Let her glow!

img_3212

This week has seen us with many doctor’s appointments as we transition from Val’s last chemo session tomorrow and onto the next steps of treatment.  We met early this week with the radiation oncologist to talk through the next treatment plan along with her on oncology doc to map out a long term follow up plan.

Val has an appointment next week where she will sit absolutely still for a very long time while they scan her body to map out the treatment area.  After that scan is complete, the doctors will go away and invest several hours in building the treatment plan to make sure that they radiate exactly where they want to and nowhere they don’t.  I like to think of it in terms that they will go and “engineer” the process.  She will also get some new tattoo’s that the team will use to line her up in the machine for treatment.  In my best Austin Powers voice, they will use a high intensity light source also known as a “laser” to line up the tattoos with the machine to make sure she is in exactly the same position for each treatment.

The actual radiation treatments are very short and probably only take 30 minutes from the time she enters the building to the time she exits.  She will get radiation treatment for 5 days a week and probably last 6 to 7 weeks.  The actual radiation treatments won’t begin for a few weeks yet while they let her recover from chemo a bit.  For side effects we have been told to expect her to be a bit fatigued and probably have some skin irritation where they radiate.

With much consulting, thought and prayer we have decided to forgo trying to get her expander put back in before starting radiation.  After talking with the docs to weigh the pros and cons, it seems best take the more conservative route and not introduce a process which may result in unnecessary complications.

The main goal is Val’s long term health by making sure all the cancer cells go bye, bye.  On the back end, Val will have a more extensive reconstructive surgery after waiting 6 months or so after radiation.  Our plastic surgeon is a very skilled doctor and if there was one person who we would want to do a more complex plastic surgery, he is it.

With Val’s last chemo treatment coming to and end tomorrow we have been told to expect it to be a bitter sweet time.  We are very excited to be done pumping poison, but have grown really attached to her oncology nurse and the entire oncology medical staff.  In some sense, we loose a little safety net with her not being seen weekly by this team.

On that note of medical team, Val’s breast surgeon, who we absolutely love and have not seen for several months called out of the blue yesterday to congratulate her on being done with chemo.  How cool is that!  A very busy doctor who we have not talked to in months, taking time out of her busy schedule to make a phone call to a patient!  It just goes to show you that very small things can mean an awful lot!

On the philosophical side, this transition to the next treatment phase brings about renewed thoughts of prognosis and what will happen in the future.  We have had our “heads down” plowing through chemo and now get a chance to come up for air a bit which allows a place for those thoughts to grow.

Val used to be very interested to know the percentages of this or that with a possible re-occurrence.  We had a good talk the other day about this subject and thinking through how we would live our life at two extremes.  The first extreme being that if we could know for positive that the cancer would return and the second extreme being that if we could know for positive it would never return.  We have really come to have peace with this thought and with the uncertainty.

 

In actuality, we have continue to learn how to just live one day at a time, taking each day as a gift.  My prayer is that we continue to live together with that mindset for many, many years to come.  Living this way helps me personally not get so “wrapped around the axle” on little things that used to really bother me.  One of my personal concerns on the far side of this experience is that I will lose that perspective and go back to old thought patterns.  It is easy to forget and I will need to continue to work at this mindset because my default setting is the opposite.

We continue to lean heavily on the Lord, knowing that HE is GOD and we are not!  He has a plan and holds us in his care.  He has continually met our needs in the very smallest of ways that are very tangible evidence of His watchful eye and love for us.

Thank you to all of you for your love and support as we walk this journey of faith together!  Let’s get on with the next steps!  Let her glow!

 

 

 

 

 

 

 

 

 

 

 

 

 

5 thoughts on “Let her glow!”

  1. God is with you along this journey. Guiding, loving, and giving direction. We will continue to pray on your behalf. And yes, let her shine! A beautiful heart you both have.

    Like

  2. We are so pleased that you are now at the end of the chemo and getting ready for radiation. We remember those days very well and at least in our case the radiation was easy after the chemo. Love your attitude about things, the mind can play some evil games at times and with my chronic and severe COPD I clearly understand the challenges of maintaining an even keel and trying to live one day at a time. Prayers continue for all of you and for your doctors and technicians. Keep the faith!

    Like

  3. Thanks for being so honest and sharing with us! When I see you in church I always want to run over and give all 4 of you bear hugs…..but know you all wouldn’t appreciate them at that moment. But please know we love you four—-always have— and we count it an honor to pray for you all and cheer you on.
    Hugs! The Huizingas

    Like

  4. Marc and Val, we are celebrating with you in this transition and being done with chemo today! Your words are very encouraging as you process the steps in this journey with a heavenly eternal perspective. God is good! Enjoy this break from treatment. We will keep you in our thoughts and prayers
    your friends,
    Todd and Lori

    Like

Leave a reply to Kay VanDyke Cancel reply