How did I get here – again?

I know I face an uphill battle – but surrounded by love of family and friends I will fight, laugh, kick, scream and dance my way through – Again!

Let me restart from the beginning! Many will remember that in 1982 I was diagnosed with Hodgkin’s Disease. I was 20 – a Sr. in College . The treatment I was given had some unwelcome side affects – though most didn’t appear for almost 20 years. And, frankly, I was happy that I survived and never really thought about these side affects until they began popping up. But I wasn’t until 30 years later I was diagnosed with my 2nd type of cancer. This time it was Breast Cancer. I was told tat it was a potential side affect, but I had been fine for so long – I thought I had beaten the odds. After 6 months of chemo, I was confident that I had beat that as well. Which, for all intents and purposes, I had!

Now, 11 years later I have been diagnosed with Lung Cancer. And again, they can almost definitely trace it back to the original treatment I had in 1982. I know some would be furious or outraged or angry – but that’s just not me. Like with the last 2 I have every intention of fighting this with the same kind of positive, open, direct and humorous attitude that I used the last time! But since that one only kept me healthy for 11 years — I will have to work 3 times harder for it to last for at least 30 more years. I am willing – So for those that followed me before or to my new followers let me give you a recap of how the last 2 months unfolded…..

So, I January I had the weirdest kind of exhale/cough combo. Almost unnoticeable to anyone else. I actually felt annoyed by how ridiculous of an affect I thought it was. But, after 2 cancers I am pretty attune to my body and, well, I kind of knew something wasn’t right. So I called my Dr. and set up an appointment — At first glance, I looked and felt (for the most part) fine. So I was given an inhaler for a week or so. It just so happened I had my annual physical scheduled for 2 weeks from that point. But the Nurse Practitioner said if it isn’t better in a week, call.

Needless to say I called. I went for a chest x-ray, they thought maybe it was walking pneumonia. To double check they sent me for a CT Scan – with contrast. Once they mentioned that – I knew where I was headed – sort of. So I need to digress for a second and talk about my Dr. He is about my age – and I have known him for almost 20 years. He is funny and unflappable. He was also my parents Dr. So we really have a history. Two weeks earlier he learned (from my husband) that my Mom had passed away 6 months before (she was living in Florida at the time). So on this day, I decided to great him with the outcome before he could tell me. He walked into the room where my husband and I were waiting – and I blurted out “So tell me am I going to meet my mother soon?” I totally shocked him – I knew and I knew he knew that I was not going to be coddled. I want to know what I am fighting — that way I can prepare myself for battle totally and appropriately. Anyway, the next series of events was quite the rollercoaster.

The scans showed a mass dead in the center of my mediastinum – my chest cavity. The immediate diagnosis was Thymic Cancer and it was a pretty severe diagnosis. I read about it – and never lost hope but the reading wasn’t so great. But I continued to look for the hope. When the biopsy results came back my Oncologist – Sarah Sadan – said – “you are an enigma” . While everything about your disease points one way – your test results point another. It turns out I have typical Lung Cancer. Instead of the mass growing inward into my lung (like most do) mine grew outward from the lung wall into the chest cavity. The positives here are many. They have made many strides in treating lung cancer’s – new therapies, new drugs, which gives me new hopes for a cure. Lung Cancer is not a walk in the park but it is better than what was first thought – and with all of this what isn’t factored in is me.

I am not willing to look at a negative outcome. I have learned that my attitude, my drive, my desire and fight is my Superpower! Today is day one of the new blog, it is day 60 of this battle. Over the next few months please follow along with me — 4 weeks ago at the Oprah 2020 Vision Tour, I learned so much — She gifted us with an affirmation – I CAN, I WILL, WATCH ME – that is my purpose right now! SO all of you WATCH ME! CAUSE I AM HERE FOR THE LONG HAUL!!!!!!!!!

More to follow – xoxo Carol @funnycancermom

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Author: funnycancermom

I am Better not Bitter! I want to laugh not cry! I am not perfect, nor do I want to be! I am The Funny Cancer Mom - If I can laugh through cancer - imagine what else I dan do. Follow, share, comment - I am here to listen and help @funnycancermom.

7 thoughts on “How did I get here – again?”

  1. Oh my lord Carol, as your friend from 1982, watching the lines they drew on your body for chemo, to hair and taste bud loss and strange strong foods showing up in my fridge at 10 Jamaica Way, I’m thinking how can this beautiful soul be third struck. I know it’s not the same but we lost our sweet black lab at 6.5 to spleen cancer in January. My dear closest Maine friend was recently diagnosed with an anal cancer. I thought immediately of you, always my first. May the Gods and Goddesses bless and keep you hear with us so you can see the twins graduation and whatever comes next for them. I love you, and truly the next time I’m in Ridgefield I’ll be coming you way to hold you and hug you well.

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  2. YOU can, YOU will, WE’RE watching…And loving, and laughing, and praying, and surrounding you with even more positive juju than you already have deep within you. Every honest word, emotion,and joke is just so quintessential magnificent Carol. Please note, that all the loving supportive replies that you’ll get are not one and done. In my household, you are clearly one of our most favorite peeps on the planet (including our Shih Tzu’s vote!!) The most powerful words that you wrote were “with all of this what isn’t factored in is me.” So beyond true!!! How the hell could YOU be factored into the equation since YOU are one of a kind. After the dust settles we would love to plan a playdate, a support date, a whatever date so we can cheerlead in person. We adore you dear Carol. And don’t forget you have Bernice hocking God so much that She/He probably has a migraine!!!!! xxxxx Laurin & Planey

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    1. Laurin – I and we feel the same about you both (and Mookie of course) – you are welcome here anytime – post apocalyptic coronavirus of course 😀😀😀😀!

      I draw as much strength from incredible lights – like you and Planey – I love you both!

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  3. I will never doubt your ability to fight. I really wish you weren’t called upon to use it again. You Can and You Will!

    Sending strength and support.

    Liked by 1 person

  4. Carol, I am so sorry to hear of your lung cancer. I feel very sure you will beat this one too! But I am sorry that you have to fight it out again. Praying hard for you xoxo. -Anne

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