gratitude

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Having Enough

Years ago, when my son was a toddler, we were on food stamps and WIC for a short period of time after my husband had been laid off. (If you’re not aware, WIC stands for Women, Infants & Children and is a federally funded supplemental nutrition program for low-income pregnant women and children.) My husband’s unemployment had run out, he was depressed, and he couldn’t find a job. It was a horribly scary time.

Yet even with that kind of stress at home, what really made it unbearable for me, was how I was treated at the grocery store when I used WIC. There was an older woman at the grocery store in the town I worked in, she waited on me and made me feel like absolute garbage. She scoffed when she saw my WIC paperwork, yelled at me when I had something on the counter I wasn’t allowed to get through WIC, and never once looked me in the eye.

I felt humiliated.

I left the store in tears, holding the bag of the few items my child needed to keep growing and thriving. The next time I used WIC, I didn’t go back to that grocery store, but went to a larger one near my home. It was a little better, but not by much. The clerk was closer to my age (I was in my mid-30s at this time), but she was efficient, did what she needed to do, and finished the transaction. There were no extra niceties, but at least she didn’t degrade me.

Now here we are, 15 years later. My son is still a growing boy, but a teenager. My husband is out of work and will be permanently. Although the disability paperwork has been filed, he will not have an income for 1-3 years. There is no WIC or food stamps for us, because in the eyes of the government, I make too much money.

So what do we do? Each day when I go home from work, I pass a local church that has a food bank every Tuesday morning. My husband and I had talked about it, and we both knew how fucking hard this would be. You work your whole life, you try to help others, but when it’s time to go for and accept assistance, it felt…wrong.

The morning he was going to go to the church for the first time, I said to him, “Remember, you’re doing this for your family. You’re doing this because our kid, god help us, is still growing. We are going to survive, damn it, and this is how we do it.” He kept nodding his head, “I know. I know.”

And off he went. I’m sure every food bank has their process and I know each one has slightly different rules. This one is in our town, but many folks who go are not from our town. They drive in from other places, but that’s how they survive. Each person or household is given a box to fill, but you can still only take as much as you need for the number of people in your home. For instance, he picked out 3 potatoes the first visit and 3 oranges, because we have 3 people. It’s been quite a humbling experience for all of us, but especially for my husband.

Each week the items are different, and you have to pick numbers to see how far down the line you are. If you get a low number, you have the better choice of produce or any of the goods. If you have a higher number, it’s often slim pickings by then. But it’s fair.

What’s interesting is the choice of items. This past week there was sliced swiss cheese with the expiration date of that day and yogurt a week past the expiration date. Usually the produce is about to go bad or you might have a few days to eat it. But so far, we’ve made sure nothing has actually gone bad. We’re trying to be creative with whatever food he brings home. He’s made hash browns with a few potatoes or sliced and baked them until they’re like potato chips. We’ve received spring mix a few times and have placed greens in nearly everything to make sure it’s eaten. I feel like I’m living in that commercial with chefs who cook gourmet dishes with food scraps…except without the chefs. We’re not making anything fancy, but we’re trying to make meals and not get sick from them. (I’m not gonna lie, the swiss cheese did taste a little odd, but I figured swiss cheese tastes a little weird anyway so it’s fine!)

But one thing that was seriously sweet about last week’s haul, was this rose. I guess the church gave it to my husband to give to me. I don’t know why, but I don’t care. I kinda love it. I’m not typically one who likes to receive flowers, but honestly, it was just nice to get something….lovely. Something that could brighten my day, even for a moment.

Someday, I hope we’ll get to the other side of this. I’m not sure what kind of shape we’ll be in financially by then, but I’m really trying to find ways of cutting costs. I make my own laundry detergent now, we switched from regular cat litter to these pellets that barns typically use, and I’m always scouring my basement to look for things to sell. This isn’t where I thought we’d be at this age, but shit happens, right?

One thing I know is that if we ever do get to the other side of this…no. WHEN we get to the other side of this, we will donate money or resources to local food banks. Even if some of the food items are a little sketchy, we still accept it with great gratitude. They are truly saving our bacon.

Eat well, my friends, and as always, hugs to you. ❤

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Dreams (and Nightmares) Do Come True

It actually happened.

Two weeks ago, I went on vacation with 4 of my favorite humans. To say we had the time of our lives was an understatement. When you laugh so hard each night that you cry and have a belly ache, you know you are surrounded by people that you not only love, but love spending time with.

We traveled to Belize and had the most amazing time. I can truly say it was the best five days of my life. Things at home were not wonderful while I was gone, but I had to keep telling myself that I just needed to let it go. Mostly I did.

Here are some highlights: saw numerous creatures at the Belize Zoo, including spider monkeys (where I cried because I felt like my brother was there, feeling just as excited to be so close to these lovelies); had a beach day where we all swam in the warm water, drank margaritas on the beach, and played cornhole in our bathing suits; went to the Xunantunich Mayan Ruins with a very informed and funny guide, climbed the massive structure and saw lizards and bats along the way; experienced cave tubing; visited a cacao farm and had a hand in making chocolate; swam under the waterfalls; had a massage (thanks, Trish!); ate delicious dishes and fresh fruit each day; heard and saw so many different types of birds that I’ve never seen or heard before; swam in the pool; went for a run; shopped a little; tried to speak Spanish a teensy bit; and drank and laughed each night.

There are hundreds of more photos that I get to look at each day. I did not take a ton (maybe 100), but thanks to my friends, we had over 500 (probably much more) to look at and do what we want with. Many of the ones I haven’t shared are all of us hanging out at the pool on our last full day in Belize. Looking at photos from that afternoon just gives me such good feelings. We were warm and our bellies full and we were enjoying the water and each other’s company. Hell, that was really every day of the vacation.

I know how lucky I am to have been able to travel to another country, to take a vacation, to spend it with my friends. I know how lucky I am to have these friends (and many others) that I have known for most of my life–over 35 years–and still love them and call them my family. They bring me joy and so much damn laughter.

I knew that when I came back from this dream vacation, I would need to hold onto the memories because life at home was and is hard. I cried the day before we left Belize. I knew that my life wasn’t going to feel this carefree and fun for a very long time.

My husband was not able to work while I was away and is now no longer working at all. Between congestive heart failure and now the neuropathy in his feet due to diabetes, there is no other way around it. Our health insurance ends this month and I will start paying for insurance that isn’t as good through my work, but at least it’s something. We will lose our doctor, our favorite doctor we’ve had for years, because he doesn’t take this new insurance. And now we’ve contracted with a lawyer to help my husband apply for disability. If all goes well, he might be able to receive SSDI (Social Security Disability Insurance)–the thing we’ve been paying for all of our lives–in a year…or two…or three.

We, in short, are all grieving so many things this week.

I’ll be able to look on the bright side of things tomorrow. Or maybe it’ll have to wait another day. Either way, I did have Belize. For that, I will be forever grateful.

Take care of each other, friends. I appreciate you.

Hugs to you all. ❤

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Until Your Love Runs Out

“With gratitude, optimism is sustainable.”–Michael J. Fox

I heard Fox say that once in a recent interview. It takes effort for his body not to shake or move due to Parkinson’s Disease, yet he’s still grateful for and optimistic about his life. I immediately found a scrap of paper and wrote this quote down because I knew I’d need it at some point. And now here I am, trying my best to embrace those words.

Your comments, messages, emails, texts and phone calls in response to my last post, was the best explosion of love I have felt in quite some time. I am not only grateful for y’all, but finding others that have been or are currently in the same situation, lightened my stress by just a bit. Thank you. So much!

Because of my blog post, my husband and I had some honest conversations, including his daily fears and what the future will bring. We added to our vision board with our own hopes and also YOUR words of encouragement.

When I asked my son what he wanted on the board, he said to win the Calvin Coolidge Scholarship. This is the one he’s been working really hard on–reading Coolidge’s autobiography, writing 3 essays and 3 short answer questions. I helped him with his resume and he got the two letters of recommendation he needed. The deadline is Thursday, so much of his life will be consumed by this for the next few days. He said, “You know, Mom, I really doubt I’ll get it, but I’m really proud of myself for trying.” I’m so damn proud of him, too. He set a goal and he’s kicking ass trying to achieve it. ❤

We’re feeling some hope this weekend. I was able to buy groceries yesterday and filled the house with healthy foods and now I’m cooking up a storm. I paid most of our bills and with a bit of juggling, should be able to pay the others around their due dates. (I know many of you know this juggling I speak of. We’re basically fucking financial experts, aren’t we?) Today my husband looked at bars for the shower and toilets that are higher than what we have. With help from one of my colleagues, I now have a short list of attorneys we may want to talk to soon about the process of applying for disability, but he’s not at that point quite yet. He has to stop working before he’s even able to apply. I really, really hope that isn’t this year.

But if it is, then we’ll deal with it. Because that’s what we do and what you’d do, too.

For today, though, we’re going to move forward and hope we can continue to keep putting one foot in front of the other. We’re going to listen to this positive potato. (My son gave this to me yesterday as my late Christmas present. I LOVE IT!)

So let’s do our thing, friends. I believe in you, just as much as you believe in me. Let’s keep chugging along until the love runs out.

Hugs for all!

Thank you, One Republic, for letting me borrow and edit your lyrics for my blog post title.

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How I Am. Really.

As many of you know, recovering from any kind of surgery takes time. It’s typically not pleasant. There are wounds to care for, pain to manage, and a wide variety of little issues you may have never had and now have no idea if it’s “normal” or if something is wrong. For instance, my chest hurt quite a bit while I was in the hospital having the tail of my pancreas removed (distal pancreatectomy). When I asked one of my doctors about it, she informed me that my pain was legitimate since they were up in my ribcage at one point and she could see where my heart was beating. 😳

It’s been 2 1/2 weeks since the surgery and I’ve really been recovering well. I did feel awful after getting home and I was frustrated and angry and sad. My husband was sick with some kind of infection, and he did not have the capacity to take care of me. I’m not gonna lie–that was heartbreaking for me. I needed him and he just couldn’t deliver. Our son helped me tremendously though and one of my dearest friends in the world visited me with treats and conversation and it gave me a great boost. All in all I didn’t think I was doing that badly. And then I took a survey the surgeons sent me. And when I finished, they told me to call the doctor. It was because I wasn’t moving much, I was in pain and trying to go by what they did in the hospital, and I was honest about my depressed state. But I was grateful for the survey because it made me look at what I was doing and feeling, and I had to change.

Instead of calling the surgeon, I got up and moved every hour, took mini walks with my son, changed my pain meds to make sure something was always in my system (only Tylenol and ibuprofren). But I started to feel a bit better, or at least more in control. (And I wish I could tell you more about what I can eat and can’t eat, because it’s still a crap shoot.)

The next day, 8 days post-op, I went to see my PCP like you’re supposed to. I think I’ve talked about Dr. Lauer here before. He’s a great guy, my age, and has become like a family friend. I have his personal cell phone number and I text him with concerns and he actually responds. (We should all have doctors like this!) When he walked into the exam room, he first told me how great I looked. “Umm…you look 7 weeks post-op, not 1 week.” See why I love him? 😉

He did an exam, we talked about the surgery, what I was doing, etc. He asked me to not run or train for anything for 12 weeks, and for the first time in my running years, I was happy to say yes. The thought of running right now is painful. We talked about my spleen, and the hope that the few blood vessels going to it now can keep it healthy. We discussed the possibility of diabetes and having to take enzymes, but right now we just see how I heal and go from there.

Then he went over the pathology report with me. When Dr. MacGillivray removed the tail of my pancreas, he sent it to the lab for them to dissect it and see what’s what. Dr. Lauer was reading it out loud and then stopped. At this point, I’m still lying on the table after the exam because I’m tired and didn’t want to get up yet. I looked over at him as he’s reading and I said, “I’m not sure what that means.” He repeated part of the report and said, “You just sidestepped pancreatic cancer.” If I had put my surgery off, which is what the great doctors at Portland Gastro told me to NOT do (they said to please get it done within a year, but preferably before fall), then I might be talking about chemo in this post instead. I knew the lesions on the tail were precancerous but having my doctor (and then my surgeon) say that I was able to avoid pancreatic cancer, at least for now, was a bit mind-blowing.

Dr. Lauer then went on to give me this lovely philosophical speech about letting go of people or situations in my life that I’ve been fretting over. “This is a new path forward,” he said. He had a few medical situations in his own life recently and it’s made him look at his life and everything around him a little differently.

As he was giving me this talk, I got very teary of course. Not just because I was feeling grateful and proud that I took charge of my health and that my doctor listened to me when I had problems, but also because I was sitting in my doctor’s office at the age of 49 and being told that I had a new lease on life. But my beautiful, funny, big-hearted brother never got this speech. Instead, he was being told at 49 that he had to choose to either stay on those machines to keep him alive or die.

To say I was feeling a huge mixed bag of emotions is an understatement.

But…I was and am grateful.

I hugged my doctor before I left, then told my son who was in the waiting room the news and he smiled a big smile and hugged me. My husband had a delayed reaction, but there have been lots of “I can’t live without you” moments. Plus we’ve agreed that he has to die first so there’s that. 😉

My appointment with my surgeon the following week was not so joyful. The physician’s assistant was awesome, and she told me how fabulous I looked and was happy with my numbers. The surgeon, Dr MacGillivray, doesn’t have the best personality. He knows his shit, which is what matters, but he did tell me that it’s possible the rest of my pancreas could still become cancerous, and we have to scan it each year to check on it, as well as my spleen to make sure that it doesn’t die. I asked, “Since I had precancer in my pancreas, what about the rest of my body?” But he couldn’t answer that, and it left me feeling bereft.

When I left that office, I ended up going to Holy Donut and eating a gorgeous gluten-free donut while walking around a park in Portland. At first, I was like, “Ok, Holly, just enjoy this delicious treat and the sunshine and the beautiful space.” And I did. And then I ended up angry eating the last half of it. I should have thrown part of it to the ducks, but I said, “Fuck it” and ate it. (These are delicious and large and expensive, so the thought of throwing away any of it seemed insane.)

Later that day I cried and cried with a dear friend about the whole situation. We talked about it and I had to just let all of that news settle. I had been on high, thinking I had dodged this big bullet, which I did, but then the surgeon was waiting for more rounds to shoot my way.

So what did I do? I texted Dr. Lauer. He reminded me of the major scans I had done in the spring that showed no cancer anywhere else and I didn’t have symptoms of other cancers. He told me that he’d let me know when to worry, but now wasn’t the time. 🙂

And so I’ve taken his advice. My job now is to heal. I have definitely been doing way too much–I was walking up to 2 miles at a time, and that would have been fine if I didn’t try and do other things during the day. But I did and this past weekend I was really sick. Naps helped but overall, I felt awful. Today, though, I started my day with a half mile walk, then went to work for a few hours. Came home to rest and worked some more but am able to take more breaks than I could at work. I’ll keep pecking away at it and do my best to get stronger.

I’m not sure what I’ll do with my newfound lease on life or wake-up call or tremendous gift. I don’t want to squander it, you know? Maybe it just means I keep going down the path I started before the surgery–doing more activities that make me happy and making my voice heard about issues that matter to me like LGBTQ+ rights and being pro-abortion and that I want to fight for a longer bereavement leave for people in this country. (Having a 3-day bereavement leave that most organizations “allow” is a slap in the face to every human being that has lost another human being.) Maybe it means cutting more people out of my life, or maybe it means letting even more in.

Whatever my “path forward” will be, I hope some of you will join me. Or who knows? Maybe I’ll join you instead. ❤

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Thanks, Y’all

Tomorrow morning at 8:40am, a surgeon in Portland, Maine will be removing the tail of my pancreas along with those nasty precancerous tumors that are attached to it. He may also be removing my spleen, but we’ll keep our fingers crossed that won’t happen.

Having a distal pancreatectomy has been frightening to think about, but I’ve felt quite calm about it since yesterday. There’s nothing more I can do now, right? I have my workplace as settled as I can, I finished the password book for my family, and yesterday I ran my last 5K in what I expect to be at least 3 months.

Pretty happy to get the run in.

So as they’re prepping me tomorrow, I will pretend I’m back in that sensory deprivation tank I tried out a few weeks ago at Float 207. It was really lovely. I chose the purple light and I’m so glad I did.

But after imagining this calm space, I know I’ll be thinking of my boy, my family, my friends and all the incredibly kind words and thoughts you’ve sent my way. Thank you.

I’ll see you on the other side. ❤

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Be Seen

“Showing your vulnerability is how we get stronger, right?”

I was at a library conference last week with loads of other Maine librarians. For me, it was one of the best Maine conferences I’ve attended due to a number of factors: I was on a panel with folks I consider my new friends and we discussed having community conversations (yup, we were talking about talking and I loved it), I got to hug and chat with some colleagues and friends I haven’t seen in person in some time, and I met new colleagues and did my best to welcome them into not only the library conference world but into librarianship and some of the beauty of it. (Which is kind of funny since I’ve been thinking about changing careers at some point. But that’s for a future blog post.)

The commonality among everything I loved about the conference, were the people. Meeting new people, getting reacquainted with others, talking about our libraries–both the successes and challenges, but also just talking about our lives–our interests, our children, our families. And in these conversations– sometimes in hallways or at a table before a session began or over a drink and a meal–many of us were vulnerable with one another.

Now, maybe this happened because this is me. When you “wear your heart on your sleeve,” it means you often advertise how vulnerable you are–you show your feelings even when you could be hurt. You’re willing to say “I love you” first, even if it feels like you’re stepping off a cliff. It’s scary shit, but my word, it can be exhilarating. And if you’ve read many of my blog posts or if we’ve been friends for a while, you know that I tend to put most of my feelings out there for the world to read about. But maybe people were willing to share more because we’re living in frightening times and we were willing to say, “Hey, my friend died of Covid last year and I really miss her,” or “Thank you for saying you don’t think you know what you’re doing as a librarian, because I think that every day” or if you were me, in front of a large group of people in a session that you were attending, you admitted that you cried in a meeting with another colleague because you felt overwhelmed and lost and needed help.

Because, you know, I REALLY put it ALL out there.

But after that session, the person leading it came to me to say, “Thank you for being so vulnerable. And showing your vulnerability is how we get stronger, right?”

I think I nodded my head and thanked them but then walked away thinking, “Really?!? Then emotionally, shouldn’t I be freaking She Hulk by now?”

I let the phrase “showing vulnerability begets strength” simmer in my brain this week. (And yes, I’ve read and/or listened to a LOT of Brene Brown, but for some reason it never quite clicked like this.) So, I tried it out. I shared some information with some people that I might not typically and was happy with the results. I felt more connected with them then I had in some time or ever. A few friends have also shared some deeply tough issues and emotions with me recently, and besides feeling that wonderful connection it has created, I feel so much gratitude towards them for trusting me, for letting me really see them.

I know this isn’t for everyone. And I’ll be honest, it hurts like eternal papercuts when you open yourself up to someone and they don’t want to hear what you have to say or see who you are. But my friends, when someone DOES finally see you? To me it’s like taking a bite of a pie that you’ve been dreading because it sounded awful but you knew you should because it’s supposedly healthy and recommended by a friend and it won’t kill you so just friggin’ do it already. So you take that bite…and it tastes like the best ice cream you’ve ever tasted. You’re so happy because it made your mouth and tongue sing and you’re relieved because you can tell your friend that you ate it and it was delicious.

Yeah, that was a stupid analogy, but I hope you get what I mean.

I know you see me. And I can see some of you.

Please know I’m glad you’re here.

Take care, my friends. ❤

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Voices of the Past

Holidays can be tough for those missing their family–either if they’re no longer near you or are no longer on this planet. Last week was the 5th Thanksgiving without my brother and the third without either of my parents. Typically, my little family of three spends Thanksgiving by ourselves and my brother used to come over to spend it with us, while his partner slept during the day (he worked nights). After my brother died, we always brought my mom over to spend the day with us. Now, though, we invite my brother’s partner to have dinner with us and it remains the four of us. On Thursday we toasted our lost family with our drinks and chatted about all of them throughout the day. It wasn’t a horrible day.

That night, my son and I sat down to watch a movie, and we got on the subject of my mother. My boy was comparing the grandmother on the Garfield Thanksgiving special to his grammy, my mom. We started to talk about Mom’s laugh and I realized that I couldn’t remember it. At all. I could picture her laughing, like this photo when she tried out our Bowflex for the first time back in 2001 and it nearly catapulted her backwards. But every time I pictured Mom laughing, it was silent. I just could not imagine what her laugh sounded like. I started to tear up, grasping at my memories of her, trying to find something that would trigger that laugh in my head. I could hear her voice, I could smell her perfume, even feel her hands in mine. But her laughter was gone.

When my teenage son saw my eyes and the look on my face, he tried to imitate his grandmother’s laugh. He could clearly hear it and was doing everything he could to share that with me. After a couple of failed attempts, he found it. He created a laugh that was enough like hers that I could hear it again. I closed my eyes and listened.

I cried a little and thanked my son. He was so relieved–not only because I didn’t break down into sobs, but also that he could find a way to share Mom with me, to share *his* memories of his grandmother with me. If anything could warm the cockles of my heart, it was that!

Unfortunately, as I write this, I still can’t remember her laugh. I’m hoping someone has a video with a clear laugh track of Mom on it. I hear my brother’s laughter nearly every time my son laughs, and I can easily hear my father’s deep, gruff chuckle. But not my mother’s. So until I find that video, I’ll have to consult my boy whenever I need to hear Mom’s laughter. I envy his gift.

If you do have the opportunity to record your loved ones’ voices or laughter, I suggest you do it (and have others do it to you). It may sound like a morbid activity, but if something like hearing your parents’ laugh can make your day, then wouldn’t you want that to listen to after they’re gone?

Have a good week, friends. Find laughter wherever and whenever you can. ❤

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Finding Community

Let me begin with thanking so many of you for sending your good thoughts, vibes and prayers my family’s way last week. My husband got through his heart surgery and everything looks great. Two stents were placed in his arteries instead of one, since they found a clogged artery they didn’t know about, but now blood is actually getting to a majority of his heart. His energy has skyrocketed and I think he may be on his way back to the living. Now he just needs to clean up his act by eating right and exercising. Not everyone gets a second chance, so hopefully with encouragement he’ll be ok and take advantage of this rare opportunity.

And now…back to running. 😉

Sundays are typically my long run days. I was up to 10 miles a few weeks ago, but ratcheted it down to just 4, then have slowly been building back up again. Today was a 10K (6.2 miles) day, and although I felt good and ready when I left my house, the feeling didn’t last. I had a hot flash around mile 1, which is a weird thing to have when you’re already sweating. I felt completely depleted by the end of mile 2. I almost called my husband to ask him to bring me a banana or maybe drive me back home, but then in my head I heard my friend Heather say, “I take walking breaks. It’s really ok!” So I stopped beating myself up and walked for a few minutes and sipped from my electrolyte drink that tasted awful. But the combo gave me a bit of energy and I pushed on. By 2.5 miles, I started to feel better. I was tremendously slow and walked up nearly every hill (except the giant hill I tried to run up and then realized I was so hunched over that I could touch the ground), but the run was finally feeling good.

I was ok with being slow today, but I wanted to feel good. I wanted those endorphins to kick in. Hell, I just wanted to feel like myself. I’ve had so many moments in the past few years when I don’t feel like me. Do you ever have that? Like you feel out of sorts, like something isn’t right but you don’t know what that is? Now that I’m perimenopausal, I certainly feel like that more and more. It’s not just the physical–the hot flashes, the 15-20 pound weight gain since 2017, the occasional lethargy. But also the mental and emotional changes and challenges that are not necessarily due to perimenopause–the occasional emotional outburst, the grief, the anger, the stress of so much loss–and trying to find a way to not only take care of myself (which admittedly I’ve been pretty bad at), but also to take care of my son and husband AND to be a support for my friends and the rest of my family.

After living through the deaths of my brother and parents, watching my husband nearly die twice and supporting a stressed and grieving child, then managing to get through (and currently going through) all the logistical shit people don’t tell you about (burials, funerals, wills, estates, financial loss while recovering from illness), I have learned a lot. But I also received a HUGE load of emotional support from my friends and family. And I want to give that back in spades. I know I still don’t have the right words to say to someone after a loved one dies, but I often say that I’m here if you need anything and often suggest a meal or time together or even $20 if I have it. I don’t say any of that unless I mean it. Occasionally someone will take me up on it and ask for help. And I’m grateful. When I was desperate, I did reach out to my friends and asked for help. Nearly every time they were more than happy to lend a hand or an ear. That’s what being a friend is. (And more than once I did NOT ask for any assistance, yet some friends helped me anyway. Because they are that awesome.)

Reach out to your friends and family this week. Contact the ones you want to. I give you permission to not bother with those folks who continually disappoint or hurt you. I know that the holidays can mean being forced to spend time with people you might not want to. Admittedly, I had a great family and loved to spend time with them. Not all the time, mind you, but enough. I know our family was lucky that way. But if you don’t have that kind of family but one that is toxic and treats you badly, I hope you get to have dinner with your chosen family this week. If you can’t do that, then please find SOMETHING that makes you happy this week, ok? Preferably nothing that can harm you. Go for a hike, pet a cat, read a great book, have a glass of good wine, walk a dog, eat pie, bake a pie, have sex, go for a run, buy new shoes–whatever makes you feel good!

And if you need a hand or an ear, I’ll do my best to lend you one or the other. I’ll try to be here for you, as you’ve been there for me.

Until then, I’ll try to keep running amidst hot flashes and cold mornings. You’d think they’d cancel each other, right? Sadly, no, but at least your voices in my head will keep me going. (I’m standing up straight, Sonya!)

Happy Thanksgiving, y’all. ❤

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Power of Positive Thinking

On my run today, I started working on my posture. It’s truly awful. I’ve always been a sloucher. When you’re over 6 feet tall and a majority of your friends are “average” height, you find yourself hunching your shoulders and slouching to try and shorten yourself. My brother was 6’6″ and his posture was just as horrible. He had a little hump near the end of his life and I can see that happening to me, too. (As I’m typing this, I’m sitting ramrod straight just thinking about it!)

Since I was trying to relax my shoulders and run tall, I didn’t worry about my pace this morning. But the route I took included a long, steep hill, and normally that’s when I feel my shoulders meeting my ears and my gaze aiming at the ground. Not today! I kept thinking, “Ok, you can do this. Don’t worry about your pace, just keep those shoulders back and look straight ahead. And relax, damn it!” So I talked to myself in my head for a few minutes, then started to think about the week ahead.

Tomorrow, five months to the day since his “widow maker” of a heart attack, this guy is undergoing another cardiac catherization and a stent inserted into a 100% clogged artery.

As I was slowly ascending that hill, I thought about this blog and the outpouring of support I’ve received because of it. When my husband was on a ventilator and in a coma in 2020, people around the country were sending him healing thoughts and prayers. I’m not exaggerating. We know a lot of folks between the two of us and they’re all over the place. And due to this blog and at least one dear friend’s move, we now know folks all over the world. So, once again, I am asking for those positive thoughts sent this way.

When Husband had his heart attack in June (the day after my birthday), he was told he might need this upcoming surgery. But he didn’t really remember that. I did. He was a little surprised in the fall when his doctor told him he’s need this stent fairly soon. And then in October, what little energy my husband had, he was losing quickly. He wasn’t (and isn’t) well. Then one day, while I was away at a conference, both his doctor and his boss told him he needed to take a break from work. His boss’ words were, “You’re not having another heart attack on my watch.” Our family doctor has been concerned and thought he might need to stop working…possibly for good. But Husband said “no.” He’ll stop working until after the surgery, but he’s too young to stop all together. We hope! (Meanwhile, he’s been getting shots in his eyes due to his diabetes…and those shots have advanced his tiny cataracts into full-blown cataracts. So that surgery will be next month!)

Tomorrow morning, we will head, once again, to the hospital. This time, though, they won’t have to save his life while quickly putting a stent in. This time, the operation will take three hours and the surgeons can take their time, look around, do what they need to do. Hopefully it will extend my husband’s life. Hopefully his energy will improve and he’ll be able to do things again. Maybe he can do yard work without having heart palpitations or take a walk with me without having to nap afterwards. I thought those things would happen this summer or fall, but they didn’t.

So let’s get this shit fixed, ok? Let’s raise my husband’s quality of life.

Let’s get him living again.

Love to you all. Thank you in advance for sending those good vibes our way. ❤

by

Thank YOU

Let me first say that the reasons I blog are because I love to write what I want and I typically use this as a no-cost therapy tool. I vent my anger and frustration with the world. I grieve my brother’s death and my parents’ memory loss. I discuss my love (and hatred) of running and my continuous battle over my weight and my eternal body issues. BUT, I also like to use my blog to express my love and gratitude for particular people or things or situations.

My post last week brought a HUGE amount of love and support from my friends and family and I cannot begin to thank you enough. I had co-workers and friends and family members all bring us food we could freeze and put in our pantry, several friends gave me money to finish Christmas shopping for my son, and the amount of hugs and good thoughts and prayers were nearly innumerable.

I have been fortunate enough to surround myself and my family with so many wonderful, big-hearted people like yourselves. If you’re reading this, than more than likely we actually know each other–have met in person–and probably think highly of one another. Or I do you, at least. But if you’re reading this and have enjoyed what I’ve had to say and we don’t know each other, I certainly hope we meet someday. We need more love and friendship in our lives, don’t we? (Cue “All You Need is Love” by the Beatles.)

My husband is still looking for a job–it’s only been about 2 weeks–but we do have hope. We’re hopeful that this is just a bump in the road and we’ll be able to stay in our home, pay our bills and feed ourselves. We know we can’t live on love alone (that would be nice, wouldn’t it?), but with a little luck, we’ll be ok.

Thank you again, friends, for caring about me and my family. Your love, support and friendship is something I hope to never live without.


a baby giraffe sitting down and says "Thank You" at the top of the image
I borrowed this photo from the South Australia Zoos. (Thank YOU!) If you don’t know this about me, I have a thing for giraffes. My brother wanted to be one when he was 4 years old (he ended up being 6’6″ so he kind of succeeded), and I’ve always loved them, too. And since I’m 6’2″ and baby giraffes are typically 6′ when they’re born, then I’m like a toddler giraffe! ❤