Live, Love, Laugh...Imagine

Sunday, June 24, 2007

Paola and Lucas Recovering

I just talked to Paola. She is doing better although she overdid the walking yesterday and is now sore. She's still in pain from the raw wounds caused by removing the tape. Also, she's still anxious to see what her "new body" looks like, but it is still too early to tell because she's still swollen from surgery. That said, it sounds like she's doing pretty well. Lucas is likewise on the mend, having had to go to the animal hospital for two bowel obstructions. Lucas is now home again.

Friday, June 22, 2007

All clear to contact Paola

Hello all,

Paola is feeling better today. Lucas is ill. I did not get an update on Rosie.

If you would like to call Paola, feel free! If you would like to visit Paola, please call her first and see if she's up for it.

Thursday, June 21, 2007

Drs are pleased with their handiwork

Paola and her mom spent this morning at the hospital for a post-op check-up. The doctors are pleased with Paola's recovery thus far. They removed the dressing and the drain - a good step forward but a painful one, given the conjunction of delicate flesh and stubborn tape. Paola was in pain from the surgery and is now in further pain from the tape removal process; nevertheless, she has been able to eat and take limited walks, so she is in far, far better condition than after the previous surgery! For a month she will need to wear a tight bodysuit-like contraption. Hopefully she'll be able to get some stitches removed in a week. So, all in all, things look good. She is still not up for phone calls or visits yet. Maybe tomorrow - I'll let you know.

Wednesday, June 20, 2007

At home

I just spoke with Paola's mom. Paola is at home and had a good night, but she is still in pain. Tomorrow she goes back to the doctor for a check-up.

Tuesday, June 19, 2007

Heading home

Paola has been discharged, and her mom is taking her home. Paola is tired, in pain, and generally not feeling fabulous. Once Paola tells me she's up for visitors or talking on the phone I'll let you know but for now, please let her rest. If you feel compelled to do something for Paola, send her a card or a note - she'll enjoy seeing them while she's recooperating.

Still at the hospital

I just spoke with Paola. She is still at the hospital but is likely to be discharged today. She has not yet seen her surgeon. The hospital would not allow Paola's mom to stay there last night. Paola is in pain but is able to eat - she had just finished a bagel when I called.

To the recovery room

Paola's mom called me at 10:19 PM EST (June 18th) to report that Paola was awake and had been transfered from the recovery room to room G10.

Monday, June 18, 2007

Out of surgery

I just got a call from Paola's mom. Paola's out of surgery and headed to the recovery room. She'll stay in the hospital tonight, and Paola's mom will remain there as well.

Headed into surgery

Paola just called - she's headed into surgery now.

I'm not afraid, Part 2

Paola and I just spoke. She's at the hospital, sitting in the ambulatory surgery waiting room. Continuing her tradition she declared for the record "I'm not afraid! I'm not afraid!"

Surgery Round Two

As you all likely know, Paola's scheduled for her second round of surgery today. This surgery will focus on breast reconstruction. I am in New York, so I'm facing the challenge of trying to stay up-to-date -- and keep y'all updated -- from afar. Paola's mom, the wonderful Rosie, is with Paola.

Paola's surgery is scheduled for 1:30 PM today. Once I know anything, I'll post it to the blog.

Saturday, June 16, 2007

Allie's back!

Just checking in - I'll be updating things while Paola's undergoing this next round of surgery.

Tuesday, June 12, 2007

Bringing the Blog back to Life

Despite my best wishes I found it very hard to blog throughout the later part of surgery recovery, chemotherapy and radiation. Instead I sent updates out to friends via email at intervals updating everyone on latest news. Though I do hope to resume blogging at some point soon, I want to share these emails here, clumsily fast forwarding the blog and bringing you all up to date on my treatment and recovery.

Here's a time line of my treatment for reference:
  • Double mastectomy and initial breast reconstruction: 16 August 2006
    • Estimated surgery time: 10 hrs. Actual surgery time: 20 hrs.
    • Lymph nodes removed from breast and left axila
    • Stage III cancer diagnosed
    • Estimated that without operation, I would have died by February of 2007
    • Food prepared by Joey's kitchen team is delivered daily starting 24 August.
  • Chemotherapy--8 sessions every other week: 1 Oct 2006 - 9 Jan 2007
    • Lost my hair by 15th of October; shaved my head 21 Oct 2006
    • Lost eyelashes, eyebrows, and pretty much every other hair strand (except in my legs) by the Holidays
    • Couldn't eat any raw vegetables, everything tasted like metal, survived on cheese, pasta and other bland foods including ice cream
    • Gained 20 lbs and made Oncologist upset when I complained about it
    • Immune system completely shot, couldn't fly, attend concerts, crowded restaurants, or theaters for the duration (though I cheated a bit and went to the mall and movies on occasion).
    • Spent 4 months essential on house arrest. Friends and colleagues delivered lunch, movies, helped around the house and stayed overnight when needed.
    • Took 5 weeks of recovery time before Radiation started
  • Radiation Therapy--25 daily treatments (excluding weekends): 5 March - 6 April
    • Severe internal pain, skin rash, and fatigue
    • Due to radiation angle, permanent damage to left lung leaves lingering dry cough
    • Heart tissue is safeguarded
    • Took 8 weeks of recovery to allow skin to heal prior to second reconstructive surgery
  • Breast Reconstruction Part II: 18 June 2007
    • Estimated surgery time: 4 hrs. Actual surgery time: we'll see, I'm expecting 5-6 hrs.
    • Scar tissue will be removed and breasts reshaped.
  • Breast Reconstruction Part III: TBA
And now, the emails. Please see following posts.

Radioactive Update (2 April 2007)

Dear All,

I hope you have all been well these past few months, and the beginning of a New Year has brought the changes you had hoped for on New Year's Eve. Even if your resolve to stick to your resolutions has been lackluster, you still have ¾ of the year to make them all come true…including the weight loss! (You know who you are…)

As Passover, Easter, and Pagan Spring Fertility and Renewal festivals approach, I wanted to take this opportunity to wish you all a wonderfully blooming time and give you a little update on things here.

Though chemotherapy officially ended on January 9th, some side-effects remained; most notably my total lack of hair and the weight gain. As I have mentioned before, chemo drugs completely obliterated the flora in my intestinal track forcing me to eat very bland and starchy foods for the duration of treatment. I guess the steroids I took to withstand the pain didn't help either as they made me very puffy. In the end, this translated into a 20 lb (~9 kilo) gain...@#$%&!

Once chemo ended, my body completely hairless, immune system destroyed (AND trying to fight the flu), I headed for a restorative sojourn to the beach and spent some much needed time with family. I was happy to soak up the sun, disconnect from the world, swim, sunbathe, meditate and read. It took me some three weeks to start feeling better, but after much sleep and surf, I felt like a person again. I finally went for walks and started eating more normally—especially vegetables, fruits, and other raw foods including sushi. (Yay!)

The steroid puffiness faded soon after my energy started to slowly return, but there was no sign of new hair still. Even worse, the waves knocked out every last lash and eyebrow which made my eyes sting violently without any protection against the acidic mix of sun block and saltwater. On the upside, I was incredibly aerodynamic in the water; which aided my first few attempts to swim. Gleefully my stomach muscles engaged and I was able to swim for the first time in over 8 months. I was terrified my torso would just sink like a log and I'd never do another triathlon again. I didn't get very far, mind you—given my weaken state, diminished range of motion in my arms, and the salt water in my eyes—still, my stomach HELD UP!!! One triathlon sport down, two to go.

A steady fruit and fresh vegetable diet also kick started the slim down, but it's been a painfully slow process. My body is a little whacked; some weeks I am up, some down. It seems no matter what I eat or do, I can't get the weight to stabilize. My doctors keep telling me I have to be patient and let my body heal itself slowly. Intellectually this makes perfect sense, but emotionally the weight gain simply added insult to injury, and it hurts.

Upon my return in late February the docs checked everything out and deemed me ready for nuking. I have never been this excited about radioactive isotopes! It's totally spacey, and duly complicated. You see, this stuff can kill you, so they need to make sure that only the cancerous parts are nuked, and at the right levels too, lest the treatment give me MORE cancer…crazy science! But how does one prevent adverse effects? Sadly, one doesn't…only prayer (and potent drinks to induce denial) can possibly account for all the unknowns. Still, glowing in the dark is much better than being dead, so I agreed and on we went.

First there are tons of x-rays from every angle to pinpoint the specific field to be nuked. I guess this also serves to give the body an early taste of radiation. Then comes the simulation. This generally involves you laying down semi-naked for hours, and hours on a gooey platform that eventually retains the contours of your body. I am so glad they told me how long the test would last BEFORE we started and I COULDN'T move AT ALL…no wait, that's the one detail they left out! The simulation, then, doubled as a test for my bladder capacity and control. Turns out I can hold it for over 3 hours without moving—and you thought my talents were relegated exclusively to the classroom!

Aside from the near-bladder explosion, the "test run" went very well. They determined the coordinates to align me with the machine and promptly tattooed markers on my body. These would then be used every day for 30 treatments to assure we were nuking the exact same area. Why is this important? Well, we wouldn't want to further damage any surrounding tissue, like for instance, the heart and lungs. Unfortunately, part of having been an athlete for years is powerful (namely big) lungs. Though they tried their best, and were able to avoid radiating the heart, they couldn't avoid nuking part of my left lung. Thankfully this will only mean a constant cough I may never be able to shake. Fun! And thus the nuking commenced on a Thursday morning promptly at 8am. I pleaded for a more humane time, but sadly other pesky cancer patients had taken the good slots! Alas, the nice tech promised me 10 am nukings after the first 10 treatments. (Score!)

If this treatment had a warning label, it'd read something like this: Extreme hazardous materials. Use only under insufferably overqualified adult supervision and confined to a vault-like room with foot thick steel reinforced walls and doors. Upon administration be sure that all non-cancerous personnel leave the premises to avoid exposure. Extreme hazard if subject moves even a millimeter during administration. Subject may experience extreme fatigue, dizziness, claustrophobia, muscle spasms, sunburn-like symptoms including itching, scaling, severe rash, cracked skin and intense pain. Subject may also experience electricity-like pain emanating from affected area and radiating along limbs and nerve-endings. Finally, treatment may cause cancer at margins of radiated field, and may in no way prevent further recurrence in areas outside the said field. Treatment may be given only once with an acceptable level of risk to deem it "safe." Subject, though mildly radioactive, does not glow in the dark; is not dangerous to babies, puppies, small rodents (including tiny doggies) or plants; subject cannot power her own house, or perform any cool party tricks.

On the positive column, radiation does in no way impede hair growth. My overachieving follicles (did you really expect anything less?) are so ahead of schedule they'd managed to fold time, as a mere 8 weeks after the end of chemotherapy I had TWO rows of eyelashes and full eyebrows that once again required grooming. My hair started growing in inconsistent patches about 4 weeks after chemo. After much shaving to strengthen the lint that first appeared atop my head, growth has finally stabilized and now covers the entire head evenly for a soft brush feel at about ¼" inch (~0.5 cm). Another cancerous joy is the guess-what-color-and-texture-your-new-hair-will-be game. At the moment my once medium ashy brown has turned into deep charcoal black. As for the texture, given that the hair is not sticking straight up, it may indeed be a bit curled rather than its original straight self. Most patients tell me I should be happy it's black rather than entirely gray—which is the other popular option.

And thus the past few months have gone between recovery and radiation. My first blood test some 6 weeks after chemotherapy showed that my immune system is back to normal and firing on all cylinders. The doctors were also pleased to see that all blood particles are regenerating normally, which amounts to an amazingly fast systemic recovery. I am currently at the very tail end of radiation and the conclusion of the cancer-fighting battles that started on 16 August with the tumors' removal. We'll know if the war is won in about 12 months though. In order to improve my survival chances by 50% I'll have to make it to 4th April 2008 without remission. Thereafter, my chances of survival will increase by 12.5% for every year I make it without cancer for 4 years. This will bring me to 5 years of remission upon which my overall chance of dying from cancer will diminish from 100% to a mere 30%. Simply put: if I make it to 5 years and I am still in remission, there's a 70% chance that I'll become the rocking old (and all around cool) broad I know I can be.

So what now? In the long term: wait and live. In the short term: visit with family and friends, and retreat again to give my body a chance to heal in preparation for a second round of surgeries. In June & July I will undergo two more surgeries to finish out the girls and assure that all pesky cancer cells are vanished. I am yet to fully discuss the complete follow-up plan with my docs, but they assure me I will be under intense observation for the first (and most critical) 12 months. But no fear, as I have mentioned to so many of you, cancer will not kill me…I've decided this and it will be so.

Though I remain steadfastly positive, I am tired; actually physically, emotionally and spiritually exhausted. Being sick and generally incapacitated for this long has been a test of will I hope never to endure again. This prolonged house arrest and inactivity have been incredibly hard on my spirit. I want nothing more than to be training as the triathlon seasons gets underway, I miss my work colleagues, and friends, and want to finally stop being in pain. And though I know these side-effects are temporary and inevitable, I still long for my body to allow me to do the things I enjoy. But, as my dad says: "La luz de 'alante es la que alumbra" (The light ahead illuminates the path); so I march onwards undeterred, though at times frustrated, to the light.

I want to thank everyone who through their actions have made my treatment bearable and my recovery possible. May you continue to turn your words into deeds, and never speak in vain.

Until June…Lots of love as always,
Paola

PS: If you made it this far, thanks for indulging my very, very long update…Chag Same'ach Pesach! Peace to your home and joy to your heart.

Chemo update and Happy New Year (29 Dec 2006)

Dearest All,

As 2006 draws to a close I want to take this opportunity to tell you a bit about what's been going on here and bring you a little holiday cheer…ok, who am I kidding, this is a cancer update! (But one with a happy ending so far)

As many of you have pointed out, the blog continues to show wet pictures of Lucas since September. I know this is cruel and unusual, not just to the poor creature, but to many of you; sadly I really have no good excuse other than "I've been having a little chemo"…hasn't gotten me out of any speeding tickets, but hopefully will allay your fury and get me out of Jury duty in Santa Clara County—got summoned this week! For now, this update will have to suffice until I am able to finish and upload a more comprehensive narrative detailing the joys of Cancer treatment.

Speaking of silver linings, one of the most remarkable things about this process has been the opportunity to learn how to receive and appreciate help, and experience first hand, what amazing people I am surrounded with. As many of you may know, I had a double mastectomy in August and by the end of September my mother had already gone home. I started chemo on October 2nd and have since relied entirely on a vast network of friends in the Bay Area to get me through it.

My colleagues and friends at Google have dutifully delivered lovingly prepared meals by the kitchen staff every day since August and through all of chemo. I should mention that some of them have waited months in line to make such deliveries as apparently I've become a hot excuse to get out of meetings :) Others have offered themselves and their parents to drive me to and from chemo infusions and follow-up doctors' visits. Some have volunteered to spend key nights with me each chemo cycle to make sure I have someone in the house should I need help, medical attention, water, a laugh or just some company. The Gray's Anatomy viewing club has been a roaring success offering up weekly McDreamy-Steamy sessions and even an excuse for a chocolate fest when the ban on cocoa products was finally lifted by the docs on Nov. 16th.

Little things from weekly cards with encouraging messages and hilarious tag lines, to a brand new pill box that actually fits all the supplements I'm on, a free subscription to NetFlix, weekly help with my garbage and recycling, Lucas bathing, head shaving in solidarity, unending errand running—especially to get Pedialyte and other bland foods, and finally, endless rides to various places and gatherings have made these last few months bearable and in some cases even enjoyable. I have been overwhelmed and immeasurably thankful for the vast show of support and love I've received. But most importantly, while learning to receive unconditional help gracefully, I have also had brazenly honest and profound conversations with many of these people, and have gotten to know them in a way I think our normal day-to-day circumstances never allowed before. Somehow, cancer destroyed a wall around us and allowed all of us to be real in a way I've seldom experienced before, but have the joy to embrace daily now.

But not everything has been rosy—just in case you thought this was turning into a Hallmark moment. Cancer treatment in general, and chemo in particular, can be summed up as a tedious and repetitive test of one's will to endure pain, discomfort and, unexpected and profoundly disconcerting side effects, with the hope that you'll be rid of every last evil cell and come out the other side alive.

I have lost my hair pretty much everywhere, including inside of my nose which irritates my sinuses and has thrown me into a permanent state of sneezing, YET I am still shaving my legs! I know, this proves that g-d cannot possibly be a woman, I'm most disappointed. On the up-side, I have managed to keep most of my eyebrows and about 30% of my eyelashes. Since chemo kills all rapidly dividing cells in your body—cancerous or not—I have also lost all the lining in my mouth and stomach rendering me almost incapable of digesting a raw vegetable or any kind of spiced food without great pain and other unspeakable side effects that I'll spear you. As a consequence, I have lived on a very bland and starch/dairy laden diet that has made me GAIN rather than lose weight on chemo. Yes, you heard it, I managed to PLUMP up…I complained to the doc and he almost killed me as this is a very desirable outcome—except when you are the one logging the outcome poundage around…sigh.

The first set of chemo drugs made me nauseous 24-7, but thankfully the latest set simply give me lots of pain and hot-flashes. Yes ladies, if you've ever made fun of your mom, aunt, grandma, or random stranger reaching for anything in sight to fan herself, please say a little prayer to yourselves that you'll actually have to wait until menopause to experience your body's amazing ability to make you think you are going to actually combust, and then make you sweat uncontrollably. The more chemo I get, the more often hot-flashes come, and of late they've been happening mostly in the middle of the night, which happily interrupt my sleep regularly. Oh how I wish there was a better way to target and kill only cancer cells in the body instead of putting patients through all this hell—it's like using a nuclear blast to kill a mosquito, it also obliterates and contaminates everything within a 500 mile radius.

The good news is that chemo is almost done. I have just completed my 7th infusion and on January 9th will go in for the last one. After that, I will take some time to retreat and heal in preparation for 6 weeks of daily radiation. Following the nuke fest, two more surgeries await. But I am taking this one step at a time, one day at a time. Chemo battle is almost over, and I am halfway through the Cancer war with relatively few casualties—unless you count hair strands individually. I have been lucky to have the support of my friends, family and work to allow me to take the time I need to heal. My body has taken a beating, but my spirit remains strong. Mostly, I've learned to appreciate the present more, as it's become increasingly clear to me that's all we really have.

I want to thank all of you for your support—whatever shape it's taken—and wish you the kind of love and encouragement I've felt this year to overcome any challenges you may face in 2007. Remember to look around and recognized how loved you are, tell others how much you love them, go out there, kick ass, and go for what you REALLY want—life's too short not to play hard!

Lots of love, health and happiness in the New Year!

Many hugs,
Paola

Back Online: First email after Surgery (11 Sept 2006)

Dearest all,

I apologize for the long silence, but rest assured that all your messages, flowers, gifts, encouragement and thoughts have not only been received, but have been an integral part of my recovery. As I have already told so many of you, knowing that you are thinking of me--and sending positive energy and love my way—has carried me through the tough days and allowed me to enjoy the good ones a bit more.

I had been waiting to feel "good" before resuming my blogging duties, but then I realized two things: a) This might be a LONG while and b) "Good" is a very relative term these days. So after my writing hiatus I wanted to take this opportunity to give a quick update and once again point you to the blog. Though I may not be able to write every day, I hope to blog at least once a week—comments on posts and the wonderlust group/forum are ALWAYS welcome.

The past few weeks since my release from the hospital have been marked with small triumphs and occasional setbacks, for an overall positive balance on the recovery front. The docs are happy and want me to push a bit harder on the physical activity—which is very painful. Mom is cautious and wants me to cut down on pain meds—since they are narcotic and generally bad for you—but this diminishes my ability to increase physical activity. So it's a balancing act every day between my doctors' orders and my caretaker's wishes.

I should also mention here that mom doesn't really believe in western medicines and thinks them all generally poisonous to the body. My docs have never heard of any of the homeopathic remedies and herbal treatments mom has so laboriously researched. So I try to take the best of both worlds and I'm happy to report that some of mom's treatments—though they generally taste like ass—have been quite effective and haven't really interfered with the course of the "traditional" medicines.

Still, I am unwilling at this point to go to an all raw diet mainly consisting of sprouted cereals (it is as gross as it sounds), no dairy or starches, and go to bed at 9 pm(!) each night. I have, however, conceded on the refined sugars—drastic reduction of pretty much everything that's yummy—and moderate to actually non-existing simple starches in my diet. In addition to mom's mission to get me to fight cancer through a rabbit's dream diet and a monk's lifestyle, the docs have summarily prohibited any caffeine containing food, especially CHOCOLATE!!!! I know, this is torture! Oh, did I mention I can't drink either? Yeah. So I guess I am closer to the monk and the bunny than my normal self…

But I am taking it all in stride and immensely enjoying the time with my mom—though admittedly frustrating at times. She has given herself over to my care with the outmost love and devotion, to the point that I have to push her to take better care of herself. Like a good Latina/Jewish/Italian mama, she is very protective of me and wants to make sure that nothing in my surroundings will cause me harm. This has translated into a manic cleaning frenzy that never seems to end, including endless loads of laundry--if something touches the floor it must be immediately washed in piping hot water! I am afraid she is single handedly diminishing the fresh water supply for the whole of the Bay Area.

The most concerning of her wellness strategies for me is her firm belief that Lucas is somehow radioactive, and I shouldn't AT ALL come in contact with him. At first she advocated for having him (and all his belongings) deported from the house for an indeterminate (I believe "forever" was her goal) period of time. After a long and tearful negotiation I agreed to not hold him or in any way cradle him and stay completely clear of him, his toys, food, and living space. In turn, mom agreed that if he spent the majority of his time in the backyard and was only allowed in the house a brief period of time in the evenings—completely away from me, of course—his contamination would be properly contained and thus I could be saved from its ill effects. She then made it her mission to disinfect and thoroughly wash absolutely everything the dog has ever come in contact with. I still have to restrain her desire to bathe the poor animal on a daily basis.

Lucas, in turn, thinks that *I* am radioactive and begrudgedly (but obediently) stays clear of my bed and person. He still gets his kicks, however, using his big brown eyes and batting tail to guilt mom into long petting sessions and extended belly rubs. Mom, I believe, has secretly fallen in love with the little guy, and though she maintains her resolve to keep him (and his supremely infectious doggy dirt) away from me, she seems to thoroughly enjoy being the ONLY person in the house permitted to pet the monster. Conspiracy perhaps?

And so the days roll in intervals dictated by the meds schedule and are colored by mom and Lucas' antics. There has also been quite a bit of chanting, candle and incense burning, heartfelt talks and some tearful arguments. Mom is settling into her role with gusto and I am trying to be a good patient. It's a tough road to travel, but we are marching on and leaning on the help of so many to make it through. Mostly, I am thankful to be so loved and to have so many of you by my side.

For those of you who are in the Bay Area and would like to come and visit, I'd love to see you. So please give me a call 650-xxx-xxxx (don't just stop by pls!) and we can coordinate a time that works—generally evenings after work are a good time :) I will let you know in as much advance as I can if I am not feeling well and can't see you, but as you well know, I am a social butterfly and hardly miss an opportunity to hang (unless I am REALLY, REALLY sick!)

For the rest of you, I've loved receiving and reading your cards and smelling the lovely flowers you've all sent. I have tacked all cards to a board Rob & Allie created for me, so they are my inspiration every time I wake up, feel down, or just need to refuel my courage cell. Thanks so very much (and keeop them coming if you are so inspired)!!!!

Catch you all in blog!

Lots of love,
Paola