Treatment is OVER

Good Morning!  I am glad to say that my life has gotten back to being busy... and fairly normal.  I finished radiation last Friday and it was a wonderful feeling to walk out of those doors knowing that I didn't need to come back.  No more afternoon drives to Dallas!  I won't be going back until March 5 for a visit with my oncologist.

I am feeling great.  My hair is growing back, slowly but surely.  I'm not quite to the point of going hat-less but I'm getting closer every day.  I don't know if that's because I actually have an adequate amount of hair or I'm just really tired of my hats.  I went back to the gym for a spin class on Saturday and that felt great... although it was much harder than the last time I did it in October.  That was another step in getting back into my old routine.

I'm up this morning getting ready for a Tuesday with second graders, getting ready to pack lunches & wake Zach up... and happy to be doing it.  Life is good.

Updates

I know it's been a little while since we've written anything.  The days have gone by so quickly.  I have eight more radiation sessions to go... yes, I'm counting down.  My treatment was cancelled one day last week because the machine was down and again today because the roads getting to the hospital were icy.  Now, my last day will be Friday, Feb. 6!

Radiation is going well.  I haven't had any burns yet, but my radiation oncologist told me that those may start this week and get worse as we near the end of treatment.  I've got some lotion that they have prescribed to help with that.  I've definitely had some fatigue, but it seems that once I make it past the middle of the week I'm okay.  I've also noticed in the last couple of days that I'm starting to lose my eyebrows & eyelashes.  Strange timing, they are falling out just as the hair on my head is beginning to grow.  I met a girl yesterday who had chemo & rad on the same schedule as me and she's noticing the same thing.   It will be interesting to see how much disappears.  Every day is a new day!

Mom & Zach went to the oncologist with me last Friday.  I wanted Zach to be able to see where I've been going... he decided that he liked the fish tank there best of all.  It was kind of fun to actually take the time to stop and look at the fish with him, I've walked right by it many many times.  We took him for a nice lunch and a stop at the mall for some new shoes.  I think he had a really good day.  My oncologist said that everything looked great that day.  He'll schedule a scan in two months to check treatment progress.  His plan is to run a scan every 3 months after that and do a physical check of my lymph nodes every 6 weeks... for the next 2 years!  

Thanks for continuing to check in on us - God Bless each of you!

Whew!

I've finished my first week of school and radiation and last night I finally realized that I am tired! I laid on the couch and fell into a sleepy stupor after we got the boys to bed. I think Michael and I had some sort of conversation as he was trying to convince me to get up and go to bed... but I don't remember a word of it!

I am actually really happy to have a reason to be this tired again. My anti-nausea meds would make me ridiculously tired too, but this is much better! :) My week at school was wonderful. My long-term sub., Sarah, came in a lot to help me out and take over when I needed to sit. She's a gem and I appreciate her so much. Everybody at school has also been so supportive and I continue to see that they are taking care of me. I LOVE being back there.

Radiation is weird. It's hard to find another word to describe it. One thing I do enjoy is that since we all basically have the same appointment times every day so I have seen the same people in the waiting room. We actually sit and talk while we're waiting, more time to get to know each other than when we would pass & smile in the hallways. Sharon & Rosalyn, I'll see you on Monday for our daily zap! The radiation itself is not at all what I expected. It's a lot like an x-ray machine that rotates around the table. No laser beams, no heat, just some clicking & buzzing. The longest part of the process is getting me lined up & in the right place. The actual radiation (once the techs leave the room to run the machine) takes about 5 minutes. The drive to Dallas is the hardest part. But, I enjoyed that this week too. My brother drove me on Thursday & Friday so we had some time to visit. I don't know the last time that just the two of us had almost 3 hours of uninterrupted talking. I don't know that he enjoyed it as much... he was driving! I just got to sit & enjoy the ride.

One more time, I have to say that I'm so thankful for everyone who has been praying for us & helping us! We continue to have people sending prayers, cards, money, meals... the list goes on and on. We love you all and we are happy to share this road to recovery with you!