Everyday Aspergers: THE BOOK

I invite you to take a look inside of my book Everyday Aspergers.

Take a look here.

(I just deleted an entire paragraph explaining why I am uncomfortable with self-promotion. I’ll spare you the details!)

My publisher, Your Stories Matter, took great care to provide this ‘book-to-look’ version of the second edition of Everyday Aspergers.

(I’ve truly failed at promoting my own book. I usually promote Steve Silberman’s book in my travels and teachings. Typical me!)

Over a year ago, I decided to move my memoir from one agency to another. I made this decision to ensure the paperback was available outside of the USA. Here are ten facts you might not know about E.A.

The second edition of Everyday Aspergers : A Journey on the Autism Spectrum can be purchased on Amazon in several countries. It makes a great gift!

The new book cover is by a talented autistic author and writer. The pages, of the new edition, have photos and images from my childhood. I added a new end chapter. The layout, pages, and style are different. It’s the same story in an enhanced casing.

https://www.book2look.com/book/KRksrIxTxr

My three sons and me in 2018.

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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.

10 Years in the Making! Everyday Aspergers

This Blog Everyday Asperger’s by Samantha Craft is retired. Her company website is myspectrumsuite.com  Thank you for the community and support you have offered through the years.

 

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In 2004, I was called to write. I dedicated myself to write every day for a year. I only missed one day and completed a 250-page memoir. I often wrote 4 to 10 hours a day. I spent the next years editing because my dyslexia and dysgraphia make it very challenging for me to detect errors. I knew nothing of writing. It was pretty substandard material at the start. I didn’t even know when to capitalize the word ‘mom’ or how to use a semi-colon. It took me three years of writing and editing to find ‘my voice.’

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I taught myself to write by studying other books, relentlessly. I took notes and would write pages and pages of words I found (in other books) on notepads. In 2012, I started Everyday Asperger’s (blog) and  wrote almost every day for a year. I then continued posting blog posts several times a month, for another two years. Each Everyday Asperger’s blog post took a long time to edit. Then, after it was online, I would reread the words for an hour (at least) trying to find all the small mistakes that I couldn’t find the first time. (I didn’t mind; it was a type of stimming for me.) At the time of writing the blog, I also reedited some of the original (year 2004) childhood stories.

Recently, after 3.5 years of writing over 1,300 pages online, I began the process for my book: Everyday Aspergers (EA). I tore through 1,200 single-spaced pages of this blog, some of which were my childhood stories, picking and choosing, and then piecing the posts together like a puzzle. This took a solid two months of working almost daily. From there, I refined and refined, trimming most posts to 1/3 original size; some of those posts, if not most, were originally two to three pages long. Next I found little parts that got cut but were still gold nuggets and found places to sprinkle them in.

After that I polished and polished and polished, and began to edit. Soon the final editing took place from December to today. Most weeks I spent the equivalent of a full-time job editing. I also employed the help of a professional editing team. To date, the manuscript for Everyday Aspergers has gone through four editing rounds, in which I read the words (at first 717 pages, then 615 pages, then 417 pages) from start to end. Each page was reedited each time! I’d spend marathon days, up to 12 hours straight editing. Some of the childhood stories have been edited and polished at minimum 15 hours per page! Counting the years before, I’d say the book itself has well over 5,000 hours of editing alone. That doesn’t count any of my writing time. It’s a HUGE accomplishment. It’s not just something I threw together. It has a huge heart and huge effort behind my endeavor.

I cannot wait for the book to be in my hands. More so, I cannot wait for those who wish to have the book to hold the story in their hands! I’ve been waiting since 2004, when I had a dream.

Much love,
Samantha Craft

I updated the Checklist for Females with Aspergers here

Me on Twitter: aspergersgirls

More about the book on  new website

 

 

 

 

506: The Risk is Worth it. Thoughts on Friendship.

I don’t believe I have any answers that anyone else cannot find for himself. Or to non-negate the previous statement: I do believe I have no answers that another cannot find for himself. I have a hard time reasoning in my mind the authenticity of any self-proclaimed or manmade accentuated leader who hints, dictates, or infers that he has the answers. I am quick to steer away, and feel quite many a qualms, when I hear of anyone who thinks they have found the answer, the truth, and the way. I know too much to be a blind sheep, and too little to proclaim I know enough. This is not to say I diminish or shake a finger at modern religion or any new up and coming spiritual fashion, only that I seriously question and outright deny the fact that any human can foreseeably house the answers for another; and certainly without the answer, he has no right, if rights be the matter, to dictate to another how to live or present oneself.

I find the purest souls to be the most delightful in their attempts to literally do nothing but be, and to let be. Those that don’t pursue fame, recognition, reward, and esteem are the ones I gravitate towards, the ones who are actually repelled at multiple levels by anything to do with being in the spotlight. Those are the ones I tend to uphold as seers and seekers of truth.

Secondly, I know enough of myself to know that I am highly influenced by my environmental and physical condition, including my own stamina and mental-conditioning. What I present as reality, and perhaps a semi-temporary-truth one day, will likely be obsolete at another juncture in time.

I don’t like to sway people. I don’t even like to ‘not like.’ Still I don’t like to form judgments, or to reach conclusions about others. Of course some things, some actions, and some people (because of said actions), stand out as recognizably out of the arena of blandness. I mean to say, they make a mark that is recognizable to both my heart and mind. Mostly, it is the things that seem mean, spiteful, unjust, and not lenient which stand out, particularly something that might be deemed ‘evil’ or ‘perverse.’ But even then the lines (and labels) merge into this gray area, and I find myself neither here nor there, trying to counter both sides of an argument that has converged inside my mind.

With all of this said, I offer a few things about my thoughts on friendship. And if that wasn’t an Aspie preamble, I don’t know what is!

Aspie and Friends:

1. I prefer online friends. Online friendships eliminate much of the burden of communication. I have time to think, to edit my thoughts, to respond in a slow and delicate manner, to take time, to get back, and to not be seen physically. Most of my challenges with communications come in the mode of sensory overload and in my evaluation of what I am seeing. Yes, I still evaluate with online friendships, but about 75% of the stress of communication, particularly nonverbal processing, is eliminated. That’s not to say online communication doesn’t offer it’s barriers and weaknesses, but overall, particularly when I take the time to check for clarity, online communication scores high above face-to-face encounters. I mean I could lose myself in a freckle or hair color and miss half of an entire conversation. And forget about the background noise and nonstop monitoring of my tone of voice, inflection, and talking speed.

2. I make online friends. It’s scary but I do it.

3. I support some friends, when I am capable, and they support me when able.

When I am at my lowest, I will sometimes reach out to three or four people at one time, most of whom are Aspie or whom have Asperger’s traits, and if not Aspie then people whom I deem for the most part trustworthy, nonjudgmental, and possessing the capacity to love unconditionally.

4. I reach out to several people at a time because someone might be busy and I also don’t want to overburden one friend with my intensity.

5. I am not blessed to have many friends. I don’t mean that in a bad way. Of course I am grateful for people in my life but no one blessed me with them. I made the friendships, day after day, year after year, risk after risk. Yes, it is hard. Yes, I mess up, and yes sometimes I get super hurt. But I am not fortunate, or even lucky to have friends, because I have worked HARD to make and maintain these friendships. And I have worked hard on myself to learn how to be the best friend (person) I can be.

6. I accept my faults, frailties, and entire humanness. I am far from perfect but I avoid beating myself up. Yes, I allow myself to have a pity-party sometimes, especially when many changes are occurring in my life. However, I have friends that understand these aspects of me.

7. I only interact with certain friends during my most vulnerable times. I choose a select few friends to confide in about particularl things, especially subject matter in which I want no advice or solution finding quests.

8. If I am not careful, and I talk to a friend who offers advice or her view of the situation, the conversation can do me more harm than good. I have learned to be selective. It is a survival mechanism. Some friends can handle my intensity, others my insecurities, others my wild-imagination, and a rare few the complete me. I have learned I can’t be the complete me around everyone; I will get hurt. I have learned I can be complete by dividing myself amongst many friends. I don’t think this survival skill is specific for those on the spectrum, but I do believe Aspies are vulnerable in their ability to be strongly wounded by others, and that they often find themselves in positions of offending or shocking, without that intention.

9. Friends are not easy for me, for there is a part of me who, despite an inconceivable amount of self-reflection, insight, and work, will always think I am not a good enough friend. This isn’t a self-esteem issue. I do like me. It has to do with the extreme ways in which I can psychoanalyze myself and dissect conversations. I am always, and will always be, an observer of others, twice removed from discourse and continually dissecting and evaluating and reliving over and over past conversations.

10. I have one friend in which I can just spill my guts and fears and anxiety and she will JUST listen. She doesn’t do tit for tat. In that I mean she doesn’t ask me for advice, expect me to listen or to return the favor. She just lets me process. I think every Aspie (and every human being) needs someone who will just listen.

11. I recognize I will always feel like I don’t give back enough in friendship. It is just the way it is. When people give to me, in time or other ways, I feel an immediate want and obligation to equal the score. It’s not that I mean to keep score, only that I naturally don’t want to take advantage of anyone.

12. I love to have friends from all backgrounds. I am not picky. Or maybe I am, if you think the capacity to love without conditions, to be honest, to be giving, to be kind, and to be genuine is picky. But with that said, and a little trustworthiness thrown in, I am capable of being friends with many, many people. There isn’t a checklist.

13. I think I need friends. I think everyone does. I think the risk is worth it.

I don’t neccesarily think the introduction matches the list. But, oh well. My friends will understand. 🙂

13 is my favorite number.

Looking for aspie friends? Join everyday aspergers Facebook like page to the left.