A long few days………………

Last Friday I was up bright and early, 0500 hours, in order to see the Police Surgeon.  He asked when I was due to finish chemo (around 6 weeks) and asked if I’d be ready to be placed on limited duty at that time.  I said it depended on when I was getting my reconstructive surgery.  If I was getting the surgery soon after I finish chemo, then I couldn’t go right back to work.  If I have to wait a few months for my skin to heal, then I could go back to work (at least until surgery).  The Police Surgeon also went over the blood tests, pulmonary (lung) function test, and EKG I had done a week prior for the NYPD World Trade Center follow-up.  My bad cholesterol is a little high, though my good cholesterol is OK.  This change started after the chemo so hopefully it will get back to normal once I am finished.  My calcium levels were also slightly high.  This may also be chemo connected.  We will see.  My EKG was fine.  No problems with the ticker!  My Pulmonary Function test- Not so good, only 81%.  Normal is 100%.  I’ve got to get back to working out and singing.  Hopefully it doesn’t get any worse.  Everyone needs to breathe!  I guess the thrice daily Xopenex nebulizer and once daily Singulair aren’t doing the trick.

I had a lovely weekend with two of my sisters, the default sister and Liz.  We had nice dinners, did cool crossword puzzles (the family joules!!), great conversation (LOL), and bluegrass.  I also realized that reading glasses are in my near future.  I could do without the muscle cramps in my left calf, ankle, and foot, while lying in bed.  The pain was so bad, I was in tears.  That lasted 3 nights in a row!  On Sunday, I went to an afternoon wedding with Gillian and she wore the “Freshman Formal” dress (shake your booty baby).  I wore a nice purple dress with a silver shrug.  I tried to use the expander that Dr. W filled for me to even out my appearance, but the bra was uncomfortable & I could see the expander. I went to the wedding one-breasted.  Oh, and I wore the Chicago wig with long earrings.  About halfway through the reception, the wig came off and the cool hat went on.  I talked to a bunch of friends and had a good time. Everyone asked how I was feeling…….can you guess?  BUT I LOOK GOOD.  (I took it as a compliment).

On Monday I went to acupuncture.  I was stuck with even more needles than ever before.  I looked like a human pin cushion.  I picked up a black dress for Gillian for her chorus concert and an ice cream cake for Gillian’s 15th birthday, which was also Monday.  We sang Happy Birthday and ate cake.  Christian kept trying to steal everyone’s “crunchies”.  The kid is addicted.  I then spent a couple hours listing magazines for sale on Amazon, while watching Dancing With The Stars (Kelly and Derek’s freestyle dance was amazing!).   I still have a bunch of magazines and books to list.  We are cleaning house.  Getting rid of things we no longer need.  Our sons will both be in college in the fall and college isn’t cheap, neither is breast cancer.  I plan to donate some of the proceeds to breast cancer charities.    I also watched the news about the devastating tornado in Oklahoma and said a prayer for the victims.

Tuesday was tough.  I woke up early to go to the High School for the Scholar Athlete Breakfast. During breakfast I spoke with some of the other parents (I didn’t talk with my mouth full mom nor did I chew with my mouth open.  Mom, you taught me well).   The Crew Team along with a number of sports teams were recognized for the academic achievements of the athletes. On the way home, I stopped at the soon to be closed King’s Elementary School to vote for the school budget (higher taxes).  Then Charles and I headed to my chemo appointment.  (Xavier had to go to body shops to get estimates for one of our cars.  It was struck in a parking lot).  My appointment was for 11:45 and I showed up at 11:45 and checked in.   Dr. D hadn’t arrived yet so I waited.

At about 12 pm I was called in to the exam room by the nurse who took my vitals.  I then waited some more & checked my emails.  Dr. D came in, we started talking, and he received a phone call.  He apologized and stepped out of the exam room.  I played a couple games on my iPad and answered a few texts from Charles.  He was waiting in a chemo cubicle for me with some lunch.  Dr. D came back, examined me and checked my scar.  I am concerned.  On part of the scar, the edges don’t meet.  Dr. D wasn’t too concerned.  He feels the scar is healing from the inside out.  He gave me the OK for chemo and I headed to the chemo area.

I waited for what seemed like a while, eating the harvest grain and Portobello soup, Charles had bought for me.   A nurse came over and asked if the first nurse drew my bloods.  “No”.  She came over and accessed my port.  Flushed the port with saline, and ………………………………………………. she didn’t get blood return.  She hooked me up to a bag of saline and let it run for about 5 minutes, and……………………………. She didn’t get blood return.  She let the bag of saline run through the port for another 5 minutes…..NO BLOOD! She then had me lean over and practically touch my toes (I can), NO BLOOD.  I lay back on the recliner, coughed, and turned my head.  NO BLOOD.  We tried all the tricks and nothing happened.  So, she had to stick me in my left arm to get blood for the CBC. We had to see if my counts were high enough for chemo.  She actually found another vein in the crook of my elbow.  Hooray! She ran some heparin through the port.  The bloods were sent down to the lab.

Charles and I talked while we waited.  My daughter participates in Tae Kwon Do, and she takes dance.  TKD is a sport.  It’s in the Olympics.  Though she is a scholar and has been recognized as such, she isn’t considered a scholar athlete as TKD isn’t a school team or club.  It’s disappointing.  Maybe she can start a team!  We want her to try Crew next year, so she has more opportunities for college.  (On an aside, When I was at the wedding on Sunday, I spoke to a cousin I hadn’t seen in a while.  His teens are home schooled  but even though my cousin and his wife pay school taxes, his kids aren’t allowed to participate on their local high school sports teams.  I don’t think that is fair as part of the school taxes they pay support athletics.  Just my opinion!)

The labs work came back OK and the procession of IV bags began.  Steroids-15 minutes, Benadryl (we don’t want an allergic reaction)- 15 minutes, and Zantac- 15 minutes, and last but definitely not least…………the Taxotere– over two hours.  During the Benadryl/Zantac run, I fell asleep.  I was awakened so that the nurse could hook up the Taxotere.  I was sleeping on my side and she couldn’t easily make the change in the position I was in.  The heat and drugs were making me tired.  It was over 80 degrees outside and pretty damn hot inside.  The AC wasn’t working.  The nurses were offering the patients ice packs but with my luck, I’d start freezing, so I declined.   I drifted a bit during the Taxotere as well but after I while, I started having hot flashes and gave up on the sleep.  I played ChickCoop, and read for a bit.  When the bag of Taxotere was finally done and the needle removed.  It was 5 pm.  We had spent hours and 15 minutes at the chemo center.  It was my longest chemo of this course of treatment yet.  (I had been hospitalized for 3 days for each of the 6 cycles of chemo, the first time I was diagnosed with breast cancer).  I put my light purple All-Stars back on, went to the bathroom (again), and Charles & I headed home.

I didn’t stay home long though.  Gillian needed to be dropped off at 6:15 pm at the High School for the chorus concert.  Xavier drove.  We dropped Gillian off and headed to Café ala Mode for chocolate chip cookie dough ice cream (Xavier’s treat).  We headed back to the High School and watched a lovely concert.  The kids are so talented and the choir directors are great teachers.  The kids sang beautifully.

We drove home, I had some cereal, did the dishes, and watched most of the Dancing With the Stars finale.  As it is a chemo night, I am still a little wired though I will try to get some sleep soon.  Tomorrow is another day.  More human pin cushion time and more time to spend with the family and friends.  Though these last few days were long days, they were days I was able to spend with family and friends and watching my children grow and mature.  I am alive and plan to keep on living.  Each day spent with family and friends is a gift.

I love you guys!

Sleep is overrated!  I tried to sleep for a couple hours but couldn’t.  I came back downstairs at around 0420 hours.  I am drinking tea and editing this post.  I’ll try to sleep again in an hour or so.  Happy Birthday Bernard.  Happy Birthday not so little Chris.

Chris at Scholar Athlete Ceremony

Chris at Scholar Athlete Ceremony

Mothers, kids, and chemo!

Once again I am trying to type this on my iPad during chemo, but the iPad keeps wigging out.  Sometimes the keypad works and sometimes not.  Xavier showed me how to use the “talk to type” but there is too much background noise and I am getting some crazy sentences!! Oh well…back to Candy Crush, Chickcoop (Damn it Jackie.  It’s all your fault. LOL), and Words With Friends.  I can’t get anything productive done.

I went down to the city and saw Dr. G last Thursday. He is my main medical oncologist.  (But first a stop at the precinct to see the new CO-but she was out & second, to stop at “Tea and Sympathy” to see my friends, Nicky and Sean, and for a delicious lunch…Scones with clotted cream, salad, and delicious iced tea. . I told Dr. G about the allergic reaction I had to the Taxotere last Monday.  He stated that I will have to get more steroid and Benadryl for future infusions.  He checked all my blood work and examined me.  He said everything looked good and we should keep on with the course of chemo.  My right shoulder, right elbow, and wrist are still hurting.  Apparently I have a lot of scar tissue under my arm.  It must be doing something to a nerve.  I have numbness in my middle finger.  I also have a pain in one spot in my back.  I’ve had it since the double mastectomy.  If you were to draw a line from my scar, around to my back, that’s where the pain would be.  This may also be nerve related.  Damn scar tissue and effected nerves! The pain in my elbow went away for a few days, but came back.  Ugh!

I was supposed to go up to Saratoga Springs for the weekend with Charles and Christian, so mom came up on Friday morning to watch Gillian, so we could head up to Saratoga by 1 or 2 pm.  Christian had a crew tournament, starting very early Saturday morning.  He rows in an 8 man boat.  This is Chris’ first season participating in crew.  He was already one of the faster members of the team.  (I’m so proud!)  However, Gillian had the “freshman formal” Friday night. She seemed a little down Thursday night because she didn’t like the dress she was originally going to wear, so Charles & I decided that  I would stay home and help Gillian get ready.  I had been helping her straighten her hair Thursday evening (a two-hour job at minimum).

Mom accompanied me to Dr. W’s Friday morning.  I arrived at his office wearing the cool hat/long earrings look.  Dr. W smirked and said, Nice Hat!”  I think the man likes busting my chops.  That’s OK, because I give as well as I get.  Dr. W removed the stitches and placed some steri-strips on the scar.  I am hoping the lovely scar doesn’t tear again.  I have been very good about not stretching the area too far.

cool hat/long earrings look

Mom and I went for a nice lunch at “Charlotte’s Tea Room” .  I love that place.  The staff is great.  (The day after my last surgery, they were closed for a private party though I didn’t know this, but they still put together a lunch for me when Charles went over there!) The scones are scrumptious.  Mom and I had the Mary’s grandmother’s secret recipe artichoke pie.  Delicious! Mom and I picked Gillian up from school & took Gillian to get a manicure and pedicure. One hour before she had to be at her friend Matt’s house, we were at “Style Counsel”  and I bought Gillian a dress (the 2nd one she tried on).  We came home, did some finishing touches on her hair and make-up, she got dressed and we left for Matt’s.  We took a couple of pictures and then followed Matt’s mom to the next house, where more pictures were taken.  I was glad that I stayed home with her.  She was very happy and told me so more than once.  (The dress definitely helped).  I was starting to get tired so mom and I headed back home.  I definitely did too much that day.  I put my feet up, iced up my chest, and relaxed.  Gillian got home after 10 pm.  She had a great time. (I knew she would). She said she danced the whole night.

The dressMom and GillianGillian and me

Mom stayed over Friday night.  I was going to go up to Saratoga on Saturday afternoon.   If Chris’ boat made the finals, he would race again on Sunday.  Charles called about 11 am.  Unfortunately Chris’ boat was disqualified for interference (not yielding to a boat that was overtaking them).  I felt really bad for him and his team.  They had been working hard all year for this big race and it ended prematurely.  From what Chris told me later (if this is wrong, I probably mis-remembered again),  that because there were so many boats, there were staggered starts.  There were 4 lanes on the lake, but the rowers were only using the two middle lanes.  If another boat was close behind, they were supposed to steer to one of the outer lanes.  The rowers on Chris’ team were never told to move so the boat coming from behind had to move to the outer lane to avoid a collision.  Because they were disqualified instead of excluded, the crew could not participate in any other races.  They were done for the weekend.  Christian’s team had only participated in one race prior to the NYS finals in Saratoga, because of poor weather and water conditions.  The one race they did participate in, his team came in second place.  Since the weather up in Saratoga Springs was absolutely shitty and Chris wasn’t going to be participating in any other races, Charles said he and Christian were going to leave Saratoga early on Sunday (we had booked the hotel for two nights).  They would be home for Mother’s Day.  Mom went home a couple hours later, after stopping at Gillian and Christian’s dancing school (North East Dance Movement), to pick up tickets to the recital.

Chris at Crew

Chris at Crew

saratoga 2013 016 saratoga 2013 024

After I hung up the phone with Charles, I spent the next 15 minutes looking up the rules for US Rowing  (http://www.usrowing.org) .  I couldn’t find any information regarding who was supposed to move the boat in the situation aboe.  I did find Rule 2-204, Interference or Foul.  It states that the referee is supposed to instruct the offending boat to move, if it has left its own water.  The referee can also use a white flag.  I don’t know if any of this occurred.  I’ve got to talk to Chris again.

Mother’s Day was lovely.  Gillian made me different colored pancakes for breakfast.  I ate the pink and purple pancakes.  I gave Gillian the blue pancake, and Chris ate the yellowish pancake.  Christian bought me lovely flowers.  Gillian and I went to church (where we saw and congratulated her friend Shannon.  Her 4 person crew team came in second place in the novice category at the NYS Finals).  We picked up some flowers at the Mother’s Day plant sale and headed home.  Christian tried to explain the Saratoga fiasco.  He drew me a map of the course, while I worked on trying to get all my medical bills together so I can submit them in order to get money from my Healthcare Flexible Spending Account.  Charles and Christian made a delicious dinner of porterhouse steak, asparagus, corn on the cob, and potatoes.  Way too much food.  I couldn’t finish the steak & I didn’t eat a potato.  Lucky CJ…she got a bone!   I spent some time weeding my garden, but I could do only so much with my right arm bothering me  and dirt getting wedged under the nails of my left hand (and I still haven’t picked up gardening gloves)!

Flowers from Christian

Monday I went to acupuncture again.  I wore yoga pants this time.  So Dr. S put a bunch of needles in my legs in addition to the needles that she puts in my arm, ears, face, and the crapload she puts in my almost bald head.  I am very sensitive.  Every time she put a needle in my head, I got a tingly shock running down my spine.  She covered me with a silver “space” blanket and I relaxed to the soothing music. I then stopped at Kohl’s to return the blender I had purchased.  I discovered a crack in the blender on the day I bought it.  I’m back to using the juicer/blender combo for my smoothies.  It works, there is just more to clean.

On Tuesday I had lunch at my friend Jackie’s house.  I had a great time catching up.  It’s crazy.  We grew up together in Staten Island, both moved off the island and we live within a half hour of each other.  But life is so busy for both of us, that we haven’t seen each other in months.  It’s hard to find time when dealing with all the drama that surrounds a cancer diagnosis.  I see my doctors more than I see my family and friends.  Another of our friends was recently diagnosed with oral cancer.  I would love to go see her, but at this point in time, I can only text her, message her, and I referred  her to a friend who also had oral cancer.  I hope it helps.  When I got home, Charles and Xavier were back from Philadelphia.  It was good to see Xavier. We last saw him on Easter (just for the day).  Gillian and I also took CJ to the vet.  CJ had blood in her urine.  We thought she had a urinary tract infection, the vet agreed and gave us antibiotics to give to CJ.  CJ seems to be doing better.  She stopped peeing in the house (Thank God!)

Today (now yesterday), I had chemotherapy.  Xavier came with me.  The chemo went well.  Dr. D was on vacation so I was examined by Dr. P.  When I told him about my allergic reaction last week, he seemed concerned and was wary about giving me more Taxotere, even after I told him that the Benadryl worked well.  He suggested possibly switching with Abraxane.  I told him that Dr. G wasn’t too concerned when I told him about the allergic reaction, so I gave Dr. P, Dr. G’s cell phone number.  Dr. P left Dr. G a voicemail.  I texted Dr. G as well.  Dr. P went to see if they had any Abraxane on site.  I didn’t want my chemo to be delayed if we were going to go that route.  When he came back, he told me that Abraxane caused increased neuropathy.  Thanks, but No Thanks.  I’ve already got enough neuropathy.  Dr. P told me that he spoke with the nurses and he was more comfortable with the Taxotere.  I would be given the steroid infusion, then  the Benadryl infusion and then a Zantac infusion.  When all that was complete, I would be given the Taxotere over two hours instead of one.  I went back to the chemo area, grabbed a couple packs of Honey Maid Grahams, a Nature Valley granola bar, and a ginger ale, found a cubby and grabbed a recliner, kicked off my All Stars, and waited.  (I don’t know why this paragraph is now italicized and I tried fixing it without success).  
 
Xavier and me

Nurse G came in to the cubicle.  She is one of my favorites!  She got me prepped, and accessed my medi-port.  I tried to keep talking because last week, she was able to get blood from my port without a problem, when I excitedly told my surgery story.  It didn’t work so well this time.  She flushed my port with a few syringes of saline.  She then tried to get blood return.  She got a little blood & then it stopped.  She flushed my port with a few more syringes of saline.  She got blood return & then it stopped.  I went to the waiting room and got Xavier.  He had dropped me off and stopped at the mall to pick up a video game and get a haircut (the mall is very close to the infusion center).  She then tried the saline infusion route.  10 minutes of saline running through my port.  She she came back, she got blood return and was able to fill the vials for my blood tests……I waited for the blood test results.  She started running the steroid and Kytril infusion. Next up was the Benadryl,  followed by the Zantac.  I was then hooked up to the Taxotere.  With all this fluid running through me (along with the ginger ale, hot tea, and iced tea I was drinking), I must have hit the bathroom about five or six times! Xavier and I listened to some music, played some games (Chickcoop, Jackie), and talked.  He told me that he was going to take me to the rest of my chemo appointments to give Dad a break.  Isn’t he wonderful.  I love my kids.  I guess Charles and I did something right. Approximately two hours after the Taxotere started, I was done.  A nurse (not G) came and removed my port, I went to the bathroom..again, then Xavier and I left to head home.

We were going to go from chemo to Greenwood Lake for Christian’s crew race.  But, guess what…..it was canceled because the water was too choppy!  Poor kid can’t catch a break.  Christian wants to take up crew when he goes to SUNY-Maritime and we are hoping that he will have some good showings in some races.  I think his team only has two races left for the season.

Gillian and Christian went to Hip Hop dance class, Gillian taught Tae Kwon Do for an hour as well (NorthEastern Martial Arts),  I did some reading, Xavier went food shopping, Charles and I watched the second episode of the first season of “Dexter” (Hi David!), Gillian and Christian went to bed, Charles went to bed, I worked on this blog (I have a very hard time sleeping on chemo days), Xavier went to bed, and now I am going to try to sleep.  I have to be up in about 1 1/2 hours  because I have to see the Police Department doctor at 7 am.  (I feel like I live at doctor’s offices).

Goodnight!

 (http://teaandsympathynewyork.com),

(http://www.facebook.com/pages/CharlottesTeaRoom/348704950474)‎,

(http://www.stylecounsel.net/),

(http://www.dancendm.com/),

http://nemartialarts.com/website/),

Correction on prior post

My friend Lynda informed me that the quote “It’s better to look good then to feel good” was actually Billy Crystal as “Fernando” from the Saturday Night Live Skit “Fernando’s Hideaway”  and was based on Fernando Lamas.  It had nothing to do with Ricardo Montalban.  I mis-remembered.  Damn chemo brain!!!!!  I stand corrected.  Thanks Lynda!

How are you doing? ….Well you look good!

The drain was removed last Wednesday.  I was laying in the exam room & Dr. W told me to take a deep breathe and another & Fu*k, it hurt when he pulled the drain out of my breast.  He covered the little hole in my side with a band-aid.  I didn’t realize until later that some blood leaked out onto my shirt.  Oh well..just had to pre-treat and the blood came out.  I spoke to the doctor about the different  reconstruction options.  I’ll probably use my own tissue for reconstruction instead of going with an implant, especially after reading that implants aren’t recommended for radiated skin.

I saw Dr. W again yesterday morning because my scar was looking a little red and I noticed fluid under my skin.  Dr. W took a syringe and removed about 25 cc’s of fluid.  I see him this Friday to get the stitches removed.  It seems like a little more fluid has settled under my skin.  The doc thinks the redness was just from the stitches.

My right breast (or lack thereof) looks bizarre.  I still have stitches.  My chest looks sunken and deformed now.  I don’t know if the appearance will get any better.  I will be without a right breast for a minimum of 4 months, probably longer.  It’s weird.  I don’t really like wearing wigs as they are hot, itchy, and I feel that they don’t look natural.  But since I got the tissue expander removed and I am now lopsided, I am wearing my wigs more often.  When it appeared that I still had two breasts, I didn’t mind being bald. I could pretend that everything was OK.  Now, if I don’t wear a jacket (and it’s starting to get warmer), anyone can see that everything is not OK.

sunken chest (pirate's dream)

Prior to my latest surgery, I had a woman ask me why I shaved my head.  She also noted that my daughter had shaved the side of her head.   She thought it was something that we just decided to do as a fashion statement.  She had no idea I was being treated for breast cancer because I didn’t look like I had cancer.  (Though I’m not sure what a cancer patient is supposed to look like). As for my daughter and her “undercut”, my son Xavier and his fraternity brothers from Sigma Alpha Mu, held a fund raiser where they shaved their heads in public to raise money for the American Cancer Society and for Breast Cancer Awareness.  Both Xavier and my other son Christian shaved their heads, as did a number of Xavier’s fraternity brothers.  My husband Charles’ head was already shaved.  Gillian has a head of thick, curly hair.  We weren’t keen on having her shave her whole head, so she had the side of her head shaved.

Xavier head shaveXavierthe undercut

Chris and X head shavesammy head shaveGillian and her crazy hair

What does a cancer patient look like?  There are a number of cancer patients that appear sickly (pale, yellow, gaunt, etc).  But there are also many cancer patients that don’t look “sick”.  We look pretty good.  We aren’t gaunt (contrary to popular thought, most people gain weight on chemo, usually from the steroids given prior to the chemo drugs).  Someone who didn’t know us would have no idea what we were going through.  He or she wouldn’t know that we were going for radiation 5 days a week, or were receiving chemotherapy drugs once a week, once a month, or in some cases, everyday.  Or perhaps we were recovering from another surgery.  Many of our scars are in places that don’t show.  You can’t always see our fatigue or pain.  I know that in my case, I try to do as much as I can.  I guess if I can still run errands, visit friends and family, go to lunch, take the kids to dance or Tae Kwon Do (TKD) , I am not sick.  I am just another mom doing “mom” stuff.  Though I must admit, when I do sleep, I usually sleep late and when I run around doing errands, I tire very easily.  By 5 pm, sometimes earlier, I am done.  I just want to put my feet up, put an ice pack on my chest, and just “veg out”.   I am lucky that my son Christian drives because he has been a godsend.  He usually drives Gillian to dance and TKD.  (Unfortunately I won’t be able to do any TKD for a while.  As per Dr. W, I can use a stationary bike.  He doesn’t want me to do any exercises that will involve my chest muscles).

“How are you doing?”  How do I answer that question?  I usually say “OK” or “fine”.  I don’t think people want to hear, “Actually, I feel like shit today”, on those days that I feel especially crappy or “craptastic”, crappy and fantastic, as my niece Julia would say.  The “craptastic” days are usually chemo days and sometimes a day or two after.  I can usually tell my family and close friends how I really feel, but not my acquaintances.  There have been times when I’ve said, “I’m feeling like crap today,” and invariably the response is, “Well you look good!”  Every time I hear that response I think of Ricardo Montalban from “Fantasy Island” and I remember a line from a commercial?? where he said, “It’s better to look good than to feel good.”  It’s usually the reply that I give, though I can’t say I totally agree with that statement.  I’d like to look good AND feel good.  Why can’t I have both!  (I’ve been advised it was actually Billy Crystal on SNL.  See next post)

Yesterday was definitely a “craptastic” day.  First I saw Dr. W and he removed the fluid from my deflated breast.  I went home, tried to straighten up a bit and work on this post.  Unfortunately I couldn’t get the words to flow from my brain to my fingers! Charles and I then went to my chemo appointment.  I waited a bit, took care of some billing issues, waited a bit more, and the nurse finally called me into the exam room.  She took my vitals.  I actually lost about 4 pounds (woo hoo!), probably from the combination of no chemo for two weeks and the fact that I started juicing/ or drinking a healthy greenish smoothie for one meal a day.  (I usually juice beets, cucumbers, celery, kale, apple, lemon, and ginger and my smoothies have all of those ingredients plus unsweetened almond milk, flax seed, vanilla protein powder and/or vanilla yogurt.  I am drinking a smoothie as I type).  She didn’t realize that I was supposed to have chemo so she had to check with the doctor and make sure there was a space for me in the chemo area.  I waited…Dr. D finally came into the room and apologized for the delay.  He checked my lungs, my stitches, and said that I was starting cycle 5 (of 6 cycles of chemo).  I noted that I hadn’t finished all three weeks of cycle 4 because of the infection and surgery.  His response, “We don’t know how much chemo you actually need or if you need anymore chemo.  If you are a religious person, God doesn’t come down and tell us how much chemo you should be given.  You had a local recurrence.  No tests have shown cancer anywhere else.  This is cycle 5.”  That was cool with me.  I was afraid chemo was going to last through the whole summer at the rate I was going.

I make my way back to the chemo area and find my husband waiting for me in a cubicle with a nice sandwich.  I grabbed a few Honey Maid graham crackers and a ginger ale from the snack area (these are  my usual chemo staples).  I sat in the recliner, and I waited and ate half of my sandwich.  Nurse G came in with a new hire and started to access my port (sticking the big needle in).  As I mentioned in previous posts, it is usually quite a process to get blood return from my port.  As I was telling Nurse G the story of my surgery and explaining to the new nurse the  problems with my finicky port, Nurse G accessed my port and shock of shocks, she got blood!!!!! No lying down, turning my head, coughing a lot, or having a 7 minute saline flush going through my port to get blood return.  I guess all I have to do is excitedly tell a story! I’ll try that next week.

I didn’t have to wait for my blood counts to come back since I hadn’t had chemo in a few weeks so Nurse G hooked up the IV with the Kytril (anti-nausea medication) and the steroid.  When that bag was finished, she came back with another nurse and my bag of Taxotere.  “What’s your name?  What’s your date of birth?”  The Taxotere bag was hooked up and was supposed to run for an hour.  About 20 minutes in, I was eating a graham cracker and I had to stop, my throat felt weird and I started getting real itchy on my upper body and head.  Off went the Taxotere bag and on went the Benadryl.  I got real woozy and I passed out for a little while.  Then I started getting tingling in my lower legs and feet.  Off went my light purple Converse All Stars and off went my socks.  The itchiness went away though!  When the Benadryl bag finished, the saline bag was started.  When the saline bag finished, back went the Taxotere bag.  However, the remainder of the Taxotere was run through the IV at a slower rate than before.  I didn’t have another allergic reaction.  When the Taxotere back finished, Nurse G came back and removed the needle from my port, slapped on some gauze and tape and Charles and I headed home.

Before all the itchiness started, I was working on my iPad trying to finish this post.  I don’t know what I was doing wrong, but when the keypad came up on the iPad, I wasn’t able to type anything.  If anyone can give me pointers on how to edit a blog with an iPad, I’m open to suggestions.  Charles was using my laptop to watch a movie, Crank 2.  He was laughing so hard that I wasn’t going to ask for my laptop just so I could work on my blog.

I don’t know if it was the after effects of the Benadryl but I was pooped when we got home.  I brought our dog CJ outside in the front yard and lay down on the hammock on our front porch.  I couldn’t sleep though because my legs were still all tingly and I was nauseous!   I was exhausted and I couldn’t sleep.  Argh! Damn steroids and damn Benadryl and damn damn nausea. I took my Zofran and Compazine but they didn’t really help.   I was up most of the night as well.  I tried to sleep but couldn’t.  I went downstairs around 1 am and ate some toast and crackers.  I had a cup of tea.  I read some “Sookie Stackhouse” on my iPad.  I went back upstairs to bed.  I tossed and turned.  I finally gave up trying to sleep at round 4 am.  I went downstairs and had some mango sorbet.  I should have tried that earlier.  It actually calmed my stomach.  (Either that or the anti-nausea drugs finally kicked in).  I read more “Sookie Stackhouse” on my phone.  Around 5:15 am, Charles, Christian and Gillian came downstairs.  The kids got ready for school.  I fell asleep on the couch around 6:30 and woke up to a veggie omelet from Charles at about 9:30 am.  There was to be no more sleep after that.  An 11:30 am appointment with Dr. F (my regular surgeon).  I told him about my blog and about the woman who thought I shaved my head as a fashion statement, and what did he say, “Well..you really do look good! Some women shave their heads as a fashion statement.  You look good bald and unlike me, your hair will grow back.”

Dr. F made me feel so good that I took my bandanna off and spent the rest of today running errands bald (wearing long earrings of course).   I had to stop at the bank.  I had a 1 pm appointment with the acupuncturist (I’m not sure if it is working yet, but I have only been to her around 8 times and my sinuses seem better).  I then went to return some cans and plastic bottles, got gas for my car, and stopped at Kohls to get a juicing blender.  I got home and made a smoothie  (realized that the new blender had a crack in it), brought the dog outside, sat on the porch and started typing until the mosquitoes started attacking.  I am now inside on my recliner,with my feet up, finishing up this post.  I am done.  Exhaustion has set in……….But I look good.

me and my hoodylong earrings, bald head

Xavier