It’s All About the Ovaries (Second Edition of Everyday Aspergers: Part One)

So, I’ve been procrastinating on this post since December 2018.

I’ve analyzed why and have come up short. It’s likely that I don’t care much for self-promotion. Indeed, in the last 6+ years I can count on one hand how many times I’ve asked folks to share about my Everyday Aspergers Facebook page. (And that counts the mention here!) If you haven’t checked it out, please do.

I could blame my procrastination on the countdown to menopause, which I hope and pray arrives tomorrow, as I’ve been dealing with the complexity of endometriosis for years, including the 2018 road traveled of chocolate cysts. Don’t let the name fool you; it’s all about the blood. And now that I’ve over-shared, I will switch gears.

 

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Recently, I’ve had a profound peace — could be hormones shifting and my lady parts semi-retiring — could not. (Oops, focus Sam!) I’d like to think it’s something to do with my faith and spirit. It’s likely a combination of coffee, getting older, and finally getting fed up with not speaking up for myself and finally understanding boundaries! That, and I do feel the presence of an angelic spirit. But that’s another story.

Not much has changed (with my brain) in the past years, since I started writing Everyday Aspergers. Which now has over 1.4 million hits! Well, yes, some of the reason behind the high ‘hit’ number is because there are over 500 posts! Omgosh — write much?

My point being, I still digress to a close-to-annoying degree.

That’s likely why I typically get called to interview for a job, based on my awesome resume, skills, and experience, but don’t seem to ever get the job! (In fact, I don’t even get a rejection letter — just GHOSTED.) Picture me bungee jumping off a high cliff of ‘tell us a bit about yourself,’ and swirling in rapid circles, giggling like I’m twelve, raising my voice in high pitch, fidgeting about, announcing how proud I am to have ASPERGERS, and then correcting myself: “I mean to be on the autism spectrum.”

I leave an interview feeling like I either nailed it and they absolutely LOVED me, and want to be my best friend, or convinced I terrified the living daylights out of them. It’s likely the latter. As I mentioned: I don’t ever hear back. Thank the lord for my job at ultratesting.us, where being neurodivergent is the norm! Thank my lucky stars. (< Madonna video)

Ironically, I have studied 1000s of hours of best hiring practices for my vocation, and can’t seem to keep my Aspie-ness in a bag when under distress at an interview. There must be a pill I can take. (Now picturing Violet in Willy Wonka and the Chocolate Factory, and now must Google to find an image.) “. .  . because Charlie she’s a nitwit.” Not to say I’m a nitwit.

 

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Okay, alas the REAL point of this post is to tell you THE SECOND EDITION OF EVERYDAY ASPERGERS IS HERE! And it’s now available in paperback in many countries. Check out Amazon or ask your local library to see if they can order it. Look at the PRETTY cover by an autistic artist (and my friend and colleague)!

USA amazon

UK amazon

AU amazon

10 Facts You May Not Know About the Book Everyday Aspergers

Are we friends yet? (Facebook link)

 

Okay … done! Although, I don’t think this is what my publisher had in mind.  (scan down for more.)

 

 

On a side note, I will speak to you as if you and I are in a cafe, and I’m catching you up with my medical stories. Sorry for the monologue, and the white-haired man sitting kitty-corner to us that is blushing because I am talking too loud.

This here ^^  … that’s an image of a chocolate cyst. Funny story … after an ultrasound in early 2018, when I found out I had at least one chocolate cyst, (and had gone to the emergency room in excruciating pain, and was curled up on couch most days for weeks) in typical Sammy-fashion, I researched with hyper-focus about the chocolate cysts and implemented some home treatments — including essential oil, strict dietary change, etc.

When I returned months later for a follow-up ultrasound, the technician confirmed indeed the cysts presented (3 of them) exactly like ‘chocolate’ cysts! Immediately following, (literally a few steps down the hall), my OBGYN doc informs me, “The cysts are shrinking, and that doesn’t happen with chocolate cysts, so we can’t call them that anymore. They don’t shrink.”

I was dumbfounded.

Surely, in some cases they can? And I’d done so much, including talking to my body, to ensure healing.

My scrunched up face demonstrated I was confused, as I asked in a high-pitched voice, that no longer suits my age: “Well, what would we call them if they weren’t shrinking?”

She responded, “Oh, definitely chocolate cysts.”

I then got that familiar feeling in my gut that means ‘NO ONE on this planet is truly an expert in anything and most of the time professionals are talking out their donkey.’

(“vulgar slang To say foolish things; to talk of nonsense. Don’t pay Jonathan any mind, Mary, he’s just talking out his ass again.”)

The next time I went back in for a check up, with said Doc, she informs that my chocolate cysts are shrinking or stabilized.

So I guess we are back to calling them that?

Anyhow, it reminds me of the time I had a dead front tooth, when I was in my early 20s, and I went to a dentist that a colleague had suggested I see. It was 1992, a sunny day. The dentist’s recommendation for my dead tooth’s discoloring was to darken all my teeth to match!!! Yes, that’s right. And, noooo, I did not!

I have trouble believing this actually transpired, especially after I told my dental hygienist the story yesterday, and she said that’s the worst telling she has heard to date. Also, because decades have past with my pretty veneer tooth. (The other dentist I saw bleached all my teeth to match the new veneer. Yin and Yang. Dark and Light. Theme of my life.)

(On another side note: I found out this week I have no cavities and an unusually small mouth [which matches my usually small head]. And I warned the dental hygienist not to say she has a small mouth despite what her husband says, because that can be interpreted in different ways.

She was appreciative, and said, “We’re going to get along just fine.”

I always find it to be an interesting phenomenon when I give out unsolicited advice to non-autistics about social graces.)

Needless to say, I never went back to that dentist who wanted to darken my teeth! But the young, inexperienced (terrified) me did shake hysterically in her car afterward. The same way I shook after seeing a ‘specialist’ a few years back.

That time a doctor would diagnose me with ‘a close cousin to POTS syndrome,’ (as my blood pressure acted a bit different from typical POTS, but the tilt table test confirmed the condition.)

This was after 5 ER visits wherein my pulse would go to 160 upon standing, wherein the IV would add sodium to my blood, and remedy the POTS-like reaction, making me seem better; only to be sent home and the symptoms to come back (160 upon standing, weak, shaking, etc.); only for me to return to the ER and be told I must be inventing it for attention.

Yes, hysteria is still widely falsely the diagnosis for women! No wonder I have white-coat syndrome.

Fortunately, my then-husband Bob (now-good friend) was in the patient room with the ‘specialist’ (notice the quotes) and me, when the Doc told me my diagnosis and prescribed an exact treatment plan, e.g, constricting stockings, raise bed, exercise regime, salt intake, etc.

A year later, I came back, feeling super pleased I’d followed the Doc’s directions, and was able to sit up for long periods of time, and return to life as normal (well atypical normal). BUT THEN . . . she SCOLDED me, accusing me of making my condition up, and saying I didn’t have POTS, and didn’t have to do all that. That I wasted my money on salt pills and where did I get the idea I had POTS?

I had to phone my ex-hubby from the car to avoid a nervous breakdown; literally thought I was losing my mind, until I realized the doctor was …

(Scan down for book reviews.)

So . . . I likely should write another post soon that is more about the book. I will. I think. Can’t wait to see what pops out of LV’s mouth then! Sir Brain is shaking his head in shame. (He doesn’t have ovaries.)

Samantha Craft’s Updates August 2016

last updated August 2018

You can find me at Spectrum Suite LLC  and email me directly at marcellelinn @ icloud . com. Spectrum Suite will soon be offering vocational coaching, life coaching, and spiritual coaching. Stay tuned!

Thank you for your support through the years. I couldn’t have wished for a kinder and more accepting community.

This blog was open from 2012 – 2016. I make updates from time to time with new news.

Sam’s other blog can be found at Everyday Aspie.

Both blogs are retired, after many years of writing, except for occasional updates about happenings related to autism, the autistic community, and the book Everyday Aspergers.

New book I contributed to here

BOOK INFORMATION
· Amazon US link
· Amazon UK link
· Amazon Australia link
The soft back version is available in USA on Amazon here.
Current updates can be found at my company Spectrum Suite.
Please consider posting a review on Amazon and/or Goodreads.

THANK YOU ~ SAM

Marcie Ciampi, M.Ed   (AKA: Samantha Craft)

Craft is best known for her prolific writings found in her well received book and blog Everyday Aspergers. A professional educator, she has been published in peer-reviewed journals, been featured in various literature and venues, including Aspien Women, Autism Parenting Magazine, The Mighty,  Spectrum Women, Project Aspie and Different Brains.  She is coauthor of the book Spectrum Women: Walking to the Beat of Autism and speaks on the topic of neurodiversity around the world, including at the Love & Autism Conference (Fall 2018) and Southwest Washington Autism Conference (Fall 2018).

Craft was the Community Achievement Award recipient at the ANCA World Autism Festival (2017), her works have been translated into multiple languages, with her list of traits for females on the autism spectrum shared in counseling offices around the world. Since 2012, she’s had the opportunity to correspond with over 10,000 individuals on the autism spectrum. Her blog Belly of a Star features her paintings and drawings and over 100 poems and spiritual writings. Craft also serves as the Lead Job Recruiter and Community Manager at ULTRA Testing, an innovative technology company with a neurodiversity hiring initiative.

Balancing the World; thoughts on leadership and autism

My entire life, like many on the autism spectrum, I have oftentimes been misjudged, misinterpreted, and misunderstood. When I finally, after over four decades on this earth, located individuals with like minds, I was overcome with mixed emotions. I’d finally found “my people” and at the same time lost a piece of myself that I thought was extremely different. Lost in the sense that I came to realize, after conversing with other autistics, that I wasn’t so different and “unique” after all. However, this was okay—extremely okay. Finding a home base community in which I was at last understood, accepted, and supported far out weighed any sense of loss of elements of self.

Four-plus years later, after an outpour of online writing, and I am navigating another aspect of my journey. I am entering another unfamiliar zone—a place of no predictability. I am facing a wide-open space of new people and new encounters. In addition, I am trying my best to maneuver in rarely frequented territory: that of an autistic leader.

Autism, in my case Asperger’s Syndrome, comes in all shapes and sizes, multiple colors of the rainbow. It is truly a spectrum. With autism, there are the typical “gifts” and tribulations. For me, the beneficial attributes of my ASD are profound empathy and insight, prolific writing, poetry, and the ability to put into words my suffering in a way others can understand. In this way, I am able to make the loneliness of some less of a burden, and I have been able to serve as a sort of gateway into a supportive community of other autistics. A community in which we find ourselves in one another. I don’t say this lightly. There have been streams of individuals filtering through the pages of my blogs and social media pages to essentially say that they now have at last found hope—and some a reason to not end their life. I don’t say this to brag, either. Those that have known me, know my heart, and it is for them I speak.

The trouble today is not so much my tribulations related to ASD, such as peak moments of heightened anxiety, bombardments of feelings that at first look are hard to decipher, the jarring reminders every hour of my waking day that I am somehow not built like most others, the intense heartache and lack of breath from searing pangs of empathy, and the worries brought on by my minds ability to steer off into complex, multi-level corridors of discovery. No, it’s not so much in that—though “that” still consumes me. More over, it is this new place I find myself, in where I am exposed.

I am a natural born leader; I always have been, despite my own qualms and misgivings. Despite my protest. Despite my quirks and challenges. Overall, I tend to end up as a voice of some sort–usually for the downcast or underdog. And it’s not amongst my favorite of tasks—this speaking up for myself and others. Indeed, it would be fair to say, I dread many moments beyond the comfort of my home. Still, there are mornings of great hope and gratitude for my ability to reach out, and with this comes waves of great peace; but there, on the other end of the pendulum, is the bareness of naked vulnerability, the removal of shield, the entranceway for stinging spears. There, in the darker zone, lives my fear and weakness, and the very brittle fight to survive exposure. For I’m not the average person, I’m not made the way of the masses. I am very much, despite where I stand, still autistic.

I am hurt daily, by my own accord, by the acceptance of others’ truths as mine. By the energy it takes to abstract and remove everything that doesn’t ring true to me. And to then wade through the muck of others’ ideas, input, feelings, insights—and on an on—to hopefully decipher what is valid and necessary at this time. I am not only balancing myself, which those on the spectrum readily know is a gallant effort, I am also balancing everyone within my reach. In this way, it is hard to be outside exposed in the “real” world.

It is especially challenging when outsiders (who do not know me and often see a reflection of their own self) try to pin their tail of identity onto me. I feel smothered, unrecognized, and brought back to the bastardized halls of my high school years. Brought back to the pettiness, the name-calling, the finger pointing, and relive the nightmares over again. It is equally difficult when another, particularly in the autistic community, starts proclaiming how I should tailor my words to suit their needs—the current societal trends—the current “right way.” To see this conglomeration of “do-gooders” with supposed good intention in mind, attempt to steer me into what is the most well accepted approach of the day is excruciatingly exhausting.

I can only be so much. I can only do so much. And I don’t understand why my own tribe would not see this. They forget that I am autistic. They forget how dreadfully scary this is. How frightening to attempt to build a bridge from the autistic world to the non-autistic world, and to appear “normal” enough in the typical arena to be heard and listened to, and “autistic” enough to be trusted in my own community. It is a fine balancing act in which I am continually on a high wire with a long heavy pole. Constantly pushed off balance while attempting to get to the other side to the unknown. I am walking step-by-step toward something that is neither a goal nor destiny, but rather a calling. I am serving, I am giving, I am loving, I am supporting, I am being my all. Yet no matter how I struggle, no matter where I step, to some, as is this world—it is never enough.

 

(I normally post at my blog Everyday Aspie, but my WordPress options were not working accurately there today.)

 

Sam’s book Everyday Aspergers is now available internationally on Amazon.

More information can be found at her company: myspectrumsuite.com

What’s Up?

buns

Hello!

I have missed you. Everyday Aspergers (EA), the book, is coming along quite well. It’s in the final draft stages and I hope it will be ready for your eyes by this early-May. (And the cover is awesome!!!)

As some of you know, I have spent countless hours editing . . . I recently had a huge aha moment: being dyslexic I ought never ever try to edit! But alas, it’s a bit too late for that. I have ‘literarily’ (notice the non-risqué double entendre?) edited my book more hours than I can calculate. And the book started off at 1,200 pages! Don’t worry, I have a professional editor. Good thing because I still have trouble with sneaky homophones, like verses and versus. Who ever invented the English language sucks.

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What’s been challenging is grammar rules—there are lots and lots of rules, and not everyone is in agreement. In addition, commas hurt my eyes, if they are not placed in the correct place; correct as in where it seems I ought to sprinkle a little dash based on the rhythm in my head; not ‘correct’ as in rules. So that’s been an interesting predicament. Also, hyphenated words fall into a similar spot as commas: the inconsistent box. And it doesn’t help that I went through a happy-to-hyphenate stage and a put-a-comma-everywhere phase. I am still recovering.

The other, (likely Aspie-related), recent challenge has been chopping up my previous blog posts,(there’s over 500), rearranging, refining, omitting, rewording, embellishing and realizing that this process is not LYING or being dishonest in the slightest degree.

And the most laughable moment to date, regarding this book journey, (at least according to my autistic partner), is when I said, “I don’t think my book is autistic enough,” with weeping puppy-dog eyes, and he adamantly responded (after asking if I was PMSing), “If you are not autistic then I am not autistic.” So that set things straight. He then added, in his arrogant Aspie-genuis tone, “Plus, you’re like the poster child for Aspergers.” Still processing that one.

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Publishing a book is kind of like childbirth—had I known the pain, I doubt I’d ever have started; however, once I see my baby, it will be worth every agonizing moment. At least that’s what I keep telling myself.

I do have to say that my psychological metamorphosis has been fascinating: One moment confident, next moment terrified. One day never wanting any human to read my words ever again, next day, over sharing my works. It’s kind of like the publishing process has intensified my autistic extremes! Go me!

Oh, and I’ve had ample opportunity to sit back and listen to LV (little voice inside my head) burst aloud fret after fret. I think she’s grown a small pink cape monogrammed with ‘insecurity.’ First off, I apologize for the short phase (about 1.5 months) in which we (me, LV and Sir Brain) we’re never going to have ANYTHING to do with AUTISM ever again! This was largely due to the ebb and flow of opinionated jerks online (something I swiftly swam away from), my tendency to hyper focus almost to the tipping point of my sanity, the way my life drips and oozes of autism (partner, son, ME, job, writing, reading, social media platforms, blogs, book, research, friends, so forth …), and my forever search for balance (psychological and hormonal!).

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For a short stretch of time, I figured I’d be a hermit in the back room, behind my garage, and just obsessively paint, never to resurface, except out of loyalty for the occasional chocolate bar left outside my door. After some retreat and reflection, I realize autism is in my bones—and most definitely in my genes—so not really a smart plan to try to escape it, entirely. Still, I am attempting to not let my special interest consume me. But alas, I likely will always have my all or nothing tendencies, despite my best efforts.

With all that said, my prolific abilities for writing and off beat wit seem to have resurfaced. This following two years of gradual rehabilitation from a weeklong hospital stay, in which the trauma to my system greatly affected my executive functioning ability; I mean I couldn’t even open an envelope for months. Took me three months to be able to sit up for more than an hour. There was some major healing that had to take place. But thankfully, I feel about 95% back to normal. Except now, my premenopausal brain-frying hot flashes and hormonal extremes–seem to be affecting my dyslexia and dysgraphia. Kind of like someone turned up the omitting words, mixing up words and letters, and forgetting thoughts dial to about the umpteenth power. So that’s been fun. Good timing, don’t you think?

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Talk soon,
Sam the Ham
(Now I want to list words that rhyme with ‘ham.’ Yep, I’m back!)

My recent interview about females and autism:
http://www.blogtalkradio.com/positivelyautistic/2016/03/05/positively-autistic–jeanettes-autism-show

To support this book journey please join our Facebook Community listed on this blog in the side section or follow this blog. Here I am on Twitter

360: The Ashes of Discovery

Photo on 3-31-13 at 12.07 PM

I pulled myself into church, today.

I have been searching within about where to take my next steps, in regards to my calling and passion for service. I believe spirit planted in my heart a connection that will lead me through.

Just yesterday, I was able to slip out of a depression brought on by PMDD, a condition I believe to be common with women on the autistic spectrum, and a condition that quadrupled my pain and quadrupled my thoughts of unworthiness.

I am recognizing that the first twenty-days, following my cycle, I have energy, renewed hope, an abundance of radiating light, and confidence in my journey. Interestingly, when sorting through my blog posts, I noticed a definite trend. Through my words, I can readily see how I become sad following a cycle of hope.

It is very surreal for me to step back and become the observer of self, to see what has transpired in the last thirteen months, and to reflect in the place and places I stood. The experience teaches me that indeed I am continually transitioning and continue to be increased in my faith and vocation, despite the set backs and the challenges, all which derive from my own self (ego, self-form, lack in faith.)

In recognizing this PMDD and how it affects my moods, and thusly my ability to remain steadfast in hope and courage, I am understanding I would benefit from putting support in place. As the last ten days of the cycle following ovulation, (I follow the exact cycle of the full moon.), I seep day-by-day into a greater degree of pain and disheartenment. I have found, though, through review, if I am surrounded by family and/or friends, I am pulled out of isolation, and therefore the depression is lifted and I am filled with love.

In seeing this, it makes sense for me to put into place a support system, in which my friends and family understand what is happening to me at a biological level. I am working on creating this space for me, of love and nourishment of soul, in the next weeks, while I am in a “good” place, not yet exhausted or immobile from the various “syndromes” I am healing from.

This has brought me much clarity, the recognition of the PMDD and how in effect I am not governed by my mind and/or spirit when the hormones shift rapidly. Knowing I am a part of the percent who feels an actual sensitivity to my hormones makes complete sense. And to a lesser degree has, much like the discovering of Aspergers, led me to several ah!-ha! moments, in which I review the past in flash backs and recognize that though I struggled repeatedly for answers to my pain and suffering, and dedicated my efforts to “controlling” my moods and pain through faith, that in fact, some things were beyond my control.

I see this as a direct parallel in how I searched for decades for answers about why I felt different from the majority (Aspergers), and wearily came up with few answers. In the past, increasingly, as I dedicated myself to finding solutions, increasingly I was disappointed, and sometimes shunned and criticized. My strength in self faltered in stability, as my hormones shifted, and I can see this in photographs of myself where I am bloated, discouraged, and have a sadness in my eyes that radiates lost and abandoned.

I now understand that why for some thirty years I have struggled monthly with a feeling of being lost to myself. To a degree I have been. For during these ten days, I develop a skewered view of my physical body: I believe that I am extremely fat, ugly, disproportionately put together wrong, and unworthy of recognition. I essentially hide from the world and the fear of judgment, becoming immobile and unable to leave my house, even to step into the yard. This confusion of my appearance is a trait of PMDD, and possibly a result of a variant enzyme in my body. This makes sense.

However, for so long, with both Aspergers and my mood “swings,” I blamed myself and my inability to rise and conquer my own mind and weeping spirit. How funny to think I was my worst judge and worst enemy, believing if I only tried harder and hard enough I would create the person I wished to be.

In truth it was the process of surrender and exposure of self that led to the underlying waves of causation, e.g., admitting weakness and loss of control led to answers. This recent last week of self-discovery was patched with confusion and doubt. Yet, I am thankful I gave up long enough to find the answers. Too, this past week, was filled with fear, which I am certain affected my pain-threshold and outlook.

The fear arose from illusion: that of death, illness, and surprise. I have carried with me, since a small child, the inevitable feeling that death will surprise me. Perhaps this dread surfaced from the dreams of prophecy I had in my youth wherein I predicted the death of my beloved pets. Perhaps the fear was constructed from the experience of continual change and loss of people in my life. Maybe, the fear took root when my kindergarten teacher died. Or just maybe the distrust and feelings of doom are genetically or spiritually a part of who I am at this moment.

Regardless, fear of death is a constant battle, an aspect of my life I am releasing continually. I have learned to recognize this fear before both feet are through my threshold. I acknowledge this existence of up most illusion.

“Fear,” I whisper.
“Fear,” I say.

And then I retreat back, a gentler part of self, and watch with much release as the messages spin and play, some forgotten record moved again by some forgotten will. In this way I survive. In this way I live.

Recently, in observing this fear all week, revved-up by the revelation of an inherent physical “flaw,”—that of PMDD—I was able to again and again surrender to my higher power and wrap my heart around the concept of submission. I feared, certainly, as the illusion came knocking again and again. But something remarkable has happened in the last months. In essence, I am so highly aware of fear’s calling that at first knock I am already removed, letting only a part of self dance and the rest set about to learn, as if placed in classroom by something beyond chance.

This is a level of transition from where I was before; and though I tremble and weep inside, experiencing moments of extreme bouts of forsaken soul, the rest of me, a greater mass, retreats into the echoes of truth, beckoning the light at the end of the bleakness to move forward and touch me before I step to touch light.

And this is glorious. For as I am in the mold of shadows, I also dwell in the light of goodness. And I know, with this flicker of hope, I will be alright. I am learning, slowly and steadily, to hold onto the glimmer, the slimness of glory, and learning in time, with the passing of days, I will return.

Is this still frightening, this purging of fear?

Yes, extremely so.

But am I growing and reaping benefit?

Yes, I am.

In all ways I am the embers in the fire pierced in pain, releasing to the cold black of coal, and then being rectified, removed from the flame ash, and brought back to the earth of goodness. And this is what I hold onto: The ability to continually rise from the ashes.

In saying all of this, I will release my fear, as I have been taught in vision that beyond fear is where I find love’s adobe.

When I abide in love, I am free. And so I tell you, my listener, what I fear.

I fear that I am creating a book and that in this book will be a history that is all of me, and that is to me frightening in varying degrees.

First is the judgment that will be set upon me, as writer, as woman, but beyond that as spirit. But this I can conquer, this fear is limiting and unsubstantial in its potency. For I know I am love and light, as I know you are.

The second fear is found in the process of building a foundation of support. I will be led, and have been led, in direction in regards to this journey; a journey which I now hesitate to call mine, as so many of you reading are affectively part of this journey now. In being led, I know I will hit walls and ditches and even waterfalls; I will tumble and fall; I am human and shall not be perfect. And in this fear, too, I am ready to breathe. I can breathe here, in this illusion of failure and wrong turns, possible deceit, and survive. I see this as only shadows and a necessary part of my path, much faced already and much climbed. So, yes, this fear I can release, too.

Thirdly, and perhaps the biggest fear, is found in the potentiality of being separated from others.

I am fearful I will non-intentionally create a path that others interpret as rigid, narrow, and religious. And that is not my intention. I welcome all walks of faith and walks of life. I have been shown in vision the discrepancies of spirit filtered through the falsehood of judgment and pride. I have been shown that my path is never the right path and never the right way. That my perception and my very comfort and haven of safety, have been self-created based on circumstance and what I choose to see and make my foundation and truth. In essence my truth can never be anyone else’s truth unless the all of us are one.

And in this way, I hesitate, in the way of a one wanting to be a helper to all and not a select group. I want to be a gift to all who need refuge and retreat, and not a one who would by appearance, and appearance alone, be an illusion of someone who segregates and isolates.

Thusly, in connecting any of my works to a title or an establishment, I also at the same time connect myself to a “label,” and to the judgment of others based on that label.

And it is in this judgment my fear lives. Here in the heart of me who weeps knowing that by choosing anything at anytime, others are automatically left out by their own doing.

But left out of what? Left out of what? Is what I ask.

In truth, I imagine, they are actually left out of nothing, beyond my own journey.

And so is this my fear: The fear of being separated by my perceived actions?

Is this fear not once again the same fear that is the irrigation and fertilization system of Aspergers?

The fear of being left out by another from his or her perceived judgment of my action. That of his energy shifting, his thoughts, his opinion, his view of me, in fact the existence of me (as I only exist in interpretation), being altered without my control.

Yes. This is the deepest fear. The loss of control.

In reviewing this with audience, I see that in stepping out and making choice in the direction for my book, I am at the same time creating a space for my deepest fear of separation based on others’ views. And thusly, I recognize that this, too, this journey to create my story into book form, like my genetic makeup, like my view of the world, like the way I communicate–literally crying and shaking in my boots—is yet another mirror exposing fear bred from the beast of longing to control.

And today, on this day of resurrection, I release, I let go of this part of self, who so longs to unite and join, but still hovers under the illusion and want of control.

I let go of this self who wishes to dislodge judgment and rigidness from her own being, yet still formulates and categorizes in hopes of solution.

I release this frightened child who thinks that like before the rest of the world will rebel against her way of existence. And I give to myself the gift of removal of control.

With deep breath and settling awareness, I set about to create a place for my mission that is not predicated by fear, not paved by intention beyond love; a path that circumvents all thoughts of separation.

In doing this, in proclaiming my truth, I again dismiss fear to the outer barriers, where he waits to teach me more. And I celebrate his fire, his flame, his ability to mold me again and again into the ashes of discovery.

I know not who I be anymore than another. I know nothing more than my brother. I know only that I am called, and in so doing will no longer hide in the shadows of fear.

Because I know by faith I walk, and in this way of the child with passion, I continue forward to meet the next imagined stranger who is already friend.