Monday, November 26, 2007

My Friends

I received a text message this morning from a friend of a friend. I thought I might clarify some things in another post.

My friends are my lifeline. Especially when I have moved to a new area, I have found myself leaning on them more than ever... even more so now that I've been battling cancer once again. The friends I mentioned, went far above the call of duty and helped me out. I in no way wanted to discount them by mentioning the help I got from my folks. I understand, a friend can only do so much... and actually what I meant to say is they did so much. I wouldn't have known what to do with myself if it wasn't for them.

I have to say, in the past my friends have been as helpful as parents and close relatives. I consider my friends my family.

I also want everyone to know, I have been speaking of my illness a lot lately. It inevitably has been in most of my conversations. Those who know me, know it's not in my character to talk so much about myself. I suppose I've been left with no choice, because it's what I see everyday when I wake up, but the truth is, in a normal state -- I'm a selfless person 364 days a year. Those who know me, know that. So, please know that I'm not trying to bury you in the details of my battle with cancer, it just has unfortunately been at the forefront of my life now. And once it's gone, I know my friends, family, and acquaintances will be getting a lot more of the regular 'me' once again.

One more thing, I've had cancer before, and unlike before, this time I was not scared...

-LB

Sunday, November 25, 2007

My Favorite Aunt

My favorite Aunt is Pat Zbylut... talk about a strong woman. I got to share some thoughts with her over Thanksgiving dinner. She knows what I am going through. She has been battling rheumatoid arthritis for several years now. We have watched a once physically strong person be handicapped by this horrible condition. As awful as it has been for her, she still has plenty of spunk mentally.

As I waddled in for Thanksgiving dinner, I immediately went for my parents reclining chair, knowing it would be the most comfortable seat in the house. While most everyone stayed in the kitchen and talked, she came into the living room to see how I was doing. It meant a lot to me. She told me how unfair it was for me to have to go through all this, and that she knows what I am going through. But sadly, I can see what she is going through as well, and I find it as equally unfair for her to go through what she has.

We both joked -- with the absence of Terry (her husband, my uncle) -- that her and I actually got to talk for a change. Normally, Terry and I trade jabs the entire dinner and joke about how much we enjoy "hanging around with the dysfunctional family." But this time I had a real meaningful conversation with her, one that only both her and I could have... because we are both experiencing some of life's injustices, but at the same time we learn from each other and have become really strong human beings as a result.

I just wanted everyone to know what a cool aunt I have, and this one is for you Pat. Thanks for being there for me, like no one else could -- because they have no idea what it's like!

Top Ten for Week of November 24, 2007

  1. Michele Sawin
  2. Virginia Sawin
  3. Carl Bobbitt
  4. Debbie Bobbitt
  5. Pat Zbylut
  6. Sterling Shetler
  7. Alyse Fischer
  8. Chris Gamboa
  9. Robin Ness
  10. Jonathan Stephens

My Burnt Nerves

**WARNING, THIS POST CONTAINS
GRAPHIC PICTURES AT THE BOTTOM**


***IF YOU SCROLL DOWN TO LOOK,
DO NOT SAY I DIDN'T WARN YOU!***


A short time after my last post, I went through some of the most horrific pain of my life -- correction: the most horrific pain of my life. If the swelling wasn't enough, it felt like my foot was being burnt alive. I think my foot just stopped burning, and my last radiation treatment was a week ago.

With that much pain, I felt like I was starting to lose my mind. I did not realize that a human could reach such a point to where the pain could start eating at one's brain... this is exactly what it was doing. I felt like I was losing control. I've had two days in my life that have been unbearable, days that I wish not to have to go through again. Those two days were last week.

My friend Jay Watts was with me when I was losing grip. He would be the first one to tell you that I made myself very clear to the docs at the OHSU Radiation Oncology clinic that things were not working, and they had better halt the radiation asap or do something immediate to get me out of the painful hell I had been living. Unfortunatly, the addition of pain medication did no good, and in fact started giving me breathing problems. Being swollen up all over my body, feeling burning flesh, and the added breathing difficulty were proving to be all too much. In the days that followed, friends Michele and Virginia Sawin could tell I was starting to come apart not only physically, but also mentally and even emotionally. They were brave enough to put up with me a few more days. Driving me back and forth to Portland each day. There was one day when I thought I would have to cancel my appointment, but Michele showed up at the last minute and saved my bacon. I missed a day and a half of work from that week, then got through the weekend without too much difficulty. This past Monday proved to be yet another challenge with more pain and swelling. By Tuesday I had huge blisters forming on my foot, this is when the doctors halted my radiation treatments. Those who were around me knew I wanted it to be much sooner than that.

In the beginning I was told I would have 17 radiation treatments, with a possibility of going to 20 if things held up all right. Things held up all right at 17 treatments, but in the 18th and 19th treatments, things got extremely painful, and by the 20th treatment I saw those nasty blisters. But at the 20th treatment, I was told that I would be having another 3 treatments. My response was "what?" -- and even the radiation oncology nurses said they were surprised by it too, but my radiation oncology doc ordered it literally on her way out the day before. She went on vacation the day after, so obviously no one could ask her what the reasoning was. Fortunately, due to my complaining the nurses got me in to see the other docs, and they agreed, the radiation needed to be stopped, probably long before this point.

The Tuesday and Wednesday of Thanksgiving week I was forced to stay home from work, as my foot was turning into one big blistery mess. It was at this time that some new medication (liquid morphine and 40mg of Oxycontin twice a day) was finally starting to curve my pain. FINALLY.

Wednesday night I went on a "death mission" and drove myself to Hood River, even against the doctor's recommendations. It was one of the dumbest decisions I have ever made as I had tremendous difficulty driving, the pain and swelling almost prevented me from driving all together. I finally reached the hotel about 8pm where I waited for my mom to meet up with me. She got a ride down with Keithanne who was going to see her daughter in Beaverton. We figured Hood River would get us out far enough to make it home at a decent time for Thanksgiving dinner. She arrived about 10:30pm and we left the next morning. By this time the swelling had paralyzed most of my body. We arrived, and I waddled into the house with each parent by my side helping me in and up the steps where I would sit in a reclining chair for the next four days straight. With foot above the heart, drinking plenty of liquids, and having the TLC of my parents by my side I am happy to say I have improved by leaps and bounds.

Most of my swelling has subsided. There is some areas in my waist that are still swollen, but my chest, legs, and feet are nearly back to normal.

Simple things like using the restroom and taking a bath have been a chore. Things that normally took minutes took twice if not three times as long.

Now, back to the blisters. I have some pictures below that might gross you out... but if you've read this far, you probably can handle it, right? Well, we will find out... but basically when I was getting into the bathtub the other night, one of them opened. The ooze that come out was disgusting. I can describe it as a bright yellow clam chowder discharge. Oh, and the horrific odor, I can't even describe it, it almost made me gag myself. The second blister that burst had a more typical yellow liquid and poured out like a hose. It was a both disgusting and amazing thing to see. The human body is a very interesting thing, and I can tell you that first hand now.

After talking with my friend Alyse tonight, I had a better understanding of people and how they are when you are sick. She has been through quite a battle over the past two or three years with her illness. I will save her story for another blog entry, but basically it comes down to needing help when you are down. She said you basically can't rely on others when you need them. I have learned that statement is very close to true. It's sad but true, and you learn who your good friends are and your truly great friends are. To be all out honest, I have "friends" who didn't even respond when I asked for help. Then I have great friends like Virginia and Michele who helped me out immensely, driving me to treatments everyday -- until they got burnt out. Jay Watts and Thane Shetler spent time whenever they could to help me as well. This coming week I'll be in good hands with them as well as my mom who is going to be staying the entire week with me in Salem.

But the true award goes to my parents, who spent the past week waiting on me hand and foot. Helping me in and out of the chair. Making sure my foot was propped up like it needed to be. Changing my dressings twice a day, and keeping my overall spirits up. It was exactly the kind of TLC I needed after this whole ordeal. I can tell you that good health is that light at the end of the tunnel I can now see because of the rest, good diet, and treatment I got from my folks.

In writing this (now very long winded) blog entry, my supervisor from ODOT called. To my relief, she said they are behind me 110% and to not worry about a thing except to get healthy. She stated how well I have done in the past month and that they just want me to get healthy and to return when I feel it is best. Luckily she had checked her voicemail this evening at her office and got my message -- said she wanted to call to relieve me of any worries. I know with a supervisor that caring, that I have gone to work for an incredible organization.

Now with all that being said, here is the visible proof of the pain and ordeal I have gone through... ahhh, yes, the pictures of those God awful blisters:







JUST GIVING YOU MORE SPACE JUST IN CASE YOU CHANGE YOUR MIND












OKAY, IF YOU ARE SURE....












THEN, HERE THEY ARE...







YES, HERE THEY ARE, AS PROMISED:

This first picture, you can see the very large (almost fake looking) blister at the base of my toes.

A closer look offers a different perspective on how big this blister truly is. There is a gauze pad stuck to my skin below it.

This one is a little better with some flash action

Blurry, but still a different view


You can see my second blister down in the bottom left. Both really big blisters right? Have you ever saw blisters this large before? Didn't think so.
An attractive shot to show you the discoloration of my skin post blister explosions. At least I was nice enough to not show you the yellow gue, right? I washed it off before I took this pic, common courtesy folks.

As you can see the once large and mighty blister at the top is now just a sunken layer of dead skin.

This picture is a bit washed out by the sun, but you can see my skin is almost black near my big toe.

Here you can see just how raw my skin is after part of the blister's skin is now gone. That red section above is a PAINFULL area, even if air hits it wrong, I'm screaming!

Just a closer view of the burst blister. And that's just a towel my foot is sitting on -- no reason to be alarmed!

A closer view of that painful red, raw, and exposed skin from the blister.

So there you have it folks, you can now see almost first hand of the ugliness I've had to deal with over the past few weeks. This is something I've been dealing with since early August actually. Then, it just looked like a larger than normal zit, but unfortunately it grew, to the point of being a Lymphomatoid Papulosis spot. Since I've had this condition from 11 years of age, I was not alarmed... but then it kept growing. Things got scary when it opened up and just never showed any sign of healing. The local doctors in Wallowa County hadn't ever seen anything like it. Finally, with my urging, I got into OHSU, where there was a doctor who knew what it was... Dr. Eric Simpson. Probably one of the brightest guys in the state of Oregon, and a darn good dermatologist, too. He had enough common sense to take a biopsy of it for the first time. Something that didn't happen in Wallowa County (but should have). Just days later, the biopsy that Dr. Simpson took, revealed tissue of Lymphoma. From there, I saw Dr. Craig Okada, another brilliant mind in Oncology who recommended radiation. Then I saw Dr. Marquez, who put me on the stint of radiation (which worked like it was supposed to), until about 20 treatments, and went south. Things got ugly... and finally Dr. Holland stepped in. We got pain under control and stopped the excessive radiation. Now that I'm bouncing back, I am questioning what all this ridiculous extra radiation was for, and why my body's reaction to it was more or less ignored -- even after my repeated complaints. Thankfully Dr. Holland took me seriously and I'm here today telling you yet another tale of LB. So what happens next? Well I'm going to get to the bottom of the mistake that was made, and will save it for future blog entries in the coming weeks. Also, I'll let you in on my return to work and tell you just how much I love my job, friends, and family, and perhaps in the not so distant future... life in general.

-LB

Thursday, November 15, 2007

A Setback

Just when I thought things were looking up, things took a turn for the worst. I woke up Monday morning with one very swollen leg. I have no clue how it started, and the docs and I are still trying to figure it out. Tuesday I got through most of the day without a hitch, but the swelling was getting worse, and signs of it showing up in my left leg. I saw the docs at OHSU on Tuesday evening after my treatment, and they talked about putting me on medication, but due to it's severity on the kidneys they opted to just caution me to keep my legs up overnight. There was no relief by Wednesday morning as I hobbled around work. I felt nauseous and decided to go home after lunch. Kept my legs up in my recliner all afternoon and didn't see much result. Went to treatment Wednesday night and they paged my doctor almost immediately when they saw my swollen legs. My doctor suggested we take a blood test first thing on Thursday (today) before my treatment. After putting my feet up for several hours last night, I finally noticed some relief, and when I woke up this morning to my surprise a lot of the swelling had gone away. Out of caution and request of the doctors, I took today off from work. Even though the swelling has gone down considerably, I am keeping optimistic that it's on it's way out. I am still obviously going to get the blood lab to find out for sure what is going on. I hope that it is just a reaction to all the radiation. My doctor said it's very possible, but kind of unusual for both legs to swell like that. I am just glad to have some of my mobility back, but my foot hurts really bad now that the radiation has taken hold. If all my swelling goes away, then I will be fine if that is the only complaint I have. The other possibilities could obviously be kidneys and liver problems causing this kind of swelling... naturally I am keeping my fingers crossed it is not. Thanks to everyone praying and thinking of me at this time. I'm doing my best to take care of myself.

-LB

Sunday, November 11, 2007

The Verdict Is In: I Love My New Job!

You find out what you are supposed to do each day, and a person figures out how to do most of those things. You feel like you belong. You have a sense that you generally know what you're doing. People tell you that you're doing a good job.




(My desk - note the Oregon State logo in the bottom left)

(A closer view)

These are the events that are making me love this job. I'm going to go out on a limb and tell you that I think my coworkers love having me in this office as much as I like being there! I am starting to feel like I'm fitting in. One lady (one of many employees) has been there for over thirty years, told me "you're going to love it here, it's just like a family." I knew at this point I had made the right decision. It is definitely confirmed at this point that I've landed in the right place. They are keeping me more busy now as well, people are finally discovering that I'm the new technology coordinator. It's a good feeling.

(I frequent the nearby Subway at the Capitol with friends Michele and Virginia, who took a pic of me feeding my face as I only have a half hour lunch break while I'm going through radiation treatments -- this allows me to leave work early in time to make it to OHSU)

(There's one of the guilty party - Michele, who has been known to mess around with my cell phone at lunch time! BELOW: Our insane server room at ODOT)

I am also starting to make some new friends with some pretty cool people. One guy, Jonathan Stephens I got to know pretty well in the past couple of weeks... I guess as well as you can get to know someone in two weeks. He works in the GIS unit (where my cubicle is), and this guy loves maps. That is a good thing, because it means he likes his job too. I look forward to getting to know him even better in the coming weeks and months. I also got to know Laura, Robin, and a few others a little better in the past couple of weeks as well.

A fellow by the name of Ryan Johnson, was a senior when I was a freshman at Joseph High School... he is literally feet away from me in the same office. To have two guys from Joseph working in the same office in Salem is just strange! Anyhow, I didn't know him hardly at all when we lived in Joseph, but I'm getting to know him better now too.

(view of my desk from where I sit in the GIS unit, notice the maps all over)

This weekend my folks came down and we had a delicious dinner at McGrath's... which is probably my favorite seafood place in Salem now. We also hung out and watched a few movies this weekend and they left this morning. Unfortunately my mother had a dentist appointment scheduled for Monday, so they had to leave today. Oh well, in just another week I'll be home for Thanksgiving.

By the way, Monday is the observed Veteran's Day... it's a HUGE mark in history for me -- it is the first ever paid day off that I have ever had in my life. Don't you worry, I'm going to enjoy it immensely!

(ODOT server room)

Another thing I'm enjoying about the Mill Creek ODOT office is the internal "war" between Duck and Beaver fans. Yours truly has always been a Beaver, and to my good fortune, Ducks are outnumbered in this office... including Ryan Johnson.

(Laura's Oregon floor mat, that I like wiping my really muddy feet on)










(blurry picture of Ryan Johnson and his Duck paraphernalia)

(Laura has a U of O blanket on her chair)

(Laura's baby -- who is no longer with us, was also a Duck fan)

So I've met a lot of new people down here in Salem, but oddly enough, I wouldn't mind seeing more of my Joseph friends once in a while. I've been going up to Portland everyday for radiation and it has been making me extremely tired... but one of these times hopefully I'll get to see Dylan, Thane, Jay and Ellie. Which by the way... radiation is just about to wrap up in a week and a half. I should be completely done the Wednesday before Thanksgiving. They were going to finish me before that, but since my skin has been holding up so well (in other words not falling off), they are going to nuke the living crap out of me apparently? I guess it's worth it as long as this version of cancer doesn't come back!

(my view from the doc's office when I have radiation checkups... you can see the new condos going up on Portland's waterfront)

(Parents new F-350 Ford pickup they just bought a couple weekends ago while they were down visiting me... this pickup has power everything, a navagation system, 6 disc/mp3 player, ipod hookup, usb ports in the console, electric rear window, sunroof, you name it, it has it).

(My old man walking by the new pickup)

It's funny how life works. I was just thinking this week on how things worked out. There could have been a pretty good chance of me staying in Wallowa County. As many of you don't know, I applied for a job at the Education Service District... a job I was overqualified for. I didn't so much as even receive a phone call from them (don't know why except it could have been someone internally responsible and small town BS); then low and behold a couple of weeks later the state of Oregon is interviewing me. I now know why I didn't get the ESD job in Wallowa County... and am thankful that I didn't because a much better opportunity came along, fate or not, some things work out the way they are supposed to.

-LB

Top Ten for Week of November 10, 2007

1. Jonathan Stephens
2. Robin Ness
3. Michele Sawin
4. Virginia Sawin
5. Laura Strauch
6. Debbie Bobbitt
7. Carl Bobbitt
8. Christian Ambroson
9. Sterling Shetler
10.Tim Dunn

Saturday, November 03, 2007

My Foot: Before & After - WARNING: Graphic!

WARNING: The pictures below are graphic. So if you are the faint of heart, DO NOT LOOK!

I know the docs have pictures of my foot from a while back when it was a pussy hole all puffed up and totally disgusting looking. Unfortunately, the pictures I have weren't taken until after the treatments started. Below is a picture after a couple of radiation treatments, and then a picture after nine treatments (taken tonight). Even the first picture is about a hundred times better than what my foot originally looked like! But even with these two there is a comparison and you can definitely see healing starting to take place (which hasn't happened until now during this entire ordeal).

Again, this is graphic, so if you're not into that sort of thing, don't say I didn't warn you!



My Foot after a couple radiation treatments:

My Foot after 9 radiation treatments:

So Tired, So Sleepy

This radiation is kicking my butt! I am so damn tired it's not even funny. Several times this past week I caught myself beginning to fall asleep at my first week on the new job. Fortunately, I was able to pull out of the daze just in time, but I had some close calls nevertheless. My goal this weekend was to do just that, sleep. I spent most of Saturday sleeping. My friend Thane came down to hang out Friday night and Saturday and left this afternoon. As soon as he left, began my sleeping marathon. I woke up this evening still tired. It seems no matter how much I've been sleeping, I am still tired. Some people can usually attest to that feeling. This is a different kind of tired though, I'd almost call it chronic. What is weird is that I just spend a couple a minutes a day under this radiation gun and immediately it somehow drains my energy. It's weird! Fortunately, I only have eight more treatments, ten at the most. I am excited, because right after that I'll have a three day weekend to recoup! That's right folks, as a government employee I will get Veteran's Day off. Additionally, we have an extra hour this weekend because of the time change and I'm totally stoked about having that extra time for you guessed it: SLEEP. Who knew I would love sleep this much? I look forward to getting my regular life back, which isn't far off. I might even utilize the fitness center here at my apartment when my foot heals up. Energy is going to be a great thing!

Plus, the sore on my foot has gotten much, much better according to my friends and docs. I can't tell because I look at it everyday, but that is what I'm told.

If it feels like I haven't been in much contact with anyone, it's because I'm tired. I'm very sleepy. Soon the hours of sleep will wake to a new life in which I will have enough energy to realize what a great change I have made.

-LB

PHOTOS