Skip to main content

Radiation Week 7

Episode LXIV: It burned like fire, this burning desire


It was suppose to be my last week. With last week's weather causing me to miss an appointment, I was going to have to wait until Monday for my final radiation treatment. I really wanted Friday to be my last treatment day. However, I still was so close... so very close... to being finished with radiation.


week 7 & 34 zaps down...


I was definitely feeling rough. I was tired. The fatigue was truly exhausting. Any time I could fall asleep I did. I was finally understanding the point of taking an afternoon siesta... and I really needed one.


Now that I was only receiving booster radiation I was suppose to get a "break" from all over treatment. That my skin would hopefully be able to heal in areas that did not get exposure. Even with that break, I was feeling the radiation burn. My entire chest area was ranging in colors.


My skin was fried, peeling, & all round irritated!


Some of my skin was drying out quickly too. That caused a new set of problems, but I tried hard to keep my skin covered in lotion. Plus, the levels at which my skin peeled ranged from barely to oh-my-gosh-a-lot. I was grateful that I got a small sense of relief after my skin finally did peel some. The new skin was sensitive, but less painful. The Repara gauze strips caused my skin to peel faster and it would fall off without pain. I really wish I had started using Repara sooner. (See my Radiation tips) Much sooner!

Even with the skin problems I refused to stop doing things. Often I wondered why I continued to do things when it caused me great discomfort. Overall, I just refused to stop living... to stop continuing on with my life. I want to continue doing things I would normally do... sometimes, I would just do them for less amounts of time or with less energy!!!


The family about to go on a nature walk!

In my head...


I wished I was finished, but I was glad to be almost done. It was so close!!!

The past few weeks of treatment have really pushed me to fight through the side effects. I think the toll of the many treatments (chemo, surgery, radiation, etc) was probably the biggest cause of my extreme fatigue. The radiation was still eating away at my skin and chest. However, the main focus has been my desire to keep up with two very active kids... I am still trying to keep up!

Now, all I can think of was that I had 1 more treatment. 1 more treatment! 1 more treatment!


“Even the darkest night will end and the sun will rise.” 
- Victor Hugo, Les Misérables


Episode Reference: Still haven't found what I am looking for, U2 song

Comments

Popular posts from this blog

my longest hardest day yet

Get ready boys and girls... today is a doozy. And a long post too! But before we begin on one of the toughest days I've ever done, let's recap. Mon: Irritating Onc day where I was not told about suspicious fluid around lung/heart in time to get a biopsy & I got contradicting info from his NP the week before.  Tues: Spending the morning getting Immunotherapy and 2 Chemotherapies before going straight to the airport to fly to Houston and enduring long rental car lines and afternoon heavy traffic. A few more checks off this weeks list... a few more to go: Now back to my Wednesday... the Humpday I would like to forget! So, after 8 hours of cancer treatment, flying, and travel in congested Houston the day before, I didn't have much rest because we had to start Wednesday early. My husband and I decided to walk to the medical center since our hotel was close. However, it was not necessarily the easiest or closest walk - tons of traffic, intersections, and some strange indivi...

the red devil strikes again

My Second Battle with Chemotherapy They say what doesn’t kill you makes you stronger. But sometimes, it feels like the journey to strength comes with a hefty toll. Facing the “Red Devil” a second time, I was prepared for some of the more notorious side effects—hair loss being the most talked about—but I wasn’t quite prepared for the onslaught of additional challenges it would throw my way. As the clock ticked past midnight, signaling the dawn of a new day, I found myself wide awake, grappling with the weight of a familiar foe. This is my second time undergoing chemotherapy, and the dread of the "Red Devil" has once again become a part of my reality. For those fortunate enough to be unfamiliar, the "Red Devil" is a nickname given to the chemotherapy drug Doxorubicin, known for its potent and aggressive nature. Back in 2013, the first time I faced chemotherapy, I was filled with a mix of fear and hope. I clung to the belief that the treatment would work, that the side...

christmas cheer and chemo chairs

Picture this: It's Christmas morning, but instead of unwrapping presents by the tree, I'm unwrapping IV lines in a cozy chemo chair. Talk about a plot twist, right? A Holiday Like No Other The hospital was eerily quiet, the usual hustle and bustle replaced with a calm serenity. The nurses, bless their festive hearts, were decked out in Santa hats and reindeer antlers, spreading cheer even as they administered my final doses of my previous month's partners in crime: Taxol and Carboplatin. Soon, I'll be enduring the Red Devil, a Chapter I am all too familiar with - yikes. The Gift of Resilience As I settled in for my last Taxol and Carboplatin treatment, I couldn't help but think how surreal it all felt. I decided to embrace the uniqueness of the moment. After all, what better time than Christmas and New Years to start a journey of hope and healing with my switching between my chemo companions? Deck the Halls with Humor The cancer center had turned the place into a mi...