Category Archives: motivate

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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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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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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That’s Life!


I can’t tell you how happy I am that 2011 is over. I was ready to start fresh. Of course a new year can present with a whole new set of issues…but nothing we can’t handle…

I made some resolutions, like everyone; and I hope to be able to stick with some of them…I want to lose weight, and get in shape, and get a job, clean out my garage, get organized, and I want to enjoy myself, and just continue to be happy and healthy. These are my resolutions — not unusual..I will make an effort to achieve each and every one of them….but I don’t think I will beat myself up if I don’t…Okay maybe I will but That’s Life — and isn’t it grand!

My daughter came home from school yesterday, she has the stomach flu! It really put a crink in my plans for the week. I had a Doctor’s appointment, and a million errands I had to take care of, I wanted to work out, but nothin’ is more important than taking care of her. She is ‘sick’, but it’s the good kind of sick. Sick that goes away in a day or two…and That’s life. And isn’t it grand!

A week ago, I was cooking and I went to grab a dish out of my cabinets. It was on the top shelf of a cupboard by my stove. I grabbed it, but unfortunately didn’t have a good hold on it and it plummeted to the counter — actually on the cooktop stove to be exact. And ‘poof’ cracked 1/2 the stovetop. I beat myself up for a day, because I really was so annoyed with myself…but after a day or two I realized…things could be (and have been) worse, so I refocussed on how to get the problem fixed, and again I realized That’s life! And isn’t it grand!

Tomorrow my dear friend comes in to town for the weekend. Along with her is her daughter (who is my daughters best friend.) They don’t get to see each other often…2 times a year at best — Though FaceTime certainly makes that easier to deal with! We have family plans all weekend, but I have made sure they will at least spend as much time together as they can. Because plans’ don’t always work out..That’s Life, and yes, isn’t it grand!

Life is filled with ups and downs. We get what we want, sometimes, and sometimes we are left empty-handed. We achieve our goals and strive to fulfill our resolutions, and unfortunately, we are not always successful. We dream big and want the best; and along with those hopes we can be disappointed. But take it from me, That’s life, and yes it is grand!

Here is to a Grand New Year!

Enjoy Today!
Carol

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Tomorrow


Since Saturday I have had a stomach bug, a colonoscopy, my son got the stomach bug and I lost my voice…and yet I am certain tomorrow will be a better day…

Come to think of it, my last five years have been pretty much like the last week, and I still believe that tomorrow will be bright…go figure! Today I realized that the holiday season hasn’t been particularly good to my family or friends over the past 5 years, and yet I still believe that tomorrow will be a better day….

I was talking with someone this morning and my friend Sharon came up. Sharon was a glowing, beautiful woman who was truly happiest outside in her garden, on a beautiful day, toiling the soil, playing with her dog, and chit chatting with her family, her husband (her true soul mate- Steven) her friends and our kids. She always said a perfect life would be owning a flower shop and bringing her dog to work everyday. Nothing ever really dampened her joyous, sparkling, warming and loving personality…That is until the cancer did almost 5 New Years Eve’s ago. Our circle was devastated – and my children even more so, for they had lost a true “angel” in their life. So with every ounce of strength I could muster for my children and my husband, for Sharon’s husband and children, I picked myself up and once again believed that tomorrow will be a better day….

Steven, a therapist, had truly lost his partner. I love my husband and I know some unbelievably wonderful couples — but these two were in a class of their own. They were truly each others better half. Steven’s sense of humor began to come back about 6 months after her death. Little drips and bits would emerge. My husband was overjoyed, because even though he has lots of friends, he had no one as close to him as Steven. Steven became the 5th member of our family. Not a meal was eaten without him seating in his seat next to my daughter. His daughter, Lauren, also got to join in in whenever she wanted. Once again, we were a happy crew. We were back to our regular crew dinners with Wendy and Doug and the boys…so light once again began stream through…that is until cancer took Steven Almost 3 January’s ago.

SHARON

STEVIE


And once again, I thought my children and my husband must believe that happiness is always possible (pretty much because I believe it to be true), so I strapped that smile on and went about the business of helping them get through it all. Laughter, happiness and joy had returned to my kids, and my husband (thought he still struggles with that from time to time). I would often wonder where I got this attitude from…and that would be my mother. She always believed in a brighter outcome. Especially in October of 2010 when she went to the dentist for, what she thought was and absess in her tooth. That day, a long one, yielded us with the diagnosis of Mouth Cancer. And on December 13th, 2010 she underwent surgery to remove a small portion of her jaw and right hard palate. But as luck with have it…having 2 people with positive attitudes is double the boost…and with nary a complaint or bad day we finished out another holiday season believing that tomorrow will be a better day…

All of you know my story…Since I was diagnosed on Valentines day 2012, I consider this year a good one. My Mom and myself enter the 2011 Holiday season healthy and happy. Happy because I refuse to think of it any other way. Steven and Sharon would be annoyed at me for being any other way. My children would not benefit from me being any other way, and my husband would not want me to be any other way.

I realized I started thinking about all of this stuff today because, as I nurse my voice back to health, I prepare to be a guest on Paul Fiener’s radio show tomorrow (12/9/2012 FROM 10 A.M. TO 10:30) on WVOX – 1460 on your AM dial (or streamed live on your computer at http://www.WVOX.com). And I realized what it is I wanted to talk about…because even though I was invited to talk about my blog and it’s future. …As we enter the Holiday season again, I just want everyone to know that TOMORROW WILL BE A BETTER DAY!!!

ENJOY AND LISTEN IF YOU CAN!

All the best,

Carol

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House Cleaning


Holidays are coming. Gifts are being wrapped, and I am making room for the new purchases. I am always surprised at how great it feels after I have finished a good purge. I feel accomplished, I feel organized, and ready to take on anything that comes.

The last few days I have done a different kind of house cleaning. Today I am going for my colonoscopy. So when I talk about cleaning out the house…I referring to my own inner house. An odd thing to write about, but let me assure you I wish I knew more about it before my first one (20 years ago). The preparation is key and really the trick to make this not so bad – and yes, like my chemo, can have some real upsides!

First of all — know your “prep” options. Some gastroenterologists still stick with the old fashioned “go-lightly drink” In my opinion absolutely fowl!!! Another drink is the Magnesium Citrate (just a medical term for YUCHY!) Now I am not saying these two methods aren’t affective,; cause they are! But they also take a toll on your whole body leaving drawn, tired, and generally feeling poorly.

About 10 years ago, I was introduced to a new method – “Visicol Pills” This was a huge improvement. They are horse pill size and you have to take a lot a short time (along with a gallon of water)…but I didn’t have to drink that nasty stuff. Then 3 years I was introduced the Miralax and Gatorade prep. It absolutely does the job, while simultaneously replenishing your electrolytes. You do not get that same draggy, yucky feeling.

Okay and here is the pitch to get your colonoscopy when you are supposed to — Early detection is the #1 defense against colon cancer. And if that doesn’t convince you here is the other reason (and my favorite one)….

Yesterday when I started the “prep” I weighed 7 pounds more than I do today…THATS 2 WEEKS ON WEIGHT WATCHERS!!!!!

So when it is time for you to get your intestinal house cleaned, remember there is a light at the end of the tunnel…or just know you are lighter at the end of the procedure. In my book, either way, a win win! Viva La Purge!

Enjoy today

Carol

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Birthday Wishes


Many of you already know that I am turning 50 on September 18th. so I sent out this email to my entire contact list.

Dear Friend,

I am not trying to be pushy, but I really would love you to be a part of a very significant day in my life. On September 18, 2011 I turn 50; and on September 19th I will get my final chemo therapy treatment that will hopefully irradicate any left over signs/cells/remnants of breast cancer that may have still been left in my body after surgery.

The walk is important because it brings together other Survivors, Family members, and/or friends that have been affected by this disease. And as one community, we walk/run together to put an end to it!!!

I know that I have emailed already, but if you are walking with me I need to know as soon as Monday August 29th…for I am having T-shirts made for our team, and that is the deadline. To do that you MUST sign up online through http://www.komennyc.com, and search for the race page for team THE CANCER MADE ME DO IT. Their is a sign up charge and then you start getting donations by emailing it to all of your friends. If you have any questions please feel free to email me and I can walk you through it.

If you can’t make it to the walk, I hope you will support one of your friends that is walking, or support me by going to my race page and donating. I am shamelessly asking you to donate — make it a Birthday gift to me if you must….

Please log on and join or donate as soon as you can. And if you become a team member — start fundraising as soon as you can.

Thank you for all of your help.

I hope to see you on race day!.

Click here to visit my personal page.
If the text above does not appear as a clickable link, you can visit the web address:
http://www.komennyc.org/site/TR?px=1268984&pg=personal&fr_id=1230&et=UBxXw1GoP9jiqbtUmSY95g..&s_tafId=61036

Click here to view the team page for The Cancer Made Me do It
If the text above does not appear as a clickable link, you can visit the web address:
http://www.komennyc.org/site/TR?team_id=44251&pg=team&fr_id=1230&et=aAKRY2N-Uax1JxOfVi0J1A..&s_tafId=61036

If you no longer wish to receive email messages sent from your friends on behalf of this organization, please click here or paste this URL into your browser: http://www.komennyc.org/site/TellFriendOpt?action=optout&toe=31c8fd68afe0f5ca6b25114ec2935f95

The response has been unbelievably heart warming. Even those who can’t make the race have found ways to be a part of my team. My friend Kathy (who owns Katherine Winters Salon) is cutting for the cure. On September 9th she is donating her profits to my team. So if anyone wants a haircut – aside from the fact that she is AWESOME at what she does – she is a woman with a gold heart.

You have heard the expression “it takes a village” I live in a great one. Wow what a great feeling — This is going to be the best birthday ever….And you all helped make it great. I am forever grateful and I thank you all. You are the ones who are awesome and who have inspired me…

With great love and respect for you all!

Carol
@funnycancermom

Enjoy today!

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Past, Meet Present


I live in a town that I never visited as a child. Even though it was very close to the town I grew up in. So I found it strange that when I moved here, I have met many people who I knew from different parts of my past. The first time I would run into a person that I knew, the memories came flooding back. I would stand talking to the individual while simultaneously visualizing the last time I saw him/her, the last place I was when I saw him/her, and the circumstances surrounding me at the time I last saw him/her. Now that doesn’t happen the next time we would run into each other, but that first encounter always opened the floodgates.

Tuesday, Scott and I decided to take the kids to Boston for a few days. Through a friend we had gotten Boston Red Sox tickets. Somehow my son has become a Boston fan — though I am not sure how that happened. Anyway, after I got the tickets, we thought we would go and spend a few days there. Seeing the game, walking around Fanuel Hall, seeing the Aquarium, going on the Duck tour…the fun touristy things…which where not the usual things I did when I went to BU. The kids were thrilled – especially when I told them about Anna’s fired Dough. Anna’s fried dough was a Kiosk at Fanuel Hall (back in the 70’s and 80’s) that served fried dough with powdered sugar. REALLY WHAT IS NOT TO LOVE ABOUT THAT! I loved them so. I remember that during my Senior Year, when I had to go to the Hospital for Blood Tests or weekly check-ups, I would swing by and treat myself to one. It was my way of rewarding myself for being a cancer patient; and frankly being 5’10 and only weighing 126 lbs,I figured I could use the weight gain. I am ashamed to admit that my present day “cancer body” is a little jealous of my past “cancer body”. But eating what you want whenever you want to — doesn’t Suck — just sayin’.

Anyway, Tuesday morning we packed up the car and off we went. The kids were in the back enjoying a movie, Scott was in the passenger seat enjoying a snoozy and I was driving and listening to my country tunes. We had been driving for about 2 hours when we hit the Mass. Pike and out of nowhere, I began to cry uncontrollably. I couldn’t stop myself. Thankfully my kids were wearing headphones. My head was spinning with thoughts. I realized I hadn’t been back to Boston since college. I left in 1983 – Cancer Free! And yet here I am returning No longer Cancer free. It was as if I was meeting an old friend and the memories came flooding back. At first I couldn’t figure out what brought the tears on and then I saw a Billboard like sign (one that I had seen a few miles back when the crying started). It was the sign for Tufts Medical Center – the place I was treated, the place I went every day for 60 days. A place that I credit for saving my life, and for also bringing me back full circle.

I regained my composure in a few moments, but it was a real watershed moment. When we got to the Hotel I told Scott all about it, and he sweetly told me I should have woken him up. But this was one of those private moments I needed to face and deal with on my own. These were emotions hidden so deep, that they even shocked me as they appeared. I needed to face my past, by concentrating on my present. So I put the past away and looked in my rear view mirror to see my present and future still enjoying their movie in the back seat; I deal with my life the only way I know how…I enjoy what I have — and that what I have is a life filled with people I love.

I am positive about one thing though, the next time I come back to Boston, my memory will not be about cancer, but rather about the great 3 days we had as a family, and the amazing Red Sox Triple Play we saw at Fenway.

I know where I have been and I know where I am going…and I hope that my future leaves all of my cancer memories in the past.

Enjoy today

Carol
@funnycancermom

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HEAT


We have had record temperatures for the las few days, and it got me to think about the heat.

We have heard about heat indexes and actual heat versus “feels Like” heat, heat stroke, heat related illnesses, record heat, and scorching heat…

Heat is funny because when you have it (or rather to much of it) it you want it less, and when you don’t have it you want it more.

During the winter you seek the heat while simultaneously wishing summer would arrive quick.

During a summer heat wave you wish the heat would break, while simultaneously wishing for the cooler temps of a beautiful fall day.

If you are a Pitcher all you want to do is bring the heat, and strike the batter out.

And if you are a Miami resident the Heat can be a blessing and a curse – depending on whether you are talking climate or sports.

If you are a criminal you have to avoid the Heat;

And if you want to stand up for a mistake that you may have made you have to take the heat!

If you in back, neck, or knee pain you seek a pad of heat,

and to bring life back to a frozen Lasagna you need to re-Heat.

People who live in Arizona don’t mind it because they say it is “dry-heat”

But my treatments haven’t been so nice lately, and I feel like I am running a dead heat to beat the side affects, and not always winning. The fevers and chill this week weren’t the greatest, but just like all good things – even a heat wave, it comes to an end, and this morning I woke up felling like myself again!

So like most of us I am staying inside — I am just trying to beat the heat.

And may cooler heads prevail.

Stay cool and enjoy

Carol

@funnycancermom

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KEEP IT MOVIN’


Please forgive my absence for the last several days. The duties of motherhood superseded my life as a cancer patient. And frankly it was a great diversion; especially after the awful week I had prior due to the double dosing. And as I had said, I did that so I could be full strength when my family was back together in August. Right reasons, wrong decision, and we are moving on.

Having to go and do for the kids this week was great. Visiting day was yesterday, and I wanted to get all the things they wanted (or really I wanted to bring them) – so, it gave me a reason to get back on task. So I decided it was time to get my schedule back to the way it used to be. Back before “Chemo” was part of my daily life. So Monday morning I went back to Pilates. It used to be part of my weekly routine. It was awesome. Being stretched and pulled in ways you don’t really think are “anatomically” possible has true restorative powers: Even if my muscle’s seem to wobble for a few days after. That one act of ambition, lead to many more. I walked on Tuesday and Wednesday, and Friday; and even went back for another pilates session on Friday.

All that excercise had “steroid like powers”. After a week of feeling good and exercising I truly felt energized. Friday I basically left my house at 8:30 and didn’t get home until 6. Then friday night I went out for dinner with friends. And I still had energy. Saturday morning Scott and I got up at 5:30 (yes a.m.) drove 2 1/2 hrs to camp; where we spent the day doing activities with the kids (I admit I watched a lot more than I participated), and in the afternoon all 4 of us went swimming in the lake. And just as a side note, for me it is a lot easier to be seen in a bathing suit in front of people I don’t know, cause I won’t see them till next year and they may not remember that I was the white whale in the cheetah print (sublety is my speicatly) bathing suit in the water. After we said our good bye’s we drove home changed and went out to a party. And I still feel like I had energy. I can honestly say, I am a little tired today, but I think after a few days of running like I had — even a “non-chemo using” 49 year old adult would be tired.

So it got me to thinking – maybe exercise is good for the mind as well as the body! HMMMMMMM! It is a concept, and one I will take under advisement. It is not that I want to be rash and exercise every day — but this can truly be the start of something great — and maybe even take off some of this chemo weight. I just want to lose a pound, OK, maybe eight. Oy did that additional drug cause a glitch in my mind — I seem to want to rhyme. Oh, I will worry about that another time.

I’m back and happy to be so!

Enjoy the day!

Carol
@funnycancermom

2 Comments

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The wish you want can be the one you don’t!


This week I learned that “Getting what you want” is not the same as “Wanting what you get.” I was so hard pressed to move up this one treatment to a two week “dose-dense” treatment, I never really thought it all through. I wanted to move them closer together for a few reasons.

First, my husband is taking a week off when the kids arrive home from camp. I was thinking that if I had chemo that week, it wouldn’t be much fun for the family. I think that it would be nice to have everyone home and happy and energetic..so that we could be a “normal family” for a week.

Secondly, I thought it would be sad for the kids to get off the bus, and wee me the next day all yucky from chemo. MY intentions were all solid.

And the final (and, yes, selfish reason) was that it would move up my FINAL treatment to the day after my 50th Birthday. What a great Birthday gift for me it would be.

Now that I have done it, I am not certain I really thought all of this through. It will be great to be all together the first week, but the week after I have chemo and no back up. The kids are not in school, and many friends will be away – so they will spend the week inside and bored. They will get to see me “sick” first hand. Not that they haven’t seen me up until this point, but this is just 24/7 of me not great…and I didn’t want that. I have enjoyed “Supermom” status up until now. I am working on a solution this problem though.

Moving up the chemo 1 week also overlaps with my husbands birthday. And while that may seem okay, he really has been so great that I think he deserves a night to celebrate him and all he has done for me. But I kind of messed that up as well. He isn’t upset about it, I am.

And lastly, and the biggest issue I face today (and the last 2 days) is this course of treatment has really made me feel pretty weak and gross. I have gone through this whole thing feeling relatively okay, and because of a desire to finish “a little” earlier — I have lost a little of my “swagger” so to speak.

None of this is awful, or debilitating, but I am definitely not myself. I am neither happy nor sad; I am not bubbly or blue; and I am not spunky nor sick…I am feel achy and abnormal. I am just BLAH! Not a word I would ever really describe myself as. I am sure that I will bounce back in a day or two…but, admittedly, I wish I would have just left well enough alone.

During this whole time I have never wished for not “being sick”…because I am and what would the point be. I have not regretted the decisions or the path I have taken with my illness. And I most certainly don’t take any of the moments with friends and family for granted. I cherish each and every one. This illness has motivated me in ways I could not have ever imagined…and I am so thankful for that. So I got a little greedy in a way. I wanted my chemo and my wine too — and I have learned that I can’t “always” have both – just because I want to. So I will not up my treatment again. This is a one shot deal, and I have learned much from it.

So I guess the old saying is true “Be careful what you wish for. Because it just may come true – but not the way you think!”

Enjoy today.

Carol
@funnycancermom

4 Comments

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