Tuesday, December 4, 2007

OHSU Appt

Sorry this may be a little jumbled or fuzzy...it's been an extremely long day. If you have any other specific questions, please feel free to email me @ toryccarnahan@gmail.com or tccarnahan@yahoo.com

Today we had dad's much anticipated appointment. Dad had his radiation "simulation" first. He was tattooed. Yep, really marked permanently. Hopefully, Aaron can fancy the plain boring dots up a bit, eventually. He was injected w/a dye & was put in a Cat Scan machine thing & was fitted for his "cast." The "cast" (I truly have no idea what it's called) and dots are so for every radiation treatment, the beams go in the exact same spot so the Drs. can zap the tumor good.

After he went through that process (an hour), we met w/Dr. Hung (the radiation expert that will be treating dad). He informed us that after much deliberation w/his peers at MD Anderson, he felt that chemo would be the most positive place to start. He said that if he was in dad's position, it's what he would do. There were obviously many things to think about w/treating w/chemo before radiation. The obvious side effects of chemo as well as putting off the radiation treatment & risking the tumor increasing in size, or spreading. Dr. Hung said that there is a large chance that chemo won't work, but the 25% chance that it does work would make radiation that much more effective. He said that there may be a chance chemo doesn't work (obviously a 75% chance), but radiation will work -there is no doubt, but it's a matter of how much radiation can zap the tumor...the point with chemo is to throw everything at this cancer before starting the radiation.

Armed w/that info & Dr. Hung's recommendation (he's a great Dr. w/an incredible bedside manner, by the way), we headed down to see Dr. Ryan (the chemo expert). Some of us took the tram...others wussed out & drove down to the waterfront because the tram was too scary. Not naming any names...you know who you are. :)

When we met w/Dr. Ryan he was pretty bleak (or should I say that he was just blatantly honest & told us things we have all read & heard before). He reiterated all the negatives, rather than focusing on the positive chances & the positive things the chemo could do for dad. He was very honest (which is definitely a plus - there will be absolutely no surprises when treatment begins), & obviously chemo is VERY rough on your body. It's meant to kill the cancer cells & any possible "micro" cells that are floating around & haven't visibly appeared.

Long story short....dad starts chemo either Thursday or Friday. He will be hospitalized for 3 days (most chemo treatments are administered as out-patient, but nothing but the most intense for dad) for the type of chemo they are administering. He will have his first treatment up at OHSU & depending on how his body reacts to it, the remainder of them may be at the Salem Hospital. He will have treatment for 3 days, go home for 3 weeks & then have another treatment for 3 days. In another 3 weeks, they will run tests to see if the chemo is working (blood tests - these will also be given weekly, especially after dad's transfusions & scans). If it is working, they will continue with this regimen for another 3 sessions, I believe (3 days on, 3 weeks off). After that, they will start the radiation. If the chemo isn't working after the first 2 sessions, they will start w/radiation at that point. The radiation (in either circumstance) will be for 7 weeks. Monday thru Friday for 15 minutes. Where the radiation is (it'll be in the sacrum/back & pelvis), there shouldn't be any severe side effects - which will be so nice for dad!

We did find out today that angio sarcoma is rare...which we already knew...cases exactly like dad's - there has only been 1 recorded & it was in Japan. The Drs. did say that dad's case would probably be published in medical journals...that's how rare it truly is. There are no numbers & chances they can give us because they've never come across it.

Only our dad/husband/friend/mentor/brother/son/etc. would be diagnosed with this. &, more importantly, he's going to beat this! It's going to be a very long tough road for all of us. Remember that none of us are in this alone. We thank all of you for the offers to help out in any way - around the house, grocery shopping, tv watching, cooking us meals, etc. As well as the cards you are constantly sending dad and mom...it definitely is the highlight of their day. Mom & dad have them displayed on their mantle. The words of encouragement, support, & love are vital to both of our parents. We all thank you and are very thankful you are in this amazing support system we have.

7 comments:

Anonymous said...

The doctors are really persuing this aggressively - It goes to show you how strong your dad is. I'll be praying the Chemo works and that the doctors will be wise.

Anonymous said...

I really appreciate the update. It is important that we all get behind Ron in the next few months. There are many, many people thinking positive thoughts! Ron, you will have plenty of support from us all. You are certainly able to meet the challenge!!

Jon

Bruce & Becky said...

Tory thanks for the blog and all your work keeping everyone updated. Ron, our positive thoughts and tons of prayers are with you for success with the treatments. We expect to see you on your bike in Eastern Oregon next summer! Live Strong!

John said...

Hang in there, Ron. The scummies are pullin' for ya!

Anonymous said...

My Dear Ronaldo,

So you got bored of retirement and decided to tackle some health care issues. If you're going to visit OHSU, make sure you leave the doctors smarter than when you found them. After all, they're not used car salesmen, you know.
Now...GET WELL SOON. Remember, you promised Betsy and I a trip to Black Butte at your beautiful Aspen Cabin.

Anonymous said...

Careys, You all sound as if you're heading at this challenge straight on and full speed...way to go! I'm in Salem once a week (sometimes more) and would love to help with yard care, shopping, food preparation (I'm actually a pretty decent chef) or anything that would lighten the load a tiny bit. We all love you guys and want to be everything we can be for you. Go RON!!! The old Slugs are with you.

Anonymous said...

Is this CAREY family amazing or what? Tiffany was great at keeping me informed and this blog site is awesome, Tory. I needed this as we head into the chemo stage. Every day I was thinking "How is Ron". I stopped by and talked to Betty yesterday. SLUG it out Ron. We are all praying for you and there are so many positive thoughts headed your way.