Just another cancer blog

Inappropriate, you say?

I have had this discussion since  I was in high school and decided strong words should be used when strong feelings are expressed – they loose their currency when flung about with abandon.  And so, although I have been known to use them on occasion, they still grate.  However- we always used to dance around the word cancer.  Some people would not even utter the work and whispered when someone contracted it.  We can’t do that anymore – we have to shout and share and  acknowledge so that we can help any and everyone get through this and know they are not alone. Words get attention.  This awful group of illnesses needs all the attention it can get.

 

Two years ago I decided to take spring break to get all my appointments in order.  Turned 65 so signed up for Medicare.  Saw the eye doctor and learned I have the start of cataracts.  Saw the gynecologist who declared tests and a D&C were necessary – scheduled that Friday so I wouldn’t miss work.  Got my two month late mammogram,  Wham.  World tilt.   They wanted to do a biopsy immediately, my doctor said he wanted to see me first, he saw the results – I got the biopsy.  So the next week the doctor calls and tells me I should consider scheduling a prophylactic hysterectomy because of a thickening of the uterine lining and a slight irregularity in cells.  I will call.  He calls back and tells me I have breast cancer.  Small tumor, Triple Negative – a type of cancer most frequent in  young African/American  women – not hormone receptive – not expected-  which is aggressive and I need to get a surgeon.  He also said ‘”fuck cancer.” ” I had non hodgkins lymphoma and here I am. ”    (And the word struck the right note in those circumstances.)  And he proceeded to tell me his story and that I need to fight.  I lined up all the doctors, consulted two oncologists for opinions and lined up the radiologist after I had contacted the surgeon.  Needed only a lumpectomy with two sentinel lymph nodes removed Not affected), localized radiation through a Savi port and cycles of chemo . . . would lose my hair, etc.  OK – they said girls continued to work while doing child care.  I decided to work and share my story with my associates and some of the story with my kid with their parents permission.  Best thing I ever did.  Preadolescent and teenage boys in a treatment center and not one unkind remark.  Some prayed for me at home with their families.  I was teaching summer school – four shortened  days a week – and felt this would work. Work was hard when it became full time again.  Got through it all.  Had some chemo brain.  Had a few uncomfortable days – but it wasn’t so bad.  Check-ups with a scare here and there but in August it had been two years since my last chemo- my hair was shoulder length – and I could put it up again.  Feeling good!

 

Labor Day I felt like I was breathing in a green house.  Didn’t think that was right and saw Dr.  Got a Z pack for the lungs and a prescription for a chest x-ray since I had had breast cancer – just checking.  Then a contrast CT scan- then a lung biopsy for several nodules in my left lung.

Adenocarcinoma.  Often found in women and NON SMOKERS.  Go figure.  Pet scan and MRI followed.  Okay except for flare in lymph gland on right side and several nodules in left lung .  All small.  Here we go again.  I started radiation on Monday and chemo on Tuesday.  Will have six weeks of daily radiation and weekly chemo – with the possibility of surgery and perhaps three more cycles of chemo thrown in after.     By the way, the original symptom cleared up with the Z pack.  Just lucky again.   Something caught early.  And last week my radiologist and oncologist both cautiously, optimistically used the word  “cure.”  Interesting, but my genetics are getting me into trouble.

 

And so, I have begun again.  A port was placed last week for chemo infusions since they are not able to use my right side due to two lymph nodes being gone – and the veins in my left hand are very unhappy because of the chemo there- was not a comfortable procedure but feeling better this week.  I was able to go to my 50th hight school reunion on Saturday and spent Sunday at a farm and grilling with the family – all of whom overwhelmed me with support.

 

My sister kindly took me to my first radiation appointment on Monday.  I had radiation and chemo on Tuesday and after radiation today I am feeling pretty good.  I haven’t told a lot of people.I am grateful for the support I have received from them.  I am just putting this out their for those of you who have an interest – and to keep the word out there that there are things that can be done,  Fight early and fight hard.  I f you feel you want to pass this one on, please do so

4 Comments

  1. Nancy Thomason

    Nice writing.
    I’m so glad we will all be able to keep up with you through this blog, and not pester you too often for the latest updates. Should save you from endlessly repeating things over and over.
    Your positive attitude is an inspiration, as is your determination. It’s a brave and generous thing to put this out there. It’s going to be a trip, and I see you emerging from it triumphantly and cancer free !

  2. lisa

    Thanks, Nancy I see the typos after I corrected and recorrected. Where was autocorrect. Even spelled inappropriate incorrectly. I’m going to blame it on chemo fog already since I have no other excuse. Thank you for your kind words. I do intend to give this a fight.

  3. Suzy Thomason Richman

    THANKS for sending on notice that your amazing blog is now posted! I think this is going to both really help all of us on the ‘outside’, and I think this is also going to be a great place for you to really explore all of this in a meaningful way. Yep, inspirational, Lisa– and yep, that fighting spirit is going to be so important in all of this. Haha, and know that *all* of us make typo’s when posting anything– I do it all the time in my online class I teach ;-). We’ll all be looking at *what* you are saying.

    Keeping you in prayer!
    Suzy

  4. Karen Clinton

    Lisa, what a wonderful idea. I know Koka keeps me updated but this is such a nice way to keep everyone posted so we all know what’s going on as I don’t want to bother you. Just know I’m thinking of you & keeping you in my prayers. I agree with your comment that sometimes that word is the only appropriate one at the time. I too dislike it immensely but use it when nothing else seems to address the situation adequately. Keep on keeping on. You will beat this

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