Tuesday, November 21, 2017

The Year of Firsts

Surprisingly, we are half way through our "year of firsts". It doesn't feel like it at times. Sometimes it feels longer and sometime it feels like we lost her yesterday. We've already been through some tough firsts - birthdays, anniversaries, events that she was a huge part of. They were hard. We are coming up on a season of really tough firsts. The thing about them is, we know they are coming. Thanksgiving, Christmas, New Year's - we know they are coming and we know they are going to be hard - there's no getting around them but at least we kind of have a heads up.

The firsts that get me are the ones that sneak up on me. The first time I was sick and wanted my mom. The first time Cole got a home run and the game ball and he wanted to tell her. The first time I figured out how to "do" my hair so that I looked like I just rolled out of bed... but in a cute way... not like how I actually roll out of bed. The first time I made a recipe written out in her handwriting. Those sneaky little ones are the ones that really get me. And those are mean because you don't see them coming - you don't get a heads up. 

That being said, there are some "firsts" that come and don't make me sad but rather, make me smile and sometimes even laugh. Tonight was one of those nights. Tonight, we played Wii baseball which is not a new thing. The thing about it was that tonight, I was really paying attention. Tonight I realized that mom's Wii character was on one of the teams. Tonight, Cole got so excited that Jahbee was on his team. Tonight, Jahbee played her ass off getting a home run and several outs in the outfield. But the best part about her character popping up on our Wii is, she built this character. I remember her doing it. We had taken the Wii to their house - probably pre-Cole - and she built her person, complete with glasses and a big grin. Then, she named it. Seeing the name she picked pop up on our TV tonight gave me the giggles and reminded me of just how dang funny she was! You see, one day, probably 15+ years ago, Mom got a piece of junk mail addressed to "Merlin Blankinshit". We laughed about it and threw it away but, when it came time to name her Wii character... she went with "Poop Wizard" - you get it? Merlin = Wizard, Blankinshit = poop... Poop Wizard! I mean, that is hilarious!! 



So those are my favorite firsts. The firsts that pop up and punch me in the gut but make me reflect on what an incredible person she was. She was spectacular. And based on the baseball game tonight, she still is spectacular. 

I miss you, momma. More than words can describe. I hope you know that we are doing ok. That you left us with enough love and funny to get us through. I love you. I'm thankful for you. io

Tuesday, May 30, 2017

Prolonged Grief

From Catron:

It blows my mind that we haven't done a post here since January but, I love that our last post was mom's VERB post. It struck such a chord with so many people, I think it was right that it be there at the top for a while. But now, I'm back. Writing is therapeutic for me and, I have a lot of things on my mind so, consider yourself warned.

Today I want to talk about grief - about grieving. It has been 3 weeks (and 4 days) since mom died and I told Wyatt last week that I felt like maybe something was wrong with me, that maybe I wasn't grieving the way I should be. I felt like my heart wasn't broken enough, that my world wasn't shattered enough, and I felt a bit like an asshole for not curling up in the corner and crying all day, every day. I felt like my love for mom, our relationship, and her amazing-ness was/is worthy of absolute heartbreak and world-rocking sadness, but I didn't feel it, at least not to the extent that I thought I would or should. Now, don't get me wrong, I cried big ol' fat tears when she took her last breaths. I cried big ol' fat tears when I had to leave the Hospice Facility. Hell, I'm crying big ol' fat tears right now. But, my point is, more often than not, I'm happy. I'm laughing. I'm head-over-heels for my husband. I'm inspired by our kids growing up. I'm amazed by my sweet family and friends. I'm ok. And I was feeling guilty about that.

Then, Wyatt and some of my bests pointed out a few things to me:

1. We have been grieving for almost 2 years. We started grieving the minute we realized she wasn't tripping all the time because she just clumsy. We grieved when she was diagnosed with ALS. We grieved when she lost her ability to write. We grieved when she lost her ability to walk. We grieved when she lost her ability to talk.

We have grieved so many little losses and so many big losses over this time that yes, perhaps the "final" grieving stage may look and feel a little different than had we lost all of these things, and her, suddenly. We've talked often about which is worse, a sudden loss or a prolonged loss and there is no right answer - loss is loss and grief is grief no matter how long it takes.For those of us in the prolonged grief stage, we may feel some relief that she is free from the body that had stopped listening to her. We may feel some relief that we don't have to fear what the end looks like for her anymore. Relief is ok; I know she is relieved.

2. We gave it our all. From the moment she was diagnosed we poured every ounce of love that we had into her and she poured it right back into us. I think we've, for the most part, always lived that way but we really turned it up a notch these past 2 years. I know, without a doubt, that we left nothing on the table. Of course there will always be things I think of that I wonder if I said, little things I wish I had said, but, the big stuff, the stuff that really matters, she knew and she felt and I have complete confidence in that. She was loved. I was loved. We loved.

3. She was ready. Mom was always very clear about how she wanted to leave this world long before ALS ever came into our lives. When she was ready, she wanted us to let her go. More specifically, when she was ready, she wanted us to make sure that the covers weren't tucked too tightly around her feet, that her hair had some volume, and that she didn't have any whiskers on her chin, and then we could let her go. Mom was a do-er, and even though ALS stole most of her verbs, she DID until she couldn't any more and at that point, she was ready. We knew it in our hearts, we could see it in her eyes, and we knew it specifically because she told daddy she was. The amazing thing is that, she told us she was ready, and then waited long enough for all of us to get our last hugs and last words of love in before she left. She prepared us, as best anyone can, for this day and, once again, she went above and beyond.

So, no, my grief doesn't look like I thought it would and that's ok. It's there, I'm not in denial, I feel it, but I feel her more than that. I feel comforted and supported and loved by the people around me and by the people that knew her and loved her, too. I see her - in my kids, in butterflies that show up randomly, in pretty skies, in my dad. It's been 3 weeks and at the same time, it's only been 3 weeks. I know this could all change tomorrow and perhaps there will be days I spend crying in the corner... but I also know that if/when those days come, the next day I'll get up and I'll go VERB like my momma!


i.o. - Cat


Tuesday, January 24, 2017

Verbs - from M

I wake up almost every morning feeling normal. Before I try to move and discover I can't, I think about what I would like to do today if ALS was just a dream.

Here's today's plan:

I will ROLL OVER on my side and CURL UP in a fetal position for a minute, then JUMP (really) out of bed. Both feet on floor, I will RAISE BOTH ARMS over my head, look up at the ceiling and STRETCH my back. I will STANDUP HUG Bill with 2 arms for a long time. CALL my whole family to come home. I will GO POTTY all by myself. BRUSH my teeth STANDING in the shower with hot water pounding on my head. RUB lotion all over me. DRY my hair, BRUSH it one hundred times and maybe PAINT my face a bit. DRESS in tight blue jeans and a not-stretchy shirt and relish every ZIP SNAP and BUTTON. PULL on my socks and my cherished cowgirl boots. I will HUG Bill again and PLAY-GALLOP to the kitchen. POUR a cup of coffee and HOLD the mug in two hands. COOK and EAT runny eggs and crunchy toast. DRINK a glass of water. I will CALL some of the people I love and TELL them I love them.  Bill and I will WALK around and look at the outside of the house and hold hands.  I will PLAY the piano and KNIT for five minutes.   I will DRIVE too fast with the windows open and WCPE playing too loudly on my way to meet Deede at a restaurant on Person Street for pork-belly sandwiches. I will go home to HOLD my family. KICK the ball with Cole. CHASE Beckett. PLAY hide and seek. Ask lots of questions. SQUIRT shaving cream in the air. FLY airplanes and RUN kites down the street. TALK about stuff. ROLL in the grass and HUNT for bugs. WASH my hands with hot soapy water. HUG. KISS. SNUGGLE.  SING Cowboy Joe with Catron and Phoebe. For hours. Family dinner date. I will DRINK a dirty martini. Order caprese salad, veggie pizza, sea bass, roasted Brussels sprouts, popcorn, hotdog, cashews and bacon. I will EAT as much as I can.  Another martini. More I love you calls. Then home with my family to SIT in my Mama's old chair with somebody else and laugh and TALK and TELL stories until my day is almost over. I will HUG and SAY I love you one hundred more times. Then I will CLIMB in bed unassisted, put my head on Bill's shoulder and go to sleep. I'll wake up in the morning and wonder what I would like to do today.

ALS kills motor neurons.
It also kills VERBS.