, "Honestly, Rodney, I don't know, I really don't know. How does one get along with someone like a Congressman who talks about 'legitimate rape'? I don't know, Rodney, makes me feel kind of blue."

Peace anyway.

Update and news...

A brief update re post-cancer treatment news and other NEWS. First, it has been an almost doctor-free summer, and wonderful for that. Dr. R's office called some time ago and postponed my appointment almost a month from late July to August 21st - tomorrow. Meantime I met with a PA in the colo-rectal practice as prep for scheduling a colonoscopy together with another vaginal biopsy. A two-for. One out-patient procedure and two doctors: the Butt Doctor and Dr. M. Can't say I'm looking forward to it, but it'll be good to get it over with.

Anyway, I see Dr. R tomorrow, first time since she failed to answer phone calls or give me results from the CT scan for 4-1/2 days. Oh well, not so important given my other NEWS.

Only a couple of the people who may still be checking in on this Blog now and then know this news, because it isn't yet fixed in stone - but getting there. I'm trying to buy a house in Rockland, Maine. The closing is scheduled for September 20th and - assuming all goes well with the rest of the process - David and I (and Ella) will be moving there some time in October, hopefully the first week or so. It's a smallish old house in decent condition right in town, about 7-8 blocks from the coast. Not a big yard - which is okay, we don't really need to take care of a yard. It has 3 bedrooms, so there will be a guest room for visitors. Anyway, it's a big deal for us. A big life change. I will be keeping my job, and working remotely, and David hopes to transfer to a store location in Maine.

Here's the "coast" we're near - Rockland has an almost mile-long breakwater - beautiful:

This impacts my medical situation because I'll be telling Dr. R tomorrow that it may be my last visit to her. I had already raised this with Dr. M months ago, when David and I began considering the idea, and Dr. M referred me to an oncology gynacologist up there. It's scary to be leaving the doctors who cared for me during the cancer treatment and have watched over me since then, but I can either go forward and live my life, not always looking over my shoulder anv expecting the worse... or not. I'm choosing to go forward and live, as well and as long as I can.

More later re medical after the visit tomorrow (if there's any news) and more re the house and relocating as the closing approaches.

Meanwhile we look forward to a week's vacation the first week of September, going back to WoodenBoat School, where I'll take a kayak class and David will relax. Then the butt-etc. thingy the week we get back, and hopefully, the closing week after that.

One friend - truly a FRIEND - mentioned that she actually misses my partisan political rants here since I haven't been posting much. I'm gearing up to get back into that mode. Check back soon if you're thirsting for rants.

Peace. Peace. Now if possible, and as soon as would be convenient to all of humanity otherwise.

Two years +

Again, so long since I've written - back in March. Since then I had the CT scan - the results of which were good, but were a pain in the ass to obtain.

In the "old" days - a year ago - Dr. R would call me the day of or the day following the CT scan so that I "shouldn't worry". This time, I had the scan on Tuesday morning and didn't get results until Friday after 5:00 p.m. The most troubling thing was that I tried calling Dr. R's office over and over, leaving messages, and didn't get a call back for days. Then when I did speak to her, she said she had not received any of the messages. I'm not sure what is more troubling: to think that I left 5 or 6 messages my doctor didn't get - or to think that she got one or more of the messages and didn't find time to call me back for 4 days. Anyway, done now.

I had to reschedule the appointment with Dr. M for a follow-up internal exam because I inadvertently scheduled it for 3:00 in the afternoon. I didn't want to do a bowel prep and then not be able to eat all day, so I rescheduled it for a morning appointment, but that pushed it back to the end of May. Finally I did it. The bowel prep was ... not fun. The internal exam ... sort of inconclusive. He thought once again he detected a "thickening" and asked if I would mind if his colleague also did an exam. What the hell? What's another hand up your vagina anyway - just another 5 fingers. It was a woman doctor, older (e.g., maybe 5 years younger than me or my age), and very nice. She did the exam and said she didn't feel anything unusual. That was a comfort.

To be really careful, though, Dr. M recommended - and I agreed - to go ahead and schedule a colonoscopy - which I've been putting off just because I couldn't stand the idea of yet more doctors, yet more procedures - and when I do the colonoscopy, Dr. M will come in and do another exam under anesthesia (and presumably another biopsy if the exam suggests it would be appropriate); that way I get a two-for: one bowel prep, one anesthesia and 2 procedures. So Dr. M's office made an appointment for me for a consult with a ... bowel doctor (actually a PA). I'll see them in July and agreed to schedule the colonoscopy etc. in September. Dr. M agreed that this is all just being super careful and there is no reason why I can't have a doctor/procedure free summer. Hurrah!

And that's pretty much the cancer-related news - thank god. No more CT scans until next April. Seeing Dr. R in the fall sometime, and not "seeing" Dr. M at the September procedure, but he'll be "seeing" me. I've come to really love Dr. M. On the one hand, he seems very confident that I am doing well. On the other hand, he is clearly very conservative and wants to be very careful to watch for any possible reoccurrence of the cancer. I guess making 2 years post-treatment is "a" milestone, but really that's all. It's hard sometimes to keep in mind, when I feel good, healthy - old and creaky sometimes - but good, that I HAD cancer and therefore my chances of having cancer AGAIN are greater than someone who hasn't had cancer. I still have never asked him - or looked up on the web - to see what "statistics" say the chances of reoccurence are for a cancer such as I had. I continue to think that for the foreseeable future, that information isn't helpful to me. Say the chances that cancer WILL reoccur are 50%. How does knowing that help me? What would I do differently? Assuming the cancer does NOT come back for at least several more years, I sometimes think that there may be a future milestone at which I may want to ask the question and seek the answer. Maybe at 5 years post-treatment; maybe not until 10 years post-treatment. I guess when I find out the odds, I'd like to already pretty much be on the side of having beaten them.

Finally - for anyone who is still even occasionally checking this blog to see if I have posted here, I apologize for the long delay. I think the lead-up to the CT scan, the sort of "semi" results from the February exam by Dr. M, the CT scan, the wait for the results of that, the follow-up internal exam by Dr. M - I just didn't want to sit down and write about it at the time.

I've gotten through it, now, and I kind of look forward to writing about the colonoscopy experience here - that's not exactly true: what is true is that I look forward to having that experience be behind me (no pun intended) and writing about it will mean that that has happened.

But I expect to be posting more often over the coming days, weeks and months, not about my health necessarily, but just generally about my life and thoughts and feelings. I MISS writing here, for myself mostly (and certainly by not writing here, I likely have driven away most of the few people who were regularly checking in). And I understand that this blog began as a way for family and friends to know how I was doing - when facing a life threatening disease. I understand if the pedestrian meanderings of my brain on daily experience do not rivet people. Nonetheless, I'm going to write. Feel free to read if you care to.

Peace. Peace. Peace.

Sunday morning

It's been so long since I wrote here - January 31st I think - that I hardly know where to start. Let's start with cancer-related news.

I saw Dr. M on February 29th. Like Dr. R, he too graduated me to seeing him every 6 months. Except...

Except that during the internal exam he once again thought he felt a "thickening". I mentioned to him that - not to be too too graphic, but remember, this blog began as a way to communicate my experience and feelings about dealing with a cancer diagnosis, so grit your teeth or jump to the next paragraph - I felt like I had to go to the bathroom. To be frank, that I either had to take a crap or pass gas. He was actually happy to hear it, thought that might be what he was encountering. So he asked me to come back another day, after using a bowel prep the night before. I asked if it would be okay to wait until after the CT scan - scheduled for April 16 - and he said sure.

So the CT scan is on April 16 - that will be my 2 year post-treatment CT scan. And I made an appointment to see him on April 18 but since then I've been scheduled to attend a 6 hour meeting at work that conflicts with my appointment with Dr. M, so I need to call him and reschedule it.

As the CT scan date approaches, again I feel that place in the back of my throat and in my chest, the tightening up, the flutter in my stomach, from time to time. I've just gotten over 2 bouts of "illness" - first a regular head cold, and then 10 days later, something more flu-like, 36 hours of fever, chills, ending with chest congestion that I"m still feeling the lingering effects of. The good thing about being "sick" is that it's kept my mind off of other, deeper fears. Actually, although I feel the nervousness stirring and beginning to rise, like sap in the early days of spring, I actually in some weird way look forward to this CT scan. First, because it is a true milestone, the first chronological milestone the medical profession seems to mark: 2 years post treatment. Second, related to that, it means no further CT scan for 12 months. And only 2 doctor visits in the intervening months.

So that's the cancer news.

Other news, let's see, the 200 residents of Alligator, Mississippi, where my father was born, elected their first black mayor by a decisive vote of 37 to 27, I think.

The Republican primary rolls out across the months like some coldly reptilian slithering snake. It does appear to have turned back on itself, found a juicy morsel of "prey" to feed upon and is now busy swallowing its own head and consuming itself. Nonetheless, I find I have boundless faith in the Democrats - that is, in their ability to snatch defeat from the jaws of victory. My grandmother, whom we called Big Mama, used to tell me: We're all entitled to be wrong. Indeed.

Green is creeping out the branches of trees, silently signaling spring - which newly arrived migrating birds are joyously announcing. Seems early, but I haven't gone back and looked at this blog from last year to check dates. I do know that I saw the first robin in the park as long ago March 6, and red winged blackbirds on the same day. Ella and I were at the park Friday (I took the day off), yesterday and again this morning. Many, many robins, red winged blackbirds, downy and hairy woodpeckers, black capped chickadees, and other birds I heard but didn't see. Spring is a feast for the ears.

Peace.

Tuesday night

A milestone: I saw Dr. R this afternoon. My next CT scan will be at the end of April but - BUT - but I don't see Dr. R again until July - I have graduated to seeing her every 6 months. How about them apples?

As I walked from the cancer center, the sun was setting, the sky glowed that shimmering blue fading slowly to black except in the west, glowing pink-red-orange. Overhead a murder of crows flew from north north west to south south east. Flew and flew and flew. They were continuously streaming overhead for the entire 25 minutes I stood and waited for my bus. How many were there? Thousands upon thousands I'm sure. Where were they going? Do they fly in family groups? Where were they? Why did they leave?

Now that the Republicans are - presumably - leaving Florida since the primary is over, perhaps the crows have decided to really go south.

I'm grateful for good news today. I'm grateful for good doctors, for having a job, for having health insurance, for being ... healthy.

Peace.