Category Archives: humorous breast cancer blog

SYNTAX


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What do you mean by that?  How many times have you said that?  How many times have you heard something come out of someone’s mouth and can’t believe he/she said that?  We have to leave The President out of this because everyone would say that about what he says.  This is about people in your day to day life.  Syntax, how a simple statement is made to reek of negativity, condemnation or condescension.  Syntax,

Syntax refers to the composition, or the arrangement of words used to portray a meaning.  Bad Syntax, in my opinion, doesn’t just refer to poor word arrangement, but the arrangement of words to portray a poorly emoted meaning.  I think it was my Mom who always used to say, “it’s not just what you say, it is how you say it!”  Me, I am all about that.  Lately more so than ever.  These days everything seems so dark and dreary in a way, so why not take any chance possible to lighten or brighten things up.  For example, instead of asking the question “WHY would you do it THAT way? That makes it look smaller!”  Maybe phrase it, “I ‘m curious as to why that is the better style? Does that make it seem bigger?” Here you are asking for the same information, just with a lighter approach.  Again, it is how you say it.

Most don’t hear themselves when they speak.  So, when you point out that they sound harsh or stern (angry even) they are taken aback.  Often becoming more argumentative.  I have been accused of that from time to time, and when pointed out I quickly look for the better way to say the same question (and apologize for using poor syntax). Nobody is perfect – and now there is even a slang for it…MY BAD! But if we all just took a second to hear ourselves (maybe even record yourself once in a while) you may learn how you sound to others.

I often use a story form 1982.  I was 20 and just diagnosed with Hodgkin’s Disease.  The next morning, I was being operated on – I was losing my Spleen and part of my Liver. Not feeling particularly light (though I was optimistic about the end results). I was having this done at Tufts Medical Center (a teaching hospital – you know with all those seemingly clueless interns like you see on the TV shows).  So, before Dr. Detterling was to arrive, a young intern came to explain what was about to happen.  He spoke fast and curtly and in ‘medical talk’ that I couldn’t understand anyway.  Trying to lighten the mood I asked: “It’s all gibberish to me, so could you just tell me am I going to live or die?” (I was joking of course).  This Intern looked me straight in the eye and solemnly said: “I cannot predict the outcome, Cancer is a very serious disease!”  I was actually too stunned to talk.  Frozen actually.  Luckily as I sat there on the precipice of an emotional breakdown, Dr. D walked in.  His hands and body shaking (in a put-on kind of way), he says “Do you need the scare to be perfectly straight?”  Some of the interns giggled and I relaxed as much as possible.  That lightened the mood immediately.  It isn’t what you say it is how you say it!

This is such an important lesson for everyone.  Interpersonal relationships, business relationships, co-dependent relationships J, can benefit from understanding this.  How many times have you walked away out of a restaurant, a store, or after dealing with a rude person?  Aren’t you soured on that place or person?  And all it would have taken is for them to tell you the same thing in a different way.  These days we read the papers and are meet with Shock and Yawn.  We don’t know whether to cry or hibernate for a while.  If we could just learn that what we say and how we say it matters.  If we could just learn to be positive and light- instead of Angry and Argumentative we can emerge shaky yet optimistic!  I hope for that! The Sun WILL come out Tomorrow!  Bet Your Bottom Dollar that TOMORROW they’ll be Sun and Syntax!

Enjoy, Be Happy and Be Understanding!

Carol

@funnycancermom

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ASKED AND ANSWERED, AND NOT A WORD SPOKEN


dad at busch gardens

Sometimes firsts are good.  The first time you ride a bike, the first time you eat ice cream, the first kiss, the first kid (just kidding both of my kids are terrific).  Firsts are meant to be moments that you will always remember.  But honestly, some firsts you just want to forget.

This is what I am feeling today.  Tomorrow is my father’s birthday.  He came so close to making it to 85.  His death in October was surrounded by such craziness, that I am not sure anytime was really given for grieving.  I mean we mourned, but so much went on in just a few short days of his death that all of those extra emotions kind of got lost in the hubbub.

At the end of September we planned moving my parents to Florida.  Nov. 5 was picked.  Flights were booked, movers were scheduled…and the packing was able to begin.  The process was physically daunting, but even more so emotionally.  My Father was already beginning his final decline (though we weren’t as steep his decline was).  I am sure he was able to register what was happening, and I believe it caused him to withdraw into himself even more.  Many have said he didn’t want to go to Florida…Maybe they were right!  He died on Oct. 21, and the moment the “Shiva” ended, we were hit with Hurricane Sandy; which didn’t even stop the packing and moving process.  Nov. 5 we were on that plan, and off to start a new chapter in my Mom’s life.

My mom and I were speaking earlier.  We speak both talk him all the time, and today my mom said, “but he doesn’t answer.”  Which made me realize something.  He certainly does answer.  He has allowed you to Segway into this new, exciting and privileged chapter of you life, without the heartache of feeling guilty (and you don’t have anything to feel guilty about).  This is his parting gift to you, the woman he loved for over 60 years.  Be happy and enjoy he says…without ever uttering a word.  You and the children deserve it!!!!

So I guess this first birthday with out you dad is also a memory…Know that I wish you here with us…But every day you are thought of fondly, and cherished even more….

 

Happy Birthday Dad….

Enjoy!

Carol

@afunnycancermom

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HOPE


Hope…What an incredible word.  It is what holds us in anticipation, and it is what can spark your individual greatness from within.  It is always looking forward at the possibilities, and cannot be held back in the past.  You hope for the future, you look back at your past.

 

Cancer has taught me a lot about hope.  Of course there is the obvious things to hope for.  I hope I get better, I hope my treatments are not “horrific”, I hope I make it long enough to see my children grow up (that was a big one this second time around), I hope I don’t get sick again, and finally, I hope that I not only get better…but I also hope that I don’t get bogged down by the ramifications of being “afflicted twice”.

 

Hope is what I wake up with every morning.  Some of my hopes are whimsical and shallow.  And that is okay.  While it would be great if those hopes were achieved sometimes, I don’t hold my breath for those. – rather, I enjoy the frivolity of the hoping.  You know those thoughts…”I hope I can lose 30 pound by Friday”, or “I hope I can eat this gallon of ice cream and still fit into my jeans tomorrow”, and of course, I hope to have the chance to meet Hugh Lurie, Hugh Jackman and Zac brown, because I am a huge fan.  These are delicious little nuggets that help me smile on days that aren’t always filled with smiles.

 

Then I have hopes that aren’t necessarily about me, but are about my family.  These are ones that really affect my emotions.  Because these are things I hope for my children, my Husband, my brothers and sister-n-laws, my nieces and cousins, my friends.  I want, no I hope, for them way more than I hope for myself.  My hopes for them are lofty and rich. I hope for them to get what they want, because I hope they will always be happy.  I know that it is important not to always get what you want, but I am a mother first.  And I hope, all the time, I can take away any pain or sorrow my children go through.  But I can’t always do that.  But I am aware that my children also have there own frivioulous hopes…And I encourage them…I think these are what is meant by “Hope springs eternal”…

 

My daughter, for example, hopes to be a star.  Her hopes don’t have a pathway to achieve this, or a definite area in which she chooses to become a star…She just hopes for stardom…and I hope she becomes one as well.  Though, she has no definitive pathway as to what type of “star” she wants to become…her hopes are lovely and endearing (and not unlike many teenage girls), and I hope to help her head that way (though honestly, I hope she finds another hope as she gets older).

 

My son hopes for more simple things.  New videogames, to be better at certain sports, and his biggest hope is that he never has to do homework again.  But of course this last one is not gonna happen.  But he can always Hope.

 

My mother, well I think she hoped that she would be okay when she moved away.  Well we were there this week, and boy she is okay.  She has a brightness and lightness to her spirit.  One which I haven’t seen in so long.  Her melancholy is present, but is being trimmed with hope that her next stage in life will have joy and adventure.

 

So I guess I just hope all of those I love to get what they hope for.  Because then I get what I hope for.  Who could hope for more!

Enjoy Today.

 

Carol

 

Funnycancermom

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Who’s In Charge Here?


Recently, my kids and I were talking about the show “The Biggest Loser”.  There was a commercial clip on showing Jillian screaming at one of the contestants.  I said, “wow she seems so mean, how can that be motivating.”  I was sure my children would agree with me (since they are forever telling me I’m a yeller, and it definitely isn’t motivating for them).    But, yet again, my kids surprised me.  My daughter said, “Mom what she is doing is changing their lives.  She is helping them get better for their kids and that is a good thing….you just yell about homework and stuff.  Totally different!”  Matt said, “having to answer to someone all the time is good for you when you are trying to change something about yourself.”  And while I wanted to tell them that cleaning their room or doing homework, or even being true to yourself are also good ways to change something about yourself…But I thought better of it!

 

It did get me thinking, however, is being accountable for our own actions and being true to ourselves the same thing?.  For example, I was on Facebook the other day….just roaming through to see what people (“friends”) have posted…I like to go on a few times a week and check-in.  There are always the same 3 “friends” that post 20x times a day.  No exaggeration…If I were being true to myself, I would send them a message saying, “99% of the stuff you say is absolute drivel.  Why do I need to hear that your dog is tired, or you were tired after taking her for a walk, or that I should be Happy because it is Sunday, Bitches!” Really, what is the purpose of that?   But, I am accountable for these words, and I realize they seem harsh and uncalled for (though true).

 

These Facebook dwellers live their private life in this public venue but instead of being angry at them, I should feel more sympathetic towards them…I guess it is a modern day depiction of Shakespeare’s soliloquy in Macbeth…

 

…Life’s but a walking shadow, a poor player

That struts and frets his hour upon the stage

And then is heard no more. It is a tale

Told by an idiot, full of sound and fury

Signifying nothing. — Macbeth (Act 5, Scene 5, lines 17-28)

 

Accountability is something I struggle with.  I believe it has a much-needed place in our daily lives, but often gets over looked.  Should we be true to our self or accountable to others?  Are they mutually exclusive?  In being true to myself as of late, I realize that I need to be more accountable to others for things.  Which brings me to my latest project. And back to The Biggest Loser for a second.  Since being sick, I have struggled with my weight.  And weekly I became more and more unhappy with the fact that as disgusted with my weight problems as I am, I have no one to blame but myself.  I have avoided the gym, I had given up on “healthy eating”, and I had found every possible excuse to let myself get this way.   I need to be accountable for that if not to myself then to someone I believe can help me.  So I have joined a group of 28 others on this journey.  I officially start Monday, but I am getting myself ready this week.  For the next 8 weeks, I have to answer to 7 other team members’ about what I eat, and how many times I work out, and how hard I work out and yes, even what I weigh.  I need to prove weekly that I am committed to this and to the team.  There are 4 teams pitted against each other, and I need to pull my weight (metaphorically and physically). …And while this is not the televised version, the benefits can only make me feel like a star.

 

So I have chosen to use my accountability for Good instead of Evil…Personal growth instead of Public ridicule…I will keep you all filled in.  And while my blog may appear on Facebook….My weight never will!

 

Go team Black….

 

Enjoy today

 

Carol

@funnycancermom

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Thank You Nannette Stueck – The Follow Up


IMG_2078Well after I wrote my November 30th blog about Nanneette Stueck, I received over 100 public and private comments on potential ways to find her. I listened to several comments and tracked a series of addresses to Maine.  I sent off a few letters hoping that at least one of the addresses I got would be hers.  But as you see from above, all of my letters were returned …NOT DELIVERABLE AS ADDRESSED.  It seemed to be a dead end.  I wondered if I was going about this the wrong way…But in the end, odd as this may be, it was her that found me.

 On December 17th I got a note posted to my LinkedIn account from Nannette, that simply said she was trying to find me and gave me her email.  I was thrilled.  The next day I got this…(I have taken out the personal details).

 

Oh finally, No, my cousin forwarded your blog Sunday.  I have been attempting to contact you since. Here’s some of the mail I’ve been trying to send you. I tried to post to your blog but it said something about needing moderation and now is gone,  linked in must have worked, I tried  Carol@fXXXXXXXXXX but that didn’t work

Carol –

Last night after watching / helping my daughter XXXXXXX decorate our tree I launched my email, The usual advertisements to be deleted, a note from my sister to call my mom in the face of Friday’s tragedy in Newton, and a note from my cousin Eileen in Pasadena, CA.

She stumbled upon your blog and found your note to me, and she forwarded it, in case you hadn’t found me.  She said she was later night, should have been asleep internet searching….I should probably ask what brought her to a cancer blog….

You are the first person I think of when someone says, “IF you know someone who has been affected by cancer,” but of course I had no idea how many new ways it would touch you in the 28 years since I’d seen you last.

I remember our quick and easy friendship and our talks, I remember our brief rooming while you continued your treatments at Tufts.  I remember too, the odd way people reacted to your cancer and I remember your strength.  I also remember how when you had beaten Hodgkins and graduated that you broke down and cried to me on the phone so scared about the future, and I was in such awe of it, like after all the bravery, why now??  Why is she so scared now, and so brave in the thick of it.  I have cautioned everyone I have known since when they have struggled with cancers, mostly breast and said be careful – watch your thoughts, be ready for the crash, and call me if you need to talk.

I, to date, have avoided the cancers personally as well as with immediate family members.  Great girlfriends and neighbors have had lumpectomies and mastectomies, all very brave and beautiful survivors! But, you were my first….and so you remain the first thought.

Great to find you and I’d love to stay in touch!!!

Love, Nannette

And even greater gift was that she was relatively local over the holidays, and we got to meet for breakfast.  I got the chance to meet part of her family.  They are as warm as Nannette.  And if I didn’t say it to you that day Nannette, you look great…and happy.  I have done nothing but talk about re connecting with you.  I know I owe you an email,.  I have been so busy telling and re telling everyone about that I don’t  didn’t even email to say what a great breakfast it was, and I look forward to many more meetings.

I realized I got a few details wrong, Like Nannette went to Simmons not Northeastern, but we figured why I thought that….But all in all our memories coincided.

What a great Holiday Gift it was to reconnect….It was a real great feeling finding you and thanking you.  I believe it completed  closure on that time in my life.  And gives me the chance to create a friendship with someone I know has a great heart!!!

New Resolution #1.

*Be grateful and always say say thank you to those you feel deserve it!

CHECK

 

ENJOY TODAY!

 

Carol

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Thank You Nannette Stueck


Over Thanksgiving weekend, my children, my husband and I were talking about sleepovers.  My son asked if I liked them and/or if I was ever scared to sleep somewhere else.  It was seemingly innocuous question.  Yet it caused the flash of a memory that I hadn’t thought about in a longtime.  It was almost movie like.   The memory was so vivid, and the emotions it conjured were so real.  So real I wanted to tell the kids all about it.  This is what I told them…

There was one time that I was afraid from being away from home.  As you know, I was diagnosed with Hodgkin’s disease when I was a senior in College. I was operated on around mid-December, and Christmas break was coming up.  It wasn’t easy or quick, but I made the decision to stay in Boston, and have the treatments there.  Away from my family.  The dorms would be closed for the holiday, so I needed to find a place to live for the month.  I guess I could have stayed in a hotel, but I didn’t want to be totally alone.  There was this other college senior I worked with at Copperfield’s.  Her name was Nannette Stueck, and we worked together at a bar between B.U. campus and Northeastern (where she went).  She and her boyfriend (now husband) Scott all worked together, and we had become somewhat friendly.  When I told her what was going on, she immediately offered me a place to stay for the month.  Her roommates would be going home for the break, and she didn’t want me to be alone for the holidays.  A single selfless act…

I was touched by her invitation, and moved in the next day, because two days later I was to start treatment.  I woke up at 5 a.m. and travelled via Trolley, then train to get to the hospital.  It was bitter cold, and dark, but I went.  After about 2 weeks, I began to feel the side effects of treatment.  Initially, food became tasteless. Everything I ate scratched my tongue and throat.  It was like swallowing extra course sandpaper.  Nannette decided to spend a day trying to cook different things that I could eat.  She made puddings, and jello’s and just a whole bunch of stuff.  It was unbelievably sweet.

A week later, I woke up because I felt a draft on my neck.  It was about 4 in the morning.  I got up and checked the window, but it was closed.  I checked the door to my rom, but it too was closed.  I couldn’t figure out what it was, but it was almost time to get up anyway, so     I went to switch on the light to the room.  It was then that I realized why I felt the draft, and I began to weep.  There, on the pillow, was a thick clump of my hair.  I couldn’t imagine that it would fall out like this.  But there it was Nanette must have heard me crying.  She came into my room and sat with me.  Told me you could hardly tell.  I knew she was lying, but she said it in a way that made us both laugh.

Nannette Stueck was my hero then.  She made me laugh and forget what I was going through!   Most people thought my decision to stay in Boston to get treatments was odd, at best.  But I knew I would never have gone back to finish my degree if I left.  I needed to continue, to go on as though nothing was wrong.  Because the alternative was that everything would stop.  My college career, and my life…And Nannette got that.  She saw I was right to do it, and made that month okay…Fun even!

It has been years since Nannette and I were in contact.  With Facebook, I have hoped that I would find her over the years.  I try.  I put her name in, but nothing comes up.  So Nannette Stueck of Ridgefield, Ct who is married to Scott from Sudbury, Mass (maybe Swampscott…I don’t exactly remember where in Ma. Scott was from.  Though I do remember the gorgeous church you got married in).  Because of you, I put every effort out to help others; whether I know them or not.  It is a truly fulfilling feeling to help others.  I thank you for introducing that to me!

Nannette, I hope you are well and happy!  I would love to find you, but understand that I may not.   I want you to know that I tell my kids about your kindness all the time!  I hope to one day say THANK YOU in person!  Your selfless act o kindness changed me forever.

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BUSY LIFE…and loving it


What a summer I have enjoyed.   With my kids in camp, and not a Dr.’s appointment scheduled…Well except for a yearly Gyno appointment, I had an “worry free and health issue free summer.”  I know that is how most people enjoy life, but for the past three summers, as many of you know, either I, or a family member, has undergone one sort of cancer treatment or another.  And this summer…that was not the case…Now, this is not to say that I don’t have friends being faced with this awful disease and treatment, because that would not be true.  And this is alos not to say that I don’t think about what they are going through, or ways I can help them get through it.  I have, however, enjoyed a summer of appointments, and errands, and meetings, and tastings, and dinners out, and visiting friends, and visiting family, and planning for the kids 13th, and…well just all things I have not been able to do for the last 3 years.  All things that are just part of LIFE….and boy was I thrilled to do them all.

With that being said, with my new found freedom, I gave up on the blog for a spell.  And honestly my schedule for the next 3 weeks doesn’t let up much, so my blog may lay dormant until the beginning of October (or maybe even November).  But fear not, I will return and with new inisght into just about everything.  Even though the title remains The Cancer Made Me Do It, I will begin to tackle all different “life” issues, from the same humorous (yet sometimes cynical) perspective.

My summer has also presented a new emotional turmoil.  My Mom and Dad, who I have written of often, are moving to Florida just after Halloween.  This move will give them a new and improved lifestyle.  I am so thrilled for the opportunity my brother and sister-in-law have helped to create; but I can’t help but feel sad about loosing my constant, and loving lunch mate.  Of course, now I have a reason to go to Florida (one other than Disneyworld).  I am thankful to Facetime, Skype and all of these other technological marvels because that will make it a little easier.

So while I am busy with so many things…helping to pack them up and move them just adds more to my schedule.  But, again, a busy life is better than no life at all…

So I bid you good-bye for a few weeks.  And wish you all well…

I will be back.

Enjoy today

Carol

@funnycancermom

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CONSUMPTION


What can I say, this is my summer to enjoy.  My children started at sleep away camp 4 summers ago.  Honestly the 1st summer I was to consumed with whether the kids were enjoying/having a good time or not.  The 2nd summer, I had it a little easier — but my sister-in-law had been going through chemo so I  travelled out to help her a few times, so it was not a totally relaxing summer (no complaints though, I was happy to go and help).  Then of course last summer was my turn…and needless to say, 0% relaxation was involved.  Chemo, my Mom, and other family issues made for a summer I never want to repeat (though the kids enjoyed camp).  So when it came time to think about what I wanted from this summer there were a few different scenarios.

1st – I wanted the kids to have a great and stress free summer….With nothing to worry about….CHECK

2nd – I want everyone to be healthy and happy…CHECK CHECK

3rd – I want to relax and do what I want, when I want and how I want….CHECK CHECK CHECK (so far)…but this last has lead to a small issue….

When I was young, I remember hearing stories about relatives (usually my grandparents siblings) had been taken by CONSUMPTION.  It all seemed so common, and I could nt really understand what it was they were talking about.  I gathered what they were saying was that CONSUMPTION could kill – and often did.

We since my children have left, I have consumed massive (yes I mean Massive) quantities of food…I have been eating with abandon (an odd old saying, but seems fitting).  And as I got on the scale this morning…I THOUGHT I WAS GOING TO DIE….FROM CONSUMPTION OBVIOUSLY!!!!

I am back, and I missed writing to you all, I am going out for a walk now (because won’t that take off a good 5 lbs?)  Health and Happiness aside, I really plan on enjoying this summer…but maybe I will get out more and consume less  OR NOT!

ENJOY

Carol

@funnycancermom

 

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Pound Foolish


I believe that honesty is the best policy.  If you can’t admit to it, then you know it is wrong.  Well I will admit it…Over the last year I got BIG.  30 lbs bigger than I was before Cancer.  And it really sent me into a tizzy.  I know how silly that sounds that my weight can phase me more than my health.  But it can.  I am the type of individual who cares about my appearance.  Not in the “designer clothes” sense…just in my appearance.  How that appearance is perceived.

It is along the same lines as when I lost my hair.  I gave off the appearance of being “sick”…and even though I had cancer, I never considered myself “sick”.  I may be generalizing, but I believe women feel that Hair and Weight are also personality traits — I mean a bad hair day can alter your personality for the day.  Now, due to the cancer, I won’t have bad hair days anymore.  No, not because I don’t have hair…because I do.  But because the way it grew in is so cute, that I am going to keep it short and silver…A friend called me a Silver Fox the other day,  and I liked it.  So that part of my appearance is in check.

So lets get back to the weighty issue at hand.  Weight.  I am not here to say that I am obese, but I am large for me.  My bones ached constantly from the additional weight they are carrying; I would loose my breathe easily when walking up stairs or exerting myself at a rapid pace.  And my internist and cardiologist confirmed it…(and to think I call these two my friends as well)  — I suffered from DECONDITIONING.  Over-weight and out-of-shape for us laymen!  As he said in the movie NETWORK…”I was mad as hell and I wasn’t going to take it anymore.”  So off to Weight Watchers I went.  That was 6 weeks ago.  I have had good days and bad days on the diet but this morning I got on my scale (not their’s yet cause I wear clothing there…Thank god!)  But on my Scale I reached 169.9 Lbs.  That is down 13 LBs.  13 is my new lucky number.  I have been doing exercise and dieting and it is really making a difference.

I was so happy when I saw that I went right down stairs and had a donut…JUST KIDDING! But I thought about it!  I have 17 Lbs to go before I hit my goal…which honestly was the heaviest I had been in 10 years, but right know that weight will be fine.

So I guess, after my anniversary from surgery was yesterday (if you remember, I had re-named my double Mastectomy day “Erin go Brahless Day”) I  didn’t worry about my weight during treatment (MUCH), but it has weighed heavy on my mind (& body) since…So I see this as another step in my recovery…

I will soon “Tip the Scales of Time” in my favor….and once again will be as “light-hearted” about this issue as I was about my cancer.

Even my puns have gotten a little thin….

Enjoy today!

Carol

Funnycancermom

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Stop writing and talk to me


Well I have been talking and talking…scratch that, I have been writing and writing to you for almost a year now.  Wow!  My posts have been read over 11,000 times…and that is pretty cool, as well.  But I thought it was time to put a voice to these words and let you know what I am up to…Luckily enough two unbelievably talented photographer/videographers were interested in my story – so they have created this to help me launch my new Charitable foundation (My Mission and vision is below).  Thank you all for being here with me!!!  You inspire me!

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Blog Mission and Vision

Enjoy today!

Carol

Funnycancermom

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TCMMDI


What can I say.  I got nothin’.  I have actually been ecstatic about it.  Writing this blog is a passion of one, but so is life.  I have not written as often as I used to, and I am finding myself apologizing to a few fervent followers for that…But I am not sorry.  I am just living!

I have finally and officially set up my Charitable Foundation.  Yes, THE CANCER MADE ME DO IT, INC.  is an official charity (501 (c) 3.

THE CANCER MADE ME DO IT

A new 501c3 charitable foundation

And news of a

 Golf/Tennis event to raise funds for Research grants in the following areas:

Breast Cancer, Hodgkin’s/Non-Hodgkin’s Lymphoma, Multiple Myeloma, Head & Neck Cancer (THANC), Leukemia, and Parkinson’s

Some have asked why I chose these ‘diseases, and I that is easy to explain.  While I can switch the “grants” year to year, I wanted to begin with these that have effected my life directly.  Breast Cancer and Hodgkin’s for me, THANC and Parkinson’s for my parents, Multiple Myeloma for my Mother-in-Law, and Leukemia for some very dear friends….How I wish there was no need…but that is just not the case.

So, at the beginning of March I will hold my first meeting to recruit friends , family, neighbors, co-survivors and supporters to help with (what I hope will become) our signature charity event.  A golf/tennis outing – followed by a wine tasting and cocktail party.

I am nervous as Hell!  I am like a scared little girl navigating a playground at a new school on the very first day.  I know I want this to be successful, and I know I want people to want to be involved, but I worry that I can’t pull it off, and that I don’t get the support I need.  And then the whole thing falls apart.

But even with all of this nervous energy…I am going forward with it.  I am Lucky enough Cristie Kerr (#3 Golfer on the PGA Tour) as a “face” of the event.  Pride Family Vineyards – and Curvature Wines as sponsors, I am even in contact with the owners of one of a popular “fashion house”.  SO I think like I handled being sick, I hope to handle this next project…Eyes straight ahead and focussed on the end….reaching my goal and not letting any of the many hurdles I will face slow me down….

Yesterday my Mom told me of a conversation she had with my oldest brother.  She said he was certain that I would be successful at this.  His confidence in me is truly heartwarming and is a real bolster for my nerves.

For now, I am researching these kind of events, and gathering information.  I look forward to any help anyone wants to offer.  Whether it be in knowledge on how to run these events or just interested in being involved.  Or just listening tome talk about it for a while.

I am just glad to talk about it, and spread the word.  Who know’s maybe one day it will be as large as the Michael J. Fox Foundation…Or even better, I look forward to crossing off disease’s as cures are found…Then I can hold a Golf/Tennis event just for the fun of it!

Enjoy the day

Carol

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Now I have gone and done it!



Alright it is official, I have submitted my first article for consideration in the NY Times! YIKES! They probably won’t pick it anyway, but as they say at the Oscars “It’s an honor just being nominated.” In this case, it is enough for them to even consider my article. Nobody I grew up with would have ever pegged me for a writer – EGADS!

I finished the editing process this afternoon — I had written the piece 3 weeks ago. And after getting some “editing” help. I nipped and tucked it into its final form. And then I read it, and read it again, and just to be sure…I read it 1 more time. Cause all of you know “SPELLIN’ AND GRAMMAR AIN’T MY THANG!” But I thought for the NY Times, I should try to do my very best. I am actually scared to go back and read it again, for fear (now that I have submitted it) I made a silly error….Anyway, I sat at my computer with my finger floating over the “enter” key which would send it soar through cyberspace. Should I do this? Why do I want to do this? Screw it! I am doing this…and

Well, I will not hear for a few weeks; I find solace in that somehow! And then if it doesn’t make the paper…atleast I have a future blog written!

I have got my fingers and toes crossed!

Enjoy today!

Carol

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This has nothing to do with it!



I know it is random but I was thinking about Tim Tebow. Why you ask, well let me tell you.

I was watching his post game speech…you know the one in which he Thanks’ “Jesus” for his platform. Anyway, I was wondering. Is this really what the “savior” is doing on Sundays…Watching Football? I can think of other things he should be doing…don’t you! I mean if he/she can’t tear themself away from the TV, than at least perform a Half-Time miracle or something – cure cancer, stop world hunger, somethin’!!! I mean Really!!! Mr. Tebow is getting paid a hefty sum of money to perform…If you, as his leader, are doing the work for him, isn’t that cheating – Whadda got money on the game?

Just a thought!

Enjoy

Carol

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I have my reasons!


My friend Audrey called me today, to say hi and check in. During the conversation she asked me if I was going to write a book. I told her I had my reservations about doing so – and gave her a few reasons. She said it would be great if I could share my story with others, because she found it so inspiring. I am not bragging, but I have heard this before. But every time I hear it I have the same reaction. Discomfort, awkwardness, and utter confusion.

I assure you, I am neither humble, nor self-sacrificial… I just don’t get it! Inspirational, why? Admirable, really? I have had cancer…twice? Not so admirable, believe me! If I was given the option, I would wish to “not have a reason to write a blog!”.so not so inspirational. What I do have is the desire to make it easier for someone else, after me. That is a maternal thing I believe. Didn’t your mother always say “If I knew then what I know now…” (Yeah, I know I hated when she said it too); but she was right, and that is all I am trying to do. Give someone in the future a little hindsight into my past!

Some of my Dr.’s have had patients call me to talk, and some friends have passed along my blog to friends, or have asked me to speak with a friend or relative. I am an open book. I don’t do it for admiration, or for adulation…I do it because I know how scary it is. I know what it is like to be young and diagnosed…I know what it is like to be old (older) and diagnosed. I have had full body radiation, and chemotherapy. I have had internal and external organs removed, (and yet I still gain weight! Go figure). I have definitely earned my credentials as an expert patient!

So for right now, no book! I would be happier if no one needed to seek this kind of information, the “cures” are still a ways off. In the mean time, I am here…to give you advice, or just to listen, to tell you a funny story, or an embarrassing one (of which I have many). I am who I am – and that is all I want to be – for now anyway!

Enjoy the day!

Carol

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