Spread the Dread

Many bloggers I read here in CancerLand speak of how their mother and/or other relatives had breast cancer–or how there was NO cancer history at all, cementing their shock at their own diagnosis. I always viewed my own story as a bit odd: my maternal grandmother, her sister, and her youngest daughter (my aunt), all had breast cancer. Then me, too.

One would think, that with a mother, a younger sister, and an only daughter getting breast cancer within months of each other, my own mother would rocket into the doctor’s office, demand screenings. Nope. My mother refused my numerous requests that she at least get a mammogram. I use “refuse” and “request” to be polite. I’ll just say the conversations were NOT polite, and I eventually stopped bringing up the issue in the interest of saving myself a lot of fussin’ and fightin’. I think sometimes my mother thinks not getting tests equals no bad news–ignorance is bliss. I can understand that trap a little. There’ve been times I’ve wanted to delay my doctor visits, until it becomes the battle of which is worse: not knowing at all, or potentially facing bad news. But my mother takes the cake: at least a decade since her last mammogram. She is almost 70. Isn’t 60-something the average age of a breast cancer patient? Basically, she refused to heed the once a year, 1 in 8 message Pink shoves down throats. And the irony? I still have to explain my anti-Pink views every now and again. Oh, she approves the Pink message—just, not for herself. Her frame of mind is that classic: “breast cancer is very real threat, but it won’t happen to me”. Ah that denial, I once knew it well.

Needless to say, this personal situation drives me nuts, which is one reason I rarely share it.

In the past year, her diagnosis of having a hereditary kidney condition (that no other relatives we know of have–go figure), has opened her eyes. She finally relented and had a colonoscopy—only 15+ years after the recommended age one should start having them. Yes there were polyps, removed and proven benign. Then finally her GP twists her arm enough to get a mammogram. And yes, there was an area of concern, and she was called to schedule a sonogram.

I pause here to say for all the stereotypical “I’m turning into my mother” things I notice about myself each day, how we approach medical issues is the one place we will always be vastly different. She is from the old school, revere the doctor’s word as near deity-like; I challenge everything. I prefer to attend doctor visits alone—cancer was awful in that necessity of always have an escort to help write down/ask questions/don’t drive after treatment. I’m a royal impatient bitch in waiting rooms, so I really don’t like company. Mom likes to have someone with her. Mom usually thinks all is well; I’m a typical post-cancer person—convinced each scratch is a sign of recurrence.

The other difference is I generally mean it when I say, “no don’t come with me”. Mom will say those things and really mean, “please escort me”! (Typical for her age and upbringing.)

Long story short, I took her for her word, did not go with her, and yes experienced the guilt only mothers can force on their daughters afterward. I am further frustrated because I know I would’ve advocated for her harder. The radiologist told her he didn’t think there is cause for concern at present—come back in 6 months. She is relieved and thinks all will be fine. And maybe it will be.

But, given my nature, I have doubts. Just to review if you missed the first paragraphs—imagine my mother as a dot in the center of a triangle. The 3 points of the triangle are occupied with her mother, her sister, and me, her daughter. We all had some serious breast cancer. If you were a gambling sort, what are the odds, hmmm?

Obviously, I’m not inclined to think all will be well even if two of those triangle points were removed. My own cancer was a story of falling into the smaller percentage: (false negative mammogram, E/P negative and HER2+, 1 in 233, NOT 1 in 8….). Of course I am pressing the panic button. Of course I expect bad news in the next 6 months.

But what can I do? The doctors, with more knowledge, think it is not time to panic. The media is full of stories of over-diagnosis, over-screening, false alarms. Who am I to disagree?

I do not know how to be a cancer mentor, as I mentioned in a previous post. I am not the one who will tell you or anyone: “hey it’ll be OK, just fight, be positive, and things will work out”. I will never join a local or online group as a breast cancer survivor that newly diagnosed women can turn to, to comfort and share knowledge. I’m an idiot that barely handled my cancer my own self. It is all I can do, when others around me begin to spiral, to not follow them down the drain (talking about even more folks I know than my own mother).

I’m sure most cancer patients have at least one or many people in their circle saying, “don’t worry, it will be fine”. For me, the problem was I ONLY had those types around me, to the point that every single time I expressed fear or other so-called negative feelings, I was shut down. The result of that for me was that I felt dismissed; it impacted me to the point it reverberates even today. That’s kind of what this entire blog is about: reassuring myself that those feelings are common, normal. And when the kind folks who comment on my blog posts comfort me or share their own feelings of “negativity”—well, that is another reason I keep this blog. This can be a safe place to vent, without the fear of being shut down and told to think positive, it will be OK. I do not know that it will be OK, so I will never say that. I will just try NOT to feed anyone’s panic.

I realize most people in my life need the “it will be OK” thing said to them. I do not know I can bring myself to do that every time. All I can do is try to keep myself from piling on. My stern message to myself: “don’t spread the dread”.

Posting This One Again for Reasons Part 1

One Reason: LOTS of chatter on the interwebz about positivity lately. Advice that cancer patients should “be positive”. And I’m seeing a very disturbing lack of understanding for those who are labeled “negative” (although I do NOT label myself that way). My new favorite quote applies here: “You have your way. I have my way. As for the right way, the correct way, and the only way, it does not exist.” – Nietzsche

Another Reason: I’ve been really, really, REALLY busy—too busy to write. I sit down each day and skim stuff to read and then fall asleep before I can get started. Hope to change that next week.

Take the Mythical Image of the Strong Warrior Breast Cancer Survivor And Bury HER Once & For All

Posted on March 28, 2013 by Cancer Curmudgeon

Author’s note:

If you are a breast cancer “survivor” who embraces that ideal image–the pink products, the racing for the cure, etc.– I am truly happy for you. I mean that sincerely, without my usual dose of sarcasm. And just as sincerely, I beg you to stop reading this post, you will probably find it offensive. As nearly always, there will be foul language, because that is how I speak.

This post is for the ones who got breast cancer, and went into it doubting, or maybe at first embracing, what I shall henceforth refer to as The Image. It is for those of us who at some point realized we could not live up to The Image. And for those patients lost and unsure, feeling set adrift, away from the pink anchor. This post is for them–you–us. -anotheronewiththecancer, AKA cancer curmudgeon

Why do I propose this burial? Because I think this mythical image is dangerous. I’m tired of hearing or reading about women who feel they cannot live up to The Image; becoming depressed, maybe suicidal, because of the way this pressure made them feel. I’ve encountered this sort of despair a few times recently, and enough is enough.

I’ve used this comparison before, I think. Let’s say a gun is pointed at your head. Maybe you get shot. There will be blood, there will be pain, and you might die. At the most basic level, cancer is just like that, a gun pointed at the head. You get cancer, you will bleed, you will have pain, and you might die. Most people, when having a gun pointed at the head, would shit themselves. Breast cancer patients however, are expected to run a race, smile, and fight, fight, fight! Like a good little girl. Whoops did I just say that? So when these women cannot live up to the expectations, not only do they feel awful because they have cancer, but they feel like they are letting EVERYONE down, especially those who’ve supported them, but also the world at large that expects certain behavior from the breast cancer she-ro.THIS IS WRONG.

I get it, there is a desire to fit in, to find support somewhere, and the smiling pink parades look inviting. Some women find solace in the support of a sisterhood. (BIG ALERT: I’m an only child and glad of it, so the notion of sisterhood baffles me.) We all want to belong. One of the many problems is, The Image pretends to invite everyone, but it does not; it is actually quite exclusive–I’ll stop short of using the d-word. Dissenters and doubters with breast cancer are ostracized. Don’t believe me? Read Barbara Ehrenreich’s Bright-Sided: How the Relentless Promotion of Positive Thinking Has Undermined America. The first chapter is Ehrenreich’s description of her breast cancer experience, called “Smile or Die: the Bright Side of Cancer”. Some of the incidents she described were all too familiar (hint: a breast cancer patient suggested Ehrenreich get professional help for her “bad attitude” I got similar advice while making what I think is a valid point on Huffington Post). In my humble opinion, it should be required reading for ALL newly diagnosed breast cancer patients.

And notice I only mentioned breast cancer patients. But even not all breast cancer patients are invited, I’ve learned by reading blogs. I’ve read some ugly stories about the ones with Stage IV getting shut out of the “support system.” But of course, they are the awful reminder that breast cancer is not totally beatable, as we’ve been led to believe. “They” can never fit into the The Image. *I use they in quotes not to reflect how I feel about those with mets, but to reflect how I believe The Image machine views those with mets.

Guess who else is not invited to the pink party? Patients with ANY OTHER KIND OF CANCER. I hate that. Why are they excluded? That is a can of worms to open on another day, another post. I will offer this thought to ponder: is it because we just expect them to die, and by that I also mean get out of our sight, as an embarrassment like the mets breast cancer patients, because they cannot beat cancer and fulfill that stupid warrior stereotype? Ask your nearest ovarian or pancreatic cancer patient, they can tell you what’s up, in language you may not want to hear.

I knew pretty much from the get-go that I would not live up to The Image. For those who’ve read some of my other posts, it is pretty clear I was never the cheerleader-joiner type. So of course I’d be the glowering dissenter in the corner. Honestly, I did try to be a good patient (not just a good breast cancer patient). I followed orders, took tests, showed up at appointed times, eventually joined a support group. As treatment progressed I learned some hard lessons about following doctor’s orders, like the need to challenge medical proclamations handed to me, because mistakes were made, but that is another post.

I think I rejected the Pinktober stuff even before I was diagnosed. As an alt-punk Gen-Xer, I hate it when I am being sold to, and tend to look for the lies beneath all shiny images, and I knew The Image, along with the pink crap, was being SOLD to me. These days, as a breast cancer patient, the Pink just infuriates me, rather than simply annoying me on an intellectual level.

When some acquaintances walked in a pink event in my name, I was gracious, I love the little pink rubber- duckie they gave me, and I will never forget their kindness. But I won’t EVER walk or run, I won’t buy pink crap. I don’t need to go into the reasons why walk/runs are not effective fundraisers, nor need I explain that cancer simply cannot be shopped away. Other bloggers have done that, and if you’re still reading this post, you already know this.

That said, this post is not me saying, “Oooo look at me, I’m so clever and strong to have rejected The Image without ever falling into the trap”. On the contrary, the marketing, the peer pressure, in cancer communities is so prevalent, it is amazing anyone ever questions anything. No, this is me defending the ones–us–who don’t want to, or cannot fit into this distorted ideal, The Image. I mean that with more conviction than nearly anything I’ve ever said in my life.

I’m not going to go into how The Image developed, there are some good books out there about that. I am aware the advocacy movement started as a way to support women’s health, bring breast cancer out from the whispering shadows, so women could demand better treatment. This is a good thing. But in a few decades, the pendulum swung completely to the other side, to the point that we shout about breast cancer from the rooftops, and there seems to be subtle pressure to be damn near proud of having it while sporting pink clothes and bald heads.

Of course I’m glad breast cancer is out of the shadows, but in keeping with the insane American ideal of “if a little of something is good, a lot of it is better”, now it has gone over to the ridiculous. We need to bring the pendulum back. We need to slow down, find the middle ground. No more ideals, no more she-roes, survivors, warriors, no more hollow “you’re so brave” compliments. I’m no she-ro. I am no warrior. I am not brave, I screamed and cried raged often enough I assure you. I am simply a woman who found out she had a life-threatening illness, made logical, somewhat informed decisions to eliminate that threat, and tried to deal with all the emotional crap that came with it. I made these choices because I wanted to live, not die. It is that simple. Don’t ascribe these words and their hollow meanings to me and my experience, it is not your right to do so.

So to those breast cancer patients, or survivors or whatever you call yourself, who are struggling because you don’t think you are “doing cancer right”, I doubt this silly post will ease your pain. I can’t remove the pressure of The Image from your back, and maybe no one can do that but you. You will need to be the one to take this mass delusional Image and chuck her out the window, where she belongs. The only way The Image will cease to exist is if enough of us ignore her.

I am sorry if I come off harsh. A lifetime of being unable to conform to much has made me a bit rough around the edges at times. The cool kids or the mainstream (in breast cancer, in life) tend to be intolerant of “the other”, and since I usually fall into that category, I cannot help but be a bit snide about being an “outsider” all the time. I tried not to criticize or judge, but at times I feel criticized and judged by the mainstream pink community and it is hard not to reciprocate. I am ashamed of that because I am truly trying to be a better person.

I do not have any proposals on how to solve what I think is a problem (and yes, it is a problem if someone goes through cancer treatment successfully, and then wants to commit suicide for being unable to live up to The Image–no matter how you spin it). As usual, I am the jackass in the corner pointing out what is wrong without much of a constructive suggestion. I don’t have a degree in Sociology or Anthropology, which is probably what is required to understand the nature of the cancer subculture. If I could lead an army of like-minded folks down the highway in October, destroying every hint of pink I saw, I would do it, but I doubt that will ever happen. All I can think of to do is reject it for myself, and offer a helping hand to anyone else who wants to do the same.

Hamster Wheel

 

Reposting Hamster Wheel.

The title of Marie’s Weekly Roundup today jogged my memory–I’d tackled the subject of my most recent post over a year ago. Wow. Still pretty much feeling the same…

 

 

Heeeere’s Cancer!

I cannot take a break from cancer. It pops up even in my escape plans.

Several weeks ago I wrote a post about watching “60 Minutes” specifically to see Anderson Cooper interview someone much cooler than himself—Dave Grohl. Before the Grohl segment came on, I sat through a segment on embryo manipulation—removing the faulty BRCA mutation to end breast cancer. My little respite from cancer was invaded. Then a few days ago, I tuned into “The Daily Show” to see Grohl discuss his awesome History of American Music Cities again. And whaddya know, before his Royal Grohliness was interviewed, more breast cancer!

It’s not that I disliked the piece mocking the Komen-fracking-pink drill bits, indeed I loved it. I’m just fussing because every time I want to take a break from cancer and indulge in other interests, it pops up.

Grrrr.

I’ve discussed in older posts the concept of “getting over cancer”, how friends and family expect patients to just be “done”, they think that after treatment, things like recurrence, lingering side effects don’t matter. I’ve read many other bloggers discuss this topic. People ask, “aren’t you tired of talking about breast cancer?” Duh, yeah! But not talking about it does nothing to reduce risk for recurrence or a new cancer. Writing about it is the only thing helping me recover emotionally. Furthermore, look how unsuccessful I am when I do try to forget about it. Watching TV, escaping into music or whatever, cancer creeps in. I hardly ever get to the movies anymore, but the one I managed to take in, “Guardians of the Galaxy”, don’t ya know, opens with a scene of the hero as a child, his bald and weak mother in a hospital bed, dying right before the hero is whisked off into space to become this Guardian. I loved the film, but was very upset for those first few minutes.

Take a break from cancer? Yeah, I’d like to. Doubt it will ever happen tho’.

here cancer

Note to Self

“You’re still going to get criticized, so you might as well do whatever the fuck you want.”— Kathleen Hanna

“Just because you’re offended, doesn’t mean you’re right.” — Ricky Gervais

From Mopey to Dopey to Sleepy

Wow. It’s been over a month since I last posted, or even wrote. Last post, I wrote about how my ongoing recent health issues had sent me reeling back into my fresh-outta-treatment panic and blues. I’d started blogging in the wake of those initial post-treatment blues two years ago, to help rid myself of them. That had worked for a long while, and I was getting much better. But this regression motivated me to do the opposite. I just felt like any post I would write in the past month would just be infected with my mopey views.

So I chose to just try and do a little self-care. I took medications and started an exercise (stretching) routine to prevent muscle spasms and numbness. I figured out that the dizziness was caused by my old allergy medications suddenly failing to work. I had to get new ones, and adjust. So I was doped up for a little while and of course, some sleepy side effects ensued. I slowly started to feel better, to the point I actually had several consecutive days mid-July of total well-being, actual feeling normal (well, post-cancer normal wellness, anyway). I planned to get back to blogging, but first I wanted to take time to make up lost work time, lost fun time, lost beach time.

Then last week I got a wicked summer cold.

It is just endless—like my body insists on being sick. And I am sick of being sick!

All this time I have indeed been reading others’ blogs and trying to keep up at least a little bit, even if I didn’t have the mental energy to say much. I’ve been thinking and pondering. I always have opinions and thoughts, and hopefully, I’ll get my act together enough to return to blogging soon.

Until later, then.

The Line

I, and many others, have often spoken of the fears that haunt cancer patients upon completion of treatment. Every little ache, twinge, hangnails even, can induce great fear in a cancer patient: “Is this a sign? Is this cancer coming back?”

For the most part, I’ve been capable of knowing when something is just a normal issue, not a signal that cancer has come back. The first time I had a little 24-hour flu after cancer, for example. It was weird, to have such a normal episode of nausea and vomiting not related to chemo. (Unluckily for me, this episode happened right after having a large Thanksgiving dinner—geez, of all the lousy times to get sick…) I know when I’m having allergy problems rather than a cold; I know that even though I’d never had a UTI prior to last fall, I knew it was a simple thing. I felt pretty secure that none of these minor illnesses signaled the return of cancer.

In short, I’ve remained on this side of my imaginary line that divides normal illness or signs of aging versus abnormal symptoms that indicate I need an oncologist. That is not to say I am or ever will be “over cancer”, I know the risks, the likelihood of recurrence and that I am not “all better”—unlike those folks who like to tell about their friend of a friend who had a little cancer that one time and now she’s “all better”.

But I have lost sight of the line lately. Or maybe I keep jumping back and forth over it, or I’m straddling it.

When I had my suspicious mammogram last March, I found myself back in that place of cancer terror, the place I occupied upon diagnosis. I had a brief reprieve after the MRI proved the suspicious area to be scar tissue and not a tumor. I breathed easy, thinking I’d dodged a bullet this time. But every health blip I’ve had since then has sent me over the edge—especially since it all seems ongoing and whack-a-mole; each time a symptom is quashed, a new one pops up.  All remains unresolved.

Given my history of medical professionals misdiagnosing me (my first mammo was all clear when really I had a giant cancerous tumor; I was told I had shingles when really I had a staph infection), it is hard for me to trust my GP when she tells me stress has made my muscles contract to simple muscle spasms causing my limb/finger/toe numbness. How do I know it is not something more sinister? If not cancer, perhaps something just as serious and catastrophic?

How do I know or trust that that my issues are not something more serious? I’ve lost sight of the line—the line that says trust the doctor that it this problem is not serious versus advocate, push, ask for tests that prove my worst fears.

I’ve been living in that dark hole of fear and terror lately. I’ve not been communicating or writing much, I just cannot focus when my mind is busy contemplating the horrible possibilities. I don’t like being in this place. I thought I had my post-treatment blues, my walking-with-fear-of-cancer’s-return in hand. But I do not.

So back to the drawing board. Back to counseling. I’m angry at myself that I took one step forward and have now taken several steps back.

Because Sunday

Because Sunday

Last year National Cancer Survivors Day was over before I even knew it existed. I kind of shrugged it off. This year I was alerted to its approach via social media. And this year I’m decidedly not enthused about it.

I see the website, with tidbits like: “On Sunday, June 1, 2014, cancer survivors across the globe will unite to show the world what life after cancer looks like.” (Aside: that confuses me—is it “national”, which nation, but the around the globe quote seems it should be called international day????) Or, the tidbit mentioned on other blogs that the day is show life after cancer can be better?

Admittedly, I’m in a very bad mental space lately. Since March, I’ve had one health issue after another, starting with a suspicious mammogram that led to a relieving MRI that showed no evidence of recurrence-at least in my breasts. But after that it’s been other health issues, drugs with bad side effects, or maybe not—still trying to figure out what is going on with me. Meanwhile, I feel crappy, and I am torturing myself that all this indicates cancer is back somewhere else. I felt kind of “blah” the summer before I was diagnosed. And yes, I had that clear mammogram a mere 5 weeks before I was diagnosed with a big ass tumor that first time. So sorry, but I don’t have much patience in this process of trying to figure out my health problems without considering what I fear most.

So I’m not up to showing the world what life after cancer looks like—for me, it has been just riddled with fear, anxiety, and panic. Even if what is happening to me now is not recurrence, the fact I’m having such a difficult time tolerating or resolving new, other health issues just shows how much cancer has damaged my body—made me weaker and not as able to shake off what someone my age who has not had cancer might be able to do so easily. No, I don’t think the folks behind this event want me as a poster child for what life after cancer looks like. I wish I did look and feel like those smiling people in the survivor pictures, swimming, being active, oddly resembling ads for feminine hygiene products. Oh yes I went there.  I may feel terrible, but I can’t stop my sarcasm.

As for that word survivor, once more for those in the back row—I do not consider myself a cancer survivor until I die of something else. I do not use it because my friends with Stage IV are not “losers”, and they are too often shut out of the rah-rah survivor discourse. I’ve written about this, and other cancer labels and language many, many times, so I’m putting links below to some of the ones I remember—I’m sure I’ve written about it in other posts that I’m just not remembering.

One final, parting shot thought: I’ve been merely re-posting old pieces lately. Yes, I’ve been too tired and feeling too crappy to write much. But that is not all. I find that I still feel mostly the same about all these issues. My mind has not changed too much. I used to think if I just kept writing and talking, the conversation about cancer could change. I no longer think that. I merely hope that at some point, the world will see there is not one single, happy story of cancer, there is not one “THE way” to do cancer (I’m thinking about that TV news person who introduced the clip of the dancing mastectomy woman by proclaiming her dance as “THE way to do cancer, folks”). At some point, I hope society will understand that there are thousands (millions?) of cancer stories out there, and no two are alike. And none of them are wrong. Taken together, they are the real, whole story of cancer.

What Do I Call Myself?

The Other Other Language of Cancer

Why This Smart Ass Does Not Kick Ass

The Curmudgeon Formerly Known as Cancer Patient

Remedial Course

Read something in the blogosphere that made me remember writing this. Might have to repost now and again until at least the media gets it right–internet “experts” never will.

Somebody Needs to Buy These Media People a Dictionary

So I’m watching GMA Friday morning and there is a brief segment about this co-host on Dancing With the Stars, Brooke Burke-Charvet. Now, I do not watch the Dancing show, know nothing of this woman, and have not bothered to look into her story on the internet, not interested enough. My complaint is the way the dark-haired female reporter, and her producers at GMA, presented the info. This Burke-Charvet woman has or had thyroid cancer, and is doing some promo thing on some health magazine about how her cancer scare means she no longer worries about looking young, and she wants people to live healthy, exercise (the usual crap), and get check-ups with doctors. Now, I do not know if it was Burke-Charvet who actually said people need to engage in preventative practices by getting annual check-ups, I will give her the benefit of the doubt. But certainly the GMA reporter said that the idea behind the campaign is for people to prevent health issues, like cancer, by going to their doctor. Apparently this Burke-Charvet has always lived healthy and had no symptoms, and it was on a routine visit to her doctor her thyroid cancer was detected.

In what universe is early detection equal to prevention?! Going to the doctor and learning she had cancer did NOT prevent cancer. She already had the cancer, therefore, it was NOT prevented. It was detected early, and that is great, but it was not prevented no matter how the media spins it.

This is the kind of thing the media does that drives me crazy. Throw around words like “prevent” so people feel in control or empowered. How many times will I have to write this? Some things are out of our control, if cancer had a motto it would be “shit happens”. This idea we can control every single thing that happens to us, cancer included, is just extreme hubris.

It is important for the media to get this language of cancer right. By suggesting to viewers that “prevention” is within our grasp just by getting regular medical check-ups is damn near negligent. I repeat, if a regular doctor’s visit (as in a visit not instigated by symptoms), reveals the presence of cancer, that is EARLY DETECTION, not PREVENTION.

The media needs to pull their collective act together. I am especially annoyed this segment was on GMA, a show featuring a news anchor with well documented bouts of cancer. She and her cast mates should know this difference all too well. Shame on you, GMA.

Agitated

I want to write a thoughtful post about all that is happening with my current issues, but I am unable to do so right now. In a nutshell, I have “some kind of cystitis” that is causing a high, almost unmanageable urge to urinate, VERY frequently. This has been going on for over two months and I’ve been bouncing around with the doctors, and dealing with scanxiety (see past few posts). A frightening episode with ultrasounds of my kidneys and bladder yielded “good” results. As in, no tumors (yay), and everything seems normal (not abnormally retaining urine). That’s great, except I still have a problem, and it seems undefinable, at least according to these imaging results. I’ve been informed that these “good” test results do not necessarily mean I do NOT have cystitis.

In the meantime, while going through the tests and waiting for results, of course pharmaceuticals were prescribed. Of course insurance would not approve the doctor’s first choice, and I’ve been forced to jump through hoops. Nothing new, that happened a bit during cancer treatment. But the drug that was finally approved came with dreadful side effects. I have been suffering from these for the past week and it has been as bad as the effects of chemo, maybe because I did not expect them to be so drastic. Dizziness, blurred vision, heart racing (although that one is not listed), weakness…the list goes on. The one that “got” me though, was: agitation.

Yes, I’ve been very agitated, which is why I’m late in getting this post out, and why it took some time for me to respond to comments on recent posts. I was too weak/fatigued to spend energy on anything but working. And I still do not trust myself to communicate in a level-headed way, even now.

Let me put it this way, the side effects were so extreme, I was sure cancer had returned, everywhere in my body. Despite an all clear MRI two months ago, I’ve been convinced that a giant tumor is lurking in my breast, under the scar. I’m convinced cancer has spread to my brain. I’m a bit calmer now that I understand that I’m agitated because of the drug, but I’m still a little “off the rails” even now. I was on the drug for a week, and I ceased taking it a few days ago—a choice I made even before I understood all these side effects—I stopped taking it to rule out the drug as a cause of what was happening to me. I’m glad I had the presence of mind to do that, and looking back at how bad the beginning of this week was, it is amazing I did have that presence of mind.

I’m still not “right”. I still have upcoming doctor’s appointments….and the original problem of urgency and frequency has returned. My frustration level right now is VERY high. So I’ll stop this post here, because I can tell, even just writing this, that my mind is still not right. I only wanted to let everyone know, given the fears I’ve written in recent posts, that at the moment, they seem unfounded.

But my problems are still not solved, so my quest continues.