Showing posts with label jeff sv. Show all posts
Showing posts with label jeff sv. Show all posts

Saturday, June 26, 2010

Last Love Infusion No. 6

My last chemotherapy was today and I almost could not believe it. I can take down the countdown counter I've had for almost three months on the right hand margin of my blog. It was a day for extra adventures for sure!

I got up at 5am, got ready and wrapped the cake pops I made for my surgeon before making breakfast for my aunt who stayed over and Tawny who came at 7:30am. As we were walking out, my aunt was distracted from the large leaf plants outside my apartment and then took a tumble on the pavement. She nearly gave me a heart attack! She was okay and mainly felt bad because I gave her such a worry that I was raising my voice at her (with curse words) on the way to the cancer center. Tawny was the referee and told me to pipe down as I drove us which was only less than 10 minutes away.

My blood was taken for the tests results my doctor would see an hour later. We went to get my refill for aftercare meds and then we sat by the cafe for a few minutes before the research worker found me and said if I checked in early I could get done in time so that I could have my stress test in time. She admitted she had to go a wedding a few hours away that evening and had to be on a time schedule. I didn't mind because so was I.

Off we went to check in early. A nurse soon whisked me away for vitals and then let me back in the reception area with the girls. We didn't have to wait long for me and my entourage to be escorted to a bigger exam room. A different doctor asked me questions and did the physical exam. She pressed against my lower lymph nodes and I giggled a lot because I am very ticklish which made her giggle, too. For a woman, you'd think she'd be more gentle on parts she has, too! My surgeon has really big hands and I have never felt any discomfort with his physical exams. AND AND AND -- she used latex gloves before I realized it. Guess who is allergic to latex?! She left to get my surgeon so I could complain to the girls.

My surgeon received about 30 cake pops. My aunt helped me make mine with chocolate cake and frosting mixed together, rolled into balls and chilled. Lollipop sticks were then dipped into melted chocolate and inserted into the balls before chilling again. They were then dipped into more melted chocolate and placed into mini-cupcake liners. I found four different colors in a polka dot pattern. These were on a tray to let set overnight.



In the morning I packaged them in to cellophane bags and put silver twisty ties on them. I also added another layer of mini-cupcake liner before packaging them for aesthetic reasons.



This is the end product my surgeon received. I placed some red crinkly paper inside a red tin before placing 30 cake pops inside. A giant cellophane bag for baskets was then wrapped around the tin and then adorned with the red with white polka dot satin ribbon. My surgeon loved it!



Tawny and I had stopped at Ikea on Wednesday night to get an apple-flavored sparkler drink for our faux champagne toast today. I had to take this picture after we got back home. Sometimes the big events in your life is about creating an "experience". I know today I created an experience for me and perhaps for the first time for my surgeon. How many patients would think to bring faux champagne and plastic champagne glasses to celebrate her last chemo? He did the honors of toasting us. I loved it!



I had my stress test which went well. My entourage looked on while I was hooked up to various electrodes and breathing masks Afterward, we picked up lunch from the cafeteria on the premises to bring back upstairs outside the chemo section. We wolfed down our lunch because we were hungry and everything was good. I was happy to not to have to rush my lunch for once before my chemo. You may recall that I am usually rushing against the anti-histamine drugs before my chemo cocktails. It makes me sleep no matter how hard I fight it.

Here are some views I will not miss:

This is the area of my port on my upper left chest. A one-inch needle is inserted and connected to tubes that is connected to other tubes for my chemotherapy.



These are my actual chemo cocktails. Two bags come before these for pre-meds. The total actual drip is 4.5 hours except today. More on that later.



These machines keep track on how much time is left and beep if there is anything wrong or when the bags are empty.



This was a view from my chemo chair as evidenced by my running shoes. The chair across the way is what the chemo patients sit in. I need two pillows to sit comfortably -- one for my lower back and one for my head. The chairs recline to give your legs support, too.



Halfway through my last bag of chemo, I had an allergic reaction that could have been really serious had my nurse not come by for me to ask about the temperature of the building. I was felt hot. I then told her I felt like I could breathe through my nose, like I had a cold. My chest was heavy. She asked me if it was getting better and I said no. She stopped my chemo and gave me oxygen tubes for my nose.

My nurse ended up calling my surgeon and he said to stop it completely and give me some more of my pre-meds for the allergic reaction. (This particular cancer drug shows some allergic reaction in some patients during the seventh cycle. Super overachiever that I am, showed it in cycle six.) I told her I needed to empty my bladder which she said would give her enough time to get another IV bag set-up. Another nurse escorted me to and from. When I got back my aunt was sitting in the chair with a worried look in her face. (I could only have one guest at a time so Tawny and my aunt took turns keeping a vigil or sat outside together why I slept through my chemotherapy.)

My face had been swollen and flushed. Within minutes of receiving the anti-inflammatory drugs, I was relieved to breathe some and the heaviness in my chest was gone! Wow. It was amazing and almost instant relief. The bag was only for 15 minutes. By this time, my aunt had gotten Tawny who was allowed to sit by me. Tawny knew I was getting better when I was giggling again. We stayed an extra 10 minutes just to make sure I was back to some kind of normal.

Tawny drove my car to a Mexican restaurant where we met her husband Jeff for dinner. Jeff left after our dinner to deliver something downtown and us girlies went to my favorite place for boba drinks, slushy fruit drink smoothies with tapioca pearls at the bottom we brought home.

This day went very quickly. My aunt and I talked about the whole day after Tawny left. She spent the night again on my couch. I made it to bed determined to get seven hours of sleep and to take my medications in time in the morning.

My lovelies, I am relieved. I have a CT scan for my chest and abdomen in three weeks to see if there is any cancer left lingering within my body. Another week after that is the appointment with my surgeon to discuss the results. Before that, next week, I receive the results for the thyroid biopsy from this past Wednesday morning. I don't anticipate anything wrong with that. My nodule is 1cm large. When you're a cancer patient and anything else crops up, you can guarantee there will be some kind of further investigation to rule out anything. This is my story and so far I am okay with it.

Thank you for my love and support! I am wickedly blessed.

Love,
Sarah xxoo
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Saturday, June 19, 2010

Feeling Good

Changes at work and my feelings of fatigue have kept me from updating my blog. I thought about it each night, but I knew I just had to rest to manage my energy...

Our temp is gone now; her last day was Tuesday. She was re-hired temporarily because I was going through my chemotherapy. I now find myself busier than ever. I would love it extra if my brain and fatigue would cooperate, but I just do the best I can.

For the past three days, I've felt so much better. My good energy has been extended in the evening. You can't imagine how wonderful that is! Yesterday I left work at 7:30pm and still had enough energy to go grocery shopping by myself until 9:30pm. Dinner was served at Sprinklesville at 10pm. Not too bad...

This morning I made the resolve to see my hairdresser Tania so I could get a couple of packages of Korean brand faux eyelashes. She was ecstatic to see me judging by the long hug she gave me. As we talked and I updated her on things, she couldn't keep from hugging me. She ended up giving me four boxes of eyelashes and trimmed my wig a little to her satisfaction for free.



Tania is a very Christian woman. She kept telling me how great I looked and how she could see an inner glow about me. I told her I was wickedly blessed and she agreed. I was humbled when she told me that I have a rare heart especially when I can go through what I am going through and still find a way to give to others. She had no doubt I would receive continued blessings.

My next trip was to the craft shop to buy some components for the gift for my surgeon next Friday, my last chemo. Oh -- I didn't tell you -- Tawny is coming to my chemo along with my aunt. I am very excited to have both family and friends represented. Tawny is working extra hours to make-up for taking the day off. I appreciate her sacrifice for me.

For my last chemo, I am buying some sparkling cider and some plastic champagne glasses to toast with the girls and my surgeon. I can't wait to complete my last chemotherapy, but I am reticent to see how I will feel the following week as the chemicals work through. Sigh. I just have to get through it.

I also have to get a biopsy on my thyroid next Wednesday morning. My primary care determined to rule out anything that may be there. I had my ultrasound at a separate facility last Tuesday morning and in the afternoon I received a call from my primary doctor's office with the recommendation. Many people have benign nodules on their thyroid. I am releasing my feelings on the outcome whatever it may be. There is no reason to worry about something I know nothing about right now. I just make the necessary appointments and show up.

This evening was time for some fun. Jeff and Tawny came over for dinner and Scrabble. I made a creamy lemon garlic chicken with pasta and broccoli and some garlic bread to go along. We feasted like kings! Oh my gosh was everything good. For dessert, I scooped some fudgey chocolate ice cream and for a lame attempt at healthy, I topped each heaping bowl with fresh raspberries. Hee.

We went two rounds of Scrabble. Tawny and I each got to start the board. For some reason, when we start the board we are actually able to branch out, but when Jeff starts the board, we get pigeon holed into a corner of the board. Next time, we are playing with nine tiles each instead of seven to make it more interesting.

This coming week is jam packed with stuff but I will try to update you with something even if it is just with pictures. I am doing mighty fine thanks to your prayers and support.

Love,
Sarah xxoo
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Saturday, May 29, 2010

Word Play

Do you remember the last time I cooked a meal for visitors that didn't involve my chemotherapy? Me neither. Tonight was the first time since last year I am entertaining purely for fun.

I started out early by going to do some shopping and ended up at the grocery store. By the time I finished around noon I was wiped out. I put my groceries away and ate lunch before taking a nap for some recovery time.

Tawny and Jeff came at 6pm to enjoy a home cooked meal of broiled marinated flank steak. It was accompanied by seasoned green beans, a wedge of cold lettuce for the quickest and simplest salad and my lazy (yet healthier!) mashed potatoes. Red potatoes were boiled until fork tender then placed on a sheet pan lined with aluminum foil and drizzled with some olive oil that has been spread out to coat pan. I then smashed each potato with a potato masher once. More olive oil was drizzled on the bed of mashed red potatoes followed by a good seasoning of kosher salt and freshly ground pepper. Finely chopped fresh rosemary was sprinkled on top for flavor. The oven was heated to 450 degrees and the potatoes were cooked until crisp about 30 minutes. I added some chopped red pepper and scallion rings for color and a fresh finish before scraping the potatoes off the sheet pan and into a large serving bowl. Yes, all of it was yummy!!

For dessert, I made what I now call my Raspberry Angel Napoleon. I sliced angel food cake and layered them with sugar-free whipped topping and fresh raspberries. I topped each serving with shaved 70% dark chocolate and some disco dust because I like sparkly. You've heard that before, haven't you?



The rest of the evening was spent playing Scrabble. We did two rounds that involved painful deliberations from Jeff. Where I play for a certain flourish with words, he was playing for high points. He won both rounds. Bastard. Ha. At some point when there were less tiles to choose from, my letter choices started to spell out Russian words or for Tawny what she perceived as Vietnamese words. She did have one set that spelled out "SO NASTY" and used the word NASTY on the board.

I was very interested in playing with these two brainiacs since we have never played Scrabble in the 12 years we've known each other. More importantly, I wanted to spend some quality and normal time with them. I am sick of having our only communication via instant messages or cell phone texts. It is just not the same when you are in person. Our recent get-togethers have also involved something with my cancer treatments. My treatments are almost over and I need to start transitioning into normal. I don't know if that is the appropriate word because my life is no longer normal and I can never return to what I knew as normal...

Cancer changes your perspective in life. It makes your world both myopic and expansive. Myopic in the sense that it weeds out the bullshit that used to bother you and expansive by lowering the fence on what you can accomplish. Things I thought I could not do before are doable. Getting back my health -- my strength and building upon that will be key. I've staged mini-milestones (in three phases) for myself for the next six months. Of course, the milestones need to be flexible because I don't know how my body will react to my last set chemotherapy. I believe I've built enough of a cushion before the second phase. The skeleton plan so far makes me feel good of what I can do to get ready to shape the future life I will lead. There is no word beatific enough for me to describe how I've imagined that life will be.

Kisses,
Sarah xo
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Friday, April 23, 2010

Love Infusion No. 3

Knowing that a chemo day was not going to be easy for once didn't make me feel any better. I've known intuitively for weeks it was to be so. With the knowing, I made sure to be up early or my 5am regular time. By the time Tawny's husband Jeff came to accompany me to the cancer center, I had eaten before 6am, but I had waffles, bacon and coffee ready for him at 7:30am. Lunch would be a long way.

I drove us and checked in to have my blood drawn and as usual my port would not give up any precious drop. My right arm was stuck with a needle and another 1" Huber for my port plus a cocktail to loosen up whatever was making it not work for the draw. It would be in preparation for my infusion later. We made our way around the corner to pick up a refill for after chemo meds before walking a full length back to see my surgeon.

My appointment with my surgeon ended up an hour later. He was never that late. I surmised that later when I was told why my infusion was later, too, due to a machine being down for one of my blood tests (which had to be done manually!) that was the cause and he ended up seeing me anyway. This time he had a medical student interview me before she came to get him so she could perform a private exam in his presence. He seemed pleased of my progress and we talked about the issues with my port which he says is not uncommon and attributed my chest pain from recovering from the surgery, etc. We also discussed my wound and gave me another alternative to care for it so I could start fully exercising my lower body.

During all this time, Jeff was able to log into work in the waiting room thanks to the wifi at the center and he was able to find an outlet when his laptop battery was getting low. He didn't end up burning a vacation or sick day thanks to the access. I was happy he had something to occupy himself and a means to IM Tawny and others.

While we waited to be called for my infusion appointment on the 4th floor, I noticed a man in the midst of a complicated cross stitch work. I must admit I was sexist and thought him a gay man at first. Something compelled me to introduce myself and ask if I could snap a pic for my blog to show how others were coping with their chemotherapy and cancer in general.

Here is Dave with his amazing Victorian houses:



Dave ended up a great guy to talk to before we were called in. Jeff was in the corner logged into work and plugged into a different outlet. He was close enough to listen to the conversation.

At 55, Dave was a special case with three different types of cancers; needless to say, he was on a special team. The one cancer has him carrying an ostomy bag that with a permanent marker, he drew a smiley face and words below it that says, "Shit Happens" which caused the nurses and doctor to laugh today when they examined him. He has to go through radiation and chemotherapy, but will get to keep his full head of hair. Lucky duck!

I liked Dave. He talked about his wife and how they use to own a bed and breakfast in St. Petersburg, about an hour away. Dave got his start doing needlework 16+ years ago to pass time away on a ship that transports to the oil rigs in the Gulf of Mexico. In fact, the rig that just blew up was a sister rig to the one he went to before his health issues. He has other needlework projects waiting for him and takes pride in his progress.

We agreed on our approach to cancer -- lots of humor! He said he sat on our side of the waiting room because the other side was filled with "doe in the headlights" type of people. I decided then and there that our side was where the "cool kids were sitting". Yeah!

My little angel Serina took time out from her research schedule to come to sit a while before she took our lunch order. My lunch was a tortilla wrap filled with ham, brie, and apples while Jeff had a zesty buffalo chicken wrap. I was thankfully able to eat mine right before the Benadryl drip took me to sleep. Maybe I woke up twice? I know I woke up when my bladder decided it needed to be emptied. Jeff was not in sight. I figured he was in the waiting room logged into his laptop. When I returned, he was waiting for me. Serina came again -- it was about 4-ish and she stayed a while before she had to pick up pretty dog Belle from doggie daycare. Kimmee was out of town and she was helping care for the pooch.

My last bag of chemicals was completed around 5:45pm making my stay at the hospital almost nine hours. It was a little rough but went quick. I felt groggier and slower than the last time. Jeff was a good cookie and continued to carry my extra bag. Before we left the elevator well on the bottom floor, I could have sworn I saw a red heart sprinkle. How could it have traveled that far from the other building and still exist from mid-January was my first thought? I backtracked. Jeff did too when I told him what I thought I saw. We found nothing. Jeff said it was meant for me only. I smiled at the phantom image. Perhaps a soul letting me know something -- giving me a soul kiss to cheer me?

I asked Jeff to make one stop at a fast food place so I could get a salad for dinner. There was no point in me trying to make dinner for myself as tired as I was this time. Jeff had dinner waiting for him at home with his family. I was grateful he lasted all day. Three more chemotherapy cocktails or "happy hours" to go, my lovelies...

Love,
Sarah Sprinkles xxoo
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Tuesday, April 06, 2010

Better Yet Fuzzy

I debated about posting today. Thanks to a couple of hours yawning in front of me, I will.

There was nothing earth shattering today. I woke up a few minutes before my 4:30am alarm. I was more than ready when Jeff and Tawny came around 6:30am. What I was not prepared for was how empty my office was at 7:06am. I had to use my badge to get past the 8th floor reception and walk around semi-dark halls. I could have sworn I heard crickets!

Lights flooded my floor within 30 minutes. By this time, I was about to get my second cup of coffee to wake-up. My meds from last night were still in effect. I would do anything today to facilitate flushing the last effects as well as chemo working through my system.

My work today was more focused on easy ended tasks which was a great way to get back into the swing of things. Projects that I was involved with were put back in my lap. I will have to devote the next several days to learning our new accounting system since it has been months since I first touched it. My buddy Bridget will be training me.

My return to work will allow for my other team members to feel that they can start taking time off since they've had self-imposed moratorium on time off. Next week, my boss' kids' have Spring Break as do Bridget's son. My boss will be off all week while Bridget will take Thursday, Friday and the following Monday off. All this means is that I need to get up to speed. My chemo brain should be much cleared for new learning and handling things starting tomorrow. I am anxious to be a solid and productive member of my team again.

If it were not for the brain fog, I think today would have felt like normal. People were still coming around and that's how I know it is not quite normal. I have to learn not to be so hard on myself. My journey to wellness is a big deal and will take time. Living with it, at least in my case, makes it seem less. It is my attitude and the immense love and support I've received that have made it easier to bear each day.

Jeff retrieved me at 3pm and I was definitely ready to go. It was another early day and because I didn't take a nap after getting home, this day seems a lot longer. I just have to take a shower and head for bed. Three hours more until bedtime. Yawn.
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Monday, March 29, 2010

A Cut Above

I couldn't remember the last time I left my house without brushing my hair. Seeing the clumps of hair clinging to the brush so easily was becoming more annoying than traumatic so I didn't brush it at all. I hid my head under my cap again before leaving the house.

Jeff and I made our way to the cancer center pharmacist first to drop off my refills for after chemo on Friday. We then went to the floor below to the salon for my shave. I didn't feel sad and I didn't give any tears. There was only a sense of surreal about the whole process. My scalp was tender and that's what I concentrated on.

The salon hairdresser offered to turn the chair so I wouldn't have to see the process but what was the point? I would have to see my bald head eventually. Seeing half my head shaved was weird. The razor could be felt buzzing around my head and I could feel it being moved around. My only thought was that it wasn't me -- it wasn't happening to me but to someone else.

Jeff said it was hard to watch the shave though he knew it was for the best. He agreed to video the floor and the back of my head so I could get snapshots for my blog. Oh -- Serina, Kimmee's daughter came to see me and give support during the whole process. With Jeff, Serina and the salon hairdresser, I was able to get a consensus on how the wig looked after it was styled.

Hair on floor:


Deed done:


My new wig is not me -- I am growing to like it. The following shot is awkward, but I wanted to show you the cut. The bangs came with the wig and were cut further so the whole thing wasn't straight across and some of the long strands in the front were cut more to the shape of my face. Had I kept it, the look would've look harsh. Jeff said the hair make me look shy?? I think that is what he said.



For being there for me, I took Jeff out for lunch and then he accompanied me to the grocery shopping I have been wanting to do for a whole week. I spent $150 but saved $41. My coffers were almost bare and I needed to make sure I have food on hand especially since I will be recovering from my second chemo next week as I try to assimilate back to work.

I took Jeff back home after he helped me carry groceries. There was another errand I needed to complete so I did that while I had my wig on. My wig was replaced with a snood later, but on me it looks an oversized beret with my big head. I am not comfortable yet going without any head covering at home. Seeing my head bare again didn't produce any tears. I was pleasantly surprised that my head shape was actually not bad. My head was not shaved to the skin. It is more like a 5 o'clock shadow which will soon fall out. The scalp is still tender and I was told the sensation will go away.

The shave is done. We can all breathe again. Thanks for all your support through messages on facebook, texts on my phone, e-mails and comments on my blog. All of it helped me get through this difficult stage of my cancer cure. xxo

Love,
Sarah
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