A couple of definitions are in order, courtesy a medical dictionary at Teens Living With Cancer:
Neutropenia: Less than the normal number of neutrophils (leukocytes) or "polys" in the circulating blood.Everything has been low, okay, blood counts, platelets, polys, red blood cells, white blood cells, weight, energy, whatever. You name it, I didn't have enough of it. Nature of the beast.
Polys (neutrophils or granulocytes): The group of white cells that is important to your ability to resist bacterial infection. A "poly" count of less than 1,000 indicates less than normal protection and considerable risk of infection.
We're getting technical, though, learning new words all the time. This isn't just throwing all the medicine available at me hoping some of it sticks. There is science involved, here, culled from decades of research. That's why we notice when things change. It's not an obvious shift, but it does mark a difference in how we'll need to approach my treatment. Details matter. Precision matters.
We're all about numbers these days, watching the steady drop of so many different counts. We watch my polys closely. They're a leading indicator. When they dropped low enough, they announced that I'd become neutropenic. A colored sign was placed outside my door -- probably red -- to remind everybody coming in that they would need to take extra precautions. It's a simple thing: when I'm neutropenic, my body will not be able to fight infections by itself. I'll need lots of help to keep any infections at bay in the first place, but even more help, in case I happen to get an infection somewhere, to actually get rid of it.
So it makes sense that I've been getting fevers. They arrive out of nowhere, though, with increasing frequency and strength. They are very mysterious. Very sneaky. We don't now where they're coming from, but it makes perfect sense that I'd be getting them. It makes even more sense when you know that I'm not "just" neutropenic anymore. Those extra seven days of chemotherapy did a serious number on my internals. Whatever straggling polys I had left were quickly eradicated by the chemo. I've bottomed out. My poly count is a big fat zero. I've got nothing.
Every return fever, then, is cause for concern. It's why I'm hooked up to so many different antibiotics, why Cindy and Anne and Mary and every other nurse on the floor spend so much time in my room. They're constantly swapping out meds, monitoring my temp, trying to head things off before they get bad.
Things change when your immune system has stopped working.
We're more aggressive, now, about finding out what's been causing all of my fevers. They can't just show up on their own. They're symptomatic of something else: one or more infections, somewhere, kicking me when I'm already down. But where? Nothing is obvious. We've kept my Hickman clean; there are no festering sores or oozing puss around the entry site. When I take two deep breaths with a cold stethoscope on my chest, then two more with the stethoscope on my back (one more, please, deep again, deep breath, please) my lungs are clean and clear. We've started scheduling multiple x-rays to validate that there are no infections in my lungs.
I should expect these fevers, right, with the neutropenia and all, but while it's okay to expect them, my doctors absolutely will not tolerate them. Unless I'm able to magically stop them on my own (which I can't), then everybody will continue to search relentlessly for the source. It's not good enough to just keep on keeping on. Demoral helps, almost instantaneously, with my convulsive chills. Tylenol manages to ease my throbbing headaches and lower my high temps. Together, they form an effective one-two punch against my fevers, but they don't do anything about eliminating the source.
That's what my doctors are after. That's the mystery they want to solve.


DEAR SIR,
MY 5 YEAR OLD SON HAS BEEN DIOGNISED FOR ACTUE LYMPHOBLASTIC LEUKEMIA.
HE IS BEING TREATED AS PER PORTOCOL - MCP 841.
HE HAS ALREADY BEEN GIVEN THE INDUCTION PHASE AND NOW THE TREATMENT OF CONSOLIDATION HAS BEEN STARTED FROM YESTERDAY 26TH MARCH.
I WOULD LIKE TO HAVE MORE INFORMATION AS TO THE FOLLOWING.
1.WHAT RESPONSE WE SHOULD SEE IN THE CHILD DURING TREATMENT.
2. WHAT WOULD BE THE SIDE EFFECTS
3. WHAT PRECATIONS SHOULD BE TAKEN TO PREVENT INFECTION DURING CONSOLIDATION PERIOD AND WHAT MEDECINES IN PARTICULAR AND GENERAL SHOULD BE ADMINISTERED TO PREVENT INFECTIONS.
4. IS RATIATION REQUIRED TO BE GIVEN AFTER THIS TREATMENT AND WHEN THE SAME SHOULD BE GIVEN.
5. WHAT ARE THE LONG TERM AND SHORT TERM EFFECTS OF THIS TREATMENT
6. WHAT IS THE SUCESS RATE.
WE WOULD ALSO LIKE TO HAVE A OPINION ON THE DIOGNISIS AND TRETMENT AND REQUEST YOU TO SUGGEST US THE BEST POSSIBLE HOSPITAL/PERSON AT ANY POINT OF THE WORLD FOR THE SAME.
(PLEASE PROVIDE POSTAL ADDRESS/E.MAIL ADDRESS, NAME OF CONTACT PERSON WITH TELEPHONE NO.)
KINDLY ADVISE US YOUR INDIAN COUNTER PART ADDRESS WITH DETAILS OF CONTACT PERSON AND TELEPHONE NOS FOR PERSONAL MEETING.
REQUESTING YOUR COOPERATION AND EARLY RESPONSE.
THNAKING YOU,
MR GIRISH. B. LODAYA.
13, MOHANLAL MANSION,
264/C L. N. ROAD,
MATUNGA.
MUMBAI - 400 019.
INDIA
TEL : 91 22 24142643
MOBILE : 91 98202 92949
E. MAIL : girishblodaya@hotmail.com/primex1@vsnl.com