Hi there happy people. I hope you’re happy people. It is Friday after all. That means it’s the weekend, right? I don’t care so much about the weekend anymore since I hardly work these days, but it does mean that people are available to do things, which they typically are not during the week.
So I could tell by the number of new views on my Peckalicious facebook page that people were wondering where the most recent post is. While they share the same name, that page is for shit I make and want to try and sell. When I actually thought I could make a side income from making shit. What I learned is that people want handmade shit for like pennies, unless you claim to be Amish, or “country”neither of which apply to me. So now I just make shit to give people. And beside, having to make things for money kind of kills the joy for me. I do it because I like to; money is nice, but I like the creative process.
If you are a facebook friend, you got the condensed version of the Dr. visit on Monday. I get tired of typing it out again and again, so I usually send a group message after my visit and post a synopsis on Facebook. Sometimes it just seems like it’s redundant – things don’t change much, or there’s waiting for things to change. But before I continue, I’d like to make a request or perhaps, just an comment, to people who frequent doctor’s offices, and particularly those who are only there for a damn blood test: YOU DON’T NEED AN ENTOURAGE. Really, unless this is your first blood test ever, you don’t need to bring your whole family. Even if it is, you don’t need more than one person to hold your hand. And pay attention to the instructions at check in. Just because you didn’t listen to the helpful staff who told you what to do with your purple or yellow folder because you were talking to YOUR FUCKING ENTOURAGE, doesn’t mean that because you sat there with it for an hour and now you realize you were supposed to put it in the bin so they know you are here, that the world should stop and you should be called next. Also, to all the fucking whiners in the waiting room. You have cancer. You are here to see the Dr. Threatening to leave because your name was not called in the 10 minutes since you sat down, (with YOUR FUCKING ENTOURAGE) is gonna hurt no one but you. You should be grateful you have time to wait. I know I would personally prefer being at home on the couch with my medication, but hey, you drove here, you parked the car, and came inside, commit. I’ve rarely been to a Dr. where I have been seen on time. The nature of medicine itself does not cooperate with linear time. Bring your happy face with you. And if you are in a hurry because you made other plans (with YOUR FUCKING ENTOURAGE), then you can cancel the plans, or the reschedule that visit. You and YOUR FUCKING ENTOURAGE took up seven seats in this waiting room. I have to sit out in the hall on a bench, with a sweet grandma and her grandbaby (this is sort of a blessing because the baby is muffling your bitching and moaning). I’m not complaining. I brought a book, and my phone to listen to podcasts. There’s a damn refrigerator with drinks for those of us with cancer. Get a fucking cranberry juice and shut the fuck up. I’d like to clarify that it is usually one or two people complaining, not a large number, but they always have a FUCKING ENTOURAGE and they are always loud. You know this waiting room is small, and there is limited space, but please, make sure that you and your FUCKING ENTOURAGE spread out as much as possible. AND WHATEVER YOU DO, PLEASE MAKE SURE THAT YOU AND YOUR FUCKING ENTOURAGE STOP DEAD RANDOMLY IN FRONT OF PEOPLE WHO ARE WALKING BEHIND YOU. Here’s a tip – if you are just there for a blood test, try showing up in the morning. Early. BEFORE YOUR FUCKING ENTOURAGE GETS UP.
My appointment was at 2. That’s “the get here on time” time. The appointment is really at 2:15PM. I am feeling week and tired, but am having a lovely conversation with the sweet grandma I met who was also a patient of Dr. K, and was scheduled for 2:30. Her grandbaby kept us all amused. I had enjoyed a brownie on my way to the Dr. so I was rather mellow, which I should bring for the whiners and their FUCKING ENTOURAGES, come to think of it. I was finally called around 3:05, which was pretty good for Dr. K, because unless you are one of the first three appointments for the day, you typically wait. No med students today. Just the nurse, Anne, and the Dr. I have no fever, I am not depressed or suicidal, and my blood pressure after a few moments of meditation, is a sweet 124/83. Dr. K and Anne come in, and I tell him about the continued bleeding and my exhaustion and blood craving. I’m not having any pain. He’s super-stoked when I tell him I’ve been off the opiates since Christmas Eve. My herbal medication does that job, although I’d rather have a brownie or some tincture. Dr. K says he’s pretty sure that the pufferfish exploding and continuing to drain is a good thing at present – at least it’s not crushing anything and forcing the intrusion of tubes into my body. I think Dr. K is trying to impress upon me that my experience with tentacles is not forever over because then he starts talking about the possibility of a fistula pushing into my bladder and then requiring double nephrostomies. I remind him that it’s quality over quantity and I’m on a no-invasive-tubes mission. What’s the point of being housebound and miserable in order to extend your life a couple or three months? Better to burn out like a fucking comet. This should come as no surprise is you know me well, even if it makes you uncomfortable. There’s a huge difference between living life and existing.
Anyway, I tell him I want to go to Ireland in April, and I need to know if that’s a reasonable expectation or should I put things in motion sooner, and Dr. K says he thinks it’s reasonable and he’ll work with my treatment to help it happen. It still doesn’t mean I am getting some delicious rejuvenating blood. He says we’ll wait another month and see how the chemo pills have worked, and then I get to have another thrilling CT scan and then we’ll talk about what’s next. My next appointment is February 1st. It’s almost like the pufferfish will be pelvic groundhog, letting us know if there will be six more weeks of bleeding. It’s not even like a period, it’s so random and weird. There’ll be hours of nothing and then it’s like the tide’s coming in. He asks how many pads a day…I guess at 4, but then when I get home, I realize it’s more like 6. Oh wait, I forgot to do my “THIS IS GROSS” warning. Oh well, suck it up ponies. Anyway, we chat and he says we should probably do an exam, considering there’s a hole in my vagina that spewing internal muck and we should make sure it’s not become a disaster area. I agree as much as I hate the probing. I really do. If you ever get cancer, which I sincerely hope you don’t, wish that it’s in your toes or left pinkie, or ear. This internal examination nonsense never becomes an enjoyable part of the visit. I know that some guys think that we ladies enjoy having things in our vaginas, no matter what that might be, but no. We don’t. Especially not while at the gyno. After we have agreed, he and Anne leave so I can get undressed.
I do what I need to, and notice there has been no bleeding since I took a shower at like 10am. Odd. I hop up on the table (when will a woman doctor design a more exam friendly table? There’s nothing remotely comfortable or relaxing about it.) At least, there are no inspirational quotations on posters that you can stare at while being probed. However, if anyone at the PSH Cancer Institute powers that be are reading this, a small TV screen featuring the food network, or the ID channel, or even South Park would be far more effective in distracting me. I sit there on the edge of the table, swinging my seriously unshaven legs back and forth, when – well, hello there tidal wave of blood. At least Dr. K can now see what I am talking about. Gross. I keep waiting. I hear Dr. K on a phone somewhere and then hear him in another exam room. It seems likes it’s been a really long time that I’ve been waiting. Did he forget me? Time is always a little skewed when you are fueled by a brownie, and I am sorta ready for a nap. I don’t want to lie down, because that’s just weird, but I am nodding off. Finally, after what seems like 2 hours (it was 20 minutes) Anne comes back and asks if Dr. K came back. I say nope, so we both sit and wait and chat .Finally, Dr. K returns and we get to the business of ramming instruments of torture into my vaginal cavity. He confirms that there is still a hole in the vagina, but again, comments that this could be a positive thing, and, once again is pleased that I do not try to leap off the table in pain while he does his exam. As long as there’s no pain, that’s a good sign. He says that fistula word again, I shush him. He says that there any odor is probably just because it’s old blood. Double gross. But I’ll take it because anything is better than tentacles and pain. If I have to start wearing Depends to deal with this, I’ll take it, because ANYTHING is better than dragging a catheter around all day and having it cause you even more pain. I don’t think Dr. K or anyone can fathom what it felt like to have that fucking tube jammed in my bladder and constantly abraded by the movement of the cyst. Anyway, we wrap up the exam, I get another prescription for oxy, and sent on my way. It’s 4:10pm.
I gave a brief thought to getting Indian food for dinner, but that would mean exiting the warm car to fetch it. Nope, it’s 20 degrees. I’m not getting out of the car until I am home. As I am exiting, I see Alice, the sweet grandma, and she has still not been called back. I give her a fist bump and tell her I hope they call her soon. I was smart and used free valet parking today, even though I always tip, and stand inside while some poor soul freezes getting my car. I hop in, pleased to find that the root beer I purchased earlier is still delightfully cold. Dinner will be Arby’s. It’s on the way home and no need to exit the car. I’m exhausted. I just want medication and sleep but I still gotta pick up the faux beef sandwiches. Finally, I made it home, and the comfort of my couch. And that’s mostly where I am, except when I am in bed, or at work, or out.
Dr. K is always surprised that I continue to try and work. He said he’d be happy to say I can’t but I tell him I need those couple hours of socialization. He’s fine with that if it’s what I want. I was a little concerned that he didn’t want a CT scan right now, but then I realized, what’s the rush? If the cancer is disappearing through the hole in my vagina, that’s a good thing; if things are status quo, we already know that; and if things have gotten worse, there’s not gonna be a lot to do about it, and the knowledge isn’t going to make me feel any better. So I can wait a month. Bad news is that the scan is on the 27th, and the appointment is on the 1st. Five days of knowing what they find, without being able to see the doctor until Monday. I supposed I should be used to that though.
Well that’s all for now people. I am going to work this afternoon from 2:30 to 4:30 if Andy ever returns home with the car, since, of course, I have work and he decided that he needed to get an oil change NOW and oh, by the way, the check engine light is on and he thinks it’s the O2 sensor. That was two hours ago. So I’m gonna grab a little nappy nap and wait. Have a good weekend, and week, and life, and such. Peace!
Update: I was sitting here thinking how pretty sweet my life has been lately, no drama, bills paid, plenty of oil, etc. Then in walks Andy. There’s a cracked tire rod, blah, blah, blah and it’s going to take at least $1000 to fix what they know is wrong, and that’s not including what is the source of the engine light being on. Car = undriveable. Fucking yay. Well, I’m not dead. That’s a plus. And we didn’t die in a fiery crash when the tire fell off, so that’s good too, I suppose.
8 January 16 | Categories: c-monster, Philosophizings, Profound Insights, Random Rambling | Tags: appointment, blood, cancer, ct scan, cyst, doctors, flying monkeys, funny, gratitude, humor, pain, positive, treatment | Leave a comment
I’ve written a bunch of blog entries since the last time I posted. I just didn’t want to post them until I could formally (or actually I guess it’s informally) thank everyone who worked together and attended the benefit held for me on November 7th. It was beyond amazing, the food was fabulous, the decorations were fantastic, seeing so many people that I love come out to support me, it was beyond incredible. And can we talk about the donations? From the amazing baskets put together and donated by friends at work, and all the other fabulous baskets donated by friends and businesses (there were about 80!!) as well as all the businesses who made donations either in prizes or food – to the amazing friends who not only organized this “shin dig” as my dad was calling it, but also spent the time cooking, setting up and cleaning up, soliciting donations, putting up with my demands, and can we say boarding planes and flying three thousand miles to either sleep on my couches or in our fine local establishments? And seeing some other friends who I have not seen or hugged in months or years. And my brothers. You all conspired to give me a fantastic day, and I can never thank you enough. I was astounded by how many people came out. I know I say it a lot, but there aren’t words (or words that will be allowed usage by the chemo brain) to properly say thank you. It was a great time, and even if not a single dime was raised, it was enough to just be there with so many people I love. That’s what really mattered. (And that no nuns were offended by my shirt)
This is my best attempt to thank those who organized and donated their time and/or resources, the businesses that made donations, and everyone who helped set up and clean up and cook and bake and just make the day wonderful. PLEASE PLEASE PLEASE if I missed someone, either comment here on the blog or send me a text or email. I will fix it. And feel free to print this out or refer people with a link who don’t have facebook or twitter to read it for themselves. I am hoping to put a thank you in the paper, because let’s be honest, if I were to send thank you cards, Andy would find them in a stack to be mailed about six months after I’m dead, because in order to send a thank you card, I would have to make it (yes, I know they sell them, but this is me we’re talking about) then I would go full tilt on card making until I had half of them done, and then lose interest or get sick and then I would say, I’ll do it tomorrow and then it’s May and people think I am an ungrateful bitch because I didn’t send a thank you card, but really I will still be working on them. So without further ado…
First and foremost, without these people, the benefit would never have happened: Lori, Lisa R, Anne S, Heidi E, Michelle G, Lisa S, my brother Stanley, KY, Mary B, Gina, Renee, and B aka Mary Bridget. (And Louise, and of course, Erin) Also thank you to the adult and minor children who were volunteered by their parents to help out. Thank you for all of the time you put into this, and being my friends. More for being my friends, because without your support, I would not have survived this journey as well as I have for so long. You may not think you did anything major, but just knowing you are there means the world.
Next, I need to thank my amazing friends at work, too many to name here. If you could only have seen the baskets they donated for the basket auction – they blew me away – and probably raised a good chunk of change. Special thanks KY, Sue Y, and Patti M, for also making individual basket donations as well. Every unit in my office created a basket by their unit and they were incredible. The generosity didn’t end there – my CYS friends also donated drinks, made food, bought paper products, had fund raisers, and just gave moral support.
Major thanks to the California girls, Debbie, Jeanne, Catherine, Cindy and Dianne (and her boy toy) for braving TSA and flying east during the beginning of fall/winter hell. We fell back into conversation like the decade or more since I’ve seen some of you was never there. I am sorry I was still too weak to be a better hostess, but I think pizza buffet night was pretty awesome. I missed our easy conversation and endless laughter. And to my beloved hummingbird friend, and her awesome mother, thank you for choosing to stay at Chateau Pecky, some of the most curious accommodations you will ever experience – where lights turn on in the middle of the night for no real reason, and just as you fall asleep the furnace kicks on. It was a delight having you as guests in my home. I’ll get some more cancer if it means you girls will visit again. And thank you Ashley, my shark sister, and Roy for making the long journey to the ‘hood to hang out with us as did my wonderful cousin, Ginny. Sharky it made my day to see you. And to Joe, Amanda, Danny, Tom, and especially my surprise guest, Stormy, thank you too, for making the trip – you will always be like my very own children and I was glad to see all of you there. You always make me smile.
And Andy – thank you. For putting up with my idiosyncrasies, my whining, and for your diligent cleaning even after I freaked out. You know you bear the brunt of my moodiness, and I am sorry, but thank you for your help in all of this.
And thank you Stanley for the awesome birthday cake. It was delicious.
And thank you Lori and Denise for your part in making me able to allow people in my home again.
Now for the list of donors and businesses:
- Anthony’s Pizza in Frackville
- Friendly’s in Pottsville
- Capitol Food Market in Shenandoah
- Kowalonek’s in Shenandoah
- La Casita de Familia in Shenandoah
- Lucky’s Corner Deli in Shenandoah
- The Pizza Shop in Shenandoah
- Who’s Place in Shenandoah
- Vernalis’ Restaurant in Shenandoah
- Boyer’s Food Market in Shenandoah
- Walmart in St. Clair
- Melissa’s Hair Design in Shenandoah
- Little Venice in Shenandoah
- Francesco’s in Shenandoah
- The Lyric in Shenandoah
- Pet Brothers in Shenandoah
- Yuengling Brewery in Pottsville
- Dunkin Donuts in Pottsville
- Angie’s Hair Salon in Shenandoah
- Kay Lex Salon in Shenandoah
- Park Restaurant in Shenandoah
- Boran’s Bakery in Shenandoah
- Antz’s Refrigeration in Shenandoah
- Chris Ozcoustic Oslar in Ringtown
- William Penn Fire Company in William Penn
- Gaultier’s Distributor in Shenandoah
- Denise D in New Jersey
- C&L Creations in Shenandoah
- Green Loving Naturals in Pottsville
- Liz Noon at Trio Salon in Pottsville
- West Street Pub in Shenandoah
- Kidspeace in Pottsville
- Kathy H at Access Services in Orwigsburg
- Eddie M
- Kayleigh L
- Brenda S
- Olive Garden
I tried to put hyperlinks for the people/businesses that I could – please give them a click if you can, and if you are local – please support them as you can. Again, I am so grateful for their generosity.
Additionally, the Shenandoah Knights of Columbus gave me a very generous check, as did the Chris Antz Memorial Fund. Thank you to my long time friend Denise D. who donated Flyers tickets and to Kellie for my Fuck Cancer shirt. Also I received very generous donations from Jeanne and from Catherine’s massage therapist who wants me to go to Ireland as much as Catherine does. Well, ladies, we’re going!
Most of all, thank you to all the people who came to the event, or shopped and dropped. Thank you to ever person who made a donation, whether it was to me directly or to Gina’s Pennies for Pecky drive. I was astounded at the monies that were raised. I can’t thank each of you individually, because frankly, there were so many people at the benefit or who just made donations, that I can’t name them all. But know that whether it was pennies or T-bills, your contributions made a difference, and if you attended, I hope you had a great time, ate a lot of good food and enjoyed the people, I know I did. Until I had to go puke outside. But that was over pretty quickly.
I, of course, have a shit camera on my phone, so I didn’t take pictures. Andy used my dad’s camera, but all of the pictures he took were blurry. So I am posting what I have received from friends, Thank you for taking them. There are pictures of the baskets, me, my cake, my friends, the tables and some of the people who attended. I wish someone got a shot of the food…it was incredible – roast beast, fried chicken, chicken parm, mac and cheese, mashed potatoes, scrumptious filling, blind pigeon casserole, polish meatballs, italian meatballs, pierogies, baked ziti, porketta, chicken and dumplings, hot dog, salads, veggie pizza, subs, meat and cheese trays – there was food for days. And then there were the bacon wrapped bang bang meatballs that Michele made especially for me. And banging they were.
Anyway, I started this at 9pm and it’s close to 3am. Wow. I just want to say one last time that I am so grateful for the amazing generosity, love and friendship that was so obvious from everyone involved in, and attending the benefit. I really really really appreciate it, more than you know, and you are making it possible for Andy and I to have experiences that we would otherwise not have if not for your kindness. Yes, the benefit raised enough money for Andy and I to do the only thing I really had on my “things to do before it’s too late list” – go to Ireland. There was also enough money for me to splurge on a 32” flatscreen. (yes, you read that right, 32”), get a new vacuum that does not spew the dust back out as soon as it sucks it in, and to make sure our electricity remains on for many more months.
I only put first names and last initials if necessary to allow people privacy. I’ll be happy to add your last name if you want. Enjoy the photos, and Happy Thanksgiving. I have so much to be grateful for – a roof over my head, the day with my son, food in our fridge, no one blowing up our house and the love of amazing friends. Thank you for everything – the laughs, the texts, the couches to lounge on and watch football at your house, etc. etc. I can’t describe what that kind of support feels like. Love to you all and a pleasant day with the people you love. Stay tuned for several posts in the next few days. Sleep a happy sleep. I’m off to attack the ham before I pass out. I got a turkey to stuff in a few hours.
26 November 15 | Categories: Philosophizings, Picture Perfect, Profound Insights, Random Rambling | Tags: amazing, benefit, cancer, flying monkeys, friends, funny, gratitude, support, thanks, thanksgiving | Leave a comment
Tonight was The Menzingers at Union Transfer in Philly (awesome set, nice venue) with Mewithoutyou (great performance) and two other bands…one I missed because they closed a road in Fairmont Park and put up no signs causing mass chaos and delaying us. Got to hang out with Lizz and Blaine and had a mostly painless night. It was a rough day emotionally, so I’ll take the absence of any kind of pain.
Picture it – 2am, there I was, driving home in the rain, Andy passed out in the passenger’s seat. I was listening to the Jealous Sound, enjoying the dark, wet night, singing (or wailing as some might say) when I notice something that looks like a leaf crossing the road. It bounced 3 times before it I realized it was no leaf, it was a frog. A very brave frog who decided to cross the road. She was just a wee thing. But it reminded me that life is tough and all, but it’s got cute little surprises now and again. A brief bit of joy in the night. AND then I saw a second one. Double happiness. Two tough little buggers.
But because I am me, I immediately thought perhaps this is the apocalypse, and it’s raining frogs? Or does it rain blood? I forget.
In other news, I bought a panda suit today. Because life is too short to not have a panda suit. Really I just wanted the head, but apparently all the available panda heads are just ugly. I can’t wait to sit on the porch and wave to cars.
And I’m thankful.
And now, I’m going to crawl into bed, and watch last season of Vikings again. Goodnight pumpkins, Dr. is Monday, so I’ll be back soon.
Well here it is, Tuesday. I feel like I have slept most of this month away. I am up and awake now, before 10 am, out of bed, which is crazy, because the only reason I was getting out of bed before 10 am for the last three weeks was for dr. appointments and to puke. It feels strange and wonderful, and shaky. I’m craving a mint hot chocolate, but today is shower day, which I can’t take until Andy is awake to do a new bandage on my back.
So what’s new in my world? Lots and nothing. I’ve been down with the sickness pretty much every day. I feel better one day, and think I can actually be social and do things, and then someone is unknowingly carrying a rare virus that is usually defeated quickly by your immune system until it gets to me, and then hello, it’s a human with very little resistance, let’s dance. I am sure I’ve endured the black death the last few days, and probably some extinct pox. I’ve puked more in the last 30 days that I have in my whole entire life. And that’s with using appropriate nausea control techniques. And the things I have puked in and on are countless! Plus let’s not forget that tube in my back that gives me an added thrill every time my automatic nervous system spasms. It’s good times.
The tube in my kidney. What a pleasure source that bad boy is! I did get a mini-reprieve with it, though. When I went in for my tube change, I laid down my case for why it should come out, and almost won. But using logic, my plan was confounded. We agreed to leave a tube in, capping it off, sans the pee bag, for two weeks – if my kidney goes back to doing it’s job without complaint, then they will pull it. In the meantime, I’ve discovered the sweet spot on my hip where I need to place my hand when I need to cough, sneeze or breathe deeply, so I am not thwarted by pain.
But let’s talk about pain. Last Wednesday, I went in to interventional radiology to have the tube change done. I took a couple oxy and some medicinal herbiage before the ride so I’d be more comfortable when I got there. I was. Then they promised me some more medicine, when they did the procedure. Unlike the draining of the cyst, I don’t believe they give you any medication to help you be drowsy. No, they are very kind to you, promising pain relief until they wheel your ass in the procedure room. Then they tell you to get on your stomach, put your arms above your head and trust they will not hurt you. They lie. First they start poking you in the back with needles they claim are local anesthetics. Just a pinch they say. Just a pinch. Just a pinch of the claw of giant crustacean tearing into your flesh like it intends to eat you. I stay surprisingly still for the first two shots. Then the third hits a nerve or something and I elevate three feet from the table and mutter “ouch”. I think the team realizes that they might have hurt me. Now, I am shaking from the pain, and it’s freezing in there, so I shake for the rest of the procedure. They took out the old tubing and put a smaller less cumbersome tube apparatus in there. They did a really good job with the bandage. I get to roll back on my back and go to recovery. I’ve done really well they tell me. I just want to go home. They must have given me fentynal at some point because I’m mostly not in pain now. I get dressed and they even let me walk up to meet Andy.
I was hungry. I wanted one of those turkey and cranberry sandwiches from Panera. I went in with Andy at first, but realized I needed to be back in the car, so I gave him my order and went outside. He brought out the goods and I ate a cookie and some lemonade. I thought I was going to be fine. Just not really hungry. The sandwich could wait. Then the meds started to wear off. I didn’t bring any with me. In the next ten minutes, my pain went from 2 to 2.4 trillion. Every inch from my waist to my neck on the right side of my body was a fucking minefield of pain. I do not exaggerate when I say that speaking hurt me. Breathing hurt. Coughing was some primitive torture activity. I couldn’t cry, I couldn’t talk, I could only whimper like I was hit by a car and left alongside the road to die. I wanted to die. I wanted fucking morphine.
Finally we go home, I thought I was going to be okay. Then I tried to get out of the car and walk into the house. Every fucking step was a new adventure in torment. I got in the house, and faced the steps where my safe bed and vial of oxy were waiting for me just a few hundred steps away. And every step found me crying and moaning and doubting that I would ever get to the bed. But I did. I shoved some oxy in my mouth, and advil, and tried to smoke but couldn’t really inhale. Then I tried to lie down. That was not easy. I literally had to throw myself down on my right side and not move from that position. I told Andy if I didn’t get some relief in an hour, that we would need to call an ambulance. I was having really bad pain in my chest and back and I was scared it was serious. But I also tore cartilage in my chest before and it often would be painful if I was in a position that pulled at it again, so it could have also been that. I was hoping it was that. I nodded off for an hour and when I woke, I wasn’t in as much pain, so that was good. I was still paralyzed and unable to move, but I was no longer in fear of imminent death. Another four hours of sleep and I was almost able to move. By morning, I could actually sit up. A few more hours, and I could walk. Things were improving.
I couldn’t make my appointment with palliative care. Reschedule. I didn’t have the strength or the energy. I had to blow off the Bouncing Souls show that I was so looking forward to. I shouldn’t complain, my kidney was working and I could move and most of the time, breathe. I was still having trouble coughing and sneezing. Then the black wave of depression crept into the space where pain had been hanging out in my brain, and down, down, down, way fucking down, we went. If you don’t have depression, you can’t understand. I try to make it as visual for the untainted as I can, and this was like the La Brea tar pits of depression and I was a fucking woolly mammoth. It was all over except for suffocation. That sucking quicksand of sorrow ate me up, and the crying started. Without belaboring the incessant crying and snot-blowing, let’s just say thoughts during the breakdown run from “I’ve failed as a mother, and Andy will hate me for the rest of his life” to “what the fuck have I done with my life?” to “I’ll never get that PhD, great work dumbass.” Until you really spend a lot of time reflecting on your life and the possibility of a very short future, you can never understand that level of sorrow or failure. People can tell you otherwise for hours, but you can tear any positive self image down to smoldering ash in a matter of minutes when you start to consider things that will most likely never happen because there’s just not enough time. I’m just now starting to realize the psychological impact this disease has on me. I keep it together most days, but when this shit crumbles, it goes down hard and and fast.
I hate to keep harping on this but I feel I have to remind people that I write this to sort through what is in my head more than anything else. If the details of this fucking monster inside me helps someone else, I am thrilled, but writing is always for me. I love that people read it, I love that people comment on it, but I love the way I feel drained and empty when I stop writing, like all the shit that swirls in my head has finally been released or at least organized. Writing also scares me – when I see what I have only been thinking appear on the page it’s like tearing off a scab and wondering if it is ever going to stop bleeding. How raw this gets depends on how much pain I am in when I write – and sometimes I hold back because I can’t face another entry that is just all about my grief, and I know I shouldn’t. I can’t – because there’s no where else I can go with this. I know there are therapists, and I know I have friends, but let’s be honest here, very few people pour out what is really inside to anyone else, because we all want to keep our pain, our shame, our fears hidden. If you don’t, I admire you – I know I have secrets no one will ever know.
So now it’s evening – I went out for a bit today in the car. Visited work until I started to feel nauseous and then took a ride and spent some time in a cemetery until I felt better. Then I drove and cried and screamed and came home exhausted. Smoked my nausea away, and hoped for sleep, but no, my feet are twitchy and my legs are restless and so is my brain. Part of it is knowing that next Monday we’ll be talking treatment and progression (or hopefully, lack of progression) of this stupid C-monster and the damn pufferfish. And as many of you know, my friends are hosting a benefit for me on November 7th here. Some of my oldest and dearest friends from California are flying in and I am thrilled – it’s going to be amazing to see them all again. And I am sure many of my dear friends that live here will also be there and I am so blessed and grateful that they are doing this for me, but there’s a huge part of me that realized just now that it’s like saying goodbye to my loved ones and I don’t know that I am ready for that. I know that sounds negative, because anything can happen, and I do believe that, but I am also very much a realist who prepares for the worst, and the very thought of maybe never seeing them again after that weekend tears my fucking heart out. Just like every day that I wonder if I have told Andy every thing I want him to know – and hope that he knows that he changed my life and I love him more than I have loved anyone in my life. That, my friends, is my nightly terror – leaving my son alone in this world. I don’t care about anything else. I just want to make sure that my baby is going to be okay and that he knows how sorry I am that all this has landed in his lap during the time of his life when he should be discovering what he loves and who he is and he’s stuck taking care of me. And the tears flow again.
I was trying so hard to keep this light and fucking positive and I can see that that has been a huge fail. So much is undone. And you’ll think to yourself, well get out there and do it! And the reality is that there are somethings you don’t just “go out and do.” When faced with what you are going to do, you have to let go of the dreams you had that can’t possibly fulfill because it’s just not possible. And you grieve for all of them. So much grieving. And even as I type this I’m trying to self-talk myself calm – I want to bolt and stop writing because it hurts so much. But this kind of pain is progress. Unlike the physical pain – which is nothing more than annoying. And at this point, more of an annoyance than a hindrance. There’s that at least.
Well, I am spent for tonight. I’ve tried to enhance this post with some cemetery pictures from today. It didn’t work. Maybe I didn’t save them in the right format. Who knows. The featured image was supposed to be this crazy tree that is way at the back of a pretty hidden entrance to a cemetery I frequent. It always has artificial flowers attached to it. And it’s updated regularly for the season. I like to sneak into the cemetery that way so I can check out the tree. People don’t appreciate the subtle beauty hiding in the places most people ignore. I’m always going to find my happy in an interesting cemetery. It’s like water is to my soul. Maybe Saturday when we go to Philly, I can convince Andy that we need a stop at Laurel Hill…it’s such a beautiful place in the fall. Just so I can take a drive through and enjoy the trees and death and decay. I am going to head to sleep, so I wish you sweet dreams, cupcakes. Thank you and come again.
21 October 15 | Categories: c-monster, Philosophizings, Profound Insights, Random Rambling | Tags: afterlife, anxiety, benefit, cancer, cemetery, chemotherapy, cyst, death, depression, driving, endometrial cancer, fear, flying monkeys, friends, gratitude, pufferfish, sick, sleep, sorrow, tumor | Leave a comment
So as I was shoving that third piece of pizza into the yawning chasm of my mouth, I finally gave in and accepted that I am sunk in blackness and I was stuffing my feelings. Also why I have put off writing for so long again. Because I’m a scaredy cat. Not like a cheetah or a lynx, but like a big ol’ cowardly lioness. And it’s paralyzing.
I promised myself that I would write first about the good things, because there have been a lot and when I look back at them, I feel like a whiner for feeling the way I do. Of course that doesn’t make my pain and weakness go away, or make it any less valid, but I am grateful for so much and for the people in my life, and I don’t say it enough. So let’s do this, and if I am not ready to pass out when I get through the good, then we’ll move on to the bad. If not, there’s always tomorrow.
So first there was the fabulous road trip to Minneapolis. Once again, Andy and I hit the road for punk rock adventure. Andy got me tickets to Dillinger Four’s 21 birthday 4th of July Show at the Triple Rock in Minneapolis. We drove straight from home to Minneapolis, speeding through the dark night through the states of Ohio, Indiana, and Illinois. Well, okay, it was getting a little light out as we drove through Chicago, but for the most part, dark Indiana, Illinois, and Ohio are similar to the daylight version. Wisconsin was pretty and has a curious number of large animal statues at different roadside shops and hotels. Like a giant moose. Or a giant mouse with cheese. There were more, but Andy wouldn’t pull over for everyone. Minnesota is also quite lovely. We hit the aquarium in the Mall of America, which was small but very cool, unlike the Mall of America, which is, though large, a mall. Okay, okay, it has an aquarium, and that Nickelodeon amusement park area, and a way cool lego store, but bottom line, its a mall, and the massive amount of people and the mindless consumerism reminded me of why I shop online. Of course, that was the first time during the trip my body betrayed me and we headed back to the hotel, which was fabulous. My sore sick body fell in love with the bed, and even more so after I swam for an hour in the pool. The next day, we went to the Minneapolis sculpture garden which was very cool. (Note to self: EARLY mornings and LATE afternoons are best to be outside when your body likes to randomly overheat to 1000 degrees throughout the day.) They have a giant spoon with a cherry on it that’s a fountain, and a bell that doesn’t ring, for which Andy and I posited theories about what a silent bell represents before moving on to two sculptures which we both decided were representative of vaginas. Once again I had to retire to the hotel to rest before we could go to the D4th show. After a quick nap, we headed out to the Triple Rock. The show was amazing – albeit hot – and I hid behind a tree most of the time avoiding sun. Even cooler than the show was getting to meet Ranae and hang out with her at the show, not to mention that Ryan gave me an awesome gift of the vinyl Jesus and Mary Chain’s Darklands, which is my favorite record of all time. I also got to meet a bunch of great people and make fun of a selfie stick. After the show, Andy and I went back to the hotel to catch a quick nap before the after party, but Andy is a still a young pup and he fell asleep so I ended up going back to see The Underground Railroad to Candyland by myself, which was a big deal, since I never have gone to a club in a strange city by myself. I was glad I did, because they were amazing. Really, every band that played was excellent, we missed some of the openers, but thanks to seeing the line up posted on FB, we got there in plenty of time for OWTH. We also saw Toys That Kill, Dillinger Four, Lftr Pllr (the special guest whom I never heard before but were amazing) Scared of Chaka, Tim Barry and Against Me! It was just one of the best days ever, and after the show, I went back to the room and tried to trick Andy into letting me sleep in, but no, he was up and ready to head back at the crack of dawn. So with a stop at the cheese shop where we bought a ridiculous amount of snacks, we headed home, tired, bruised, but happy happy happy. And Andy and I had only two screaming matches at each other during the whole trip – once at 5am when I needed to pee and couldn’t find a bathroom and the second when we were stuck in traffic in Chicago for 2.5 hours because of those damn hippies at the Grateful Dead thing going on there. Still, it was a fantastically fun weekend and I am so glad we did it. Plus spending the time talking with Andy always is worth it. And Andy got a ton of fireworks that could not be purchased here, so he was very happy too.
Then I got to see two of my oldest and dearest friends, Donna and Denise, who were in town for a wedding. It was 15 years since I’d seen either of them, and it was like we never had been separated. We drank and laughed and looked at photos to point out all the people we knew who were dead. I also got to see all of the kids, which was great. Then we also got together for breakfast which was another laugh riot. It would have been complete if our friend Anne could have joined us, but she had an event that she needed to prep for, so hopefully another time. Nevertheless, we had a blast and we need to not wait so long to hang out the next time.
After that, my friend and former common law domestic partner, Debbie, her husband, kids, and her parents, brothers, sister in law, and niece and nephew came to Hershey to meet Andy and I to hit Chocolate World and get some dinner. I hadn’t seen Debbie since Andy’s graduation, and I hadn’t seen her family since Andy was 10. It was a day of great hugs, great laughs, and fun. The girls, Tyler and Kylie, are gorgeous and I adore them. And again, it was like the miles and the years between us just disappeared, I only wish we had had more time to just hang and talk, but I’ll find my way home to the west coast eventually.
Then was my surprise trip to DC with my friends from work. We left early Saturday and got to DC around noon. After a fun drive with mimosas and my breakfast of brownie, we parked and headed off the Natural History Museum. Now, you may or may not know that the National Mall is under construction which means if you want to get to something on the opposite side you must walk ALL THE WAY AROUND. Now, had I known this I would not have worn my black OWTH shirt and would have applied sunscreen, but I trudged through the heat (and it was fucking hot) darting under shade trees as we traveled along. We paused for rest and put our feet in the fountain on the mall, which was enjoyable until you realized how warm the water was. I saw my favorite strange bunny sculpture, but my phone died so there are no pictures. We checked out the museum, which was crowded but fun, and then took a pedicab back to the hotel which was ultra fun, as I waved, queen-like, to the masses as we traveled. The guy who pedaled our cab was interesting and it made a great way to get back to the hotel. The hotel was very cool, and I had my own room, with another one of those comfy beds. When we got back, we grabbed some drinks and headed up to the rooftop pool, and I got kicked multiple times by a rambunctious child without parental supervision. My leg buckled under me after getting out of the pool, and I had a major cramp, but it went away, and and after a nap, I had a brownie and we headed out to the dinner cruise on the Potomac. Our cab driver was an idiot and it took us twice as long to get there as it would have if we walked, but I couldn’t handle anymore walking. The cruise was very nice, the food was awesome, and I ended up hanging out with Jenn on the observation deck most of the night, just enjoying the night air, the lights on the shore and sailing. Unfortunately there was non-stop “cool jazz” playing and it was making my eyes bleed by the end of the night. After the cruise, we’d planned to go to the hotel bar, but once I got to my room, I was cooked. The next morning we got up and headed out to the National Zoo where we rented me a scooter and began the zoo adventure. Unfortunately, the red pandas were unavailable, and the elephants under quarantine, but the Komodo dragon poked his head out when I got to his enclosure. We got to see some special “double turtles” (see photo) and vultures. I tried to race a cop who was on a segway, realizing after I dared him that I had had a brownie for breakfast and probably shouldn’t have been driving a scooter at all, not to mention racing cops. There were three lazy pandas there though and that was pretty awesome. We made it through the zoo by noon before it got REALLY hot (it was already blazing by then, and not even mid-day). After the zoo, we were all really tired, and headed back home. We stopped to get some fabulous Thai takeout and have lunch at Quaker Steak and Lube, which none of us had been too, and now having been, really have no desire to go again. Tired, and full we finally made it home. It was very fun, and I am just glad none of us were arrested. What was even more special about this trip was that ALL my coworkers contributed to it – they had a pot luck luncheon where we all paid $5 for lunch and we brought a dish, and then the next day, we had a reduced lunch for $3 – which was actually a fundraiser to raise money to do something fun for me. I know I’ve said it before, but I can’t say it enough, I work with the best people – our job may suck, we may bitch and moan, but my friends at work have the most generous hearts, and the fact that they did this for me made the trip even more special – I only hope I can return the kindness for others later. Needless to say, after the trip, my body decided I needed to stay home with crampy legs and nausea, but it was well worth it.
And that brings us today. All that goodness took the edge off the gloom that’s clinging to me. I expect I will write more over the next two weeks as I stress about my upcoming CT scan and Dr. appt. I am bummed that my CT scan is the day before Andy’s birthday, and I am going to try not to read the results until the day after, but let’s be realistic, I’m gonna be hitting refresh until the scan is posted on my online med portal. The next couple months will be busy too, we’re planning to go to Riot Fest, and then I have OWTH tickets for September in Philly and Baltimore, and we got Bouncing Soul tickets in October, and if I can manage it financially, and physically, I want to go to Fest in October too. I’ve been putting these things off for years and I need to do it now or it may never happen, especially since I think there may be chemo ahead and the pain that was my constant companion last year, has returned and PA is still lagging on the medical marijuana bill. Sigh. Call your local representative.
But before I go, I strongly encourage you, if you are a fan of OWTH, or Bad Religion, or good music in general, to go to Ryan’s Anxious and Angry web store and buy something so you can get the free flexi of OWTH covering Bad Religion’s Sorrow. It’s amazing. Just buy something from Ryan even if you don’t want the flexi, because he’s a good guy and is super generous, and is always willing to help people out. And because his cat Stray Charles is blind. Or don’t buy anything and just make a donation to suppor the podcast. And listen to his podcast, which is very interesting if you like punk rock and mental health issues, and has helped a lot of people dealing with mental health concerns know they are not alone. Really, it’s worth the listen. And now it’s time for bathroom trip 5 tonight and then try and sleep. Let’s hope it comes quickly. Sweetest dreams, my dahlings!
4 August 15 | Categories: c-monster, Philosophizings, Picture Perfect, Profound Insights, Random Rambling | Tags: alcohol, amusement, anxiety, blackness, cancer, co-workers, ct scan, Flexi, flying monkeys, friends, gratitude, happiness, Off With Their Heads, road trip | Leave a comment
Yes, I know that spring is still a few days away according to the calendar, but you really should go by my feet. I’ll explain. I hate shoes. I used to be barefoot all the time, but then I moved back to good ol’PA, where life is not cooperative with my need for foot freedom. This means that at some point, I can not longer plod through the snow in sandals. My foot liberty is curtailed when the temperature gets into the teens, or snow accumulated that it covers my toes. On my little escape to Maryland this weekend, my wiggly toes realized that the temperature was above freezing, and plotted an escape. Monday morning, my fake super cheap ugg boots were set aside for an old pair of Doc’s sandal and I called “Spring.” (note: I still think ugg boots are stupid, but I can say they are warm and when they are only 19$, you can’t go wrong – at least the snow doesn’t soak them as quickly, as say, sneakers) So there you have it, I have declared winter to be over. Today I wore capris to work too…
There are other signs as well here in Northeast-kinda-Central PA. Some are clearly evident, others not quite yet, but my springy senses tell me that even those will emerge by the weekend. Mounds of snow are nearly pure black as they always are within a day or two after a snow; the melting snow on the highway reveals tons of garbage pitched out of car windows by nasty pig people or overturned big rigs who can’t drive in the snow. Firecrackers ring out at night. Bath salt heads screaming the street increase in number. The vampire children emerge from their winter slumbers. And before you know it, the pajama pants parade will commence on the main street of town, when all the teen mommas who proudly announce their job is “stay-at-home-mommy” on Facebook will don their finest pajama pants, pop their spawn into a stroller (first dressing the little in seasonally inappropriate garb) and march proudly, sprag smoking twixt their lips with the ash dropping on the kidlet’s head, up and down the avenue. What a sight the herd of future and/or present CYS clients are! Trying to act like they aren’t pushing a baby buggy, their posturing screams “look at me, I’m a fertile breeder” as they try to attract the attention of their next baby daddy. The cluster of children who have children will then mass together at either the notorious One Stop Shop, where you can get birthday cards, cut rate sunglasses, cold cuts, beer, and all of your bath salt and paraphrenalia needs met, or they will move to the corner closer to the town’s main intersection, and sit on the curb, alternately ignoring or screaming at the little person, while they wave to the potential absent fathers as they walk/drive/stumble by. That very same corner where I once hung out with my girls in my wicked youth, when we would wait to be notified where that nights party was, or for some older boys to stop and ask us to go for quarts or to burn one. Things harder to do when you are pushing a stroller. Although from the looks of Team PJ Pants, I somehow believe they probably manage to push those stroller along narrow wooded paths or up slippery slate banks to get to a bush party. Some nights I wish I had a van and the authority to just scoop those poor babies up and get them to safety – but alas, as a caseworker I don’t have that authority without a court order. The final marker of spring will come when the days final hit 60 degrees, and the pajama pants are replaced by shorts and tank tops that would make Miley Cyrus look modest, and those poor tots being carted about are still roaming the streets at 11pm. Then you know, summer is just about here.
Pennsylvania black snow mountains…way to make winter even more depressing that it already was…
I managed to escape the my mesmerizing hometown, and came down from the tower to visit with my brother and his wife this past weekend. As wonderful as it was to get away, and spend the weekend eating, drinking and watching my family drink to excess and give me tons of great blackmail video on my phone, it was exhausting and I was glad to come home. My brothers, as wonderful as they are, should never sing. They can dance, but the singing…no, never, nyet. But it was a good time, and amazing to be out of my bed, and socializing with humans, and Bailey, my brother’s playful and willful boxer, who was so excited to see so many people, jumped all over me while I was lying on the couch and gave me multiple bruises from his paws as he attempted to lick my head. I am seriously hoping I don’t have to have an exam tomorrow when I see my Dr. because I may end up in a psych hold for real this time because I am so bruised. No Dr, I wasn’t trying to hurt myself, my brother’s dog threw himself on me, and assaulted me. And then it’s a 72 hour involuntary with chemo. How super would that be?
Yes, tomorrow is chemo infusion number 4. It was a little sketchy earlier, because I came home from work and took my nap only to wake up feeling nauseous and with a low grade fever, but it passed. I probably have one now, because I am now on my second dose of my pre-chemo decadron, the lovely steroid that makes me feel 20 degrees warmer than I actually am. Which is why I am up writing at 5am, instead of sleeping. Decadron is also responsible for keeping me from sleeping. It’s intent is to keep me from getting violently ill from the chemo, but as a steroid will, it gives you a sense of invincibility. So, instead of sleeping, I watch the same episode of Vikings three times, did two digital jigsaw puzzles, sorted my snacks for tomorrow, did two loads of laundry, looked for claw clippers, because the toe and finger claws are growing quickly, cleaned out my purse, packed monka-monka, lotioned my feet, scanned some receipts, updated my C.V. with some additional training info, and ate some crackers. I am sure I did other things, I just can’t remember them. Oh right, I made seven hundred trips to the bathroom as I slurp water to try to plump up my veins for the good time poking tomorrow. I am sure anxiety has played a role too. Since I have to leave early today with my chemo-buddy for the day, Ms. Crystal, I might as well stay awake and just forgo sleep. I did have a few naps, after all.
It’s amazing how great my family, friends and co-workers have been, in being my chemo-buddies, giving me rights, cards, gifts, food (especially food). And even what might seem like little things, like text message and calls, just to see how I’m feeling – it means so very much. I am blessed with astounding people in my life. And I can’t forget how much Andy has stepped up to help too – he’s been working a lot of overtime to make sure bills get paid, and buys groceries, and brings me food when I ask. I am very proud of him – he can still be an asshole sometimes, but he’s still a kid – and feel bad he has to sacrifice to help care for his mom. And don’t tell me I shouldn’t, because that’s what moms do. So thank you for all of you who are there for me, even if I tell you I don’t need anything – I appreciate it all more than you know.
It appears that it is nearly time for me to get ready for today’s fun and to eat some breakfast. I’ll be back again soon – til then, aloha, sweet friends.
My sister-in-law, hiding under the table because she didn’t want me to take her picture. Then I explained that cameras can take pictures of people hiding under tables –
My baby brother, my dad and my sister-in-law rocking out to Eminem
12 March 15 | Categories: Uncategorized | Tags: amuse, Andy, anxiety, bald, cancer, carnivorous kangaroo, chemo, chemother, chemotherapy, children and youth, family, flying monkeys, gratitude, pajama pants parade, spring | Leave a comment
So here we are, 2:49 am. I’ve clipped my finger claws, restrung my mandala (someday I will figure out how a bead fell off and left me with 107 beads…and the bead that fell off, perfectly normal), took a stroll through the house, and had some quality time chatting with monka-monkey and zombie monkey, listened to three podcasts at Anxious and Angry (you should too) and gave some serious thought to laminating something. So I decided, hey, I’ll blog a bit.
There’s snow on the satellite dish, and I felt guilty asking Andy to go out on the roof and clear it off, so I’ll hope the sun comes out tomorrow, and melts it off. Today was a snow day…although I was already in the car on the way to work before I found out I could have stayed in bed and savored the warm comfy comforter. Needless to say I turned around and hit the grocery store, because naturally, it might be 24 hours before I could again go to the store and buy milk and bread. Or less, because quite frankly, the roads weren’t really too bad on my way home. So there was no TV all day. Not really a bad thing, but I couldn’t get motivated to read, so I started watching Helix on Netflix, and then a quite troubling movie called “Come Back to Me” (you should too). I planned a whole bunch of projects in my head that I will do someday when the energy returns to my body, ate some crackers, and then some more. Such a busy day. Right now, I’m busy hoping there’s a delay in the morning because I am clearly not going to get a lot to sleep.
My weekend plans have fallen apart. There’s a leak in pop’s furnace, which means he’s not going to go, so since taking pop to my brother’s house was the reason we were going, now means we’re not. I was lamenting remaining trapped in the tower, and I realized I have been too much of a whiner lately and need to refocus on being grateful, because quite frankly, so many other people are in far worse straights than I am – I still have a job, I work with a wonderful group of generous, kind, caring people who make being at work bearable. Andy has really stepped up and taken on the responsibility of paying most of the bills, as I have little bitty paychecks since I burned through my paid time off back in December (yay for paid snow days/delays!). We have heat, I have a bed, there’s food in the house, we have a house, a roof, clean running water, indoor plumbing. I have boots. A computer with internet access. I have health insurance, actually, I have excellent health insurance. I have a good education. I like myself, mostly, and I am comfortable being alone. I have multiple talents. I have a nicely shaped skull. I understand the secret language I talk to myself in. I’m kind, funny, and have a vast amount of useless knowledge. These things so far outweigh the negatives in my life, I sometimes get too caught up in those.
So is life hard? Yes. But it’s not the worst place I’ve ever been.
And with that said, I’m gonna try to hit the bed again, not because I think I can, but because my toes are cold.
And spring is only 14 days away. 14 days.
For the first time ever, I completely scrapped the post I was writing and decided to start over.
I’ve started and stopped writing entries several times these past two weeks, (there’s extra bonus writing at the end – a longer post I started and didn’t want to keep writing so I’ll just slap it on the end of this one as a bonus). I don’t know what’s keeping me from writing – anxiety, exhaustion, procrastination – I mean I know it’s not because I don’t have anything to write about. Sometimes I think that I avoid it because I don’t want to have to keep whining about this cancer nonsense. I just can’t help that the stupid monster inside of me just kind of pervades my thoughts every day.
I do think of other things – like getting a pet goat, what book I should be reading, how I wish I had a maid, how I am hungry for brownies, that the season premiere of Vikings is next week, how I would rule the world when I am Empress of the Universe, calculations for the diameter of watermelons at the store – you know, important things. It’s not that I don’t want to write – I do – but half of the time, I find myself slipping into medication-assisted sleep, and the other half, I nod off, unmedicated. Some days I am all fired up about some social issue, I get ready to write and then I get distracted and next thing you know, drool is slobbered all over my cheek and my own snoring wakes me up.
Which is exactly what happened after I wrote that last sentence – I fell asleep, laptop in lap, and woke up this morning at 7ish. I had my wonderful morning cancer killing tea, and just finished some yummy oat meal. I realize I have little to complain about this morning – I feel okay, I can make tea in my bedroom with my loverly keurig, and oatmeal too. I am warm, and comfortable, and I can just spend the day doing nothing, which is what Saturday is often about here lately. I’m still undeniably anxious and restless about next week’s events but I’m grateful that I have such amazing health care that I don’t have to worry about the financial side of this. This whole cancer thing does put things in perspective, but I’m still not in that “live every minute as though it was your last” mindset. I am still too scared about what is to come to get there.
But let’s move away from this cancer nonsense and talk about what is going on in the world. I am sure we all know it’s cold. Well those of us in the snowy areas of the northeast do. My county has finally established a foot hold for a shelter for the homeless, but it’s causing quite an uproar because the shelter is part of a store front in the business district of the biggest town in our county, or I guess what has been formerly known as the county seat. The frightened townspeople are afraid that the existence of shelter will lead to more homeless people. Really? Like a funeral home would lead to more dead people? I often wonder when stupidity and hatred became the norm. Why is there so much opposition – I mean there’s already a drug and alcohol rehab on the main thoroughfare, and we still have the same amount of salt heads as ever. The homeless are still gonna be here, people…they will just squat in vacant buildings or spend the day in the library or the night in a laundromat or Wal-Mart , doing what they need to do to keep warm and alive. How stupid people are that thinking helping people who are in danger of hypothermia or frost bite will lead to more people wanting to live on the street. I just have such a hard time reconciling the emphasis in this area on being good Catholic and Christians and then in the next breath not turning your cheek, but rather turning your back on the people who need your christian charity the most. I feel like hell when I am driving my fat ass to work and I see someone walking in this cold, and people here are too worried about their “things” than they are about another person. These are the same people who will wax poetic on the value of a fetus, until that fetus is born and homeless and grows up in poverty. Then they will call my office and ask someone to go out and “take those kids away” forgetting that this was one of those fetuses that they insisted be born into to poverty. End of soapbox tirade. I have others, I’ve just decided if I am going to post anything, it’s gonna have to happen quick.
Round 4 of attempting to finish this – this is just an example of how tired this stupid chemo makes me. This is my fourth attempt to finish this post. I fell asleep three different times. Even after I drank coffee This is why nothing gets done around here. I get all excited with plans, I get all the stuff out for whatever project I have planned, and then before I know it, I’m under a blanket, dreaming about being attacked by a vicious and violent kitten I am supposed to be pet-sitting. Needless to say, that did not improve my opinion of cats. But on a night like tonight, being warm in bed with many blankets is not such a bad thing. Of course, since Andy is out on the road somewhere with friends tonight after a hockey game, I am now awake because I am worried about his safety on this hellishly frigid night. I couldn’t fall asleep easily anyway, with this howling wind. My multiple layers of blankets on the windows isn’t even keeping the icy breeze off my adorable bald head. I don’t want to text him because I don’t want him checking his phone wherever he is driving considering there is little visibility with the blowing snow. I just hope he had the sense to stay put wherever he is. Motherhood. It’s like an itch you can’t get rid of.
Well, since I have failed at humor and don’t have much else to write about until after my Dr. visit on Monday, I’m just gonna put this lame excuse for a blog post out of its misery. But not until after I share this facebook post from a young man who was one of my students when I was teaching at Lebanon Valley College…it’s nice to read these things when I often wonder if I have made a difference in this world…and according to this, I apparently have:
Everyone please keep Diane Pietkiewicz in your thoughts, prayers, etc. I’m not one for religion, but I’m making an exception and praying to the big guy. Diane is the most memorable part of my Academic collegiate experience. Best professor ever. She consistently made me look at the big picture, taught me never to settle, and that the history of our nation is far from that which we’re taught in highschool lol. She is fighting a bullshit disease, and deserves all the support in the world!
And since Joe talks about praying, I just want to say this…all of you lovelies should know by now that I tend to follow Buddhist philosophy, rather than religion. I am not one for praying although I do chant daily but I do appreciate prayers, in whatever faith and form they come in, because I believe in the power of focused attention. For me, putting positive vibes and thoughts out in the world can’t do anything but good, so I am grateful for whatever words or thoughts you put into action. I spend time every day visualizing this damn puffercyst inside me shriveling up and dying. So pray on, or chant, or just think good things. As a matter of fact, I am really grateful for everything people have done/are doing for me while I endure this latest go with chemo – everything from offers to run things up from the netherworld of the office so I don’t have to, to sending me surprise packaged, to simply asking me how I am. And I apologize for not being as shiny and happy everyday as I have been in the past – I try, but as I’ve whined about, I am so tired all the time. In fact, today as I was rolling over in bed, I realized I would have made a damn fine bear. But not a polar bear, because apparently they don’t get to hibernate. But a grizzly. I would be a fine grizzly. I could be a panda too, but they aren’t really bears, and they also don’t hibernate – but they are pretty lazy, which if me right now.
And with that, I shall try get comfortable and warm in bed, while I wait to find out if my kid is safe. I tacked on the post I tried writing the other right at the end of this one – I promise to try and rein in my adult ADHD next time and stay awake from start to finish when next I write. So stay warm and dry my darlings. Bonne nuit.
(I started this on the 29th of January, or so)
On the first day after chemo, chemo gave to me…so far, nothing that I can’t really complain all that much. I ate some chili (not always nausea friendly, but I am not known for always making the wises decisions), had some tea and ginger beer, and some nuts. No fever, took a couple oxycodone and a zofran (super effective anti nausea drug) and I am drinking water like a camel ready to hit the desert. Of course, that means I am spending a lot of time running to the bathroom, but if it means I don’t get sick, I’ll do laps. Andy cut off his dreads today and then I buzzed the rest of his head, because he wanted to show his solidarity in the current situation. He was pissed that I buzzed the last of the zombie grinch or some other weird Dr. Seuss character hair without him, but I explained I couldn’t go out in public to chemo looking like that…I love making and wearing funny hats, but hats get hot pretty quickly inside, and frankly, I love my bald head. It’s a weird time of year to be bald because it’s freezing outside, so when I am in the cold, I need to wear a hat, but at home it comes right off, and now that I don’t look like I wondered out of a nuclear bomb blast, I won’t be wearing hats indoors at all except to make my doctors, nurses and small children laugh.
The day was long yesterday, my doctor was running late and then I found out my co-pay went up, and I got to chemo late. It was quiet on the infusion unit yesterday, but the day was fun since my friend and co-worker Heidi took a vacation day to drive me to chemo and hang out with me. We played the Chupacabra: Survive the Night Game which could be very fun in you add alcohol and make it a drinking game. Otherwise, playing to best three out of five is enough. But between the game, and conversation and people watching, the day went quickly. My nurse had a bit of hard time getting my IV started…she didn’t want to go with the vein I thought would be a good choice at first, so she tried my hand – no go. She then decided to try around where I thought would work, and hit one, but today it has a huge bruise, which doesn’t typically happen for me, so on my point scale of 1-10 where ten is I feel nothing and 1 is “oh my god are you doing this for the first time????”, she only gets a 4.8 downgraded from the 5.2 or 5.3 she got yesterday. I knew I’d have a bruise on my hand, but I didn’t think I would have on my inner arm. (as of February 14th, I still have remnants of this bruise) It doesn’t hurt, it just looks ugly. But the doctor did say that my blood work looked good and I looked good and let’s just see what happens by the 3 cycle to see if this thing shrinks, and that it’s important for me to just stop what I am doing when I get tired, and walk away from it. I know I don’t now, because when I am at work I don’t think like “I’m sick” and just do the work, and exhaust myself so I suppose I am just going to have to remind myself my body is in a fight, and I need to put it first. Alas, I also need to work to have health insurance and to pay the premium. I am very excited about my first paycheck since December tomorrow. I am going to do something crazy with all that cash…like pay rent.
And speaking of crazy, a couple weeks ago, there was a contest on the facebook group, Saving Money, Living Smart, that I belong to…at Christmas, there was wish list to put on the items that you wish you could get for Christmas, and I put down a Keurig. Well a couple weeks ago, the group owner asked a few of us if we got our Keurigs, and then had a second chance contest to nominate someone who we felt deserved it. Well I felt I did…I mean, especially today, the day after chemo, and then next week, when Andy is sleeping after work, and I am too sick to get out of bed myself and I want a cup of hot tea and can’t go get one and have to wake him up. I don’t know if anyone else entered me too, but I told my story about how I found out about the cancer two days before Christmas and blah blah blah, and today, the FedEx guy shows up and what? Whoa. I now have Keurig from Saving Money, Living Smart and the Keurig Company. How awesome is that? As soon as Andy gets up from his nap, I’ll have him take a picture of me and my Keurig…what a great surprise and what perfect timing. (Even though I bitched all the way down the steps about who was knocking on my door because don’t they know I am resting.) This is fabulous…I can’t wait to take it out of the box and check it out once I get a picture. I just need to get one of those reusable cups for my ginger honey tea. I am excited. (and that’s where I fell asleep that time)
15 February 15 | Categories: c-monster, Philosophizings, Profound Insights, Random Rambling, Soapbox | Tags: amusement, chemo, chemotherapy, cold, cyst, endometrial cancer, flying monkeys, gratitude, postivity, sick, side effects, sleep, snow., tea, tumor | Leave a comment
That’s right, my lovelies – I did not run over any armadillos, I did not get a cat, I did not mix vodka with orange juice, I did not become a brain eating zombie, I managed to stay awake for at least one hour a day, I resolved to clean the house when absolutely necessary (which it never truly was), I did not use a drone to attack the neighbors, I ate no cauliflower, I checked my phone once a day, and I never told facebook what city I live in, no matter how many times it asked. 10 Resolutions made, 10 completed. Completing such daunting tasks gives me such a sense of satisfaction. I don’t know that I can top this in 2015, but damn it, what’s live without challenge?
I’ll get to this year’s resolutions in a moment. I really want to give the real ending to the attack on the cyst, because I couldn’t before I told my dad (aka pop) the facts – I didn’t want to ruin the holiday for him or for my niece – I mean I had to ruin it for Andy and some of my brothers, co-workers and friends, and of course, it was a bit of a downer for me too, but I couldn’t do it to my dad. I think I’ve told most people, if I haven’t and this is where you get the news first, I’m sorry. It’s not the thing you get any enjoyment out of telling people and one thing I’ve learned is that no matter how many people I tell, there’s always going to be someone that I forgot to. I can think of five or ten or fifteen now. Fact is, I’m tired of telling people. Here’s a fact: Telling people you have cancer (again) is fucking hard. You feel bad that your are giving people bad news, you feel you have to make them feel better, they always ask how they can help and it’s just generally a bad thing. If I tell you, just tell me that you love me. Or if you don’t love me, just say, hey, whatever you need. I’ll keep talking if I feel like talking about it, and if I don’t keep talking about it, and you have questions, ask me. I have a blog, seriously, it’s not like this shit is secret.
Anyhow, I read the CT scan before the surgery. I saw the words “possible malignancy” – I saw the look on the ER doctors face when he had to tell me there were some concerning items on the scan. I know my body. I knew something was wrong. After surgery, when Minion 1 arrived, and I asked her about the offending nodule and if they found cancer, she danced around it, saying that they “don’t think” anything is wrong, but they are only using human eyes. I much preferred the way I found out the first time – the resident held my hand and said it straight up, we can’t confirm it yet, but from the preliminary pathology, it looks like cancer. This time, I knew I was going to hear not very good news at my appointment. I know when they take a biopsy, they look at the sample to make sure it’s a good one. They don’t just randomly snap out a bit of tissue and hope for the best. And while they are checking, they can notice whether they have good cells or abnormal cells. Sure, they may not know if it’s malignant with certainty, but they know if something’s up or not. Minion 1 needs to work on her delivery. I should give lessons.
I also knew I wasn’t healing as quickly as I have in the past. I had some pretty hideous bruising. I lost my appetite. I knew things were different, but I wanted to believe what the Minion 1 told me. So when I got to my appointment on the 22nd, I was ready for the news, or at least I thought so. I went by myself because Andy was in Pittsburgh with my nephew and brothers for a Steelers game. I didn’t want him to not have fun because I had an appointment. I asked my niece’s mom to go with me last minute, but she couldn’t. So I just resigned myself to going it alone. I got there on time, checked in, and waited. I got weighed, and found out I’d lost 40lbs since October. That’s a lot. And then I waited. My blood pressure was almost normal, but there was much excitement by the nurse when I told her I was off the morphine and just taking percocet. I wasn’t in pain. That’s good. Yay. No need to undress. Hang out, Dr. will be in. Now, Dr. K is a presence. He’s a tall, funny guy, with a southern twang to his voice and he’s always cracking jokes with nurses and staff and patients. I suppose you have to when you have to give the news he’s giving. He’s almost never late. I can sometimes hear him talking to other patients when I wait for him. Today I can hear him telling one that they will beat this thing, and that they will be in to review the chemo and radiation schedule with her, etc, etc, etc. Not good. It’s still taking a while for him to see me. I wonder where my treatment coordinator is – I have presents for her and Nurse Sue and Dr. K – just little holiday gifts to say thanks. I don’t hear Anne outside either – not good. Finally, Dr. K arrives with Minion 2 from the ER nightmare. They sit down. Sit. That doesn’t usually happen, so yes, it’s another harbinger of doom. Dr. K looks at me and doesn’t mess around – the biopsy shows cancer, and launches into how we could treat it. No surgery, no radiation, two different ways to address it with chemo, there’s no protocol for cancer in this area, quite frankly he doesn’t even know how or why it came back, it shouldn’t have at this point, once you pass two years, there’s a much less likelihood of recurrence. I just kinda look at him, and tell him I don’t have dying on my agenda. He said that’s good because he hasn’t, and isn’t, giving me permission to die. I’m not crying, I’m almost relieved because now I know – I awkwardly hand him the card and ornament I brought him – tell him I don’t know if he Jewish, or celebrates Kwanza or Christmas, but he can hang the ornament on his Hanukkah bush if he wants to – and thank him for taking such good care of me. I can tell this is as hard on him as it is for me. I think the Minion 2 wants to bolt, but is glad I am not crying and that I am, matter-of-factly, addressing what I need to do. Dr. K tells him to talk to me about the MRI, since he hasn’t staged it yet, and needs the MRI to determine what all is happening in the dark recesses of where the stupid pufferfish lies. I tell him I think the unwieldy beast is starting its dark resurgence because I’m having some discomfort in the area, and he says that’s what he wants to see on the MRI. Minion 2 has ceased sweating, I truly believe he thought I would lose it like I did when they offered my the psych hold in the ER. I maintained calm. OK, I was in shock, but it still didn’t involve crying.
You are never really prepared for the news. I’m still not sure I have accepted it, and probably won’t until they hang the poison bag on the rack and it starts dripping into my arm. Dr. K and I hug, he assures me that we will kick cancer’s ass and be laughing about this in no time. He tells me this is a shitty way to end the year, and a shitty way to start a new one, but go home, enjoy the holiday, and they will call me with the chemo schedule the day after Christmas. I tell him I trust him, he got me through it the last time and will this time. I shake the Minion 2’s hand, and like a scared bunny, he hands me the packet of papers for checkout and flees the room. I head to checkout. As I stand there, alone, having just been told my body has betrayed me, it hits me, and I tear up. I have cancer. Fuck. The receptionist asks me about the papers – I tell her all I know is I have a 4 week appointment on the 5th, and Dr. K wants me to have an MRI. She asks if it is scheduled – I tell her I don’t know – I was just handed papers by the Minion 2. She looks, and doesn’t have a clue why I have been handed all of Dr. K’s results and notes. I suddenly realize I need a note for work, and another prescription for percocet. I ask if she can get that for me when she asks him about the other papers. She does – he tells me I’m off until after my 4 week check up. I realize we never even looked at the incisions. Good thing I heal OK. She comes back with all my papers – I ask her if she can give Anne and Sue my cards and ornaments. She will. I’m still not really connecting to any of this. I get my appointment for the MRI and visit summary and head for the elevators.
I don’t break down until I am in the car. Then I am a snotty, sobbing, weeping, sniveling, snorting, coughing, choking mess for about five minutes. And alone. Horribly alone. And also very glad to be alone because I don’t have to worry about making anyone else feel better about my breakdown. I text who I need to text. I need to get groceries while I am down here. It’s funny how the trauma and the mundane activities intersect here. I need to get food. I also need to get home. I start the car and go to Giant, and mindlessly wheel the cart up and down the aisles, tossing shit in I don’t really need, but I have a fuck-it-you-only-live-once attitude and decide we’re having a fucking rib roast and ask at the butcher counter for a small incredibly expensive rib roast. Two hundred dollars later, I’m checking out of Giant with my rib roast. I forget to buy water. I’m not even hungry. I need to go home and that’s the last place I want to be. My iPod won’t fucking charge. I’m not going home until I have the opportunity to sing loudly with my iPod, and preferably with OWTH, until the pain inside is purged. I must also see my friend, Pony-Pony. I need some normality in this surreal scene. I also need gas. Actually, GAS first.
So I drive – first to a gas station. I fuel up and head to the MHS barn to see Pony-Pony. He’s not there. They probably are making him be the stupid donkey is some live nativity somewhere. I keep driving. I see my friends, the goats, at the goat barn, and I yell “fuck you” at the sheep in their pasture. My iPod is still not charged. I see some cows. I see another pony, and another, none of which are Pony-Pony, but at least I saw them. I keep driving. I realize my blood sugar is quite low, and I am a little shaky – I’ll got to Hardee’s. This whole time I feel like I am in weird freaky film where my character is in a dream world unbeknownst to everyone who sees her. It’s like none of this is real. I finally get the iPod charged enough to commence screamsinging. Fortunately, RTE 322 is not busy and I can cry and sing and drive all at once with no worries. It’s not real. It’s not real. I get to Hardee’s and order some sort of burger and onion rings. I manage to choke down the onion rings. I head home.
The drive was cathartic. And pretty scary. Occasionally I would look down at the speedometer during pauses between songs. I pushed 100+mph more than a few times. It’s not really my fault the car goes that fast. I slowed down several times. I wanted to get home and then I didn’t. I would have to tell Andy and then other people. This is the part that sucks. I finally drove home – I walked in and Andy was all excited to tell me about his trip and the game – and I killed that with a look. He asked how the visit went and I lost it. I sobbed and cried and told him how sorry I was he had to go through this all again. My kid is a good hugger. He told me I was the strongest person he knew and it was just cancer, and I could beat it. Then he proceeded to hug me some more. When he was adequately covered in snot, he went and got the groceries from the car. I didn’t want my expensive rib roast being stolen in this neighborhood
The C-monster is such a fucking burden. Not only do you have to worry about being sick, but you have to worry about bills and work, and the house and telling people and not upsetting people all while being told that this is the time you are supposed to focus on yourself. If there are people who are able to do that, I wish they would have a network where you could find out their secret. Because once you recover from the shock, you have to think about who to tell, and when and where and how and how are they gonna react and if they are old, like my dad, are you going to kill them? And then there’s the logistics – appointments and chemo and food and laundry and the joys of all the changes in smell and touch and taste. And when you have been the head of household for the last 24 years, that just doesn’t stop, you still worry about that. It’s just a lot. And no matter how much you have people tell you they will do whatever they can to help you, you don’t want to ask, because you don’t want to be a burden, and you want to be strong and tackle this yourself.
I’m tired of writing tonight, and I am tired of watching this fucking pathetic Steelers game while I type. I’m tired of being sick and doctor’s appointments, and not wanting to get out of bed. At least there’s minimal pain. At least there’s plenty of food in our house and we have functioning utilities. I can still write. My bed is comfy. I have a new blanket to take to chemo with me. It’s all gonna be over in 18 weeks (it better be). Tomorrow is the MRI – it will be a whole new experience for me, so look forward to that blog entry. I sure hope there’s no metal inside that suddenly gets torn from my body like I’ve seen in horror movies.
Good night my happy people…I’ll be keeping you updated – hug on your loved ones and do something fun with them before they can’t, or you can’t. Sleep well. Oh, about those resolutions, still working on them. I won’t be bound by your constrictive linear timetables. Kisses.
Oh yeah – three years ago yesterday, I got my first diagnosis. Happy Anniversary. I didn’t know the 3rd anniversary was also cancer.
4 January 15 | Categories: c-monster, Philosophizings, Profound Insights, Random Rambling | Tags: anniversary, annoyances, anxiety, bald, biopsy, cancer, chemo, chemotherapy, children and youth, cold. flying monkeys, ct scan, cyst, diagnosis, disease, doctors, family, fear, flying monkeys, gratitude, happiness, health, hope, hospital, humor, ipod, life, malignancy, mass, mri, narcotics, New Year, pain, positive attitude, procedure, pufferfish, selfesteem, side effects, surgery, survival, treatment, uterine cancer, whining | Leave a comment
Ah my friends, I have returned, later than planned, but back nonetheless. It’s early morn on Christmas eve, and I am still a little amped up from crafting like a loon as if I could ever finish everything I want to before Christmas day. As we know I am a grasshopper in all things. I did however, finish a project for the tree I have moved from project box to project box for two years now, so I’m kinda stoked. Now the tree just has to go up. Again, another attempt to get Christmas right gone awry because of the stupid pufferfish — which leads us to today’s entry where the minion encounters the pufferfish for herself in the operation remove and apparently realizes that I wasn’t kidding about the torture it was inflicting on me.
When last I wrote, I left you with a cliffhanger about how I was going to see Dr. K on Monday to discuss the future of pufferfish residing in its pouch. I hope you googled pouch of Douglas so you can visualize the pain I endured from leaving the ER and enduring the rest of the week lying on my side because it was no longer possible to sit or stand for very long after that no good horrible very bad day. Monday arrives and Andy drives me to my appointment. LONGEST hour of my life. Every bump stung. We could not get there fast enough. I am sure Andy was doing at least 80 but it felt like 40mph, and every stupid person who could possibly be on the road was on in front of us slowing us down. I get to the appointment. Dr. K is running late. I can’t sit. It hurts too much, so I am standing and pacing and squirming and just generally miserable. Did I mention by this time I have also run out of percocet? Yes, well I was out on Saturday. I have seriously pondered removing this thing myself. FINALLY my name is called. I jump on the scale, and guess what? I am down 30lbs. Since October. Being unable to eat has its benefits. Onto the exam room.
Again, no one is taking my pain as seriously as I am, even when I tell the nice nurse I am at an 8, pushing a 9 on the 1-10 pain scale. I am lying down on my side on the exam table, my blood pressure is “going to pop a blood vessel” level. I am rocking and crying and waiting for Dr. K. He will save me. He arrives. I blubber about how this is now unbearable and I cannot go on, this monster has to come out. He nods and says, yes, I agree. Finally!!! Someone is taking me seriously. He’s gong to get me on the surgery schedule for tomorrow. YAY!!! And even though this means I cannot have anything to eat or drink from now until after I am gutted, I am elated. I would not eat for weeks if it meant I was going to have some relief. Whatever it takes, I tell him, just get it out of me. I pause in my blubbering to complain about his new associate and the minions and how they wanted to keep me overnight on psych hold and how his associate should never ever use the words sympathize and/or empathize ever again because she is clueless about what my pain was like and it came off as cold and uncaring, and they sent me home in the exact same pain I arrived in. And also, please let them know I know the difference between “the pufferfish is trying to assassinate me” and “constipation”. So there.
I meet with the necessary folks to get all my surgical ducks in a row and get some sodas and water from the kind nurse Sue. She’s the best. They will call me with a time for the surgery tomorrow. No more eating and no drinking anything after midnight. Fine, what ever, just give me another ‘script for the happy opiates and I’m on my way. Oh wait, you need to go to anesthesia. No, not them, Dr. Doogie will say I have a heart murmur again. Damn. Okay fine. Whatever it takes to be released from my bonds of pain.
I go find Andy in the parking lot and give him the news. Now we have a dilemma. Do I go home, an hour away and usually 20 degrees colder than Hershey with a winter storm pending, and risk having to drive at a super early hour to the hospital in snowstorm, or do I stay in Hershey? It seems logical I stay here. I have clothes in the car since the ER trip. I have friends I could call and stay with, but with a storm swirling off the coast, I don’t want to inconvenience anyone, so I decided to book a room. I get one at the Simmons Motel which I will plug here as a very nice, quaint, clean and comfy room and a 50’s feel and a super soft bed. And quiet except for the damn train. But I am getting derailed. (see what I did there?) In the meantime, Andy makes arrangements for his friend Tom to pick me up and get me to the hospital in the morning so he doesn’t have to come down and just sit around all day. Now some may say it’s odd that I don’t want anyone with me – but frankly, it’s easier to be by yourself, in my opinion, you don’t have to make anyone feel OK, and comfort them. You can just get shit take care of. We go hang out with Tom for a while, I get my pain under control with some medication, and head back to anesthesia. I meet with the goofy anesthesiology associate – I think you have to be a bit odd to work in that department or working in that department makes you a bit odd, because she asks me this litany of questions but doesn’t put down the answers as I tell her as I find out later. She asks me about my “heart murmur” and I ask her to keep reading so she can see that I had an expensive EKG after that diagnosis, and that there was no heart murmur. Her response? Oh, right I see that now. Then she asks me about my anemia following my surgery. I tell her continue reading, so she can see that I lost a ridiculous amount of blood from my tumor and that once I got some blood bags hooked up, anemia gone. Again, Oh right, I can see that. Then she asks me about my thyroid. Again. I tell her to read ahead, and again, she sees the answer I was going to give her. It takes forever. I want out . I just want to go to the hotel and sleep until I get the call. Let me go. Please. Finally, she leaves and the Dr. comes in. She checks to see that I am still breathing and I still have a heart. I sign the papers. I get to leave. I go to the hotel and check in and send Andy on his way. All is going to well, see you in two days. We hug, and give the usually mother/son affection. I tell him, no worries not gonna die.
I find that my surgery is scheduled for noon. Oh good, I could have gone home – but hell, the room was only $50, I don’t have to worry about being tempted by food or drink because I have none, and I can just lie there, in an opiate haze and do my bowel prep. Those of you with previous abdominal area surgeries or in the medical profession will understand that this means a lot of time running back and forth to the bathroom, typically in the middle of the night. I drift in an out of pain riddled sleep, literally counting the hours until I will be rid of this nightmare inside. I finally doze off for a few solid hours until BOOM. The medication for the bowel prep sends me running to the bathroom. Now the fun starts for the next 4 hours. I get through night, and though I’d like to remain in this super soft and comfy bed, I have to go. Tom comes and picks me up and takes me to the hospital around 10, because he is squeezing me in between work, and I wait. Counting. I am all checked in and they tell me a volunteer will come get me when I need to go to the surgical wing. I am stoked because I can then get a wheelchair ride instead of having to make that long walk. I connect to the free wifi, and get down to the business of saving baby pandas from the mean dragon. I will save you baby pandas.
Noon. Gee, all the volunteers have gone home, so here’s a map and off you go to same-day surgery, ma’am. What? I have to take myself? No wheelchair. Walk? Oh fine, and I head off. (please make no mistake, I love Hershey Med Center, they are awesome and I would not go elsewhere for my health care) I get to the elevators when I encounter on of the Sons of Anarchy Pennsylvania motorcycle club members. I can tell this by his hoodie, that reads “Sons Of Anarchy – Pennsylvania.” He has a pager. He must be a MD too. Why else would he have a pager, being in a biker club? He notices my Spamalot t shirt I am wearing from the musical. He shares with me that Spamalot is one of his favorite musicals too. If only I wasn’t about to have surgery, I may have just met my soul mate, a biker who loves musical and is clearly a doctor to boot! But as my luck would have it, after we exit the elevator on the surgical wing, he turns left and I go right, and our potential love affair is over. Sigh.
At the unit, I am escorted to my prep area and given a gown and some special washing clothes to prepare. The nurse shows me the chart and tells me how to wipe down for surgery and says when it comes to doing my back, ring for her and she will do it for me. I do that and a different nurse comes back to help. I tell her what I need, and she says to open the last package, place the pad against the wall and rub up and down against it like a bear scratching its back on a tree. I look at her surprised, about to question her, but still ready to follow her instructions, when she says, “just kidding”. I laugh with her and said that I guess they have to get their fun anyway they can, and she said she was gonna see if I was going to do it, but she decided against it. I told her had she not stopped me I probably would. I hope on the bed and entangle myself in my blankets and listen to an Anxious and Angry episode on my iPod I guess my laughing to myself troubled the nurse and one comes to hang out with me and get all my vitals and shit. She hangs out for a while, and finally I am ready for the big surgery, when they ask where my ride home is. I said I am not going home til tomorrow, and she’s all – well it says here that you are going home after surgery – I look at her and say, uh no. That’s not what the Dr. said. She leaves to go get that worked out. Time check. 2:20PM. Technically I am supposed to be in the ER in ten minutes. She comes back to assure me that I am indeed staying overnight and informs me that surgery is running about 45 minutes late. I tell her it’s cool, I was a last minute add on, and as long as the pufferfish is dealt with, I will wait. I pick a movie to watch on Netflix and wait.
3:45. Still waiting. Me and another woman are the only people left in this holding area. She’s crying and whimpering, and I am am just happy that gutting will occur. 4:30. I’m on my way. Next stop the OR. I tell the operating room nurses that they better keep Dr. K focused and don’t let him mess around, I want be in and out and in recovery before the Season Finale of SOA at 10pm, so no dilly-dallying around in there. They assure me they will keep in him in line and before you know it, I am waking up in the recovery room to another nurse asking me if I want ginger ale. And this Mennonite lady in a rocking chair smiling at me. I wasn’t sure what was going on at first and then I slipped into full awareness once I noticed there was no pain. JELLO!!! I could have JELLO!!! It’s JELLO heaven. I immediately order up a few orange jellos and some water and eat like I haven’t eaten in days. Oh wait I haven’t eaten in days. I inhale the JELLO and begin to keep the nurses and the nice Mennonite lady in stitches with my sense of humor until they determine I can go to secondary recovery down the hall. The doctor will see me then. My “sister” Paige calls me and we chit chat for a bit as the anesthesia wears off. I assure her I am fine, and think about getting more jello. The little boy in bed across from me belongs to the Mennonite woman, and needs to go to the NICU, but there’s a problem getting enough people to help transport him – I tell my nurse she can go help, I have things under control, I’ll be fine. She is about to do when word comes down, I’m off to the next stage of recover and away we go. At this point I realize I still have a catheter. I am not please by this. I ask for its immediate removal. Denied.
I get settled in my room. I have some sort of inflatable bed. It’s very comfy. I have the special massaging boots I love so much on, and my phone. Rudolph the Red-Nosed Reindeer is about to start and I can have all the Jello I want, and when I am ready, even a sandwich. I make sure I am not dead, because it seems like heaven. Especially the no pain part. No pain. Did I mention NO MORE PAIN. I get a new nurse. Like all of the nurses, she is super nice. She tells me I am staying there all night as there’s been some sort of influx of patients on the Women’s Health wing and there’s no room for me there. I see all kinds of people walking the halls – they aren’t stuck with a catheter. I ask again for mine to come out. Wish Granted. I am even allowed out of bed. I get up and head to the bathroom, just for fun. I have no pain. I am so happy I can’t even explain. I jump back in bed, watch the final episode of SOA, call Andy and eventually get my sandwich. I take several trips to the bath room, roam the halls for a while and finally fall asleep around 2 am. I still have no pain. If I didn’t know better, I’d say I’m still not awake and this is all a dream.
I get up around 6 when the female minion arrives. I remind her that in the ER she said she said she would not be gutting me. I ask her what happened in the ER, because none of the nurses knew the exact details. She tells me that they went in, it was hard to get to, they just drained it and did a bunch of biopsies. I ask about the C monster due to the what I read in the CT scan and she tells me that they are pretty positive that things were normal, but they won’t know until the reports come back, because you can’t tell those things with human eyes. I ask where Dr. K is. She tells me they will be back between 8 and 9 to discharge me. At this point I am starting to think he called it in, and let her do the surgery because I didn’t see him before surgery or in recovery and now he’s sent her in here and I am not even sure he didn’t go back to Disneyland. But I’ll wait to see.
I alert Andy to come fetch me. I am starting to have pain from surgery but not pufferfish brutality. I am told to wean of the perocet first and then the morphine. I get up and head to the bathroom to produce enough pee to be allowed to go home. After succeeding in that area, I am provided with a delightful breakfast of eggs with salsa. I can’t really eat, but I try. The nice nurse who was with me through the night tells me that Dr. K and the minion aren’t coming back but I can go home. I find this odd, and now I am sure he is just a figment of my imagination, but I am going home. I get freed from all of the IV tubes and machines and dress to go home. Run to the bathroom again. When I get back Andy has arrived. I am free to go. Still no pain. It’s a early December miracle. The minion comes back with my note for work, and a pretty prescription for percocet and I am turned out into the cold. Andy and I head home, after stopping for chinese and a chocolate croissant. I am cured.
This brings us to today. The pufferfish remains. He is still under the watchful eye of Dr. K and my close monitoring of my body. There are more tests to be run, but I remain pain free. I am weaned off the morphine (yay) – I have no debilitating pain – I had my one week check up – wounds are healing very slowly, and there was a lot of bruising inside and out. My incision did not start spouting fluid like they did during the last surgery. I can eat a little and sleep a lot. I have lost 40lbs now. Things are looking okay, but I cannot go back to work until the 6th after my 4 week check up and I can’t lift things. This means no holiday baking, not decorating, and only doing things that require sitting or lying down. I drove the car to the Dr. yesterday – I am still recovering from that, but the bottom line is I am recovering and will be able to enjoy the holiday with NO PAIN.
And that my friends, it the second part of the story. I will relay the story of my one week check up at a later date, but it involves minion 2 (the male one). It’s time now for me to return to watching White Christmas and sleeping. Have an awesome holiday and be sure to savor every minute you are with those you love. Eat, drink and be merry. I know I will be when I am gnawing on the bone of my rib roast on Thursday. Tomorrow (actually today) is the annual family Christmas eve dinner. Pictures will be forthcoming and I bought a special surprise that will bring joy to the hearts of many and make the family photo spectacular. I will share that debacle with you all later. Merry Christmakwanzakuh. I hope it’s all you wish for an more.
24 December 14 | Categories: c-monster, Philosophizings, Random Rambling | Tags: amusement, cancer, ct scan, cyst, diagnosis, doctors, flying monkeys, funny, gratitude, health, holiday, hospital, humor, minions, pain, peace, pufferfish, random, restless, sleep, surgery | Leave a comment