How Becoming a Mom Changed My Nerdiness

Of course I heard from everyone with an ounce of experience that becoming a mother would change my life.  I was prepared for this in most of the big, important ways, but one of the things that’s surprised me is how being a mom has changed my life as a nerd.

First, I obviously don’t have 8+ hours a day to spend writing.  That just ain’t gonna fly anymore.  I was also never a writer who carried around a notebook – I took notes here and there, but never actually WROTE in a notebook.  Now, that’s the easiest and/or only option I have.  When you’ve got one arm pinned under a sleeping monster, straining to reach a nearby notebook is a lot easier than trying to escape and get your laptop.  (In fact, as I write this – on my laptop – I have to keep distracting little hands from pulling out my power cord. And this post will take me approximately 8 times longer to write because I have to keep tossing her over my shoulder to look out the window at the dog, who I’ve just noticed is eating his poop… BRB.)

I also was never a huge phone app person.  I’ve added at least 5 now, all related to being a mom or using baby gear, so in that little way I’m becoming a little more of a techie.

And you better believe I plan to pass along love of my fandoms to the little squirt.  We’ve already binged the new She-Ra, and she at least stared at the transformation hair, so that’s a good start.  I look forward to first viewings of Star Wars and Dr. Who, first readings of The Chronicles of Narnia, and teaching her to side with me over her dad about Hogwarts houses.

Something I didn’t expect was that, for the first time in my life, I’d be able to easily relate to other women.  I grew up on a hunting preserve, writing science fiction – I’m just not wired to connect with most women.  But with the shared experiences of childbirth, babies that just will not sleep, the inevitable poop explosions – suddenly I feel LESS like an outsider and more like one of the tribe.  By creating a tiny human, I too have a non-nerdy thing to talk about that’s actually relatable.

BUT, at the same time, I’ve found that being a nerd AS a mom is a pretty common thing too.  I stumbled upon a couple Facebook groups for nerdy parents, and that’s my new favorite use of any free minutes the mini-tyrant allows me.  Nerdy memes related to parenting, nerdy discussions about our favorite nerdy things, and of course occasional parenting questions – it’s all great.

That’s not to say that I don’t miss being a more active part of my other favorite community, my author peeps.  To those of you who’ve put up with my endless social media posts of baby pictures, please forgive, as it’s the only way to keep our friends and family up to date who live 2+ hours away.  I promise I am reading your books and watching videos and generally lurking as a fan/friend even when I’m too exhausted to comment.

So, until the next time I have a minute free of screamed, nonsensical demands, here’s AI taking in Star Wars the only way she knows how…so far.

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Raffle for a prize of 50+ eBooks!!

Hey, readers!

There are only 11 days left to enter the raffle for my Book Charity Event for Mental Health Awareness Month.  The prize is an awesome collection of 50+ eBooks from various donating authors, so why not enter?

Here’s the link:  https://www.rafflecopter.com/rafl/display/5acd3f201/

Book Charity Event Raffle Pic

May – Mental Health Awareness Month

TPH Charity Promo Small
This month, I’m donating all proceeds from my novella, The Poet Heroic, to the Patient Assistance Fund for Pine Rest Christian Mental Health Services, which is a  local facility that helps people with counseling, detox, etc.  Absolutely 100% of this fund goes towards helping people pay for treatments they might not otherwise be able to afford.

Why I’m doing this: 
Last Fall, one of my close friends committed suicide.   I was writing The Poet Heroic at the time, and I constantly thought of my friend as I wrote because he was a twin and my main character is a twin.  This book affected me emotionally in ways I wasn’t expecting as a result.  It was only fitting that I dedicated the book:

“In loving memory of Jeff, and for anyone else struggling to find the light.” 

No one knew my friend was struggling.  As far as we know, he never asked for help.  His loss hit us all very hard – for many reasons – but one of the hardest things is that he never asked for help and so we were never able to help him.  Many of us were left with this feeling that we just wanted to DO SOMETHING.  We wanted others who might be struggling to know it’s okay to ask for help.  We wanted others to be able to get help.

So, this is something I can DO.  In the few weeks I’ve been working on this month-long event, I’ve heard touching stories from many people who have suffered with depression.  I’ve heard touching stories from people who have a loved one struggling with mental health issues.  I’ve had many people join me because they too want to DO SOMETHING to help.  I’ve been very touched by all of the support and donations, and we’ve got a few weeks to go!!

If you’d like to be part of this event, join us at http://bit.ly/MentalHealthAwarenessEvent

If you’d like to enter a raffle for 50+ ebooks! and help spread the word, enter at https://www.rafflecopter.com/rafl/display/5acd3f201/

If you’d like to add to my donation to the Patient Assistance Fund, (THANK YOU!), see http://bit.ly/ThePoetHeroicBonusGiving

If you’d like to buy a copy of The Poet Heroic and donate that way, go to http://bit.ly/ThePoetHeroicPurchaseDonation

Please, use this month to raise your own awareness, maybe ask for help yourself, and be especially supportive of those struggling with mental health issues.

About my vague health posts lately…

Here’s what’s been going on with me:
 ***
A few weeks ago while in the shower, I thought I got shampoo in my eye because I had sudden patches in my left eye’s vision.  This stupidity seemed very typical of me, and I didn’t think too much of it.  After a week, these grey patches had quieted into a small blurry spot in the center of my vision. Then, while trying to relax in a jacuzzi at my parents’ house, the patches suddenly returned. The next morning I went to my mom’s ophthalmologist, and thus began one of the scariest times of my life.
  ***
The ophthalmologist took pictures that showed my left eye was hemorrhaging “like an eye mini-stroke,” and the pooling blood was causing my blind spot.  (You know when you have a vision test and you’re supposed to read the letters?  I couldn’t even see the giant E at the top.)  I was sent semi-emergently to a retinal specialist in Grand Rapids, and there further pictures and an angiogram confirmed that my eye was hemorrhaging in about 8-10 places.  The pics of my eye looked like craters on the moon.  Also, for some reason the blood flow into my eye was slow – 20 seconds when it should be about 4.  It wasn’t inflamed enough to suggest an arterial occlusion, so that was some good news.  But if it developed into an occlusion, that could mean I’d lose my vision entirely.
  ***
Thing is, this should not happen in someone my age with absolutely zero risk factors.  (I’m pretty sure the specialist thought I was lying when I kept answering “No” to his ROS questions.)  So, the specialist ordered about 14 blood tests and an MRI/MRA to sort out what the hell could be causing this.  He sent me home – my eyes fully dilated for 10+ hours and exhausted without any treatment – with the knowledge only that “it could be something pretty scary.”  (A terrible thing to tell a medical transcriptionist, btw.  Knowing the multitude of things that COULD be wrong = hypochondriac freakout.)  Then, because of some office snafus, my MRI wasn’t properly scheduled and no one bothered to call me for 4 days until my mom called to yell at them.  So I went from being treated as an emergency on Monday to not hearing anything for the rest of the week.  DID.  NOT.  HELP.
  ***
Since my eye externally looks completely normal and I’ve had no pain whatsoever, this all would’ve gone completely undetected were in not for my blurry vision.  But something is “seriously wrong” as an underlying mystery diagnosis. Plus now I’m afraid to bathe because that seems to be a hemorrhage trigger.  So that’s awesome.
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This has all been completely new to me.  Aside from having strep so often as a child that I had to have my tonsils out, I’ve had near-perfect health my whole life.  I’ve sprained several ankles, sure, but I’ve never been diagnosed with anything, never been on medication, never had a cavity, and I’ve never worn contacts or glasses.  I have NEVER taken my health for granted.  I have felt incredibly blessed my whole life to have the health I’ve had.  So maybe I’m due, I don’t know.
  ***
As an avid reader, as a writer, and as an artist, the possibility of losing my sight is heartbreaking.  As someone planning a wedding and finally making plans for a future I’m looking forward to, being told I might have something that could kill me (“do not exert yourself” was expressed, as a blood clot was another possibility) is even more terrifying.
  ***
I don’t do well not having control, and I was properly freaked out for a good while.  I hate not knowing.  At least if I knew what this was, I could find a way to cope, to prepare, or to move forward.  But the not knowing is the hardest part for me.  (They HAVE ruled out the random test for syphilis, so I guess that’s something.)
  ***
But here’s the thing:  It’s always during times of freaking out that I feel most held.  You are free to not believe in God, but I do.  During my times of fear, I always feel like God goes, “Ah-ha, see? This is what I’m here for,” and then I feel cocooned in a love/peace that I can’t explain.  This has happened time and again, and it’s happened now.  I again have reached a place of acceptance that I’m not in control, and “let whatever happens happen” is an incredibly freeing headspace to be in. I don’t want to go blind or die; I want to live.  But at least I’m being given time to evaluate and appreciate the life I’ve had.  This too, in a way, is a blessing.
  ***
And that’s not all.  For a long time in my life, I didn’t let people in.  I didn’t let people help me.  (I certainly never would have publicly acknowledged that I was terrified.)  Now, going through THIS crisis, I feel incredibly blessed to have so many people who genuinely care about me.
  • I have a mother who’s been a saint through this whole process.
  • I have a dad who I know would do anything for me.
  • I have a brother who was willing to watch my monster-cat while I stayed at our childhood home because he knew I needed to feel safe.
  • I have a fiancé who’s called every day to check on me while he’s been out of state for work, and I know he’s worried but trying to joke and keep me calm.
  • I have future in-laws who’ve taken it upon themselves to become MRI/MRA experts.
  • I have friends I’ve known since childhood who demand updates. (My phone now knows to auto-fill “hemorrhage.”)
  • I have college friends who’ve expressed concern and willingness to help however they can.
  • I have a friend in Florida who called because she figured out that that might be easier for me than emailing since the whole problem is my vision.
  • I have a church family who prayed for me the second they heard the news.
  • I have family who’ve expressed their love in a variety of ways.
  • I have online friends I’ve never met who don’t know what specifically is going on but express unquestioning compassion whenever I post something about needing mental/emotional/spiritual support.
Please know that I do not take any of you for granted.  Your kind words and thoughts are extremely appreciated.
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During my checkup this week, a visiting retinal specialist from the Philippines was shown a picture of my retinal hemorrhage and said, “Wow, that’s so rare I could have gone my whole life without seeing one.”  My specialist reviewed my blood work and found basically nothing (thereafter getting creative and ordering a test for what is essentially cat scratch fever).  I did finally have my MRI/MRA, and fortunately that came back as a normal study free of occlusions or vascular malformations.  (Ever had an MRI?  It was very hard for me to come out of the machine and not say to the tech, “I know Kung Fu.”) But basically, nothing so far hints at the cause of this anomaly.  We decided/joked that maybe I would have this named after me, although we agreed “Sunshine Disease” doesn’t sound scary enough.
  ***
So now?  My left eye’s vision has improved to 20/40, so that’s something I can live with.  But it might never get better, and at any time I could hemorrhage again so it gets worse.  On the one hand, it is wonderful to hear all the negative results of these tests.  On the other,  there is NO diagnosis and I’ll never know if this could happen again of if something worse could happen.  Right now, there’s no way to treat this mysterious underlying cause.
  ***
So I’m still a bit freaked. I still need your prayers, bright thoughts, positive vibes – whatever you’ve got to throw my way.  But I’m trying to hold to that feeling of being held and reminding myself to trust and let go.   It helps nothing by being tense.  And I think it’s important to appreciate the blessings I have, now more than ever.
***
  • I feel fine and still “have my health.”
  • I can see well enough.
  • I’m not in pain.
  • I have a God who probably knows what He’s doing.
  • I have my people.
  • And at least I won’t die of syphilis.

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