The Family Curse: Growing Up in the Shadow of ALS

Yeah, soโ€ฆIโ€™m still fucking sick. Recovering, but much slower than Iโ€™d like. Lame. Please bear with my foggy brained rambling ๐Ÿ˜†๐Ÿ’š

I decided to scrap my last โ€œloveโ€ post for February. Cuz, wellโ€ฆIโ€™m just not interested in it anymore!

This month (ironically), Iโ€™m planning a few โ€œhealthโ€ related posts.

Not at all like โ€œhow to be healthyโ€ posts.

More likeโ€ฆthis is some shit Iโ€™m dealing with, or have dealt with in the past, posts.

Itโ€™s been in my neverending collection of stuff I wanna post about eventually, soโ€ฆhere we go! ๐Ÿ˜‰


“Holding Hope” – Image created with Gemini

Some families pass down heirlooms.

Some pass down traditions.

Mine passed down ALS.

And if the pattern in my family holds, thereโ€™s a chance the story isnโ€™t finished with me.


The Family Curse

A few months back, I wrote a little bit about my teenage experience as a caregiver for my mother after her ALS diagnosis, & the personal fallout after sheโ€™d passed away (ALS, Grief, and Growing Up Too Fast: What October Means toย Me).

For those who donโ€™t know, ALS runs heavily in my motherโ€™s family. To the point where our genes are sought for study. Itโ€™s pretty scary.

Let me map out some of what little I actually know :

  • It comes from my momโ€™s dadโ€™s family, traceable back as far as the late 1800โ€™s when it was referred to as โ€œcreeping paralysisโ€.
  • My mom was the oldest of four girls, the middle two were twins : The youngest doesnโ€™t carry the gene; the other three passed away, all from ALS, at around the ages of 35, 45, & 55.
  • The three sisters had a total of six kids between them, myself included. Out of those six, three have already passed away from ALS, most recently about two years ago now. I havenโ€™t been tested for the gene, but my remaining cousins were & they do carry it.
  • Here’s two of many stories about about a couple of my cousins :

Existential Crisis

My odds probably arenโ€™t great. But as long as I donโ€™t get tested, thereโ€™s still a strange kind of hope in the uncertainty.

However, one of those remaining cousins was recently diagnosed with ALS. Sheโ€™s only a couple years older than me, soโ€ฆcue the amplified existential crisis.

I’m tired of being so rudely reminded of my mortality, as I’m sure were all of my ancestors before me.

I’m tired of all this grief, and fear.

That possible genetic time bomb has been ticking a little too loudly in my ear latelyโ€ฆ

And I resent the fact that my family isnโ€™t as close as it should be. Itโ€™s always been kind of sickening to me, because we all know thatโ€™s not the way it should be.

Shitty Instincts

For some reason, hearing this news makes me want to reach out to my old friend even more. (If youโ€™ve been around a while, youโ€™ve heard me mention him. And you may have heard me mention that Iโ€™ve tried reaching out to him, to no avail.)

Why.

Because I don’t wanna go out without resolution. Such unresolved tension. Especially since thereโ€™s no good reason for it in the first place.

And because I want his support; because sometimes he could be the most enlightening perspective in my life.

He was around when I first started learning more about the tragedy surrounding this gene, and he said to me one day, โ€œseems you already count yourself among the deadโ€. Which wasnโ€™t any more true then than it is nowโ€ฆ

No One Makes It Out Alive

I donโ€™t consider myself among the dead.

I consider myself among the cursed.

Cursed with immense loss & fear ingrained in my genetic code.

Cursed with being faced with the harshest of realities, such as the fact that no oneโ€™s there when all is done – โ€In the end, you’re measured by how you treat the people closest to youโ€œ – Ryan Holiday.

Cursed with shitty genes & a constant reminder of how short life can be.

But also immensely blessed with a sense of urgency that most people donโ€™t realize until itโ€™s too late. If they even get the chance.

All I can do is love my family, keep trying to live vibrantly, and keep trying to help others.

โ€œLife is long, if you know how to use itโ€ – Seneca


Celebrate life. Honor your ancestors.

If ALS has touched your family too, you already know the strange mix of grief, fear, and urgency that comes with it.

If youโ€™re able, consider supporting ALS research – or simply reach out to someone you love today. None of us are promised tomorrow.

Click here to learn more about ALS or to donate toward finding a cure ๐Ÿ‘‰ ALS Association

Stay real. Stay loud. And rock the fuck on. ๐Ÿ’š๐Ÿค˜๐Ÿป

What is zen BLITZ all about?

zen BLITZ is still in its baby phase, & it’s been quite an adventure so far!

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I think it’s important to reevaluate everything in your business as you go along, including your brand identity! This post is to share a little more about who I am, my brand’s themes, and the projects I work on.

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As for me… I really love that wig; it’s just too cute, lol! I have a history of being a caregiver in my family, for my parents & grandparents; currently for my father. I also have an employment & education history in healthcare. ALS runs heavily in my mother’s family, so I’d like to be able to donate some of the profits from my shop toward treatment & research one day! I’m currently engaged to a super awesome guy whose love has set me free; the only thing really holding me back is myself.

 

I have a bit of a problem sticking with themes, lol! I’m a Libra, so I have a bitch of a time making decisions in general. Themes varying from vague (fun, spiritual, classy) to more specific (witchcraft, buddhism, steampunk, rave, hippie boho). I know I need to pick specialties & focus on a certain audience, but…that’s not me! That’s not very zen BLITZ. zen BLITZ is calm & crazy, spiritual & steampunk, yin & yang. Right now, I’m just testing what works well, & what doesn’t.

Another problem I have is sticking with any one project. Really, I’m “in too deep” with my jewelry making, especially since that’s what my fiance has been supporting most. However I’ve always been into all kinds of crafts, because my mother was super craftsy. I tend to have a few different types of projects going on at once, but I do also tend to finish one thing before adding another. So far, my shop is mostly jewelry – necklaces, bracelets, rings, & earrings. I also added some wine glass charms. I’m currently working on a set of crochet wine glass and water bottle lanyards, & then I’ll start working on some more jewelry. I just finished a set of ATCs (which were a bit of a flop…learning experience), & have been working on woodburning a plaque for my sweet deceased kitty.

Seeing as jewelry is a very saturated market, I figure it wise to venture into other handmade markets wherever my talents lie. The only constant in life is change. It’ll be fun to watch my shop evolve over time!

“It’s important to reevaluate everything as you go along”

That’s advice I carry throughout all areas in my life. It’s always a good time to shed things that weigh you down, & change the things that aren’t working for you. “Every day is a holiday…”

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That’s my brand identity!

What are YOU all about? Freewrite some random words, & let’s chat in the comments below!

And be sure to check out all the fun stuff in my Etsy shop at zen BLITZ

May is ALS Awareness Month

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learn more & donate here

ALS, aka Amyotrophic Lateral Sclerosis, aka MND (motor neuron disease), aka Lou Gehrigs Disease, is an increasingly common neurodegenerative disease. Very little is understood about it, & it is inevitably fatal. Continuing research is necessary to put a stop to this awful affliction.

In this week’s article, I’ll tell you a little bit about ALS, point out some famous people affected by this disease, explain why ALS awareness is important to me, and share a special promo in my Etsy shop!

More than 20,000 people in the U.S. alone have ALS at any given time. Only 10% of those cases are due to an inherited genetic mutation, while 90% have no family history of the disease. As a neurodegenerative disorder, ALS kills the motor neurons throughout the body, leaving muscles paralyzed while the mind remains intact. There is no testing for this disease, only ruling out other diseases. Life expectancy is 2-5 years after the onset of symptoms.

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Stephen Hawking

Odds are good that you know of at least one famous person who’s had ALS. Lou Gehrig, of course, the famous baseball player whose name became extra infamous for this disease. Stephen Hawking, the super famous physicist, just recently passed away after suffering from ALS for over 50 years! Steve Gleason, as well as many other professional athletes. Wikipedia has a whole list.

ALS actually runs in my family. I think the statistic was 25 people in 3 generations, but 2 or 3 more have been added to the tally, 2 from my generation (the 4th). No one has lived more than a year and a half after the onset of symptoms, so it’s pretty quick, but no less horrific. It’s traumatized many of us who have had to watch this happen to our loved ones. My mother had bulbar onset ALS, was sick for about 11 months, and passed away due to respiratory failure (which she was fully conscious for) 4 days after my 15th birthday. I’ll refrain from whining, but encourage you to learn a little more about my family’s story in this interview on YouTube.

So, to support ALS Awareness, here’s a little gift for you :

ALSA May promo

“Continuing research is necessary to put a stop to this awful affliction”

ALS is a devastating disease that can seemingly strike anyone, especially if you have a family history. Your help in funding research is greatly appreciated – donate directly to the ALS Association, or any foundation of your choice, or buy something from my shop & I’ll gladly pass along the good vibes from my wonderful customers!

Do you have any experience with ALS? (Friends, family members, personal, etc). Let’s chat in the comments below!! โค

And don’t forget to stop in & check out all the new stuff in my Etsy shop : zen BLITZ