Tag Archives: diabetes

Hello! Life calling.

I think I’ve had more than a few moments like Saturday night’s.

I think maybe the timing of Saturday’s moment was particularly unique.

We started out by going to a birthday dinner for my sister-in-law (in the yellow shirt in the photo). She’s the Mom of The (former) Live-In Niece (third from the right). We had a great time eating, laughing, and generally enjoying each other’s company.
Sat1

As we finished up dinner, it started raining. By the time we made it out to our vehicles, it was really coming down. About five minutes after we started home, we heard one of the local radio stations announce a tornado warning. By the time we made it home, the tornado warning was gone, but we were still under a severe thunderstorm warning for some time.

The first thing The Great Spousal Unit did when we got home was let the dog out (like he would actually want to go out in stormy weather like that). When she came back inside a couple of minutes later, she said she heard one of the big trees in the neighborhood fall down. If you’ve ever heard a hundred foot tall oak tree fall, you remember the sound, so she knew.

Well, it was too dark out to go and check where it happened, and I wasn’t about to get back in the car again, so we waited until morning to find out where the tree came down.
Sat2

We had just driven down this street, exactly in this spot, about three minutes before the tree came crashing down across the road. Three minutes later getting home– the time to wait at one or two extra traffic lights– and that photo could have included us underneath that tree.

I don’t generally believe in signs. I believe in reminders, though. And I needed this one. Because I already know these things, but I’ve lost sight of them in the general slog to get through each day.

What are the reminders?

Life is short. Don’t be afraid to pursue what is important. Don’t wait to do something meaningful. If people can be helped by what you do, don’t make them wait while you… wait. Because their lives are just as important, and just as subject to the possibility that anything might happen at any moment. You might not get the chance later.

Advocating for People With Diabetes is something I’ve grown into over the past few years. It’s easy for me to feel like what I do doesn’t mean much. Until it means something to someone. Or until I can lead someone to someone else who makes the difference for them. But you never know when that’s going to happen, or when the opportunity will present itself. So you have to be ready.

Also: Never miss an opportunity to experience true, in-the-moment joy while it’s happening. For so many years, I’ve been guilty of recognizing special moments, even in the smallest of things, and moving on with my life like they never really happened. There are reasons for that, not good ones, but I am so guilty of not fully letting myself go for fear that someone will recognize I’m happy and do something to crush it. It’s happened before, and it’s conditioned me to where I felt, I don’t know, like I was 60 or 70 percent happy about something I should have been 100 percent happy about. I’ve been feeling like I’m missing out on 30 or 40 percent of my happiness for a while now. I don’t know if that makes sense to you, but it does to me.

It’s okay to sit on the sidelines for a while, watching the world go by. But don’t sit too long. Live your life. Make it special. For you, and for someone who needs you.
 
 
 

Dude, where’s my motivation?

I’ve got to tell you… I really hated writing this. I’m nervous about publishing this. I don’t enjoy thinking about this or talking about this.

I just have no motivation to accomplish anything related to diabetes right now.

Actually, that’s not true. I have had the motivation to do a number of things, but every time I get ready to do them, I just give up. I think to myself, “Well, maybe this isn’t a good idea, I don’t know if I should do this, maybe I should just think about doing this another time”. Or maybe never.

That’s not like me, generally. I’m more the guy who thinks, “So what? If I want to do something, I should just do it, hopefully I’ll help someone, and I can enjoy it as long as it lasts”. It’s the difference between things being fun, and things being competitive. I don’t do competitive anymore. I don’t like myself when I’m competitive, and I don’t usually do my best then either. When things are fun, I look forward to them, obviously, and yes, I seem to do my best work. Because it doesn’t seem like work. It’s just fun. And I feel a sense of purpose in what I’m doing, like there’s a greater meaning.

But it’s more than that. It’s really more a feeling that I am one step behind the curve, so to speak. Like those dreams where you’re running, but no matter how fast you run, you can’t run fast enough. I hate that feeling.

At the same time, my BGs are on the roller coaster more than they are off. My weight is at a very (for me, anyway) uncomfortable number. And as bad as it sounds, I’m really not interested in working to iron out the wrinkles in my diabetes at this point in time.

I don’t want to confuse lack of motivation, or lack of competitiveness, or a feeling of being behind the curve, with a diminished sense of advocacy. I’ll still fight for my rights as a Person With Diabetes, and for everyone living with diabetes, regardless of my state of mind. There is no time to lose. But there are some things I’ve started and stopped lately, and though they were never even given a chance to be failures, they still feel like failures. That’s bad medicine. It’s reflected in my BGs, how I look, and how I feel about literally everything.

Add to that a work schedule that has absolutely blown up over the past few months and promises to stay that way for the remainder of the year, and, oh yeah, knee surgery and the lack of chances to work out for a few months. I could really use a couple of days off, but nothing is on the horizon. And those workout-high endorphans, well… sometimes they’re just the right medicine. But that won’t be part of my regular routine for some time yet.

It feels utterly ridiculous to be whining about all of this right now. I’m not dealing with anything that anyone else doesn’t deal with, probably more often than I do. When it comes to having to live with diabetes, I’m one of the lucky few who has many options at his disposal to treat, get healthy, and keep on going. I’m just really tired right now, mentally more than physically, and being tired makes me feel less motivated to stay healthy, get stronger, and look for new stories to tell.

Ultimately, I need to downshift into suck-it-up mode and plow through. This is one of those times when I have to remind myself that I’m not doing great, but where would I be if I didn’t try at all?

Perspective: my problems are not really problems. They sure as hell don’t feel like opportunities right now, either. But, things usually go in cycles, and this is likely just a temporary bad cycle. Truly, things could be much worse.

I don’t have any predictions, promises, or insights to share today. I only have my continuing dedication to a better life for everyone living with and affected by this disease. However that happens, whenever that happens, I hope to contribute in any way I can. I want to help, and I want to do it with a sense of empowerment and a joy for life. I want it to be fun again.

Because, why not?
 
 
 

Thank you for your support.

It’s that time of year again… the time when riders are out on their two wheeled vehicles, getting ready for the ride of a lifetime. Or lifetimes. Yours and mine.

These riders are training for the JDRF Ride to Cure Diabetes, which is held in several locations throughout the year. Today, I’d like to feature five riders, most of whom you probably know already, especially since four are also diabetes bloggers.

A rider needs to raise at least $2,000 to be allowed to join one of these rides. That’s the kind of money I can never even hope to raise, so the least I can do is support the riders who can (or who are close). I hope you’ll click on the links to their pages and help support their rides. The money they’re raising will go toward research to help make a future with less, and then hopefully no, Type 1 Diabetes. Here they are, in no particular order.
 
 
– Our first rider does not write a blog. But he has been featured on other blogs, including this one back in February 2014.

Bob Parant will be riding in Burlington, Vermont again on July 25. Bob’s a 43 year veteran of living with Type 1, and he never lets it get him down. Read his inspiring story here. And:

Support Bob’s Burlington, Vermont ride
 
 
– Moira McCarthy Stanford writes a compelling blog at Despite Diabetes, chronicling her life as the mother of a young woman living with Type 1 Diabetes. She’s been a tireless advocate for a long time, and three years ago, she participated in her first Ride to Cure Diabetes. This year, she’s participating in two rides—LaCrosse, Wisconsin on August 15, and Death Valley on October 17.

The best part for Moira will be in August, when her daughter Lauren will join her for the first time. Their stories are amazing, and you can help them both get to their destinations by supporting their rides. Here are the links:

Support Moira’s LaCrosse, Wisconsin ride
Support Moira’s Death Valley ride

Support Lauren’s LaCrosse, Wisconsin ride
 
 
– Jeff Mather is a beast of an athlete. He writes a very interesting blog at Jeff Mather’s Dispatches, and right now, he’s diligently working on training for a complete ironman triathlon: 2.3 mile swim, 110 mile bike, and a full marathon. All in the same day. All with Type 1 Diabetes along for the ride. He’ll be taking a break from his training (who takes a break from training with a 100 mile bike ride?) on July 25, when he’ll be in Burlington, Vermont for his latest JDRF ride, one of several for him in the past decade.

Support Jeff’s Burlington, Vermont ride
 
 
Jeff will probably spend part of his time in Vermont riding alongside Victoria Cumbow. Victoria writes at her self-titled blog about life with Type 1, her life as a new homeowner and resident of Nashville, Tennessee, and her absolute love of transportation on board her bicycle. Her first JDRF ride was two years ago in Death Valley, and she completed the Nashville ride a year ago. This time, she’ll be in Vermont, after already completing a sprint triathlon and a half marathon this year. Just… wow.

Support Victoria’s Burlington, Vermont ride
 
 
Last, but certainly not least, is Alecia Wesner, writer at SurfaceFine. In years past, she’s been a top fundraiser for JDRF walks in New York, where she lives and works. This year, she’s decided to give up sneakers for bike shoes, and head to Vermont for her first 100 mile ride. When I read what she writes about it, I think she may be unsure if she’ll make it. Regardless of what she says though, I think she’ll do great. And she’s bringing her sister along for the ride too!

Support Alecia’s Burlington, Vermont ride

Support Paige’s Burlington, Vermont ride
 
 
I’m not sure I know what else to say except how much I appreciate what these athletes are doing to help all of us living with Type 1 Diabetes. I hope you feel the same way, and I hope you’ll either join them or donate to help them on the ride of a lifetime. Many lifetimes. Yours and Mine.
 
 
 

Mid-Season Garden Update.

To say I’ve been insanely busy these last few months is quite an understatement. Right now, it’s work… all day meetings, but don’t forget to get the rest of the work done, rinse, repeat.

I’m not really complaining. Every so often in a job like mine, you have a year when a lot of things happen, and you’re depended on to give the extra measure of devotion for the good of the team. This is one of those years. It happens.

All this extra work makes it even nicer when I can come home and eat out of my garden. Here’s a mid-season update:
Garden

The big thing you notice here is the yellow squash plant, which I should never have planted there. They get pretty big after a while (like “Feed me, Seymour” big), and if they can, they’ll steal sunlight from any other plants in the area, like my tomatoes and my peppers. So I have to trim off a leaf or two now and then to make some space.

The bad news is that there seems to be evidence of some creature (squirrels, probably) eating the flowers (which come just before the squash), which is what helped me maintain a healthy plant that bore absolutely no squash last year.

The good news is that I have a couple of squash that have survived anyway.
GardenSquash

But, more bad news: In Monday night’s thunderstorm for the ages, my red leaf lettuce plants got pelted and fell over. This looks like the beginning of the end for these guys, which is sad because I’ve been eating salads nearly every day for over a month. I mean, these guys were the gift that keeps on giving. We’ve already eaten the romaine… there are just a few secondary shoots that have grown back, and they’ll make good salad. In addition to that, most of the radicchio (to the right of the romaine) has done very well.
GardenLettuce

Other than that, it looks like my pepper plants are surviving and thriving, and two of my three tomato plants are going gangbusters. I don’t know what happened to the third one, but it just stopped growing up a few weeks ago. I’m still holding out hope, but not much.

Oh, and I almost forgot: I’ve managed to get a few strawberries this year from a secondary garden. Most of them are smaller than what you’ll find in the grocery store, but they are so amazingly good! I can’t find enough adjectives to describe how mouthwateringly fresh they are.
GardenStr
 
 
So that’s what’s happening in the garden so far this year. Things aren’t perfect (like diabetes, gardening rarely is), but there’s still a lot to look forward to.

How ‘bout your summer? What are you up to, and what are you looking forward to?