April 19, 2009
Just When I Thought I Was Out of the Woods . . .
Posted by booklady under Uncategorized[10] Comments
. . . my ankle says, “uh, not so fast, there, Booklady.”
I really had thought that this next post was to be my contribution to all the good news of healing that’s going on AchillesBlog.
I too could do my towel toe scrunches, marble pick-ups and windshield wipers easily, and being assigned to only 5 minutes on the recumbent bike barely got me sweating. After 2 weeks of four physical therapy sessions, I could walk on to a BOSU with my bad ankle, and rocking on the BAP board with 1 pound weights felt good. My PT file was running out of lines to list the exercises I was doing — after all, it only HAS been four months! Like a puppy being trained, I was taking it all in except for those 30 challenging calf raises. My exercise classes at the Y were modified not to stress my ankle, and after several sessions of abs and upper body work, my body felt as if it were waking up, feeling alive again.
All the while, my PT and I were very cautious and conservative to keep waiting until my then-scabby wound was truly closed and and to be given a final clearance from my Infection Specialist to undergo ultrasound therapy. I was really looking forward to that two-week follow-up with the ID doc.
Between my Friday and Tuesday PT sessions, however, out of the blue, a discharge oozes out from under my hardened scab, and I pray that it stops there. It doesn’t, and through the weekend, my ankle swells and turns darker by 10 a.m. My scar area feels warm and other the sensations from previous infection bouts felt all too familiar. My last PT session was cut short because my wound truly looked angry and my therapist did not want to aggravate it any further. Needless to say, I had to make that call suspending future PT appointments until further notice.
That was about a week ago, and it took this much time to scrape myself off the floor to begin to share it and much more to write and reflect about it. I often cried myself to sleep in the dark these past few days, as I was truly feeling that I was in the shadows of the valley of death.
I returned to my ID doctor in pain, he looked at his pages of notes of my near-weekly visits since February. He determined that I be scheduled for a bone scan to confirm that my infection had not reached my bone. I was able to get a hospital radiology appointment on Good Friday and had to go in two phases.
During the morning phase, I was put under an imaging machine which took pictures of my ankles every five seconds for about 15 minutes, and they already revealed the hot spot where my infection was. I was then injected with a low dose of radioactive isotope and instructed to return in three hours when my bones would glow under imaging. And glow I did. My hot spot showed brighter and it was very close to my bone. The radiologist had me linger a few more minutes to take additional x-rays of my ankle to confirm his suspicions.
Though it was a great Easter weekend, it was a long wait to call my ID doctor on Monday, and when I did, his nurse told me to come in immediately. In my gut, this was not to be good news.
I was his first appointment the next morning when he told me I had early stages of osteomyletis and confirmed I had a bone infection resulting from my lengthly wound infection. Sigh . . . my mother’s and other caring ones’ warnings to ”take care that your infection does not reach your bone” reverberated in me, as I was indeed not well, literally, to the bone.
Doc told me the antibiotic therapy for bone infections was intensive and was not to be any different for me. I started these processes this same day.
- I have a foot-long PICC line (a fancy intravenous tube) coming out of my left arm. It was inserted under hospital conditions by a radiologist and his team of nurses. It follows one of the major veins up my arm and leads to my heart. It was amazing to watch the live x-rays of it being done. I saw my ribs and my heart beating in real time (I do have a heart after all! God, please protect my little heart!). The tubing looked like a parabola or the St. Louis Arch in me.
- Rather than being admitted into a hospital, I was assigned a home nurse who walked me through my intravenous process. Her handout listed the 21 steps I needed to do at each dose administration, which will be exactly every 12 hours, twice a day, for the next 6 weeks (or 8 weeks, if my bones are not cooperative).
- My home nurse brought her pharmacy with her. I have syringes of saline and heparin, boxes of tubes and alcohol swabs, bags of Vancomycin antibiotic in my refrigerator and sterile syringe caps. I have learned how to disinfect my work area. My day now revolves around these doses, or infusions, as they require about 2 hours of drip time.
- She’ll be visiting me weekly to draw blood samples to make sure my kidneys are functioning well, to change my PICC line and to deliver supplies.
So as not to bore you with the mundane details, I’ve learned to make light of the observations I found in this process:
- Although my infusions are supposed to take 90 minutes at 10 drips per 10 seconds, my first one took 4 hours because I had an allergic reaction to the Vancomycin. I felt a huge hive attack coming on, with severe itching on my scalp, face, chest and joints. I had the red (wo)man’s syndrome and learned what a real hot flash felt like. I had to reduce the drip rate to 1 drip every 3 seconds. My nurse had to observe me for our full consultation and did not leave until 8 p.m. that evening. She must have been climbing the walls. Sorry!
- To counteract the Vancomycin reaction, I have to take 2 doses of Benadryl 30 minutes before each infusion. The irony is that I have to wake up at 3:30 a.m. to take the Benadryl which makes me feel loopy for the next 12 hours. Yes, I’m not good for much anything at work and home. Driving under this influence is not advisable. I’m trying to wean myself off these bennies but paying for it with longer infusion times until my body gets more adjusted.
- The doc says that there is another drug available if I’m unable to adapt, but because bone infections are treated “blindly”, Vancomycin treats a wider range of bacteria than the other drug. The other drug also requires thrice-daily infusions and very frequent diarrhea attacks. I think the vanco will be my drug of choice.
- By the end of the treatment, I will have had 84 infusions and 168 hours of drip time, not including loopy time. This is more than a part-time job!
- Though it’s tempting to sleep through the infusion, I have to be lucid at the last drop because if I allow the IV bag to drip until dry, the pressure will then cause my blood to be drawn into it, and I don’t intend on being a blood donor at this time.
The photo above is of me and is my newest dance partner. I haven’t named him yet. We’re quite clumsy together at our 4:oo a.m. AND p.m. dance sessions. We keep waltzing into door posts, ceiling fans and light fixtures. Though the tall and slender type, I’m finding out he’s quite a drip and a drug user; it would be great if he had wheels. I’m already trying to nicely figure out how to pass the time away on this lengthy, obligatory blind “date” — maybe over a jigsaw puzzle, beginning to watch LOST from Season One or Korean soap operas, scrapbooking, reading with my feet up, Face Booking, blogging, meditating or learning Italian, perhaps?
These are the things I know:
- My hubby’s quite the ham when he asks me, “did I shoot anything up yet?”
- The medical field truly produces a lot of plastic waste, which I have to learn how to properly dispose of.
- I’m so thankful for my hospital chaplain friend who walked to the doctor’s office to be with me when I received my bone’s prognosis. My hubby was out of town on business and visiting our oldest son.
- My friends who have known of my achilles journey shake their heads in disbelief when they see the newest bandage on my left arm and ask, “What now?” What they don’t know is that I wrap BOTH my left foot and my left arm with plastic at each shower. Put together with a shower cap, I become Plastic Lady. I’m quite a sorry sight to see
- When all this is over, I definitely will get over my fear of water and learn how to stand-up paddle board.
- My appointment with my ortho this week will be interesting, as I had my radiology report sent to him too. I’m really one for his case studies.
- I’m taking the next two weeks as medical leave — three, if need be — thanks to my work partner who holds the fort so well, especially at this time of the school year. I am not allowed to lift any weight, including textbooks, on my PICC arm. I guess carrying books are now a workplace hazard for me. I did bring home work that I can do on-line.
- I’m still thankful for good medical insurance that keeps me in good care, though this round will require a $200 out of pocket co-payment per week (there goes the tax refund).
- I barely could keep it in when my ID doc told me he was praying for me, as is for those closest to me. I’m receiving it intravenously and divine interventionally.
Cheers, Aloha and God bless until my next post; you know where I’ll be at every 4:oo hour –
Booklady



