More about how MS and cancer hang out
Warning- if you are struggling with cancer, know someone who is struggling with cancer or have lost someone to cancer, you may not find this blog amusing. Please know that I’m not minimizing cancer at all. It’s just how I deal.
BUT, if you have kicked cancer’s ass, you may find this hysterical.
This cancer thing has gotten real. At first it was one little, new spot with a great prognosis. A little day surgery, a little radiation, no big deal.
That’s what I heard anyway. And what my multiple sclerosis brain heard. Cancer, no biggie. What’s there to freak out about??
Everyone said I was brave- how could I not be worried? I appreciated their compliments. I like being brave. I feel like I’m kicking MS ass, so why not kick cancer ass too??
But it turns out, I wasn’t brave- I was MS cognitively defunct. Cancer is scary you big MS dummy and this could really suck.
Upon closer inspection one spot turned to two, day surgery turned to 1-3 days hospitalization and radiation is off the table and the dreaded C word is uttered. No not cancer, chemo!!
(How much cognitive damage does MS have to give you for you to be more afraid of the chemo word than the cancer word.)
But the chemo is not definite, both spots are still small, and the prognosis is still excellent. Things are just going to suck for a while.
Ultimately, I made the decision to remove both breasts and begin the work to get new ones. I dealt with this by thinking hey, free boob job! I never really liked my boobs too much anyway.
But when the brain fog cleared, I had to face the reality of how much poking and prodding and medical stuff was going to transpire.
(I may not be able to take a real shower for weeks! I don’t even know how to take a sponge bath.)
I think I liked the brain fog better.
Suddenly my jugs are in the forefront of my mind.
Last week at church I was leaving the ladies room and entering the tiny hallway outside of it. The elderly man in the hall didn’t see me and, in his eagerness to get of the way of the lady entering the hall across from me, he moved, swinging his arms and punching me right in the left breast. The one that is still somewhat ok.
Several days later I was trying to chop something and the knife in my hand flew up and came crashing down on the counter, just missing my right breast. If it hadn’t missed I probably would have saved my insurance company some money- do it yourself home mastectomy.
I swear I’m not making up either of these stories.
Still, I’m determined to face this challenge with humor and by doing all that I’m supposed to. I learned on my MS journey that it’s important to follow doctor’s orders but sometimes the orders are confusing. You have to decipher the meanings of what they tell you in a way conducive to your own treatment plan.
Here are some things I’ve discovered. For this list the doctor’s recovery instruction is in italics and my translation is in bold lettering.
No driving for 3 weeks
Limo service is a must!
This is when you need to rely on your friends
Party time!!
Ask them to bring you food so you don’t have to cook
Guys, pick up a pizza on your way
They’ll be happy to help
Hey Ben and Jerry, I’ll be here all week- whichever times work best for you.
And keep hydrated
Stock up on Pino Grigio beforehand.
A recliner can help with the healing as it will keep your chest elevated.
Time to buy new furniture per doctor’s orders! Will insurance cover a sectional with a recliner built in?
You need to rest and relax as much as possible, no strenuous housework.
Hey friend, would you clean my bathroom for me?
But Yvonne your surgery was six months ago.
Didn’t you see the note where I’m not supposed to do strenuous housework after surgery?????
(True story- I actually got of gym for 6 weeks in the 8th grade with one doctor’s note saying I had swollen glands. If you remember the horror of gym in the 8th grade you know what a feat that was. If I can manage that at age 13 who knows what I can get out of now!!!!)
All of this is to tell you that while I will kick cancer’s butt, I may be out of the blogging loop for a bit. I’ll try to post repeats here and there but don’t worry if you don’t hear from me for a while. I will likely be resting, reclining, and conjuring up all kinds of new MS weirdness with perhaps some cancer weirdness thrown in!
And don’t worry about me losing my sense of humor. True to the spirit of using humor to heal, some friends threw me a “goodbye to your boobs” party. One friend baked me this delicious boob cake, Hershey’s kiss nipple idea courtesy of her 16 year old daughter, and another wrote me a boob poem. So, for your amusement, here is a boob poem written just for me, and now for all of you.
Two Boobie or Not To Boobie, that is the Question
By Kristin Perry
A Boob by any other name is what?
Tits?
Maminhas?
Two ways to get black eyes if you run?
No.
They are a way to feed a child then and now.
And a way to entertain a grown up child.
But will losing them make a difference?
Hummm, think of the advantages…
No more “over the shoulder bolder holders” for a while.
You may get to decide what size you want.
No sagging boobies.
You don’t have to worry about rolling up and tucking in the boobs when you get to old.
And you can actually say you have balloons in your your body that you didn’t swallow.
But I digress…
You can do this.
You are strong, independent and a hell of a woman.
Boobs don’t make the woman,
They just give the guy a few more minutes to do his job.
One more thing friends-something I’m looking forward too as I recover is delving more into this anthology, When Bodies Break. I know it will offer a lot of inspiration and support as what I have read thus far has been fabulous!! It’s totally worth checking it out yourselves as it’s available on Amazon and all proceeds from the sales go to the Benaroya Research Institute.
Thank you all for your support. You guys rock!!!!!!
Yvonne, what a horrible medical journey you are on. Sending you love and light and laughter and offers of whatever help I can provide. Donna
Thank you so much my friend!!
Pick a C cup !! Hope you got a second opinion or that you truly trust your doc. Hopefully they will do the reconstruction and removal at the same time. Guessing you carry the gene that’s why you opted for mastectomy. The new model Yvonne – Yvonne 2019. You know Lemtrada and Ocrevus as well as Rituxin are chemo drugs and used in MS. I just know in my heart you will be fine and back on your feet in no time. Keep me posted. Sending you all my best.
Thank you so much my friend!!! Will definitely keep you in the loop.
Boobalicious funny!
Make’em big—make Stormy Daniels envious, I say.
Boobalicious-I love it! I don’t know about going the Stormy Daniels way. I don’t know how the poor thing even stands up!
You did Great keeping the laughs going. Hope you got a new living room set that’s comfy that you can kick back on. Have a nice Rest for awhile.
🙂
Thank you so much my friend!!!
So can I be the bad influence and bring the not so healthy things to eat?…. thinking maybe brownies?… I mean Chocolate is good for you right ?….. All kidding aside I am so sorry what we thought was going to be a simple procedure instead has turned into so much more, but you know us ladies will be there for you to help however we can…. Maybe we will bring some silly 80’s movies too..
Chocolate is definitely good for you! I think I read a study. You know what’s even better for you? Silly movies and good friends! Very grateful for you my friend!
Yvonne your bravery is inspirational and your humor turns tragedy into black comedy, my favorite kind. And to be honest I also feel more frightened by chemo than cancer. I blame some terrible movie from around 1980. I had 8 pounds of breasts removed due to neck pain and the ability to buy cheaper bras and occasionally skip wearing one is a bonus as is the free lift.And the scars do get better with time. That said you know where to find me if I can help in any way. 💜
Thank you so much Jennifer! I didn’t know you had a similar procedure done. I’m adding slight weight loss to the positive list now. Miss seeing you at the office my friend!
Your sense of humor is GREAT & it makes you a very strong person so you can handle it all with a smile and a laugh A side advantage for the new “jugs” is that you and my sister-in-law will be the only two standing up (not sagging) at the nursing home Lol Stay strong Yvonne😊😊😊👍👍👍
A another definite plus! Thank you so much my friend! Do I know your sister-in-law? If not, we need to hang.
Thank you for sharing your story Yvonnne! Love your perspective! I respect you so much for giving people facing chronic illness and/or cancer (2-fer 🤣) permission to say🖕! Bottom line is “it sucks”..”it’s not fair”…but it is “what it is”! I hope you take lots of limos, eat chocolate ice cream, drink 🍷, hire a housekeeper and most of all…enjoy your new “rack”! You’ve got this! You are a warrior! 😘
Thank you so much my friend- I really appreciate it! I think you are a warrior too. Hope you and your beautiful family are doing great!!
I truly wish you the best! I have MS and survived lung cancer and at first I thought you were complaining but I realize now the humor in our situation. Keep being positive! We are really OK.
Thank you so much my friend!!! Big hugs to you!
Well in true Yvonne style, you’ll definitely kick cancer in the pants! And at the end of this temporary muck you’ll have tons of new material AND perky new lady lumps! You’ve got this! XO
Too true and too funny Gina!!! Excited for your upcoming exciting news as well! Can’t wait to read Stumble to Rise which will be released in March my friends!
Yvonne I am very grateful to have you as a friend on the surface we seem so different and yet it works.. We are both strong in our own ways, but we each try to use humor to tackle the stuff we deal with.
Absolutely my friend!!! Love you and am very grateful for your sister/friendship!