All posts by Tom Bird

Week three update:

Well three weeks ago I had this lump cut out of my head. Friday was not the best of news as to what it was. The weekend was one of the worst two days I have ever had. But today I am feeling pretty good. Physically I feel great. Just a little lingering wobbliness from the vertigo episode. Really looking forward to that eventually going away. It has been nice these last two days to have activities to distract and keep me occupied. Jessie went into work and left me alone for a few hours yesterday and today. It is weird to be alone since I have had someone by my side almost continually since the operation. Yesterday I did a light workout on the bike trainer. Road for an hour and an easy pace while I watched the Ken Burns documentary Cancer, The Emperor of All Miladies. Today I decided to walk as my ass is a little sore from the bike seat. I figure I will alternate between the trainer and a fast walk. Went 2.5 miles and was out for 45 mins or so. After that I puttered in the yard a bit. It looks fantastic thinks to the help from my sister Dianna and Jessie’s Uncle Don and Aunt Bobbi doing so much work. While eating lunch I received a call from my case nurse at Cigna. Her background was working with Neruo Tumors. She was very positive and has really helped perk me up a bit. She also reiterated most of the information you see on the internet is very old 10+ years so it is hardly applicable anymore. Plus she said me being active is a huge boon to treatment and recovery. Just gotta keep that mentality going!. My scar is looking good. Jessie said 6 or 7 stitches have already dissolved. Since people have been asking and are curious I will post a picture.
 
Also, I have to give a shout out to Frank for putting me on to my Ugg Slippers. I love wearing slippers all day. When I go back to work I may have to ask if they can be added to the dress code. You just feel good wearing slippers all day. Plus I can go outside and not worry about them. Heck I forgot I had them on last Thursday and wore them to dinner.
 
And I want to reiterate what Jessie said before. All the visitors have been great. I feel so lucky to have such great friends and family.
 
Oncology visit is tomorrow – will update with new news once we have it – I am expecting GOOD news from now on. My plan is business as normal ASAP.
Scar HydrangiaOh and adding a picture of my favorite Hydrangea in the yard. I just looks so good right now.

And now for the Debbie Downer news….

We had our two week follow-up with the Neuro Doctor.  While he is very pleased with my progress from the surgery the results from the tumor are not good.  They have classified it something much worse than we originally thought.  What really sucks is to have everything going so well we were positive the news today would be better than we expected.  Now that they are worse it is like a punch in the gut.  There is nothing positive about this thing they pulled from my head other than it was removed before it was causing me any serious issues.  That is the only good news so far.  The treatment will be the same as what they originally thought it was so Radiation and Chemo here I come.

The one good thing is I can start some light exercise so get on my trainer.  I am still not supposed to lift anything greater than 15 lbs but at least I can get my heart rate up.  He said in 4 more weeks I should be able to do normal activity and all the stitches should be dissolved by then.

Everyone has been so great so far with both Jessie and I thought this and we really appreciate it.  Going forward we will really need that love and support even more.  We have a tough road ahead.  The plan is to become the outlier and prove all the statistics wrong.  My goal is to look at this 20 years from now and say what was the big deal….

Oh and the Meal Train is AWESOME!

First the food has been great.  One less thing for us to stress (well Jessie really) about.  She is the one that needs our support.  I just get to lay around and heal and read and eat and read and heal some more.

While the food has been fantastic, seeing everyone each night is something I really look forward to.  It is very positive and uplifting as we go through this.

Probably starting chemo and radiation next week – we see oncologist Wednesday.

Time to research all those cancer fighting foods!!!

Humbled by this experience

Every day I am amazed at the generosity of my friends and family.  I have no idea how I would have gotten through this without such awesome support.  I got my call today regarding my oncology visit.  Unfortunately the girl was just a scheduler and could not tell me anything.  I am scheduled with the head of the department so he should be well versed in treating and should be up on the latest and greatest treatments.  Dr Edward A. Neuwelt

My followup with the surgery group is next Friday.  Not sure what they are planning to discuss.

Tomorrow I will have been home a week. I have been so lucky to have my big sister Dianna here to help out.  I would have been going crazy just sitting around.  Not sure how I am going to last the next couple of weeks.  My ass is tired of sitting down.  You can only read so much.  Glad the pain meds are dwindling.

I cannot wait to go to the gym.  The hardest thing is to try and stay somewhat healthy when you cannot lift or pull/push anything greater than 15 lbs.  And all the amazing food everyone is bringing does not make it easy to keep the weight down.

And thanks everyone the food has been a fantastic gift and has been so good.  I look forward to the visits every day.

Physically I feel like I can go get on my bike or go for a hike but every once in a while a cough or bending over reminds me that some serious work was done not too long ago.

One week ago

One week ago i was waiting to go into surgery. They told me you will not remember any of this. Well they were wrong. I remember all the presurgery checkout. One of the funny things is you are in a large room with 4 other beds and a sheet for privacy. All you can see is peoples feet. And their shoes. My surgical nurse needs new shoes. They were pretty ratty. To me they were filthy and not something you should wear into surgery. I wanted clean fresh shoes. That tells me you have an eye for detail and are clean.

Getting wheeled into the operating room. They could not get the table to move up and down.  The anesthetist did not want to knock me out until they got the table fixed as it would be easier to move me if I was still wake. Eventually someone realized it was not plugged in. I yelled out reboot it. And they got a kick out of the patient telling the operating room staff how to fix their problem. 

On the way to the operating room i was freezing. I chatted with one of my anesthesiologists about biking. Mtn vs road and about Cyclocross racing. He had heard of cyclocross but never been to a race nor was he interested in trying it.

I don’t remember any of the surgery just everything leading up to it. I remember bits and pieces from the recovery room.

They also said put me in feet first as the room was very small and I had to scooch over on to the surgery.bed. My nurse screwed up and put me in head first and they gave him a bunch of crap about which side my feet were on. (they were the bits with the socks on)  The surgical bed s cold and uninviting. All stainless seel, narrow, had a little air pillow for my head. Straps to hold me in place just in case I try to roll out of bed i even remember what looked like a mesh drain.

I was also shivering uncontrollably. Not sure it it was nerves or just feeling cold.

To this day I am amazed how fully functional I am. All of the “stuff” we read and expected did not really come true. That makes me optimistic about future as everyone is so different and react differently than others. If I did this well with the first surgery how will I react to everything else?  I hope just as well.

Glad to be home.

What does Dorothy say, “There is no place like home” I agree. While everyone was wonderful at OHSU it was not where I wanted to be. When you have to go somewhere. It is never as fun as the place you choose to go to.

While I finally pooped and was allowed to go home. Great news. We saw on the release papers something that we were not too happy about. They still think my tumor was an Oligodendroglioma. They think it is a stage III Anaplastic version that is a bit more aggressive than the typical run of the mill Oligo.

They are still waiting on the genetic testing to determine the treatment plan so fingers crossed it is the type that is more susceptible to certain types of Chemo and Radiation therapies.

So not out of the woods yet. Still a long road ahead and this was just the start. So glad we did not take the wait and see approach. And again everyone is different and might not have the same situation we are in. So what may work for us may not work for others.

Time to study up on my chemo treatments.

I should be in the maternity ward

Trying to give birth to my food baby. Have walked the halls, having contractions, it is kicking like mad. When you ingest a bunch of food and all the tools to move it along and things are just bound up the cramps are horrible. Done all the recommended treatments but to no avail. Stubborn food baby. At least I know it is mine. Good god this sucks. I can go home if I just drop a duce. A bouncing food baby.