Morgan

Release

October 27th, 2009 at 6:23am MST by Morgan

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!

Melissa

Beautiful day!

October 21st, 2009 at 9:56pm MST by Melissa

…still coming off a high from U2 last night.  It was a family plan to enjoy it together, however, Morgan wasn’t able to make this one.  He entrusted Kasha to Nick and I and we got out for a nice dinner then met up with Michael and Shauna for the U2 concert.   UNBELIEVABLE!  What a great concert!    Next one, red zone- with Morgan!

Today- is a beautiful, happy day!  I’ve learned a lot over the last four months, at the top, celebrate the good and enjoy the happy, up days.  We are celebrating today!

Morgan’s surgery went well and he is in great spirits.  When he called me just before lunch time he was in such a good mood.  He was full of joy and so alive~  it reminded me of the days he was hitchhiking and had just come off a great ride or had reached his destination early.

You go Morgan!  : )  I love you.  Let’s keep celebrating!

Melissa

Brave

October 20th, 2009 at 12:02am MST by Melissa

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-adjective
1. possessing or exhibiting courage or courageous endurance.
2. invulnerable to fear or intimidation: “audacious explorers”; “fearless reporters and photographers”; “intrepid pioneers”.
3. Archaic. excellent; fine; admirable.

-noun
4. a brave person
5. a warrior

–verb (used with object)
6. to meet or face courageously: to brave misfortunes.
7. to defy; challenge; dare.

Synonyms:
1. bold, intrepid, daring, dauntless, heroic. Brave, courageous, valiant, fearless, gallant refer to confident bearing in the face of difficulties or dangers. Brave is the most comprehensive: it is especially used of that confident fortitude or daring that actively faces and endures anything threatening. Courageous implies a higher or nobler kind of bravery, esp. as resulting from an inborn quality of mind or spirit that faces or endures perils or difficulties without fear and even with enthusiasm. Valiant implies a correspondence between an inner courageousness and external deeds, particularly of physical strength or endurance. Fearless implies unflinching spirit and coolness in the face of danger. Gallant implies a chivalrous, impetuous, or dashing bravery.

~ Good ole Webster dictionary~

Morgan~ our living picture of brave, courageous, valiant…

I am in awe~ and amazed everyday ~ at your bravery.  Your Courage!  I am so proud of you.  Everyday is a fight and you continue pressing on.  You inspire me!  I love you- Go Morgan!!

*****

It’s a roller coaster ride~ and it’s miserable !!!  … so much can change in a day.

He has been in the hospital since Friday, October 9.  He mentioned in a previous post how the week prior had been quite scary- he was very weak and had been very ill.  Friday he was picked up by a non-emergency ambulance service and brought to the hospital to start chemo.  He was too weak and hadn’t eaten much during that week he needed to gain strength and see what was going on before chemo started.

Monday rolled around and he was feeling better, had friends coming and wanted to get chemo going.  The chemo began.  He had a great week of chemo and was feeling well, received his last dose of chemo on Friday and Friday night went downhill quickly and hard.  His fever reached 103.5.  Morgan had developed another MAJOR infection.  It was very dangerous, but was caught and treated quickly and it is being studied further, but is managed again.  He is on an antibiotic, had a transfusion and he is gaining strength again.

His close friends Dan and Ben were here for the weekend.  They were able to have some good laughs and I know it meant so much to Morgan to have them in town and to be able to visit with them.  I was delighted to get to share in some of the conversation Sunday evening.  I really wanted to meet these friends Morgan talks of often.  They both have been so good to him and their journey together as friends has had influence on his life and shaped Morgan’s world.

In looking through my photos for a picture to post- I am amazed at how time has flown by- yet stood still.  I can’t believe it’s been four months- all that has changed and happened in four months.  And then I think our world has stopped- there is loss, pain, mourning this new life with cancer.  I need to unload for a moment.  Cancer Sucks!  It’s horrible!  Cancer is what has been tormenting Morgan for all these years.

I know that it was even worse than he led on because he isn’t one to complain.  We thought it was back pain from a fall.  It was cancer- that makes me SO MAD.  Cancer has been living inside of my brother- robbing him of fully LIVING.  He lost years to pain.  This diagnosis has changed us.  You live differently.  We have had to let go of expectations, making plans and celebrations have become so different in just four months.   We have had so many fun things planned to look forward to and they ALL have been rearranged or postponed.

I’m learning a new brave- outside the box.  We will press on and keep making plans!   We support your dreams and believe in your future Morgan!  : )

Tomorrow is a big day, surgery and some major changes.  They will replace his kidney stints and remove his urethra catheter to replace it with a suprapubic catheter out his belly.  This will be better for long term and it is believed will help cut down on infection.   In the next couple days his  (CBC) blood count will drop  and he will go into the neutropenic stage.  This is where his white blood cell count drops and it is difficult for his body to fight infection.

If you are our praying people~ here are some requests:

* Doctors in surgery * Chemo/PacMan eating Buster & friends * Morgan~ strength, hope, courage, faith, peace, comfort, FIGHT. * Kasha- see and feel our love and appreciation and that she would have continued strength, health, peace, comfort.  * Pain management * Continued favor with doctors and nurses treating and caring for him. * Wisdom, clarity for next steps.  * Protection during Neutropenia-NO Infections!  * our Mom’s~ loyal, faithful, loving and serving.  *

Morgan is brave- over and over again~ a warrior with enduring courage.

Thank you for continuing to journey with us ~ our faithful family and friends~ Team Morgan!    : )

Morgan

Sleep, glorious sleep

October 15th, 2009 at 6:40am MST by Morgan

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!

Morgan

Chemo continues, flying friends and U2 360

October 13th, 2009 at 10:37am MST by Morgan

I’m beginning Day 2 of Round 3 of chemotherapy today and I feel better than I have in a few weeks. My energy has returned and I have something of an appetite again. One big change I need to make is to get back on an exercise regimen. I’ve fallen off the wagon and my body- especially legs and feet- are suffering as a result.

Last week was a really rough one and in all truth I was scared. I had never felt so weak, and I believed I would get no better from that point on. But new days, hydration and pills (not to mention a renewed optimism) brought me back around. Kasha and my mom have been overlapping schedules to be with me almost around the clock. It’s been so great for me, to have that support. It re-energizes me. Right now Ruth, my mother-in-law, is here at the hospital. I appreciate her companionship, and she’s able to help me with little things throughout the day so I don’t have to wait on the nurses.

I haven’t been having any noticeable side effects from the chemotherapy so far, just like last time around in September. Usually my levels all drop around the beginning of the 2nd week. We’ll see what happens. It shouldn’t be too bad.

My amazing friends, Ben and Dan, will be coming in this weekend to visit me. It’s a shame I won’t be able to leave the hospital while they’re here, but I hope they will take my family up on some hospitality to see the city a bit– go out to dinner and see a little of what Phoenix is about. I haven’t seen Ben, from outside Portland, Oregon, in over 5 years. Unbelievable. He’s been such a vital friend over the years. Dan I was able to catch in California back in August, but the visit was brief. Glad he and Ben were both able to sacrifice family time to spend it with me all weekend.

I was originally supposed to go to the U2 360 concert next week, but I now know my chemo schedule won’t allow it. I’ve told Kasha I still want her to go, since Melissa and Nick will be there, and possibly some other family members. It’s silly for her to forgo the concert just because I can’t be there. I want to hear all about it! Plus, no reason for my family to sacrifice everything on my account. I did get to see the U2 360 movie, which was amazing, so I know the concert will be incredible.

It has been a long time since I’ve personally checked in with you all on the blog. Thanks to all of you for your patience. I’ve got some work to catch up on this week from the hospital bed and also hope to write some emails and letters. We’ll see how far I can get. One thing’s for sure, my spirits are higher than they’ve been in a long time and I’m motivated by it!

Melissa

Companionship

October 10th, 2009 at 12:00am MST by Melissa

*Written by Mark to celebrate Morgan’s wedding toast*

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My brother Morgan and I are separated in age by slightly less than 3 ½ years. By adult life standards, that’s practically the same age. Growing up, however, that span of time created a hierarchy in our brotherhood/bunkmate arrangement of which Morgan assumed the lead role.

I recall the EARLY mornings where I would awake to find Morgan perched on my bed in the room that we shared. He was looming over me- incessantly requesting my assistance with his paper route that day. It wasn’t actually help that he desired. It was companionship. I eventually gave in… most of the time.

Back in those days, paperboys had to do their own subscription fee collections- a bona fide nightmare for an introverted people pleaser like my brother. So what would he do? Drag me along. Not for muscle, but for companionship.

I knew that at the end of that abhorrent task we would go and blow the loot on video games at Alpha Beta or Appetito’s. We shared a compulsion for those “Machines” as our grandpa would call them. “Now don’t go and put all of this in The Machines!” He would admonish us anytime he handed out a little pocket change. But boy did we.  All of that and then some. Personally, I enjoyed the games that pitted us against each other, Street Fighter, Mortal Kombat, etc. On the screen our size and strength was evened up. So I could beat him pretty much all of the time. He was frustrated and would gesture physical retaliation. But I couldn’t help it. I was compelled to beat him to assert myself- even if there was some potential harm on the horizon.

And those who know Morgan well know that he also finds it very important to fiercely, albeit quietly, assert his own values in the face of potential adversity. While many of us might not relate always to his means and methods, we can recognize his passion. And his loyalty. And his strong sense of honor. In fact, the rest of should be so lucky as to emulate his commitment to family and friends. Many people say “There is nothing more important than family,” but Morgan walks the walk. He is as empathic and supportive as one can be with never a foul word to say about anyone.  I believe that people often give gifts they would cherish in the own lives.   And for those of us fortunate enough to recognize and accept it- Morgan’s companionship is his greatest gift.

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In closing, I want to say to Mrs. Kasha Strub, thank you for accepting Morgan for all that he is. In good times and in bad. In sickness and in health.  God bless you both. We love you. Salud!

***

This speech moved me.  It was so touching, fitting and enlightening.  Companionship; a true quality and one of my favorites of Morgan’s.  I have many sweet memories of Morgan and I just being together.  He has comforted me, been there for me, shared wisdom, made fun memories and saved me on several occasions.  I love my big, little brother~ our gentle giant.

I am reflecting on the memory of June 10, 2009 tonight.  We celebrated Morgan and Kasha getting married.  It was a sweet calm before this storm.  A long awaited day and so treasured.   I never imagined all of this.  I am broken. I am changed.  I can’t even try to help you understand, it’s truly indescribable.  

I wish I could put into words the appreciation I have for Kasha.  Morgan chose her to be his companion~ long before they wed.   She has been there for him for years and has encouraged him to follow his dreams and passions when the rest of us were scared or unsure.  She has been there for him in ways we weren’t.  We are all blessed and so thankful to have her in our family.  A forever sister to me, this one is here to stay! : )    We love you Kasha.  Thank you for all that you do~ all day, everyday.   I can’t tell you enough, but will try for the rest of my days.

I’m proud of you Morgan!  I’m blessed to call you my brother.  You continue to gift into my life; Kasha is one that I treasure.   I love you Morgan.  I am here for you.  Always!

Melissa

let’s laugh

October 7th, 2009 at 8:51pm MST by Melissa

Monster Mash

Melissa

cancer SUCKS!

October 4th, 2009 at 10:19pm MST by Melissa

I think about writing everyday.  often.  I just don’t always know what to write…  I try to keep you up to date with details, but never have all of them.  There is so much that goes on behind the scenes- …. and when it looks like we’ve got it somewhat figured out… WE DON’T! 

Cancer sucks!  I know this in my head and my heart.  and CANCER SUCKS more. than. I. know.   You  just can’t wrap your head and heart around all that is going on in Morgan’s body, heart, head… minute by minute- everyday.  He is living it.    Please pray for;  Strength, Peace, Fight… wisdom…   God be near…  healing… 

Quick update:  Morgan checked into the hospital Saturday and stayed until Friday.  They were trying to figure out where his fever and possible infection was.  During the week they changed out his catheter 4 times.  Did a needle aspiration in his foot to biopsy/ grow a culture to check his foot.   Monday, he is scheduled to see visit the oncologist in his office.  We are waiting to hear if chemo will start this week.    

Yes, I’m a bit scattered and random.  I just wanted to touch base tell you we’re still here.  Don’t stop checking in, give up or stop praying- sometimes it’s just overwhelming and indescribable.

Melissa

Team Morgan

October 4th, 2009 at 10:15pm MST by Melissa

Team Morgan 2september 039Team Morgan

Morgan

Happy Birthday

September 26th, 2009 at 8:15am MST by Morgan

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!