Why I Run

An old friend wrote to me today and said that my running was an inspiration to her and she was going to get out there and just do it.  Since I have run out of time and must write my daily blog, below is an essay I wrote a year before I was diagnosed and explains why I love to run.  Hopefully it will inspire my old and new friends to get out there:

Upon turning 40, I did two things.  I started writing and I signed myself up to do a sprint triathlon.  Two accomplishments I had always wanted to obtain. Two goals to take my mind off the inevitable march of time; one to tune my mind, the other to tune my body.  Training for the triathlon was daunting. I knew I could bike, this I have done all my life.  The swimming was something I had to contend with and I am still, 3 triathlons later, trying to master.  Running, I hated. For many reasons, one is a bladder control issue that after 3 children just, as they say, “happens” to some women. I had tried in years past to run instead of going to the gym. Usually after my husband complained of the fees I was paying to go work out.  But running never lasted. 

 

Oddly enough, 3 years later, I have become a runner.  I love to run. It’s free and quick. It allows me to eat cookies –lots of cookies, guilt free. What started as a bet to myself, a challenge to say I did it, has turned into an obsession. When I run, I reflect.  I ponder all the problems that have started to become overwhelming. Most days, I walk a tightrope of sanity. Running is the Velcro that secures my sneakers to that rope. It helps me avoid the tumble into the abyss of insecurity and paranoia that waits to swallow me. While I run, my head gets cleared of all the negative thoughts about my friends and my family.  It allows me the time alone with my feelings to understand that life can be hard but that there is so much to appreciate as well.

 

With each step, I replay the fight I had with my 12 year old son.  I scroll through it in my head like a movie scene editor and realize that maybe I was overreacting to the situation.  I make a mental note to apologize when he gets home from school.   

As I jog by a broken down brown 2-family for sale,  I imagine that my husband and I buy the duplex and live side by side as amicable divorcees. That way the kids could see us both all the time.  On some days, while I lope along, I piece together the particulars of a friendly separation with visitation, and on others I imagine my husband and I together through retirement and old age.

 

My mind turns to a fight I had with my friend yesterday. It was a trivial matter we fought about, but there was definitely some underlying tension. Or am I being paranoid?  I try to understand why we are not connecting these days. I decide to call her later and ask her to the movies.  As my thighs start to burn and the sweat begins to collect at the base of my neck, I turn up my I-pod and sprint along the straightaway of Summer Ave.  A beautifully wide, tree-lined street with large Victorians that rest far back on meticulously cut lawns.

 

 

 Some days as I run through the streets of my suburban town, I list my blessings, as my mother always tells me to do.  I have 3 beautiful and healthy children, a house, a family, some truly supportive friends, and my own health, which without; would make running impossible.  My feet and knees are still intact so I am lucky in that respect.  This feeling of thankfulness particularly happens on cool crisp fall morning runs.  Although I now run year round, it’s the fall days that bring my spirit back.  The late morning sun warms my back while a brisk breeze cools my face. There is nothing like jogging through newly fallen leaves and inhaling the smell of burning wood to make you appreciate the seasons and remind you why you live in New England.  

 

Running can seem somewhat voyeuristic. When I run at suppertime, the smells give away secrets.  The folks in the white Colonial are having roast beef, the English Tudor –spaghetti. Sometimes I can picture them eating and imagine their lives and invent stories that I can use someday. In winter, I often must run in the dark of the early evening.  Then I can actually see inside the houses, my neighbors moving about in their curtain less sanctuaries, unaware that I am watching.

 

I am always relieved to see the bridge, once I am over that I can see my own house at the peak of the hill. I am usually tempted to walk the remainder of the way but I force myself to keep moving my lead filled legs for the last stretch. When my run is finished, often I have worked through a story or a poem in my head; so I immediately sit at my computer and write it down or scribble some notes to finish at a later date, or type out my feelings previously buried too deep for retrieval. I am tired and sweating and exhilarated. Even though my legs are burning, my lungs hurt and my back aches; my head has been cleared. And I don’t need my body to write.  All I need is a clear mind and an idea.  Running gives me both.

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Now How Much Would You Pay?

Yikes.  The day is almost gone and I nearly missed my daily blogging promise. Time to write.

 Let’s talk about the outrageous cost of having cancer, can we?  Since my diagnosis last year I have paid quite a lot of money out to Brigham and Womans, Winchester Hospital, Dana-Farber and then of course the separate bills that come from each doctor: Christian, Hergrueter, Anderson, as well as each resident and intern that assisted in the surgery rooms, anesthesiologists, pharmacologists, pathologists….the list is endless. We are lucky that we have insurance, an 80/20 plan that on the surface sounds reasonable, but with each procedure and each subsequent bill, my 20% is starting to add up.

Here are just a few of the numbers that came in the mail this week just for the last surgery I had (remember I have had 5):

Breast reconstruction – $1968.00 – for Brigham Woman’s hospital

Breast reconstruction $7401.00 – for Dr. Plastic

Implant – $2625.00

Anesthesia -$2210.00

Recovery room -$2530.00

And my favorite of all:

Operating room services, which I guess is just for the luxury of lying there unconscious:  $23,075.00

The total for this bill was $32,155.47

 

Now mind you this is just one week’s worth of bills for one surgery.  The numbers boggle my mind.  Here is another that I just can’t get my head around.  I don’t even remember what the bills were for the first 6 rounds of my chemo but this week when I got the bill for my Herceptin I almost passed out. I get Herceptin every 3 weeks for a year –one treatment, just one ,cost $12,500.00!!!  This is why the US is the only country that authorizes Herceptin treatment for a year.  Other countries are fighting for it but their governments will only give the drug for 9 weeks — though I think the Aussies just won that battle.

So my question is: How in God’s name does anyone without insurance pay for all of this?  I don’t understand it.  It doesn’t seem right, the cost of health care is out of control. Even with insurance the payments are huge.  There are too many people out there who forgo medical procedures for a lack of funds. If it comes down to a choice of putting food on the table for your family or getting a much needed MRI, many will choose the former. It’s a shame.

Good thing I got that waitressing job. I wonder if tomorrow  night I can make $12,500.00 in tips to pay for my Herceptin.  To do that I am going to have to serve an awful lot of Martini’s.

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A Step in the Right Direction

 

There was an article in The Boston Globe yesterday about Mass General Hospital. It seems that MGH will be the first hospital in the country to do mandatory genetic testing on every cancerous tumor they encounter.  This is very cool.   What they have found is that many of the tumors have similar characteristics to others and by treating them more specifically then they can do away with unnecessary over-treatments.

This type of testing is already done on most breast cancers now which is why they have Herceptin that treats specifically the her2/neu type of tumor (the kind I have).  Herceptin will not work on non-her2 fed tumors.  Hopefully the testing of each tumor in all sorts of cancers, lung, colon, etc will call for the invention of other herceptin-like drugs used as targeted therapy and save patients the agony and side effects of many Chemotherapy treatment drugs that are not working.

Ten years ago herceptin was not around and many died from their her2/neu type breast cancer.  Now, with the help of the drug, many live long and happy lives.  It is exciting to think that steps are being made toward more of these targeted drugs.

I often hear people complain that they think it is big business for drug companies to NOT find a cure for cancer.  I don’t believe this. It just takes time and patience. Sometimes growth in any area of life comes in spurts. There are times it seems our own children will never grow up and then suddenly overnight, their shoes don’t fit and they need new jeans and they can talk in full senetences.  I feel that this new step in cancer research is like a growth-spurt.  Once we tap into the genetic make-up of these tumors, it will open up a whole new world of possibilities for treatment.

They say necessity is the mother of invention. Since personally I seem to know way too many people battling cancer right now, the necessity of MGH’s new plan seems obvious.

Read the full article here:

http://www.boston.com/news/local/massachusetts/articles/2009/03/03/mgh_to_use_genetics_to_personalize_cancer_care/

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Oh,Pooh

I wonder when it will go away; the terror which occurs every time I have an ache in my body.  The assumption that the cancer has nestled in the receses of bone or blood. When does it stop becoming my ‘go–to’ self-diagnosis?  Or is it simply part of the new me.  The post-cancer me.  The me that lives with a small black cloud hovering just above my head waiting to turn me into Pooh as I hum, “tut-tut, it looks like cancer”?

And I realize now that I am not the only one in this household that thinks that way.  As I writhed in bed last night, unable to lie flat because of continuous muscle spasms in my back, I know that Mark was thinking the same thing I was; “It’s a tumor in her back, or lung, or bone.”  I ended up sleeping sitting up on the couch since every time I tried to get horizontal, the pain was excrutiating.  Before I finally and thankfully fell asleep, I spent quite a few hours thinking about how even if this was only  a muscular issue, that if the cancer does return, it could be like this.  I know many people now, through the Mother’s with Cancer blog that live with chronic pain due to their recurrance of cancer.  They live out their life on pain meds just to try and get by.  It is a scary thought, one I will try not to dwell on.  But I do wonder if there will ever come a day when a pain in my back will again be as simple as that, or if I am destined to always think this way.

Today the pain is still present but is being dulled by a  heavenly warm Ben-Gay patch .  If the pain continues another day or so I will have to eventually get it all checked out but I hesitate to put myself through a battery of  tests at this time as I know that with my history they willl probably scan my whole body.  Today I will assume it is just my back.  Tonight, in the dark, the fears may return, but for now I will assume the best and not be as Christpher Robin might call me, “a silly old bear.”

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Every Day

I was going to give up candy, specifically Rollo’s and Peach Rings, for Lent this year, but I decided that I would never follow through anyway, so why bother.  Besides, I really, really love Rollo’s and Peach Rings, so forget it.  I guess it would be a little hypocritical of me, since I never give up meat on the supposed ‘meatless’ holidays — which I think are absolutely ridiculous. I consider myself a Holiday Catholic and actually enjoy going to Mass on Christmas and Easter — the days ‘real’ catholics usually hate going to church because all of us sinners are taking up the good seats.

Anyway, this was not supposed to be a rant against organized religion, which, could be a very long one, but I am not looking to get into a theological argument.  For me personally,  religion is something that should be there when you feel inspired or need it — not as an obligation — unlike my writing which needs to be written every day instead of just when I feel inspired.

 So what I did do, instead of ‘giving up’ something for Lent was that I decided to ‘add’ something.  I have decided to write a blog post every day during Lent.  Usually I have waited for some news or for something inspirational that happened to me before I write a blog but I am going to try this.  I will write every day until Easter and hope that my writing is jump started since it has been quite lax lately.

I will not be alerting you all by e-mail anymore when I have a new post so if you feel inclined to check in here on occasion please do.  I am sure some days I will have more to say than others.  But even if I have little to say, I am going to post.

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Good News

I got a piece of good news yesterday. When I went in for my treatment, Dr. Anderson walked in the office (late as usual) with an ‘I-know-something-you-don’t’ grin on her face and handed me the results from my last echocardiogram which was done two weeks prior. 

“Your numbers are up!” she said.

And indeed they were. My left ventricle heart function, which was down to 40-45 from a baseline of 60 had made a slight rise to 50-55.  Phew.  This is indeed good news.  This means maybe, just maybe, it was a temporary effect of the AC and maybe, just maybe it will rise even higher.  Most likely it won’t rise higher but 50-55% function is good (no one has 100%) and can be considered ‘low-normal’.

So bring on the training.  Time to get swimming, running and biking. No more blaming my heart for being lazy.

Speaking of excuses, back in November I wrote down some goals on this blog in an attempt to get on with my life after my hellish year of cancer, surgery and chemo.  Let’s check back in and see how I am doing, shall we.  I said:

1. Stop procrastinating and blaming my cancer for my messy house and lack of organization.

***I think I have done that.  I am still not as organized as I would like to be, but honestly, before cancer, I wasn’t very organized either. As far as blaming the cancer…I can see that the farther I get away from it, the easier that will be.

2. Get back on the Zone and lose 15 lbs.

***Well, I am trying to eat better and  I think once I can train harder the weight should come off.  For now though I have to get comfortable with my new, menopausal, shape.  It’s a little rounder in certain places, but nothing that 50 miles a day on the bike won’t cure.

3. Publish my essays and turn them into a book that will inspire and help others.

***  Let’s just skip this one for now. I need to work on my writing, this I know.  Maybe I should have stayed off Facebook which seems to eat up an inordinate amount of my free-writing time. I have to remember that  if I want to be an official blogger, then I need to post more often. I am having the same problem with my writing in general.  Unless I feel inspired by an idea or thought, I tend to stay away from the keyboard. From now on I will try to add stuff more frequently — even if it is not so profound.

4. Get a job.

***  I am happy to report that this one I accomplished.  Although it is just a waitress job for now, I am working at a local restaurant which is very convenient and the money should be decent.  This was a tough one for me.  After being out of work for a year it was hard to go back.  Plus I am feeling like I look old with my stupid hair and many of the staff are far younger than me.  It will be fine though.  The first week I was a nervous wreck and felt sick to my stomach going in but hopefully that ‘junior-high-no-one likes-me’ feeling will go away.  As strong as I thought this cancer has made me, deep down I will always be the 12 year old new girl at school.

So that is it for now.  Since my treatments are standard now with no big surprises (thankfully), I am considering putting some of my other writing on here for your reading pleasure–or displeasure–and test out some of my memoir stuff.  We’ll see.  At this point your reading of this is completely voluntary, so that is good.  If you don’t want to read my dribble, than you don’t have to.

Thanks for listening.

Posted in breast, breast cancer, chemo, goals, health, heart, heart function, Uncategorized | Tagged , , , , , | 5 Comments

This Time Next Year

Tomorrow is my birthday. The fact that it is on Friday the 13th makes me very nervous.  I am considering not leaving my house, which is quite impossible as I have to run a Valentines Day craft in my daughters class and my friends are taking me out to celebrate later that night.  Still, I could very easily stay under the covers and not surface until it becomes Saturday the 14th.  I suppose, though, it can not be worse then my birthday last year. I don’t like remembering my birthday last year but unfortunately it has been on my mind all week, playing out like a b-rated movie:

  I see myself sitting on the edge of my bed. I remember feeling happy that my mastectomy surgery was almost two weeks behind me and that I  finally had my 2nd drain removed.  Soon I would be running again.

I remember hearing the phone ring and walking to the hall to answer it, knowing  I was alone –Mark had  gone back to work after taking care of me for so many days and the kids were in school.

I smiled when I heard Dr. Christian’s voice assuming he was checking on my well being, returning to the chair next to my bed to sit and chat with the surgeon I had become so fond of . Forever indebted to him for removing all the cancer from my body.

But he did not call to chat.

“The lymph nodes which on initial inspection were clean, showed, on further investigation to be cancerous,”  he said.

“What?”

“You will need to come back in for further surgery.  We will need to take more lymph nodes to see how far the cancer has spread.”

I remember the panic and devastation.  I remember crying, thinking there was no way that I could handle another surgery. More surgery, more anesthesia, another drain, the possibility of lymphedema– thoughts that bounced around my brain, exploding like popcorn kernels in hot oil. 

I remember the rain. A heavy and hard driving rain  that lasted all day. The kind of rain that makes you think about Arks.

Friends starting showing up to console me, family members called.  Everyone wanted an explanation.  How could this be. We all thought the lymph nodes were clean; we had celebrated that fact.

“But it’s my birthday” I said to anyone who would listen.  It didn’t seem fair.

The next day, I remember talking to my angel, Maryanne, from the Brigham who you may remember, helped me so much with the first surgery.  She tried to console me and allay my fears of more surgery, more cancer, and the increased risk of lymphodema. She said something that at the time seemed so far in the distance that it was unfathomable.

” This time next year” she said, “when this is all behind you, you should plan a trip, go somewhere and relax.  Try to focus on that now and think about a year from now when this is all said and done; focus on a vacation or  getaway.”

She was right of course.  At the time I still had so many hurdles to jump, some I couldn’t even see, so it didn’t seem possible.  But she was right.  She knew that a year is a long time and that people recover, scars heal, hair grows back, and life goes on. So here I sit facing down another birthday a year later.  And I am ok.  I got through that surgery and 3 others after that.  It truly amazes me when I remember this past year and what I have been through. Sometimes the memories make me sick to my stomach, sometimes they make me cry, and sometimes, they make me smile when I think of just how strong I have become.  That day was only one of many disappointing days filled with bad news but somehow I got through each catastrophe. Instead of each blow making me weaker,the opposite happened.  With each scary premise I faced down, I grew more resiliant. 

Tomorrow it will be “this time next year” and I am taking my family skiing  for the weekend, just like Maryanne said I should.  It is not a trip we can really afford financially but emotionally I can’t afford NOT to take this trip. And tomorrow, instead of worrying that it is Friday the 13th, I will be thankful that I am a year older and many years wiser.

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Living in the Moment

I learned an important lesson as I was running through the icy streets yesterday.   I realized that If I think about how much fartherI have to go until the end or even visualize a hill that I will be be ascending a few streets away then my run becomes very difficult.  I become tired and weak, my legs feel heavy and, I begin to think that I won’t make it through the whole route. If, on the other hand, I concentrate on how my legs feel with each footfall and how pleasant the cool air is against my face, or how much I love the song that is reverberating in my ears, then I feel invincible ; like I could run all day.

It is the difference between living for the future, or living in the moment. Even though I know where my run will take me and even though I know that I have the ability to change directions at any time, the thought of  what lies ahead and my possible inablity to deal with it saps my energy before I have even given myself the chance to run 5 miles. When I enjoy each minute of running and am truly thankful for the strength to be able to do it, I am light and energetic.

Living in the moment has become such a catch-phrase these days, bordering on cliche. Everyone knows that they should do it, but in this life,fraught with difficulties, it is far easier said than done. I know that I have spent most of my motherhood half-listening or half-playing with my kids for years.  I may be with them physically, playing cards or baseball,but my mind wanders, worrying about bills or my health or what I am going to make for dinner.  And make no mistake, my kids notice : “Mom, you didn’t even hear what I said!” gets uttered quite often around here and it isn’t just because I am losing my hearing.

So I decided yesterday, as I weaved in and out of snowbanks, feeling the sun on my back, and being grateful for my continued ability to lace up my sneakers and hit the pavement, that I would vow to try to live my life the same way that I take my runs.  I am going to treat my time alone with my family and friends like I do my runs.  I will not think about what lies ahead; only what lies right in front of me.  Because when I start to do that, then a game of cribbage with my son, an hour long talk with an old friend that I have missed, a cup of tea with a neighbor or a walk  in the woods–  will all leave me feeling as  refreshed and satisfied as I feel after a long  jog. And that’s about as good as it gets.

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An Opportunity to Help

Now  that I am feeling healthy again I figure that I need to take advantage of it since I now know how fleeting health and well being can be.   I am registered for 2 triathlons this up coming season and am anxious to start training.  I am back to running but mostly inside because I have become a total wimp about running in the cold.  As much as I hate the treadmill, it is better than nothing.

With my newfound understanding of the evanescence of life, I also need to check off some of these lifelong goals that have been just beyond my reach.  My aspirations are right there in front of me, like the plastic rabbit at a greyhound track, it’s just that I can never seem to quite catch them. It’s time to change that.

One of those goals that I have decided to stop talking about and just “do” is the Pan Mass Challenge. This 2 day 153 mile ride  raises money for Dana-Farber Cancer Institute and the Jimmy Fund.  Their mission statement explains:

 

 

The Pan-Massachusetts Challenge raises money for life-saving cancer research and treatment at Dana-Farber Cancer Institutethrough an annual bike-a-thon that crosses the Commonwealth of Massachusetts. Since its founding in 1980, the PMC has successfully melded support from committed cyclists, volunteers, corporate sponsors and individual contributors. All are essential to the PMC’s goal and model: to attain maximum fundraising efficiency while increasing its annual gift. Our hope and aspiration is to provide Dana-Farber’s doctors and researchers the necessary resources to discover cures for all cancers.  

 

 

 I had considered doing the breast cancer walk but I would much rather ride 150 miles then walk 90, especially while I still can. What I love about Pan Mass is that 100% of the proceeds go directly to the cause —  there are no corporate hands in the pot.  Also this race covers all cancers, and I have been touched recently by many different forms of cancer, not just breast cancer.

My oncologist asked me to join the Dana-Farber riding team, but I declined. I am riding with Susan C, who has become invaluable to me as a friend and a bike partner over the past few years. Susan asked me to take her biking a few years back when an injury stopped her from running.  I begrudgingly agreed since up to that point, I was a solo-biker. I preferred to exercise alone, not wanting to bend to anyone’s time or speed. Susan took to biking immediately and quickly started mapping out long rides for us, anywhere from 30-60 miles at a pop.  Without her I would still be riding my measly 15 miles. Susan was patient with me as I tried to pedal through chemo treatments, offering to do shorter rides and slowing down to accommodate my shaky muscles and palpitating heart. I would not even consider doing the Pan Mass without her.

I run many races that sponsor great causes but I have never had to actually raise money.  So the tough part here is asking you all for donations.  Both Susan and I need to raise $3400.00 a piece.  We are committed to this amount and if we don’t raise it, we are obligated to pay the balance.  This makes Susan very nervous but I told her that I would put this message out to all of you my friends and ask for help.  The race is the first week in August which seems very far away, but I figured I would ask early so I can alleviate Susan’s fear and we can train with a clear head knowing that we have covered our butts.

I am riding not just for myself but in honor of my mom who died this year of colon cancer, my dad who died of complications from esophageal cancer, and my brother-in-law Bob who died of kidney cancer.  I would be happy to add any of your loved ones to my list and bring their spirit with me on my ride.  From what I understand it is an intense experience to ride with all these loving, caring people who are also carrying their loved ones in their hearts.

To the right of this post under My Links you can click on where it says “sponsor me for the Pan Mass challenge”.  There are many ways to donate, and they walk you through it.  My id# is FK0012.

Thank you.

Posted in breast cancer, cancer, chemo,coping,running,herceptin,mastectomy, health, Uncategorized | Tagged , , , , | 2 Comments

Notes from a Mother with Cancer

“Ever since you got cancer you are so mean!”  

Theses are the delightful words of my teenage son, who truly thinks that because I have cancer I am taking it out on him.  That I am just pissed off at having cancer and that he never does anything that deserves to be yelled at. He also feels that he should be able to do whatever he wants and that I am far too controlling.

When I tell people that I have a 15 year old son, the comments I receive sound oddly familiar to the one’s I got when I told people that I had cancer:

“Oh you poor thing.”

“This too shall pass.”

“You will get through this with time.”

“I will pray for you.”

The double whammy this year of dealing with my illness and also with the hormone laden mood-swings of my eldest born self-serving-entitled teenager has all but blown the roof off my house. This past week brought our frustrations to new heights when the doctors told him he had a knee disorder and ordered my jock son to rest the knee for 4-6 months causing him to quit his beloved JV hockey team and sit around the house playing X-Box 360. This coupled with the fact that the doctors have ordered me to lay-low for 2 weeks after surgery has turned our house into a battlefield.

I hate X-box.  I hate all computer games.  I always have.  This year was the first time any gaming system was introduced into our house and now we have two –the Wii, which I bought them last Christmas and the X-Box 360 which my son purchased with his own money thus making him believe he can play it whenever he wants for however long he wants. This on-line live contraption means he sits in our playroom for HOURS talking into a Janet-Jackson like headset to his friends who are sitting in their play rooms and play these games together.  No human contact…no outdoor fresh air. It came to a head the other night when I found him on it at 2:00 am, 7 hours after he started!

My other two kids,age 12 and 9, seemed to understand my need for peace this year.  They were easy on me after chemo and surgery and generally have really tried to be good.  My 15 year old — well, it seems like he has gone out of his way to irritate me.  He claims that I am meaner since I got cancer. What he can’t seem to understand is that even if I didn’t have cancer, I would still be angry about X-Box and I would still be telling him what to do.  It’s all about timing.  He happened to head full fledge into teenager-dom at the same moment I got cancer. Unfortunately, as a typical first born, his only perspective on things is about how they effect HIM. My cancer has been an inconvenience to him on more than one occasion.  Also unfortunately, he, like my husband has a difficult time expressing his feelings and therefor much of what he may be feeling gets swallowed up into a world of inane sports facts and weather talk.  This is something I continue to work on daily.

As I pondered our fight the other night it dawned on me just how difficult it is to be a “Mother with Cancer”. I blog on a website that goes by that name; and there is a reason it needs it’s own special site. Mother’s who have cancer have an extremely difficult time. No matter the age of the children.  Each phase of child rearing brings with it it’s own set of problems and when you heap on the sickness and fatigue of battling cancer and dealing with treatment not to mention the impending feeling of anxiety over “what if”…the combination of mothering and cancer is overwhelming.  Yes, it is horrible when father’s have cancer, but no matter how involved Dad is in the family, it is always easier for him to take to his bed when he is not feeling well.  Mom always has to be “on” no matter what.

Weather it is the physical exhaustion of chasing a toddler or the mental anguish of dealing with a teenager, mother’s who have cancer are a special breed.  Tough as nails as my mother would say, we have no other choice.  Every day we put the needs of our kids before our own (as do all mothers) and wait till the wee hours of the night to think about our own worries.

I know that eventually my teenager will outgrow this phase. I also know that I have many things to work on when it comes to dealing with him. Since he is my first I do a lot of “test” parenting on him. Sometimes I have to change my expectations and my tactics when things start to go awry.  Eventually too, my cancer, will fade into the background of our lives; He will find something else to blame my “meanness” on; maybe it will be my new job, or my book tour (ha), something other than cancer.

For now though, my hats off to all Mothers with Cancer and their ability to get through another day.  Lord knows it aint easy.

Posted in breast caner, cancer, chemo, chemotherapy, family, Uncategorized | Tagged , , | 2 Comments