Well hello all, sorry it has been nearly a month since I
updated this blog. There are a lot of things to catch you up on, and mostly
things you have already heard.
Round 4 (aka Half
way)
·
This treatment wasn’t scheduled until 2 in the afternoon,
I had all morning to sit and think about the hell I was about to endure and it
seemed too much to handle. My poor husband literally had to drag me out of the
house to attend that session. Once we arrived it was business as usual. But I
found myself very angry instead of appreciative. (Something I am not proud of,
or even something I am used too).
·
The treatment too nearly 3 hours, and it doesn’t
hurt, just annoying. The worst part for me is the smelling and tasting of the
different meds. For example, the saline solution they rinse through the drip
bag taste just like metal. But worse than metal is the Heparin they need to
inject before and after every treatment. That tastes like pure rubbing alcohol.
I literally almost lose my food every
time.
·
The recovery from round 4 was one of the hardest
I have dealt with thus far. I asked the doctor as to why this might be, and due
to chemo build up in my system, the treatments will just continue to get harder
not easier (so I’m not crazy, but that stinks).
Round 5 (start of the downhill slide)
·
This round I did meet with the doctor, so I didn’t
have the luxury to “prepare” for the madness, considering the time was had to
arrive. They took my blood and weight, and then I waited for the results.
·
When the doctor finally came in, she assured me
that I “looked” healthy regardless of the situation (pretty sure she tells us
all the same thing, regardless, it did lift my spirits). None the less, my
white blood count was low yet again, which means I need to be continually
careful with whom I come in contact with.
·
She assured me that she thinks the treatments
are doing what they should be, however we won’t have concrete answers until
after my 8th treatment. Naturally I have been stressed thinking,
this hell was all for nothing and I might have to do it again, however
according to the doctor, that risk is so minimally we don’t talk about it. (WOO HOO-that made my day).
Side Effects:
The newest side effect that has arisen
in the last month would be the ulcers that are lining my esophagus and stomach.
They are extremely painful and make eating very difficult. Which would led one to think (or at least in
my head) that more weight should have been dropped, on the contrary my friends.
I have actually gained nearly 5 lbs. Which according the doctor’s office they
love that. I on the other hand, am ready to start a smart healthy diet. I’m
considering “Game On”. My best friend
has been doing it for a long time now with great results. It promotes healthy
living, while eating all the necessary foods your body needs to thrive. I will
have to tweak it a tad, due to the chemo regimens, but hope it will be a good
fit!
As for my hair, well it’s still
there, but I have had many people comment on how they can tell it’s thinning,
which means I can no longer pretend it still looks good! Haha. My doctor said
that if I haven’t lost it all yet, then I probably won’t, it will just get thinner
with each treatment. Which is why I
can’t decide if I will just leave it or continue my strategic comb over look? I
guess that decision will ultimately be made my hair. And I’ll leave it at that!
Activities
We recently received our Rosetta stone,
for Filipino. Chase served in the Philippines, and uses the language for work,
so I decided I wanted to learn as well. This will be a fun experience that we
can grow closer too, and hopefully I can one day be as fluent as he is.
We were able to take a 4wheeler
ride up by the Bountiful B, while Chase scouted for Elk. It was a long ride and
my poor dog was exhausted, but it was so much fun. We hadn’t had a lot of time
for fun this summer, with everything going on, so it was a nice break.
Well I always try to end with a
positive note and this post won’t be any different. I have been angry more than
anything else lately. Which I know it part of the healing process, and is
actually healthy to let those pent up emotions out. However, a lady that I love dearly gave me
this poem and it couldn’t have come at a better time. It really helped me put
things back into perspective and be grateful once again for the many wonderful
things that I am blessed with daily.
THE MONUMENT
God,
Before He sent His
children to earth
Gave each of them
A very carefully
selected package
Of problems
These,
He promised,
smiling,
Are yours alone. No
one
Else may have the
blessings
These problems will
bring you.
And only you
Have the special
talents and abilities
That will be needed
To make these
problems
Your servants
Now go down to your
birth
And to your
forgetfulness, know that
I love you beyond
measure.
These problems that
I give you
Are a symbol of that
love.
May God bless
all of you, as I know he has blessed me in this great time of need? Remember
that we are not alone EVER. I hope you will all take as much comfort in this
poem as I have.
Remember Love conquers cancer, XoOXxx
I love your pic...I love the poem, well said! Bre, you are a shining example to all, I love you much, mom.
ReplyDeleteI can’t imagine what you are going through physically and emotionally, but I have no doubt that you will conquer this, because you are the strongest person I’ve ever been around. I’m so very proud to be your father. I love you very much! Dad
ReplyDeleteGoing out to dinner was fun last night. I am happy you felt well enough to go. We need to do it again, and as much as possible, to get you to eat something...love ya, mom.
ReplyDelete