Michelle’s Story

Site created on June 15, 2018

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On May 27, we found a painful lump in my left breast. Since it was Memorial Day weekend, I had to wait until Tuesday to call the doctor.  It was also the week of post planning, so I forgot to call Tuesday.  I called on Wednesday, and they were able to get me in on Thursday.  I explained that I knew it had not been a year from my last visit, so I was not sure how that would work with insurance and all, but that I thought the lump trumped the year wait.  Indeed it did!  Three ultrasounds and a mammogram later, Dr. Pettiford said, "I really think we need to look closer at that.  I want to call it a complex cyst.  We need to aspirate it and possibly biopsy it".  Her schedule was full for that day, but we returned Friday morning at 8 for what ended up being a straight biopsy - there was no aspirating anything!  So, our week of waiting and researching began.  What is a complex cyst.?  I was planning for it to be just that - it goes away with aspiration I could no longer feel the lump; that must be what it was!  Out of sight; out of mind.  Fast forward 7 days.  I was at a meeting for school; Bo had worked.  We met up at the doctor's office at 345 for the biopsy results.  I had a dog to pick up at the vet in Griffin; we are just here for a quick reading and then I will follow up in 6 months for an ultrasound to be sure there are no changes - I have been doing this routine for several years now for the other fibrous cysts we've been watching.  Dr. Pettiford came into the room and said, "We got the results back and it is cancer".  The world stopped for a brief instant, and life changed as I know it.  I guess the shock on both of our faces concerned her because then she said, "let's go down to my office and talk about it".  It probably did not help that Jimbo was in uniform; I guess that could be intimidating!  She pulled out the biopsy report and read it with me, and I completely understood everything she said.  Bo was sitting slightly behind me, and he was having a small meltdown.  Dr. Pettiford kept asking if everything was alright and if we understood each thing she was saying.  Absolutely clear.  I turned around and saw tears streaming down Bo's face, and I am not sure what happened in my mind, but I had to have a tearful moment then as well.  I guess that is what doc was waiting on because then she got up and pulled a book she "wanted me to have" - understanding Breast Cancer - and when I saw those words there in pink and white, I had a big moment.  Then I dried it up and finished our conversation.  I texted my principal and several of my coworkers that knew I had the results coming to let them know that it was indeed cancer.  Dr. Pettiford gave me the next steps - a visit to the medical oncologist, a breast MRI, and then back to see her in a week.  What a busy week and summer I was beginning to have!

Newest Update

Journal entry by Michelle Hanners

Hasn't been much to update, but I will go back and add some for mid-July through the end of August.  But here is for today.

Ok here is a complete update from today. My friend Live.Like.Lively, believes in sharing all - the good, the bad, the ugly. Feel free to follow that page as well as his personal page (he is a 20 year friend of ours that is a Clayton County PD officer currently fighting inoperable brain cancer).

I guess my post seeking someone to take my place last night was a premonition for how today was going to go. I slept pretty well last night, which is unusual the night before treatment; I have been sleeping only about two to three hours on those nights. I re-read all of the information given to me on the Taxol - none was really scary - but I woke with an uneasy feeling this morning. Nothing in particular, but very emotional. I think I cried 4 times before we even made it to the hospital, then once again while receiving the chemo. Understand now, I don't have a whole lot of Estrogen or Progesterone going on because I had pretty well finished menopause and was on HRT prior to getting my non-hormone related breast cancer (Don't judge, night sweats suck!). The HRT had NOTHING to do with my cancer, remember it is triple negative, meaning no hormone receptors of any kind. I no longer use the HRT just to be sure it does mutate or feed the cancer any further, so no worries for me there either. I will not return after I am finished, so if you use Minevelle patches, I have a few generics, I will be glad to donate to your cause 😀. So, I think I made the hubs uneasy because he wasn't quite sure what to do for me and my uber emotional self; I hardly ever have cried, especially in front of him, so he was like what's wrong......"I don't know"......YIKES! 
When we got to the Oncologist's office, we actually saw the doctor and not the NP, though I do love the NP who took my case after the first one missed the embolism. I asked a few questions about info I had read last night, got positive answers, but I did forget to ask about the parking permit. No fear - I will be back next week! On to the oncology room. He didn't go over my blood work with me, so I mentioned that to the nurse, who promptly checked prior to starting (If my white cells or red cells are out of whack, I skip chemo and get a blood transfusion instead; I used to be a blood donor and had I known that would become an option for me, I would have pre-donated to myself and asked y'all to do the same). So far, I have had no problem, only my hemoglobin and hematocrit have been slightly low - that's not part of the blood; what the heck is that for anyhow???? 🤷‍♀️So, off we go - steroids, Benadryl and Pepcid as premeds (helps with nausea, reaction, and stomach discomfort), then the Taxol. OUr understanding was that it would be a 4-hour process where they increased the dose every 30 minutes. That never happened, so I waited all afternoon for them to call back and say, "come back we messed up". They never did, so hopefully they knew my fear was real and just decided on the dose I received. I called the surgeon's office to cancel my ultrasound since we were planning on 4 hours at oncology and rescheduled for next week. Well, we were out in about an hour and a half, so I called back. They said to come right now and I was in and out before my original appointment and got the good news that the treatments had worked and the tumor had shrunk to more than half. Luckily she dropped a metal clip in the tumor at the biopsy so that she could find it later. She had a hard time seeing the tumor aside from looking for the clip. 
So, I had no reaction to the new chemo, go good news at the surgeon's office. What do I now have to be apprehensive about??? So the dark cloud of doom left; we ate some Larry's subs and came home to take a nap. I ventured out to Starbuck's to get my half-price frappucino and now here I is.
So all is well again, I guess I am entitled to a pity party once in a while, I am just glad none of you were around for it! I am back to my smiling self (that's why only my Coach Amber shirt is pictured today and not my face). It's smiling now though so no worries!
Thanks for reading to the end if you have. Your prayers, thought vibes, encouraging words and cards (shout out to my 6th-grade peeps at Lee Middle for the card I got today, that certainly helped my attitude) have been the best. Those who have and continue to provide meals - you're the best! Much love to you all. I am off to grade and side-eye the Falcons game.

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