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Monday, September 28, 2009

Blog 22: And Yet MORE Hospital FUN!!!

Work, training, and daily life consumed my world for the next month. Nothing notable happened until Monday, August 10th when something seemingly benign started to change my life like a thread beginning to fray. I had no idea what was in store for me.

As I was sitting in my office, typing away on my decrepit computer and tackling various patient, staff, and vendor issues, I started to contemplate the evil building maintenance establishment which was seemingly out to kill me. The temperature was in direct contrast to my own personal thermo-regulatory demands regarding the air conditioning. I am cold-blooded and rarely, RARELY hot. In fact, I’m THAT annoying girl wearing the sweater and coat while asking the restaurant server (or shelf stocker or what have you) to turn up the heat on a beautiful, balmy fall day. I’m the girlfriend--once upon a time, anyway--who would forget her coat and eventually confiscate her date’s jacket (or use it as an excuse to snuggle). I’m the girl who can’t enjoy the movie in the theater because the theater managers obviously use the space to pack meat during off-hours. So, as I was feverishly fanning myself and wiping the glow from my face, I joked with the head nurse and one of the physician owners that I was having another one of my frequent hot flashes. And when I say "another one" I am referring to the likes of standing in the freezer with the door open at the grocery store, having friends fan me when I would suddenly become overwhelmed with drenching sweat, and changing out of my sticky pajamas in the middle of the night. Both told me that it was pretty darn cold considering that the air conditioning was cranked down to 40 degrees (in the tradition of medical office buildings the world over). In fact, Dr. Edwards illustrated by tugging on his lab coat proclaiming, “It’s actually quite cool in here.”  This struck me as totally bizarre and was the first time that I began to consider other symptoms I was trying my best to ignore. At lunch, I approached Dr. Baquero, the young, fun, markedly down-to-earth woman doc who tends to counsel and help some of the other staff members. Upon explaining my current situation, she ran through a host of symptoms. Hot flashes? Check. Weight gain and/or failure to lose weight while exercising daily? Check. Lack of regular period even 6 months after chemo? Check. Anxiety and/or Depression? Check check. Insomnia? Check. She told me that I need to have my hormones evaluated and I left a message for the CCCST nurses to pass along to Dr. Wilks. It went something like this: “Just thought I’d mention that one of the doctors I work for THINKS I might have some hormone problems based on my symptoms….probably  not a big deal but just thought I’d let my awesome medical team be the judge. Thanks!”   

Later that night, I saw that I had missed a call from the clinic. The VM went a little something like this: “Sarah, it’s Dr. Wilks. I worry a lot about hormone deficiency syndrome and this definitely warrants a visit to see me. Please call and schedule an appointment ASAP.”

I googled hormone deficiency and soon after became deeply saddened. I did not sleep that night (which was nothing out of the ordinary, actually) convinced that I was Sterile. Barren. Infertile. Not a Woman. I turned to wine to help me make sense of this and went to bed feeling so, so, so, so sorry for myself. I think I may have even cried a little. The next day –at work--I set my Facebook status to read that drinking one’s sorrows away is never a good idea as I had gotten NOTHING accomplished, felt terrible, and had compromised my work integrity by nursing a hangover all day. I took a long lunch to run errands, during which I was able to make an appointment with Dr. Wilks for Thursday. At least something was in the works, even though my road to spinsterhood was being paved before my eyes and, as we all have come to realize at some point in our lives, KNOWING is better than not knowing. I slept well that night.

On Wednesday, August 12th I attended a TNT Recommitment ceremony and gave a speech about my cancer story. Since becoming involved with TNT I am asked nearly daily to describe my initial symptoms, how I was diagnosed, and what treatment was like. This was a great forum to explain all of that while celebrating with the “hardcores” (those who weren’t scared off in the first half of training) our dedication to the cause. The energy and loyalty was contagious and, despite my blues, was once again infected--pun intended--with fervent determination. I was ready for Saturday’s 6 miles!!!

I saw Dr. Wilks the next day to discuss my symptoms. She agreed that a complete hormone panel was necessary in moving forward but also decided to move my 6-month CT-scan from September 11th (my infamous diagnosis anniversary) to August 17th “in case this is a Hodgkins thing.” By that point I was convinced that I was unable to have children but then, in the recesses of my mind, started to worry that it was, instead, a relapse. I told her how grateful I was to her and that I loved her. We hugged and, yes, I was a little farklempt. On the way home, I called Mom. She became audibly anxious but I convinced her that I was FIIIIIINE. I was not in danger of a relapse and Wilksie was just being hyper-vigilant because she just loves me so. Still, Mom insisted on being there for my follow-up visit and I defiantly said NO. I was going to be OKAY and did not need her to waste the gas and her time to hear something that I could convey on the phone. We continued arguing back and forth until we agreed to disagree: She said the issue was not closed and we would reconvene once I’m most certainly agreeable after a few glasses of wine. Therefore, she told me, she would be calling later in the evening to settle the details. Next time I’m accused of being stubborn, please remind me that I am my Mother’s daughter.

Despite my not eating anything questionable or imbibing in anything alcoholic, I woke up on Friday feeling the desperate need to run to the toilet, dry heaving the entire way. When the feeling passed, I made it to work without incident, but almost instantly felt the overwhelming wave of nausea once I arrived, this time accompanied by shaking chills, dizziness, and body aches. I closed my office door and called Mom, telling her that I was undeniably sick but couldn’t let on to the office. I mean, let’s face facts: I have frequent doctor appointments, was out with a virus a few weeks ago, and am forever the “cancer patient” no matter my official work title.  Mom heard the weakness in my voice and insisted that I tell someone: It was clear that I’m not well and could only do so much work before throwing up and/or passing out.  As she was walking by, the charge nurse stopped to inquire about my appointment with Dr. Wilks but quickly realized how sick I was. She left me alone but soon beckoned me to the other side of the clinic: She had set up a vacant exam room for me with pillow, blanket, “do not disturb” sign, and plastic bag of peppermints (who knew they were good for nausea?). After about 2 hours of desperately attempting to sleep despite the patients, doctors, nurses, and nuclear medicine tech doing their jobs in the surrounding exam rooms, the head nurse came in. “Your Mom is on the phone. She’s been calling and she’s really worried.” I had her bring my cell phone to me and I called her while still huddled in my little manmade cocoon. Even as the phone rang, the pictures danced on the wall and my stomach tumbled. I realize now that they didn’t send me home precisely because they knew I couldn’t drive. After a few minutes on the phone, despite the fact that she had planned an all-day offshore fishing trip with Gary and friends, Mom persisted that she was coming to see me. I was emphatic: “Mother! I don’t have cancer anymore. I’m just a regular person with an illness. You would NEVER have been this insistent before. What’s the deal?”

            She paused for a moment and then quietly said, “Things are different now.”

            I convinced her that she was being paranoid and returned to my office. About 5 semi-lucid e-mail replies later to various vendors, Dr. Edwards and the nurse came into my office, closed my door, and grilled me.

            “I think you have the flu and I wouldn’t be surprised if it’s H1N1—which is swine flu--based on your symptoms and the time of year,” Dr. Edwards said. He quickly called in a prescription for Tamiflu and sent me home. I want to say that I LITERALLY slept all weekend, but that is a huge grammatical pet peeve of mine. Literal means literal. I did wake up a few times between noon on Friday, August 14th and 6:00 a.m. on Monday, August 17th. Still, as literal as I can get while figuratively speaking, I slept a LOT. All the while, Mom would call and beg for permission to come. If she couldn’t be there for me while sick with the infamous, media-hysterical swine flu, she wanted to be there for me during my follow-up oncology appointment. I told her—YET AGAIN--that the news would be good and she didn’t need to waste precious gas on something that would be conveyed by telephone. End of story.
The joys of Swine Flu.
            I was still pretty pathetic on Monday but had a morning CT scan that I was determined to make. If I was still in remission I needed to know; if I was relapsing it was IMPERATIVE that I know. I mean, of COURSE I wasn’t relapsing….of course. But…..still. It doesn’t hurt to know, right? And, I mean, there are always doubts…..

            I returned to work on Tuesday but left a voicemail for Dr. Wilks that I had likely just had Swine Flu but that, thanks to Tamiflu, I was getting over it (miracle drug!) but that perhaps she should take that into consideration when reading my blood counts and CT scan. I never thought I’d be freakish around CT scan time, but I admit it: I was definitely becoming paranoid. I had begun to think that every symptom was a symptom of cancer. In my core I KNEW it wasn’t back, but in my mind I couldn’t help but overanalyze…..  Still weary from the battle my body just fought, I decided to come in during the mornings but take the afternoons off to recuperate. Dr. Wilks called me back late on Tuesday afternoon while I was sleeping and, when I answered “hello?” she simply said, “STOP GETTING SICK!” I laughed and she said, “Can you feel the love? I’m insisting that you stay FAR AWAY FROM ME but I still love you dearly.”

            “I know you do,” I said. “This is why I love you.”

            “And you better not put this in your blog!” She said. (Yeah, sorry Dr. Wilks. I’m nothing if not a vigilant and honest blogger).

            “So you read it!!!!” I beamed.

            “Yes……AND I KNOW YOU CALL ME GENERAL WILKSIE!!!” Said General Wilksie, laughing.

            “It’s only because I love you and had to give you a nickname.” She pretended to be offended but we both know that it’s a HUGE compliment. I love my Wilksie. We agreed that I would keep my appointment for August 24th versus gracing the cancer clinic and its vulnerable patients with my germs. Of course, this completely abolished my TNT training plans of spwogging 6 miles. I felt deflated, defeated, and like a total loser. I’m not gonna lie when I say that I considered dropping out. I knew I wouldn’t but I still totally needed that extra encouragement.

On Sunday morning, August 23rd, I called Mom around 7:00 a.m. after a sleepless night. The abbreviated conversation basically stated that I did, in fact, need her here. I was terrified, even though I did not want to admit it and I cursed that weakness within me. I told Mom that I was scared that the Swine Flu symptoms were really those of cancer but that, in my heart, I knew I was fine. Logistically I had about a 5% chance of relapse (and everyone knows how I do so love graphs, charts, and statistics), but that I couldn’t shake the irrational fear. She told me that after she was fully awake she would call me back. At 9:00, showered and dressed, she informed me that she’d be here that evening. Have I said this before? She is my rock and I’d be nothing without her.

I went to work with full-time Practice Administrator capability on Monday morning but had to return home at lunch where my Mom was awaiting me for my 6-month appointment. I felt fine because I was certain that I was healthy yet, oddly, my blood pressure read 165/100 when the Medical Assistant took my vitals. Perhaps I was slightly concerned??? And yet, Wilksie said that my CT scan looked GREAT (“normal!”). While Mom gasped with utter relief and became teary-eyed, I continued to wring my hands as Dr. Wilks then left for a few moments to retrieve my blood results.

Upon entering the room and flipping through the report, she paused. She frowned. She commented something to the effect of: “Oooh, yeah. It’s just no wonder you’re not feeling well! Ummm okay, you’re not producing any hormones at all. Everything you’ve described is right in line with what I’m reading on this report. No estrogen, progesterone, testosterone….” I wanted to cry. I was both elated that my problems were acknowledged, and saddened that my female-ness had all but given up. “This is indicative of someone in full-blown menopause,” she said. I just nodded. I knew. She told me that she’s not comfortable handling hormone issues as that’s not her specialty and encouraged me to make an appointment with Dr. Gonzalez, the wonderful primary care provider who initially spotted the Lymphoma. As my regular doctor, Dr. G would be better equipped to take on the problem and has had success in treating patients post cancer. I was fortunate enough to have scheduled an annual exam months ago, and therefore had an appointment lined up for later in the week anyway. Knowing this, the ride home was astonishing: I felt that I was validated and on the way to recovery. Yet, my fears were heightened: Would I ever be able to have children? Without female hormones, am I really a woman? Who would want me now??? Of course, true to form, Mom spent the evening telling me that it would all be “figured out” now and that this was “good news.”

On Tuesday morning just before leaving for work, I saw my Mom in the kitchen as I was pouring a huge travel mug of coffee and she was going for her first cup of the day before returning home. She asked how I was doing and I laughed that I had a huge, bubbling blister on my ankle. I told her that I remember nicking it the previous night with a razor in the shower but I had never known a scratch to result in anything more than a minor irritation. I had applied Bacitracin and a band-aid and hoped for the best, limping (literally) to my car the whole time. All day Tuesday was fair game for staff fodder. Everyone had a right to ridicule the boss woman for hobbling around the large clinic due to a really nasty case of…a blister. I admit, I deserved it. Dr. Edwards switched my nickname from “Sir” to “Chester” (“Sir” because I was in command of the clinic and he is an extreme liberal who loves to tease me about being a girly-girl while sporting some serious work cojones, and “Chester” as an old Gunsmoke reference to a character who dragged one of his leg behind him). As my foot segued from generally painful to throbbing radiation up my calf, I approached Dr. Edwards and BEGGED him to take care of it for me. He insisted that I should leave it alone (after all, it did appear normal looking and the surrounding area was not hot to the touch) and commenced teasing me. I smiled weakly but cringed at the distress I was secretly in….something had to be done. That night, while painting my toenails, I sterilized a needle and tried to pop the offending blister. It wouldn’t give. I once again applied Bacitracin and a band-aid and went to bed. Attempting to sleep that night was just short of slow, torturous murder. 

I woke up on Wednesday morning with a magenta foot—hot to the touch—and the blister now raging and festering. The difference today, though, was that it was black. Yes, my blister had turned black. I almost vomited. After a shower, I applied a fresh Bacitracin-laced bandage and went to my appointment with Dr. Gonzalez, hobbling from home to the car, car to the office door. I was definitely a mess and in no shape to be vertical.

Back to the main issue at hand, Dr. Gonzalez looked at the labs that I had brought with me and gasped, “Oh dear. You’re not making any female hormones. Like…. at all. Even though they didn’t test all of your hormones, it looks like you’re not producing anything and I’d bet that you’re having trouble just doing daily tasks. Wait…….Oh. My. God…….Your B-12 is low.”

            “I know,” I said. “I’m on injections every month.”

            “No, your B-12 is 256 and needs to be at a minimum of 900-1000. This tells me that you have no immune system, probably feel depressed, and are at high risk for Alzheimer’s Disease in the future.” At this time, she rolled the stool toward me and put her hand on my knee. “This is serious. We need to get this up—and FAST.” I nodded absentmindedly while she insisted that I’ve likely been experiencing memory loss (check), loss of cognitive skills (check), lethargy (check) and anxiety/depression (check check). Dr. G prescribed an estrogen patch, Progesterone capsules, and DHEA. Meanwhile, I was sent home with a very official hormone-testing kit. I was tasked with collecting saliva four times a day in plastic vials and following various other strict rules. I am to send in my specimens using an official air-tight plastic bag wrapped in special plastic bubble-wrap and, a month later, we MIGHT have specific numbers on my hormone levels, at which time Dr. G will alter my prescriptions according to bio-identical typing. Thank god my insurance pays for it as it costs $700-$900 for lab interpretation. And yet, this was absolutely, positively necessary. Without hormones I am also at risk for all reproductive cancers, mental and emotional problems, infertility, among other problems…. Fab.

After she notated the obvious and gave me strict instructions, I showed Dr. Gonzalez my black heel and red foot and she immediately proclaimed that it was infected. No surprise there. In addition to the news that I was reproductively a 65 year old woman, I was also informed that my blister would be lanced and the fluid collected for a pathologist to examine. So sexy and SO what I needed…. GREAT start to a Wednesday. The lancing was actually done by her Medical Assistant as I lay on my stomach, ass in the air, feeling vulnerable to the world. Once again, I lost my dignity. On my way out, Dr. G handed me a box with the specimen tubes, instructions, and other paraphernalia. I went back to work feeling slightly more confident: At least today, despite the immense pain, I was treated and expected to get better armed with ammunition of the antibiotic Keflex, hormones, and self-assurance. World, I’m ready for a comeback. Or, in the words of LL Cool J circa 1991, Don’t call it a comeback, I’ve been here for years.

On Thursday, August 26th I hobbled into work over an hour late. Despite waking up at the usual time, I required the additional hour to get ready AND to walk Lola as I extended my left foot, swept my swollen right foot, and swiveled my hips. My triage nurses blatantly laughed at me (I feel the love) as I limped around the office. The head nurse arranged another makeshift footstool for me with a pillow placed atop a large trash can. Nothing helped and the pain intensified. I removed the Ace bandage, showed her the nastiness, and delighted in her gasp: My foot was disgusting: The stuff of horror films…possibly some sort of highly communicable necrotizing fasciitis. She instructed me to NEVER GET UP before lunch. Meanwhile, I was on the phone with the practice bank while Dr. Edwards arrived. He could not see the complex foot contraption under my desk and therefore walked away before I could indicate that I was on an important call (and I was) and to hang on. A few minutes later I paged his office, “Dr. Edwards, I usually don’t require my bosses to ‘come hither’ but can you come here please?” In 20 seconds he was opening my door and, like the nurse, audibly gasping.

            “You need to go to the hospital now. That’s bad…..really bad.”

            I nodded stupidly and told him that I’d call my doctor for an appointment.

            “No, you have to go now. We want you better and we don’t want to lose you. I’m calling next door so they know you’re coming.” I called Mom and told her that I was on my way back into the hospital (this time a Methodist facility connected to the office building); she was having her hair done and therefore told me that I’d have to wait my turn (I mean, it is a hair appointment). I love her even more for prioritizing her hair over me (“Sarah, I love you very much but you put these gray hairs on my head. My hair appointment comes first”). Yessss, my Mom rocks….. Not that she needs defending but, in her defense, we both thought I would be treated and out of there in a few hours.

            Mind you this is, arguably, the best endocrinologist in south Texas telling me to go straight to the hospital. Moments later, one of my triage nurses was wheeling me across the skyway to the Metropolitan Methodist Hospital. By then, Dr. Edwards had alerted the ER and they basically whisked me away with VIP status. By 10:30 a.m., Cutie Dr. Larson treated me with antibiotics and morphine. As he said, “I’d give it a 90% chance that it’s MRSA. It looks like MRSA, sounds like MRSA, and acts like MRSA. We’re treating it as MRSA,” MRSA being Methocillin-Resistant Staphylococcus Aureus, or a potentially deadly and very stubborn staph infection. After asking how they will determine it for sure, he told me that a fluid test would be the primary indicator. Since one was taken the day before in Dr. Gonzalez’s office, they were game for proceeding with extreme caution while awaiting the results. 

After two doses of morphine, my foot was still throbbing. When the nurse re-entered to deliver another dose, I asked her if she could first help me to the bathroom. Saline IV’s make me have to pee like a racehorse. She helped me to sit up, I swung my legs over the side of the bed, and then unintentionally cried out in pain. As I waited for the hot pokers to STOP SINGING MY DAMN LEG from ankle radiating to knee, I was shocked (literally—I felt temporarily paralyzed) to find that it only intensified. Tears sprung from my eyes as she helped me into the wheelchair. My foot, ankle, and lower calf were searing—as if being charbroiled. To this day, I still cannot adequately explain what I had experienced, but I know that I have never been in such despair….not even during cancer and the dreaded bone pain from white cell boosters. The nurse helped me into the bathroom and assisted me with lowering my pants and sitting on the toilet. Once again, tears streamed down my face and, once again, I cried out in agony. She left me alone until, from the other side of the door, she heard me wailing. Without hesitation, she opened the bathroom door to find me struggling with my pants. She helped me into the wheelchair, flushed the toilet, and assisted me back onto the bed. For another five minutes the ensuing pain was undeniable. I was in excruciating agony.

At his request, I called Dr. Edwards to update him. When he inquired about how I felt and I responded that the pain was unbearable he said, “I’ll be there in a few minutes.” “No, you don’t have to,” I slurred. “Nope, I’m coming,” he insisted. “I’m in the ER,” I said. “I know—I just spoke with them.” Within 20 minutes, he was pulling open the curtain and sitting at my bedside, instructing the nursing staff to give me “whatever pain medication she needs” and to treat me well. All the while, he was apologizing that he would be out of town over the weekend and not physically able to be here for me. Of course, he still verified that I have his cell phone number and was comfortable with me calling it any time. So grateful for the concern and attention, I embraced him before he left. I am blessed to have an amazing boss: Thank you, Dr. Edwards.

By noon I was transferred to a room in Oncology because, as they explained, I was still technically a cancer patient. Because neither Dr. Gonzalez nor Dr. Wilks admit to, or have privileges with, the Methodist system (Baptist all the way for them), a hospitalist named Dr. Randy Panther admitted me. Back in my room nurses Shad (yes, SHAD, like Chad with an S) and Tiffany gave me more morphine for the obvious pain (there is a cap on the amount of narcotics that can be given in the ER; once followed by a treating physician on a medical floor, the doctor can determine how much to give) and brought in a potty chair. Reminder: I had experienced the aforementioned dignity sapper last winter while hospitalized with pneumonia. When they inquired as to whether or not I’d use it, I said, “hell yeah,” and welcomed the easy route to relief. Thank you, handicapped toilets ;). And, just for effect, I offer you a new visual: By this time, when I lowered my foot from an elevated position, I instantly connected with one of my favorite shows. I own The Tudors seasons I and II on DVD and have frequently watched an episode during which the cook who was found guilty of poisoning some of King Henry VIII’s advisors was boiled alive in an “eye for an eye” attempt at punishment. As with my trip to the ER bathroom, my foot and lower calf felt as if it were being slowly lowered into a boiling cauldron….no joke. The pain was that immense.
That's my leg inside the cauldron.

By lunch time, and because I missed the nasty food cart, my TNT friend Amanda offered to bring Quizno’s to my Morphine-happy ass. She arrived at 12:30 and left at 2:00, during which time my new doctor visited. Dr. Miller, on-call for Dr. Panther, confirmed that we were dealing with MRSA and used a ballpoint pen to mark the red lines along my heel and calf. This, by the way, is a perfectly acceptable and standard form of indicating the lines of demarcation to determine whether or not the infection was spreading (ie: responding to treatment or not). After she finished her artwork, I asked her if this was a simple case of 24-hour observation since I was, in fact, talking, breathing, and conscious and, pain aside, mobile.

            “Uhhhh….no, no….you are really sick. You’ll definitely be here until Saturday, if not through the weekend. I know you feel okay with pain management but this is still very serious.”

            Yeah, so I’m on strong drugs I feel much better so allow me to digest this little tidbit….
Typical case of MRSA

            After Dr. Miller took her leave, I left a message for Dr. Wilks to call me back seeing as I was IN THE HOSPITAL and NEEDED HER. While Amanda and I were eating and chatting, my phone rang. It was Cancer Care Centers of South Texas and I took the chance that it was my hero.

            I answered: “Dr. Wilks…………………………WHYYYYY?????”

            “I don’t KNOW!” responded that familiar voice. We talked for a few minutes and she told me that she would ask her good friend to check in on me. Since Dr. Wilks doesn’t have privileges there (Metropolitan Methodist is nowhere near the CCCST), Dr. Dham would be stopping by and providing regular updates. Even though I would miss seeing her, I was comforted that she was putting me in the care of someone she fully trusted. She told me to hang in there and continue fighting. “I love you,” she said.

            “I love you too.”

            After hanging up, Amanda’s eyebrows furrowed. “Was that…ummm….your doctor?

            “Yes, yes it was,” I said defiantly, totally defensive of how much I cared for Dr. Wilks. Everyone can SUCK IT for being judgmental--the woman saved my life. A few hours later, long after Amanda left, another TNT friend named Tom arrived to keep me company. Because I was on 5 doses of Morphine, our conversation was cut short.

Only an hour later, Mom arrived from Rockport. Her glamorous “hairs did” and whatnot, in juxtaposition with my football-sized foot marked up with blue pen, made us quite the pair. Needless to say, she had no idea that, upon leaving my apartment the previous Tuesday with a sudden--albeit average--blister, she would be returning to me in the hospital on Thursday with MRSA. Oops. While still there, Dr. Edwards returned to my room. He and Mom finally met as I was draped in a lovely hospital gown, bejeweled with sexy tubes. Don’t hate me cuz you ain’t me. Moments after he left, the head nurse made an appearance. She and Mom exchanged stories about me as I lay there, confined to my bed and a victim of verbal abuse (“oh, and this one time you’ll never guess what she…..”).

Mama left that evening at 5:00 to take care of Lola. Moments later, my Triage Nurse from work, Regina, arrived and kept me company for about 30 minutes. I so appreciated her efforts and, between us, she is one of my very favorite staff members (out of 30). Thanks, Reggie, for making me laugh while held captive! Oh, and don’t let my watching King of the Hill taint your vision of me as SuperBoss. Ha.

Mom returned that evening to bring my toiletries after my FANTASTIC(-ally horrible) dinner of hospital roast beef, vegetables, cold roll, and iced tea. Though nasty as the food was, I will not complain. I will, however, require certain amenities. Even in the hospital I can only function on Cetaphil cleanser, Neutrogena moisturizer, toothbrush, toothpaste, floss, lip balm, deodorant, and hand cream for my cuticles. It may seem excessive but remember that said needs were reduced to a mere Glad freezer bag of items plus some underwear and previously-confiscated hospital scrubs (from Iowa) to sleep in.

That night, I met my 3rd shift nurse, Jack. He introduced himself by throwing open the door, standing in the entryway, and instructing me that it was TIME TO PROVIDE A BLOOD SAMPLE! After nearly a year of encountering oncology nursing, I’ve NEVER met someone so blunt and rude. Oncology nurses are, in fact, notorious for being wonderfully selfless and loving. Taken aback, I simply nodded and attempted to joke with him. Alas….Jack does not joke. Instead, he remained at a distance in the doorway (to prevent transfer of any remaining cancer germs I presume) and asked how I was feeling. Wait, no he didn’t: He asked if I was “okay,” and if I had “peed” that night.

            “Actually,” I said, “I’m itching a lot. A LOT.  I’ve had a few doses of morphine and some antibiotics, but the itching is actually becoming uncontrollable. I can’t help it…..seee?????” (I revealed to him my newly-scratched, self-brutalized arms). Jack told me that the Morphine is the most likely culprit and called Dr. Miller, who prescribed 25 mg of relief via Benadryl, although I still continued to itch like crazy. In fact, I resembled a dog with fleas. (Seriously, days later, Mama Jackie would imitate/ridicule me).

And yet, despite Benadryl, I was still itching on my scalp, neck, chest, belly, calves, and feet—even my infected, painful-to-the-touch foot—just two hours after my previous cocktail of Morphine and Benadryl. At hour three, Jack scored me an additional 25 mg of Benadryl, but warned me that I had met my max. NO MAS would be called in. According to Jack: Stick a fork in me…I was done.

At midnight, I dared to summon Murse (read: Male Nurse) Jack by way of call button. I was still itching and, by this time, in distress. In fact, I had managed to climb out of bed and limp into the bathroom (seriously against orders) to inspect my face. I had scratched it terribly and, upon returning to bed, found blood on my pillow, gown, and sheets. I had scratched myself to the point of bleeding: I had scratched myself silly. Upon entering the room, Jack acknowledged my obvious allergy and determined that this was “just part of it. You are clearly allergic to something,” he said. “I mean, I can call your doctor if you want, but she has only approved 50 mg of Benadryl. It really won’t matter.  Sorry.”

Rethinking what he just said, I responded without hesitation. “Yes, I want. I am bleeding all over the bed. It may mean nothing to you but please—AT LEAST—record it in my chart.” I pleaded. “I am miserable. I can’t stop myself from scratching my body, my face, and my scalp!” I said, pointing to the scratch marks on my cheeks for emphasis. Jack said that I was just “adding to the doctor’s schedule” and that my distress was, again, “just part of it.” He reminded me that I was not in a hotel; I was in a hospital. I explained to him that I didn’t expect miracles (or a mint on my pillow) but that I did expect him to address my medical issues…..I’m a mess and, as my nurse, he’s accountable.
It's REAL--the biology of morphine and its Pruritis side effect
            Two hours of itching misery later, I called the Nurse button again. Jack emerged, visibly pissed. “What do you need?” he asked (and, might I add, quite irritated).

            “I am seriously in pain. The itching is unavoidable and I don’t know what else to do. I do have an MHA and I do work in healthcare with nurses and I do understand how hard you work but I really can’t deal with it anymore!!!” I felt so vulnerable and so helpless.

            “Well,” he said, I can’t change anything about that.” I stared him down with my poison-dart-shooting eyes (and severely infected foot with toes pointing directly at him in an attempt to exterminate him with my nastiness) until he left. Shortly thereafter, I welcomed my new nurse Nicola.

“I hear you were having troubles with side effects,” said a cheerful British accent, “and I’ve already called Dr. Miller. After all,” she said, “It’s part of my job.” I later learned that she was the charge nurse. I proclaim now that I HEART NICOLA!!! I explained my issues, showed her my bloodied linens, and she secured an additional 25 mg dose of Benadryl for my itching, managing the impossible: 75 mg of Benadryl and regular Antibiotics = decent night sleep. She also switched my medication from Morphine to Dilaudid, after Dr. Miller assumed that the offending allergic reaction was to Morphine. That night, Nicola pushed Dilaudid into my central line for the first time. The effect was JUST as amazing as morphine; In fact, I made a conscious attempt to NOT react as the drug entered my system every four hours knowing that, if I seemed too satisfied, I could be accused of drug-seeking. I acted nonchalant…this was nothing….just some basic pain relief (aside from the incomprehensible sensation coursing through my circulatory system, reverberating in my muscles, and settling into bliss). Because Morphine and Dilaudid are friggin’ awesome, I will describe the effects: Imagine your whole body relaxing, going numb, and eventually tingling. This initial response only lasts a short time but the “floaty” effect lasts for at least an hour. After that, I am left with a space cadet sensation of pain relief and relaxation. Later, I found out that Dilaudid is the lesser-used drug because it is highly addictive. Can’t imagine… Needless to say, Nicola is now SuperNurse, with or without the UNBELIEVABLE drugs.

In the wee hours of the morning, as two other nurses were discussing how to treat my pain even though it was clearly between dosages, one suggested that they try Tylenol. The other asked if they still had some on the floor and the other responded, “I think so. We can get some down the hall though.”

            This is when my drug-induced dementia got the best of me.

            “We really do. I just had Regina bring some from the pharmacy last week. Go check at the triage desk.”

            Both nurses stopped what they were doing and stared blankly at me. “What?” It was at this point that I realized I was between two worlds. Normally, I’d have been horribly embarrassed but I was too stoned to care.

            “Oh nevermind.” I said. “Just do what you want. I don’t care.” That ended that. (Must stop thinking about work…)

On Friday morning, August 26th, I met Dr. Dham, the friend of General Wilksie whose CCCST clinic is in the Metropolitan Pavilion and who therefore has privileges with the Methodist Health System. What she said affected me tremendously. She told me that, unfortunately, this may be the way my life would proceed—like, forever. In fact, I may be at the mercy of Hodgkins Disease, which, even when treated, has a history of “chipping away” at one’s health. In other words: Don’t give up hope but don’t be surprised or dismayed if I get sick again, and again, and again, and again……. 

“I hope you’re not a frequent flyer,” she said earnestly.

After she left (and I actually found her to be lovely, funny, and sweet despite the unsavory projection), I took a few moments to reflect: This really could be my life. This really could be what I’m up against every flu season, every highly contagious case of strep throat, every minor virus, every routine cold, and every MRSA. This could be my life whether or not my cancer decides to try me again….this could be my eternal prognosis. Instead of being angry or saddened, I was surprisingly matter-of-fact and decided that no step was too minor to prevent the seemingly inevitable. I decided that I will eat according to the food pyramid, I will resume exercising (since stopping when I became too weak to continue), I will take doctor-recommended vitamins and supplements, I will wash my hands religiously, and I will use hand sanitizer. My pledge, from this point forward, is that if I do happen to get sick it will not be from lack of trying to stay healthy. Take note: If I get sick, it is not my fault.

Mid-morning, I received a bouquet from my Team in Training group. THANK YOU!!!

At lunch, Drs. Lee and Dons visited me from my clinic. My Mom and I were both overcome with emotion after they left as we acknowledged that they cared enough to visit me while I was still confined to the hospital. They are both so sweet and I felt validated in my career.

Later that day, Dr. Miller emerged once again. Because Dr. Gonzalez had taken a fluid sample, Dr. Miller called her while in my room to obtain the results. During the conversation, Dr. Miller threw me a ‘thumbs-up sign.’ Upon hanging up, she told me that the tests revealed NEGATIVE for MRSA and POSITIVE for STAPH. We all exhaled with relief and cheered that I was not, in fact, harboring a gross--sometimes deadly--flesh-eating bacterial infection. She decided that we would continue treating with various antibiotics until the infection responded. “I have to warn you, though,” she said. “This type of infection usually gets worse before it gets better. That’s why I think you’ll be here through the weekend. Once you get over the hump, we can talk about letting you go home.”

That evening, I slept on and off as nurses, aides, and other healthcare workers continuously woke me for vitals and bloodwork. On Saturday, September 27th, Drs. Miller and Dham came to my room at almost the same time. Both observed that my foot was getting NO BETTER and even indicated that my infection was progressing past the line of demarcation along the left-side right ankle. Swelling was increasing, redness was intensifying, and the pain was just as bad, if not worse. Dr. Miller said that this was NOT indicative of the get-worse-before-it-gets-better plan (indeed, it was worse than that) and arranged for an Infectious Disease specialist to treat me. Within minutes, she reported that Dr. Kim Moran would be visiting me soon. And yet, they suddenly realized that I had been treated by her on-call partner, Dr. Wood, who saved my life from succumbing to pneumonia only months before, and asked if I would be more comfortable seeing him. Since they all have my best interest at heart, I determined that Dr. Moran must be just as amazing. Mom commented that ALL of my doctors are females and proclaimed: “GIRL POWER!” Yesssss for Drs. Gonzalez, Wilks, Miller, and Moran!”  Later that evening, Dr. Moran assessed my ankle and determined that, despite the fact that a rudimentary test determined I had a Staph infection, my illness was not responding in kind. In fact, she said, it was, indeed, acting like MRSA. Combined with Dr. Larson’s assessment that it looked, felt, and acted like MRSA, Dr. Moran declared the test to be incorrect and confirmed that I did, in fact, have MRSA, a deadly disease. She put me on a hardcore antibiotic known for its compatibility with treating the infection and told me to hope for the best since the other six antibiotics were clearly not working.

By Sunday morning, September 28th, I was slightly better. The lesser-used (for its intensity and possible long-term side effects including hearing loss and renal problems) all-powerful Vancomycin proved to be helping and Dr. Miller realized that this positive reaction was proof of MRSA. She agreed to keep me on Vanco, Levaquin, Dilaudid, and Benadryl. Under the circumstances, Sunday was uneventful, albeit a tad more productive disease-wise, and Dr. Moran decided to test the waters. She would kill the Vancomycin IV altogether to test the Levaquin alone. In fact, if I could tolerate oral Levaquin and my foot still improved, she would feel assured that she was on the right track. The remainder of Sunday and all of Monday proved to be successful while solely on oral meds (Levaquin and Darvocet every four hours—at a VERY weak dosage I might add) and Dr. Moran recommended my discharge on Tuesday.

And, might I add, it had been nearly a week since I shaved. With multiple doctors coming in several times a day examining a sick fuzzy leg and comparing it to a healthy fuzzy leg, I was beyond self conscious. I begged for a razor but was ignored. I PLEADED for a razor but was shot down. Eventually, I just ever so sweetly demanded one but Dr. Moran agreed to only let me shave while a nurse was nearby and only if I promised to proceed with extreme caution. Every doctor I know has expressed how little they pay attention to body hair but I don't buy it. Like, at all. What I find most precious is the juxtoposition of massive growth of hair on my legs in sharp contrast to the patchy chick-fuzz on my head. And the razor they gave me? Yeah, it was the standard hospital issue cheap plastic medieval torture device. I later suspected that was the reason for the bedside anti-shaving campaign seeing as anyone could find themselves mistaken for a victim of a knife fight after using one. A person who landed in the hospital precisely for a catastrophic shaving nick, on the other hand, would behoove herself to wait until she gets home and can use her Gilette Venus with soothing aloe strips. It was worth it, though.

On Tuesday, most of the doctors and nurses were prepared for my release as I hobbled around my room gathering my take-home bag of toiletries and confiscated hospital items (plastic pitcher, emesis basin, etc. because you just never know and each costs like $100.00 in hospital pricing and I’ll be paying for the damn things). I waited all morning for Dr. Panther, my admitting physician (and therefore my discharge doc), to give the A-OK. My vitals were taken twice. My nasty lunch was delivered and my nasty lunch was eaten. Work calls were made. FINALLY, at 2:00 PM, Dr. Panther ordered my discharge and I was graced with five pages of paperwork. I was home by 2:30 and asleep in my bed by 3:00 while Mom retrieved my Levaquin Rx from Wal-Mart. I was elated to stretch out in my queen-sized feather bed, watching good trash TV and reading my book (irresistible wiener doggie at my side the entire time).  

And yet, still afflicted with hospital-grade narcotic-induced fatigue, I slept most of Wednesday and emerged that evening to open a bottle of wine at 4:30. Mom made BBQ pork and we enjoyed a homemade dinner after we had both mustered mass-produced hospital nastiness for nearly a week. On Thursday Mom followed me to work so that I could pick up my car that was still parked under the building in the physician lot (just a work perk of working for prominent docs). We went to my office so that Dr. Edwards could examine my newly shrunken (yet still curiously red) foot. While there, I checked e-mail and hugged my staff as they came in to check on me. I felt loved and blessed to have such an AMAZING team to work with. Dr. Edwards agreed that I had “turned the corner.” Mom was supposed to follow me back home but was surprisingly late. I later learned that she had found the office building pharmacy. While it does, in fact, sell OTC and Rx drugs, White Cross Pharmacy also sells the most FABULOUS local jewelry and accessories. An hour later, Mama came home and gushed about the bejeweled necklaces, woven shirts, and funky handbags. This is just one of the many things I love about Texas….where one can find intricate artisan works in Mom & Pop shops. And yet, the most effective and meaningful comment she made was that my staff really loves me. “They adore you,” she said. Awwww…..I really try to be a great boss (fun but firm, steadfast but understanding) but it’s nice that someone else recognizes it.

That night, Mom and I headed to India Palace for our beloved Indian food. Aside from visiting the office, it was the first time I had been allowed out in public since being banished to the hospital for a deadly, highly contagious infection. People are so touchy. Of course, we enjoyed our spicy and saucy foods and browsed the store next door for bags, jewelry, and shoes. While she gushed over the finds, I felt miserable in my inability to purchase anything for ME. My income first covers living expenses and then pays off portions of both my numerous medical bills and grad school. Whatever leftover funds I am delighted to find in my bank account are stocked away for savings. LITERALLY, folks, you never know when you’ll need it. Take it from me, Ms. Paranoia speaking from solid experience. Like cancer.

This is why she sleeps with me:
She requires 2 pillows and
multiple blankets
Mom left the next day, Friday, September 4th. I spent the weekend doing little more than visiting the toilet, grocery store, and fridge in favor of storing up sleep in preparation for a full week of work ahead. On Sunday night, I awoke to Lola’s unaccustomed movements and shaking. Lola was having a serious elderly accident—like, the liquid kind. Instead of chastising her for something she could clearly not control (bladder and bowel incontinence), I set her in her dog bed as I stripped my bedding (yes, she sleeps with me—she would have it no other way) and simultaneously thanked God that the next day was a blessed Labor Day holiday. This visual obviated why I was still single….my dog rules my house and, as an old lady, has some THANGS to SAY….  Seriously, though, while the washer and dryer worked hard at de-nastifying the Egyptian cotton, Lola and I took two walks and moved to the guestroom (formerly known as “Jackie’s Boudoir”), a clean, furnished, perfectly respectable alternative. The problem was twofold: I was not in my own bed (even though I owned the bed and was quite comfortable) and my child was ill. These two things kept me awake. I spent Monday morning sleeping and completing chores, wondering where the last of my time-off went and cursing the start of the week, as necessary as it is…

Without further incident, I chalked Lola’s illness up to a toxic ingestion of leaves, twigs, or other substances while frolicking outside. Case closed. The rest of the day Lola was weak but otherwise displayed a healthy appetite and zest for playing. Still feeling depressed, I called Mom on Monday morning while drinking coffee and attempting to watch daytime TV. I told her something that had been on my mind for weeks, if not months. I asked her to vow never to laugh at or judge me for saying what I was about to say. I told her what had been consuming me: Based on the fact that I am seriously immunosuppressed, I was not going to live long. That, in fact, I took what Dr. Dham had told me to heart. Not BECAUSE of what she said, but because it was ringing true and contributing to a feeling I’d been storing in my heart. A few weeks prior, I wondered why I was still the way I was. On the outside, I was a decent looking single woman with a Master’s degree and a pretty agreeable personality. And yet, I (and others) questioned why I was still alone. I mean, I didn’t exactly MIND being single, but why was I not desired? Why was I not already with someone who loyally stood by me through my hard times OR who was interested in investing a life with a “real survivor?” I’ll give ‘em the hair thing: I mean, I am sporting a mad whitegirl afro. My fro now reaches 2 inches up and out, but has yet to fall downward in an attempt at an actual hairstyle. Please wish it luck as it continues to channel Blanche Devereaux from the Golden Girls. I digress. I really did think I’d figured it all out: I was single and ready to mingle precisely because I wasn’t expected to have a long lifespan. I was connecting with an inner emotion that I realized had been lurking there all along. It seemed clear to me now: I was not long for this world.

I returned to work on Tuesday with a few dozen “Welcome Backs” from my staff and the docs. I am truly blessed to have such amazing employees and couldn’t wait to get back into the full whoa-it’s-already-lunchtime and juggling-five-separate-but-unrelated-issues swing o’ thangs. Despite the massive stack on my desk, however, I was still charged with issuing payroll. This is no easy task as I must first calculate each employee’s hours, then determine time-off statuses, and finally calculate everything into our payroll system. I usually shut my door for this daunting task (I would hate to screw with anyone’s paycheck—including my own) but felt compelled to keep my door open this week as opposed to alienating the staff under the recent circumstances. I happily accomplished payroll on Tuesday before deadline, but was still faced with other looming deadlines. A folder filled with bills-to-be-paid still mocked me with a menacing face and I tackled said items on Wednesday by filling the printer tray with Quickbooks printable checks, inquiring with both banks about the account statuses, and carefully calculating what we could afford to pay. Even the most lucrative businesses have a cash flow pattern that must be monitored carefully throughout the month. In fact, I started from the bottom (due soon) upwards (due later) as it would represent the time-lapse factor in a more accurate manner. As I pulled out Dr. Edwards’s American Express bill, I double-checked his review. Each month, he carefully determines which expenses are to be allocated to his personal needs, his winery (a very reputable and exclusive establishment located just north of San Antonio but known throughout the country), or his medical practice. In turn, I pay his business expenses with a company check and the remaining balance with a personal Edwards check. In reviewing this, I found that he had overlooked a business expense thus causing me to nearly allocate said (high dollar—like, in the thousands—you figure the interest and do the math) amount to he and his wife. To make sure, I called his cell phone. When I told him that I was concerned that he almost paid for a medical conference out-of-pocket, the usual jovial and laid-back Dr. Edwards had a startling, out-of-character response.

Having a meltdown
            “I told you to pay that a long time ago!”

            “I’m sorry…..I’m just now getting back to work and able to pay the bills.”

            “That’s no excuse. Now I’m going to pay a very large late fee because you neglected to pay.”

            “I will call them and explain the situation. It is totally my fault.”

            “You need to pay it!” Click.

I sat there, stunned and rendered completely immobile. Motivated (by humiliation) into action, I printed the check and continued my bill-paying process, all the while growing incensed that I was blamed for a problem that was NOT created by me. In fact, every time I’ve been rightly accused of wrongdoing while on the job I have sucked it up and admitted it, stating that I had “dropped the ball.” This was not one of those situations.  He gave me that statement on Monday, August 24th. Because I was told to ONLY pay bills twice a month (after payroll so that my awesome staff was cleared first), I KNEW I would include it with the pile of bills remaining to be paid after payroll was processed. All bills, still current, would be paid that morning and received midweek around the 1st of September. And yet, just a day before my self-appointed bill-pay, I was admitted to the hospital. While confined to the prison sentence of 3rd floor Oncology, I accepted calls from the Charge Nurse, Billing Supervisor, and various doctors. I even accepted a call from the bank inquiring about an account issue. In other words: I continued to monitor daily activities and handle situations as they arose. I heard nothing from American Express or that particular physician and, upon being discharged on August 29th, felt relatively certain that things were A-OK in the clinic. And yet, now I was deemed culpable for a potentially devastating mistake. The doctor could be charge a 20% (very sizeable) late fee for my inability to pay on time. As I pondered this, I thought….wait…I was back to work within 10 days—even fewer when you consider regular call-ins from my hospital room. If it was late, that was only due to the fact that the doc withheld it, sitting on his kitchen counter for weeks, before handing it off to me, rendering it a last-minute bill. This was NOT my doing.

            The next morning, I entered his office with the intent of explaining myself-- particularly after a sleepless night of rehearsing my talking points ad nauseum. Before I could open my mouth, Dr. E launched into me. “You failed to do as I asked. I told you to pay that RIGHT AWAY and you didn’t. That’s gonna cost me.”

            Calmly and with practiced composure, I said, “Please let me explain. This is not an excuse but an explanation. You wanted me to pay the bills AFTER payroll, which was made expressly clear to me. Payroll was on Friday and I was admitted to the hospital on the previous Thursday. By the time I got out, bills were ready to be paid but by no means overdue. I had no idea that your AmEx bill was critical. I am so, so sorry. If you want me to make it the exception to your rule, I will.”

            “It ALWAYS needs to be paid immediately. I told you that.”

With sweaty palms, I chose to not say, “FALSE: You told me to pay it soon and ‘soon’ to me referred to 3 days later with the other bills, as you had requested. And Oops!!!….I was put in the hospital.” Instead, I admitted defeat and apologized yet again, taking full responsibility and assuring him that it would not happen again. He dismissed me, coolly.

I was enraged. I called Mom. She talked me down. I settled down and took a xanax. It was over.

The rest of the week I regained self-confidence as tasks were accomplished and staff expressed their wishes and entrusted me with new issues to attack. I was BACK, BABY! The following two weeks were seamless and I continued about my job as if nothing happened. In fact, a second late notice appeared for the infamous AmEx bill and I took it upon myself to call and inquire about any late fees as the paid check was well on its way. None were incurred (he is a loyal customer) and I reported this to him, as well as the fact that his newly-arrived-on-my-desk albeit late cell phone bill had incurred a $6.00 late fee but I successfully (and very easily) had it removed. He was pleased, but did not hesitate to remind me that this was MY FAULT. I walked away kinda pissed off.

So here I am, decompressed. I’m back to work and trying to make sense of my body’s complexities. Thank you for all of your kind wishes. My infection is cured and I am still awaiting some sort of response to the hormones and B-12. Some days are better than others but every day is a learning experience. I do love my job and my staff but—I can’t lie—I still long to be independently wealthy so that I can work part-time (to, you know, stay mentally sharp) and spend the rest of the time pursuing my dreams, whatever they may be. Until then, I will count my blessing and be glad.

Monday, August 17, 2009

Cancer Free....Seriously....Now what??? (Blog 21)

Blog 21: Okay Really, Now What???

The following week of June 15th was typical in that I felt as capable as I did idiotic. In other words: A usual day for Sarah involving as much confidence as wild, pathetic guessing. On Saturday, the day before Mother’s Day, Mama Jackie called me to say that she had received my bouquet of yellow roses yet she emphasized how unnecessary the gesture was while I cried (literally) about how necessary it was for me to attempt to demonstrate my love of--and gratitude toward--her. After a few minutes of reassuring “you didn’t need to do that” combined with a few glasses of wine and “yes I did; you’re the best Mom ever” sentiments, I felt confident that she understood the emotions I had attempted to convey via a $50 bouquet.

The next day, I called the veterinarian. Lola has been acting like a teenager for months and I had met my limit. NO MAS!!! I had lately come home from work to find a present awaiting me at the porch, in my bedroom, or outside the guestroom. It never failed. The vet tech explained that, given her age of nearly 10, she may be experiencing a physiological problem. I left work early that day to take my little queen bee to the vet, during which they examined her, took blood, fecal samples, and urine and then told me that she likely has fatal renal disease given her age and sudden behavioral problems. They would have more tests later but, until then, I was at least allowed to take her home with me that night. Instead of thinking about my new job, family matters, or attempting to start working out by way of a half-hearted power walk, I held her in my arms at home while we both fell asleep.

The next morning, after rushing a fecal and urine sample to the vet on my way to work, I noticed a missed call from Dr. Wilks. She told me to call her back “ASAP” with regards to some blood results that need to be addressed.

Oh God. Lola is dying of kidney disease and my cancer is back.

I called the clinic number but, despite the fact that she had already called and told me to return the call at that number, the answering service responded. Yeah, to answer your question, I was ABSOLUTELY FREAKING OUT.

I made it in to the office with a carafe of coffee in hand and a bundle of nervous energy. I recall dealing with the following: An angry patient, a newly proposed managed care contract, and a high-strung doctor who wanted me to address the dictation issue ASAP. I FINALLY received the much anticipated phone call from Dr. Wilks herself explaining to me that my Vitamin B was pretty low and that I needed regular injections. (Seriously? That’s all? Good lord, doctors need to learn some message-leaving etiquette.) With a MASSIVE exhale of relief, I agreed to make arrangements and I called my mom to calm her anxiety (of COURSE I had called her on my way into the office after receiving that seemingly fatalistic message). I felt somewhat relieved but my focus then shifted to my much-awaited response from the vet: Tell me I’m dying again and I’m relatively okay; tell me my dog is sick and I’m a mess. Later that afternoon, the vet called and explained that her tests revealed that Lola is old (duh---I adopted her at 7 weeks old in 1999) and has a highly treatable form of colitis and exhibits the early stages of hypothyroidism. In other words: she is fine and just needs a course of antibiotics and a new brand of food.

On Friday, June 19th I left work at noon and returned home to find Mom coddling sick little Lola on the couch. Mom was my designated driver seeing as had been prescribed a large bottle of white liquid chalk (barium) for lunch on the day of my 3 month CT scan. Note: I had previously experienced this culinary delicacy the night prior as a post-dinner nightcap. It was berry flavored and it was vile. At the clinic, I undressed from the waist up, donned the gorgeous cotton gown, and was scanned from the top of the neck to the bottom of the pelvis.

As per usual while laid flat—not seductively, sorry to say--in a plastic tube, the entire event seemed completely pointless given its fast in-and-out nature followed by a handsome bill. Indeed, a few minutes after being scanned, I dressed and we left, ready to have a glass (or 5) of wine before going to dinner. For the next few days we decided to eat out as much as possible, clean house, and run essentials errands a la Pier One, HomeStore, Best Buy, La Cantera outdoor shopping mall, and Target. In other words: I had energy. No, seriously: I was able to make it through a full day without stopping, napping, or bitching whatsoever. Mom and I accomplished what we needed without incident and we both commented in the car that I was remarkably more energized than she had seen me in a year. I was happy, I was healthy, I was gleeful. While at Francesca’s, an outrageous knockoff store in The Rim, it occurred to me that I was filled to the max with both RED and WHITE blood cells….so hot. But seriously, I had a great time trying on ridiculous plastic rings and huge pins while Mom laughed and imagined me approaching my MD specialist boss—wearing said massive, obscene faux jewels-- while casually tossing an invoice or EOB in his direction. Neither of us could keep a straight face. “Ummm…..Dr. B? Yeah, so we need to talk about this Medicare refund request…?”*BLING!* We had a great time and we both acknowledged that this was a new beginning. A new me. A new Sarah.

The following Friday morning I returned to the clinic for my early morning CT results. As soon as I arrived the receptionist told me that Dr. Wilks wanted to see me “immediately.” With trepidation, wringing hands, and sweaty palms, I inquired as to WHY my cancer doctor insisted on convening with me at the earliest possible time. “Oh, she has a meeting later in the morning,” she responded quite casually. I exhaled a huge sigh of relief. Only moments later, Dr. Wilks bound into the exam room: “Sarah?” she asked. “You’re here……” followed by: “Ummm….Why are you here?....Oh, because of your B-12?” she asked.

“Ummm…..I had my 3 month CT scan?” I informed her most nervously.

“Oh, you did? When?” She said, flipping through my enormous chart.

“Last week? The 3-month scan?” I offered again.(Allow me to interject here: my senses tell me not to worry while my environment tells me that everything is ALL effed UP!!!)

Dr. Wilks thumbed through my chart feverishly and then…….recognition!

“Your scans look GREAT!” She said.


“YES! Your lungs are looking pretty good and the spots on your lungs are indicative of scar tissue. Everything still looks good!!!”

I continued to the nurses’ station whereupon I was showered with love and hugs from five of my favorite people. They gushed that my hair was growing in “beautifully,” (even though it wasn’t) and that I looked great. To Shannon, Maxine, Ann, Ann, Marion, and the others: Thank you for your love and encouragement.

Dr. Holt, my former employer, had purchased a gift for me that would finalize my entry into the World of Healthy People. She arranged for me an appointment with a local Natural Healer. I had no idea what that meant but I willingly drove myself to a surprisingly sophisticated part of SA on Saturday morning (let’s be honest: I was expecting a hippie-dippie commune with fairies and gazing balls gracing the front yard). The woman there ushered me in and proceeded to conduct a “healing session” on me. She was awesome!!! I am not exaggerating when I say that my limbs were reverberating against something static: I was rendered an unwitting slave to the massage table. She didn’t make weird noises, she didn’t burn incense, and yet her hand motions a foot above my flesh caused my whole body to vibrate. I am not kidding. By the end of the 60 minute session, Gail told me that my chakras were surprisingly open and healthy, but that my circulation may be compromised (how did she know that I was having neurological issues?). I thanked her and left, feeling physically rejuvenated but still emotionally cautious about the entire experience.

That Thursday, I attended an LLS support group at La Madeleine. My new friend Clarisa told us about her long, horrifying experience regarding a potential bone marrow transplant, lung tumor biopsy THROUGH BONE, and questionable doctor who refused to take the advice and expertise of other MDs, namely an interventional radiologist and MD Anderson lymphoma-specialized oncologist. All signs pointed toward RECOVERY but this doctor tried to convince countless specialists—and the patient herself—that she was dying and needed further treatment. In my world of healthcare administration, being cautious is called Defensive Medicine. In this case, it was just excessive and unnecessary. At the behest of family and friends, Clarisa journeyed to MD Anderson for an in-person consultation to make more sense of this controversy: her oncologist tells her that she requires a serious bone marrow transplant and invasive, painful biopsy because the treatment is failing and yet every other doctor who has been consulted furrows his brow, scratches his head, and says that her scans and labs look great. Everyone involved agreed that her Hodgkins was responding well, that she was in remission, and no further treatment (aside from finishing the standard ABVD protocol), was needed. Clarisa thanked them and quickly agreed to stop seeing her quack of an oncologist. WTF was this woman—her doctor--thinking????

Also that night at LLS Happy Hour, the LLS reps informed the Hodgkins kids that we can never, ever go scuba diving or involve ourselves in similar activities that require oxygen saturation level changes. Most Hodgkins patients have been exposed to Bleomycin, the chemotherapeutic agen that often compromises lung function. One scuba session and we could be history. Sad and interesting….. In a weird twist of fate: It is fortunate that I was highly allergic to Bleo and was taken off of it midway through treatment.

On Friday night, as I was hanging out in bed and checking e-mail, I discovered that the Leukemia & Lymphoma Society’s Team in Training program was having an informational meeting on Saturday at my church. I knew the time and the place and therefore had no reason not to attend: I was guilted into going. While there, the program quelled any hesitation regarding whether or not to join: Raise money for an amazing cause, have access to expert coaching/training to get into shape, and meet amazing people. Two hours later I was hooked, and by Sunday night I had committed to doing the San Antonio Rock ‘N Roll ½ marathon. 13.1 miles = huge, huge imposition on Sarah’s daily schedule and massive challenge to her current physicality.

Jazzed to start this new venture, I shouldn’t have been surprised when, at the grocery store checkout line, an epiphany led me to believe that now is the time to start going wigless. Sayonara Veronica and Noreen: Now it’s just Sarah and her (albeit short and spunky) hair. I recall standing in the checkout line seeing people around me of varying shapes, sizes, abilities, and follicular lengths. I then dreaded the idea of wearing an itchy, synthetic wig for another hour, much less another day. Still in line, my phone rang and I talked to Mom, explaining that I think I just made up my mind: I was done with the head coverings. She summed it up so simply: “It’s a new day, a new week, a new month, and a new dawning for you: This is the time to do it. I think you’ve made up your mind!” With that, I had a new resolve: I was no longer a slave to my hair—or lack thereof--anymore.

With trepidation on Monday morning, June 1st, I walked through the back door of my office nervously anticipating a reaction. One of the doctors (a young, cool female) has an office near the back entrance and is usually there early after dropping off her kids at school. We said hello and I tilted my head in embarrassment, subtly pointing go my short, spiky new ‘do. “Oh! I thought your hair was pulled back! I forgot that you were wearing a wig before. Wow!” Huh??? The day continued in a similar fashion: medical assistants, nurses, doctors, and pharmaceutical/medical device representatives stopped short when they saw me and then explained that my hair looks great, they hardly noticed, etc. It was so sweet. But, the best part was that I would frequently pause my day to acknowledge the fact that I felt FREEEEEEE! I was no longer finger-combing through nylon hair that had gotten tangled, no longer itching my scalp, and no longer adjusting a wig that had a tendency to ride up, slip back, or otherwise fall out of place. I felt liberated.

On Wednesday, June 3rd, Dr. Edwards came back into the office after a few days off for vacation. As usual, he stopped at my office door, began to say his hellos, and then stopped short. His eyes dilated into saucers and he said, “Wow….your hair!”

“Oh my gosh. I am so sorry that I didn’t warn you. Yes, I guess the secret is out: I’ve ditched the wig!”

“It looks great,” he said. “You look like a French movie star!” With that, I blushed, accepted the compliment (I think it was a compliment anyway?) and moved on. I had clearly crossed into new territory: That of a Short-Haired-Girl-Who-Could-Almost-Look-Butch-But-Was-Clearly-Feminine-Because-She-Wore-Makeup-and-Jewelry-and-Girly-Clothes. What to do with that??? I needed some time to adjust to my new dichotomous look and frequent trips to the bathroom would reassure me that I could NOT be mistaken for a 12 year old boy.

A few days later, Nicole Bell from LLS called and asked if I would agree to be this season’s Team in Training Honored Hero. Taken aback, I of course said that I would, understanding that my responsibility would entail attending certain team events, sending notes of encouragement to participants, allowing my picture to be plastered on various materials, and be otherwise available to the Team. Within moments, an Honored Hero questionnaire made it to my e-mail inbox and I completed such self-indulgent queries as “What do you like to do in your free time?” and “What is your favorite movie?” And yet, on Thursday June 4th while making dinner, my phone rang. Sheri asked if I would be this season’s Team in Training Honored Hero. Wait…what? I told her that Nicole had already approached me and she laughed at the coincidence: “Nicole asked you on behalf of the organization and I, as a TNT Mentor, asked you as a personal friend!!!” Seriously….I’m truly HONORED. Why would I get special attention for having cancer? I did not CURE cancer. Nor did I rescue a child from a burning building or invent something worthy of a Billy Mays infomercial (R.I.P). I cautiously informed Sheri that I had made plans to actually COMPLETE the ½ marathon and she told me that, not only could I maintain my status of Honored Hero, but that my participation (ie: struggle) with the team would be even more inspirational.

I attended the seasonal TNT Kickoff party on Saturday, June 6th whereupon I learned that my training mentor would be my dear friend Heidi and I met my other teammates. The TNT colors are purple and green and—let me attempt to convey this accurately—there was a WONDERFULLY ABSURD amount of clothing, hats and other accessories, confetti, and d├ęcor decked out accordingly. It was like a G-Rated carnival. The speakers introduced me along with the other honored teammates (Clarisa being one of them!) and a few people approached me afterward telling me that they would need all the inspiration they could get as they took on this unbelievable personal challenge. There was a lot of clapping, cheering, and chanting “GO TEAM,” and I left feeling recharged. Not only was I there to motivate, but I was there to DO IT. Here goes nothing…..

On Monday, June 8th I hit my gym and managed 20 minutes on the elliptical machine at a Level 1. I think I burned off a stick of gum, and yet, I sweated my arse off and panted until my lips cracked (again, not in a good way). The adventure begins!

Armed with a PURPLE folder stuffed with information on the following: Training schedules; Training tips and tricks; Nutritional, Injury Prevention, and Gear Clinics; and info sheets on coaches and mentors, I marched into UNKNOWN FOREIGN TERRITORY (Read: Academy Sports & Outdoors). I had a mission to purchase dry wick shirts, shorts, hat, and socks, fuel belt and bottles, sunscreen, and interval training sports watch. Two hours of hemming, hawing, and total confusion later, I paid my $200 transaction and left feeling inept and intimidated. Still, this was one for the books: Sarah Brannon shopped at Academy. My stepdad Gary will be so proud!!!

With absolute trepidation, I attended my first TNT practice on Wednesday night, June 10th at the San Antonio zoo (how fitting). We were doing 2.5 miles and I looked to my mentor Heidi (yes, that Heidi from book club and my benefit) with dismay. She just nodded with confidence and turned her attention back to the announcements, conveying to me that it was allllll good and I was in excellent care and could DO IT. I began my maiden voyage speed walking and enjoying the absolutely gorgeous scenery around me when I encountered a familiar face from the kickoff. I saw that her jersey was already blinged out with her name, and I made casual conversation with her. Amanda and I quickly became friends, bonding over healthcare (she works for an imaging facility), girly stuff, and TNT. In mere moments she informed me that she runs intervals. Oh….God. As her first running interval approached I agreed to try it, testing whether or not I had it in me to follow through. Afterall, I was healthy but unathletic prior to my illness, unhealthy and incapacitated during my illness, and now relatively healthy and semi-capacitated afterward. Which means…..what? Suddenly, the interval was upon me and I was running….and feeling the slight (nearly nonexistent) breeze in my face….and my muscles flexing……and the sweat beading upon my forehead. Was I really doing this??? We continued the 4:1 program—4 minutes walking followed by 1 minute running. Not FloJo-worthy but a win for me! Along the way we engaged a fellow TNT teammate in conversation. She had kept up with us and we learned that her name is Diana: thus developing the Trifecta of Amanda, Diana, and Sarah: SPWOGGERS United.

Amanda said that last year she and her pace partner had described themselves as Woggers, as in Walkers/Joggers. This is meant to differentiate themselves as hardcore walkers aspiring to running status. And yet, I decided that our sweat accumulation, motivation, and athletic prowess propelled us to SPWOG status. We are now SpeedWalkers/Joggers. (NOTE: From this point on Spwog will become a common reference, if not yet referenced by Merriam-Webster). As we spwogged, we also encountered long-time TNT supporters and hardcore runners along the way. As these people proceeded to SMOKE US, I still felt invigorated by their calls of encouragement: “Good Job” and “Go Team!” and “Yay Sarah!”

The entire team met up at the original starting point to stretch and bond, during which I informed my new friends that I would miss the first Saturday practice to attend my annual family reunion. Everyone was supportive and positive and I left feeling empowered as I called Mom to explain to her that I just completed 2.5 MILES!!!! 3 months after inpatient hospitalization!!!! CAN YOU BELIEVE IT???!!! Yes, she could. She was so excited for me and supportive of my pathetic attempts to become fit. By the time I got home and checked Facebook, I saw that my new friend Amanda had decided to announce that, from now on, she would formally spwog in honor of me: Her new friend Sarah Brannon. I was humbled once again. I couldn’t help but brag to my own Facebook crowd about the amazing experience I had with TNT. It had only been a few hours and I was hooked!

To prepare for my annual family reunion, I left work early on Friday, May 12th, and headed to my brother’s south Houston home in time to have dinner and go to bed--an evening characterized as both pathetic and delightful all at once in Sarah’s world.

Actually, we had dinner at a local Mexican restaurant and retired to bed predictably early, irresistible 2 1/2 year old nephew nugget & all. Brannon Christopher Gay had rocked the restaurant booth with his baseball, dinosaurs, and kazoo in tow and, while the food was mediocre, the company was primo and rendered us all exhausted.

Let me state this plainly: The Somers family reunions are pretty lame by conventional standards. We secure a room at a suburban Houston conference center, load four tables full of food, inhale said food and make polite conversation, and leave four hours later both bored and uncomfortably full (or hungry if you refuse to eat deep-fried everything). We milled around for a few hours hugging each other, reciting our past-year accomplishments/troubles, and paid extra attention to the babies and toddlers of the group who were too young to defend themselves and tell us to back off. Yet, during the blessing and announcement I felt strangely compelled to speak up and thank everyone for their love and support. Most of my relatives who attend the reunion are elderly and thus on a fixed income, so I thanked them for their dedicated and heartfelt phone calls and cards while I was in the hospital as it boosted my spirits and helped me to get through the most difficult time of my life. Suddenly I was tearing up and wondering where this emotion was coming from! Sniffles and tears abounded and, with that, we broke for food and I felt yet more resolution. If I haven’t said it enough I’ll say it again: Thank you to my sweet family who prayed for me. I love you.

Arriving home the next day, I shifted into mania mode as I did dishes and laundry, took out the trash, ironed, and made dinner: Preparation for a full week of staffing, managed care, and TNT training challenges. And yet, I started the week knowing that it would be a short one as Mom was due on Thursday and I had a scheduled surgery for Friday: I was getting my port out on June 19th. On Thursday night we had County Line BBQ and on Friday morning, at 6:30 exactly, I woke up to “SARAH!!! It’s 6:30.”


“NO….It’s 6:30 AND WE HAVE TO LEAVE AT 7:00!!!”



10-4. Go Away.

I checked in at 7:30 as requested but was told that the interventional radiologist performing the procedure was running very late. I commenced a text message marathon and moaned about my lack of coffee and water (NPO before surgery) and was finally taken to a room in Cardiology at 9:00, whereupon we settled into a bad court TV show marathon (“I’ve missed you soooooo,” I mused while gazing into the wall-mounted television set). Sidebar: I was in Cardiology because that’s where the equipment needed to do my surgery is located. At just before 11:00 the murse (read: Male Nurse) arrived to discuss the procedure and at 11:30 the doctor arrived to repeat everything he said.

“Ummm…..excuse me but I have a really crazy, morbid question,” I said to the doctor.

“I’ve heard it all. What do you need?” Dr. Rohweter said.

“Okay, so I’m sure you’ve had a lot of absurd, nutty requests from patients so this won’t be weird at all. Buttttt………… I was telling the nurse here….ummmm…..I have my camera. And I’d really like you to take a picture of my port when it’s out.”




Breaking the silence: “That’s not weird, is it?” I asked. “……Is that weird?”

“In all my years of practicing medicine I’ve never had THAT request,” he insisted.

“Awww COME ON!!! You’ve never had anyone ask to take something home or take a picture?”

“Well, I once had a guy ask for his gallstone but—I mean—that was IN HIM for months! Why wouldn’t he want to see it?”

“But I had my port in me for over 9 months and it helped me get through the chemo that saved my life!” I argued, quite desperately.

“I’m at a loss for words,” he said. “You are right. I hadn’t thought of it that way.” Dr. Rohweter explained that this is an extremely straightforward procedure and that the easiest part is getting it out. “Once it’s out, it’s out,” he said, quite poignantly. “The hardest part is cleaning out the pocket that the port was in…most of the time will be spent making sure we avoid infection.”

With that, I was wheeled out of the room. We paused in the surgical waiting area and the murse tried to make idle chit-chat with me, telling me that he was a Baylor student during the Waco Standoff against David Koresh. Awesome, but not exactly appropriate conversation, considering….

Eventually I was in a surgical suite as techs prepared for my procedure. I was awake but sleepy, aware but indifferent (I had been through worse), ready but cautious. Doctor Rohweter came in and they discussed with each other details about my procedure as in preferred equipment and doses. I was told that the worst I’d feel would be the lidocaine shots but that everything after that would be painless. I recall recalling nothing from my port implantation (during which I underwent the same conscious sedation and had absolutely, positively no complaints) so I wasn’t worried about feeling and/or remembering any pain. Of course, you’ll recall that the anesthesiologist that day had told me that I was a very expensive date and needed a LOT of margarita meds….more than they could ever have expected. I don’t like to brag, but yeah……..Within moments they were apparently doing the procedure and asked me multiple times how I was doing. I was later told that I responded “okay,” then “just fiiiine,” and eventually, “great,” until I actually said, “Ummmm….I’m okay but I think I need more. Can I have more?” He responded with, “Do you feel us working on you?” I was on a sedative that is also known as a truth serum (I guess the part of your brain that registers stress is also suppressed from lying, or something???). I answered, “No, but I’d like more.” I guess they blew me off. Later, when asked how I was feeling, I asked again for more. I remember this clearly and someone responded with: “No, honey. You’ve had enough. We’re just about finished.” I felt deflated, as though the bartender cut me off and told me that they were closing soon. IT CAN’T BE 2 AM ALREADY!!!!



g o n e.

et voila!

At one point I was wheeled back into my room and my Mom was brought back from the surgical waiting area. I wanted water, water, water, water, water and, since it’s after 1:00 and I hadn’t eaten for 19 hours, perhaps food. When they presented me with a paper menu and asked what I wanted I remember thinking that the chicken salad sandwich was edible from my lengthy stay last March. I was brought some chicken goop on white bread (I only eat wheat) and Baked Lays, thus constituting “lunch.” A few minutes after my tray was removed, the murse emerged.

“How are you feeling,” he asked.

“Super!” I said.

“I know,” he said with a smirk. “We asked you in surgery how you were feeling and you said you were on a hammock in Cabo. That must have been good.”

“Shut UP!!!!!!!! Did I say that?..........Whatever!..........No I didn’t!”

“Yes, yes you did. We’ve heard worse but we got a lot of humor out of it.”

That night, we ate a quick dinner and I retired to my bed. Yet, I couldn’t sleep. Dr. Marks (“David” now) called at just after 8:00 to make sure that I was okay. I thought it very sweet and chivalrous of him.

“Do you need anything?”

“Yes, just some verced.”

“I’ll be right there,” he said as I silently gushed and laughed, barely conscious.

I lazed around all day Saturday while Mom ran errands and left on Sunday during the early afternoon. As usual per my OCD self, I completed my chores despite feeling half-drugged, and returned to work on Monday.

While most of my staff was oblivious that I was even absent on Friday (not feeling the love), a few asked how the surgery went and how I was feeling. I was exhilarated to be metal-free and ready to take on the world as a CANCER SURVIVOR. For some reason, this now made it official, as if the doctors did not expect it to ever return. Life was awesome and I was ready. Bring it…

The subsequent weekend and following weeks were much to be expected as I felt largely intact and healthy with only a few twinges of pain here and there, easily managed by Tylenol. On Thursday, July 2nd I arrived home from work to pack for a long weekend in Rockport and yet on Friday, July 3rd I woke up with a raging headache--borderline migraine--and opted to ingest a muscle relaxer as I was forced into a deep sleep. I managed to wake at noon, leave by 2:00.

When I arrived around 5:00, no one was stirring and I grew tired, so I lay down in my bed….the office futon, to be exact (whilst Brannon lazed in the guestroom crib and thus claimed the entire guestroom as his OWN), and read my book. Before dinner, I entered the kitchen to find my nephew, Brannon, stating to the world that he was, in fact, looking at a STRAWBERRY in the KITCHEN. I’m sure in toddler talk that meant something significant. Upon laying eyes on my 18 month old boyfriend, I scooped him up, phlerberted on his belly, and told him how much I missed him. We ate ribs that night (I believe Brannon had his constant diet of chicken nuggets and fries—don’t get me started), and went to bed early. On Saturday my big brother Scott, sister-in-law Sarah, Mom (Mimi), and I met Gary (Poppy) at the Rockport Marina for some fishin.’ Gary baited Brannon’s plastic CARS (or was it Transformers?) fishin’ pole with shrimp as we watched the boys pull in some 1/8 pound whoppers. Have no fear, PETA people: They all lived to see another day.

We smiled into the camera, squinting into the sun, and enjoyed our 4th of July realizing that the majority of the day would be spent indoors given the blazing sun and penetrating heat. At the annual 4th of July party, my Nugget Brannon swam with the other kids and I was overjoyed to witness the simplicity of life as a little kid. If I had a bathing suit—and didn’t fear inducing mass chaos when the other partygoers saw their first beached whale—I would have jumped in with him.

We all progressed to the marina and then to a friend’s huge boat while we watched the fireworks. No explosion was too great for Big Man Brannon.

I woke up fairly early and left by 10:00 AM with a sendoff kiss from Brannon. I love my nephew so much and he will never understand how much he inspires me to keep up my strength..

I did make it home relatively early and was able to complete my chores (laundry, water plants, wash and empty dishes, etc, etc, etc, etc, etc) before imbibing. Wine is my savior and I enjoy it immensely.