Enough ranting, now for what else is going on:
- I am having bladder problems yet again. Urgency, frequency, some dribbling. It's been pretty annoying, but inconsistent. This has been going on for over a month, yet Dr. Rivkin can't find anything wrong. I has told him about it and that's why he rushed to order my PET scan. He kept joking about how I was getting older and needed diapers and this really pissed me off. I am 30 and should not be having bladder problems. Especially since this was one of the symptoms of my cancer. But the PET SCAN SHOWED NO EVIDENCE OF TUMOR, which was a relief. He then ordered a culture of my urine to see if I had an infection, but that was negative. So as of now, he says that my symptoms may be a result of damage and fibrosis from radiation. I am still skeptical because I thought that this area was irradiated as much as everything else. Plus I thought that these changes would occur much later, rather than after only 2 years. But he explained that symptoms can occur anytime following treatment. I already have constipation most days, which I never had problems with before. Anyways, he brushed the issue off as no big deal, which was frustrating. So my next plan is to talk to my primary care doctor and get a referral to a urologist, because I think that's the proper route for my insurance to pay for it. It's cancer-related though, so I don't know why Swedish can't handle it. Another insurance issue, go figure
- Avastin side-effects.
- My urinalysis showed a small amount (1+) proteinurea, or protein in my urine. Doc said that I was dehydrated and needed to drink more water. He will continue to monitor it with pre-treatment pee tests, but presently it is low-grade and may be resolved with hydration. Here is what the Avastin website says about proteinurea:
- Proteinuria/nephrotic syndrome (Warnings and Precautions)
- The incidence and severity of proteinuria are increased in patients receiving Avastin compared to controls
- Grade 3 and 4 proteinuria ranged from 0.7% to 7.4% across clinical trials
- The overall incidence of proteinuria (all grades) was only adequately assessed in AVOREN, in which the incidence was 20%
- In AVOREN, median onset of proteinuria was 5.6 months (range 15 days to 37 months) and median time to resolution was 6.1 months (95% CI, 2.8 months–11.3 months). Proteinuria did not resolve in 40% of patients after median follow-up of 11.2 months and required permanent discontinuation of Avastin in 30% of the patients who developed proteinuria
- Nephrotic syndrome occurred in <1% of patients receiving Avastin in clinical trials, in some instances with fatal outcome
- In a published case series, kidney biopsy of 6 patients with proteinuria showed findings consistent with thrombotic microangiopathy
- Monitor proteinuria by dipstick urine analysis for the development or worsening of proteinuria with serial urinalyses during Avastin therapy. Patients with 2+ or greater urine dipstick reading should undergo further assessment, eg, a 24-hour urine collection
- Suspend Avastin administration for ≥2 grams of proteinuria/24 hours and resume when proteinuria is <2 g/24 hours
- Discontinue Avastin in patients with nephrotic syndrome. The safety of continued Avastin treatment in patients with moderate to severe proteinuria is unknown
- Hypertension: My blood pressure readings are pretty inconsistent. At my appointment I had a reading of 139/78- my highest yet. Yet, before my infusion it was back down to 110/68. I've never experienced "white coat" syndrome- where readings are higher than normal when patients are in the exam room. I'm going to dig out my blood pressure cuff and start taking it myself.
- Slow healing: This month I went camping 3 weekends in a row and developed "camping feet" (or dirty hippy feet) from going barefoot, hiking, mosquito bites, and just being around scratchy plants and rocks. I now have a lot of lovely cuts, bruises and callouses on most of my lower extremities (Mark you would run from me if you saw them). Anyways, I had a really really itchy mosquito bite on my ankle, which my big toe scratched raw while I was sleeping. This spot became an ugly blue-purple-red splotchy ulcer (yet painless) which is still healing. It's the kind of cut you would expect from a patient with diabetes or arterial insufficiency (lack of blood flow to bring healing white blood cells and oxygen necessary to make new cells- exactly what Avastinbandaid and my little 5 & 6yr old noticed and became obsessed with my boo-boo. Every one of my other cuts are also healing pretty slowly, so I have awesomely hideous camping feet.
- Vision: I've had no more problems from the Tamoxifen. Only those two incidences of blurriness months ago. BUT, after developing a lingering summer cold with 2 weeks of laryngitis, I also had conjunctivitis (pink-eye). I have a couple days of antibiotics (prescribed myself) left and then I can take off my awful glasses and wear contacts again
- Sweet tooth: It's back, but now I believe it's completely unrelated. I read dozens of posts from other survivors with taste changes after chemotherapy. Tons of people who went from salt to sweet like myself. They never tell you these things in the clinic- thank god for the Internet and great network of survivor blogs! Unfortunately my teeth are taking a toll (see previous article), and I am planning on visiting an urgent care dental clinic in the next few days to get a filling for a previous cavity and relieve a toothache :(
That's it for this long post- I'll post an update on what's going on in the rest of my life soon!
