#seriously ive had to pee since i woke up like an hour ago and yet i keep getting sidetracked just scrumbling
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semiotomatics · 1 year ago
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hey can everyone stop posting for a sec i gotta pee
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nikkithomas · 4 years ago
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Here’s the deal. I started having a lot of pain in my lower back, legs and hips. At first, I went to the chiropractor and he did some adjustments. I seriously felt so much better.
My regular doctor had prescribed some medicine for me for an unrelated thing and it made me so sick. I’d be so nauseous that I’d have to go get fresh air...walk it off...or even splash water on my face. That had been going on even when I was in Knoxville.
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Aircheck had asked me to talk about my ACM trip to Vegas when we won in 2019. I’m sure there were people who thought it was funny or maybe even crass...but they asked what I thought or what was going through my head at that ceremony...and I think my answer was something to the effect of “I was trying not to throw up” or something like that. My stomach was on fire and I felt so dizzy. My face was all flushed and hot. I thought about going to the ER there in Vegas...but I was afraid I’d miss the reason I was there...to pick up the ACM for our station. I think it was win number seven for the station...as a PD it was my third...and it was still a pretty big deal. Honest to God, I didn’t want to let anyone down. I also wasn’t sure if it was food poisoning or something. When I got back to Knoxville, went to my doctor...they ran tests...gave me some medicine...and I thought that was the end of it. They still couldn’t figure out what was going on with me, though.
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I left Knoxville and moved to the Tri Cities. Best decision I’ve made in years, by the way. I truly love these people. They’ve done a phenomenal job of protecting their product and their people and I believe that’s why this station is still so healthy when many other legendary stations have suffered. The stress level dropped substantially. It’s amazing what can be accomplished when the station and the people are a priority. Which by the way...XBQ has been so much like KAT Country. It’s been everything I love about radio and thought I’d never experience again. These people couldn’t be farther apart...yet be so much alike. It’s a good thing.
The main thing bothering me then...was my back and legs. Kept having some really nasty pain. The pain was so intense sometimes that it made me nauseous. My face was flushed...I had a fever...then I didn’t have one. Maybe it was my weight? I was getting up to pee a lot at night. Only sleeping one or two hours in a stretch. It was all these things that I never put together.
I wanted to get healthy. Told my doctor I wasn’t going to take that medicine that made me feel so bad...just in case that was the problem. My endocrinologist was cool with that. I started the keto diet. Actually...I did keto up until right before Thanksgiving.
I was so happy. My thyroid is absolutely hateful...so losing weight is the hardest thing to do it seems. On keto...I dropped over 30 pounds. Wow! I thought that was great!! Everything felt better. My energy levels were up. I’d get up at 4am and wouldn’t stop until 11pm...and everything was good...until my hip, back and legs started hurting again. It was so bad one morning that the guys I work with called chiropractors for me. It was awful.
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The pain had never really stopped...but at a certain point you just get used to the pain and move on as best you can. That’s what I did up until a few weeks ago. If you know me, you know that I love Toys For Tots, St Jude, Second Harvest, etc. We were out with the marines working on Toys For Tots and I ended up having to miss one day because I hurt so bad. Now for me...that’s bad.
It never let up. I’ve just pushed through and tried to “suck it up” since then. That was a couple of weeks before Christmas. Y’all I seriously thought it might be psychosomatic. Maybe it was all in my head. If it hurt...I’d try to stretch or move and work it out of my body...but that NEVER worked.
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So...I go back to the chiropractor. Those guys were so good to me. They can electrocute me anytime they want. (All hail the TENS unit!!) That seemed to be working...and then we had a little bit of a COVID scare at work...(everyone is okay, thank goodness). Around that time...I was running a fever off and on. Low grade. There were some other things that weren’t feeling quite right...so...just to be safe...I got another COVID test and quarantined. Still...I felt like I was ALWAYS in pain. Sometimes it was so bad...I couldn’t move or do anything in any way to make it stop. It made me want to cry. It was embarrassing. It was frustrating because I couldn’t get it to let up. It got so bad that last Saturday I drove myself to the ER to get checked out.
Urgent Care said they couldn’t help because I needed “imaging”. Well...I got that imaging done folks. Turns out...I have a scary mass on my right ovary. It’s pretty huge.
I went in Saturday night...terrified of being around sick people...but it had to be done. The pain was so intense...that my blood pressure shot sky high...and my nose starting bleeding. The doctor ordered morphine, Norco and a CT scan.
The guy doing the scan was a travel nurse. He went from being pretty chatty to sort of quiet and reserved after the test. When they injected the dye into me...he was telling me it would hurt...and it was nothing compared to what I was feeling.
I woke up two hours after the scan to the doctor on call sitting next to my bed and looking sorta weird at me. She told me they’d received my test results and everything I’d said was right on the money.
The burning, pressure, aching, tension...all of it...was related to what she referred to as “not the biggest mass” she’d ever seen...but “one of the largest”. She was surprised I’d been walking around with this thing in me for God knows how long.
Now here’s where the story goes off the rails.
That doctor at Ballad mentioned the word “cancer” about nine times in that room. That was the “suspected” diagnosis. She said I needed to follow up and see another doctor because of what could be “cancer”...and told me they’d have to see if it had spread anywhere.
Now...that was a LOT to take in. So...I did what any other person with an iPhone, an unlimited data plan and tons of morphine in their system would do...I looked that crap up on “Dr Internet”.
The next time a nurse came in...I asked her...”Umm did you guys do a CA 125 test?”
That same poor sweet nurse, who would go on to blow a vein...and push the medicine through the IV into my skin, thereby causing a monster of a bruise and making my vein get rock hard...she said in this really hushed tone...”I don’t know...I’ll ask. I saw your report. I’m so sorry.”
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At this point...I’m facing my mortality. I just wanted out of there. I wanted this damn thing out of me...I wanted answers...I wanted everything to be okay.
I still want everything to be okay.
By the way...she never came back in with the answer to that CA 125 test question. So I took that as a hard “no”...or “they did it and don’t want to tell me”.
Monday I was back in the ER. Doubled over, in tears.
The doctor ordered pain medicine...that never came in the four hours I was there. That was NOT a fun time. The nurses just let me sit there. To her credit...the doctor was pretty furious when she found out they’d ignored her orders. Once again...this other doctor looks at me and says...”You know they think this is cancer?”
No. Still no test...but she made an appointment for me with a local oncologist.
Now...that CA 125 antigen test is not infallible, nor is it the end-all-be-all test for ovarian cancer. It is a marker though specifically for ovarian cancer.
So if they’re telling you that you have a massive tumor and it could be cancer...(two doctors over two visits..the word has been dropped about a dozen times...it’s also in the CT report...you’d think someone would bust out a needle...draw the blood...see what that looks like...and get you in the right frame of mind in case it is this horrible bastard of a disease!! Right? Wrong.)
The mass at the time was 10.3cm x 10.3cm x 7.1cm.
The oncologist couldn’t see me for a week...the gynecologist couldn’t see me until February 1st.
Yeah. No big hurry. I’m just having trouble walking. I’m in tears. I’m peeing...like a teaspoon at a time. I know that’s graphic...but if you don’t pee...you need to get checked. I felt like I was (and still feel, by the way) in the middle of a massive labor pain that wouldn’t ease off. It’s pain that makes you want to throw up sometimes. It’s super intense.
I went home that second time...sat down in my room...and I couldn’t help but tear up. I’ve cried two and a half times over the “state of things” since this started. Those are the “what am I going to do” tears...totally different from the “oh Lord this hurts like hell...dear God make it stop” tears.
Talked to our friend Eric who told me it was a shame I didn’t live in Nashville...because I could probably call Vanderbilt and be seen pretty quickly. Eric...was right. I’m three hours from Vanderbilt...but only an hour or so from Knoxville.
I called UT. (Go Vols!) That football situation isn’t ideal...but that hospital ain’t half bad.
Within less than an hour...the head Oncologist had looked over my CT scan and was working to get me in there ASAP. They’d have taken me that day...but it was too late in the day and I’d never make it down there in time. So...they scheduled me for Wednesday morning.
Before I walked out of the room that morning...they told me they were going to operate and get this out of me by Monday at the very latest. The schedule was full...so they needed to check on a few things before I left the hospital...just in case there was torsion or whatever.
I had a CA 125 test. That looked good from what I understand but my CT scan and sonogram looked sketchy. The mass appeared to be even larger since Saturday?!? (It showed up as being 12.6cm x 13.3cm x 8.3cm) They gave me a COVID test and told me to self isolate until my surgery...which is scheduled for tomorrow.
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It was upon learning how much larger this thing had become...that I named it...”Larry King”.
I don’t know why...but that seemed to be the name that fit whatever this thing is inside me. In my mind...it looks like Larry King...holding two shot glasses. One shot glass is filled with Dewar’s...the other is filled with Metamucil. He has a cigarette hanging out of his mouth...but I don’t know if he’s a “smoker” yet.
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If it officially comes back as cancer...I’ll let you know. If it doesn’t...I’ll let you know that, too.
I’m not writing this for pity or attention...on the contrary. It’s all a lot for me to take in...and I’m just not sure how to process it all. Writing it out sort of helps.
In the middle of all of this over the past week...Tom Starr passed away. He was such a sweet man. There’s a picture that he took of us at CRS...it’s me...Tom...Lisa McKay and Heather Davis. I think Heather wrote a caption that said something like “it’s so hard to believe half of the people in this picture are gone”.
That was pretty heavy.
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I’m still trying to process that actually. I thought the world of Tom, loved Lisa McKay (she got me when so many others didn’t)...and just to the left...there I was. I felt like a jerk for even taking a moment to feel bad for myself. There are so many other people who have it so much worse than I do. And what if there’s nothing to this thing? What if it’s just some sort freak thing? There are so many people who’ve fought so hard and powered through so much and here I am...maybe worried for nothing...getting ready to have surgery...and it feels wrong to worry about myself. Whatever is done is done and I’ll fight whatever I need to fight. If it’s not cancer (oh God please let them all be wrong) then I have a lot of things that I need to do...and other people’s opinions and judgment that don’t have any place in my head or the right to exist in my life’s body of work or otherwise. I’ll just keep praying for them.
I keep telling myself those doctors could be wrong. Until I see a pathology report...this isn’t real.
While I appreciate and am thankful for any prayers you can send up on my behalf...please don’t feel obliged to write anything on this post. Seriously. I just needed to get this all out and behind me.
I HATE “bleeding on the internet”. It’s a serious pet peeve. Not everyone is worthy of knowing everything that’s going on...nor should they be expected to care...but I realize sometimes people need reinforcement and support. I still don’t like sharing MY business on here. It feels weird. I’ll talk about things on the air...that I don’t care to regurgitate on Facebook.
I’ll talk about award shows, TV, things that are funny...pictures...but it’s not my business who you vote for or what you believe in. I’m just glad that you DO. Better to have convictions and purpose than be apathetic. Over the years...it’s been amazing to see how a simple picture I’ve posted or link (without even commenting on it...just a pic or simple URL) how it can make people lose their minds.
You will never solve life’s problems on Facebook or any other social media platform. It controls you. You/we are merely the peanut gallery from which billions of dollars are “mined” every single minute we’re on here.
The smartest thing I ever had laid on me about social media was from an interview with a Silicon Valley person that said “If you’re not creating the product...you ARE the product. Think about that.
Our world is so messed up right now. And no matter what party you’re affiliated with...it just seems very wrong to lump everyone together and vilify them all. Not everyone is evil. Not everyone is right or wrong. Writing people off is so inhumane. You really can disagree with someone and not hate them.
I remember being at a concert in a few years ago and had just learned some pretty tough stuff that was impacting a competitor, and shared that with one of the leaders that I worked with. They’d taken a huge blow...which was awesome strategically...but it happened at the same time the competitors PD had lost his mother. I remember expressing that I felt bad for the guy (specifically about losing his mother)...and without batting an eye...the guy I worked with said he didn’t feel sorry for him at all. “That’s just too bad!” He said other things but I won’t go there because that would reveal who that person is...and the person for whom he was speaking about that day. Now...in my heart I hoped that guy who up until then I’d had so much respect for...did NOT know what happened to this guys mom. It just felt gross talking to him. I never looked at him the same way again. It was all about depth. There was nothing there. Very disappointing. I once cared what this guy thought about me...but that was done. And living through this now underscores that feeling and reminds me on a personal level what really is important. That’s a lot for a workaholic like me to process.
I’m signing off now. It got sort of “ramblesque” there at the end. Sorry about that. As for all the other stuff...I’ll let you know how it all turns out.
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