18 August 2016

They're never too young to learn consent

Consent is a big deal.

Always.

And it goes both ways because men can be assaulted, as well. And women can assault women.

So one of the things that's really important for Bo and I is to teach the kids about consent. Both that they must receive it and give it for things to happen, like physical contact (hugs and kisses).

There are a few reasons we want them to know this, even as kids. First of all, we don't want the kids to feel obligated to give hugs and kisses to people (like family) so that if someone, whether family or not, tries to touch them inappropriately, they will know they are not obligated to consent.

My body, my choice.

Even with family.

Another reason we want the kids to know this is because they need to know and accept that "my body, my choice" extends to others, as well. Yes, Tink, it is your body and your choice. But it is also Puck's body and his choice whether or not he will accept hugs or kisses from you. And when they get older, they'll know that they must also make sure that the person they want to be intimate with or even hug or kiss more casually wants that contact.

My body, my choice.

With everyone.

Tink is an extrovert who loves hugs and kisses. So sometimes she gets so excited she forgets. At this age, we gently remind her, and usually she apologizes (to the person she had physical contact with) for not asking first. And those instances are getting fewer and further between.

Even at five and seven years old,

my body, my choice.

16 August 2016

The scribbling family

One of the reasons I wanted to meet Bo was because I knew she was a writer. I thought that, if nothing else, we could become writerly friends. I lucked out and ended up with an amazing wife instead.

But there has always been the writing.

Life has been chaotic in the last couple years, especially with the kids' health and my own health. So writing has taken a back seat a bit (outside of my work, at least). But now that things are finally settling down and we have a good routine, Bo and I are both working toward making more time for writing. We've set up a desk for her in the bedroom, and I've adjusted my daily schedule a bit to give her a few hours every afternoon during which she can write (or do whatever else she wants to do).

Sometimes you have to be
a superhero to write a story.
It's not only Bo and I that write stories. Puck is a writer, too.

In order to teach elements of stories (protagonist, antagonist, etc.), I had Puck fill out worksheets to develop characters and a plot, and then write a story. He loved it. He's written two stories (about dragons), And last week, he saw a toy gryphon and said, "I have an idea for my next story."

I think he's a scribbler, too.

I love that our family is full of writers. I love seeing the creativity when Puck and Bo are developing their ideas. I love sharing story ideas with them and talking about how to make them better.

Most of all, I love seeing the pride and joy on Puck's face when he reads us his latest story.

I'm so proud of him, and I can't wait to see what else he's going to come up with this school year.

In the meantime, Bo and I will be scribbling away, as well.

09 August 2016

I am her first and best advocate

Photo by Brandi Gilbertson
If you've been following this blog for a while, you probably already know about Tink's health concerns. They've been going on since her birth (well, before her birth, really), and sometimes I feel like we're going in circles trying to figure out what's causing these problems.

Right now, the most important issue we're dealing with is failure to thrive. We've ruled out any physical GI problem. Her blood work (almost) always comes back perfectly normal. So we're taking her care in a different direction: psychological.

Tink's pediatrician has referred her for behavioral therapy for a probable feeding disorder. We're optimistic that the treatment plan will help her, and we'll be able to get her healthy.

The problem is that my mama-sense is still tingling.

When Tink was still in infancy (a little over a year old) we took her to see a pediatric geneticist. While he didn't find anything at that time he could diagnose her with, he had a few conditions in mind that she could have, but was too young to meet the diagnostic criteria for. There were also a couple of conditions he was thinking about, but they would have required specialized genetic testing to diagnose, and he wasn't prepared to do that at that time.

As Tink has gotten older and (somewhat) bigger, the geneticist's report keeps echoing in my mind. I've done a little research (I know), and I can see signs of one of the conditions the geneticist mentioned all that time ago.

I'm reluctant to say, "I think Tink has this" to a pediatrician or other health care professional because I don't want to sound alarmist or that I'm looking for something more serious to be wrong with her. I don't want that at all. I want my daughter to be healthy. And the key to getting her healthy is finding out the cause of these problems.

As her mom, I know I am Tink's first and best advocate. I know what's normal and abnormal. I know if she's okay or not okay. And I have to follow my instincts when advocating for her.

I do think she might have one of the conditions the geneticist mentioned. But she might not. And I definitely think the more pressing concern is addressing her probable feeding disorder. Once that's out of the way, she'll either get better or we'll move on to the next round of diagnostic testing.

And I will always advocate for her as fiercely as I can.

05 August 2016

Happy Birthday, Puck!

Photo by Brandi Gilbertson
Tomorrow my sweet boy turns seven.

I can hardly believe it.

Puck has grown and changed so very much in the last seven years. We've had some challenges and successes, but overall he's healthy and happy and on his way toward becoming the person he wants to be.

Puck is smart. When you give him something to do, he'll pick it up quickly and effectively. He likes being a helper, and he likes knowing how to do interesting and useful things. Some of his favorite toys are puzzles and anything he has to build.

Since we've started homeschooling, he's excelled in math and science. He's passionate about science, too. He reads non-fiction books (particularly those about animals) nearly every day. He can recall facts about animals easily, and it has given as a way to nurture a love of learning in him. He's an excellent student.

Photo by Brandi Gilbertson
Now that he's securely in the "school-age child" portion of his life, other aspects of his personality are starting to emerge. He's funny, and has a very sarcastic sense of humor. He loves to trick people (playfully, of course), play pranks, and tell jokes.

Puck is clearly his own person. He does things his own way, even if it means he sometimes does things the hard way. Eventually, though, he figures things out on his own or asks someone for help to figure it out.

I am honored to be his mom and to get to be a part of his growing up.

I'm eager to see everything that's still to come in his childhood. I'm eager to see the teenager and young adult he grows into years down the road. And, for now, we'll celebrate seven.





Happy Birthday, Puck. Mama loves you.

Photo by Brandi Gilbertson

01 August 2016

What does chronic illness look like?

Since being diagnosed with fibromyalgia, I've had to make some adjustments in my life. Some of these adjustments have been good, like getting medication so I'm not in pain all the time. Other adjustments have been more of a challenge.

The biggest challenge I've faced so far is adjusting how I see myself now that I'm labelled as someone with a chronic illness.

Fibromyalgia is a lifelong diagnosis. I will always have it, I will always combat pain and its other symptoms. And it may get worse as I get older.

Because of this illness, there are things I have to do differently in my life. For now (maybe not forever), I'm giving up the idea of being able to run a marathon. Or run at all, for that matter. My exercise has to be more gentle to my body.

I'm also adjusting my daily schedule to accommodate my fatigue. I'm becoming a polyphasic sleeper (not to take advantage of the benefits, but simply because that seems to be what's easiest for my body and work/family schedule).

Right now, I'm trying to find a balance between the diagnosis and the identity. Yes, I have fibromyalgia, but I am not fibromyalgia.

One of the ways I'm doing this is by reading Toni Bernhard's How to Be Sick. So far I like her approach to chronic illness.

There is illness here, but I am not ill.

This approach is allowing me to make accommodations for the illness without letting myself get pulled into a black hole of "I can't because fibromyalgia."

I am tired and I hurt. But I still work and I still care for my family and I still do the things I need to do in order to be the woman I want to be.

It's still a process. There are days I let the fibromyalgia keep me from doing what I need to do.

There are days it has to.

When those days happen, I do what I can and try again tomorrow.

I have fibromyalgia, but I am not fibromyalgia.

20 July 2016

As we near the end of summer

Summer is one of the slow times in my work. My primary work revolves around the academic year, so I have a lull in the summer and in December/January.

Image source: punsayaporn / freedigitalphotos.net
This year I had mixed feelings about getting to the lull. My workload in spring was quite heavy, and I needed the break once it finally came. At the same time, the void left by a lack of work was a bit frightening, knowing that my work is what our family relies on for survival.

Work picked up a little bit this month, and I know that the levels will return to normal soon. And eventually, I'll be looking forward to the break I get at the end of the year.

Despite the lull in work, I've tried to stay productive. I'm working on a few things that have to stay in the background for now, and this has been a good time to do some administrative work, get some elements lined up, and prepare for the fall season of work.

Each week and month that passes, I'm taking steps to move my career in the direction I want it to go. I'm closer to the career person I want to be, and I'm excited about what's coming.

In the meantime, I'm enjoying my summer lull, the extra time with the kids, and the chance to let myself rest a bit before the chaos of autumn begins.

How's your summer going?

28 June 2016

Coffee-stained health

Some of you may already know that I've been having some health problems lately.

In addition to the diagnosis of rosacea, I've been dealing with a great deal of pain and fatigue that has been increasing for the last couple of years. So I got a referral from my primary care physician to go to a rheumatologist.

I saw the rheumatologist a couple of weeks ago, and he diagnosed me with fibromyalgia. His exact words were, "Well, you definitely have fibromyalgia."

Okay, then.

In addition, he thinks I also have some kind of autoimmune condition "in the lupus family." So he ordered a lot of blood work to try and determine what else, if anything, I have. Once we know what's going on, we can develop a treatment plan that helps deal with all of my symptoms. The blood work is done and I'll get the results at my follow up appointment in a couple of weeks.

If I warn you that my veins roll, it's for a reason.
This is that reason.
The experience was not exactly pleasant. I don't like getting blood drawn. I always warn whoever is drawing my blood that my veins roll and they have to be anchored. I always bruise. Sometimes (like this last time) very badly. But if it helps get answers, it's worth it in the end.

It was abrupt, this change from "something's wrong" to "chronic illness."

In the progression of what I've been experiencing, along with comments from my primary care doctor, I had a pretty good idea of what's been going on. But hearing the words made it real. I know that I'm going to have to deal with this for the rest of my life.

There is a mental and emotional shift. There are things I just can't do anymore, and things I won't be able to do when I'm in a flare (like right now). The past few week it has been hard to accept that the reason I can't do these things is because of my body, not because of my personality. There are things that I can't change, and instead of beating myself up and getting angry because I can't do certain things, I am having to create and adapt to my new normal.

It's going to be a process. And in the meantime, I'm doing what I can.

23 June 2016

Modifying my green book

I've been using a planner (with a green cover) for quite some time. I call it my green book. In that time, I've tried different things with it here and there, and tried different planners, but I usually returned to some incarnation of the green book.

But it wasn't really working for me. I didn't have the space I needed for notes, and the layouts of the pages locked me in to using the planner in a very specific way.

It just wasn't working.

So as I was wandering around online to try and find some workarounds, I discovered bullet journaling, created by Ryder Carroll. It's a way of incorporating planning, scheduling, notes, and to-do lists all in one place. The foundation of the method is simplicity and flexibility. You can use any notebook and pen and find a way to make it exactly what you need it to be.

Here's the video on Carroll's website:


If you Google bullet journals, the image results will be full of artistically magnificent pictures of layouts and notes and oh, my goddess the pretties. And that's wonderful for those using their bullet journals as an artistic outlet. That's not me. I express myself in words, not visual art.

So I'm sticking much, much more closely to the original method developed by Carroll. I've incorporated a couple of chart-style trackers and I'm using a different method for indexing, but other than that, my bullet journal is very simple.

I can tell you that even using this method just this month has helped me stay much more organized. I have everything in one place, and the method plays into my need to write things down in order to remember them. (I ♥ analog planners!)

Because of the method's simplicity and flexibility, I'm able to make it anything I want it to be. I use it to track projects for work, it includes my blogging editorial calendar, planning and task lists for our upcoming family vacation, and even my "40 before 40" list.

I plan to stick with this planning method through the end of the year to decide whether I really like it or not. If I don't, I can go back to a different planner at the beginning of 2017.

In the meantime, I like it quite a bit.

21 June 2016

On Father's Day

I used to value Father's Day.

I was pretty close with my dad, especially after I moved back to Illinois from Florida, and during the divorce. We spoke on the phone a few times a week, and I prided myself on showing my appreciation to him every year in June. One of the last Father's Days I spent with my dad, I surprised him with a round of golf for the two of us and my younger brother. I like golf, so it was a good morning.

When I moved back to Florida, things changed. Well... I should be more specific. I started dating Bo, and things changed. I told him the nature of our relationship was up to him, and now we haven't spoken in I don't know how long. My father has clearly made a choice based on his religious beliefs about homosexuality.

The good news is that there are aspects in which Father's Day still has value to me.

I have an amazing father-in-law.

My father-in-law looking dapper on our wedding day
October 2015
He embraces me as a daughter (no qualifiers). In fact, it was less than 12 hours after I met Bo that he friended me on Facebook, and there was no going back after that. He loves me and I love him, and when I think of Father's Day, he is the one who comes to mind.

My father-in-law is a good man. He loves his family and would do whatever he could for any of them. There are no strings attached to his love. He has never once told me, "I love you, but I don't agree with your lifestyle." He just loves me for who I am.

I have lost my father by blood by his own choice, which has caused me to also lose the rest of my family on that side. But I have gained so much more in a family by choice.

I think I came out ahead in that.

14 June 2016

We are Orlando.

I live in Orlando. The Pulse is only about a ten-minute drive from my home. And though my wife and I are not clubbers, we know people who are.

We are fortunate that we were home. That we didn't lose anyone. (Our neighbor lost four people Sunday morning.)

At the same time, we have lost them, too. They were are our brothers and sisters. They are me.

I am heartbroken in so many ways and for so many reasons because of this. And while it's important to talk about the big-picture issues that have been brought into the stark spotlight (homophobia, discrimination, gun control, religion, racism, etc.), it is imperative that we don't let other important things be pushed to the shadows because of the big-picture discussions.

Every single one of those involved in the massacre on Sunday morning is important. They deserve to have voices. Those who have survived can use their own voices to take up space, but there are 49 people who must rely on us to speak for them.

Say their names. Remember them. Speak for them.

"To actively do nothing is a decision, as well." --President Barack Obama, 6.12.16

Stanley Almodovar III (23 years old)
Amanda Alvear (25 years old)
Oscar A. Aracena-Montero (26 years old)
Rodolfo Ayala-Ayala (33 years old)
Antonio Davon Brown (29 years old)
Darryl Roman Burt II (29 years old)
Angel L. Candelario-Padro (28 years old)
Juan Chavez-Martinez (25 years old)
Luis Daniel Conde (39 years old)
Cory James Connell (21 years old)
Tevin Eugene Crosby (25 years old)
Deonka Deidra Drayton (32 years old)
Simon Adrian Carrillo Fernandez (31 years old)
Leroy Valentin Fernandez (25 years old)
Mercedez Marisol Flores (26 years old)
Peter O. Gonzalez-Cruz (22 years old)
Juan Ramon Guerrero (22 years old)
Paul Terrell Henry (41 years old)
Frank Hernandez (27 years old)
Miguel Angel Honorato (30 years old)
Javier Jorge-Reyes (40 years old)
Jason Benjamin Josaphat (19 years old)
Eddie Jamoldroy Justice (30 years old)
Anthony Luis Laureanodisla (25 years old)
Christopher Andrew Leinonen (32 years old)
Alejandro Barrios Martinez (21 years old)
Brenda Lee Marquez McCool (49 years old)
Gilberto Ramon Silva Menendez (25 years old)
Kimberly Morris (37 years old)
Akyra Monet Murray (18 years old)
Luis Omar Ocasio-Capo (20 years old)
Geraldo A. Ortiz-Jimenez (25 years old)
Eric Ivan Ortiz-Rivera (36 years old)
Joel Rayon Paniagua (32 years old)
Jean Carlos Mendez Perez (35 years old)
Enrique L. Rios, Jr. (25 years old)
Jean C. Nives Rodriguez (27 years old)
Xavier Emmanuel Serrano Rosado (35 years old)
Christopher Joseph Sanfeliz (24 years old)
Yilmary Rodriguez Solivan (24 years old)
Edward Sotomayor, Jr. (34 years old)
Shane Evan Tomlinson (33 years old)
Martin Benitez Torres (33 years old)
Jonathan Antonio Camuy Vega (24 years old)
Juan P. Rivera Velazquez (37 years old)
Luis S. Vielma (22 years old)
Franky Jimmy Dejesus Velazquez (50 years old)
Luis Daniel Wilson-Leon (37 years old)
Jerald Arthur Wright (31 years old)