This week has been rough. I seem to have caught a raging cold and in the words of my hemo nurse today its 'kickin' my butt'. Today's treatment was just another issue to add to the plus column of getting a fistula. Each time I coughed or sneezed I set off the arterial alarms, requiring a nurse to reset the machine with each outburst. And each reset adds additional time to my treatment. I must not have looked so great either, because I got more questions of 'you doing okay?' from nurses and techs resetting my machine. In truth I would have loved to just burrow under the covers and slip into blissful oblivion until I was rid of this bug.
I also got word of the final sensitivity testing -- it seems I'm on the one of the few antibiotics that isn't resistent to my abdominal infection. I made multiple calls yesterday trying to expedite surgery for fistula creation. I'm having to remind myself to trust God and be patient -- funny -- I've had so many opportunities to trust Christ and wait paitiently for God's timing -- and still, it comes far less naturally then I would want. God is good to remind me of His promises, but today is one of those days when its a little harder to remember. But it is on these kind of days when I am restless because of leg cramps, but too tired to do anything about it that God uses others to remind me of His love -- so thankful for His faithfulness, even on my rough days!
~V
Wednesday, January 23, 2013
Tuesday, January 22, 2013
The Lord Has Brought Me to This Place... And Other Unexpected Expeditions in the New Year
December 31, 2012
A
Christ-centered faith has no room for coincidence – because I believe this, I
also have to believe that the Lord has brought me to this place. I’m in good company. All throughout the Bible
heroes of faith are forged in the fires of adversity – all because God brought
them to (and through) staggering events that shaped their faith. Daniel, Shadrach, Meshach and Abednego
endured enslavement before they faced their fires and hungry lions. Coincidence?
I hardly think so. You’ll pardon
me grouping myself alongside these men of faith. It would perhaps be far more appropriate to
group myself in with the Jonahs of old, but I digress.
I’ve been pretty fixated on Paul’s letter in Corinithians
describing his ‘thorn in the flesh’.
I’ve been wrestling with frustration over my bad days – using the
passage as a reminder that God can use my weakness to showcase HIS
strength. It is so true – often I am
guilty of taking credit where credit is so very not due – Any strength you see
in me is the result of my Christ holding me up – He is my anchor.
He has brought me to a place of acceptance – He used the
last few weeks to shore me up so that I could withstand today’s blow.
I’ve been battling an exit site infection for the past two
months. Some days seemed to be better and
then the last few days I began to have pain along my catheter implant
site. Yesterday I noticed a raised
reddened area along the catheter’s path.
Thankfully I was able to get in to see the doc today and subsequently
was referred to a surgeon. Several hours
passed, a visit with the surgeon and multiple expletives later, (from him, not
me) the census is - Infection at the cuff of my catheter. Apparently this is
the least favorable spot for an infection (as if there were a good spot). So, long explanation slightly shortened – the
catheter must come out.
Later this week I will have the catheter surgically removed
and a Hemo catheter implanted in my neck for the third time in 2 years. I don’t understand why this had to happen – I
don’t like it, but I am certain that no matter my understanding God has a
purpose for me in the life I have been gifted with. Before you write me off as a phony-balony or
a saint let me just say, my attitude is a work in progress. You can pray for me in this. I have a few issues to work through – I have
major issues with loss of control and trust.
But really it comes down to trusting God in the things in and out of my
control and having an attitude that mirrors God’s peace rather than my
turmoil. If I have to go back to Hemo
(and barring a miracle, Hemo awaits me) then I want to have an attitude that
reflects my Lord, His love, and His peace.
It’s my own little in-center mission field – but here the natives can’t
go anywhere if they don’t like what I have to say ;) Thank you for being so faithful in your
prayers! May God richly bless you in the
New Year!
~V
*************************************************************************************
The past two weeks has been a busy blur. When last I wrote I was planning to have my
peritoneal dialysis catheter removed. In
my pain-med drugged state I failed to blog the last two weeks’ events – so that
is where I will pick up my story.
**********************************************************************************
January 3, 2013
The day of surgery had finally arrived. The surgeon had given me a 3-day antibiotic
to stem the tide, but it had little effect on the ever-increasing pain at the source
of the infection. I was never so glad to don a vented hospital gown in all my
life! I spent the morning regaling
hospital staff with my health history, providing venous target practice for
blood work and IV, and catching my OR staff off guard. Shortly after my OR nurses began wheeling me
to my awaiting surgical audience I popped the dreaded question, “Would now be a
bad time to tell you I really need to pee?” Their stock still stance and stone
cold countances would make any Scotland Yard Guard proud – they looked to each
other and then back to me. The tension
was thick…… you could have cut it with a surgical knife. It was then I thought I better resolve this
stand-off, I mean, I make it a practice to never upset the persons who prepare
my food, how much worse must it be to tick off your surgical team? Quickly I interjected, “um, I actually don’t
have any kidneys…” No Response ….”uh, so I can’t pee…” My harried chariot bearers still just stared
at me. … “it was a joke.” Well, I thought it was funny J Apparently my audience thought otherwise,
but really, they had read my chart – no kidneys equals no pee & why else
was I getting a dialysis catheter? Just
keepin’ them on their toes J
The next two day’s events I relate to you via the info
others have told me, because, well, I was totally out of it! The surgery went well and I was released the
same day – both of which I was very glad for, but the results of the surgery
were not as good – The infection was a particularly nasty bug, which had
infiltrated my peritoneum and the catheter tract. In order to make sure the beastly infection
bugs were gone and wouldn’t take up permanent residency the surgeon left the
incision open. Hmmm open incision and Hem dialysis….. can you say Déjà vu? It was eerily similar to my summer of 2011 –
the summer I had no wishes to repeat. I
had feared this very thing happenening and had thought I would be an anxious
mess. But the Lord was so good to me, giving
me peace in the circumstance I had most feared.
The real thing was far less scary then I had imagined PTL! I would have loved to crawl under the covers
and sleep my pain medicated sleep for days, but I had to be at in-center
dialysis bright and early the next day.
Still in a bit of a haze at this point I was able to sleep through most
of my treatment which went relatively easy.
The only thing I remember is having a curious patient wheel over to my
chair and watch as I was hooked up and comment on every conversation I had with
my nurse. I think I now have a better
idea how the monkeys at the zoo feel.
The next few days I had wonderful friends and family to
occupy my time and provide pleasant distractions. A routine of sorts quickly developed… Three mornings a week I would wake to my
alarm, stumble out of bed and dress in Hemo Sheik – Long sleeved V-neck shirt,
elastic waist sweat pants, zip-front hoodie, and tennis shoes. A ponytail and glasses completed my ensemble
and I and my blankie could be out the door in 15 minutes flat. My 3 ½ chair time stretches to 4 most days
and then I spend the afternoon sleeping.
My nights are restless and I wake on my Hemo-free day still feeling tired
and tired of tired. Most of my treatment
days have been rather uneventful – I recline in my chair after having my dual
lumen catheter hooked up to concurrently drain and filter my blood and then
return it back to me in a repeating cycle.
I have a TV at my disposal, but most days I try to sleep, read my bible
and then drown out the noise of the center with audiobooks, music or
movies. My attitude this third time
around is markedly different from last time.
My mom calls my attitude last time – ‘politely rude’. I probably internalized a lot of my
irritation and beligerance, but it was always just at the surface. God really brought that to mind this time and
I was really convicted. My actions and attitudes are a reflection of
my relationship with my God. Trials are not a free pass for a bad
attitude. I think the following
conversation probably sums this up best.
I had put in my time at dialysis and was waiting to be disconnected when
a large man approached me and began
fiddling with my catheter and machine.
He looked official, but I was still a little wary. “Soooo”, I said, “what’s your name?” He replied and we made polite chit chat. As
he neared my catheter I tried to play it cool – “so what do you do here, are
you a tech or a nurse?” I suppose I need
to work on my characterization of ‘cool’, cause he flashed me a humorous smile
and wanted to know – “Why? Do I make you
nervous?” I gave him my best ‘not-nervous’
look, but waited for an answer – he soon told me he was an RN and I began to
relax, knowing I was in capable hands.
We continued talking. He hadn’t
seen me before so he was questioning my dialysis history. I gave hime the cliffs version and then he
wanted to know how I dealt with it all and who my support team was. I had the opportunity to share how wonderful
my parents have been but even more how faithful and true my Heavenly Father has
been to sustain me through each event in my life. His response wasn’t quite what I
expected, “Wow, so its no big deal then?” I think I may have snorted in an unladylike
fashion and then proceeded to tell him that it was sooo a big deal, but it was
the Lord who helped me through these big deals and allowed me to learn and my
faith to grow through these times.
The me of a year ago wouldn’t have been so convicing if she’d
said the same thing – that me was closed off, prickly and counting the days
until her in-center release. Today’s me
still has some of the old hang-ups – I still don’t like Hemo – but I am making
strides to allow God to use me where I am, even if that means while I’m sitting
in my grey pleather recliner.
**************************************************************
It seemed as though requests for my presence were in high
demand. I off-set my in-center days with
visits to multiple doctors and specialists.
I saw the infection specialist and was started on two antibiotics, and
then I followed-up with my surgeon. He
managed to keep his colorful expletives in check on this visit, but while he
was happy with the healing progress of the incision site, he was very honest
about his concern over the potential virulence of the infection. Because of the bug’s nature he made it clear
that he would not even attempt to place another PD catheter any sooner than 6-8
months from now. He felt the infection
was in-check and under control but was unwilling to consider using any man-made
products to create an access site. This
left a fistula creation to be the only option.
*************************************************************************************
January 17, 2013
Today I have the venous mapping done. This is the first step in the journey to
getting a fistula created. The fistula
is really the gold-standard of dialysis.
It is created from the person’s own artery and vein. The artery is stitched to the vein so that
the artery’s higher volume of blood is directed through the vein. This higher volume and higher pressure are
intended to increase the size of the vein, over time creating a useable
fistula. In all my time doing dialysis I
have always lamented the use of a fistula.
They are a curiosity, but far from pretty – often you’ll hear people give them the moniker of “hose”. Another rthing that makes them seem
less-than-desirable is the fact that two needle sticks are required whith each
treatment – ick! So there’s my hang-ups,
but I’ve been making a conscious effort to find positives to outweigh the
ick. I’ve found several… I would be able
to have my IJ catheter removed, thus eliminating one more avenue of infection –
big plus! Sans IJ and PD catheters I
would be able to resume showering and swimming – Major plusses! A fistula, while not pretty, is necessary –
my own badge of honor!
The venous mapping was relatively easy, an IV in each wrist
allowed the nurse to inject dye through my veins in each arm and X-ray captured
the pics to reveal what shape my vessels were in. Thankfullly my non-dominant arm possessed the
most favorable vessels for use – Thank you Jesus!
The staff were pleasant and really helpful at explaining
what I could expect with the fistula – and I was such a good girl that I got
juice and crackers before I left J
***********************************************************************************
January 21, 2013
My incision has healed enough that I no longer require
packing and I am able to do dressing care by my self. I have finally returned home and am trying to
find my new normal. I had kind of a
rough day of treatment, battling leg cramps for half of my treatment and the
rest of the day. It was strange coming
home – it was the first time I’ve returned to my home while still doing Hemo. In the past I would stay with my caretakers
until I was back on PD – It became very real to me today – This is my life, not
just a seg-way to something else.
*****************************************************************************
If you’ve made it to this point in my musings you deserve my congratulations! The New Year has been flush with activity
and changes, but through it all the Lord has been ever faithful in providing me
with the necessary strength to continue on.
He has blessed me with parents and extended family who care for me and
encourage me – they remind me of the Lord’s promises when I am too tired to
read them for myself. The Lord has
blessed me with a league of prayer-warriors – friends, family and even strangers
who care enough to bring my needs before the Great Physician and Healer. I am so blessed and humbled by the blessings
God has placed in my life.
I would appreciate continued prayers for the full
eradication of this infection. I got the
call today that I’m on the only antibiotic that isn’t resistant to this
bug. Please pray also for me as I begin
the process of getting my fistula created, that it will work well and that I
would not have difficulty adjusting to it.
Right now I think the unknown and my imaginings of what it might be like
are far worse than what I’m in store for.
Thanks again for your friendship and faithful prayers!
~ Vanessa
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