Everything Fred – Part 121

13 September 2023

I feel pretty good this morning even though it started at 3:30 am. Seems the saline solution they give me along with the drug infusion makes up for some of the fluids I’ve lost through diarrhea. I felt good enough to start on my walk and was about halfway through when I got those stomach rumblings. I barely made it back to the house.

In reality, prior to the walk I had one semisolid bowel movement and then the diarrhea hit. After the walk, I had a second bout but I still seem to feel OK. Enough OK that I decided I need to trim the Heliconia. It gets out of control quickly and the dead leaves really detract from their appearance.

I didn’t get to trim this one because I filled the yard waste container with a second one on the side yard but you can see what I mean by the dead leaves.

I trim with an old home-made knife my Dad had that still can be sharpened to a razor’s edge. It cuts through the leaf bases pretty well and I’ve learned to wear gloves (the hard way) so I don’t slice a finger.

I have no idea how old this knife is but it is home-made. I don’t know if Dad made it or he had it made. It’s a perfect cutting tool and it can take an edge when sharpened.
This is the one I trimmed today and it looks much better. I also had to pare it back so Trevor can get his lawn mower between it and the fence. Every few years, I actually cut the whole thing down and it grows back within a few months.

I really enjoy how the leaves poke up under my Bahama shutters in the bedroom and bring a little green into the room.

I’m waiting on AAA Modern Air to show up for a check up of my A/C unit. I have a contract with them and they should call between 8-12 today. They clean the coils, check the coolant, and do a few other things. The main thing is for me to order more A/C filters. I change them once a month unless it’s winter and then it’s every two or three months. As you might guess, the filters are irregular in size so you kinda have to buy them from the company. I get two service calls a year and only pay for one.

I also spent some time on the phone with my insurance company. They send you a questionnaire and then ask you to submit it. Then they call and want to know what you want. I told them I was satisfied with my coverage at present, but who knows. They insure my house through Citizens, so they have no control over that. My car insurance is with them and I don’t think there’s anything I want to change on that. I guess it’s good they at least call you for once.

I’ve now been scheduled every Friday at 1:15 for a hydration infusion to follow up on the chemo infusions on Tuesday. I admit to feeling better after the hydration infusion and since it falls on day 4 when my diarrhea normally hits hard, I suspect I need the fluid replacement. No telling how long I’ll be with the hydration but I estimate at least two hours. I’m glad I no longer need the Filgrastim every three days so I’ve cut my visits to the cancer center down from four days a week to two days a week.

Nancy and Michel came over last night and brought massive amounts of Thai food from Heart Rock Sushi and Thai on Sunrise Blvd. in Fort Lauderdale. I used to go to that place quite often for sushi but haven’t been there since Covid. They brought two containers of Nam Sod Salad (minced chicken, ginger, roasted peanuts, red onion, scallions, cilantro, lettuce and lime juice) and Beef Pad Thai and a Broccoli Stir Fry with Beef. I’ll be eating left overs for a week. It was all delicious.

Better yet was visiting with Nancy and Michel. Today was their anniversary of my introduction of them. I took them on a date to Las Olas Cafe (long since gone) and they seemed to hit it off. Imagine me as a matchmaker! I think it’s now been some 20+ years they’ve been together. They left this morning for a golf tournament in the Dominican Republic and I told them to make me proud. Nancy said about 7 are going from the Fort Lauderdale area but there are 100 entrants from all around the world for the tournament.

We discussed heading to Key West for our birthdays. Michel and I are close on our birthdates and we say all three of us should celebrate in Key West. We did that years ago before Covid and just simply haven’t gotten back. We had such a great time together when we did it before.

October 13, 2019 – just before Covid hit. This was taken in the lobby of The Saint Hotel. We had a few drinks at their Burgundy Bar before the photo. Apparently there is another hotel in New Orleans. Maybe we should try that one next.

Well, the A/C person called and the stomach is making noises.

Stay tuned!

Update to Update – Part 59

12 September 2023

Stephanie did get me out of the infusion center by 2 pm. I was happy to note that it only took 4 1/2 hours for three drug infusions. I only have one more of those to go with two drugs. The rest will all be one. The Taxol only took 30 minutes and the magnesium was 1 hour (she only gave me half the dose). The Herceptin took one hour so when I go on the every three weeks with program, I should be out of there in 2 1/2-3 hours. That’s great.

I always feel better after the infusion. Part of that is the hydration with saline they give me. I seem to tolerate the administration of the drugs pretty well. The nadir comes 3-4 days later.

Also good news is my white blood cell count is normal and I don’t have to go in three days a week for injections. I have been scheduled for a hydration infusion on Friday. Those always make me feel better. In essence, I’ve gone from four days a week at the cancer center to two days a week: one for Taxol and one for hydration. That’s a relief!

Another bit of good news was Dr. Velez suggested a 120 day prescription of Imodium AD would run around $30 with GoodRx but apparently I have great insurance and it only cost me $5.49 for 120 days script. I was more than pleasantly surprised.

Nancy and Michel are coming over and bringing Thai. I can’t wait to see them. I love their company and truthfully, I need the distraction from all my routine. The Thai doesn’t hurt either. I don’t eat anything too spicy these days because of previously mentioned issues, but spicy food is the only type that has any real taste for me.

Hope the update of the update helps understand what’s going on. Stay tuned!

Cancer Update – Part 59

12 September 2023

The Xanax last night did the trick. I slept the entire night through and the alarm waked me at 6 am. I was a little ditzy when I first got up but the second cup of coffee did the trick. I arrived at the cancer center just a little after 9 am for a 9:30 appointment and they actually took me back early.

Stephanie is my nurse again today. She’s the one with great axenic technique. Sadly, I had to ask her name because I’ve had a different nurse four of the five times. I just start calling them senior lapses. She had no sooner gotten with a saline drip that Dr. Velez’ nurse Danielle appeared and asked about my well being. I told her it had been a rough few days. I also mentioned the telephone call from nuclear medicine during the week and asked about the echocardiogram. I showed her my log of medication/diarrhea.

Stephanie had no sooner gotten the port flushed and blood drawn when Dr. Velez stopped by. He said when the echocardiogram lab gets backed up, they often go through nuclear medicine and can get the same readings they need – hence the mystery of nuclear medicine vs. echocardiogram was solved. I suspect they also charge more in nuclear medicine.

Danielle and Dr. Velez both suggested a midweek hydration infusion and a cancellation of the Filgrastim injections. Apparently, they are satisfied with my white blood cell count (how I don’t know since it was low last check) but I’ll go with it. Dr. Velez also put in a prescription for Imodium AD. He also provided a printed coupon with GoodRx that supposedly gives me a good discount. However, my insurance seems to give even a better rate for prescriptions than GoodRx. I’ll check both. It’ll save significant money. The prescription is for 120 pills with 3 refills. The cost for 120 with GoodRx will be about $30. Over-the-counter cost was around $70.

Dr. Velez wants me to take Imodium AD every four hours and only use the Lomotil every 6 hours. I’ll still alternate until my diarrhea gets under control.

I’m waiting on the blood tests to see where I am deficient. I’ll know more what to expect today once they come in.

Stephanie started the magnesium drip already since she anticipates it being low.

10:20 am
The magnesium did indeed come back low (normal is 1.9-2.7) and mine was 1.7.

The Comprehensive Medical Panel just arrived. Sodium was low, chloride was high, anion gap (checks acid/base balance of blood) was low, glucose was high (248), calcium was low and alkaline phosphatase (measures liver/bone health) was high and total protein (function of liver or kidney problems) was low.

CBC with Auto Differential showed white blood cell normal, red blood cell low, hemoglobin and hematocrit were low, neutrophils relative was high, lymphocytes relative were low, neutrophils absolute high and lymphocytes absolute were low.

Next up will be the pre-infusion cocktail of Benadryl, dexamethasone, pepsid, and zofram. Then I can start the Taxol then the Herceptin.

My IV pole with pre-infusion drug, Taxol and Herceiptin and saline solution. The small bag on the left is the magnesium. The middle ba is saline and the third bag on the right is Herceptin.

Stephanie started with the Herceptin. It’ll take around 30 minutes and then the Taxol will be an hour. They’ve upped the rate of the infusion since I’ve not shown any ill effects for the previous 3 infusions. Less time here.

Note the jacket. When you get infusions, you get cold. I’ve learned to automatically ask for a blanket and a pillow and I keep the jacket in my shoulder bag.

The Larousse Gastronomique did arrive yesterday and thankfully it was in English. I will need a magnifying glass to read it but it is everything I thought it would be. It is an encyclopedia, historical record, and recipe book, all in one.

The color plates are great also. This is chicory and endive types.
The above map shows the wine regions of Burgundy, a barge tour I did in 2012.

Also yesterday, I noticed my night blooming cereus had bloomed.

The bloom only lasts one night and if lucky, is fertilized by a moth.
This is what it really looks like in bloom. The aroma is amazing and permeates the night air. If I can smell it, certainly moths can. This photo is several years old but I stayed up all night to photograph the blooming. It was worth being hung over a little the next day in class from lack of sleep.

10:48 am
Stephanie is admistering the pre-infusion drugs. Good stuff!

Maybe, just maybe I’ll get out of here around 2:30 pm. They stop the magnesium while the other stuff is dripping but they’ll finish that up after the Herceptin and Taxol. Stephanie decided to do the Herceptin first this time.

The Herceptin finished at 1 pm and now I’m back finishing half of the magnesium and the rest of the saline (for hydration). I feel pretty good at the moment – much better than when I first walked in. I might make it out by 2 pm. I won’t know what to do with the extra time.

Now, if only my appetite for something besides sugar kicks in. I don’t need a 248 reading for glucose.

Stay tuned!

Everything Fred – Part 120

11 September 2023

Yesterday was a good day diarrhea-wise and I eventually started to feel OK towards the end of the day. This morning started with diarrhea around 7:30 am and it’s continued and I feel terrible. Not an auspicious start to the day nor a good harbinger for tomorrows double drug dose.

I called my friend Daryl and canceled tonight. I was going to see Daryl and Bill’s new place at the Vee, but I just don’t trust myself too far away from the bathroom. To add insult to injury, for some reason CVS will not refill my Losartin (blood pressure) medicine even though there is one refill left on the prescription. I called my GP’s office and had them transfer the prescription over to Walgreens. I intend to do that with all my prescriptions. Partly, it’s not CVS’s fault. The one I use is probably one of the busiest in the county and they have a pretty significant turn over in personnel, so I’m sure things get confused and lost.

Last night before turning out the lights, I watched a YouTube video of Chef Jean-Pierre cooking Beef Stroganoff (Stroganov). It’s an interesting video and he lays to rest whether the dish is French, Italian, Russian, etc. and quotes the authoritative source Larousse Gastronomique, the “bible” of chefs. It was originally published in 1938 and was recently re-issued in 2009. The dish was created by a French chef working for a Russian Count Stroganov. Somehow, the spelling evolved into stroganoff later.

I heard of Larousse Gastronomique many years ago but the 1938 version was all in French and I decided my French wasn’t good enough to think about purchasing it. I assume the 2009 re-issue is in English and I ordered it off Amazon after watching Chef Jean-Pierre’s YouTube video. It should arrive today. It’s really for professional chefs but I’ve always wanted a copy and reviews on Amazon say it is eminently readable and I do love reading cookbooks. If nothing else, it’ll serve as an excellent reference publication.

Maybe it’ll have some recipes to stop me up and help abate my diarrhea. I did Google that and found that in reality, I’m eating pretty much what I should be eating with diarrhea. I also followed the advice of Judith and boiled some eggs to add a little protein. I still do a good bit of the BRATT diet (bananas, rice, applesauce, toast and tea) along with less fiber. My two weaknesses are caffeine (coffee in the morning) and sweets.

I have no idea how long I’ll be at the cancer center tomorrow. First will be a blood test to determine deficiencies then my pre-infusion cocktail of zorfran (anti nausea), pepsid (coating stomach), Benadryl (antihistamine), and dexamethasone (steroid and anti nausea). When the blood test comes back, they’ll administer magnesium if low. The magnesium will take an hour, Taxol will take 1-1 1/2 hours and the Herceptin probably two hours. That’s if all goes according to plan.

I was scheduled to go to dinner with Nancy and Michel tomorrow but I may have to change that to a simple visit either at their house or mine. With the way I feel today, I’m unsure how well tomorrow will go. Luckily, they are flexible.

I really do appreciate how my friends check up on me. I’ve never been one to talk much on the phone but Judith called yesterday to check on me, so did Ron in Miami and Joel. I spent some time talking with Chris catching up on Tucker’s escapades and goings on in the neighborhood. My cousin Jimmie and I had our weekly phone call yesterday as well. The day before I talked with cousin Jo in San Antonio. Saturday was football day and Natalie (LSU grad) texted me about the Ole Miss/Tulane ball game and asked how I was doing. Michael in Virginia also emailed me to check on me. I feel much cared for and looked after.

There was no morning walk but I did get back to my half grapefruit routine. I decided I didn’t need the Budesonide any more. Dr. Velez suggested I needed it only for a week and as it was a steroid, it was raising my blood sugar and I couldn’t eat grapefruit while on the drug. I prefer the grapefruit. Also, whenever I took the medicine, it had a very foul smell. It’s funny how some medications have a really distinctive smell.

I remember years ago as a kid that all medications were intentionally made to taste bad to prevent kids from overdosing. Somewhere along the line that requirement was relaxed and now you can buy all kinds of kids over-the-counter medicines that taste good (or at least not bad). One bad taste that sticks out in my mind as a kid was Milk of Magnesia. Mom was a firm believer in that and it tasted like a chalk milkshake. Ugh! The worst, of course, was castor oil.

Thanks for reading my blog. Today is mostly word diarrhea. I’ll try to do better next time. Stay tuned!

Everything Fred – Part 119

10 September 2023

My cousin Jimmie reminded me that she had stage 0 breast cancer. It was her I alluded to in the last post but I didn’t want to put her name to it unless she was OK with it. She also mentioned our Aunt Edna Lee (her aunt, my great aunt) has “female” cancer which Jimmie suggested may have been ovarian cancer. Cousin Jo and I mentioned Aunt Eddie but neither of us could remember if it was cancer. It now looks like both sides of my family have the tendency towards cancer. Normally, I think mostly of strokes and heart attacks in relation to my family.

Jimmie also mentioned the DDT we were exposed to as kids. Rachel Carson published her ground breaking book Silent Spring in 1962 and before that DDT was the pesticide of choice throughout the U.S. It was quite common for towns and cities to send trucks to spray/fog the area for mosquitos. It was a broadcast spraying and it would permeate the neighborhood. It worked well on keeping the mosquito population under control.

Jimmie, Jean and Jo’s house was a long house with a garage that ran under most of the length of the house where Uncle James parked two vehicles. When the mosquito control came by, and Uncle Jame’s cars were gone, it was common for them to drive into the garage spraying DDT fog. Jimmie and I love the smell of the fog and we would run into the garage and play in the mist after the vehicle pulled out of the garage.

DDT can stay in the soil for up to 15 years and in humans, it is often found in fatty tissue, in mother’s milk, and can be passed on to the fetus. Jimmie and I would certainly have received significant doses. It was banned in the U.S. in 1972.

Again, there’s no way to determine what caused my cancer. It’s just that I’ve had plenty of opportunities over the years for carcinogenic exposure.

The good news of the day is so far I’m diarrhea free! I do admit to low energy today. I think the last few days have really taken it out of me. I slept until 8 am this morning and by the time I was ready for my walk, it was well after 10 am and getting too hot to make the effort. Hopefully, tomorrow will see me on my walk, doing yoga and swimming laps. I did manage to grocery shop today but that pretty much sums up my day.

I wasn’t going to but I ended up watching the Ole Miss/Tulane football game. It was actually a pretty good game, especially since Ole Miss won. Again, college ball has become more semi-professional than amateur but it brought back memories as a college student.

Years ago, I made it to a Tulane game in New Orleans. I think their old stadium was under renovation and the game was played on some small stadium near the campus with metal bleachers. The exciting part was not the game but going to New Orleans. If my memory serves me correctly, it was the first time I’d eaten at the Camellia Grill. Even when I was stationed at the Coast Guard Communications Station in Belle Chase, I would often take the St. Charles streetcar to the Camellia Grill for breakfast or lunch. I’m not sure the food is any better than any other restaurant/grill in New Orleans but the place has presence. It’s also two years older than I am.

Tulane and Ole Miss used to be frequent rivals. Tulane was a charter member of the SEC along with Ole Miss, Sewanee, and Georgia Tech. I also remember listening with my Dad to Ole Miss/Tulane football games broadcast via WWL in New Orleans at the Roosevelt Hotel. Saturday’s game was the 73rd in the series – one of the longest in Ole Miss history. The longest rivalry is Vanderbilt at 97 games.

Several years ago, I met my brother and sister-in-law at the Roosevelt. They took the train which turned into a disaster when they had to disembark and take a bus into New Orleans. In any case, we stayed at the Roosevelt for two nights.

The Paris Exhibition Clock in the Lobby of the Roosevelt Hotel

I had a Ramos gin fizz in the history Sazerac Bar in the hotel. It was Huey Long’s favorite drink.

New Orleans is a magical city. I’ve attended 3 Mardi Gras there, was stationed there for two years in the Coast Guard, sailed up the Mississippi River on the CGC Reliance, made lifelong friends in the city, and have eaten some of the best meals of my life there. One item that should be on the bucket list of every person is beignets and coffee with chicory at Cafe Du Monde. I love strolling the market just off Jackson Square and hitting the dive bars all along Bourbon Street. I think back to my first visit to Bourbon Street and seeing all the strip joints for the first time with hawkers outside trying to get you to come in for a drink (although I was much underage – money was money to them).

My cousin Jo introduced Jimmie and me to Pat O’Briens and hurricanes. There were two piano players that night in the main bar and they were kind of dueling. One would break out into a melody or song and the other would interrupt with snide comments and jokes. I remember that particular year, either LSU or Tulane had played Texas and lost. The piano players got into a side gig of talking football and playing fight songs for teams mentioned. For example, one player would say something about the University of Michigan and then play the fight song of Michigan. This went on for a while and they eventually included Texas and “The Eyes of Texas Are Upon You.” Then one shouted lets play a song for LSU. They played “The Eyes of Texas Are Upon You.” It was great.

Warning! Two hurricanes will knock you on your a**. It was also there at Pat O’Briens that Jo told Jimmie and me that she was going to introduce us that night to the person she was going to marry. She qualified it by saying “He doesn’t know it yet.” That was when we met Ken for the first time. So, you can see, New Orleans holds a lot of memories for me.

Stay tuned!

Cancer Update – Part 58

9 September 2023

I started out this blog as “Everything Fred” but realized as I wrote it was mostly about my cancer effects and treatment. You’re probably tired of reading about it but it is what it is..

It’s been a rough couple of days with the diarrhea. I’ve had six episodes of diarrhea in those two days and the volume of discharge is pretty stunning. The only good news is that it seems to have decided to allow me to sleep at night and get active during the day. Of course, that means I don’t get too far away from the toilet so I didn’t walk these past two days – nor do yoga – nor swim my laps. Even more distressing is that I seem to be gaining weight (without eating a lot) and my belly seems to be distending. I guess I’ll find out more on Tuesday with the next chemo.

Yesterday I was basically a vegetable. Today I was able to rake leaves, clean the pool filter, pool deck and patio and spray for weeds. Just as I was finishing up spraying it started raining, so the spraying was probably to no avail. I’m sure the weeds appreciated the shower.

As usual, Saturday is wash day and clean house day. The washing takes the longest time but that has to do with the cycle on the machine – each load takes 58 minutes. Of course, that’s a long cry from helping Grandma Searcy boil clothes in her old wash pot. I’m sure helping her was more romantic than reality, standing over a hot fire in summer.

I cleaned at the house. I just didn’t have the energy. I changed bedding, emptied trash, dusted, vacuumed, and mopped. The bathroom needed a hefty dose of Scrubbing Bubbles. That took me until noon and then I headed to bed for a much needed nap.

I was talking to my cousin Jo yesterday and we discussed who in our family had cancer. We couldn’t think of but a single person on the Agnew side of the family and the only person I could think of on the Searcy side was my Dad. He started with prostatic cancer and that spread to his lungs and his brain. As I was cleaning house, I remembered that Uncle Ray had some form of cancer, so it looks like it is more on the Searcy side of the family.

Most people ask me what the source of my cancer was. There’s absolutely no way to tell. As an undergraduate, we dissected a lot with specimens preserved in formaldehyde. Not only that, but back in the dark ages, we used acetone a good deal in experiments. Both Mother, Dad, and Archie were smokers and I got a good dose of second hand smoke. As a graduate student, I was exposed to vastly more quantities of formalin and formaldehyde and acetone. That continued as long as I taught. It doesn’t really matter since my cancer is gone and the chemo is designed to prevent its return.

The one thing I’m glad of is never having smoked. I think I’ve probably smoked three cigarettes and three cigars in my life but never took to it. When you live with smokers your entire early life, it tends to turn you off to that.

The handouts they give you at the cancer center caution against drinking. I do like a cocktail but with the chemo, alcohol doesn’t have a pleasant taste to me. I tried a glass of sparkling wine last night and ended up emptying the glass and then the bottle.

I continue having minor nose bleeds, my fingernails and toenails, which used to need trimming weekly, now only need trimming every two weeks. The edges of the skin near my fingernails seem to be splitting and getting sore. I have a sore throat every morning when I wake but it at least goes away during the day.

One benefit is I don’t have to shave nearly as frequently as before. It’s so strange to lose coarse hair all over your body. It’s a weird feeling.

Yesterday, I put in an order for a new keyboard from Apple. My old “magic” keyboard was sticking on the letter “m.” Yesterday, the “a” key started sticking. It’s kind of hard typing a sentence and not using an “a” or “m.” I paid the extra $9 for same day delivery from the Apple store at the Galleria. Of course, the delivery took place while I was getting my injection. I called the delivery person and persuaded him to leave the package at the door (Apple wants someone there to receive the package) and he agreed.

The new keyboard also has a number pad to the right side. I used to have this on the PC at the college and I learned how to use it without having to watch my fingers. It made entering grades much easier. It’ll take a little while to get used to the new keyboard but so far, I like it.

Sunday will be grocery day. Hopefully, the diarrhea will abate and life will get back to a little more normal. Stay tuned!

Cancer Update – Part 57

8 September 2023

It started with 10 hours of sleep. I guess I was trying to make up lost sleep from yesterday but I went to bed around 9 last night and waked at 7 am. I took 2 Lomotil and was starting breakfast when I got that feeling. Breakfast was put on hold until the diarrhea passed. Again, the adult diaper saved the day, so to speak.

I can tell I’m weak and not feeling well so I don’t plan to walk (not sure I could make it without a diarrhea episode) and definitely not do yoga or swim. I’ll probably just lay low for today.

I’m not sure why I don’t feel well, whether because of Tuesday’s chemo (4 days out seems to be my nadir) or the Filgrastim the last two days or the flu shot yesterday. Maybe it’s an accumulation of all three. I already feel like I could sleep another 10 hours. I noticed my arthritis in the hands acted up last night to the point of having to take Advil. Then I had a minor nose bleed this morning. All things that could have something to do with chemo.

I just got a set of Medicare Summary Notices that encompasses my mastectomy and the follow up surgery that alleviated some swelling and inflammation. Medicare was billed $70,319.73. A great deal of that was modified to what Medicare agreed to pay. The overall result is that I may be responsible for $1,677.44 of that but I suspect my supplemental insurance will cover all of that. The strangest part of the costs was the complete removal of the breast was $7,330.34 but Medicare approved the whole amount but only paid $4,412.29.

The recovery room from surgery charged $3,991.00 and Medicare approved the whole amount. Several services were not approved but were probably re-billed and approved later. I can’t imagine trying to track down and trace all these expenses and give approval. I check over the summaries but it gets too complicated to figure out every little thing. I just hope for the best and only concentrate on anything that looks suspicious.

Today at 4 pm is my third Filgrastim shot. Then Tuesday is my day for both Taxol and Herceptin (and I suspect magnesium) infusions. It’ll be a long day on Tuesday. Again, if my white blood cell count is low, I’ll add in three more days of Filgrastim injections. Tuesday will be my fourth infusion of Taxol with five to go after that.

Stay tuned!

Everything Fred – Part 118

7 September 2023

So far, it’s been a productive day: morning walk, yoga stretches, laps in pool. Of course, the day started at 3:30 am. I was out of bed by 4, and breakfast, computer stuff, and all the exercising done by 9.

I headed to Walgreens to pick up a prescription of Lomotil and while there got my flu shot. In talking with the pharmacist, I asked about the Filgrastim used to boost my white blood cell count and how that might work with/against the flu vaccine. He said it was perfectly safe but might degrade the overall effectiveness of the flu vaccine to about 50%. I know I’ll be on Filgrastim for quite a while and decided 50% protection from the flu was better than no protection. I’ll be back for the new Covid vaccine later this month.

While at Walgreens, I cruised the anti-diarrhea isle and found buy one Imodium at full price, get 50% off the second so I stocked up and purchased 6. With 24 in a package and now alternating with Lomotil, it should last me a while. Still no word on whether or not my insurance will pay for it so I’ll keep the receipts just in case I can file with Medicare.

From Walgreens, it was breakfast/brunch with Joel and John at Peter Pan Diner. That’s the second time I’ve eaten there this year. It was voted the best diner in the state not too long ago but if that’s the case, other diners must be in real bad shape. The food is OK but nothing to write about so I’ll stop.

Yesterday, Barb stopped by for a visit. I hadn’t seen her since her trip and wanted to catch up. She brought rice pudding from Publix and I made some cheese/turkey/ham wraps and we had those and coffee and caught up on each other’s lives. If you remember, she’s the one who stayed the night with me after my second surgery. She left me with the rice pudding. I have to admit, Publix does a great job with the rice pudding. Just add a dusting of cinnamon and you are good to go.

Barb is so easy to talk with. We’ve been friends for years and every time we get together we have great conversations. I really appreciated the company – and the rice pudding!

Later today I’ll drive to the cancer center and get my second Filgrastim injection. I’ll have a third on Friday and when they do my blood work on Tuesday before my chemo infusion, I’ll find out if it’s working to get the white cell count up. As it is, I now visit the cancer center four of the seven days of the week. Then, this afternoon, I had a call from central scheduling about another echocardiogram (Herceptin can cause heart problems). They, so far, have not scheduled a hydration infusion this week but anything is possible.

The best news of the day seems to be that Hurricane Lee will veer northward before getting to the Florida coast. I have no desire to go through a Category 5 hurricane. Hopefully, it’ll stay out to sea and dissipate. I did fill the jeep up with diesel just in case it changes its mind.

Stay tuned!

Cancer Update – Part 56

6 September 2023

The chemo infusion with Taxol, magnesium and saline went well yesterday. Today was a different story. This morning I had two severe diarrhea episodes. Thank goodness for the adult diapers because the first came with no warning. If it hadn’t been for the diaper, I would have been washing sheets a little after midnight. The second one at least gave me some time to get to the bathroom. The diapers are worth not having to do midnight laundry.

I thought I would have another sleepless night after the two episodes (I was waiting on the next one) but the Xanax took over and I didn’t wake until 8 am this morning. True to form, I was a little hung over with the Xanax. Just as an example, after my morning computer binge, I shut the computer down. I never do that unless there is a thunderstorm in the area at the time. It could just as well be chem fog from yesterday’s infusion but there’s no way to tell.

It’s is currently 11:12 am and I just finished my morning walk. I usually never walk after 10 am but today was nice. The temperature was a balmy 84°F and the humidity was tolerable. Today is bulk trash pick up day and I was surprised at how much people were putting out for pickup. It seems to go in cycles with some months virtually nothing and then this month seems everyone is cleaning everything out. Looks as though old couches are popular for discard.

My old anthropology teacher at Ole Miss, Dr. James, always said you could tell more about societies by their tels (dig terminology for garbage dumps) than by just about anything else. Who knows what anthropologists will determine from our mount trashmores.

I’m also determine to do yoga and swim again today, Xanax be damned. I usually don’t swim after 10 am either. Not sure why my cutoff is 10 but it seems to work for me most cases but I really do need to get back into shape. My blood pressure is running a little high, even with medication and my glucose level is in the 200 range again. Of course, I had a dose of steroids yesterday. It has absolutely nothing to do with the Tootsie Roll miniatures I keep sneaking.

I texted Dr. Velez about the diarrhea and the possibility of a script for Imodium. He had already sent off the script for Lomotil but Danielle didn’t tell him about the Imodium. He said he would try to send a script but wasn’t sure insurance would pay for that. It’s worth a try if there’s a significant difference in price. I can’t always depend on the BOGO for Imodium. Perhaps it’s cheaper on Amazon. I also informed him I’ve doubled the dose of Lomotil and now take two every four hours and alternate that with Imodium every four, so both are on an eight hour schedule. It really gets complicated keeping up with it so I have a sheet I log everything down so I know which pills to take when. I also record each diarrhea episode. When the nurse or Dr. Velez asks, I just hand them the printed sheet.

I have an appointment at 4 pm for the injection to boost my white blood cell count and for the next two days at the same time. Looks like I need to buy stock in (1) adult diapers (2) Imodium (3) and Claritin. I’m not too sure how well the Claritin works on preventing bone pain from the injections but so far, any that I’ve had has been minor. At least it seems to help with my itching problem almost as well as Allegra.

Someone yesterday at the infusion must have completed their cancer treatment. There was a bell ringing and a lot of hooting and hollering and clapping. Congrats to whomever it was. I’ve a long, long way to go.

Stay tuned!

Everything Fred – Part 117

5 September 2023

I had one of the most enjoyable evenings last night at the Pillars Hotel and Secret Garden restaurant with great friends, tasty cocktails, and a wonderful Thai dinner prepared by Chef Hammi.

View of the Pillars Hotel from poolside. It’s consistently been voted once of the best small boutique hotels in the U.S. At the upper left, you can see the state bird of Florida – the crane.

It was a little too warm for outside dining and on the recommendation of Yelena, our server, we agreed to inside dining. We had agreed to meet for cocktails at 5 pm and we requested Yelena, our go-to person at Secret Garden. She mixes some great drinks. We always like to hang out in the lobby for pre-dinner drinks.

Left to right: Me, long time friends Kurt, Holley, Tom and Jim. Holley and I had an espresso martini, Kurt a vodka martini, and Jim and Tom had margaritas. Yum!

Over the years, we’ve gotten to know Yelena quite well and Holley wanted to do something special for her so when she saw a flower vendor along Sunrise Boulevard, she purchased a dozen roses. We haven’t seen Yelena nor have we been to the Secret Garden since before March of this year. Yelena was taken aback by the flowers and kept mentioning how no one ever brings her flowers. They were a definite hit with her.

On Mondays, Chef Hammi does a prix fixe menu and tonight was Thai.

I


Among the five of us, we managed to hit every item on the menu. As usual, it was excellent. I believe this is the best restaurant in Broward County. It has everything: ambience, great food, and great service. We sat down to dinner around 6 pm and didn’t leave until around 9 pm. Yelena kept telling us to take our time and stay as long as we wanted.

On top of all that, when it came time to settle the bill, Yelena compted us with a bottle of very expensive Reserve Chardonnay. She told us that she gets to do that about once or twice a year and she wanted to do that for us.

By the time we left, the sun had set and you can see the type of view you get when you sit outside and look over the New River and Intracoastal Waterway.

Once I got home, I turned out the lights around 10:00 pm and found myself wide awake at 3:30 am. I seem to be setting a pattern here on chemo infusion days. Subconsciously, I seem to be a little anxious so maybe I need to take advantage of the Xanax prescription and take one the night before chemo treatments. At least, since I got up so early, I may be able to get my morning walk in before I have to head to the cancer center.

7:00 am

I did manage my walk down Riverland Road. It was pitch black but I met three couples out for a stroll. By the time I got back to the house, dawn was breaking.

I had a little time to kill but when it reached 8:30 am, I left the house for the cancer center and made it a little after 9:00 am for a 9:15 check-in. The waiting room was packed. I think most of those waiting were not going for infusions. Stephanie is my nurse today and she said they start infusions at 8 am and are now thinking of starting them at 7:30. I suspect Holy Cross is getting popular as a place for chemo.

I always watch nurses’ processes when getting things ready for my infusion. Stephanie was meticulous and I told her she had excellent axenic technique. She’s thinking of going for her masters in nursing but hasn’t decided what particular specialization.

10:05 am

I’m waiting for the results of my blood test. From there, they’ll determine if I need anything other than the Taxol infusion. The last two infusions they have given me magnesium and for the hydration infusion, they did the same.

10:17 am

The first test results are in. For the CBC with Auto Differential, my white blood cell count is high, my red blood cell count is low, hemoglobin and hematocrits were low, neutrophils relative high, lymphocytes relative low, and neutrophils absolute high.

10:39 am

For the Comprehensive Metabolic Panel, my glucose was high (240). Otherwise, everything else was normal.

My magnesium level was also low again, so I suspect I’ll be getting another dose of that.

Stephanie added the pre-infusion drugs: Zofran for nausea, Benadryl (nausea), Pepsid to coat the stomach and Dexamasone (steroid). After the Taxol, she’ll administer the magnesium. I’m also getting a saline solution which should help with my dehydration (magnesium deficiency is the key).

I did ask if I could get a prescription for Imodium. I bought six packs of 24 at Walgreens (their brand) and it was BOGO. That ran to over $60. If I can get a prescription, my insurance will probably cover it at a much reduced cost.

11:40 am

Stephanie began the Taxol infusion. It’s on slow so it’ll take about 1 1/2 hours. If I don’t have any adverse effects this infusion, the next infusion of Taxol will take around 1 hour. Progress! It’s also a good thing I had the dental appointment changed to yesterday instead of today at 3 pm otherwise I would not have made it. These infusions make for long days.

Noon

Danielle, the nurse practitioner in charge of the floor, came by and suggested upping the number of times I take Lomotil to the same frequency I take Imodium. She’ll write a script for Imodium and Dr. Velez will renew the script for Lomotil. That way insurance will cover both.

1:24 pm
The Taxol finished in 1 hour and 34 minutes. Stephanie is now rigging the IV for magnesium. She said my level was very low and I’m to get the full bag and that will take two hours (2 grams/50 ml).

You learn something new every time you visit. Today I learned there is not one bathroom in the infusion center but three! That’s a very important tidbit of information considering how often I have to go pee with these infusions. All three are on the same side of the building. Out of four visits to the infusion center, I’ve been in the east wing (with the bathrooms) twice and in the west wing twice. It’s not really an imposition because the farther I have to walk the better. At the moment, there are two bathrooms on either side of me in cubicle 4D so I feel pampered. Of course, one of the bathrooms doesn’t have hand towels. That particular room has a sign that says “Flush twice.” I’ve read that on some of the paper instructions they pass around but the sign is only in that one room. I’m sure the idea is the chemicals infused are so toxic that the aerosol from the flush is hazardous to people.

For example, Stephanie has just been in a regular (albeit stylish gray) uniform all day until she hooked me up to Taxol when she put on a gown. That tells you something.

Mainlining magnesium. What a rush!

I’ll probably stop at the grocery store on the way home. I need some fruit and I’m running low on Blue Bell ice cream. Maybe that’s why my glucose hit 240 today. That and the steroid will probably make it go higher. Again, I figure I need to eat what I want to eat and worry about the details later.

Looks like I’ll get out of here around 4-4:15 pm. That’s eight hours of infusions. Who knew it could be so tiring. Sadly, the Benadryl did not put me to sleep. I suspect I’ll take a Xanax tonight to make sure I do sleep and hope for no hangover. They have not scheduled me for a hydration infusion but I’ve had almost a liter of saline which they would do for a hydration infusion. They also have not mentioned any injection to boost my immune system so they are probably satisfied with the results.

Now, on to the grocery store! Stay tuned!