Tag Archives: expanders

Making a Difference & Feeling Fortunate

“This is a part of me now.  Even without religion, this would be my religion”

Tomorrow morning we will meet the oncologist and hopefully get all our questions out of the way.  What is our score?  What does that mean?  What choices are there?  What are the risks?  What are the side effects?  How will that effect my/our lifestyle?  Blah! Blah! Blah!

My wife the eternal list maker has worked on a total of 4 pages of questions.  When she passed the list to me I could only smile.  She had the energy to create one of her famous “lists”.  Also on the list was, “Will it change my relationship with my husband?”  I told her to scratch it as I could answer that for her.  The answer is “yes”.  “Yes that it already has changed our love.  It has put it under a microscope and magnified it for us to inspect and see that it is okay.  It has shown us that we have enough love to go around”.

I know that it wasn’t “that kind of love” she was talking about, but I wanted her to know that the side effects weren’t going to change anything about how I feel and shouldn’t be a reason to change her decision.

Still uncomfortable, she calls her expanders a bullet proof vest or a chastity bra.  Humor has come out of her that I’ve never seen before.  Calling herself the Bionic Woman..”We can rebuild her…stronger, faster…” and wondering where she might be able to find those Gauthier cone bras that Madonna wore in the 90s are all ways of her making light of the uncomfortable feeling she has on her chest.  I know it is her way of coping.  I think she didn’t want to watch the chemo / hormone therapy tape last night because she purposely wanted me to just tell it like it is.  That tape was like a movie both of us dreaded watching, but was a real thinking video which made us realize how much thought we/she is/are going to have to put into the treatment plan.

Chemo would be a drag.  She has gotten almost all of her energy back and her desire to take back some of the responsibilities that I had taken over are there.  The chemo would seriously be a setback so we’ll see tomorrow.  All signs point to no chemo, but I think we’ll breathe an even heavier sigh once that option comes out of the mouth of her oncologist.

Tonight she got a call from her OB/GYN, the one who discovered the cancer.  This is what medicine used to be.  Your doctor calling to see how you are doing out of the blue.  It had been a while and since my wife self-referred herself to a different medical group for surgery and oncology, she hadn’t been as visible to everything as she normally would have.  She is getting her records which is a good thing as we wanted to make sure that she knew where my wife was in the process.

The call made my wife smile as did the email from her old colleague who has been seeing the same oncologist ,that she will be going to, for the last 3 years.  Her colleague said that she lived quietly with cancer for the last 3 years and was now just ready to let it out.  She wanted to share her story like everyone else as long as she could affect or convince someone else to go get tested.  My wife said she also saw a special today on Robin Roberts in honor of Breast Cancer Awareness month and she too said it was time to make a difference.  My wife said she wants to make a difference and she is going to figure how at work, at home, and in the community.  She said cancer prevention and detection is her belief and even if she didn’t have a religion, fighting cancer would be it.

Amen.

Think , Laugh & Cry – A Loving Fight against Breast Cancer

“Don’t forget to think, laugh and cry everyday.”

 

(note, wrote this on the way down to LA this morning).

 

Those famous words from Jim Valvano came to mind as I watched Oprah’s episode with Christina Applegate and breast cancer last night.  I cried not just for our situation, not just for Christina, but for all people suffering from any kind of cancer.

 

Today as I make (made) one of my day-long trips down to Hollywood for business, I just find myself wrapped in thought and emotion.  This is a trip I was supposed to make weeks ago, but everyone delayed the meeting mostly because I couldn’t make it because of my wife’s surgery.  Short plane rides, showers and bathroom stalls are just some of those places where time stands still and all my emotions come flooding in.  Sitting on a plane and just starting to cry is a weird thing.  I think of those times with my dad in the hospital, then my mom in the hospital and now with my wife’s visits to the hospital and think how lucky I am to still have two of those three people left in my life.

 

This morning was the first day I ever recall walking as a family to school.  You see it on TV where the family unit of four walks to school together down a tree-lined street.  We held hands said hello to other kids and parents we met.  It felt so normal.  We kissed our kids, sending them off with a hearty “Take care of your body” and my wife and I walked back to our car holding hands.  We never hold hands.  Is this the new us?  I don’t know if we can do that forever, but it sure felt nice.

 

Although I’ll be back tonight, I am still concerned for my wife, wanting to make sure she is okay.  She promised that she’d take it easy as long as I made sure to immerse myself back in my work and stop worrying just a little.  I can try that.  I reminded her that I just have a whole new appreciation for how much it means for her to still be with me.

 

One of the movies showing on the plane in October is “The Bucket List” starring Morgan Freeman and Jack Nicholson.  It’s about two guys with terminal cancer who have a list of things to do before they “kick the bucket”.  We wanted to see that movie before she was diagnosed.  I think we need a good laugh now and will watch it this weekend.  We might also find it inspiring.

 

Yes, definitely doing a little laughing, thinking and crying today.  It does feel good to let those emotions out. It feels real human.  The words my wife took from Oprah’s show with Christina Applegate were those words that Melissa Etheridge gave her, “This is a blessing and you now can live your life the way you want to”  or something like that.  Well blessing isn’t really the right word here.  A wake up call?  Maybe that is it.  We had definitely started doing that and my wife was onboard with that mentality, but we had forgotten it.  She told me this morning before I left, ” I need to put the past behind and start living.”

 

Amen

Back to our regularly scheduled programming? Well almost.

“You’re not quite ready to be a full time soccer mom.”

Weekend number 3 after surgery and we started to try to get back to something normal.  Soccer season with two games across at the same time required logistical gymnastics.  Another mom drove her and our daughter to the game.  She never watches but I made her promise me that she’d stay in the car and watch the game or at least watch the whole game and not take her eye off the ball if she stood on the sideline.  I reminded her that a kid or ball running into her would not be good and that she wasn’t quite ready to be a full time soccer mom.  Of course she didn’t listen, stood on the sideline, and according to our daughter, took a ball in the hip.  Yikes!

The next day was a cousin’s wedding reception.  We have lots of older sick relatives so we hadn’t told them anything.  It was a crowded restaurant with very little wiggle room so my son and I played like offensive linemen protecting her from any blind-sided impact or overzealous hugging relatives.  Somehow we made it through the 3-hour ordeal with her being totally exhausted but happy to get out of the house.  She also had the chance to talk to a cousin and a couple of aunts who had had breast cancer.  They consoled her and reassured her that all would be well.  Their stories were all different.  My cousin had the same surgery my wife did.  One aunt had a lumpectomy and had to go back for a bilateral mastectomy.  Another had a mastectomy and reconstruction on one side.  At one point the 3 of them and my mother all took a photo together with the bride.  I alone shed a tear thinking how these 4 women all indirectly related by marriage were impacted by cancer and were sisters in a community of women who have been through a lot.  There were no shared genes.  All connected by marriage and a similar disease and very bright smiles.  I don’t think they even realized the circumstances of who was in that photo.

My wife did say that the pain was lesser and that she only seemed to be pained later in the afternoon.  She really looks great and I know part of it is her always positive style which I told her she needed to put away sometimes.  While it is good to look great so everyone can feel good for her, there might still be some tough times ahead and she might have to let everyone understand that.  We still won’t know her possible chemo plan for another week.

The week is starting off okay.  I’m still taking the kids to school and she is now picking the kids up.  I think the kids really feel better knowing mom is okay enough to pick them up and play chauffeur again.  I have to remind them to take it easy on her though.  Her mobility is good and we don’t have any visits to the PS this week so it is just a good week to get things done.  The hard part for me is to get back to work and keep my concentration.  I do worry and call just to make sure she is okay.  Letting go is going to be a hard one for me as I will not feel comfortable until she has fully regained her strength and we feel like we can truly begin the healing process.

It is hard to believe it has only been two months since her diagnosis.  It seems like forever.  And we still have a litle longer to go.

Alright a Deep Breath and onto the Next Hurdle – A Loving Fight

“We’re in a good place but let’s keep on our toes”

And off she goes….I think my wife really is a new woman.  Although she has pain and deep discomfort from her expanders, her first full day without drains seemed to go without a hitch.  Although I still made breakfast and drove the kids to school, she had energy to go for a walk with our Principal’s wife, entertain my mother and sister who came by to check on her at lunch, and drive the mile to our kid’s school, read to our son’s 3rd grade class, and then make it home.  While still in discomfort, she said her energy level was more than back and all the exercise she had done to get in shape before surgery was a big help.

I sat at work worried and checking in on her.  I thought it was too much and stood at the ready in case she needed me.  I married a stubborn fighter.  She’s still soft inside, but she’ll fight when she needs to.  I reminded her that although she is feeling good today, the road is still long and we have some uphill painful battles yet to climb and we needed to keep on her toes.  That did it, I stepped over the line.  I needed to let her enjoy the moment.  Don’t rain on her parade, you fool!

The expanders though are our next hurdle and from what i’ve read the more they get filled the worse the pain  will get.  So although she says she doesn’t need me to take her there, I think I will just be there anyway to take her home just in case.  Funny we were so focused on the drains and then now our attention is on the expanders, the schedule for exchange and lastly the looming possibility of chemo.  It really is one step at a time.  While we are aware of each potential situation my word of advice is to cross the bridge when we get to it.  I think our physicians are amused by my wife’s lists.  My wife’s lists are famous in our house.  I don’t think there is a thing my wife won’t list.  I think our list of questions though will change from previous visits now that the drains are behind us.

Today she took her first shower and re-bandaged herself  Like many said it would, it felt good just tor un water all over her.  I think we’re going to have a water shortage here in California after that marathon shower.

One other note.  Sadly, someone out there on a message board thought it was “weird” that as a husband I was being an active information gatherer and was bothered by my being an active participant in my wife’s fight against cancer.  It really angered me and when I mentioned it to my wife, she gave me this big hug and assured me that many people don’t know what it means to have great support.  She’s right but I also think it is a sad state that someone would feel that there is some kind of perverted research that I am doing.  We’re talking about someone I love deeply and there is no end to what I would do to find out what I could do to help her.  I also feel saddened but understand that there are many out there who can’t feel open about what they share.

I also think she thinks it is weird mostly because I am a guy asking the questions as opposed to another woman . Many women ask questions but when a guy asks the questions she got scared.  This is sad because I think husbands need to be more active and help their wives through this.  The day will come when I will be in the hospital and I will need all of my wife’s support and I sure hope she can do for me what I did have been able to do for her.  People!  Cancer does not discriminate! Black, white, young, old, men, women, children….we need to fight the cancer, not the people!

Celebrate the Drains are Gone – 15 days post-Breast Cancer surgery

“Take Care of Your Body means Have a Nice Day”

And on the 15th day, we all sighed relief.  This morning we went into the hospital and had the drains removed.  They used Hurri-Caine spray to numb the area.  The nurse told my wife to breath deeply and as she breathed out the nurse pulled the drains.  First the right and then the troublesome left.  They were 6 inches in length each inside her and resembled long flat extension cords with little holes that the blood entered.  OIn the left side we saw that they were clogged and thus why we had leakage.

My wife said it truly is a relief.  She already seems like a new woman.  The laughing and giggling have started again.  She is still feeling small soreness and discomfort, but when asked to gauge her pain from a 1-10 (high), she said it was a 1.  This afternoon we took the first big step.  I had her drive to our kid’s school and back to pick up our son. She did it like an old lday with some soreness, but it made me feel good that she was able to accomplish this on her own. 

Ironically we ran into her surgeon at Starbucks on our way to the school.  She was surprised to see us out of context and glad to hear we were driving again.  “Just stay off the highways” she said.  Those in our neighborhood including the Principal’s wife were surprised and happy to see my wife behind the wheel again.  In fact, we are feeling guilty about all the meas we are still getting from our wonderful class parents.  I found that the other family which lost their mother to cancer is also getting meals prepared by the other families in our school.  How wonderfully blessed we are to be in such a wonderful community.

One of the funny things we all do is pick up the quirks of our parents and pass them on.  As my father was a physician and worked for the Department of Public Health in San Francisco during the height of the AIDs epidemic he used to always write notes and messages to us in our lunch boxes, birthday cards, etc.  They never said, “Have a Nice Day” or “We Love you”, or anything like that.  They always said, “Take Care of Your body”.  These notes continued onto college and even when ending a phone call. It was like the show “Hill St. Blues where the captain would say, “Hey…Let’s Be careful Out There”.

Dring my dad’s final months, we lived with him and I’m fortunate my children really got to know their grandfather.  One of the things they picked up was his silly phrase.  In honor of him we continue that phrase every morning.  The other day as I kissed my daughter and she ran off to class, she yelled “Take care of your body Daddy!”  A teacher heard the exchange and laughed.  I could only shrug my shoulders and smile.  The phrase was still embarrassing, yet so very important to our family.

As i mentioned, our life is one long race over hurdles and so linear that we just focus on the next task.  The next task is to deal with the expanders and the discomfort that will come as the expander pushes on the chest muscle over the next 2-3 weeks.

Tomorrow she beigns to spread her wings.

Stand Up 2 Cancer (4 days to go) – Final meeting with Reconstruction Surgeon

“Be your own miracle”

– From “Stand Up” by Beyonce Knowles

Four days to go and the reminders seem to be all around us.  There were women walking in all shades of pink around the city in their Walk against Breast Cancer.  Our daughter asked why mommy was waiving at them,  “Because I am one of them and they are walking for me”, she said.  Then tonight was a major event for the organization Standup2cancer.org.   I think it was a landmark event.  It took just an hour but it was a fundraiser to bring ALL cancer research together.  Some crazy stats:

  • Cancer takes so many forms and one person in America dies from cancer every minute.  
  • Every other person in this world will have some form of cancer 
  • 500,000 Americans will die of cancer this year (1500 each day)

I actually watched the show alone as it was uplifting to the point of shedding a tear.  My wife is going through so many emotions right now we agreed to Tivo it and let her just watch it after the surgery.

I also didn’t go with my wife to her last meeting with the reconstruction surgeon.  I just thought it better that she ask her own questions and give her my questions on paper (of course she didn’t ask them).  I mostly worried about her balance and how steady she might be although I know most people are walking around the next day.  He had some good recommendations about relieving the pain and making sure not to let the drains hang too low as that is why they are painful.  He said that ticket holders (hey my profession comes in handy) are great to put them in  so they don’t pull on your skin.  He also said that the tissue expanders aren’t as painful as some people think.   It was a relatively short meeting so I think it came out okay.  My wife had a few other personal questions about the recovery but the doctor seems to have given her all the right answers or at least the ones she wanted to hear.  He told her that most of his work would be done two weeks after the surgery and just to watch under the bandages for any swelling or infections (redness).

At the end of the day we are exhausted once again, but it always is nice to catch up.  It has become our daily ritual to check in with each other and see where we are mentally.  She’s still a bit anxious, but more anxious to get this cancer out of her body and move on.  Me, I feel like I’ve been managing the emotions of two people and she knows that.  I told her that I’d rather be on the table next Tuesday unconscious because I don’t think I can spend 5 hours waiting around.  I’ll need to buy a new pair of running shoes.