Category Archives: crazy sexy cancer

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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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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It’s My Anniversary!


I can not believe that is 1 year ago (well really February 14th) that I went in for my routine Mammogram.  A day that started out like many other – though because it was Valentine’s day I knew my husband and I would be going out for dinner at one of our favorite local haunts “Mima”.  Off to the Dr.’s I went.  I had  my Mammogram, my ultra-sound and then straight to an exercise class.  I was feeling pretty lucky because I had gotten in and out in just over an hour.  No waiting.  I should have known then that this wasn’t a good sign!

I had gotten home from the gym at 10:30 and the Dr.’s had already left the message that they found something.  The rest of that day was a blur until the night.  Then, recently John, the owner of Mima, and I were talking up this upcoming Valentine’s Day.  He was happy to see that Scott had made reservations.  I said it wouldn’t be Valentine’s day with out it, but it is also the perfect way to end a year of “Tumult”.  You see last year Scott and I enjoyed a wonderful dinner.  And over coffee and dessert (I had both because my lovely, thin, husband doesn’t eat sweets) I let him know about my day.

At first I think he was shocked that I had kept this news in all day…and I hadn’t called him at the store to tell him. How awesome was he!  He put his hand on mine and said “I am sure it’s nothin’, lets’ take one step at a time.”  I appreciated his calm strength…and I never told him I could see his true feelings in his eyes.  The following week I had learned my biopsy results (Surprise, it was malignant…oh wait you know that already).

What amazes me so is that it is one year.  365 days.   I just can’t believe how much CRAP I have shoved into that little time.  But Wednesday morning I will wake up and say…Happy New Year and start over again.  Day 1…Clean Slate, Clean Bill of Health, Clean House and Clean Clothes (you know cause Wednesday is the day I have the cleaning people come).  And to celebrate, we are going on vacation.  I have never looked so forward to it as much as I do this week.

To my friend Sue (who went through this after me) and to my new friend Susie (who is just starting her journey) I can’t wait for you to be on the flip side as well.  and we can celebrate the hell out of your anniversaries…

So here’s to having Valentine’s Day as a just another Hallmark celebration, rather than one that reminds me of my past year.

 

HEARTS TO ALL.

Enoy the day!

 

Carol

 

 

 

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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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Who’s that girl in the mirror?


It is rare, if ever, that I have been happy with a photograph of myself. The photo above is the closest I have ever come to being happy about the way I look. Especially after the year I have had! I am thankful for all of the comments and compliments I have been given on it. I have even taken steps to get a copy so that I can have it framed and displayed in my home. Seeing the abundance of great and the flowing rolls at my waist gnaws at me, but overall I am happy with it!

When I see myself in the mirror, I don’t see the same individual who was there before my illness. And while friends and family tell me that what I see is not what they see; I have still felt like the lead in a Hans Christian Anderson story — you know the one about the duck.

Recently, I was introduced to a woman who has just been diagnosed. We have spoken several times over the last few weeks, and her story has touched me. She is further along than I was, and her chemo regime will be more stringent than mine; but I believe she will be fine in the end. I think she sees that now, as well. Her voice today was much calmer and more sure – which was a relief. I was concerned that her fears could become an obstacle for her, and could cloud her capacity to gather the information she needed.

She told me of some good news that she had gotten. Awesome, I thought! Then she wanted to know about my weight gain. She had asked me this several times during our talks. I told her honestly that I have “packed on the pounds (30 to be exact). I know it sounds weird that I gained weight during chemo but I did…Anyway, I know that much of what I said was helpful, but she was still focussed on the weight gain. So here is what I said. “If it is weight gain you want to focus on – you can. But focus on the fact that after you are done with all of your treatments and healthy again…you will have a new project…getting back in shape. Keep thinking about the future and what you need to do. Because no matter how you look at it…you are looking at your future – and that is a good thing. But when you have completed it all (the treatments I mean), don’t waste your time (like I have done) being unhappy with what you see in the mirror.

Because what you see is ALIVE AND WELL..and looking good in a photo or two will happen again!

Enjoy today!

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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HEY


Thursday was one of those days that keeps you wondering about for a long time – especially if you have girls. My daughter and I were sitting around enjoying an afternoon together. She got a text and began to respond feverishly. “Is everything okay?” I asked. “MOOOOMMM!” she responded with the roll of her eyes and the genuflecting of her head, and I quickly realized that my daughter was gone and another child had taken her place. To all you Mom’s of girls out there, when did SYBIL become the characteristics of a “teenage” girl? I am amazed at the speed of which this transformation happens – it is truly supernatural.

Now I have seen bits and pieces of this coming for a while; and Yes, my friends have warned me of this plague…but REALLY, she just turned 12 on Wednesday…couldn’t I get a little break – you know like a week!. I guess I can see the omnipotent’s point. I mean I am cancer free, my hair seems to be growing back, my husband is still being especially nice, my primetime shows are back from summer hiatus – but REALLY couldn’t he pick a different kind of “hurdle to jump over next – something a little easier?

My daughter really is one of the sweetest girls you will ever meet, so when she flips to the Dark side, it really is shocking. So I have begun to formulate responses that could possibly bring my daughter back quicker. If only I could pull my hair out, but I barely have any yet to do that to. I could I just break down and beg for her to return – but nay I say – that can only show weakness. I could ignore it, but face it – where is the fun in that. I mean if I have to last through this time in her life, I might as well have a little fun – right? So that leaves me with my plan of action…Embarrassment. I think if the girl I birthed decides to switch into someone I am not familiar with, maybe I can make it so this other persona doesn’t want to appear anymore.

Today I plan to try it out. If SYBIL appears, I am going to hold her hand, and ask her to “skip to the loo” with me, and I am going to text her every minute to impart on her that most meaningful words of the TEXT world “I:)”. Maybe even wear short shorts and a tank top (Well I think that is just universally cruel so probably not that). And in the end I believe she will be annoyed enough that to make my daughter respond to me and not her evil other self…I hope!

And BTW (i just learned this means by the way) the text that started it all was from a friend who screamed ….”HEY” in a text – I mean the nerve of her friend to write that!!!

Smile and enjoy todya…

I think I will

Carol

@funnycancermom

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The Flip Side


Call me crazy, but yesterday I was practically “school girl” giddy. On Friday, I was notified that my 7th chemo treatment (2nd to last treatment) would have to be postponed due to the impending Hurricane Irene. The thought sent me into a state of depression fro a few days. I have plans, I have a schedule, and I am un-accepting of that changing. All weekend long I concocted stories in my head; stories to make ensure that if appointments opened up for monday (or Tuesday) I would be the first to snag one. I thought of the child care angle (though my kids are almost 12 and I have friends her were on call), I thought about being will to sit all day and wait for an open chair, and, of course, I thought about all out begging…I have no shame — I want this done with.

Well in the end I had nothing to worry about. Dr. Mills called me 1st thing Monday and said she was there to come on over. I may have to wait for the protocol nurses, but they would definitely get my treatment in. HORRAY! So my friend Elaine drove me on up. Hurricane Irene had done damage, but it also made the office uncrowded. I was up in my treatment chair by 10:30. My nurse today was a different one than I was used to, but she did an exquisite job finding a vein and drawing my blood. I was back in my mom’s car by 12:30! And for what ever reason I was up and perky all day (and all night – Man steroids really do keep you hyped up). I got home and had some quality time with my husband before the kids go home from their friend’s houses. I relaxed for an hour or so, and then I sat on the tennis court watching my son play with my husband, My friend Wendy and her son Daniel. My Daughter and her friend rode bikes and jumped rope (which I tried but realized at 50 – I mean 49 – my jump is a little rusty).

Usually by 5 or 6 I am ready to crawl into bed for the night but I was positively giddy. So the evening continued with a great impromptu dinner out with my friend Amy and her family. We sat outside on a gorgeous night, on the water, watching the sunset. I was feeling fine and famished (as usual). Was this feeling of jubilation from the breathtaking setting, maaaybe; was it because I had 7 done and only one left – Poooossibly; Was it because The support, love and warmth that has surrounded me through out this entire ordeal has lifted me to a higher plain of being…Ok really? But that sounded poetic didn’t. 🙂 But I do think that I have found a great combination of things to get me through all of this and change my life for the better. Since my 1st treatment on May 4, I realize I having a great support system – family, friends, and community; I believe that having a positive outlook on your time in treatment as well as what you hope to achieve after treatment is a must; that getting my priorities in line and keeping things in perspective can be hard but can be life changing; learning when it is time to stand up for yourself…and not back down has helped me find (and push away) the right Dr’s and have allowed me to ignore the negative influences during this period in my life; but most important of all.. I have learned to laugh at life and enjoy what is thrown at me…because after all this was only a short bump in what I hope to be a really long and full life. Full of love, laughter, family and friendship — and, yes, even some tears and sadness. With out one you can’t understand the other.

So here I am on the flip-side of my May 4th f=post titled 1 down 7 to go…

Today is 7 down 1 to go….

Hip Hip Horray!

and ENJOY today

Carol

@funnycancermom

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The Silver Lining


What does it say about me that even though we are having a Hurricane in NY and just had an Earthquake — things are pretty good with me? Is that one of those HMMMM moments. I am thrilled that the kids are home. We have been spending a lot of time as a family — which I know will not happen as much once the craziness of “school” and “activities” start in two weeks. I have been taking advantage of every moment. Admittedly a little bribing needs to be done because unfortunately Matt has some of the same characteristics as Scott. (For example, today I took him clothes shopping – since he grew 3 inches at camp and his long pants are now board shorts on him. You would think I was taking him into a torture chamber. The moment we walk into the store – the eyes start rolling and e is already ready to leave. Oy!) The kicker is, after a few minutes he was totally into i — trying on pants and shirts, and putting outfits together. I was impressed. Later, when I said “see that isn’t so bad” He responded “it was torture.” Oh well, I still had fun.

My daughter (who could shop for a living) got her braces this week. The braces have made her a little uncomfortable, so she is staying a little closer to me than usual. I have to say that braces today are way different than when we wore them — you know back in when electricity was invented. Now there are only a few bands around the teeth, and colored rubber bands (that you can switch ever 6 weeks) – it makes me briefly jealous of the experience. Though lets face it — no matter what I wouldn’t want braces on again.

In the evenings, Scott and the kids have been playing tennis while I cook dinner. I know how June Cleaverish that sounds, but I love watching them from the kitchen window as I cook. I started playing tennis last year, but my surgery has put that on hold for a while. Seeing them play gives me the impetus to get back to playing once I am done with treatment.

The Hurricane threatens our plans for the weekend, but it will also give us more family time. Even if it becomes game night, or all of us squeezing together on the couch to watch a movie — I am looking forward to it. I know that the weather has put a kibosh on some of my friends vacation plans and I am truly sorry for them…But I am not upset about the impending storm. I know where my parents will be; I know my brother has landed safely in florida; and most of my friends are will either be home from vacation and/or haven’t left yet. So that takes most of the worrying out of it!

Next week I have chemo again and I am back to being reliant on others to help me care for my family….So, I say “bring on the rain” cause I have a family weekend coming up and it may be one of the last for a while….

Stay Dry and Stay Safe…and keep an eye out for the eye of the storm…But most importantly,

ENJOY TODAY!

Carol

@funnycancermom

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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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