The Best Laid Plans

I spoke to my older brother yesterday to tell him what time I would pick him up for Thanksgiving.  It was a call I dreaded. Not because I dislike my brother who has struggled with mental illness and depression for years, but because I had promised something I never followed through on and I was afraid that he would be angry with me.  I had promised back in June that I would come to his tiny subsidized apartment in Lowell and give it a good “spring cleaning”. I was going to replace the nicotine stained curtains, scrub down the walls and replace the fraying rug. We were both excited with the prospect of his new and improved living space. My brother has very little and this was a gesture that would bring great joy to his somewhat lonely existence. But I never went. I let the Summer turn to Fall and made excuses when I thought about it and got busy and then it just got too late. When he answered the phone yesterday he sounded genuinely happy to hear from me.

“Hey Franny, how’s it going.”

“Great Bri, listen I am sorry about not getting over there to clean, yet.”

“Oh that’s ok, I figured you weren’t feeling well.” Of course he thought that.  He has always worried about me, his little sister, since I was diagnosed with breast cancer. Brian always made time to call and find out if I was ok.

“I feel terrible that I never got there to clean. I didn’t mean to disappoint you.”

“Don’t worry about it.” he said as graciously as he could.  How could he be so accepting of this, I wondered, when I was so horrible about handling disappointment in my own life? Why do I get so upset when things don’t go my way?

I have lived through quite a few “real” disappointments in my life–like the death of my father and two brothers at young ages or the fact that I moved to a new town every 10-18 months throughout junior and senior high always right about the time I was settling in, not to mention the loss of my youth and body parts due to cancer. After enough of these major life disappointments  I seem to have become immune to death,and sickness and change in location, losing friends and loved ones with an heir of acceptance. The major blows I can handle–leaving no room  for the minor disappointments in my repertoire of coping skills.

When looking for a new home years ago when the market was red-hot and if you didn’t place a bid higher than asking price as soon as your foot hit the threshold then most likely you would lose it; my real estate agent told me to never picture my own furniture in someone else’s house so I wouldn’t be upset when I didn’t get it. But I didn’t take his advice.  Each house I entered I could imagine how my wooden bench would fit perfectly in their kitchen-nook and ,oh, wouldn’t my couch look lovely under that sunny window. And I am still doing it today.  Although now it’s with those that I love. I am the furniture and I picture myself in different scenarios surrounded by friends and family.  Whether it’s a simple lunch with a friend or a night out or a weekend away with my family where everyone gets along. I forget to take into account that other’s may have their own plans.

As I get older, my circle of close friends has narrowed considerably in direct relation to the widening of my  expectations of their loyalty and love for me. I find myself getting my hopes up about spending time with the ones I love–people I want desperately in my life–and when they are too busy for me, I become extremely disappointed. So when a friend can’t meet me for lunch or isn’t home when I visit I am heartbroken. Because in my mind I had things worked out just-so.  Last Spring I was hoping my best friend and her family would join us on a trip to South Carolina.  I got my hopes up so high and pictured all the fun our families would have together that when she finally told me no (which took some time because she didn’t want to disappoint me), I was crushed and angry.

As an adult I should have learned by now how to handle disappointment. Instead, a constant battle rages between my grown-up mind and my child-like heart . My brain does realize that I have no right to be angry at the other person for letting me down.  Since usually it is not they who have let me down but my own mental furniture moving that has gotten me into the predicamanet in the first place. But my heart acts out so when things don’t work out for me I sulk and feel sad and rejected for a while until I talk myself out of the destructive self-pitying that doesn’t do anyone any good.  At the same time I am trying to teach my children to handle disappointment. “It”s fine” ,I say when they don’t make the ‘A” team in hockey or soccer. “Pick up and move on” I say when my son realizes his bum knee will handicap him for life.  I want them to learn how to handle such things knowing full well that I, a 47 year old woman, still struggles with it.

There are solutions to this problem, but none of them sound enticing.  My disappointment revolves around people I care deeply for, who I want to spend all my time with. I am never disappointed by aquaintences or those I hold at arms distance in my life.  Only the few I have let sneak into the inner circle of my heart.  I suppose I could stop letting people in. But I would have to let the others go as well. If I stand alone, then no one can hurt me.  Just like when my oldest son was about 6 years old  and he stopped accepting balloons at birthday parties and carnivals.  When someone offered him a balloon he would say,

“No thank you, I don’t like balloons.”

But I knew he loved balloons.  It’s just that he had lost one too many to the windy skies or popped them on sharp objects and he had told me that he was never going to get a balloon again because it was too sad when you lost it. I don’t want to do that.  I don’t want to stop accepting balloons or let loose the ones that fill my heart just because they may disappoint me. It’s a jaded and cynical way to live. I think I would rather enjoy the beauty and happiness of spending time with those that I love and suffer the disappointment when things don’t work out as planned.  The alternative feels  too lonely.

I don’t want to stop making plans either. If I don’t ask anyone to be there for me then they can’t let me down.  Again a cynical view.  One I am not willing to adopt.  I think I would rather continue to make plans and get excited about things that “might” happen even though sometimes they may not work out exactly as planned. I’d rather continue to buy balloons and fill up my imaginary house and take the risk.

Because I know, deep down, that those that I love mean well–like I meant to do well by my brother. Eventually I will clean his house.  He knows that.  He trusts me. So I must learn to trust the ones I love, and like my brother, graciously accept that their true intention is never to disappoint me–only that life gets very busy and sometimes with a little patience on my part things may work out even better than I had planned.

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A Process

Aging is a natural process. Everything we do and everyone we lose adds moments to that process. Getting married, watching our children grow, losing our parents. We can’t stop it, it’s inevitable.

I remember crying one day when I was pregnant with my oldest son–16 years ago. I told my husband that I did not want to have children because their mere presence in my life would age me.  I thought that by focusing on my child’s developmental growth, I would lose track of the years and my life would fall by the wayside. A lot of my panic at the time was the hormonal mood-swings of pregnancy but there was a bit of truth to it as well.  Obviously I grew older as my children did and yes I lost myself waiting for them to walk, and talk, and ride a bike, but it was gradual enough and I was busy enough for years so that  I didn’t notice. It’s only now, looking back at pictures do I see how youthful I was back then and I can compare it to where I am now. Older, yes, wiser, definitely.  They do not exist independently.

With my children out of the baby stage there are now other reminders of my own aging.  Two years ago the death of my own mother and last month with the passing of my Mother-in-law, Virginia.  Virginia was an incredible grandmother, no better could you hope for, she remembered their favorite candy every visit, she knew about sports and how to engage a teenage boy and of course was very gentle without being condescending to my daughter. She was a beautiful woman through and through.

Although I have only had one Mother-in-Law I am pretty sure I lucked out in that department.  She was caring without being intrusive; she somehow found a way to let her opinion be known in such a way that was acceptable, and she was usually quite right in her perceptions.  I am  sure she held her tongue far more than she let it wag and when my sons get married I can only hope to follow her lead. And although I didn’t have the kind of relationship with her that boasted of daily phone chats, I knew she always understood me and I certainly knew she always had my back in any conversation that may have led to disparaging remarks about her daughter-in-law.

And now she is gone.  My children are grandparent-less–which I don’t think of as devastating since I lived my entire life, grandparent-less. I feel that they are indeed lucky to have had any grandparents at all, but to them it is a horrible fact that they throw onto the table at various times.

When my kids say, “I have no grandparents, now”, I am instantly transported to a recurring conversation I used to have with my own Dad sitting at the kitchen table;

“I am an orphan, you know,” he would say.

“No you’re not, Dad, you had parents at one point.”

“Doesn’t matter, they are both gone, and now I am an orphan.”

Well, I guess I must be an orphan now, too, which really sucks because the word itself conjures a sense of being alone and on your own in a big scary world. That’s exactly what happens when both of your parents are gone. You are in a sense alone in a big scary world.  There is no one to call when you are not quite sure how to handle a teenager with a new license, or a middle child’s insecurity, or God help me a pre-teen girl and all her dilemmas. The generational layer that laid above me, protecting me with their knowledge and wisdom has been ripped away. There is no hierarchy, anymore, they have moved on.  Now it is up to me.

Had I been a little more organized I would have thought ahead.  I should have made a giant list, as long as Santa’s, with questions to ask my parents and in-laws. Questions regarding future years, about when my daughter reaches puberty and my sons get married. There are questions about my own childhood that I never asked–like ‘did you hate me when I was a teenager?’ Or everyday questions like how Virginia made that amazing roasted lamb or what it feels like to turn 50. I would have kept this list in my desk drawer, categorized like an encyclopedia, referencing it daily. Since I was not that organized, my only hope is to try to remember the wisdom the previous generation has instilled in me and try to recall as many facts and advice that I can. I will  encourage my children to start a list, to ask me as many questions as they can and write them down–questions for me, their protective layer.

 

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I Confess…

…I have not been writing.  Here or anywhere else. .  It would be easy to blame my lack of creativity on outside events like work,school, sports schedules, funerals, car disrepair, or financial upheaval. But that is a cop-out.  I should not be waiting for inspiration, I should be seeking it out actively in the routine, the mundane, the ordinary. Instead of letting life kill my inspiration I should be looking closer at the world around me.

See, I have officially entered the Post Cancer Stage. And look at me–I am fine. Just fine. But fine is so boring. No one aspires to be “fine”. If they did you certainly wouldn’t hang out with them. Unfortunately what comes along with “fine” is a settling into routine.  Somehow between driving to soccer and hockey, filling out PTO forms, and making dinner I have forgotten about how precious life seemed 2 years ago when I thought it might be stolen from me. I have lost my edge and though I desperately want it back, I certainly don’t want to go back to the days of cancer and chemo. I have met people over the years who need that edge constantly.  These people  can’t  handle the ordinary so they create drama and tragedy to justify their existence.  When there is no more tragedy in their own lives they seek it out in others.  These people are exciting to be around at first, but quickly become exhausting.

But routine can be exhausting too. Lacing up my sneakers for a run this morning, I was feeling tired and irritated that  I had to go running– conveniently forgetting the past few years and  how wonderful it felt to run after each surgery and how excited I was for the doctor’s OK to get back at it. But  now I am back to running 5 days a week and there is no reason not to run –no surgeries or chemo or swollen appendix. As I left my house and headed up Summer Ave, I was tired and hunched over and thinking of all the things I had to do when I got home. A hotter, more humid than usual Autumn day today,  I started to feel the weight of the past few weeks heavy on my shoulders.

Right when I was thinking I would turn around and go home, an incredibly refreshing breeze blew straight at my face. It was perfect, not too strong as to impede my forward motion but strong enough to cool me off.  I continued my run and it seemed every time I got really hot this breeze blew at me.  As if I were running behind a flatbed truck with an industrial fan set on 4 minute intervals. Eventually I anticipated these breezes and stood up straighter to catch the full effect.  At one point I lifted my chest and opened my arms out wide in an attempt to capture the fresh air into my lungs.

I could have just run like I do every other day and not paid much attention to the wind.  It was innocuous enough that I easily could have taken the breeze for granted.  But somehow today that breeze lifted me up and gave me the strength to continue. An ordinary breeze. Yes.  It’s just nice when you actually stop and realize how much these short bursts of air can give you the strength to get through the ordinary, mundane, sometimes harrowing daily routine.

So I began to think of all the breezes in my life.  My breezes blow in as a bear hug from my teenager while I try to make supper, a cup of tea at a kitchen table with my best friend, a comforting voice on the telephone, or a picnic under an oak tree with an old friend.  Quiet and strong they fill my lungs with air and carry me through even the most boring day. They let me know that “fine” can be awesome and the mere fact that I can appreciate them is enough to keep me on track.  I am blessed to have them and will cherish these breezes with open arms from now on, savoring every one, never taking for granted the simple beautiful moments in my life. A fine life, after all.

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“I Want So Much To Live”

I was lucky enough to see this new documentary at The Boston Film Festival this week called “I Want So Much to LIve”.  It is a beautifully done film about the invention of Herceptin.  This short film  highlighted the young scientists of Genentech who made it their mission and passion to get this drug perfected and approved.  It was these young kids in California who figured out that something was odd in the breast cancer world; they wanted to know why after treatment some survived and some didn’t.  They figured out that 20% of all breast cancers were fed by the her2 protein and then went about finding an antibody for it.

As I was diagnosed to be her2/neu positive in 2007– 4 years after Herceptin was approved– I was lucky enough to receive this drug.  The story touches on the women who were not so lucky, who wrote letters pleading with the drug companies to let them have this new drug that was available. The film explained the clinical trial process and how a drug gets pushed through the FDA–giving us both sides to the story and showing how there was no real ‘bad guy’ because everyone was working toward the same goal–finding a safe and effective drug against breast cancer.

What struck me most about this documentary was the unbelievable commitment of these scientists to prove that Herceptin was worth the company’s time, money and effort.  They knew in their hearts that this was an important step in helping to cure cancer, and they would not take ‘no’ for an answer.  It also amazed me that it was only in 2003 that this drug finally became approved, and that had it not, I would be in a very different situation right now.

You should definitely see this film if it comes to any of your cities. It made me feel like all the walks, runs,and bike rides we do to raise money for research against all cancers is actually doing something.

Here is the link to the film’s website index.html

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Jars of Clay

My Mom, Mary Buckley, died this week 2 years ago. She was an incredibly strong person who dealt with many tragedies over the course of her life.. This was a piece I wrote about her for a Grub street class last year.

Jars of Clay

When you fill a clay jar with too much water, eventually it will crack.  It is not noticeable at first, you can’t see the corrosion inside but over time there are small outward signs –the texture changes and there are slight variations in color.  Until one day the vessel cannot hold and eventually breaks wide open. The day we buried my brother, Michael, I noticed the first sign that my mother’s jar was overfilled.

It was her eyebrows.  They were purple.  I stared at them across the kitchen table long after the mourners had left the wake, while my brother, sisters and two nieces chatted.

“It was a long day,” my mother said, tendrils of smoke escaping through the side of her mouth, “I can’t believe how many people were there. They just kept coming.”

Next to her, my sister-ln-law, Paula, moaned, excused herself, and left the kitchen.

In the eyes of our family, my brothers’ widow had not handled the day very well. Paula had spent the entire wake screaming and gnashing, throwing herself across the open casket, oblivious to her own 8 and 10 year-old daughters’ pain. Understandably, her husband had been taken from her by a drunk-driver, the day after Christmas, but our family had already buried a brother and had lost our father less than 2 years before – we were grief veterans and we wore our badges with dignity and honor. We were taught well by our mother to be stoic in the face of tragedy—never let them see you lose control.

But I saw.  I knew that she had taken careful steps that morning –picking out her classiest black suit, ironing the cream-colored Lord and Taylor blouse.  Matching her belt to her patent leather sling-backs.  This was important to her. She needed to prove to friends and family that she was stronger than anything this life could throw at her. Carefully, like a movie star in her dressing room, propped on the pink stool of her vanity, she applied foundation and mascara and then drew in her eyebrows; painting a perfect arch –not too straight, not too curved.  But in her grief, my mother had reached for the wrong pencil. Instead of the brown eyebrow pencil she always used, she grabbed a purple pencil used to line the under eyes.  When that was done she put on her pink lipstick and then with a straight back, stood up and left to bury her 34-year-old son.

To tell her would have been too much.  I feared that the embarrassment of having been around so many people with purple eyebrows would have been the final drops that destroyed her well sealed jar of dignity– feared that her jar would completely disintegrate.  So I just stared at her face, and said nothing.

It was my brother’s 10-year-old daughter, who finally spoke up,

“Grammy she said, “why do you have purple eyebrows?”

Everyone stopped talking and looked at my mother.

“Look,” said my niece, showing her a mirror.

She stood and walked to the hall.

“And none of you people told me?” she spat, turning an accusing eye on me.

“Um, well, I really didn’t notice,” I lied.

I know that internally my mother was mortified, because later in the car she lashed out at me, but that day in front of everyone, she did not dissolve.  She held fast and strong proving that my mother was made of far more resilient material than clay.

My mother stared at the mirror for a few minutes, composed herself and then spoke to her  granddaughter.

“I think it was your dad’s favorite color.”

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PMC 2010 Re-CAP

“So…how did it go?”

I’ve answered this question so often in the last week that I have neglected to update everyone here. I can’t believe a whole week has passed, this time last Saturday I was already past the first water stop.

So, how did it go? Incredible. As great–no better– than last year.  I feared that in trying to re-create the feeling of last year’s ride that I might be disappointed as can happen whenever we try to re-live a special moment.  But that wasn’t the case and it became obvious why riders do the Pan Mass Challenge again and again. It’s because you know, as you are riding by people with signs and cowbells and horns, clapping and cheering and saying THANK YOU I AM ALIVE BECAUSE OF YOU, showing pictures of their loved ones and hearing the stories from every single rider who rides for their mother, their father, their cousin, their spouse or themselves that this isn’t just a ride; it’s a ride to culminate raising MILLIONS of dollars to fund research that is ACTUALLY SAVING LIVES.  The ride is only part of it–it is the people who give–you, who give–that are the important ones here. Because the ride means nothing without the donations and THAT is what this is about.  So to see the results all along the route–people crying and laughing who come out by the thousands is what makes this the most important weekend of my entire year.  The 1700 miles Susan and I rode to train for this ride are nothing in comparison to the 1700 lives that can be saved from the millions of dollars raised.

And can we talk about the volunteers? 3,000 strong that fed us,massaged us,cleaned our sunglasses,gave us water and ice and Advil and changed our flat tires and  kept us safe on the roads.  Mark was one of these.  He changed 24 flat tires and road the course in a truck from 4 am to 6 pm on Saturday and got up at 3:30am again to do it Sunday. It’s extraordinary to see so many giving individuals.  I’ve said it before—the volunteers work harder than the riders–and without them this event would absolutely not take place or run as smoothly as it does.

So Susan and I will do this again next year.  We have decided to do the full original route from Sturbridge which will add 30 miles to our ride.  This means we will need to do a little more training for this if we can find the time but we are certainly up for the challenge.

The best words that can summarize the week-end, were in an email to Billy
Starr who is the Founder and Executive Director of the PMC.

“The greatest compliment I can make of the PMC is that if you told me I was
going to die on Sunday, which I hope of course does not happen, I would be
thrilled to have spent my last day on Saturday riding the PMC: doing
something to try to improve our world, and experiencing all that is best in
humanity: teamwork and giving of oneself for others.  The riders and
volunteers behave in a way that IF there is a God, they would all be acting
exactly as God would hope for humans –  caring more about others than
themselves on behalf of this amazing weekend!”Thank you to all who have supported Susan and I with either donations or kind words or balloons or cakes or a pat on the back–it means more to us than you can ever imagine.

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PMC update -10 hours to go

It is 9pm the night before the 7 am PMC start and yes I should be sleeping but first I have to pack.  And clean my house.  And pick up my son.  And write this blog.

Susan and I just arrived home from dropping our bikes in Wellesley and getting our goody bags replete with promotional items and our PMC 2010 shirt, which I must say, is a lot nicer than last years’ garment. I am nervous but not the same as “race-nervous”. I get a different flutter when I am going to be racing–this is just a ride, not a race per se.  Susan gets very anxious about the crowds and riding with so many bikes–I am more nervous about being able to complete the 84 miles tomorrow.  Realistically I know we can–god knows we have trained enough–but things do happen, like injuries or stomach-aches that can impede even the fittest rider.

I will be happy once we get on the road and I hear Susan yell “CAR BACK”  which she does when a car is approaching.  Others do that too, it’s a bikers courtesy call to those ahead who may be riding two abreast, but last year Susan took it upon herself , mainly out of a nervous reaction, to yell it louder and more often than the other 5,000 riders.  It became quite funny after 5 hours or so.  There was also the cry “CAR UP” and “ON YOUR LEFT” that she took on and used as a sort of personal rocket fuel to propel her through the ride.

While Susan is yelling at her fellow riders, I will be busy looking for people this year.  There are many I must find along the route. I will be looking for John Marchiony, a fellow biker, blogger and friend of my niece who I have never met but spoken to through cyberspace.  I will be looking for Team DON–a team that rides for our friend Jim’s brother Don who died this year and had ridden the PMC for 9 years.  I need to make sure I see my sister Moe who will sit with balloons and water at the “Robert Walsh Memorial Water Plant” in Mansfield that is named for her beloved husband who died 13 years ago of Kidney cancer.  There are customers of mine who will be at a campground in Truro that said they would be waving to me as I ride by.  At Nickerson I will be looking for my great friend Linda who took the time to send out my donation plea and because of her I received many donations from people I have never even met.  I will also be looking for my husband, Mark, who is riding in a PMC van, volunteering his time to fix broken bicycles and help riders in distress.

In between listening to Susan and looking for friends, I will be doing a lot of thinking.  I will be thinking about all the wonderful friends,family,and neighbors who contributed to my ride and helped me once again reach my goal.  I will be thinking about all those who we have lost to this horrible disease as well as those that we have saved by riding and raising the money we do. I will be praying for my mother-in-law who is struggling to come back from a stroke.  And I will be once again, feeling so very greatful for having the strength to pedal 163 miles and lucky enough to be given another year to enjoy this life and all of you.

Thank you.

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Another Year, Another Mammogram

I know that the yearly mammogram  you get after you are finished with all treatments for breast cancer are supposed to cause anxiety and stress but  that wasn’t the case for me yesterday.   I admit I was quite stressed getting to my appointment, because we are now dealing with 2 broken vehicles and I had to ask a friend for a ride into Boston, but once I was in the building I was calm, cool, and collected.  So calm in fact, I fell asleep in the chair waiting for my results.  Head back, mouth open, deep snooze until I heard my name from far, far, away, “Frances Kolenik”.  My head snapped forward as I wiped drool off my chin and looked around at the other woman in their starched blue and white gowns, busy reading or worrying.  I wondered if they overtly stared at me while I slept or stole fleeting glimpses of my slumbering while thumbing through their magazine.  I’m sure they thought it was wildly inappropriate.

My mammogram was over quite quickly. Done in half the time it used to take. Since I have only one real breast, they only squash and flattten one side into their heineous machine of torture.  The nurse I had was exceptionally rough yesterday, handling me like a slab of meat. “Just slap that baby up on this counter…ya come on, up here, stand on your toes. That’s it, now stand like that while I screw this vice down on top of it..one…more…turn…there now don’t move, and hold your breath.”

Like I could breath if I wanted to.

But I was spared the agony of having to do this  on the other side because they don’t check the implanted side. So within minutes I was sent off to the waiting room with the other women to await my results, and in my case catch a few winks.   My results were normal.  This was good news but nothing I didn’t already know. See, it is not the other breast that concerns me.  I don’t expect to get breast cancer in my other side.  That would be a new cancer.  What actually causes me anxiety is that a cell from the cancer I already had somehow escaped the onslaught of  chemo and has attached itself elsewhere in my body.  The area surrounding my implant particularly worries me-but they don’t check that.  Nor have they done any other scans on me like they do for others that have had the same treatment.  I am still not quite sure why.

I did see Dr. Christian who ‘manually’ checked my chest and said it seemed fine.  I told him about a pain near the sight of the original cancer and he said he had no answer and that maybe it was a “ghost” pain–pain some people get in an area of the body that has been removed or amputated. I am not quite convinced that is true,  but  for now this answer will have to do.  I will bring it up again with my oncologist in August.

So as far as the year mammogram check, which some think is a big deal, I am not feeling that great sigh of relief.  I am happy to have a clean scan in my right breast but what would make me really happy is a PET scan that would show no evidence of cancer anywhere else.  This, again is something to take up with my oncologist.

The good news is this…a full year has passed since the end of my chemo and I am here, and feeling stronger than ever.  I certainly  don’t need a test to tell me that.

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PMC update Week 7: When Maps Lie

It’s been a while since I updated you on our PMC training.  Susan and I have been logging some serious miles lately to make sure we are ready for the big event.  Last I spoke to you we had just finished our first long ride of 30  miles which at the time seemed difficult.  Now 6 weeks later we are right on schedule and finished our back to back rides of 50 miles and 80 miles.  These longs rides take us from Reading through North Reading, Wakefield, Lynnfield, Boxford, Tewksbury, Georgetown, Andover, North Andover, Billerica, Carlisle and Concord.  On our 50 miler we made it to Walden pond which is a destination I was hoping to get to last year and during the 80 mile ride we even pedaled into Plaistow, New Hampshire for a short time.

Susan at beautiful Walden Pond

We seem to be training correctly and slowly building on our previous lengths because neither Susan or I seem particularly sore after these long rides. Mostly I am hungry.  After the 70 miler I came home and ate anything I could get my hands on–for about 5 hours straight.

Where are we?

What seems to be harder than the actual riding, is the planning and plotting of our routes.  Susan (who I now call ‘my Sherpa’) spends hours and hours on Google maps and with a paper map trying to figure out roads we can safely ride on, writing out directions on a tiny piece of paper she tucks into the leg of her shorts. Sometimes though, even with her meticulous cartography, we get lost. Usually it’s because the road that exists on the map, does not exist in real life.  This happened twice last week, the first was in Middleton and was unfortunate because we were being chased by a ‘hound-dog’ who thought we were lunch.

“Faster Susan”, I screamed back to her as  my fight or flight reflex pumped my legs into overdrive, leaving my partner to her own resources.  I’m sorry, but when it comes to biting, snarling, vicious dogs, it’s every biker to themselves.  I blew past Susan, the hound hot on my heels, and right when I thought I was losing him, that he might be slowing down, the road ended in a path of rocks and gravel.

“Uh-Oh.”

Our hound friend stopped too, looked up at me with a grin and licked my leg. Then he ran off after a chipmunk, which was lucky because we then had to turn around and ride back down the road we just came and I didn’t want him following us all the way home.

We encountered a non-existant road again on our 80 mile trek at the top of a huge hill in Tewksbury. Or maybe it was Haverhill. Susan pulled her directions from her shorts and stared at the folded paper with disbelief, “But the map said that this road turns to Lilly Pond Rd!” Susan gets very upset at these mapping malfunctions because she stays up all hours of the night to ensure we have a pain-free ride.  She takes it very personally.  I stared at the gated path across the street and thought that if that’s Lilly Pond Road then we are certainly not going to be going down it.

Last year during our training we would sometimes get lost and were often filled with great anxiety.  But the difference between last year and this is that we don’t panic anymore.  I guess we have been out there long enough now to get a better sense of where we are.  The last mishap put us into Georgetown where we weren’t supposed to go that day but where we had been on another ride so we knew how to get back on track.  We are confident in our ability to find our way home.  I guess you’d say we have become “seasoned” riders and at the same time we are discovering glorious farms and forests close to our home that we never would be able to encounter in a car.

Susan is away this week so we will have to make up 60 by this weekend when she gets back.  I am kind of enjoying the break and I hope she is too, but if I know my partner, she’ll have me back in the saddle before she has even unpacked her bags.  Thankfully I picked a bike partner/sherpa who is far more dedicated and disciplined than I.

If you would like to donate to our PMC ride and have 100% of your donations go to cancer research, you can find us at:  http://www.pmc.org/profile/FK0012

Fran & Susan’s 2010 PMC Training Guide – Long Ride Goals

Week Beginning Dist
1 May 10, 2010 30
2 May 17, 2010 40
3 May 24, 2010 50
4 May 31, 2010 60
5 June 7, 2010 50/40
6 June 14, 2010 70
7 June 21, 2010 80/50
8 June 28, 2010 60
9 July 5, 2010 90/60
10 July 12, 2010 80
11 July 19, 2010 50
12 July 26, 2010 70
PMC 84/81
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Summer Bucket List

My kids are out of school at the end of this week which had me pacing the halls of my house yesterday , sick to my stomach. It’s not that I don’t want my kids around all day, everyday–not at all.  I actually enjoy the carefree days of summer with them.  But yesterday I was in a panic  about our serious lack of finances and how I can’t afford to send anyone to camp this year, especially my middle schooler who still struggles with finding friends and who spends most weekend days home alone. “What are we going to do all summer?” I kept thinking”What are they going to do?”  Drama camp costs $400, hockey camp over $200,the beach parking lot costs $25 at a pop, the movies for all of us runs over $50,the mall?  Forget it.

My panic was just about at Ativan-level when I walked by the refrigerator and saw this, posted by my 10 year old daughter:

Things to do over the Summer with Maddie(her friend)”

1) Jump in a freezing pool 5 times

2) Rollerblade up the Mineral Street hill.

3) Silly-String each other.

4) Dance in the rain in our bathing suits.

5) Plant a tree named Fred.

6) Design a new drink.

7) Put pink streaks in our hair.

8) Stay up all night at a sleepover.

9) Go in the pool at night.

10) HAVE A PARTY.

Not only did this list make me smile, it blanketed me with such nostalgic warmth that my panic melted away by reminding me that summer is not about  camps and spending money we don’t have–it’s about dancing in the rain in our bathing suits and staying up all night long because we can!  It’s about remembering what it’s like to be 10 years old when the world was safe and school was out and lemonade stands were at every corner.  Thank you Maeve, for reminding me.

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