Wow. What a week.
Mason went in for his
third, and what was supposed to be his final, round of chemo on May 1st.
Three days into his chemo, however, my mom asked the doctors to do an MRI.
Because of his previous fungal infection, which showed up in an MRI after his
second round of chemo, my mom wanted to make sure he wasn’t taking any
unnecessary medications for that infection or anything else. What they found on
that scan gave us a bit of a scare. The fungal infection was still there, or so
we thought. There were countless other things it could have been, such as a
bacterial infection, the fungus again, or even mold. Some of the potential problems
on that list were slow growing and very difficult to treat. We were very
nervous.
It’s amazing how calm and
positive Mason stayed throughout this entire mini battle. He would text my mom
inspirational little messages telling her that everything would be okay, and
that he would overcome this obstacle just like he has overcome everything else.
He was constantly reassuring my dad, Parker, Morgan and me. It seemed like the
one person who you would think needed the pep talks, guidance, and comfort was
the one giving it! Truly ironic if
you ask me.
After the discovery of
these spots, they stopped chemo and began to administer the most basic of all
antifungals. Over the weekend, they took a sample from his nose in order to do
a biopsy on that to find the cause of the spots showing up in his MRI. Because
nothing showed up there and a second MRI revealed that these spots showed no
improvement with the antifungal treatment, they decided on Monday that Mason
was going to undergo a surgery to look at his sinuses. They also needed to do a
lumbar puncture at this time to get an idea of what was going on in his spine
to make sure no fungus was there.
On that Monday, I left
school early and took a train down to CHOP. My parents had barely been texting
that day and I needed to know that Mason was okay. I got there and my dad met
me and took me to the 4th floor to the OR waiting room. They had a
big flat screen TV, which displayed the initials of all of the current patients
somewhere in the OR and their status, discharged or still undergoing surgery.
When I got there, my parents informed me that his sinus procedure revealed
nothing but inflammation. Since that did not tell the doctors anything or give
them anything to biopsy, they needed to go directly to the source. After
finding nothing in his nose, they had to open up his head. On Monday, my
brother had brain surgery.
Though waiting in the OR
was tough, we were greeted by his neurosurgeon after an hour or so (it felt
like four) with hopeful news: he did not see signs of a fungal infection in
Mason’s brain. They took a sample of the center of one of the lesions found on
the MRI, but according to the doctor, it just looked like dead tissue. It was
as if something was there before, but it was possible that his body had fought
off the infection and left only dead tissue behind. While this news gave us
some hope, we still had a lot of waiting to do. We needed to wait for the
Infectious Diseases team at CHOP keep an eye on the sample and see if any kind
of infection would grow. Waiting is too difficult, and I’m too impatient. It
was hard to not know what was wrong, but things were looking good on Tuesday
according to the doctors, and on Wednesday, we were to get the “final” results.
That Wednesday we were
informed that nothing grew at all. Wow. A weight had been lifted off of Mason’s
shoulders. Obviously he has a bunch of other ones, but this weight was a very
important one to get rid of. It weighed heavily on Mason and that weight
extended to all of the rest of us.
What about that round of
chemo? It was stopped three days in. Is Mason going to finish it? Here’s the
thing… due to this minor setback, Mason’s timeline has been slightly altered.
Originally, we were aiming for his bone marrow transplant in mid-June. Things
have changed, however, and I don’t think I will be seeing him at my graduation.
Mason’s oncologist, Dr. Greene came in tonight to inform us of the new, very
tentative, plan. Because of his special and mildly unusual circumstances, she
had gotten a very large team together to discuss the best options for Mason. These
doctors came to the conclusion that because Mason will not need treatment for a
fungus or any other infection which could take weeks or even months to heal,
they are going to keep him here and wait for his counts to drop yet again.
(They were giving him injections to boost these counts in order for surgery to
be possible and to see if his own body could fight off his problem.) After that
happens, they will take another scan of his brain to see how that is looking.
They will keep Mason at CHOP over the next three weeks, approximately, without
administering chemo.
As long as Mason’s brain
images improve and Johns Hopkins has room for him, he will be dropping in for
that transplant about a week early. It is this new development that makes me
believe that he won’t be at my graduation, which is okay with me. If he can’t
be there because his brain is healthy, his leukemia cell counts are low and
almost nonexistent, and he is in route to a bone marrow transplant, that’s okay
with me.
Mason went through a lot
that Monday. He went into surgery expecting only a lumbar puncture and a sinus
biopsy. When he woke up hours later in the ICU, he had an almost three inch
long incision on his head from where the doctors went in. He was nauseous after
the procedures and was also in a lot of pain. He’s doing so much better now,
and of course that good news only helps. I spent the night with him last night.
He was smiling and laughing, and we were goofing off. This little scare and
setback turned into a near blessing.
In times like these, it is
so easy for people to forget all of the reasons that they are lucky. My family,
on the other hand, has discovered that it is much easier to recognize and
appreciate your blessings. We were very nervous, without a doubt, but it has
gotten better. With the nerve-wracking news we got previously came good news
that filled us again with hope. That feeling is a good one to maintain: hope.
It keeps you up when you’re feeling down and ensures that you believe in the
power of prayer and healing. Mason will be healed, and through the scary
procedures that he had, we are reassured of that. He’s so strong and continues
to only become stronger. He’s our hero.
Yes, Mason and all of you are so very lucky. Not only because he emerged with good news from this terrifying week, but also because you have each other. You recognize what's important in life, and you are growing even tighter than the close-knit family you have been. My heart is with you all even if I'm not with you.
ReplyDeleteI was blessed to have some "face-time" with Mason yesterday...I even had my mom come to my house and we chatted and saw Mason for over half an hour. Mom was so thrilled that she got to see him...You know her, she thinks we are all hiding something from her...but there he was...Mason being Mason, laughing, itching his head incision...but in great spirits...We are there for you....we are family!!!
ReplyDeleteSorry to hear about the fungal infection, but I know it didn't dampen your spirits Mason. And it'll be great if you're able to get that transplant early! XOXO
ReplyDeleteI am so glad I found your blog. My son, Dylan Crunick, plays Chandler baseball with Mason and as you probably know, was diagnosed with cancer a few months before Mason. Dylan came home from Chandler's mini camp with news about Mason needing brain surgery and I wanted to find some accurate information. While I have never met your family, I feel as though our boys lives will be forever intertwined. I wear Mason and Dylans bracelet every day and think of him often. He is a hero, they both are! I am glad to hear good news about Mason and will pass it along to Dylan. Please feel free to reach out to us if you ever need anything. We will keep your family in our prayers. Love to you all,
ReplyDeleteKristen Crunick