Category Archives: compassion
I’ve been writing this blog in my head all week. I just can’t seem to find a theme I can stick with for more than a paragraph or two. Or, if I’m honest with myself, a sentence or two.
Regular readers will know a friend of mine passed away and her memorial service was this last weekend. I’m in the second or third tier of mourners. Tier one – the decision makers and those truly being overwhelmed with waves of grief. Tier two – the organizers. The ones asking the decision makers what they want and striving to make it happen. The people whose grief makes them prickly, rude, short-tempered, unclear and perfectly sure they have everything in line because keeping things in line is how they cope. Tier three – the support system for the first two tiers. The listeners. The worker bees. The one’s who are distant enough to put off their mourning until it’s convenient (at least a little more effectively).
Having the memorial made it real. That’s part of the point of course. Being gifted some mementos makes it real and personal (which it has always been, but denial is so convenient). Having nothing left to “get done” means there is no longer an excuse to put off the emotional response.
I’m sure the death certificate doesn’t say my friend died of cancer. But it is certainly the undiagnosed and untreated cancer that caused the heart failure.
I’m grateful my friend didn’t die alone at home, but had people around her who cared about her.
I’m grateful my friend went quickly, all at once, rather than having to slowly and painfully waste away.
I’m grateful her very elderly mother dared to get on a plane and put herself in the hands of a community of her daughter’s friends whom she had never met.
I’m grateful for the presence of people who spoke about areas of my friend’s life that I wasn’t privy to.
I’m angry that a cancer that large and impactful goes undiagnosed for so long. I’m angry that the complaints of a large woman (both exceptionally tall and not willowy) are dismissed by our medical community as always being about weight. I’m upset that no matter how good the insurance you’ve got, unless you know what to ask for medicine is practiced according to the insurance company guidelines rather than actual medical need.
I had breakfast today at Gilda’s Club. It’s a sort of monthly social event. At Gilda’s I am surrounded by people living with cancer, many of whom know they have no hope of a cure. I am always buoyed up by the spirit of care and acceptance. I am reminded that there is pain and sorrow, but also hope and joy.
I’m putting one foot in front of the other. Step by step.
The only thing that is certain is that things will change. When I was up at my parents (see last week’s blog) one of the things I did was help my Mother send sympathy cards. Her brother’s father-in-law passed, not unexpectedly. Thing is my parents actually had a relationship with the in-laws and my Mom still hasn’t quite reconciled with being unable to physically show up when these things happen. And of course, given the age group, they happen with some regularity.
The other passing that warranted a response from her was the second husband and truly life partner of an old friend. Again, this was not an unexpected death. All the same it’s the first time I’ve ever heard my Mother admit, “I don’t know what to say.” The reason she doesn’t know is because she’s not there. My Mother always made a point to BE THERE for the people she cares about.
Last week another friend, my age, died suddenly and unexpectedly. This has left many people in my community reeling. I’m doing what I can to show up.
There have been plenty of times in my life when I couldn’t show up. Sometimes I’ve been physically unable to. I have lost friends because I didn’t show up when they needed me. My physical limitations (up to and including being in the hospital) apparently were not an adequate salve for the feeling of betrayal.
Occasionally I haven’t been able to show up because some obligations trump others. I’ve always been proactive about trying to make sure that there is either notice or some kind of substitute in place. I’m sorry, sick kids and other family needs have to come first. Everyone who knows me well has heard me bemoan being unable to hold a “real job” because I am on call to Orion’s medical needs. Still they are surprised and hurt when that same issue comes up and impacts “sure I’ll help you with that project”.
The thing about showing up for other people is that when you do what you can, when you can sometimes you get lucky. Grief is an odd thing, and it doesn’t just stop. Sometimes that card that gets sent months later comes in at exactly the right time. Sometimes the phone call, “I can’t be there because my own life is falling apart.” provides some distance, or perspective or just an opportunity for a friend to get out of their own head. Sometimes not being there in the moment has made me available for the long haul.
Last week my women’s group did an honoring of Frieda Kahlo on the anniversary of her death. That was 64 years ago and people are still being impacted. People still show up when they can. I believe it still makes a difference.
We spent all of the 4th of July week (and both weekends) up at my folks house. It was quite the event. Small resort towns around the Brainerd Area do big celebrations. We didn’t watch any fireworks, but we could hear them. Every evening!
Because we came up, Dad got to get several things checked off his “to do” list. He went to a meeting, got his snow blower tuned up, and put new tires on the car. He also had his buddy Orion along for 3 parades and a trip up to International Day at Concordia Language Villages
Orion attended Waldsee, the German village, with his Opa as his aid for 10 years starting 20 years ago. It was fun for the two of them to return to their old stomping grounds. There were even several people there who remembered them from years gone by. The old Dean, Karl, noticed them across the way and stopped what he was doing so he and his wife could catch up with Jager and Opa.
I kept Mom occupied while the boys were out and about. Ordinarily we’d be taking things easy at home, but the air conditioning died the day I arrived. So we had our own “out and about” adventures. We decided it was too hot to be home and went out for a drive and pizza.
We collected my sister, Andrea, and ran errands in Brainerd. (That really meant lunch at Prairie Bay and Mom sitting in the air conditioned car while one or the other of us ran into the store.)
We ate pretty well at home too. When I’m there I do a lot of the cooking, or at least the meal planning. When I can stand it, I’ll enlist Dad’s help.
That’s especially true for grilling. I’m more than happy to let him set up the coals and carry things back and forth, at least most of the time. We’re still in mourning about that beautifully cooked salmon.
Dad did have a chance to redeem himself. At my request he made mussels and a fresh focaccia to go with them. Even Orion thought they were really tasty!
It was a great trip. We had a great time. It was also pretty physically demanding. The drive took at least an hour longer than usual – in both directions. The heat and humidity was draining, and it wasn’t always easy to breathe. General household chores (which I do more of up there than at home) take their toll, as do extra transfers with Orion and massage work on Mom.
Now I’m glad to be home, laying on my back on an ice pack.
Sorry about not being able to get the photos aligned properly.
So many wars, so many lives. Some were fought over an ideology, and won, and yet we still contest that ideology. Some were fought over resources, because a desperate enough people will do anything to try and survive. Most were fought because someone was afraid of losing something, and many who fought lost everything.
I have mixed feelings about this day. I appreciate the sacrifice of those who have fought for my freedoms. But I grew up during Vietnam. I understand war to be instigated by the wealthy and powerful in order to protect their wealth and power and fought by the poor and less fortunate. Give us your life, we’ll give you an education doesn’t sit well with me.
I know we did not do well by those who fought in Vietnam. We, as a country, had yet to learn how to hate a war and still honor those who served.
Is it an honor to serve in a war that was lost? I don’t believe might makes right. Just because you win doesn’t mean you are more just, or moral, or worthy. But, for example, I struggle to honor those who lost their lives fighting on the losing side in our civil war. Their families, though, certainly believe them to be honorable and do not want them forgotten.
Is any war really won? WWII, a war that had a clear moral victory, the war fought by “the greatest generation” we won. Today we can have Nazi’s marching in the streets and our president insisting they are good people. Is that what those lives were sacrificed to achieve?
As a Wiccan I do work with ancestors. When they talk about fighting the good fight they are not encouraging fisticuffs. They generally have a broader view in death than they did in life and would like to broaden my view as well. They encourage me to understand better and more fully. They want me to speak and educate and ask for what I desire. Sometimes that’s scary for me. It’s rarely easy.
That fear, of finding out that we are wrong, of learning that there is more to a situation than we thought, of admitting we don’t know everything, that is, ultimately, why we have wars. If it wasn’t so scary to find a better solution, we probably would. If a better solution than giving up your life was available, wouldn’t you take it?
So honor the ancestors this Memorial Day. Honor those who have given up their lives in service to this country. Honor them by demanding we find a better way, a real win.
Many of you know that I do regular volunteer work for Gilda’s Club Twin Cities. Gilda’s is a place where support, education, classes in healthy living, social support and community resources are made available to anyone impacted by cancer – for free. That’s not just people with a cancer diagnosis, but their families and support systems. It’s an incredible organization and a beautiful and healing environment.
Because Gilda’s does not demand anything of its members, it is supported entirely by community donations. Our clubhouse is a gift of time, talent, and resources of many volunteers, community members and business organizations. The position I occupy, Gilda Greeter, is a volunteer position that many of the group of Gilda greeters have been doing for years. There is a lot of love at Gilda’s.
Last week was our big annual fundraiser. The “Imagine a Place” Breakfast started to raise funds to create a clubhouse in our area. Imagine a Place, our founders said, where people could go to get help and support. We continue to imagine and to grow. That takes a lot of time, a lot of hands, and honestly a lot of money. I put in some extra hours last week to help out.
The Aliveness Project has been around in the Twin Cities for a lot longer. They are an organization that supports people who are living with HIV and AIDs. They were one of the first groups that offered free testing. They also provide education and support to their members.
I’ve not been as active with the Aliveness Project, although many of my friends have. One of the best fundraisers they do is called Dining Out for Life. Essentially, restaurants who participate donate a percentage of the days take to the Project. It’s fun to make a date for a night out and know that because of the timing you are also supporting a good cause.
In all honesty, we didn’t plan our night out to happen along with Dining Out for Life. (In spite of the fact that we were all aware it’s a thing.) We didn’t pick the restaurant Northbound Smokehouse because it was one of the biggest supporters of the event (a platinum level participant). We just got lucky.
We ordered big, ate really well, tipped generously and all threw a little something extra in the envelope the Dining Out volunteers provided. We were happy, and grateful, to be enthusiastic participants. It was fun, it was easy, and most especially it was a good cause.
Minnesota has one of the most active non-profit communities in the nation. We have a council that reviews non-profits and provides information about how their money is distributed. We have community events, generous business owners and an understanding that if those in need do better, we all do better.
How do you support your community?
I’ve been posting a little inconsistently because I’ve been spending a lot of weekends “up north” at my parent’s house. As they age their needs have changed. Mom is mostly using a walker to get around, even in the house. She’s really needing a wheelchair if she’s out and about.
There was a big effort in March to get Mom a hospital bed to sleep in. She can use the adjustability. It will also help to have the grab bars just to roll over. We acquired a bed from one of the relatives (in the next state over). The logistics of getting the bed here and installed have been daunting.
The biggest dilemma in all of this has been space. My parents hang on to everything. As my Mom has lost track of what she has, she’s found the need to “replace” things that never were lost. We’ve seen them using what we would call rags and bought new as well. Then we discover the problem is just that the new stuff is being “saved for special.”
We are repeatedly invoking the mantra “Use the stuff! If you don’t use it, then toss it.” We’re at the point where the hospital bed is ready to install and the white gloves come off. We’ve spent the last weekend cleaning, decluttering and tossing. The whirlwind also included putting in new faucets in all the sinks (to stop the dripping).
It’s been a little distressing, a little disgusting, and required a lot of patience. The end result is that Mom can actually take her walker into any room in the house. Furniture has been moved and cleaned behind and under that had been collecting dust for 20 years. There is still a lot to do, but this is a good stopping point.
There is a lot of disorientation, especially on Mom’s part. It will take her some time to get used to the space. Dad has to touch everything that’s been put away and make sure that his most precious memorabilia is where he can get his hands on it at a whim. I’m sure in a couple of weeks piles will begin to accumulate again. Better is still better.
Thanks to my sister Andrea, her husband Butch, her son Zac and his SO Darcy, and Andrea’s daughter Alyx (who spent the weekend scrubbing). I couldn’t have touched this job and they took the lead on all of it. I’m thankful to be able to help at all. 5 years ago, I couldn’t have done anything.
Our culture has lost track of the sacredness of caring for our elders. We don’t have the time, services, support or even the examples of how to handle this. We are trying to do this work from a distance. 3 hours is no distance from my parents compared to what many of my friends deal with. Very few of us anymore have the resources to take our aging parents into our homes. We do what we can, and are grateful for the opportunity.
Have you missed me? I’ve noticed that when I’m dealing with big events in my life I stop writing. My journals all have gapping holes during the times when I would be most interested in going back and reading about what I was thinking in the moment. I’ve blank spaces from when Orion was a baby, and each of his hospitalizations. I have holes in the record immediately after recording that I had cancer. I stopped journaling when the cupboards came off the walls.
My parents are aging and it’s hard. It’s hard on them and it’s hard on us. I’ve missed the last two blogs. The first I skipped because my folks don’t have internet, the second because I’d just gotten home. I have been slammed with emotional content and I shut down.
When I was a kid I was “sensitive”. I cried in empathy, wore my emotions on my shirtsleeve and was generally harassed about it. I made an active decision to stop.
The first trick was pretty easy, typical in my family. That is to put emotion aside while you deal with a crisis. The idea is to stay clear headed and available, and not add to the chaos while it is occurring. The aftermath, when everything is safe, comes like a tidal wave and can be very confusing as it appears to have no source.
Having that kind of emotional catharsis in public is a great opportunity for gaslighting. There IS nothing to be so upset about (anymore). It IS overreacting (because it’s all the reaction at once). Even the part about “just looking for attention” isn’t entirely false. If I’ve just spent hours offering sympathy and emotional support to others, yes I may be looking for a little sympathy and emotional support for myself.
So I learned to allow myself to be distracted. Eventually I learned never to “get around” to dealing with my emotional content. There are lots of distractions! I’ve been trying to unlearn that.
I’ve found that I’m a better writer when I can be open to emotion. I’ve found that there is strength in vulnerability. I’ve found that it’s really hard to make myself do the work and that I need to create a time and space for it. I still can’t do it in public, at least not until I have a good handle on it myself. The support would be nice, but the gaslighting I can’t deal with.
So I shut down, a little. I look for distractions (I don’t have to look hard). I pick and choose my confidants. I try to carve out some space. Please be patient with me.
I’ve spent the past two weeks babysitting my grandpuppy Minnie. She’s actually 4 years old now and much easier to have around. I was sick one of those weeks and she was warm and comforting. She’s not nearly as hyper or demanding, although she still knows Grandma is a sucker when it comes to treats.
Minnie has been through a lot this past year. My daughter has moved many times, and I had Minnie because she was moving again. All the stress and upheaval has taken a toll on the dog. She’s a lot more volatile, less trusting, quicker to say “enough”. That’s problematic.
Of course to my daughter Minnie is perfect. There is discipline, but not a lot of acknowledgement of an underlying problem. Mostly, I suspect, that’s because my daughter also feels like there’s nothing she can do about it. So I take the dog, and establish a routine. It’s easier for me. I’m home a lot more than my daughter is and just that is a reassurance.
Minnie and Orion have a love/hate relationship. Minnie is scared to death of the wheelchair and looses her mind any time Orion moves. On the other hand he often drops food while he’s eating. Orion adores Minnie, except he doesn’t actually want to touch her and hates all the noise. That’s a dynamic that scares me so I keep an eagle eye on the two of them anytime they interact. I also do a lot to make sure there isn’t much interaction, like putting Minnie outside while Orion comes to the table. It won’t solve anything, but Minnie isn’t my dog.
Karina has a few days off so she’s taken Minnie back. It’s nice to have quiet. No one barks every time a neighbor walks by or comes out of their house next door. It’s easier to have a morning where I’m not running back and forth letting Minnie in and out while Orion gets dressed and ready for his day. It’s nice to jump into the car for a quick trip to the library before the blizzard snow starts to accumulate without having to worry about getting Minnie settled or arguing about who might want to come with.
They say the best part about having grandchildren is that you get to give them back. This is true. Still, I find I’m Missing Miss Minnie. I catch myself looking for her, or thinking about her next treat. It’s definitely easier and quieter having her gone. It’s also just a little more lonely.
I got to spend the weekend up at my folks helping to make a happy birthday celebration happen for my Mom. Fragile is not I word I would ever have thought to apply to my mother. She’s the strong one, who will do whatever is necessary no matter where she is at. She bounces back. Climbing mountains after surgery is something I learned from her. She’s “in charge” and keeping track of all the moving pieces at any event she attends. At 82 today, she struggles to reconcile a self image which she can no longer maintain.
She rarely goes out anymore. It’s hard for her to get around. It’s hard for her to sit in the car for any length of time. When there are a lot of distractions, or conversations going on she gets confused. My Mom has been dealing with chronic pain for a long time. Her allergies are severe and complicated enough that medicating pain isn’t an option, beyond an occasional Tylenol. Her mouth is dry, so eating and talking become impossible when she doesn’t have water at hand.
We took her 100 miles there and another 100 miles back to go out to lunch with a good sized group. I went a few days early so we could get her showered, lay out her outfit and do some massage therapy in advance. Just my presence gives her a space to gather her resources. I make sure her water glasses are always full so she doesn’t have to ask. I put food in front of her rather than quizzing her about what she might want and what is available. I do the dishes and sweep the floors, which are both really big jobs for her. She can bank a little reserve.
For her, it was more than worth it. She had a really good day. She enjoyed it so much she didn’t want to go to bed because she didn’t want the day to be over. My youngest sister couldn’t make it, but all the rest of the female children and grandchildren were in attendance. It was a girls day out. There were lots of leftovers, but she knew I would get them home and see that they were used. The wait staff sang happy birthday and fussed over her desert. We all tried to keep the table conversation with one person talking at a time. There was a lot of love.
I am so very fortunate to be able to help facilitate that kind of good day for my Mom. I’m grateful for every opportunity I have to see her out and about and having a good time. It’s a joy to watch her relax and participate and let go of the worry of being “in charge”. I wish I could do more.
Happy birthday Mom!
The temperatures are dropping and the wind is gusting. The cold and damp are fitting for the season, they set the mood. There are ghosts walking.
I am at that age where parents die in clusters. This is the way of things, of course, but that doesn’t make it easy. I worry about my own parents as they approach their “end years”. I see that gradual decline isn’t so gradual any more. It’s getting harder for them to keep up, to get by, to get things done.
This year in particular I find myself trying to offer comfort to friends whose loss simply can not be consoled. Grief comes in waves, it takes its own time. Those “stages” are neither sequential nor independent. They can come in any order, repeatedly and sometimes all at once. And I take those phone calls. I listen. I witness. Sometimes that’s enough.
I’m looking for comfort too. I want to escape in a good book. I want a fire in the fireplace. I want a pot of soup on the stove. For my ancestors those things were just part of the days. Now I can go to the grocery store and buy mirepoix, precut and measured. (I didn’t, but I can.) Bone broth is on the shelf in boxes because much of our meat is already removed from the bones. Soup is no longer the ever present cauldron, but a can in the pantry.
Baking is part of that comfort factor as well. A good bread, warm from the oven, and I can feel myself relax into the smell. Pop-up biscuits from the refrigerator case do not elicit the same affect.
There is no time for this kind of comfort in most of our lives. We rush through our days, rush through our meals, rush through our grieving and just “get on”. Perhaps the most important part of this season is to make a point and take some time. In most of the U.S. we have an extra hour coming to us this coming Sunday. How are you going to use it?