Archive for the ‘Home Life’ Category

Release

Tuesday, October 27th, 2009

I should be leaving the hospital later today. Believe it or not, it’s been 2 1/2 weeks since I was admitted this visit. So long… I have only been outside twice in that time, to take in the sun and fresh air.

Other than that, I’ve been taking walks down the halls each day to strengthen my legs and make sure my foot holds. I’m supposed to have a brace for my right foot today, since I have what they’re calling a “drop foot.” I don’t have full control over it and the foot just drops to a 30 degree angle instead of 90 degree. It makes it difficult to walk, and my physical therapist has been tying it up to help for now.

I’ll be continuing IV use from home. I haven’t tried that yet, but there’s a company that will come into my home to help with infusions of antibiotics. They are necessary to take for at least another week, for my urinary tract infection. I’m not totally sure, but I think my blood infection is cleared up. It was a serious issue for a while, but they pumped me full of so many antibiotics I don’t see how anything could have survived!

It will be good to be home. First, I’ll just enjoy being closer to Kasha. She won’t have to spend so much time going back and forth to the hospital. Second, my home just feels better, and I have access to my big TV, Wii games and DVD player.

I need to get to writing again. Or at least some research. I’ll be going through a lot of papers these next few weeks, trying to organize, and that should help me find a lot of the papers I’ve written in the past in support of my book, American Wayside.

I’ll let you all know how things are going at home in the next few days. Thanks for your continued thoughts and prayers. I do appreciate it!

Sleep, glorious sleep

Thursday, October 15th, 2009

Yesterday was filled with sleep. While the chemotherapy cocktail was dripping into me I was snoozing. Before and after meals I snored. By the time 9pm came around I was ready to sleep the night away.

Kasha left the hospital around 9:15pm. (She had been with me since about 5pm this evening, after work.) My mom, Marsha, was here to “fill her shift” through the night. I had my “briefs” changed, positioned myself on my side, and drifted off to sleep.

Throughout the night I sometimes wake myself up with violent body jerks or loud snorts and snores. I’m not sure if it’s the drugs that lead to all this. I was always a quiet, steady sleeper before. Anyway, I managed to stay prone until about 3am when I was tempted to get up and geek on the computer. I resisted and slept even more.

At 5:30am I was finally up for good. My nurse was in to provide drugs and draw blood (that’s Cornell from Romania- one of my favorites here). My PCT (Patient Care Technician) cleaned me up and now here I am, ready for the day. About 8 hours of sleep. What used to be a standard for me is now hard to catch all at once, and I’m sure the extra winks will help. Maybe I won’t feel so drowsy this afternoon as a result.

Never underestimate the need for sleep. That’s what I’ve learned. When tempted to watch another hour of TV or stay glued to the computer, give it up and get to bed!

Happy Birthday

Saturday, September 26th, 2009

I had a wonderful birthday, thanks to everyone who came out to my party last night and also sent birthday cards this week. I’d like to especially thank my Wyoming and Colorado family, who sent over a dozen cards with creative print and messages.  Thanks so much also to Dad & Carol, the Lammers, Nick & Melissa, Mom and Vicky. Your support has been a tremendous help.

Friday afternoon, the party was switched to my place. The reason– I wasn’t sure I’d have the energy to make it to Melissa’s house. There was a chance at one point that the party would be cancelled. My doctor’s office had called and recommended I immediately admit myself to the ER at John C. Lincoln Hospital because I had been having fevers each night and a lot of pain in my right foot. I was able to call back Dr. Lo (my oncologist who had left the ER message) and explain that I was having a party. He said it would be OK to wait for the morning to go to the hospital.

And so the party went on. My living room was transformed from a semi-hospital room to a wide open entertaining area. The hospital bed was wheeled to the back of the room and a half dozen chairs  were set out. The couch looked inviting in front of the sliding glass door, and my old office- with doors opening into the living room- was clean enough to operate as a second entertaining room.

Spinato’s was delivered, my absolute favorite pizza. By 8 o’clock everyone who was coming was there. My brother, Mark, had flown out from Austin to be there. Considering the expense of such a trip I was really touched. He had just been out here a few weeks before for my mother’s notable birthday. I was also excited to talk with an old friend- Michelle- who I hadn’t seen in about 9 years. Coffee, espresso, cheesecake, fruit and shortcake were served. I had suggested chocolate cheesecake as birthday cake and it was perfect.

By 9:30pm only family remained. We took some photos and then someone recommended the party break up so I could get some rest. I had begun to feel a little more weak, so I had no complaints about ending the party. Everyone quickly cleaned up the house and then trickled out the door. The party was over, and I was grateful for all the work put into it. (Thank you Melissa and Mom!)

This morning I’ll be admitting myself into the hospital. In the next hour, in fact. I’m not sure what the ultimate result will be, but I’m hoping to get my pain pump adjusted so my right food doesn’t throb with pain so much, and figure out if I have an infection that’s causing my nightly fevers. Maybe they’ll start me on another round of chemotherapy Monday. We’ll see.

In the meantime, thanks to all of you who came to my birthday party, sent a card, or offered well wishes. It all means a lot to me!

More about Morgan on Facebook

Friday, August 21st, 2009

I’ve been using Facebook quite a bit lately to keep in touch with friends and share more about myself. There you can find tons of info about me, including photos, hobbies, personality quirks, travel notes, etc. I’ve added my reading list, music recommendations and lists of the places I’ve traveled. Check it out. Go to:

www.facebook.com/morgan.strub

(If you don’t yet have a Facebook profile you’ll need to first create one and then add me as a friend in order to see most of my info.)

Family Day – Strubs in Phoenix

Friday, August 21st, 2009

Today I’ll be meeting up with all my family for meals and merriment. Mark and Jack are in town, and they’ll be coming over this afternoon in time for my radiation appointment, then off we go to meet my brother Michael and Dad & Carol -who drove down from Pinetop- for lunch at Hometown Buffet. Later this evening, most of us will join with Kasha, Mom, Melissa, Nick and the girls.

There’s a chance that I won’t be feeling as well next weekend as I do now, due to chemotherapy starting up again, so I want to maximize the time I have and enjoy all I can. It’s been a rough couple of weeks for me- due to steroids, new pain and numbness, emotional weardown, etc. I’ve also been letting myself worry about next week, even though there’s nothing I can do about it. For all I know, everything will be smooth and fine– the hospital stay, ureter stent replacement (kidneys), and chemotherapy. No need to jump ahead in my mind or expect the worse.

For now, I just have to live in the moment. I got extra sleep last night so that I could reset myself and be ready for everything.

I have been bad about following through with communication lately. I apologize to those of you who have reached out to me lately and received no response. I am thinking about you! Please be patient with me, I’m sending word soon.

Hope to have some photos up here on the blog this weekend… and some guest bloggers among family members.

Turn It Down- on steroids, refocusing on support

Tuesday, August 18th, 2009

I’ve been getting overwhelmed, thinking about writing in my blog, and so I haven’t done much of it as you can see. That’s a feeling I’ve been experiencing a lot of lately- a sense of overwhelming- and it turns out it’s mostly drug-induced, artificial.

I’m still not used to the effects of the steroid I’m taking, Dexamethasone. In fact, I had no idea what I was getting into when it was first prescribed to me last month. No one explained its side effects, and I didn’t think to ask. Up to this point I’ve just been letting whatever drug details get through that seemed relevant and leaving it at that. (“You’re giving me OxyContin for pain? I could have severe constipation? Ok…. Lopressor to keep my blood pressure down? I might get tired and dizzy? Whatever…”)

The drug’s potency is about 20-30 times that of hydrocortisone and 4-5 times of prednisone. I take a 4 mg tablet, four times daily. As one of my radiation doctors described it this last week when I began complaining of symptoms, the shock to my system is like drinking 50 cups of coffee.

It was returning from my LA trip last week, when my doctor upped my dosage back to 4x daily, that I really began to notice extreme changes that were very UNme. Most symptoms I had been experiencing since the start of my prescription a month ago, but it’s the emotional/mental effects that have been hitting me hardest lately. Now, I wish a doctor or nurse had warned me about this scenario of side effects:

You’re going to become something of an assh*le. Your wife is going to get the brunt of this as you become more and more critical, mean-spirited. You’ll make her cry, and you won’t be able to see how your dark mood is muddling everything up.
Sleep? Forget about it. Not only will you lose it at night, you’ll convince yourself you never needed it, all the while dozing throughout the day in a mostly unfulfilling way. Any productivity gained by having all those extra hours is lost in a low-grade drug haze.
You just can’t get enough to eat. Every meal is an overkill of double portions, and snacking takes on a whole new meaning. Your face puffs up and your gut juts out.
You’ll have a general feeling of discomfort and upset. From stomach and throat irritation to cracking, unhealing wounds to annoying periods of increased sweating.

So, with all this trouble the drug is causing me, why on earth am I taking it? According to Wikipedia’s Dexamethsone page:

“In oncology, it is given to cancer patients undergoing chemotherapy, to counteract certain side-effects of their antitumor treatment… Dexamethasone is also given in cord compression where a tumor is compressing the spinal cord.”

In my case, it’s mostly for spinal cord compression. I spoke with Dr. Kukunoor on the phone today and he told me I can again cut back to 3x daily, and that next week- after I start back on chemotherapy again- I may be able to decrease to just 2x daily. I can’t tell you how relieved I’ll be- body and mind. Let’s hope the radiation is doing all it can to shrink the tumor that’s making this necessary in the first place- the one between my shoulder blades.

My last radiation treatment will be Friday. Then, back to the hospital on Monday for both chemotherapy and kidney surgery. My brother and his son will be in town beginning Thursday. I’m excited to be able to see them both, Mark and Jack. I can’t tell you enough how much my family’s support and presence has meant to me; my wife, parents, siblings, aunts and cousins. I’ve always known how important they are to me. I guess I never really knew, until now, how powerful their influence is- to facilitate healing and catharsis.

My friends have also been essential to me, of course. They inspire me, provide emotional support, and motivate me for what lies ahead. I’ve been amazed at their level of devotion, and it makes me want to give all I can in return; to show their belief in me is not wasted.

So, what gets me through these rough times– when the drugs play tricks with my mind and the myriad physical symptoms keep wearing me down? My family and friends, of course. My commitment to them, and- as a result- my commitment to heal and choose to live as best I can.

And I’m so grateful for Kasha. I can’t imagine making it through without her. We chose each other, for better or worse, and we’re able to love each other through whichever comes our way. Let that realization shine through each time Buster or any steroid tries to bite us in the ass.

Amazon Kindle – Avid reader once again!

Thursday, August 13th, 2009

Very good friends of mine have just become my lifetime reading benefactors. They’ve provided me with the money to get the new Amazon Kindle, a wireless reading device that can store hundreds of books- old and new. What makes this product so amazing is that I can load it up with free books that will last me for months on end. Classics are easiest to find for free, but I also have a bunch of e-books that can be converted into Kindle format and then sent to the device using my computer and a USB cable.

The Kindle can be used as more than just a book reader. When I was in California this last weekend, Dan was showing me his and some of the cool features, including a basic text web browser (I could even pull up digihitch.com) and instant messaging service (Yahoo! Messenger). As a wireless device, the Kindle can receive new books straight from Amazon, so if I do choose to buy a new bestseller I can be reading it on my Kindle within a minute of purchase. I can also read sample chapters from nearly any new book release without paying a cent, plus get samples/excerpts from many thousands of older books.

A few geek features I’m excited about include the ability to do keyword searches on words within the books I’m reading, as well as digital highlighting of passages. I can even store notes about something I’ve highlighted! Perfect for when I’m doing some non-fiction research. I really think the Kindle is going to make my “bed life” a whole lot easier. I’m heading over to Amazon.com to buy one now.

If you’ve been thinking about buying one yourself, use this link to do so and I’ll get a small commission from amazon.com at no extra cost to you!
Buy the Amazon Kindle Wireless Reading Device (6″ Latest Generation)

Losing hair after chemotherapy

Thursday, July 16th, 2009

Morgan's chemotherapy-related hair lossLast week I began to notice that I could pinch out tufts of hair. Looks like I’ll be bald soon, but for now I’m not bothering to shave or buzz my head. This last weekend, Kasha took photos of me on the balcony as I pulled out more hair.

Home, Rested

Friday, July 10th, 2009

I woke up at 7am this morning in my own bed. I had one of the best, most restful night’s sleep in over a month. What a gift that is. I woke just briefly a few times, once getting up to go to the bathroom. Otherwise, my catheter was dutifully filling up by the side of the bed.

I left the hospital around 5pm yesterday. Kasha went over my new prescription drug needs with Nurse Kathy and discussed nutrition. I have no dietary restrictions really, but I’m making the effort to eat healthy, green and organic. I haven’t had a cigarette since the day I was first admitted to the hospital (June 19th) but I do still think about it. There are some mornings where a coffee and smoke seem like the best thing, but then the nostalgic urge passes and I get on with myself.

Today is Kasha’s and my one month wedding anniversary. Our actual ceremony was supposed to take place tomorrow, July 11th. We still have a box of 60+ expensive wedding invitations to attest to that. I’d like to get them sent out to everyone this weekend, along with an explanation of why we moved the wedding forward and links to our websites (this blog and the wedding photo site).

There are no plans made yet today. No doctor appointments or professional deadlines. I do have a few tasks for my web business I’ll take care of this morning, but otherwise I’m free to do whatever I want today. What a wonderful feeling. It’s a good day.