Good Times

Six years ago we rescued a 5 month old Bernese Mountain Dog. Greta has been an absolutely wonderful companion all these years. Now, she has an unidentified mass in her chest and the clock is running down.

We are working to make these last months good times for her. We spent the weekend taking walks, having playdates, and visiting dog parks. She’s a strange girl. She doesn’t play with toys and barely plays with other dogs. Her entire doggy world is wrapped around Alex. She will even delay eating for a few more minutes of petting from him.

She’s a worker. She loves to walk in her backpack and I regret that we never trained her to pull a cart or wagon. She was bred to pull and we had to be choosey about her collars and harnesses because if they gave her the right feedback, she’d lean into the chest piece and pull you right off of your feet. It happened a lot when she was little and I was pregnant with Jujubee.

She’s a mellow love of a dog, and when the time comes she will be so so missed.

Family History: Uncle Hank

Our family has quite a few interesting characters. Whose doesn’t? Contributing to this is a persistent trait of mental health … quirks. My Great-uncle Hank was one of those quirky individuals.

When I knew him he was a sober and self contained older gentleman whose mother, my great grandmother Nell, lived with him. Nell was a firecracker, but there was always something a little odd about Uncle Hank. He was always thrilled to see us kids, but he just wasn’t a natural with us. That didn’t stop him from bribing us with his stash of hard candies until he was a favorite. Secret candy with no strings? Definitely cool.

I found out as an adult that the candy was my mom’s fault. Uncle Hank smoked like a chimney until Mom told him he wouldn’t get to see us unless he quit. POOF. He traded the cigs for an endless supply of Cherry and Butter Rum Life Savers. As I understand it, a generation earlier he quit drinking with the same efficiency. My granddad kept pulling him out of bar brawls when he came traumatised home from WW2. Eventually he succumbed to threats that he wouldn’t get to see my mom and uncle unless he dried out. So he did.

He was a seaman in World War Two, assigned to work on three different ships in the Pacific Theater. He survived the sinking of two of them. This is information I’ve gleaned, mind you, and is integral the image of the man as I saw him. It occurs to me as I wrote this that it may not be completely accurate. I don’t know what work he did aboard ship. I’m not sure anyone does. What information we have about it comes largely from records found in his footlocker that was uncovered when my great-grandma passed away and her house was sold. Looking back on memories of this time I was absorbing conversations the adults were having while my brother and I explored the upstairs of a house where we had never been allowed before. We were little I can’t have been older than 7.

Hank came home from the war with a tattoo, a drinking problem, and shell shock. We’d call it PTSD now. Then he was shell shocked, and a drunk, and maybe schizophrenic. Likely, he had trauma related psychosis having something to do with being on multiple battleships as they sank. He was in and out of hospitals, sometimes for long stays, until my mom was an adult. Family mythology says this included spans in the kind of hospital where they put lithium in the salt shakers.

After great grandma passed,we saw less and less of Uncle Hank every year. I didn’t know why until I was 18. We came into town for a visit; the first face-to-face visit in five years because we’d moved rather far away. Instead of the pleasantly stoic, awkward man I remembered, I was confronted by an angry soul. He yelled at my mother for things I’d never heard of and in some cases for things that never happened. He called us names, but never looked at us, and he left. It was heartbreaking. PTSD had given way to paranoia and dementia.
He passed away in 2012. There wasn’t much of a service, and I didn’t attend it. I was too sick myself at that point.

We are all more than our diagnosis. We are more than our treatments. I didn’t know Uncle Hank was sick until I was an inquisitive teen. It didn’t occur to me until even later that he lived with his mother because he couldn’t live alone. He was just him, and I loved him.

Routine

Alex’s semester is over! While we wait for his grades to arrive, we are planning our time. The a babies are used to being home alone with me, and Himself is used to being away and on his own all day. He’s spending this week home with us, then starting next week he’ll spend 3 days weekly at the library doing job hunting and prepping for his first actuarial exams.

Yesterday we sat down and planned the summer semester routine. Having a routine planned, even if we strain against it or are challenged by it, lets us and the children know what is expected of us at any given time.

We don’t tightly schedule the routine. Daily, we set up who wakes up at what time, and what needs to be done for The Morning Routine. After that we set when is lunch time, when is dinner, and when the kids head to bed. Weekly, we settled what days and times Alex with be studying and what the general plan is when he’s home. There are real challenges to his doing school full time, so we are trying to take maximum advantage of the positives in the situation. He will be taking the girls for outings once a week, giving me a chance to have some quiet, personal time to do whatever without their sweet fingers all up in my productivity.

How do you deal with the time one your hands?

Gratitude: Vacation

I am so grateful that things came together for this trip. My sister-in-law let us use her timeshare condo without charging us the fee. We found a cheap hotel for the mid-trip overnight, so I didn’t even have to boondock camp between Denver and Corpus Christi. Once we were there, it was a beautiful rhythm of visiting the pool, the beach, the fishing dock, and relaxing with videos. And rather a lot of eating.

My kiddos fell in love with fishing, which will never not feel shocking. My suburban princesses found a friend on the dock who taught them to reel, let them stroke the teeny fish he caught, and then stood with them on the dock for hours when the fish weren’t biting. Mr. Rocky was an absolute saint. He helped us with gettingout dusty rental rod into functional condition, teased us over using neon pink artificial bait, and then afterward sent us a card in the mail thanking us for sharing the dock with him.

I’m grateful for the last day we went to the beach, when the water and sky were so blue I thought I was in Florida. The wind was light and pleasant. Rosebud got over her fear of the surf when it was calm and rippling instead of stormy and gray. Jujubee made a friend with a little local girl and built a pair of excellent sand castles.

I’m grateful that this was my month to have a mild round of PMDD symptoms. I got home with my sanity essentially intact, even though I was on the road for what is the most acute phase. I didn’t break with reality at all! My worst symptom was an increase in social phobia that had me fleeing the community pool when the neighbors got too chatty.

Shoulding All Over Myself

We are just back from vacation and things are particularly chaotic. I have an idea that I should have handled our return differently. I should have done more school while we were away. I should be resuming our routine with rigor. I should be cooking more and more often, and sharing it with our friends, who are ill.

I should be better.
I should eat better.
I should workout more.
I should engage with the kids more.
I should clean more
I should be more like other people.
I should
I should

I call this way of thinking “shoulding on myself,” because it creates all of this tension to live up to impossible standards. “Should” implies consequences of not doing it. “Should” implies orders that have come from outside of myself. It is a terrible habit. It breaks up the day into chunks of false urgency and harsh self-judgement.

Sick Kidlette

Rosebud is having a procedure done under general anesthesia today. She’s having some dental work done and also her second endoscopy monitoring her EOE. This is her second endoscopy in 2 months.

She also has a condition called Mastocytosis, meaning her body makes too many mast cells. Those extra mast cells can result in anaphylactic reactions to very odd stimuli: for us this includes ibuprofen, temperature changes, and stress. Because of this, general anesthesia is extra risky. She’s on 3 extra meds to keep her from reacting today and I’m sitting in the hospital waiting room twitching. She didn’t have a reaction last time, but I have this sense of dread when I’m not able to personally monitor her.

Having a sick kiddo is worse than being sick myself. First, Rosebud is NOT a stoic patient. She’s 2, for heaven’s sake, and already greets the sight of a person in scrubs by screaming “No pokes!” More subtly, though, when Rosebud and Jujubee are doing poorly I have to ask myself what triggered them. Did I miss something and accidentally expose them to a known trigger? Are they developing a new trigger? Is this the dreaded idiopathic reaction? I can be philosophical about my health, but I have no calm at all about theirs.

Ordinary Times

Nothing special to report today. The dog lives on, sweet girl. The weather is increasingly spring-like, though we could still get snow in Denver before the month ends.

My energy is strange today. My doc suggested that I shift one of my meds to AM dosage instead of PM and it does seem to make a difference. I’m not more awake, and inertia remains an hideously powerful force in my life, but there is a meditative quality to my lethargy that is quite pleasant. Instead of being worked up over what I should be doing, I’m able to simply rest. Once I do get my butt moving I’m pretty productive.

Take today. I got up at 0845 with the girlies, arranged breakfast then laid down on the couch to doze while they ate. I was up and down, alternating between taking care of the kids and dozing on the couch until 1130. Then I got dressed, wrote a blog post, started the laundry, made lunch, played a very small amount of a video game I haven’t indulged in in eons, and now that the girls have eaten I am back at writing. I feel strangely good. Small changes in routine, med management, and lifestyle can really make huge difference.

A week ago, admittedly during the worst part of my cycle, I was self injuring and crying uncontrollably. Now i’m contemplating a walk with the kids, grocery shopping, and speaking to the neighbors. My girls have made friends with the girls next door, which is totes adorbs, but I have not yet managed to get to know the parents. I’m not good at small talk and the idea of getting to know them is terrifying. Today, though, I’m able to contemplate it a little.

Pill Box Day

For those of us on a cocktail of meds and supplements, pill boxes can really help ensure that we actually manage to take everything everyday. I have a system of 7 boxes, each with 4 compartments. I use one box for two days worth of pills; morning and evening. It used to be that I would fight the fight to keep them filled myself. Now Alex fills them for me, bless him.

Pill Box Day, when I would lay out all of my prescriptions and be confronted with the reality of my various diagnoses. I would get sucked into a vortex of excessive introspection, thinking and recriminating myself for being a sick person. I knew that this happened, and so I would avoid Pill Box Day for as long as possible. My old system could hold as much as 60 days of meds, if I could coordinate my supplies that well.

Three to six weeks in between sessions still wasn’t enough, though. I would end up off of my meds for days or weeks, and we all know that is no help at all. How does your family support you taking your meds? Do you have a special way of getting through yours version of Pill Box Day?

Inevitable Defeat

I’ve missed a week of posting. I got overwhelmed with getting ready for my mother-in-law’s visit, then I fell into the trap of thinking that this hurdle is a complete defeat. I haven’t completely gotten past it yet, and the total lack of people interested in reading here doesn’t help. I may have something to say, and the internet may give me a voice, but that doesn’t make anyone want to hear.

Gratitude Practice: Creative Outlets

I am so grateful that I have so many excellent creative outlets available to me. I write, here and elsewhere, when I’m able to focus. I sew on my machine or by hand. I quilt when I’m too foggy for the others, because chiku chiku stitching requires more meditation than active thought. I paint and color with the kids. I crochet and weave irregularly. I play tabletop role playing games when I need a more intensive escape that what I get from reading. I mend, I crochet, I knit (poorly), I weave (infrequently). I am blessed to have a spirit that finds comfort and completeness in these tasks, and blessed to have the resources to be able to create.