Treatment #4 has not been the easiest !
I have
had more uncomfortable and painful symptoms this time.
As I said on my previous
post, the neuropathy and heart palpitations were new symptoms and both are scary.
The neuropathy pain can be so painful it is life altering. But I have also been
more tired this time. I usually have a low period in which I am very, very
tired – but then recover somewhat before next treatment. This time I have felt tired
the entire 3 week period and its only 3 days until my next treatment….if I
decide to have it.
I still have not made up my mind what to do. I have done a lot
of reading and have a lot of questions for my Dr. before I decide.
When I made the decision to fight this cancer with everything we could – it
was because I did not want a repeat cancer. They say the second time around is
much harder to fight and to win.
However – with these new side effects I have to consider the quality of my
life also. And this is where it becomes each person’s very difficult decision.I truly want to beat this cancer, but I want to live a full life too.
I still have so much I want to do with Tom and my family and friends. Things
to see and do, places to visit. And I do not want to do them in a wheel chair. Tom
and I are at the age where we can spend more time having fun. Enjoying life and
reaping the benefits for working so hard all our lives.
So in my mind it boils down to this....
I can finish my chemo and possibly be wheelchair bound from the heart damage and or be in a medicated stupor and crippled from the pain of neuropathy. OR stop the treatments, maybe risk a shorter life, but be able to function, walk and do things before I die.
I am not sure if decreasing my dosage is an option or if it would even matter in reducing the newer symptoms.
Even though I am an Optimist, I still realize because of
the cancer (and possibilities of recurrence) and because of damage to my body
from the chemo, I may have a much shorter life than I expected.
Of course there are no guarantees….anyway.
I might get
hit by a plane crashing from the sky or a driving/texting teenager
tomorrow.
I hope I beat the odds. I plan to try with all my being.
I will know I have been true to myself and no regrets.
I have a picture with a saying that hangs on my wall, that I absolutely love.
“ Life should not be a journey to the grave with the
intention of arriving safely in an attractive and well preserved body; but
rather to skid in sideways, chocolate in one hand, wine in the other, body
thoroughly used up, totally worn out and screaming…. “ Damn what a ride”.
Of course now it has new meaning to me… as I have to have
small bits of chocolate and wine. Not gobs and gobs……dammit.
I need to stay healthy enough to still walk and run
and
make my journey a long one.
and
make my journey a long one.
My dear Kelly.....my heart bleeds for you. Remember......God, not the doctors, not chemo, nor anything else will determine your outcome. I suspect that you will come out better, live life to the fullest, and experience thousands more sunrises and sunsets with your hubby. And of course,spend many more visits with me!!!! Love you much. Hug, hug, kiss, kiss.......Melissa
ReplyDeleteDear Kelly........I am here thinking about you and praying for you every day. The end is in sight. Just a few more days. Hang tight. I know your life will be better than every. Love, hugs, and kisses. Melissa
ReplyDeleteThank you Melissa, I know I am on the down side to this, but it is getting harder each day. The symptoms are definitely cumulative.
ReplyDeleteI know this to shall pass. I love you.