UPDATE
{Grandpa and Brocklii Bear... who is here for his baby blessing:)}
Time for another status update on Dean's progress!! Last week we went to Huntsman for his first
MRI following radiation. The Doctors had
told us not to expect much because radiation can sometimes make the brain look
worse, as it leaves the brain swollen and spotted. So, we went in just expecting results that
were similar to the scan taken just after his surgery. I hadn't worried much about this MRI until we
were actually sitting in the examination
room, waiting for the Dr. to pull up the results on his computer screen...all
of a sudden my stomach was doing somersaults!!!
Apparently, I WAS feeling just a touch anxious!!! The doctor pulled up the images from both of
his MRI's so that we could see them side by side. It gave us a chance to see the before and
after of radiation. So....drum
roll...the results were VERY encouraging.
The Dr. told us that this scan was as good as it could look. Can I just say, MIRACLES continue to come our
way...we are SO grateful!! Every place
that had shown signs of tumor or cell growth were either gone or significantly
smaller. He said that some of the spots
that we were seeing could be possible scar tissue from the surgery. The Doctor was very pleased and said that
Dean's recovery and the way he has responded to treatment have been a bright
spot for the neuro-oncology team. He
told us that most patients have some kind of side effect or difficulty after
this kind of surgery and diagnosis. But
Dean has defied all odds and continues to amaze them all with his
"iron" like approach to this!
Not only does his scan look good, but he has been able to pass every
"mini-mental test" that they have asked him to do. As I am sitting there with him, I silently
try and do the same things they are asking him to do. I've got to admit that I have failed every one
of the subtract backwards from 100 by 7's tests and I have missed some of the
spell the word backwards tests...YIKES...I am going to study up so that next
time my score will equal Dean's. I guess
the bottom line is that Dean is smarter than me even with part of his brain
missing. BOO!
So, we move forward from here with a break from chemo until
October 30th, when Dean will start back up on a double dose. He will take the chemo for 5 days and then
have a break for 23 days and repeat that cycle for another year. At that time they will see how things are
overall and decide where to go from there.
He will have MRI's about every 6-8 weeks to monitor those darn cancer
cells and make sure they are behaving themselves. We feel SO hopeful and EXTREMELY blessed as
we have had the windows of heaven just opened up and blessings poured out on
us.
This past week as we listened to conference, I felt as if my
Father in Heaven was sending down little packets of sunshine and comfort, as he
was teaching me how to use this experience to become a better person, with my heart
more aligned to His. I was touched by the
stories of other's personal trials and felt uplifted as I heard how those
challenges opened up the way for them to feel of the Savior's love more
fully. I loved that Sister Burton said that the gospel of Jesus Christ should
be in the marrow of our bones and be the substance of our soul...Sister
Stephens reminded us that we must choose what we learn from adversity, Elder
Johnson said, that our discipleship is defined not by the trial but by how we
endure them and Elder Eyring taught that we remove the pavilion that separates
us from God when we say thy will be done and in thy time. Those are just a few little
"packets" that touched my heart.
As our family has had this "opportunity" for growth, we thank
our Father in Heaven for his endless love, His knowledge of us in a very
personal and intimate way, and His matchless power and we remember that all we
go through in this life is calculated to bless us and bring us back to Him. That is where we hope to be...together, with
Him.
4 comments:
Ahmazing!
Ahmazing!
Ahmazing!
Love, love ,love the updates!
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