Live, Love, Laugh...Imagine

Monday, August 28, 2006

Paola's doing wonderfully

Hello all,

This is my official last post. I'm headed to the airport shortly, but I wanted to update everyone that Paola's doing GREAT. She had a doctor's appointment this morning, we ran various errands, and then she, her mom, and I ate lunch out at a restaurant.

Paola reports that she is still in pain but has energy. She's definitely enjoying hearing from those of y'all who have been calling. I don't think she's been on the internet today (it's been a busy day), but she has LOVED seeing comments on her blog, so keep it up!

Paola has not been sleeping well on her lift chair so she's rented a hospital bed, which will be delivered tomorrow morning. She's really looking forward to that bed!

Thanks to everyone who has helped Paola (and, by extension, me) out in the last few weeks. Matt L., Michele T., Rob L., and Liz W. have been especially wonderful - thank you very much. Thanks also to the providers of food.

Despite the fact that the last few weeks have been rough, I've enjoyed spending time with Paola, and I've had fun meeting her friends. I also had a great time reacquainting myself with Paola's mom and brother and with Rob L. I even managed to learn approximately 2 words of Spanish! (Quite a feat, as anyone who knows my linguistic capabilities will attest...)

In closing, Paola, you are growing stronger and healthier every day. It has been inspiring to watch you tackling adversity. You've pushed yourself hard, and your rapid recovery is testimony to your willpower. Take it day by day and know that your strength will carry you, not only through this, but also through chemotherapy and anything else that life throws at you. It has been a honor to be with you during this period of your life.

Best wishes,
allie

Sunday, August 27, 2006

Headed home

Paola said she was too dirty and icky for a "leaving the hospital" shot, so this is all you get. Paola's mom is driving (white car) Paola home from Stanford hospital.

"I'm not afraid"

Paola is being wheeled into the operating room, not to emerge for hours and hours. As she's being taken away, she's yelling back at Michele and me: "I'm not afraid! I can't believe I'm not afraid, but I'm not. I'm not afraid!" (I have to attribute this outburst of euphoria to the drugs but what do I know...)

Paola and the anesthesiology resident


He of the painful IV insertion. He's pretty happy; Paola is too (of course, he'd just given her drugs). This is mere seconds before she got rolled into the operating room.

Lucas missed Paola when she was in the hospital


Photo credit: Fishstik2 (aka Rob Lojek)

Weekend update

Well, Paola is definitely on the road to recovery! This morning she and I took a long (well, for someone on a walker) walk. She's been able to take quasi-showers, and she's eating like a champ. She's been able to reduce her pain meds from every 4 hours to every 6, which means less waking up in the night to take medicine.

Yesterday she and her mom went to the ER because there was some drainage from one of the incisions, but the doctors told them that everything was fine. She's still regaining her strength, and she's still in pain, but she's doing great.

Paola is now answering her own cell phone so feel free to call her. Please don't drop by the house unannounced, but I'm sure Paola would love visitors. Just call her and see if there's a time that she'd be up for a visit.

I finally figured out how to post photos yesterday, so check them out. More to come! Also - as I'm sure many of y'all figured out - your comments weren't posting to the blog. Apparently the comments were in limbo waiting for the blog moderator (Paola) to "allow" them. Anyway, she got online the other day and did that, so the comments are finally showing up. I couldn't see them any sooner than y'all could, so I'm sorry that I didn't respond to the comments.

FYI, I'm returning to NYC Monday (tomorrow) night, so my days of blogging are about through. Once Paola's arms don't hurt her as much, she'll be able to resume blogging herself.

Saturday, August 26, 2006

Pre-surgery photo

Photo - night before surgery

Paola and her friend Emily after Thai food...

Friday, August 25, 2006

Privacy at last

After spending the last week plus with people around her every minute of the day, Paola got the gift of privacy today. She stayed home alone while her mom and I went to the medical supply store to survey the selection of chairs and beds. (Paola rented a reclining/lift chair, but she's finding it a little less comfortable than she'd hoped.)

Paola slept fairly well last night, and she's eating normally (though she can't have any caffeine). She took three walks outside today. She's still in pain but is doing much better.

Thursday, August 24, 2006

Paola's home!

Hello all,

Paola left the hospital precisely at 11:00 AM this morning. She's home now catching up on missed episodes of "Entourage." Between her new TV (a birthday gift), her snazzy rental rolling walker, and her reclining/elevating chair, she's pretty happy.

Paola's still in pain and still has limited motion (particularly in the arms), but she's doing much, much better. Nonetheless, she requests no visitors until next week. If you'd like to stop by and see her, please call ahead and schedule a time to visit.

I'm sorry that I wasn't able to return every phone call. Both my phone and Paola's were ringing pretty constantly for a few days! Please know that if I didn't call you back I did let Paola know that you called (or, if you left a message, I passed it on.)

[By the way, I'm not sure how much longer I'll be doing these updates - I assume Paola will be back on the computer sooner or later.]

Wednesday, August 23, 2006

Another good day and tomorrow: discharge!

Hello all,

Well, today marked one full week in the hospital for Paola. She's much, much better than she has been. She's down to two drains (she'll come home with those) and is able to get in and out of bed, use the restroom, sit in a chair for hours, and, most excitingly, walk the hospital hallways. She's still in pain, but she's completely off IV meds. Yesterday she had her long anticipated grilled cheese sandwich (only half). Today she finished off the grilled cheese, had yogurt, had applesauce, and then had salmon for dinner.

There was so much going on today Paola didn't have time to get a bath or a shampoo, but I bet her mom will take care of that this evening. Paola's REALLY looking forward to being able to wash her hair, so I think that's high on the to-do list once she arrives home. (She's going to be discharged around 11 AM tomorrow.) Her nurse and I warned her that she's going to be exhausted by the trip home. As such, I'm not sure that the shampoo will happen right away, but maybe Friday will work.

That's the news. To those individuals competing in the Canadian Ironman, Paola wishes you well, and so do I.

Tuesday, August 22, 2006

A very good day

There's not much to add from my earlier post. Paola walked from her room to the nurses' station and back three times today; she ate yogurt and drank juice; she remained clearheaded the majority of the day. She's off IV meds entirely. She had two more drains removed, but the doctors say she'll likely still have some drains in when she is discharged. We had an excellent nurse, Laura, today. We were delighted not to have the nurse from hell today; she wasn't on the unit today (maybe she got fired!) I gave Paola a bath and washed her hair. She felt well enough to deal with her own hair and gave herself a ponytail.

That's the latest...

Good news all around

Hello all,

Paola is doing fantastic. Her doctors are thinking that she may be discharged Thursday. Sorry, but she's decided that she'd rather not have visitors until she gets home. Even when she gets home, she's going to be in pain for a while so I think she may not be up for visitors immediately. Please schedule your visit rather than just dropping by!

In other good news, she managed to walk from her room to the nurses' station and back. (I'd tell you how far this is but I'm horrible with distances. It was a good way though.)

She's supposed to be switched this afternoon to all oral meds so she'll be free once again of her IV pole.

Paola will have a busy schedule of doctors appointments in the weeks ahead. At this time, I am planning on returning to New York around Tuesday of next week. Paola's mother will remain here for a few weeks. I envision that Paola and her mom may be grateful if anyone can help by making grocery runs or Target runs or maybe helping get Paola to and from doctor's appointments. (Paola's mom can drive Paola's car, but Paola may need to be in a wheelchair at first, so an extra pair of hands might be useful. I don't know, I'm just speculating.)

That's it for now; I'll write again when I have news. By the way, for those of you who have been frustrated in your attempts to comment on these posts: it seems that Paola has to allow each comment individually and - as she hasn't been on a computer at all - she hasn't been able to do this. Please just comment in the forum section of the blog. She's very much looking forward to seeing all of your comments when she is able to get on her computer again! By the way, the offer still stands that if you drop cards or small items by her house her mom and I will bring them to her.

Also FYI, Paola's brother left today. Raff, if you're reading this when you get home, thanks so much for EVERYTHING. We'll miss you.

Monday, August 21, 2006

An eventful day

Today Paola moved to a new unit. We are both regretting the move -- for all that we know it is a sign that she is getting better -- because now she’s just one of many patients and the nurses are less able to give her individualized attention.

I wrote “less able” in a conscious attempt to be charitable. The first nurse she had on the new unit was HORRIBLE. It wasn’t merely that she didn’t seem 100% competent; it was that she was rude. Nurse X (name changed to protect the unpleasant) was one of those health care workers who refuse to believe that a patient – or a patient’s companion – might actually know what medications the patient has received (or needs to receive), what angle of bed is most comfortable, etc. She shared her “philosophy” -- which was basically that only wimps need medicine -- with us. While I agree with her that one should strive to get off the meds, it seems that if you just had major surgery and are in pain, you ought avail yourself of available pain-relieving agents. But I digress…

Paola reports that she had a good night. When I arrived this morning, she was sound asleep and didn’t even realize I was in the room for hours. Paola’s nurse let her sleep as long as he could, but he had orders to move her to the new unit so eventually he woke her up and then we formed a merry band – Paola prone on a stretcher, a nurse and I bearing Paola’s collection of gifts through the hallways.

Paola’s new room – in unit C2 – has – yes – cell phone reception. Unbelievable! It’s a private room with a nice view; she’s happy with it. As I’ve previously mentioned, the first nurse we had to deal with was terrible. The second nurse seemed unfriendly at first - I think Nurse X had told her that we were “difficult.” Anyway, she warmed up to us over time and appeared to be a very good nurse. Too bad nurses work in shifts. I’m just praying that we can avoid Nurse X tomorrow. [Especially since she directly ignored or contradicted doctor’s offers re Paola’s care and whenever this was brought to her attention felt the need to remind all present that she’d been a nurse for 31 years. (I wonder if she’d been a GOOD nurse for any of those years????)]

Paola is off IV fluids and is responsible for keeping herself hydrated. She’s been cleared to eat whatever food she wants except anything with caffeine (coffee, chocolate, soda). She still doesn’t have much of an appetite so today she contented herself with jello, a little soup, juice, and some applesauce. Her big accomplishments of the day were: getting out of bed and sitting in a chair, walking from her bed to the door of her room and back several times, and walking to the restroom and using the real toilet. Her evening nurse (the competent one) was not impressed – her plan was to have Paola walking the hallway corridors tonight. Paola is very determined to do absolutely everything she’s told to do, so I assume she will actually walk the corridors tonight. That said, when I left her this evening, she was in a lot of pain.

Have I mentioned the issue of Paola’s mother’s bed? The first two nights that she was here, Paola’s mother stayed overnight at the hospital. Despite numerous requests, the nursing staff was unable to find her something on which to sleep. The third night, I warned Paola’s night nurse (a very competent individual) that he might have an additional patient if he couldn’t procure something on which Paola’s exhausted mother could sleep. Accordingly, he found a kind of reclining chair (think: giving blood), which we wheeled into Paola’s room.

Today, when moving units, I asked if we would be able to keep the reclining chair and was told that we would. However, later in the afternoon another nurse came and took it away, despite our protests. Pleas to the incompetent nurse to find a replacement chair (or cot) went unheeded. Pleas to every individual who seemed possibly able to help likewise went unheeded. However one marvelous nurse’s aide took pity on our plight and brought us a cot, which we greeted with much joy.

I think that’s the day’s news. Sorry this posting was so delayed. Unfortunately, the new room still has no internet, and the one time I made it to the cafeteria, I couldn’t get a signal.

Good night, and please pray that we can avoid Nurse X tomorrow!

Sunday, August 20, 2006

A good day

Today was a good day for Paola. As I mentioned earlier, she’s off oxygen and the dressing was removed from her abdominal incision. Her fever is gone. She’s still receiving pain meds, but only by request. She’s still receiving prophylactic antibiotics and anti-nausea medication, as well as IV hydration fluids. This evening she began eating again. One of the doctors told Paola that she could eat anything (meaning, anything the dietary department sends her). Paola misunderstood and thought that she could have ANYTHING. She asked her mom and brother to bring her a grilled cheese sandwich. Sorry Paola, for now it’s jello!

The biggest news is that Paola’s moving around. She sat in a chair 3.5 hours this morning, and she sat in the chair again another 2 hours while I was with her. She’s in bed now, but prior to that she walked around the room a little bit. She’s sitting up, getting out of bed, walking, and getting back into bed largely on her own power. She’s not at all wobbly – these motions hurt her, but she can do them. She’s also using the bedside toilet.

In addition to being in pain, Paola feels gross. It will be a while longer until she can take a real shower or bath. In the meantime, I gave her a sponge bath today, and I washed her hair. She also got to brush her teeth for the first time since before surgery, and she put her nose ring back in. So, all in all, it was a good day. If she has a good night tonight, she might be ready to start receiving visitors. I'll let you know. If you do plan to visit, please be aware that room for flowers, etc., is extremely limited. Thanks,
allie

So far, so good

So far today things have been much better than yesterday. Paola is off oxygen, and the doctor took the dressing off her abdominal incision. She's still in pain but is coherent and able to talk. She is able to get out of bed to use a bedside toilet. Our goal today is to walk.

Saturday, August 19, 2006

A day that ended better than it began

So, as I previously mentioned, Paola spent last night throwing up repeatedly. This, along with the resulting lack of sleep, left her feeling not too hot today. She was very drowsy the majority of the day. Sometime in the early afternoon, she felt nauseous again. This was a false alarm, but it left her troubled and unhappy.

The day had good news too. For one, Paola's off morphine. She is still on pain medications but only by request.

Most of the good news came after 4pm. She got out of bed (largely under her own power, same as yesterday) and sat in a chair for two hours. This is really important for many, many reasons, and it was very encouraging. She got back into bed largely under her own power as well. The unit was understaffed (a recurring issue) so no nurse was available to give Paola a sponge bath in the afternoon [she'd declined when offered one in the morning], so her mom and I gave her a sponge bath and Paola's mom "washed" Paola's hair. (The hospital has these cool hairnets that have shampoo inside of them. If a patient can't wash his/her hair, one of these hairnets can be pulled over the hair and the shampoo can be rubbed in via a massaging motion. Then, the hairnet is removed, the hair is towel dried and combed. Result: clean hair.)

Perhaps the best news of the day was that Paola's night nurse, Jack, (who she and her mom think is FANTASTIC) managed to locate a reclining chair. We've been asking for a cot or a reclining chair for days as Paola's mom has been spending the nights at the hospital in utter misery. Paola's mom's discomfort has been upsetting Paola so getting this chair was a really good thing for both of them.

I think that's all the news. Let's cross our fingers for an uneventful night so that both Paola and her mom can get some rest.

Bye,
allie

A rough night

Paola had a rough night last night due to vomiting. The doctors checked her stitches - nothing seems to have been harmed. She's sleeping now. The goal for the day is to get up into a chair again. If all goes well, the additional goal is maybe to start walking.

As you can probably guess, she still doesn't want visitors. Sorry for the bad news.

bye,
allie

Friday, August 18, 2006

A big day!

All,

Paola is continuing to improve. As of this evening, she still thinks she isn't ready for visits or phone calls, but there is lots of good news to report. First, Paola added chicken broth to her diet of jello and so-called "Italian desert" (i.e., slurpee). Secondly, and more importantly, she stood up today and was able to transfer into a chair. Getting into the chair was quite painful, but she did a very good job, and she stayed in the chair for at least 1.5 hours, maybe 2 hours. Then, she got back into bed with only moderate assistance. The doctors said she absolutely had to get up and sit in the chair today, so she met the goal. I think tomorrow's goal is to start walking again.

Only slightly less exciting was Paola's other big accomplishment of the day -- sleeping. While I was with her, Paola managed to get an hour of relatively undisturbed sleep, which she really needs. It's hard to sleep in a hospital - people come in and out of your room, your equipment beeps, the equipment from other rooms beeps, and your loving friends and family keep telling you to do things ("Take deep breaths") or asking you questions ("Do you want some water?"). Paola hadn't gotten much in the way of non-artifically induced sleep, so it was really good to see her take a nap.

That's the news here. As you can see, it was a big day. Tomorrow promises to be another one so stay tuned.

all charged up

Hello again,

I'm getting ready to head back to Paola's room post-lunch but am writing again because I forgot to inform everyone that the missing charger for Paola's cell phone turned up. As such, I have in my possession her cell phone, its charger, my cell phone, its charger, my laptop, and its charger. We're all charged up, so no worries about calling...

allie

nap time

Hi, nothing new to report, I just thought I'd hop online because I'm in the cafeteria having lunch. It's nap time for Paola. Everything is fine here.

bye,
allie

argh part 2

Ok, I finally got something to post! To expand on my previous update, Paola's been eating jello and drinking clear liquids since yesterday evening. She still has a fever, but the doctor I spoke with wasn't worried.

You are welcome to send non-edible items to her (Unit G2S, Stanford Hospital) or, if you like, you can drop small items off at the house and we can bring them to her when we come to the hospital.

That's the news, more later, assuming of course, that Stanford's shitty wireless internet lets me post...

allie

argh

I have written this update twice now, and the damned internet keeps cutting off before it gets posted...

Paola is still recovering. She is coherent and conversational, but in pain and sore. She still asks for no visitors. You are welcome to call me on her cell phone or mine, but she's not up for talking yet.

Posting this now before anything happens to it...
allie

Still recovering

Hello all,

This is Allie, here at the hospital. Paola is coherent and conversational, but still in pain and sore. Once again, she asks for no visitors. Feel free to call me on her cell phone or mine if you like, but she's not up for talking on the phone yet. Yesterday evening she was given permission to eat jello and to drink clear liquids, so she's been doing so. She still has a fever, but the doctor I spoke with is not worried.

You are welcome to send things to her (Unit G2S, Stanford Hospital). If you like, you can drop off cards or other small things at her house, and we can bring them to her when we come.

That's the news. More later.

Still recovering

Hello all,

This is Allie, here at the hospital. Paola is coherent and conversational, but still in pain and sore. Once again, she asks for no visitors. Feel free to call me on her cell phone or mine if you like, but she's not up for talking on the phone yet. Yesterday evening she was given permission to eat jello and to drink clear liquids, so she's been doing so. She still has a fever, but the doctor I spoke with is not worried.

You are welcome to send things to her (Unit G2S, Stanford Hospital). If you like, you can drop off cards or other small things at her house, and we can bring them to her when we come.

That's the news. More later.

Thursday, August 17, 2006

Brief posting

All,

I'm too tired to really write so just briefly (I'll post again tomorrow):

* Paola's doing well. She's still drowsy from the anesthesia, and she's in pain. To control the pain, she's taking lots of morphine. She has a fever, which none of her doctors find alarming or surprising. She's on a broad-spectrum antibiotic just to make sure that nothing is infected.

* Paola has requested that nobody call her or visit tomorrow. When she feels ready for visitors, I'll pass along the word.

* She got to see her mom and brother today. Her mom is spending the night tonight.

* Paola's seen her surgeons, and they are pleased with her recovery.

* Paola has been allowed to start taking clear liquids. She was very excited about this, as she'd been mighty thirsty.

More later (i.e.. tomorrow). Goodnight!
allie

Doing fine

All,

Sorry for the long delay in updating the blog. Paola is in pain but otherwise doing very well. Her mom is currently with her, and she is in a private room with nurses and machines monitoring her. She has requested people not try to contact her yet. As before, feel free to contact me (either on my phone or hers) but please beware that reception is not good.

Flowers are ok, though space in her room is limited. Her room number is GS201. She still can have nothing to eat or drink, so please no food-type stuff. We are hoping to start her on water this evening.

She's on high levels of morphine to make her more comfortable, and her throat is still sore but she's able to converse with her mom. She's still quite drowsy and will dose off during conversation. She's still working through the anesthesia -- after all, she had almost 19 hours of surgery.

The plastic surgeon stopped by to admire his handiwork and was pleased. From what her mom and I have seen, the new breasts look great! Michele (Paola's friend who has been AWESOME, deciphering medicalese, keeping us company, etc.) warns us all that once the swelling goes down, things will look different, but so far, so good.

That's the scoop. More once there is something new to pass on.

Allie

good news

All,

Paola is out of surgery. I saw her after an hour or so in the recovery room (so, a little after 3 AM). She was very groggy but knew who I was and asked about her family. Her throat hurt a lot, so talking was difficult. Also, the nurses told me that the pain medications they were going to give her would make her sleep.

The doctors told me that she was stable and had been throughout the whole surgery. The plastic surgeon assured me that the long time on anesthesia was not worrisome.

When I left the hospital (i.e., was told to go home), they still did not know what room she would be in tomorrow, so I have no landline contact information for her at this time. Even if I did, I would discourage calling her (except maybe later in the day/evening) because her throat will be so sore. Her cell phone is almost dead, so tomorrow I need to find the charger for it - it's not where I thought we put it. My cell phone is recharging now, and I'll have it with me tomorrow. We will likely be in a part of the building with bad reception again though. (For y'all who live here or who are affiliated with Stanford, I urge you to tell Stanford that their cell phone issue is unacceptable.) I will update this blog as more information emerges HOWEVER I am signing off completely at this time in order to get a few hours of sleep.
good night,
allie

never ending day

All,

I spoke with Paola's reconstructive surgeon around 12:45 AM. Everything is very good. She is still not out of surgery, but should be soonish.

Paola's mom and brother are in CA, but are at Paola's house, hopefully sleeping. Thank you Matt for getting them from the airport.

To those of you who are texting me, I'm so sorry but I don't know how to text. Furthermore -- except for when I run to the cafeteria to access the internet -- I've been moved to a new area of the hospital where my cell phone has absolutely no reception. Paola's phone has limited reception. Both are low on batteries.

In essence, Paola's doing well. She still needs to get out of surgery, spend an hour or so in the recovery room, and then move to the special unit. Nobody has been able to tell me yet when she'll be able to receive visitors. I have been unable to learn if there's a landline phone in the room. So please, have patience with me! I'll notify you as soon as I know things.

Thanks everyone for being so concerned.
allie

Wednesday, August 16, 2006

Sorry I'm not computer literate

All, sorry I messed up on my latest posting. I can't fix it, so it will have to stay as is for a while. Sorry...
allie

A very long day, part five

All,

The latest estimate is that Paola's surgery will not be over until midnight or later. I have been reassured that there is no problem and she is doing fine. I do not know what the delay is.

Allie

A very long day, part four

All,

The latest estimate is that Paola's surgery will not be over until midnight or later. I have been reassured that there is no problem and she is doing fine. I do not know what the delay is.

Allie

a very long day, part three

Dear all,

A surgical nurse just informed me that Paola's surgery should be over around 10 PM. I'll post at least once more tonight, once the surgery is completed.

Due to heavy call volume, my phone is almost dead. Unfortunately, I didn't think to bring a charger today. Thus, please call me on Paola's phone should you wish to contact me. Also, if you call, please take pity on me and tell me who you are. Please remember that I don't know a lot of you!

Thanks,
allie

A very long day, Part II

Hello all,

I spoke with Dr. Dirbas about 30 minutes ago. He says that Paola is doing well. The removal portion of the operation is complete. The reconstruction is ongoing and will be for quite a while longer.

Updates on other things:

* Paola's mother and brother are arriving in San Francisco tonight. Matt Lindner will take care of getting them.

* Post-surgery, post-recovery room, Paola will be in a special unit, which is kind of like an intensive care unit. This apparently is standard operating procedure, because they want to keep an eye on people who just had such extensive surgery.

*Both Paola's phone and mine have extremely bad reception in certain areas of the hospital. Please do not be upset if you call and the call is not answered. If you leave a message, I'll try to call you back as soon as I notice there's a new message.

* In this special unit, there will likely be restrictions on number of visitors, visiting hours, etc. As soon as I find out, I will let you know.

* Pre-surgery, Paola was told that she was going to feel bad post-surgery. She may not want visitors right away. Furthermore, because she is on a breathing tube during the operation, she was told that her throat was going to be painful after surgery. This may lead her to not want to talk on the phone right away. I know everyone wants to get in touch with Paola, and as soon as I hear from her or from her doctors that she ready to have visitors or talk on the phone, I promise I'll let you know. Given the cell phone situation, I'll also try to find out if there's a landline she can get calls on (in the special unit, she may not have a room). I'll pass any information I have on as soon as I can, and, if you need more, you can try to reach me on my cell phone or on Paola's. In the meantime, I strongly discourage anyone from trying to visit or call her tonight or tomorrow morning, at very least.

Thanks to everyone who's called today, offering help in so many ways. I really appreciate it and your support for Paola.

A very long day

** Disclaimer - Paola's in surgery now. I have no news to report; the following is just a recounting of the morning's events. I'll update the blog as soon as I have news. Allie **


The alarm clocks went off at 4:20 AM. We both turned off our alarm clocks; however, it quickly became apparent that Paola had gone back to sleep. I was reluctant to wake her -- after all, today didn't promise to be fun -- but we had to be at the hospital at 5:30 AM. Attempting to wake her gently, I stood in her doorway and called her name repeatedly, but my attempts were useless. In fact, as if to drown me out, Paola began snoring loudly. I had to shake her awake. As she stared at me sleepily, I reminded her that we needed to go to the hospital and she couldn't drink anything.

Yesterday, Paola's breast was injected with a radioactive dye that allowed the technician to take images of her nearby lymph nodes. Bearing these images, her medical proxy forms and lots of other random stuff, we headed out the door at 5:00 AM. I drove, and Paola navigated while simultaneously talking on the phone with her family, then Google folk in Dublin, and then some office that officially placed her on disability. We got to the hospital a few minutes before 5:30. Unable to find the parking lot where we'd been instructed to park, we raced around campus, parking in a different garage. We got to where we were supposed to be only a few minutes late. Paola checked in and then took another call while I passed the time with the only magazine in sight - Ladies' Home Journal. The cover story sang the praises of plaid wool.

After a short wait, a nurse called Paola's name, and she took Paola away. A few minutes later, she got me and took me to Paola. Paola was reclining on a hospital gurney dressed in the normal (inadequate) hospital gown, but she had on little socks to keep her feet warm, and the nurses tucked blankets around her. A whir of medical personnel came and went, asking questions, the most common of which was if she had any allergies.

An anesthesiology resident introduced himself to us and set about asking even more questions, including, yes, if Paola had any allergies. A nurse stopped by, asked which breast was being operated upon, and upon hearing "both" wrote in marker on each of Paola's breasts the word "Yes." Around this point, Paola's friend Michele, who works at Stanford, showed up. The anesthesiology resident started an IV in Paola's left arm. She didn't enjoy this experience at all, especially given the size of the needle.

Paola's cubicle quickly filled to capacity with me, Michele, the anesthesiology resident, a plastic surgery resident, a general medicine resident, and two other individuals, who I think were chief residents. These last two were women, which pleased Paola, who was very happy that there would be females with her in the operating room.

In the midst of this, Paola's plastic surgeon showed up. Some of the people stepped out the cubicle, and Paola disrobed. The surgeon took some photos of her breasts. (Michele said this was for the before and after pictures.) Then, it was the surgeon's turn to write on Paola. The material that will make up Paola's reconstructed breasts is coming from her abdomen, so he spent a while there. First, he made a dot on either end of her pelvis, near the hipbones. Then, he drew a curving lines from one dot to the other, under her tummy. As a result, Paola had a smile across her body. Then, he drew a straighter line connecting the dots, turning the smile into an open mouth. At this point, his artistic renderings became far more abstract - vertical lines, horizontal lines, etc. Paola knew what I was thinking and teased me about not being able to take a photo and post it to this blog. (She said that I could "paint the picture with words," and that's what I'm attempting to do.)

Once the surgeon was through (and had photographed his handiwork), I put Paola's gown back on her, we hugged, and she got on the gurney. I took a photo, which I'll post, once I figure out how to do so. The anesthesiology resident gave Paola some drug - my guess was an anti-anxiety something or another. Paola stated that she wasn't scared and expressed surprise at how calm she felt. And that was it! Paola and her entourage headed down the hall toward the operating room.

After Paola's departure, Michele kindly guided me to the cafeteria and gave me a quick tour of the hospital before returning me to the waiting room. Around 8:30 I approached the desk and asked the nurse when she thought I might hear from Paola's cancer surgeon. (The surgery is being performed in two parts - the removal, then, following a break, the reconstruction.) As of that time, the surgery had not yet begun. She estimated that the surgeon might be ready to speak with me around 12:30 PM. It's only 10:20 AM now but my laptop battery is low so I'll end this post and go back to the waiting room. I'll write again once I have something to report.

The night before surgery

Hello all, this is Allie making her debut on this blog. As I type, Paola is showering, hopefully savoring the experience, as we fear she may be limited to sponge baths for the next few days. Following the hospital's instructions, Paola has removed her jewelry and her nail polish.

Tomorrow we have to be at the hospital at 5:30 AM. At this moment it's a little past midnight, so you can see that we aren't getting much sleep tonight. Paola and I had a wonderful dinner (Thai) with one of her friends, Emily. It's been a busy day, full of errands and medical appointments and attempting to prepare for the next few days. Paola was pleased to find post-it notes with the pink ribbon (breast cancer awareness) logo on them at Office Depot. She stocked up!

Paola's phone has been ringing off the hook all day with well-wishers. (Or, I should say, people have been calling, but due to cell phone ghosties, the phone hasn't been ringing, so Paola kept finding new voicemails...) Her friend Grant dropped off a lovely and thoughtful gift. She's looking forward to hearing from everyone (and seeing those who are in the area) while in the hospital, although it's likely she won't be up for visitors tomorrow.

Paola's out of the shower, and she reports that she did enjoy it. Off to take a shower and head to bed as morning will arrive far too soon...

Following is Paola's email to friends and family on the eve of the operation:

Dearest all,

I apologize in advance as many of you already know much of this information. Still, I wanted to take one final pass at my ENTIRE contact list to assure that everyone's up to date. I should mention that this email is going to folks living all across the US and CANADA (go Camel!), the Middle East, Europe and South America. Between all of you, there are over 10 languages spoken and about that number of nationalities represented. Finally, you all rival the UN in your ethnic, racial, and religious diversity. How cool is that?

As I prepare for surgery in a few hours, I wanted to share with you all that I am single-mindedly dedicated to beating the *#&$*%*^ out of this cancer so I may resume my life as an all around kick-ass girl, triathlete and Googler. I have heard your fighting words, felt your supportive embraces, and continue to bask in your collective love; and though I know the road ahead is tough, I am tougher! Cancer ain't seen nothing yet!

If you have been keeping up with paolablog.blogspot.com, then you know that the surgery is scheduled for Wednesday 16 August, 7:30 am - 5:30 pm PST @ Stanford Hospital, in Palo Alto, California. Allie will do her best to blog something tomorrow telling you all how things went. Googlers and TNTers--you have your points of contacts to find out more details. If you are outside of these networks, the blog will be your best bet, but please know that *I* won't be able to type for at least on week--potentially much longer--and Allie will have limited access as she'll be by my side at the hospital. You may also call the following numbers directly (corrected from previous email) where they'll be able to tell you whether I am out of surgery or not. Unfortunately, that's the extent of what they can reveal due to U.S. patient privacy laws.

Stanford Hospital Ambulatory Surgery Center
Before 7pm: 650-498-4835
After 7 pm: 650-723-5163

I leave you tonight with the knowledge that I am most definitely loved, and the promise that I will put up the fight of my life starting tomorrow in that OR. I know that you will all be there with me along the way in my long recovery. So let's keep marching, together, and learn about ourselves and each other through this journey. Thanks for everything so far and see you on the other side of the anesthesia.

Lots of love,
Paola

Sunday, August 13, 2006

To Boob or Not Two Boobs

I have been thinking a lot about breasts lately. Ok, I know this doesn't distinguish me from guys, but I bet they never actually stop to ponder what these appendages actually represent. The truth is breasts have taken on much more than their mammary function, they represent femininity, sensuality, womanhood, and even sexuality. Breast are short hand for woman and everything that we are supposed to be--mother, lover, wet-dream, nourishment, tenderness, sustenance, life-giver, nurse. No wonder the "girls" fell ill under the pressure of their own iconography.

I must confess I had never had mixed feelings about my breasts until one fell ill with cancer. I had always been perfectly happy with them, though they have never actually defined me in any way--except perhaps as a Victory Secret junky. But when faced with a life or death decision, could I live without one? Either? Neither? One thing was clear: given the size of the tumor the left breast has to be removed in its entirety. What of the right one then? What's really at stake...just breasts or something deeper? How much of myself is wrapped in "the girls"?

Like the consummate pragmatists I went to the data first. For most things, with the exception of wisdom, youth is generally on your side. When it comes to cancer, however, youth is your undoing--it gives the cancer strength to reproduce and ample time to invade. The medical literature places a "normal" woman's chance of recurrence post-treatment at 0.5-1% change per year of life (as calculated according to approximate life expectancy). Ok, so what does all this mumbo-jumbo mean? Essentially that I have a 30-40% chance of cancer in the right breast (over the course of my life) should I decide to keep it. This, of course, is doubled if you are a BRCA 1 or BRCA 2 carrier. So depending on the genetics I have anywhere between 30% (best case) to 80% chance of a second cancer. I decided I'd wait for the genetic test results to make the final decision.

However, data only paints some of the picture. What about the possibility of breast feeding a future child? How comfortable am I with losing key erogenous zones? What are the physiological effects on my body and recovery? Never mind physical scars, how about emotional ones? What about my body image as a young single woman? Most importantly, what would allow me to sleep at night and prolong my peace of mind...in the loooong run? It seemed that most everyone around me was mostly focused on the very short term. But since I am not planning on dying young, I wanted to look well into the future and weight my options to make this impossible decision. As I worked through these scenarios and talked to survivors and doctors I started formulating my bottom line.

My friend Lisa helped solidify my initial thought that though being able to breast feed would be great, I'd first have to be ALIVE in order to give birth...so really, nursing was a minor detail at that point. Lisa also shared the less glamorous aspects of her experience. Given that, and the fact that generations of children have been successfully raised on formula, I eliminated this as a concern.

Now, what about intimacy? Many of the survivors I have been lucky to meet were graceful enough to open up about their post-mastectomy sex lives. In the immortal words of Joni Mitchell "you don't know what you got 'till it's gone;" thankfully these couples, who are living on borrowed time, have mostly strengthened their physical and emotional bond--reconstructed, implant or no breast...the fact that she's there at all is a gift in itself. The mere thread of losing a partner, then, is enough to appreciate her as a whole woman, rather than a sum of her parts. This set my mind at ease and gave me much insight into the kind of partner I hope to have once this ordeal is over. I know in my heart that this too will be my experience.

And so we come to the question of body image...every young woman's perennial torturer. It's hard enough negotiating a pudgy figure with the ultra-slender, curve-less, flat-stomached, toned, overly siliconed and botoxed ideal. Now I have to also figure out how to be a single girl with reconstructed breast? Isn't cancer torture enough? In truth, for its good parts and bad parts I have never really fully appreciated my body. I got my first wake up call when I blew out my knee and couldn't exercise for nearly a year. After a painful recovery I vowed never to spend another sunny Sunday laying on the coach. So I joined a triathlon team and learned to swim, bike, and run.

Now I realize how silly I have been--and how silly I am being to even add "body image" to my one boob/two boobs decision matrix. Any time that this body--whatever its shape--allows me to remain on the planet will be a gift, and one I will take full advantage of. I know mom is scared that no boy will want me after a radical double mastectomy/reconstruction. But if that is all they care about, then really, I am better off without them. So I am currently a recovering self-hater, and each day, though I am scared of the surgery's outcome, I tell my inner teenager, that whatever the result, I will be ALIVE--and THAT is my bottom line.

Once I came to this conclusion the genetic tests weren't back yet. There's a huge difference between 30% and 80%. Then I thought, 10 years ago women didn't have the luxury to find out their BRCA status; what if I take stock of my options and ignore genetics for a bit? How comfortable am I, truly, with a 30%-40% chance of cancer later on? What if 10 years from now they realize that while I wasn't a BRCA carrier there is some other mutant gene that only affects Miami-raised-half-Colombian-half-Cuban-brown-eyed girls? What then? Ok, so that's silly, but so is banking entirely on a single test. Truthfully, I realized that any chance of this happening again was far too high (and far too high a price to pay) to keep a breast. And so, I signed over the girls to the scalpel and medical research, and have decided to have both breasts removed and reconstructed. New boobs and a new lease on life...now it's up to me to learn to love my new body.

PS: The genetic tests came back yesterday and I am NEGATIVE. Still, I am peaceful with my decision.

PPS: I decide to have a good-bye party for my boobs. Here are some pictures!






I cook Cuban food for everyone--but they have to help if they want to eat!







Everyone gathers before eating to hear me officially say good-bye to the ladies. Many boys offer to give the twins a proper good-bye, others demand that the girls make a personal appearance. With all decorum and solemnity I tell them to go to hell.







And finally, we eat a boob-shaped cake to drown our sorrow in luscious sugary goodness.

Saturday, August 12, 2006

Scheduling a Surgery: Almost as Fun as the Spanish Inquisition!

So, remember how helpful the Stanford Cancer Center folks were when I tried to book a second opinion consult with Dr. Dirbas? Well, that same commitment to complete incompetence delayed my surgery by a couple of weeks and nearly derailed the whole process. It went something like this:

> Thursday 27 Jul: I meet with Dr. Gurtner, agree that we are going to perform a DIEP flap, possibly bilateral--but will wait for genetic testing to come back to make final decision. I immediately follow up with Gurtner's surgery scheduler who'll get in touch with Dirba's scheduler to see if we can have the surgery the week of August 7. Oh, they have to find an OR for 10 hrs too.

> Friday 28 Jul - Wednesday 2 Aug: I call and leave many messages for Dr. Dirbas and Dr. Gurtner's scheduling staff. I finally get a call back from Dr. Dirbas' office; apparently the same woman with whom I had my little "second opinion" conversation is on the case. Really? Exasperation + Sigh... After multiple phone calls I manage to convince her that I am NOT having a TRAM FLAP and that most likely both breasts will be reconstructed. She finally confirms that the surgeons have been scheduled for Friday the 18th and it's just a matter of getting the OR. I may not know for sure until the day before the surgery. GREAT!

> Thursday 3 Aug - Monday 7 Aug: Still non-committal answers about the actual final schedule, but I am assured that surgeons are confirmed and an OR will be found. Mom, Allie and Raff take the plunge and buy airplane tickets. Still no final date though.

> Wednesday 9 Aug: Hmmm...funny how I don't have pre-op appointments with either surgeon and I'm supposed to be in the OR next week. Don't they have to run tests? Don't I have to sign consents? I get on the phone. Dirbas' scheduler, who still isn't sure what the procedure will be despite me having told her repeatedly: *B I L A T E R A L* *D I E P* *F L A P*, finally confesses that there might be a problem. WHAT?!?!? Tickets have been bought, plans have been made...are you serious?

I call Gurtner scheduler. Turns out Gurtner was NEVER actually scheduled for the surgery and he is going on vacation on Friday the 18th. Gurtner scheduler actually HANDLES the situation, figures out what's happening, and gets me in for pre-op appointments (which Dirbas' staff refused to do without a "solid" date). I guess they were waiting for the Cancer Fairy to materialize herself, schedule the plastic surgeon and find an OR.

> Thursday 10 Aug: Gurtner walks into the pre-op appointment and apologizes for the situation. He had been looking for me on the schedule and was so surprised my surgery date wasn't set, he figured I'd gone with another surgeon. Meanwhile --I tell him--I thought he already had me booked. "What?" Exactly. He is very gracious and confesses he is new to Stanford and now that he understand the system's limitation he's going to work on it. "That is fabulous," I say, and I mean it honestly; "but what do we do about MY surgery?" "Well," he replies, "we move all small, non-urgent cases from Wednesday to Friday, and we operate you on Wednesday the 16th. I already took care of it." WOW! The SURGEON fixed the schedule!!!! That's unheard of, and really awesome. Had it not been for his intervention, I'd have to find another surgeon or wait an extra 3 weeks. Meanwhile, the tumor is nearly 6 cm now and encroaching on the axila (that's the armpit for non-medical personnel). Dr. Gurtner is my hero :)

To be fair, Dr. Dirbas was also apologetic and very irritated with the situation. I tried to politely tell him how incredibly useless his staff is, but really, I had to be diplomatic. He did follow up with some specific questions, and I was as frank as I possibly could without telling him outright that the stethoscope he was holding is probably smarter and far more capable than his current scheduler. I also couldn't tell him that she doesn't actually understand spoken language, that she doesn't listen to patients and that she lied to me. But I *DID* share the second opinion conversation--in broad strokes--and warned that had it not been for my absolute resolve to have him as my surgeon, I wouldn't have been seen in his clinic, at all, EVER. I finally did mention that this reflected poorly on him professionally, and though I didn't hold him personally responsible, it was a major problem. He never got defensive, but looked a bit troubled.

The most important thing, however, is that the surgery is finally set: Wednesday 16 August, 7:30 am PST, Stanford Hospital. My mom is still working on changing her ticket to arrive before the surgery, Allie gets here on the 14th and Raff most likely on the 16th. Sigh... and on we march.

Wednesday, August 02, 2006

Allie-b, and other stories of heroic friendship

There are things you can't wait for others to know: your child took her first steps or said his first word, you've just gotten the transfer to the Fiji office, you've experienced excellent customer service at the DMV, or even more amazingly, you've just been told "I love you" and this time it's real. Sadly, finding the right time to tell your friends that you have breast cancer ranks somewhere between a triple root canal without anesthesia and pulling out your own toe nails with hot pliers. If I could schedule this, it'd go under NEVER.

But part of being strong is surrendering yourself to others when you need support. And though I had been stoic about the diagnosis and clinical in my approach, I started feeling the weight of my disease. So I compiled a contact list and went to it.

The first time I blurted out the words "I have breast cancer" I was standing in the middle of a parking lot listening to the steady flow of cars on the highway behind us, and a noisy group of teenagers three cars down. Next was a restaurant, then my car, a conference room, the gardens outside my office building, a street in the middle of the Inner Sunset, a softball field, various doctors' offices, an elementary school parking lot near my house, a cafe, the Target parking lot, my kitchen and my couch (and others I am sure I'm forgetting).

This had essentially become my personal cancer announcement tour of the Bay Area. Scenic vistas--did I mention the bank's parking lot?--private conversations shared in public spaces, shock, sighs, tears and some laughter...but mostly sorrow and disbelief followed by fighting words and love, sheer love. I gave into it, and took it all in--call by call, email after email, one conversation followed by hugs after the next. I must confess I didn't realize just how loved I am. And I wondered why that is. Why don't we tell these things to each other more often? Why does it take a deadly diagnosis to verbalize our feelings? There is no perfect time, just life and it's so easy to underestimate its speed.

It's hard to single out any one of these conversations, as they have all been joyous and painful in their own way; but I'd like to share Allie's response as an example of the caliber of friends who've become my extended family--and on whose shoulders I'll be carried to remission.

The first time I met Allie she was hurriedly carrying boxes up three flights of stairs to her room in Long Portal, Brown College UVA. It was September and naturally it was 100 million degrees with 110% humidity in Charlottesville just for move-in day. She was a spirited 3rd year (that means junior for all you non-wahoos), in charge of pretty much everything as far as I could tell.

We became fast friends after we discovered a mutual love for Annie DiFranco--which she played non-stop for approximately a WHOLE year--wine, and wacky outings like the time we dressed up as ninjas, crashed a party to sing happy birthday to some girl, and then almost got arrested at the 7-11 when we came through the door totting fake guns and face paint. Allie's also been witness to the total annihilation of a manual transmission--the thing literally fell out of the car--and Ganesha drinking milk. (Look, I couldn't make this stuff up even if I tried.)

To complete the picture I should mention that Allie has two master degrees, is currently pursuing a doctorate, spent two years in Africa for the Peace Corp, has an amazing sense of humor, loves cheese quesadillas, and basically lives on Coca-Cola Classic, bagels and pizza. She also started going out with her now husband at a party I threw :)

But enough background. I had tried to contact Allie for a week and after a couple of messages she wrote an email from Montana telling me she was on vacation. She could tell something was up, but I didn't want to ruin her cross-country traverse so I filled her in on my Dublin trip and convinced her there was no emergency, though I did ask her to call me when she got back to NYC. We played phone tag for a bit, and after a couple more messages Allie knew something was definitely up--after all, I NEVER call her at 9 am on a Saturday (my time).

I was hopelessly lost in the Inner Sunset when I looked down at the phone and saw Allie's name flash on the screen. Crap! I have to take this. I pulled over in the next street, parked the car in a red zone, and actually engaged in conversation after feeling for my phone under the seat where it fell after a sharp turn. Allie was thankfully still on the line. After I caught my breath, I laid the news on her...no preamble, I think I didn't even ask about her trip.

In true Allie fashion, she immediately went into emergency mode, asked key questions to assess the situation, offered me her (and her husband's) life savings, and wanted to get on the next plane to SFO. God I love that woman! Most importantly, she agreed to be my medical proxy and execute my medical wishes should something go wrong. I wasn't shocked. This was Allie, in her truest form...the same kick-ass girl I'd met in my dorm over 10 years earlier. I know she immediately got on the computer and pulled every last article, study, pamphlet, and footnote about California laws, my type of cancer and its treatment protocol.

And so the announcements went, each response amazing in its own way--especially from my inner circle. From flowers to cards, hugs, offers to shave their head and sperm donations for the necessary pre-chemotherapy embryo harvesting. What else could a girl ask for?