Posts Tagged ‘help’

Adventures in Oncology

Wednesday, November 11th, 2009

Things are going ok. Isaac might even be doing better than I am at the moment.

I wish I could say I was the calmest, sanest, got-my-act-together-under-stress person you could find. Sadly, that is not the truth. Now, ’tis true that in acute moments of crisis, I can be steely and reasonably focused (other interpretation: numb and on automatic pilot). I wait until the worst is over before I start crying. Protracted crisis response, however, is not my forte. I might normally say, that’s what Xanax is for, but as long as I am the household’s chief chauffeur, Xanax is not an option. You do not want me behind the wheel while on Xanax.

Anyway, we’re muddling through. Isaac has radiation therapy five days a week, Monday through Friday. My understanding was that it will go on for maybe two months. A nurse I spoke to yesterday (who was handling paperwork, not working on his case) said they don’t do it for that long. I hope she’s right. Then again, he doesn’t have a run-of-the-mill cancer. Damn my taste for exotic men.

He had one round of chemotherapy while in the hospital. That goes on a 29 day cycle (or a 32 day cycle–I’m not always sure what the oncologist is counting as Day 1). The next round will begin the day after Thanksgiving. Great–Black Friday. How the heck am I going to tell the bosses I need to go with him?

Chemo is a bit of a production. A lot of people go in for a few hours, get hooked up to an IV, then go home. What they’ve got my boy on is a drip that is continuous for four days straight. However, they are going to do this as an outpatient. He’ll have some sort of regulating dispenser on a belt pack that he’ll wear round-the-clock at home.

However (lots of “howevers” in Oncology Land) in order to do the chemo, he has to go into the hospital (next week, I think) to have what’s called a PICC (Peripherally Inserted Central Catheter) line inserted.  It’s a tube they put in his upper arm that runs all the way to the heart.  He had one in the hospital, but they removed it before he came home. This one, they said, will be smaller than the one he had before. It might be left in indefinitely.

We learned a lot about this yesterday (Tuesday) at the oncologists’ office. Now, that’s a place I would not like to work. Don’t get me wrong, the staff is wonderful. They have been without exception pleasant, kind and caring. Yesterday, I came in with a bunch of paperwork that I needed for my family medical leave right at the deadline to submit it. The nurse who filled it out was pretty stressed by the rush, but she took care of it for me while I stood there. I kept apologizing for waiting until the last minute. She kept telling me, “I know you’re under a lot of stress,” while I stood there putting her under stress. I was so grateful I wanted to cry.

What gets to me is that the place is so crowded with patients. So many people with cancer! All those lives disrupted, not just the patients but their families, too. I just feel drained when I there. Poor magical skills on my part; you’d think by now I’d be better at shielding. I’m not, I admit it. I get overwhelmed by the energies of people around me.

Isaac, bless him, says I shouldn’t go if it is too much. Not a chance. It’s really important to me to be there. You’re given so much information at these medical meetings, not all of it sticks. If I have to then get it second-hand from Isaac, more data gets lost. I went through that when he was hospitalized and I was too sick to visit him. He was sick as a dog with all the infections, and trying to retain all they were telling him; I was sick as a dog on the other end of the phone trying to understand what he was telling me, while he wasn’t always remembering what he told me and what he didn’t. You need two sets of ears, at least, just to process all this stuff.

So, the oncologist says it may only take two-three months before he’s considered to be in remission. The obvious cancer is responding well to the treatments. The wild card is what else may be going on in his pelvis. The oncologist wanted him to get a PET scan, but the PET scan people said at this stage, there’d be false positives so don’t do it, but we couldn’t get hold of our oncologist because it was a weekend so another doctor at the practice said cancel the test, but our main doctor said yesterday it would have been ok, but now for sure it’s too late, so she doesn’t know what else may be happening … see what I mean? Medicine is art as much as science.

Day to day, nothing terribly exciting goes on. We go to medical appointments once or twice a day. Maybe we’ll go walk a little if the weather is nice, then he comes home and naps.

He has trouble eating because of mouth sores. Also, he’s on an extremely restricted diet. Everything has to be low fiber and low residue. That means all the things we’ve been conscientiously eating for years–fresh fruits and vegetables, brown rice, whole grains–is mostly off limits. No skins, no seeds, white bread, white rice, bland, bland, bland. Yep, he’s losing weight. The struggle is making food he can eat that has some nourishment for both of us. One strategy for keeping weight on cancer  patient is to feed them milkshakes and all the other high-sugar treats you normally wouldn’t indulge in every day. However (lots of “howevers,” remember?) he doesn’t tolerate cows’ milk all that well, which puts limits on ice cream. Still, we’re going to get a blender today so I can make him smoothies with bananas and and soy ice cream. Maybe tofu, too. If I can get out of this funk enough to bake, I’m thinking banana bread and zucchini bread. I’ll have to peel and seed the zucchini, but that’s no big deal. Of course, I normally bake with whole grain flours. Not now. Now it’s gonna be white, white, white. Did I mention I don’t digest wheat very well? Another “however.” And I’ll have to put the brakes on myself so I don’t get fat while he’s getting skinny.

Isaac, being by nature more upbeat than I am, did take one dramatic, proactive step. He was already noticing his hair and beard coming out, so he went to the barber and had it all shaved off. I thought he was just going to get it cut very short, but nope, out came the razor. He’s so cute when he’s impulsive.

before haircut 1before haircut 2bald 1bald 2

I have to get myself together enough to go back to work soon, or we’re going straight to the poorhouse.  Donations welcome. And thanks for all your good thoughts and concern. More later as I think of it.

Isaac’s Illness

Monday, October 26th, 2009

I’ve been letting Isaac take care of neopagan.net for so long, I almost forgot about our own blog. But he’s not available to update y’all, so it’s my turn.

If you haven’t already heard from our Facebook page or other sources, Isaac’s been in the hospital since last Wednesday. He’s been diagnosed with colorectal cancer, with tumors in his rectum.

This is a little different than the more common type of colon cancer. In fact, he had a colonoscopy last year and had no polyps or anything like that. What he has is called squamous cell carcinoma—more like a skin cancer—which accounts for less than 5% of colon cancers.  Yes, my darling really is a rare pain in the butt.

On the upside, it’s very treatable with chemo and radiation, so surgery may not be necessary. This is a good thing, as surgery in that location is not easy to repair.

Right now they are treating him with heavy antibiotics. Cysts, which had formed around the tumors, were causing him a great deal of pain, which is what got him to the doctor to begin with. The cysts may need to be drained, but they need to get his infections reduced before doing anything invasive like that. However, they are shrinking now and his pain is much, much reduced. He’s having more tests on Tuesday and Wednesday to make sure the docs aren’t overlooking anything. Also, his lung function is down, and they want to determine if he has COPD, which would be a permanent problem. I’m hoping he’ll be home Thursday, but we just don’t know.

Many people have asked how they can help.

Absolutely send your good wishes and healing energies. Concentrate on shrinking the tumors, increasing his stamina, and increasing his lung function. While you’re at it, send me some strength. Along with this stress, I’m getting over the flu, and until I do, I can’t even visit him in the hospital. Needless to say, I miss him terribly.

Yes, we have health insurance from my employer, although, of course, it won’t cover everything, and won’t cover lost income. Since I work on commission, and haven’t been working, my November income will be abysmal. Thus, if you feel moved to hit that “donate” button, we’d be very grateful, as will our landlady.

We’re trying to keep people up-to-date on our Facebook page, but if FB isn’t your thing (I’ve only been on it for a few months myself) I will also post updates here. Yeah, right here, the sensible place to put it!

Adopt an Elder 2009

Thursday, January 1st, 2009

I’ve just spent some time updating an essay on this topic. Here’s a bit from the opening:

Every local Neopagan community has one, two, or more older members who may be struggling to survive on a day-to-day basis. Whether thay are seniors or Elders, and regardless of what tradition they belong to or teach, or what local “witch wars” they may have been part of years ago, now they are getting old and needing help to get by. If they are Elders, the main reason for their poverty is usually having devoted most of their lives to serving a Pagan community instead of earning their livings in nice middle-class jobs at corporations with good retirement plans and health coverage. Even worse, sometimes they did have such jobs, and juggled holding them down with serving a community, and then got downsized and/or had their pension plan looted by the top executives. Either way, like most Neopagan clergy, the odds are high that they are living at an economic level dramatically lower than most of the other Pagans they serve or have served, often for decades. And, of course, there are plenty of Pagan seniors around who may never have been leaders or teachers, but who are still struggling to keep their heads above water, especially in the current economy.

January through March are the worst months for Pagan Elders. The weather is cold, there are few (if any) festivals to pay them for teaching, authors’ royalty checks from the Yule shopping season don’t arrive until late March or April, any food gifts from relatives have run out, and everybody in the mainstream culture is broke (or feels that way) . What does or should this mean to non-elderly Pagans? It means that winter is the most important time to check on your local Pagan seniors (and any Elders living in your area) to see how they are doing. Is their rent or mortgage paid, or is their landlord/the bank trying to evict them? Is there heat in their home? Is there food in their pantry? Is their walk shoveled?

For the rest of this essay, visit Adopt an Elder! I also made some updates to Our Blatant Hucksterism Page.