My last chemo treatment was on the day after Christmas – and I was SO glad to get it and have this journey start to end!


Have to admit – this last six months of chemo have been the roughest ones of my life. I have never felt so ‘off’ and ‘not good’ for so long a time. But now it was done – and I entered another hard space – now we wait till the PET scan can be done (6-8 weeks after the last chemo). Tiny bit by tiny bit I began to feel better. I honestly thought I would bounce back much faster than I have – but at this point – any improvement is huge!


Finally the day arrived – January 28 – and off we went to the PET scan trailer. Got there early (as usual), and got signed in and put in my designated chair (JUST big enough for the recliner to fit). Then I got a couple – no – three)  heated blankets to try and stay warm – it is REALLY cold in the PET trailer – guess that huge PET/CT Scan machine puts out a lot of heat!


The nurse put in the IV and took a little bit of blood to check my blood glucose – it was 85 – no worries about being diabetic there! But they check, because it must be under 200 to be able to do the scan. Then she set up the machine which measures out and delivers the radioactive sugar to me before the scan. I’ve always thought that it is interesting that they use sugar! So – got that all administered – and now had to wait again – for around 45 minutes – so it could circulate throughout my body. I also got a too large bottle of barium contrast to drink – not cold and not good – have learned to chug it down fast as possible thru the straw so I don’t taste it so much – ugh!!


Ah, it finally came time for the scan – move to the room with the huge machine (it takes up most of the trailer which is big as a semi – so it is BIG! Had to take off my jacket – but they added a fourth blanket to keep me warm – and even one for my arms – which had to be over my head for the scan. Then the nurse added the contrast for the CT portion of the scan – and the machine did it’s thing – humming and whirring like a mad scientist had constructed it. Once that was done – we moved right on to the PET portion of the scan – which took way longer – but I just closed my eyes and prayed.


Then came the hardest waiting of all – to see what the scan results were. I haunted the MyChart – hoping for instant results – ha! The scan was on Monday – no news Tuesday – no news Wednesday – No news Thursday……but ah! Friday came with the results! Not sure how the docs feel about the patients getting the test results before they meet with the patient – but I’m glad!


The reports were short – and a couple of sentences from each part of the scan fairly leapt off the page at me – from the PET portion: “Complete treatment response since 8-13-2018. NO current PET evidence of lymphoma!” And as if to emphasize it – from the CT portion: “NO CT evidence of recurrent lymphoma!” So this is a day of thanksgiving to my Lord, Jesus Christ, for bringing me through this with a complete healing! It is a day to celebrate! Thank You, Lord!!

Ode to Annie and Billie Jo…

It started out as an ordinary day…..regular trip to the oncologist – check the blood levels, and back home. Except this turned out to be anything but ordinary!


First was an ‘added-on’ appointment – the oncologist had detected sounds and told me I had pneumonia, and should go see a pulmonist – also to try (again) to find the cause of the cough I have had for literally years. So off we went, and the ‘swallow test’ was only moderately awful – you would think that somehow they could make the nasty barium taste better….ugh!


We had time left before the appointment for my blood tests, so I got to go to my favorite thrift store and get a few goodies, and we stopped and had lunch at Arby’s – these were both unplanned and made the day even more fun – found some bargains and had a yummy lunch!


We were still early – but decided to go ahead over to the oncologist – and getting there early turned out to be a good thing – got right in to get the blood tests, and then headed back to see the nurse in the infusion room and get my results. Usually, these interim test results are brought by one of the other nurses, not what I think of as THE nurse. But she didn’t come – so we waited. They were pretty busy, so I didn’t mind waiting – this was routine, after all. Then she came and sat down, and laid it on the line….’Trish, these are awful!’ Uh oh….. and they were. White Blood Count down to 4.4, Red Blood Count down to 2.71 (first time this was low), Hemoglobin down to 8.3 – and then the Platelets…..down to 8. Yes – single digit 8. My previous low on platelets had been 11 – and I knew the oncologist’s ‘bottom line’ was 10 – so….what to do. First I got a injection of Aranesp for the red blood cells – then they tried to arrange getting the platelets in time to do the infusion this afternoon – but it was too late.


I needed the platelets, so the only way to get them was to go to the ER and get them there – and then the adventure began……the oncologist’s office called over to the ER to let them know I was coming, and had JUST had my blood drawn – so they didn’t need to repeat it. They agreed (ha!)


It was around 2:30pm when we arrived at the ER and proceeded to wait. I had all my paperwork from the oncologist’s office with me – with all the information they would need, but no one was interested in looking at it. Well, maybe later. We filled the time with people-watching as they came and went in the doors. We were a bit surprised that if the employees (and there were plenty of them) were not actually talking to someone, it seemed it was ok to just hang out and talk about their own lives – joking around and chatting – and I’m thinking… they have nothing else to do when the walk-in traffic slows down? Hmmmm. After about an hour – and I think that is their version of ‘lightning speed’ – I was taken back to a room in the ER and the nice guy who walked me back also found me two warm blankets – wonderful! I was just freezing! Then in came the nurse – to whom I offered my pack of paperwork to read – total non- interest. And….just as I thought, even though the oncologist office had just done my bloodwork – they were ‘going to do our own – we just like it that way.’ Uh huh – translation – we want to bill it, not read someone else’s work. I told them I had a ‘power port’ – kind of a central place thru which chemo can be infused directly – and can also be used to draw blood for testing.  The response? ‘Oh, well, we don’t want to mess with a port someone else put in, so we’ll  just find a vein and draw it from your arm.’  And I knew this would not end well….


So – she tried – and actually got the necessary draws for re-doing the testing, and then blew the vein – giant bruise. So – tried the other arm – had to get a needle in to give me the platelets….since they would not use the port – and even using a smaller needle – instantly blew that vein…..another even larger bruise. So….she took the blood to send to the lab and said she’d find someone else to put in the needle for the infusion. And so we waited some more…..won’t even go into how incredibly uncomfortable the bed is in the ER – not to mention the chair my poor husband was stuck with…. I was still freezing, and they did bring me some more warm blankets – I am now wrapped up in four of them…..and I’m still cold….and we waited…. around 5:30pm or so – we finally got to see the doctor (who was ‘tied up with someone else’ til then) who came in and said that he was ordering the platelets and we’d get this infusion going. And I’m thinking… knew this hours ago and are just NOW dealing with it?  Ok then…. but then things really went off the rails….


I had asked that the room door be open – I just like seeing what is going on – being endlessly curious about the goings on in an ER in real time. Watched the nurses try more than once to find out what was happening with the platelets – to no avail. At some point, one of them came in and said ‘we’re having trouble locating the pathologist who ordered the platelets’ – really? Does he not work here? Does the matching etc not get done here? Yes and yes…..but no more info…. Did I mention that we are now at dinner time – and still no one had the least interest in looking at the paperwork I had brought with me? But I did get the feeling that they were unhappy that I was just watching all that was going on…..and in a little while…..they came in and said they were moving me to a ‘quieter, more comfortable room’ – hmmmm….well, ok – am not going to turn down comfort, and neither was my husband!


Got all settled down in the new room – so comfortable!! Some time in the afternoon, a nurse had mentioned that the doctor ‘might have ordered some food for me’…..but no – he did not. So Lucian was off on the mission to obtain food for us… we had already discovered that ice was a precious commodity in the ER – we repeatedly asked for – and received one styrofoam cup with ice and water. Never learned where the ice machine was – or we would have helped ourselves…..but no…..and then we met Annie and Bobbi Jo! And everything changed! Annie set off on a mission to find out the whereabouts of the platelets…and enlisted Bobbi Jo in the quest – how blessed we were to have these two on our side! Meantime, Lucian made up a sign and posted it to Facebook (my phone memory was gone after 10 minutes of FB, his did better!). It got quite a bit of attention…..




Now we are way past dinner and still no platelets…..we were hoping the sign would produce results….it didn’t, but Annie and Bobbi Jo did! Never found out where the platelets were all afternoon ( I suspect they never got ordered) – but they did find out the platelets had to be ordered from the Red Cross – contrary to us being told they were here, but just waiting for them to come upstairs…..hmmmm. Now there was hope…..they had been ordered, just not from where we were told – and finally!!!! THE phone call saying they were on their way to our floor!! This time, they told us about 15 minutes….and guess what? it was 15 minutes – amazing how a little truth can boost the spirits! Annie and Bobbi Jo sprang into action – got the infusion pump, got a temp machine to take my vitals – it was something to watch them working together to get er done! Small glitch….my temp had been climbing…..and there was concern it might be too high to start the infusion – but God stepped in and calmed that fear – and we were good to go!  And what time, you ask, did these platelets start going into me? We came to the ER at 2:30pm – and it was now 9:00pm – just a tad excessive, I think. From then on, Annie and Bobbi Jo showed up in the room every 15 minutes – take the vitals, speed up the infusion….then showed us how to find out how much time was left by reading the pump – praising God for these two women who were the fountain of good information where we had had hours of no or incorrect information!


One bonus from this extended stay in the ER was that we got to watch the entire evening lineup on Fox News – Tucker Carlson, Sean Hannity etc  – so nice to hear REAL news for a while!! At long last – it was just before 1:00am, and the infusion was done! Got dressed in record time, and the doctor gave us our exit paperwork – and we hit the road – got home just after 2:00am – and have never been so glad to get into bed and off to sleep!!! They have at the hospital – an award for nurses who go above and beyond  what they ‘have’ to do…..and boy both Annie and Bobbi Jo qualify completely!!


Wondering….what will next week bring? I’ll let you know!!!




Sometimes it’s the small gifts…..

Sometimes it’s the small gifts…..

I hesitated to come out and post anything after my last chemo treatment – somehow I just didn’t want to have another ‘downer’ type post about how tired and awful I felt – figured no one wanted to hear that….so I waited. The last treatment was the ‘mini’ (translate – all drugs were half dosages) after the really bad ‘maxi’ treatment, but even so I learned that it takes me a full 10 days to get back to feeling ‘myself’ again.


Now that I am feeling good again, my mind has been filled with the ‘small gifts’ I have been given – starting with last Friday… I still wasn’t totally back to feeling myself, but as we started off for another trip to Virginia Beach, I looked outside at the sky and the landscape and thanked God for providing all this beauty!  The first gift was that this particular trip to Virginia Beach was that it was not MY doctor appointment, it was my husband’s – so I was just along for the ride!


As we drove along, I looked out at the fields of cotton, which are now being harvested – like snowballs on stalks, they made the fields white as far as the eye could see….another gift! This made me think of all the huge bales of cotton – some big rectangles the size of semi trailers, and some fat round bales wrapped up in colorful plastic, all destined for the Cotton Gin. Had to look that up and find out exactly what the Cotton Gin did. The one we pass is in Suffolk, VA, and is a big metal building with a huge lot out front that is chock full of those bales of cotton. I found that the Cotton Gin (short for Cotton Engine), houses the machine that removes the seeds from the cotton, then dries, combs and bales the cotton for transport to the next step in what it will become. So I learned something new….a gift!


I worry each time we are on the road that there not be any accidents, and or other holdups on our trip – and this morning was no exception – except that the worry came true – there was an accident, and we crawled  forward for a good 20 minutes to get past the accident site. We always build in extra traveling time for just this kind of thing, but now our cushion was gone, and I was praying that we not be late to our appointment. And my prayers were answered – clear sailing over the high rise bridge, and onto the road we needed to be on….and we pulled in to the doctor’s with a few minutes to spare and a whole line of handicap spaces …..all empty! Another gift! The doctor’s appointment went well – all was good, and we were sent on our way for 6 months, instead of 3! Yep – that’s another gift!


After that, I asked if we could go to IHOP instead of our usual Wendy’s drive-thru – so after finishing up our errands, we had lunch at IHOP – and I got my favorite Belgian waffle (wondering when they stopped putting pecans on the bottom of it), and it tasted so very good – another positive change – it tasted good! So, yes, put it down as another gift!


Not the most fascinating trip ever taken, but I discovered that a lot of your attitude and feelings directly relate to how you choose to view things – and sometimes the best gifts of all are the small ones!

Just putting this week away…

Just putting this week away…

I did think it was just going to be a week as usual – marking mostly that I’d gotten thru another treatment – ah, how wrong I was!


I did expect to feel bad – I knew that the Neulasta shot was going to give me some grief – it is, after all, designed to make your white blood cells reproduce at an accelerated  rate –  after  a day or so of that, I really did expect to bounce back (well, maybe not ‘bounce’ ) to feeling my normal self. Next day was even worse than the first – and I was kind of blindsided. I remember clearly the bone pain getting those new cells made, but I did not expect my entire body to hurt – ears, head, throat, you name it, and it hurt.


I got through the weekend, and was hoping for a decent week – but it was not. Instead of getting slowly better, I was getting worse – and I remember thinking ‘what is going on here? I should not feel so really awful all over!’  By Tuesday evening I was running a low fever – just hoping to get some sleep – but woke up every hour or so in misery. By the time 9:00 am came around, I was feeling so bad that I woke Lucian up and asked him to take me to the ER. I sure did not want to go, but money or not, I just had  to do something. So into the car, and off we went to Franklin and Southhampton Memorial Hospital. I could not tell them why it was that I hurt so, but hoping they could tell me. They got right on the phone to my oncologist, and meantime did some tests to eliminate all they could. They did tell me that my White Blood Count was 0.4, and my Platelets were at 17. Those are some LOW counts! Word came back that the oncologist thought that I was was having really severe reactions to the Neulasta. I had an appointment with him the following day, and he said to come in.


When I got to the oncologist’s office, they did my blood counts, and they were even lower! My White Blood Count was now 0.3, platelets were holding at 17, and my ANC (which shows how well you can fight off an infection – which should be around 4-5) was 0.12. I also now weighed less than I ever have in my adult life – Wow – those were not lows that I wanted at all. My oncologist came and talked to me and said that my body just cannot tolerate the full dose of CHOP, and these levels were from that. Going back to the ‘mini’ version with the next treatment. Went back to the oncologist the next day, so they could see if the levels were coming up – and thank God! they were ! Had to laugh at myself, me, the one who has been ‘on a diet’ since I was in the 8th grade, was getting on the scale hoping that it went UP! A real first there, and indeed, it was up too. Now just giving my body time to build up after this little episode, and be back ready to fight on by my next treatment later this month.


Not the happiest of posts – but though I got knocked down pretty bad, God and my dear hubby, Lucian, have been right there with me every second of the way – and with that kind of backup, nothing can keep me down!

mini to maxi and a bad hair day…

mini to maxi and a bad hair day…

The first little triumph of the day was not having to hit the road at 6:00 am! Having been thru the entire cycle of chemo once, we had a better idea of just how long it would take, and we therefore nixed any more early morning appointments. So it was much nicer to be able to start off at 8:30am and be there in plenty of time for our 10:00am appointment.


Then came the explanation for the mysterious words of what chemo regimen I got the first time round – it was referred to as a ‘mini-chop’. And this time, it was to be different – seems that the first time, the docs wanted to be sure my body could take the chemo and handle it ok on a smaller scale before they brought on the big guns. I passed that test, so now it was on to the ‘maxi-chop!’  All right – bring it on!


The first thing I noticed was a LOT more anti-nausea pre-meds…..not the greatest sign in the world – so I could expect that was going to be a bigger side effect this time round. These would get me thru whatever went on during the treatment, and I had meds at home to get me through what might happen after. After that, it was just a progression of moving from bag to bag of the drugs that make up the C-H-O-P. Still made for a bit of a long day – and before we were ready to go, they brought out the ‘Neulasta On-Board’ to attach to my belly. It is a delayed delivery that would automatically inject the Neulasta about 27 hours after my chemo treatment. This saved us a trip back to the doctor to get that shot – it is designed to boost your white blood cell count which gets pushed down by the chemo.


Funny story about last week and the little ‘on-board’ doohickey. It is pretty small – maybe a couple inches square – and it blinks. All.The.Time. Little green light, blinking to let me know it is working. I was told it would do this, and also that it would beep to let me know when it was going to inject the drug, and beep again when it was done. Sometime during the night, I got up to go to the bathroom, and thought it was lightning outside – but there was no sound….then I realized I was the thing lighting up, not the weather! I guess I wasn’t awake enough to make the connection right away…lol! Even funnier was the next day, when, having forgotten all about the beeping that was to come, my honey and I were in the kitchen, and heard this ‘beep…beep’ – we looked all around, was it the microwave? No….maybe the oven? No….the coffee maker? No….Then we both realized – it again was ME that was beeping! Quick lesson on how to feel like an idiot! And some comic relief!


Then came the tough part – or parts – the first two days after the last treatment were not fun – but this time with the max dosage – it was worse. Beyond tired, hurting, and nauseous – what a fun combination! Took my meds, and just decided to spend the day doing absolutely nothing but napping and watching TV. Sometimes you just have to hunker down and get through it – and I did. This is day two, still not great, but much better than yesterday. The little Neulasta doohickey did it’s thing, and now just need to deal with the pain that brings – but it is temporary. YAY!


The really hard part of today was admitting that the nurses were correct, and though I had escaped it in 2010, this chemo was going to make me lose my hair. Awful feeling. I kept hoping that it would not happen, but the evidence was clear every day, as more and more was coming out. The sweet gal at the beauty salon offered to cut it all off for free, if and when I wanted her too – I so appreciated that – but the thought of sitting in a salon while all my hair got chopped off was more than I could bear. My dear husband came to the rescue, and told me he would do it for me – when I was ready. Today, I was ready, and with prayers to start and many tears, he did this for me. That is love. It was hard, but now it is done, and I have a wig, and hats – so maybe it won’t be near as bad as my imagination paints it! I know it won’t – the anticipation of something is always much worse than the reality!