I went into the
hospital Nov 6 - 21 due to recording a lung function of 35% on my testing. I
have not ever experienced a result that low and needless to say scared the 💩
out of both Ric and I. We knew I needed to be admitted and start treatment. I
had a pretty solid stay, nothing too out of the ordinary -- oh, yeah, except
that blood clot, that echocardiogram and the hemoptysis.
I am continuing to throw clots each time a
PICC line is placed. It is really uncertain the reason why. They have ran every
blood test and clotting test imaginable and each comes back 'normal or
negative'.
We ran an echocardiogram to look at the
pressures of my heart. With pulmonary disease, once your lungs start failing
this causes your heart to work harder to pump what little oxygenated blood
there is throughout your body. This can elevate the pressures in your heart and
slow down the flow of the blood movement through the heart. Speculation was
that this is where my disease was headed and that the clots might be developing
in my heart all along. Concerned that the 'shortness of breath' I have been
experiencing was due to pulmonary embolisms and not just CF - as we had
previously assumed. Thinking about this brought my nerves out, but nevertheless
-- once again, normal. A true relief this time. This allows us to believe,
my body has a quick and strong response to the "trauma" associated
with the PICC line placement and that the formation of a clot is how my body
responds to the negative stimulus.
I had my largest episode of hemoptysis ever. I
freaked my nurse out - now, it's kinda funny thinking of his reaction.
Hindsight, ya know. If you don't know what hemoptysis is, look it up. I don't
like typing it - it freaks me out.
I ended up having to stay an extra day, making
my admission 15 days, but I was still out in time for Thanksgiving. Yay! It was
great to spend the holidays with my in-laws who travelled to AZ from all over
the states.
Week prior to surgery consisted of lots of hanging out and book reading. We had our first 'Sherman Army Live Q&A' (#SAQandA). Thanks to everyone who tuned in! DM a question anytime, more Live Q&A's are in the works.
Surgery on my sinuses and deviated septum went
well. They relieved a lot of congestion and blockage in each of my sinus
cavities. This should help alleviate my headaches, reduce my nose blowing, as
well as hopefully decrease my quick recurrent lung infections from post nasal
drip. Recovery was going well, painful but well, and they told me I'd get an
early release -- I'd be home for Christmas! Oh how this made my Mama heart
happy. I had been having a hard time being happy, when I knew I would be
spending the holidays away from my 2 year old. It just didn't seem fair to him.
How I was dealing with it was maintaining the mindset that he didn't understand
a calendar yet, and would be okay celebrating on any given day.
The morning following my good news, and after
packing up some of the stuff from my room, our CF doc rounded and broke the
news that I had cultured a different bacteria from my sinuses. They wanted to
aggressively treat this infections in hopes that it would help me have a
smoother six months rather than the rough six months previous. They would also
be doing a 15 day course of IV antibiotics - requiring me to stay inpatient and
restart my "clock". I would be in over Christmas. I would be in over
New Years. I was devastated. I took my time to cry, and then realized the
only thing I could change about this situation was my attitude. Sure I'd be
missing this Christmas, but really, we take action now to hopefully have a
brighter future. We are planning for Christmases 5 years from now.
I could sit and pity or I could look for the
positive and create change myself.
I then asked Ric to bring aallll our Christmas
stuff to the hospital- we WOULD celebrate on Christmas Day and we would
celebrate in style. We had a beautiful Christmas morning with presents and
Santa came to hand deliver Hawke his toy! How lucky is that kid?! We were so
grateful that Grandma and Grandpa could be with us during this time and make
the "magic" a reality. Being in the hospital during Christmas
was very humbling. I felt much of Jesus Christ's love as I reflected on him and
his birth. I slightly hoped he would come again and heal all those in the
hospital -- maybe it really would be my lucky day 😉.
Staying longer in the hospital ended up being
a tender mercy; several days post surgery I dislodged a clot from my sinuses
which resulted in a severe nose blind (think mild hemorrhage). Because I was
in-patient they were able to have the ENT doctors come to my room quickly and
take care of this. I bled for six hours. It was aggressively coming out my nose
as well as my mouth. (Sorry for the graphics, but hey the medical life ain't
always pretty, but it sure is adventurous!) I narrowly missed going back to the
operating room and cauterizing the bleed. They put packing up my nose (think
tampon), and inflated it with air to create a type of pressure dressing. This
slowed and eventually stopped the bleed. This "device" called the
rhino rocket, earned a nickname in our room as 'T'mera the Tampon' or 'The
Wonder Dam'. She was with me for 7 days and then was removed. I hate to think
what would have happened if this incident had occurred at home, I don't think
we would have been able to make the 2.5 hour drive back to our CF Clinic and
would have ended up at a hospital that didn't treat CF or know my body. Again,
grateful we were there.
I couldn't close this post without saying
a THANK YOU to each and everyone of my family, friends (3D and from
social media) who sent Christmas Cards to help brighten my room. This holiday
cheer was so fun when I would receive a mail delivery! I love, love loved
hearing from you. To look at your photos, read and be inspired by your
stories/letters/notes. I am grateful for your thoughtfulness and taking the
time/making the effort to make my holiday brighter.
Those of you that work in the healthcare field
during the holidays, thank you. My heart is overflowing and so big for you.
Sacrificing your time with your family to care for those who aren't with
theirs. Yes, I know you get paid, and probably a little more than usual, but
still. Thank you. You efforts are noted and gratefully respected and
appreciated.
I was finally released after spending 25
straight days in the same hospital room and 6 out of the last 8 weeks in the
hospital.
Nov 6 - 21
December 11 - January 4
What I thought was 39 days, I actually
recounted and made it to 40 days in.
Here's to the New Year and resolutions of
staying out the hospital!
Xx, M
I love reading your posts. Your upbeat attitude is wonderful. - Donna
ReplyDeleteAmazing... I love reading your posts.
ReplyDeleteDr. Edmund Fisher is a leading provider of Otolaryngology treatments in Bakersfield, CA. His practice, Sinus & Nose Surgery Center, focuses on treating individuals from all over the Bakersfield area as well as those that fly into town for a quick treatment. In addition to his 20 years of combined ear, nose and throat experience, Dr. Edmund Fisher has been providing oral surgery services for seven years.
ReplyDelete