Thursday, September 1, 2011

Back in the saddle again...

Or should I say back on the cold metal table again? Either way, my throat feels back to 100% after taking last week off. I started radiation again on Monday and so far, so good, although the doctor warned me today that my throat may get sore one last time before we're done. As of now I only have 3 more treatments and I'll be good to go! I am so excited. Today I had the tech take pictures so all of you (my loyal friends and family!) can see in pictures what I have tried to describe in words.

This first picture gives a pretty broad perspective of the room. My feet are in a large rubberband to help prevent me from moving and I am in a hospital gown because I am undressed from the waist up. A light comes out of the piece of machinery above me that they use to line up with my tattoos. Yes, I am the proud owner of two new tattoos. They are small and located in the middle of my chest.

Once I am lined up the tech leaves the room and a bunch of clicking and zapping occurs. The machinery rotates around the table a couple of times as the treatment is given.

As I've described with such endearing and affectionate terms before...here is an upclose and personal shot of The Mask. Although it may look soft and pliable it is in fact solid plastic. Once I am lined up and in place, they use the bindings on the sides of my head to lock me into place. This is me in my "happy place" or atleast that's what I tell myself.


So, as I said before, only 3 more times of this lovely gig and I'm done. The Mask will be mine when I am finished and I'm debating whether I should keep it or crush it to pieces! :)









Wednesday, August 24, 2011

Radiation

I began to experience slight discomfort in my throat at the end of last week but knew it was something I could manage. As I went into the weekend the discomfort began to increase when I tried to swallow and by Sunday afternoon I had reached my limit. The liquid Vicodin I was taking didn't touch the pain so Monday morning I called the doctors office. In the back of my mind I knew what the suggestion would be but I tried to convince myself that there may be other possibilities. Painful swallowing? Yes. Blood in sputum? Yes. Choking on spit? Yes. These answers guided me to postponing this weeks treatments and I had a meltdown. I want to be done with all of this. Cross the finish line and never look back. I was given a prescription for Percocet and sent home to crush the pills and do my best to manage the pain. This was not in my plans, it postpones my finish line. After crying harder than I've cried since this journey began, I felt better. The irrational thoughts I was thinking began to fade and I knew I'd be okay. Just another little bump in the road that I can and will handle. The medication has taken the edge off and I'm anticipating being able to go back in for radiation treatments next week. In the meantime, I am focusing on accepting the fact that I don't write all of the rules and control all of the plans. On Sunday in church the pastor said something that has stuck with me, "The difference between hope and despair is faith.". I continue to have faith that I'm right where I'm supposed to be.

Saturday, August 20, 2011

Graeagle is...

...spending time with the newest member of the family...

...having my aunt play the "C" card on my behalf...

...using the Star Walk app at 5000'...

...golf for all ages...

...learning to ride a bike...

...wagon rides...

...passing out in the hammock...

...Sudoku and crossword puzzles...

...perfecting your ladder golf toss...

...being surrounded by mountains...

...celebrating birthdays and the sweet, sweet music of Taylor Swift...

...enjoying sunrises from the mountain top...

...having my Grandpa wear my wig...

...seeing a bear!...

...nature walks with my aunt...

...sister time at the river...

...an afternoon treat at Frostee...

...the gift of a lifetime...





Monday, August 15, 2011

My Grandma

I know that most of you are waiting to hear about my trip to Graeagle and how the start of radiation has gone but the thing that is on my mind right now is my Grandma. My cannonball Grandma, Grandma Joan. Two years ago today she passed away and boy do I miss her. My Grandma and I had alot of things in common, that's not something every granddaughter can say. The sun, Graeagle, "luck", laughing and cannonballs to name a few. She loved to photograph barns, cows and landscape. She learned to paint in her later years - flowers, scenery and us grandkids. She taught me to drive a stick (although she wasn't a very good teacher because I was the only grandkid to FAIL Grandpa's test). I miss her Bugs Bunny face and her laugh that turned into a squeal and then a warning that she may wet her pants! I love how competitive she was..."Whack-A-Mole", golf, Sudoku, hula-hooping...nothing stood between her and a win! I love how she addressed my cards Jen(nifer). I love how I have a voicemail of her saying, "Don't forget the buttwiper.". I love how when I would mention I had lost or misplaced something she would say a prayer over the phone to St. Anthony and anxiously wait for me to report I had found it. I'm sure having to hear of my cancer diagnosis would have crushed her but in the same moment she would have provided comfort. Comfort only a Grandma can. I love you Grandma.

The thing that amazes me is that all of these pictures were taken just a week before she died. So inspiring...








Saturday, July 30, 2011

Disconnecting to Re-Connect

Well, my day has arrived. I leave for Graeagle in just a few hours and I can't wait! I'll be taking a break from the electronic world so I can focus on quality time with my family and quiet time to myself. I will be sure to take tons of pictures to share when I get back. Graeagle, here I come!!!


Saturday, July 23, 2011

Good News (The Details)

So Wednesday brought about two appointments. One for my PET scan and one for my radiation simulation. I was scheduled to have them at separate times but when I was getting my I.V. for the PET scan done the tech said they could coordinate both tests so I wouldn't have to come back in the afternoon. I was very appreciative of her efforts (atleast before I knew what was coming!). Just like my last PET scan I was left in a dimly lit, quiet room for about 45 minutes while the radiotracer circulated through my body. When my time was up another tech led me to the familiar room and I hopped up on the table, a little anxious to get things done and at the same time at ease because I knew what was to come (or so I thought). I knew things may be a little more complicated when they but a giant rubber band around my feet so the chance of my legs moving was reduced. Last time they trusted me not to move, this time, not so much. After a few minutes I knew why. With my legs banded together and my arms firmly at my sides they proceeded to maneuver my head into a hard plastic brace so that my chin was pointed high into the sky and my neck was extended. Ok. This was manageable, not comfortable, but manageable. With not much warning other than, "Don't move! We're going to place a mold over your face that will go from a liquid to solid state. Just relax.". Uh, what? Before I could ask a question that's exactly what they did. A piece of what appeared to be pantyhose/drywall form dipped in warm white silly putty was placed over my face, from the top of my head down past my chin. Manageable. The edges of this contraption were metal and were promptly clamped down on each side of my head, near my ears. Ummmm, manageable? They were kind enough to "pinch" the spots over each eyelid - this would come in handy for me about 15 minutes later. As they were giving me the final instructions on how important it was that I not move I felt a wave of panic and flung my arm out (wanting to test whether I could break free if necessary!) and proceeded to hit the male tech just close enough to his "family jewels" to make him scream, "Whoa! Hey now!". Sorry dude. You just bungeed my legs together, put a contraption over my face that I can't move and you're getting ready to leave the room so you can slide me into a tube. You're lucky I didn't have better aim! I knew I would need to relax if I was going to live. Seriously my heart rate was high and the test was just beginning. Click, click. Into the tube I went. I could open my eyes but couldn't see anything. Panic. I hear Whitney Houston singing, "OOHhhh I wanna dance with somebody...". I can relax to that. In and out of the tube I went all the while the contraption on my face is beginning to take shape. I have moments of panic and moments of bliss. More songs are played and just when I think I can't take anymore I hear the door open and the tech says, "Just 10 more minutes and I can take the mask off. You ok?". Dude, I can't talk. Remember? I let out a grunt. He interprets that as a "yes" and leaves the room. 10 minutes means 3 more songs. I can do this. I try to put myself to sleep. It doesn't work but I try. He finally comes in again (mind you this has been a good 30 minutes from when we started) and I am so relieved to feel him undoing the clamps. He says it is crucial that I not move because the scan is not over but that I can talk if I want. He lifts the mask off and without thinking or hesitation I say, "That is the shittiest thing ever!". He apologizes and leaves the room so the scan can be finished. When I got out to my car I realized I had my camera and snapped this picture trying to show how much pressure was on my face while the mold was setting. This is about 20 minutes after we are done.

I met with Dr. K2 yesterday to go over my bloodwork and PET scan. The results are good. The larger of the masses has shrunk down considerably and he feels that the remaining spots are mostly scar tissue. The results are consistent with what a post chemo Hodgkin's patient would have. He was pleased and so was I. I will be receiving 3 weeks of radiation at an average dose (24 for 5 minutes) and getting another PET scan the second week in October. In the meantime I will get my port flushed (I hate going in the chemo room but it's only for about 10 minutes) every 6 weeks and work on getting back into shape so that my lungs will heal up faster. After I see Dr. K2 in October I am hoping to get clearance to have surgery to remove my port. All around good news. I'm not completely in the clear yet but yesterday was a big day and I am relieved to be moving in the right direction.

My ears continue to bother me so I am trying over the counter medication and hoping they clear up fast although Dr. K2 says it may be a couple months. I also received the o.k. to have my teeth cleaned - I'm hoping this week! And in case you're wondering, the mask that was created will be worn by me every radiation treatment. I'm hoping now that it's in a solid state it won't be so bad. I'll let you know!

I am so thankful for the calls, texts and emails checking up on me. I am blessed beyond words. Please continue to pray that my body continues to heal. Please also pray for my friends and their families who continue to fight their own battles against this horrific disease. Thank you.

"I am not skilled to understand what God hath willed, what God hath planned. I only know at His right hand stands one who is my Savior." - Dorothy Greenwell 1873

Friday, July 22, 2011

Good News

I know some of you have been waiting to find out how my appointment with my oncologist went and I will write more tomorrow but in short, it was good news! The remaining spots have gone done in size that is consistant with post chemo Hodgkin's. I will be doing 3 weeks of radiation beginning the second week in August. I will fill you in on the PET scan, radiation simulation (yikes!) and today's appointment sometime tomorrow. For now, it's lights out! Thank you for the continued prayers, they are working.