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Settling In: Taco Trailers and Texans

January 18, 2010

I’ve been in the nation of Texas for just a couple of weeks, but overall I’m enjoying the warmth of both the weather and the people. Austin is an odd little pocket of ex-hippies and UT students who espouse the slogan “Keep Austin Weird”. People bike to work, recycle and carry concealed weapons. I’ve noticed an unusually high number of neck tattoos and an unusually low number of over-sized belt buckles. Yesterday, I passed a guy on his bicycle wearing nothing but a g string. Not even a helmet.  I thought, “this must be my first Austin Weird experience.” I also thought, “that guy can’t be comfortable in the saddle.”

Other observations of note:

Guy in his late sixties, walking down the sidewalk carrying a full sized boom box playing hard core rap.

You can buy beer and wine on Sundays, but not hard liquor. Guess Jesus doesn’t approve of shots.

This town has more bike lanes than sidewalks. Must be that Lance guy.

Local grocery store displays Velveeta in the produce aisle next to broccoli.

You can get almost any kind of food from an airstream trailer. Tacos, pizza, crepes, cupcakes. Genius.

Lady Bird Johnson was a big deal.

Dry cleaners are downright difficult to locate.

Grocery store clerks like to chit chat about anything and everything during your transaction. Same with barristas,  ice cream scoopers, pharmacists and of course, bartenders. My husband finds this unnerving.

Best. Grocery Stores. Ever. Original Central Market and Whole Foods offer incredibly high quality foods from every cuisine. Both have embedded restaurants that serve booze. Errands are much more fun when you can reward yourself with some hooch.

Everyone knows someone in a band.

The only people that ride the very nice public busses are poor minorities, the dentally challenged, and me.

Again, these are just observations in broad strokes. Overall, its interesting that everyone seems to simply love living here. People seem generally content and relaxed. I really want to give in to this mellow happy miasma, but I can’t help but suspect its all part of an evil plot involving mind control and robots. Can people really adore where they live to this degree? I’ll keep digging and report back.

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I’m not dead

December 31, 2009

I sort of forgot that if you have a cancer blog and don’t update it for a while,  people wonder if you died.

Just wanted to reassure everyone that I am very much alive and feeling pretty good actually. Its just the Holidays kinda snuck up on me and I just didn’t feel like thinking or writing about cancer. I went to Vegas and saw my good pal run her 56th marathon (one in each of the 50 states!). Visited Mom in St. Louis for pre-Christmas. Spent Christmas Eve with friends and hosted 8 people Chez Blumer for fancy food and drink. I started my holiday toast with “Here’s to another Christmas I’m not dead!” Luckily my friends “get me” and were already lightly boozed. In the meantime, I’ve been researching my snowbird relocation spot: Austin. Yep – I’m ditching the cold and chemo combo for a balmy and chemo combo in the land of Hippies with guns. I even started practicing my “hook ‘em horns” sign, but I keep doing the heavy metal Satan sign by accident. So much to learn…

I hope to write a lot more while in Austin and have notes on several blogworthy episodes. Tentative titles include:

My Christmas Enema

The Elvis Moment

My Siberian Teenage Hair

Longest Two Hours Ever

and….Santa’s Watching so Stop the Drama Already

I promise to write soon. Right now…I have to pack. (gulp)

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Haunted by Calista Flockhart

November 15, 2009

My life is playing out on Brothers & Sisters. For those of you who don’t watch, Kitty (Calista Flockhart) a high powered politico was diagnosed with cancer about 5 episodes ago. They admirably avoided the “very special episode” crap and have dealt with issues of treatment, family and the internal mental game with particularly eerie insight. Someone on the writing staff must surely be a survivor or a close caregiver. Anyhoo, I was particularly happy and freaked out to watch the latest episode where Kitty chooses to shave her head and go the wig route. She has a remarkable moment where she just stares at herself and her hair in the mirror, as if taking one last look at her “normal” self before buzzing her noggin. I feel like I have that moment every morning. Despite my “the Donald” do, I’m too chicken shit to shave my head and move on.

For a while, she contemplates stopping treatment. (We’ve all been there.) Her family is incredulous. Only then does she let the “brave patient” facade drop and truly confess the strains of side effects to her Mother. Mom is embarrassed and sad to learn she had no real idea of what her daughter was suffering, despite sharing a home with her. I realized that I can also be guilty of an overly sunny report to my loved ones. I firmly believe a positive outlook is crucial to healing, but I could probably stand to be a bit more honest about the downside as well. How else do folks know how and when to help?

I also realize that lots of folks read my blog for some sense of commeradarie in the travails of treatment. Maybe a peek at what to expect from a similar regimen can eliminate some of the fear of the unknown rather than depress someone about what’s to come?

So, here’s my current line up of side effects. I list and detail these not to complain, but just to share and let people in a bit on my day to day.

To begin: I’m on a regimen of Folfuri every two weeks. That’s a drip of irinotecan, leukovorin, and avastin followed by 40 hours of 5FU on a portable pump. Overall, its way less awful for me than Folfox which involved oxiliplatin. Oxiliplatin is Satan Juice.

Schnoz: Every time I blow my nose, there’s blood involved. Sometimes a little, sometimes a minor nose bleed that stops quickly. Odd, but not a big deal.

Hair: Its thinning and thinning and thinning some more. I risk a sunburned scalp if I go out without a scarf, hat or my fab new wig. And its thinning everywhere. Lets just say….free Brazilian.

Mouth: Oh the mouth sores. These internal canker sore-type things are truly sucky. I had a couple on my tongue that brushed the sharp edges of my teeth whenever I spoke or ate. Ow. They make it hard to eat in terms of pain and a general oogie feeling that hangs around. And the medicated mouth rinse might actually be ickier than the sores themselves. Imagine BenGay in your mouth. Very weird.

Throat: For about two days in each cycle, I feel like I have 2 big lumps in my upper throat area. It makes it hard to swallow and I have to really really chew everything I eat. Major gulping of beverages as well. My doc admits to being “stumped” on this one. Alrighty then…good thing it always fades away.

Skin: Here’s a freaky one. My palms and the bottom of my feet peel as if recovering from a nasty sunburn. Sometimes it peels to a deep layer and my poor tootsies are red and raw-ish. Moisturizer definitely helps.

I’m also getting very sensitive around the area surrounding my port. I have major owies where the repeated use of tape has pulled away my skin. I’m totally putting my foot down tomorrow and making the nurses find a solution to this. I’m not putting tape on scabs. Duh.

I also used to get tiny pimples on the right side of my face and neck on the day after treatment. It seems the culprit was Decadron, the steriod that I get in my pre-meds. I asked doc to eliminate this from my druggy cocktail and the zits promptly cleared up. #nozitsatfortyWIN

Armpits: This one is fun. While I am free of hair in the pit department, I have developed zits in the region. I learned that it is not uncommon to develop small cysts in the area, but luckily I don’t have any. Just armpit pimples. Yay.

Belly: I’ve lost all muscle strength in my torso, so extended walking or standing can leave me a bit achy or sore. As far as nausea goes, mine is pretty well controlled by drugs. I feel most queasy on my last day of the pump and the day after, but it doesn’t interfere with my diet much. Lately though, I’m getting slightly queasy on days later in my cycle. Probably to be expected after 10 bouts with this chemo cocktail, but I plan to ask doc about this too.

Butt: Hemorrhoids, anal fissures, constipation, diarrhea, rectal bleeding – you name an ailment of the ass, I’ve had it. I’ve learned to alter my diet a bit in different phases in my cycle, but ultimately I have a regular battle with irregularity. Usually some Immodium, Tucks and a soak in the tub will clear up the issue. However, I have had 3-4 episodes of blinding, sweating, cringing pain over the period of an hour or more on the throne. Those days have been the worst in my entire experience of treatment. I’ve been planning a blog specifically dedicated to these horrific scenes, but its just so damn embarrassing I keep putting it off. This coming from a gal who has detailed the day she crapped her pants. Trust me. Its ugly.

Overall fatigue: This is a biggy. On day two of my chemo, I pretty much just sleep all day. I’ve come to accept this for the most part, but it freaks my husband out. Seriously, I’m awake 4 hours max. Its very disorienting and freaky. I also have a hard time falling asleep – mostly I just can’t get my brain to shut off. A groovy drug called Ativan helps a bunch, but my hours are still irregular and hard to manage. Most days, I need a short nap. Some days, I just can’t seem to wake up at all. This takes a progressive toll on me and I see this as my biggest challenge long term. I have a feeling exercise is key, but the ass groove in my couch isn’t shrinking.

Brain: Here’s where the real stamina is required. Yes, all of these side effects are uncomfortable but they are by no means unbearable. (Except, of course, the occasional hour long butt battle.) Everyday, I try to push myself to do at least one thing I don’t feel like doing. Sometimes its just moving from the bed to the couch, but its something. I need to add some exercise to my routine at this point, but I’m not having much luck. Hopefully I’ll have the motivation and discipline soon. Right now, I’m a mostly unapologetic lard ass.

Well….uh…there ya go.
How am I feeling? Now ya know.

But please know, none of this is too much for this Tumor Assassin. As long as I can down the occasional Bourbon; I’m good.

Peace out.

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Booty Patrol

November 8, 2009

Individuals with hemorrhoids should not ride bikes.

Never the less, it was time for this post surgery gal to get off her duff and try to exercise. So, dusted off my bike helmet and took a little ride round the hood. Checked out our new Sausage Shoppe. (No double entendre here, it really is a shop that sells sausage.) Peeked at fancy cooking stuff. (Been coveting a Shun cleaver. ) Contemplated Cold Stone for lunch. (Hmmm…probably counter-productive.) And generally enjoyed myself. Yes,  I panted like a 15-year-old boy surrounded by Venezuelan Ms. Universe contestants, but still glad I got out on this odd Indian summer Chicago Sunday. Nice to feel kinda normal. Especially since my helmet hides my “The Donald” looking remnants of hair.

I also got my fab new wig yesterday and had a date night with my hubby and 2 fellow foodie wine pro pals. Again, felt like my old self. No nausea. Ate a freakish amount of rich food, split 3 bottles of wine (after several aperitif cocktails!),  and woke up late, but not hung over. Now I’m cooking for a dear friend who is caring for his Mom, post surgery. I actually get to help someone else! What a nice change of pace. If I can have mostly days like this, the side effects are not so bad.

Suck it cancer; I’m livin large.

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A Streetcar Named Dilaudid

September 30, 2009

Somehow, I have turned in to Blanche DuBois.

I spend lots and lots of time in the bathtub and I find myself suddenly dependent on the kindness of strangers. I’ve been quiet in the blogosphere for a while, trying to wrap my mental game around some new treatment and ongoing issues relating to chronic illness. Frankly, it blows. I’ve been in a moody place that isn’t particularly inspirational, heroic or even interesting so I just decided to keep my trap shut. But, I think I’ve figured out what’s made me particularly mopey and I think its important to share.

Accepting charity sucks.

There.

I said it.

I am EXCEPTIONALLY grateful for EVERYONE who had shown me profound kindness and generosity over the last 18 months. The outpouring of love and assistance has been truly inspirational. But. Accepting help and gifts and cash from your friends, family and radio fans is a very creepy feeling. I feel totally undeserving. Not because I’m a rotten person or anything, its just Marc and I have it so much better than most. We have great insurance. Marc has an impressive job with a supportive employer. I have access to many support organizations, simply by living in a major city. Somehow, I feel like I’m robbing the truly needy.

That being said, I’ve also learned that friends and family desperately want to “do” something to help. Sadly, they can’t make my disease go away or do chemo for me so many feel quite helpless, which sucks in its own way. In an effort to help loved ones who want to offer some comfort, I suggested they send Jewel or Target gift cards. I made an effort to ask for help, as loved ones have requested.This summer has been tough all over and we can always use stuff to make mine or Marc’s life just a tiny bit easier. I’ve treated myself to new bedding to keep me comfy and a wicked cool red grocery cart that I’m looking for ways to trick out. I’m planning to get a yoga mat and try to channel some pretzel healing karma or chi or whatever it is you get from Yogis that don’t carry pic-a-nic baskets. I’m even flying to Vegas to watch my pal run her 50th marathon in 50 states courtesy of miles from a terrific pal with miles to share. My dear pals Tim and Katherine even set up a donation website where you can donate toward my future care. I’m keeping it all in a savings account, just in case I hit a cap on my insurance pay outs or I have access to a surgical procedure out of network. Those are just a few examples; there are many many more.

Having a bit of a financial cushion is extremely comforting as I look at the insurance statements that roll in every day. But I can’t separate the guilt and even a bit of shame for accepting other peoples hard earned dough. I get it. I asked people for help. But, its still weird being on the receiving end. What’s worse is I haven’t written a single thank you note. I’ve saved names and contact info, but I just can’t bring myself to do it. Not that I’m not incredibly grateful; its just so embarrassing somehow. I feel enormously selfish for not offering a simple written “thanks” to all the generous souls who have offered numerous forms of support, but I’m truly at a loss for words. (I know, it seems impossible.) And the longer time passes, the more rotten I feel.

Please know I appreciate every single gesture, note, card and check. Its just every time I try and muster the mojo to start writing, I stare at the haunting blank note cards until I can’t take it anymore. Then I dip in to my stash of narcotics and soak in the tub. Its the truth and it ain’t pretty. I’m not trying to excuse myself from the responsibility of gratitude or make anyone feel awkward. I just wanted to share my feelings in an effort to explain my discomfort and out of character behavior. And I don’t imagine my feelings are unusual. I’ll bet plenty of tumorous folks out there feel similarly strange accepting assistance in a variety of forms.

So, please don’t think I’m an ungrateful bastard. I’m just embarrassed and tongue-tied. Probably a little high as well. I promise I’ll try again, once I dry off.

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Funny Cancer TV coming to Showtime

August 28, 2009

Hey cancer peeps! I just learned that a pal of mine from college just got a new show green-lighted on Showtime. Its called “The C Word” for now and sets out to be a dark comedy about a young woman with cancer. And dig this…Laura Linney stars. How cool is that?!?

Darlene Hunt is the Writer/Producer and a wonderful chick. We were in the same acting class in college and I can personally testify to her amazing talent and fabulous sense of humor. I can only hope she’ll do a cameo or two as well, because she’s so freakin funny on screen.

Anyway, if you don’t already have Showtime, you should subscribe when the show airs. (Lord knows us tumory folk can’t have enough TV. Plus you should really watch Weeds. Its terrific and deals with another YAWC hot topic, Pot!)

Stay tuned!

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Vampire Port

August 14, 2009

I awoke this morning to find that my port has been sucking my blood in my sleep. This was disturbing. The blood in my line, nearly down to the pump, was bright red. Being 8 am in the morning, I immediately starting freaking out and rushed into the living room to grab the phone. Unbeknownst to me, we had carpet cleaner guys in the house and I tred directly across the newly cleaned and wet area rug. As you can imagine, this earned me a serious WTF look from hubby.

Once I realized my error, I simply explained “I have blood in my line and I’m freaking out…..Sorry.” Always understanding, he says “Oh. I get it. No worries.” So, I tromp back to the bedroom, circumventing the rug, to call my Home Health Care nurse, truly hoping NOT to have to go to the ER. Its the weekend AND the Air and Water Show downtown which will mean thousands of SUVs creeping around looking for non-existent street parking. It would really and truly suck.

On the phone, I am cheerfully connected to Nurse Marta, who hears from me regularly and has a sunny voice. “Hi Marta, its Chris. Um, I just woke up and I have a lot of blood in my line.” One thing about nurses. It takes a lot to get a rise out of them. I’ve always suspected if I called and said “Hi Marta, its Chris. I have a massive head wound and I’m pretty sure it was caused my this meteor that just crashed through my roof.”, she’d give me nothing short of a typical coach’s advice. “Ok honey. Throw some dirt on it. Shake it off.”

Marta quickly eased my fears with typical aplomb. “Oh, that happens sometimes. Its just the way you sleep on it.” (somehow isn’t always the patient’s fault!) She asks me if the pump is still running and on the same schedule as when I went to sleep. (yes and yes). Is the bag of chemo still deflating? (another yes) “Its fine. Now that you’re up the drug will clean the blood out of your line. If it isn’t gone in a couple of hours, give me a call.” I hung up very relieved that I didn’t have to navigate soccer moms and overstimulated children downtown. That is until I realized that my oxygen tinged blood was now flowing BACK INTO ME. Huh. I guess that’s ok.

Hubby sticks his head in the door.
“Did I overhear that everything is OK?”
“Yeah. My port just has a secret life as a Vampire.”
“Want me to go to Starbucks?”
“Yes, please.”

and so begins my day.

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Serving up Sangria tonight @ Young Adults w/ Cancer Hootenany

August 12, 2009

Got Tumors? Cancer doesn’t have to suck while your in the prime of your life. Join Kairol Rosenthal, author of Everything Changes: The Insiders Guide to Cancer in your 20′s and 30′s for a book signing at Women & Children First tonight in Andersonville. Also on hand will be Jonny Imerman of Imerman’s Angels, Matthew Zachary of The Stupid Cancer Show and ME serving up Sangria and talking about my funny little cancer blog: Chemo and Vino.

August 12

Women & Children First Bookstore

5233 N. Clark Street

7:30pm

Sponsored by i[2]y

Here’s my Sangria recipe:

2 750 ml bottles cheap, but not sucky, dry white wine

1.5 c brandy

1 c sweetened lemonade (I like Neuman’s Own)

10 oz frozen peaches

10 oz frozen raspberries

sparkling water and/or sugar to taste

Steep the fruit in the brandy and lemonade in the fridge for a few hours if possible. Combine chilled wine and brandy. Taste and sweeten if necessary. Ladle into glasses and add a splash of sparkling water to each cup just before serving.

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The Port Tan

July 29, 2009

I have captured a new look in Chemo Chic. The Port Tan. Those of you who sport an unintended Farmer Tan or any other white on tan pattern that doesn’t exactly jive with your clothing lines can understand.

Back on the 5FU, I had forgotten that “sun sensitivity” thing and didn’t lather up before I walked two blocks to the train on a cloudy day. My pasty white Irish skin was now that blush pink that makes you look constantly winded and flushed. But what really sealed the deal, was a v neck shirt at an outdoor event with my port peaking out reminding everyone that I’m toxic. “Screw it. Let ‘em see!” I thought. Until I got unhooked from my pump today.

 Now my décolletage is a paler golden color set off by a giant glaring white square just below my right clavicle. It is nicely trimmed in a pink halo of irritation from the adhesive and has already started picking up lint from my shirt for added texture and color. Yes, this is The Port Tan. A stylish square brand that says, “Hey look! I could be even paler!”

 The bright side of all of this is; I’m actually outdoors. Doing stuff. Which is mostly better than sitting on my damn couch, popping narcotics and watching cartoons. Mostly.

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better days

July 9, 2009

Hi gang!

What a difference a few days can make! Today I spent a few hours working at UIC, did a bit of grocery shopping, met my pal Jess and Marc for dinner and started laundry all by myself! I had a good 2 hours on the train, and while my eyes did water a bit , it was just because of the smell of a homeless guy next to me and not tears.

My “fake patient” job at UIC is a great outlet for me right now. I feel like I’m giving back by helping train doctors and making them more aware of their beside manor and compassion. I get to act and go somewhere else mentally for a few hours a day, while still earning a bit of cash. The part where I have to wear a hospital gown is kind of a drag, but I am a pro now in tying and draping those things for maximum coverage. Mostly, its nice to be actually doing something and contributing to society; not to mention our household income.

Speaking of cash. Some incredibly thoughtful friends have created a website to raise funds for my medical expenses and ongoing care. I am both touched and grateful for the outpouring of kindness and support. Take a look at the site here  if you like. I am overwhelmed by people’s generosity. I can’t tell you how wonderful it is to have the freedom to just order pizza, when Marc and I don’t feel like cooking. Or to stock up at Target on jumbo sized paper towel packs and detergent so that we don’t have to spend all of our time together running small errands. I’ve even got a cute, red, rolling grocery cart on the way to help me with day to day shopping. All of these things make our life just that little bit easier, but it makes a huge impact overall.

Marc and I are also going to open a special savings account to store contributions toward my ongoing care. I am keeping an eye on clinical trials and new surgical procedures that may require out of pocket expenses and/or travel. Again, it is just such a wonderful feeling to know that I will most likely have the freedom and resources to pursue this kind of treatment. Thanks to all of you, I have the luxury of just focusing on me and my eviction of these tiny invadors. It still sucks to have cancer, but I couldn’t ask for a better crew of folks to help me kick this thing’s ass.

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