I had my monthly bronchoscopy last week.
Though there was once again narrowing in some of my airways, there was less
necrotic tissue and overall things looked better than last time. Hopefully that
means things are moving in the right direction and settling down. I haven’t
started wheezing yet, so that’s also progress, as previously it only took about
a week for the wheezing to start up again. They still want me to come back next
month for another bronchoscopy, but I should start needing them less, and
eventually not at all, hopefully soon! The doctor said that this happens in
10-15% of lung transplants, because of course I would have an atypical
complication. I’m officially statistically special. We all know I like to keep
them on their toes!
During Simchas Torah I lived on the edge
and braved the crowds at shul. I of course wore a mask and was careful about
washing my hands, and spent a good amount of time outside where there was more
airflow and therefore less risk of germs. Probably if I wanted to be 100% safe
I should’ve stayed home, but what’s the point of getting a life saving
transplant if you don’t actually participate in life? I’m basically still
making the same calculations that I did pre-transplant to balance protecting my
health with living a fulfilling life. Hopefully I calculate correctly, but at
the end of the day I’d rather have a short life filled with good memories than
a long life of empty boredom.
I’m still struggling with significant joint
pain, which has now spread from my hips, shoulders, and a few fingers to almost
all of my fingers, my knees, elbows, and one wrist. Pretty much any movement
hurts, and I often hurt when I’m sitting still too. Going to sleep is really
fun, as laying in bed without distraction is the perfect time to really focus
on all my aches and pains. I have an appointment with an orthopedist tomorrow,
so hopefully he’ll be able to offer some relief.
In the CF world, the BIG news this week is
that the FDA approved Trikafta, a new genetic modulator that had huge results
in clinical trials and treats the vast majority of CF mutation combinations.
This is the triple combo drug I tried unsuccessfully to get early access to
when my lungs were failing. Not gonna lie, I’m definitely feeling some kinda
way about the whole thing. I waited YEARS for them to come out with a genetic
modulator that I was eligible for. One breakthrough after the next I was
disappointed, as my mutation combination was not eligible for any of the new drugs.
Then, FINALLY, the one that I could take was being developed – and my lungs promptly
went to pieces. From November through March I kept being overcome with rage as
my lung function deteriorated right when a promising new drug was on the horizon.
By the time we started talking transplant, I moved from enraged to resigned.
And now, here I am, approaching 6 months post-transplant, seeing that long
awaited drug finally hit the market. Yeah, I’m a little bitter about the whole
thing.
But, I’m trying not to waste time on
bitterness. For whatever reason, that wasn’t the path I was meant to take. I
need to focus on the path that I’m on and getting through this transplant life.
The truth is, I’m probably breathing better than I ever would have even if Trikafta
worked miracles for me. If we could just get my pain under control I feel like
I could conquer the world! Maybe I’m just supposed to enjoy breathing with
these lungs for however long I get.
It’s hard not to imagine the what-ifs and
could’ve-beens, especially while struggling with physical pain. But I’ll try
instead to look at what is and what will be, to keep putting one foot in front
if the other, and to get the most out of the life I have.