Posts

The Smell of Thanksgiving

Image
Tis the night before turkey day ,and all my little eaters and non eater are packed quietly away in their beds, dreaming of white turkey and pumpkin pie with mile high reddi whip on top. Some family members can't make it, others haven't made it in years, so the mix will be fun and refreshing. But here's the jib: whilst the folks frolic along the lines of food and drink, slump down in chairs to stare at a family member, or the boob tube--which ever is more attractive, i'll be counting  oral intake calories for Rhyse. Dividing those calories by the time of day and the amounts he needs to sustain his energy, and subtracting the volume of vomit along the way. I'll be chasing him with his MOOG feeding pack, and inconveniencing him as he tries to wrestle around with his oh-so-awesome uncle Josh, whom he speaks of nearly every day of his life. And finally watching for signs of severe fatigue, and finding ways to allow him quiet time to recharge until it's time to go...

The Fever that Changed the Journey Part Eight: The Answer

Image
The Answer After a couple of hours we were called into the parent meeting room to meet with Dr. D, the surgeon who had just finished the biopsy.  He handed us a picture of the procedure, and explained that although he didn’t have any immediate answers, neither did he find what he expected.  We were left puzzled by that comment. I stared at the photo page he handed me, trying to figure out if this was a good ‘unexpected’ or a bad ‘unexpected.’ As soon as Rhyse was awake and stable we were escorted back to our room on the tenth floor.  While I concentrated on comforting Rhyse who was in great pain from the three incisions, and add on circumcision we requested, nurses, doctors and surgeons flowed in and out of the room to do their evaluations and vitals.  Apparently while being under the anesthesia some fluid pooled in his lungs and made it difficult for him to breathe. His chest and tummy were thrusting up and down, trying to get enough oxygen to functi...

The Fever that Changed the Journey Part Seven: Back for Biopsy

Image
Back for Biopsy Late Monday morning my in-laws had arrived from Indiana to stay with our daughters while we were once again contained in the hospital with Rhyse.  Thank God for family. Checking back into the hospital is no easy task when you had just checked out three days prior.  Rhyse was frantic and unwilling to be taken out of his stroller, screaming and shaking from fear.  The minute we arrived on the tenth floor he was ready to fight tooth and nail to get back on the elevators.  He pointed at the doors with all he was worth, and it was a wretched feeling pulling him in the opposite direction. By the time we arrived on the tenth floor the entire staff had heard about Rhyse’s bout with the IVs a few days prior, and everyone was nervous about repeating the incident. I did, however, take great comfort in being on the tenth floor—my ‘second home’ since Rhyse’s birth.  If there’s anywhere in the 12 story building I feel most comfortable and encouraged ...

The Fever that Changed the Journey Part Six: Weekend Home

Image
Weekend Home Saturday morning was an odd time.  I had two different documents to read and sign regarding cancer research, and donating the biopsy so others could use it to ‘gain more understanding’ of Neuroblastoma.  Cancer: I could hardly wrap my brain around those words.  Rhyse’s doctors were assuming he had cancer and someone already wanted a piece for research. I wanted to keep things as light as possible for the whole family’s’ sake.  Walking around in a trance wouldn’t help anyone, especially not us parents who knew the gravity of the situation.  So with this in mind I decided we would have an hour in the morning where each parent would take a child and do something; an impromptu date. I took my six year old daughter, Maggey, out for breakfast and then just drove.  She kept asking me where we were going, and I really didn’t know.  I just picked a direction.  As we were cruising along a familiar route I spotted an estate sale s...

The Fever that Changed the Journey Part Five: Cancer Certainty

Image
Cancer, 99% Certainty In a very kind, compassionate voice she relayed the news.  The CT scan had revealed a large, long tumor along his spine and sympathetic nervous system: “homogenous but abnormal posterior mediastinal soft tissue density.” We were to be admitted to the 7 th   floor for the night and begin the day with an MRI, more blood tests, and a urine catch.  “Don’t worry until you have to” were her words.  Yea, ok.  She slipped out the door and tears slipped out of my eyes…I was too tired to think clearly, or keep my wits about me.  It was 1130pm and my emotions were already worn to the bone.  I was alone and tired and I had no resistance to fear. When the doctor walked out of the room I melted.  I was suddenly thrust back to the day Rhyse was born, October 17 th , 2011 when an attending doctor told me Rhyse was “probably terminal.”  I never allowed myself to go back there emotionally, nor did I entertain the idea that ...

The Fever that Changed the Journey Part Four: The Dreaded CT

Image
The Dreaded CT Next on the list was a CT-scan.  What an ordeal that is.  The nurse came in the room with two, monster size cups of water laced with dye to slowly administer via Rhyse’s gtube.  I sucked the fluid up into one of my 60 ml syringes and ml by ml pushed each cup of water into his stomach, over the course of two hours.  At 7pm he was finally eligible for the scan, but no one came to get us.  After nearly an hour we were still waiting. If I had the energy I would have tracked down a nurse and inquired.   But I was too tired, and didn’t want to leave Rhyse alone on a gurney with side rails so large his entire body could roll through! Finally a nurse came in saying he over-heard someone on the phone discussing Rhyse’s CT.  Apparently the problem was IV number 8, the scalp IV. Up to this point no one had experience administering the CT-scan dye into a scalp vein: they didn’t know if there would a negative reaction or not. I didn’t e...

The Fever that Changed the Journey Part Three: Calling Nurse Number Four

Image
Calling Nurse Number Four Throughout Rhyse’s 20 months of life he has had numerous platelet transfusions, more blood draws than I can count, three bone marrow aspirations, a gtube placement, several sedated EKGs, and of course a sprinkle of unscheduled ER visits and nineteen days in the NICU. IVs are a ‘normal’ part of his life. But Rhyse’s body isn’t so obliging. Between Rhyse’s small stature, petite bone structure, hypersensitivity to pain, and veins as curly and winding as his gorgeous, red hair IVs are a terrifying experience.  What’s more, finding a nurse who can stick a vein and get a successful flush in less than three attempts is next to impossible. On this day Rhyse endured the worst experience with IVs to date.  Already screaming from the effects of a high fever, complete with shivers and tremors, nurse number one scanned his limbs over and over,  careful to choose the best site; his left arm.  Historically Rhyse’s left arm has indeed been the b...