Lonely

I’m painfully lonely today. This is certainly not an unfamiliar feeling for someone as introverted, socially-avoidant, and socially-isolated as me, but it’s worse today than usual. I’m usually quite satisfied with somewhat robotically and unemotionally going through my day in solitude and that’s exactly how virtually every weekday is, except for the frequent spattering of appointments throughout my week. I work full-time from my home office and Ben and I can count the minutes, rather than hours, that we are in one another’s company each day; our schedules don’t overlap well. I don’t have kids and I don’t have any local friends I spend time with since, in the timeline of someone on the spectrum (who has trouble making friends and doing social things), we’ve basically just moved here. It’s been five months and four days, but who’s counting…

Anyway, today I’m wearing the loneliness like a full-body leaden radiation shield. It’s not the comforting and calming weighted blanket feel; it’s the heavy trapping feeling like trying to fight a strong undertow to get back on shore after a long swim. It’s days like today that the familiar welling of tears keeps filling my eyelids and I have to instantly distract myself to avoid succumbing to their flow. 

My house is cold, both literally and figuratively. It’s an unusually chilly May afternoon and the pervasive grayness has prevented any sunlight from warming the room. The thermostat reads 56, which is even colder than the uncomfortably cool 58 we permitted in the winter to save money. I can taste the figurative coldness, the loneliness, the lack of vitality. When I came back from OT this morning, it overwhelmed me as I approached the front door, the coldness in here hit me like a gust of November air with wet leaves. I could see it, smell it, taste it, and feel it. Coldness like this gnaws on my stomach and encourages me to eat, even though I’m uncomfortably full, to ease the ache and fill the void I feel from lack of human connection. 

The real reason days like today bother me is because I know they aren’t isolated incidents in that it’s not an unusually quiet day that will pass. It’s symptomatic of the life I lead and very much a chronic condition. I want two opposing things at the same time and it’s virtually impossible to rectify that in an agreeable fashion: I long for love and company yet I’m wildly uncomfortable, overwhelmed, and exhausted by it. I prefer to feel connected yet I struggle to connect. Social interaction is my constant logic puzzle or science experiment, as I must carefully observe, analyze, and try to understand and replicate the needed responses. I miss the opportunity to enjoy the moment and be present in the engagement because I’m busy “working” to make sense of it. It’s like instead of watching the production, I’m manning the spotlights and just waiting for the cues instead of comprehending the meaning of the play. It’s not until after the friend and I have departed and gone our separate ways that I can then run back through everything that happened and try to gather the meaning from the whole rather than each individual part. It is then I can assign emotional significance to what happened and not just the literal meaning of each sentence, that I so carefully followed in a calculated manner to determine my next question or response. I appear articulate and like I’m understanding (I hope) because a ton of legwork is quickly and constantly being performed in my head, but unlike a computer, it’s hard for me to simultaneously carry out all of these processes so some information gets stuck in the holding area, a backlog of sorts, that I evaluate later, even if I don’t want to anymore (like if I’m trying to sleep). Unresolved material begs to be processed before moving on to the next activity, which is one reason why social things can be so tiring: for me, they extend well beyond the end of the interaction. 

Any potential sensory overload aside (say we were out and about doing something), my brain will not cease analytic activity until it has completely finished assessing and cataloging all of the verbal, nonverbal, environmental, and contextual information from the encounter. Then, for some reason, after that lengthy and arduous process seems satisfactorily completed, it starts digging up prior social encounters (either organically experienced or observed on TV or elsewhere) and reassessing those or comparing the new material to whatever is stored in memory. There can be no obvious relation but I have to ride out the digestion because I can’t quell it. Sometimes, useful connections are made, such as relating a new discussion about a friend’s volatile freelance job situation with a prior conversation about stressful financial times. Frequently, it’s useless details or seemingly elementary concepts: the geometric pattern of someone’s earrings reminded me of the sweater of someone at the library four months ago or people’s lips purse when they are hesitant to answer a personal question (nonverbal patterns take up a disproportionately large percentage of my brain processing speed and mental attention).

Days like today are somewhat like getting a lousy performance appraisal or report card; all of my acknowledged weaknesses are directly handed to me in objective language. The insecurities I have, the deficiencies I know to be problematic, are presented in clear view and the only possible reaction is to yet again acknowledge their presence and significance. We all want to be “successful” or at least see progress, so it’s ego deflating and discouraging to get reminders of the contrary. As someone who’s naturally and habitually critical of myself, I’m fully aware of many of my challenges and must deliberately try to recognize growth and give myself credit when it’s due. This is not one of those cases. I’m lonely because I live a pretty isolated life and my good friends all live quite some distance from me.

Today, like many days, I turned to Comet for support and, as always, found her love to be boundless and her attentiveness to be unparalleled. While this is truly one of the wonderful blessings of having a loving pet, I want today’s pain to remind me to continue to make a concerted effort to reach out to people I already know and try and cultivate those friendships and also push myself to make new friends in my community. Although this is probably my biggest challenge and least comfortable position, ultimately, it is a required means to the end I desire: meaningful connections with friends who I can spend time with in an emotionally gratifying way. Loneliness carries a potent heartache; I battle enough pains as it is. Alleviating this one will not only eliminate its insult, but friendship has the transformative power to lessen other pains as well. I could use all of that medicine that I can get.

 

Am I Safe? Are You Harmless?

Yesterday, at urgent care, I had my first trauma-related mini panic attack in a long time. It used to be a disturbingly frequent problem but with therapy, time, and courage, I’ve started regaining trust in men. I’m now able to make a critical distinction: not all men are likely perpetrators of rape or attack. Most men, like most women, are good people trying their best to lead honorable and meaningful lives (or at least not criminal ones). My attacker was the exception to the rule, not the rule itself. After the attack, I feared every man, even ones I knew (except a handful of close friends or relatives). As such, any time I was in close proximity to a man, especially in secluded or isolated environments, I’d panic. My brain would flood with worries: would he touch me, hurt me, have a knife or weapon on his person, hate me for some unknown reason or have some other motive? Was he getting too close to my body? Was there an exit close by? Physical symptoms would mount just as rapidly in tandem with my spiraling thoughts, racing heart, dizziness, a feeling of facial flushing then rapid draining of color, whispers of nausea building to overwhelming sickness. Worse, as if erasing the months passed since the trauma, I’d feel physical reminders of the wounds I had suffered, as if still etched in gaping scabs and swollen bruises on my skin. Even when I’d have flashbacks while doing everyday activities like driving, sitting in class, or grocery shopping, I’d re-feel pain from the injuries I suffered during the attack sort of like when you see a graphic scene in a movie or real life when someone incurs a serious injury and for a fleeting second, you grab that same body part on your own body as if recoiling in reactive pain and verifying your body is fine.

Anyway, for the first year after the attack, any encounter with an unfamiliar man catapulted me into panic or flashbacks. The reaction was so automatic and so dramatic that I found it very limiting. I never wanted to find myself in a situation where I’d be one-in-one with a man or the only woman in a group. So, I stayed home. I avoided asking my male professors in my graduate program any questions during their office hours or while my peers were filing out of class, even if I was clueless about assignments or concepts. Email was my only vehicle of communication. I couldn’t risk it. (Surprisingly, a number of my professors turned out to be instrumental in helping me defeat this crippling anxiety by, of course, being so friendly and harmless.)

Eventually, I got over it by slowly loosening my grasp and gradually letting the fear slip away, by taking small, manageable steps at first, restoring some confidence, amassing successfully safe interactions, and continually trying to expand the “risks” I took to conquer more and more normal situations.

Yesterday, my encounter with the x-ray tech caused all the anxious feelings to flood back in and swell to a critical mass in my brain. With the door shut behind me, I felt mildly nervous, but with all my injuries in the past couple of years, it was certainly not my first time post-attack in a closed room with a male technician; I can think of at least five this year already! Perhaps it was slightly more anxiety-provoking because I had on a gown with no pants or underwear. I don’t know if this is inappropriate to admit or helpful to those with SPD but I can’t wear underwear. I’ve tried every kind imaginable and nothing is comfortable. Like socks, something seamless may first seem tolerable, but then suddenly, it becomes a screaming impossibility to handle. I’ve been known to stop dead in my tracks while out and about and frantically rip my shoes off to peel away my socks when the sensory threshold is surpassed. I rarely see it coming, but even in January, among the icy sidewalks carved into knee-high banks of snow, I’d plop right down and remove my boots to free my feet from a sock: trudging back home with cold, wet feet was still preferable to suffering the offending sock. I imagine this same solution for uncomfortable underwear is beyond socially acceptability, so it’s better to start with nothing! Luckily, the types of pants and shorts I wear and of comfortable fabrics and loosely-fitting designs (though they leave much to be desired in terms of fashion!).

All this is to say that I ended up on the x-ray table with no pants or underwear. A thin, gauzy white gown was my only shield. I lay there, staring up into the machine’s camera arm, my own arms folded over my chest as instructed waiting. Tim, the technician, tinkered on the computer to enter my demographics. With the light out, my heartbeat starting accelerating; first, it was hardly noticeable, but with my hands over my chest, I quickly realized that it was not only beating quickly, it was also pounding, visually displacing my hands up and down with each beat. Relax, I told myself. When Tim emerged from the small closet containing his desk and computer, my ears started ringing and I became dizzy. “Are you OK?” He asked. I nodded yes, unable to speak, but my spooked eyes were a tell that I was lying. “You are very crooked on the table,” he commented. “Can you straighten yourself out?” As I have terrible kinesthetic awareness and body position sense, I am never surprised to hear this and have received similar instructions almost every time I’m at an appointment. I tried my best to align my body on the table. He started gently pushing my shoulders and straightening my neck and then my feet to position me appropriately for the picture. Like a reflex or the pop of a Jack-in-the-box, my limbs recoiled into a tight tuck position over my trunk to avoid his touch. “You’re fine! I’m just getting your spine lined up here. Don’t worry I’ve done this for years!”

I pleaded with my mind to relax. I didn’t want to feel afraid of him, and logically, I knew that he was totally harmless. In fact, I felt guilty even having unintentional anxieties about the situation. We tried again to situate my body as well as possible and then he swung the overhead camera into its designated location. He reached over me to palpate my iliac crests in tandem to verify proper positioning and a level pelvis. This is it, I thought. I squeezed my eyes as if to will myself out of the situation and transport myself to safety. But, I was safe. Just as he should be and just as he should have clearly seemed, Tim was a harmless healthcare worker trying to do his job in providing necessary medical images for my care. He retreated to his computer command station, told me to hold my breath and not move, and snapped an image. As he repositioned me for the next series, I was visibly more relaxed, and a wave of relief came over me, not just because nothing had happened and I knew that I was safe, but because ultimately, I knew the whole time that I was in good hands but my anxious reaction seemed entirely out of my control. I was embarrassed by it the moment it began stewing, and struck by how unfamiliar the reaction had become to me—a testament to the vast improvements I’ve made over the past two years. What was once as natural and automatic as turning my head when someone says my name has gradually become a faint memory, an abandoned instinct like a long-forgotten nickname whose familiarity only resurfaces years later when you hear it again.

It’s easy to feel displeased with my behavior/reaction during the imaging because it feels like I must’ve taken steps back. I’m hoping it makes sense to simply blame it on the stress and frequency of my recent medical appointments. I also choose, in this situation, to recognize the progress I have made. The encounter served as a helpful reminder of how far I’ve come, how unfamiliar and removed I felt from those once-pervasive worries, and how naturally and normally I now face everyday situations without the looming fears of getting victimized by every passing man.

Mental Health Awareness Month

April was Autism Awareness Month and May, among other things, is Celiac Disease and Mental Health Awareness Month: two other causes near and dear to my heart. There’s been a boom of awareness around celiac disease, though partly convoluted by the gluten-free fad, yet I don’t feel I need to devote much attention to it at this point.

Mental health awareness, on the other hand, is more important to discuss, primarily because mental illness still seems to carry a stigma that it’s a weakness and should be hidden, something disgraceful that should be covered up—a coveted secret not to be confessed. Even when I was in graduate school last year, I remember telling a classmate that I wanted to adjust the arranged meeting time for a group project because of therapy and he replied, “oh, what injury do you have?” assuming that it was physical therapy to address a running injury (an innocent, and reasonable mistake). I said, “no, psychological talk therapy for depression and anxiety.” “Uh woah, yikes, weird. Uh yeah, let’s just pretend it’s physical therapy.” He, by no means, said this with any ill-intent; on the contrary, he was trying to protect my ego and present the “safer” or more respectable alternative to the group to spare me the assumed embarrassment.

I’m so accustomed to mental health treatment and therapy at this point that I’m not afraid to admit that I need it, use it, and find it helpful. Of course, I prefer not to broadcast it and it certainly would never have a place on a brag reel, but mental health services are simply another legitimate, and necessary facet of healthcare. Like physical illness, which can range from acute viruses or injuries to chronic illnesses like multiple sclerosis, and range in severity from mild infections requiring a short course of antibiotics to intensive or emergency care situations or terminal cancers, mental health illnesses run the gamut. Some conditions are acute and short-lived, while others are chronic; some are more of a mild nuisance while some are debilitating. Even depression can be experienced in an acute bout in response to a difficult situation and some anxieties or phobias only crop up when encountering a specific stimulus. Other people, myself included, have chronic depression and generalized anxiety (and PTSD) that are regularly present. Beyond anxiety and depression, there are probably hundreds of other recognized psychological conditions with just as many varied presentations as people afflicted with them. Also like some physical illnesses, a variety of mental health conditions go undetected or untreated. This can happen in cases where the umbrella of symptoms is hard to identify or they exist at a low enough level or persist for so long they become the individual’s “normal,” or because of lack of awareness that there is help, or one’s pride or lack of insurance/resources preventing one to seek help.

Mental health awareness, or increasing the frequency with which these conditions are discussed is therefore important for two key reasons: to increase the general public’s understanding of symptoms and available resources (to aid diagnosis and treatment so that individuals don’t suffer in silence or from an uniformed place) and to show the variety of shades and types of psychological illnesses and their common prevalence (to help reduce the stigma of it being “weird” or “shameful”). Anyone can experience mental health problems, although some people are more susceptible to certain illness than other people. Receiving a diagnosis and participating in treatment is a critical step in managing or mitigating symptoms and reducing risks associated with symptoms or behaviors of such diseases. I can speak to the fact that left unaddressed and unchecked, mental health problems can escalate to severe issues or dire situations. Like physical problems, the earlier a mental illness is addressed, the better. It would be dangerous to allow bacterial pneumonia to fester for weeks, lest it turn into a more critical condition; it is equally risky to sit with depression for weeks on end, allowing it to spiral into a more critical condition. Then, instead of responding with more conservative treatment or improving more quickly, it can stick around longer and necessitate more comprehensive measures, not to mention the unnecessary suffering.

I hope that people will continue to speak up about their battles with mental illnesses. Discussions and admissions are some of the best ways to increase awareness, educate others, reduce the stigma, and potentially help or save someone else’s life. I vow to do my part and try my best to be brave, honest, and open and engage in conversations, even if personal or uncomfortable. I’d rather be slightly embarrassed (though my whole point is that I shouldn’t be, it’s natural to be in our society’s current attitude towards such issues) and divulge certain parts of my life that are nowhere near pretty or perfect, and potentially help someone else who is suffering alone, confused or worried, or too shy to take the next step.

Here is a resource that may be helpful

:

http://www.mentalhealthamerica.net/may

 

Prosthetics & Orthotics

It is coming up on a year since I graduated from the University of Hartford’s MS program in prosthetics and orthotics. It’s amazing how much my life has changed and how different it looks today. Of course, many things are still the same or similar, but it’s been quite the year of growth, self-discovery, risk-taking and bravery, losses and gains, love and living, stumbles and achievements. I have had moments of true joy and peace as well if those of dark despair and pain, not much unlike any other year in my life thus far, but perhaps more self-aware and impactful. It has been a year that tested my resilience, courage, patience, forgiveness, strength, hope, and my relationships with others and myself. I feel like I’ve physically aged a lot in recent years: my health problems have accelerated, I’ve dealt with chronic stress, and my doctors and I have thrown a number of wrong “solutions” at my misdiagnosed problems. But this year in particular, I feel like I experienced the emotional growth catch-up that had been stunted from trauma, lack of self-awareness, and again, trying to slap an improper and inadequate solution on a gaping wound of a problem.

I had long been interested in prosthetics and providing mobility for those with disabilities. Now that I’ve learned about people on the spectrum’s tendency to cultivate “special interests,” I am fairly certain this was one of mine. In first grade, my best friend had cerebral palsy and I loved being the one who got to push his wheelchair or go to physical therapy with him and watch him practice walking. I thought about ways to design his chair to be more play-friendly so he could engage with me on the floor by lowering a special lever on the chair (this was sketched in markers in my notebook) without needing an adult to lift him and transport him into the beanbag. I wanted him to be able to do it himself. In second and third grade, I constantly drew pictures of a hospital scene that was simply a page chock-full of people on crutches, in wheelchairs, or pushing walkers. I’d draw various iterations of the same scene for weeks and staple them all into a book. I added so many pages that eventually I couldn’t staple it and had to punch holes and tie yarn through it to bind it together. There was a storyline: a central boy that was in a wheelchair and the various adventures he had (though everyone around him except his one friend who pushed his chair were also strangely in chairs or otherwise mobility-impaired. I think the world looks pretty different and somewhat isolating from such a position in reality). I also convinced my best friend to make stick crutches with me and practice going around my block in case we lost legs (the irony of this given my current injury-related mobility issues is not lost on me). I loved going to her house because she had a dollhouse with Playmobile figures, including a wheelchair and crutches that could clip on. I could play that for hours. I also purposely removed the arm from one of my little dolls, and would carry BJ lovingly in my pocket. I had a whole backstory for his struggle as well and would fashion ways for him to do things bimanually—my first prosthetic design.

This childhood fixation probably seems bizarre or disturbing, but hopefully these examples begin to demonstrate my early interest in prosthetics. I had carried a very real frustration with my educational and career choices. Although the root of my poor decisions cannot be entirely pinned to one problem, while an undergraduate, I opted to change my major from the premed track of biology to kinesiology (exercise science). To say I struggled with the transition to college is a gross understatement and, at the time, biology seemed like an insurmountable major that was not worth the fight.

Anyway, after years of schooling and working in fitness, even earning a Master’s degree in Exercise Science and Nutrition, I felt pretty locked into the path I had started down, yet the day-to-day job of being a full-time trainer was not only physically exhausting, it was somewhat unfulfilling for me because I was, in many cases, unable to effectuate the change I wanted to in my clients. All of this desire to do something different increased 100-fold after my attack. I needed to distance myself so far from training so as to lose the constant reminder of what happened and my fear that my vocation would perpetuate another trauma. My fears were eating me alive.

I applied to a host of programs and positions, hoping someone would take me and shake me out of my desperate situation, but I lacked confidence that anything would pan out. I didn’t even tell my husband or family that I was seeking a change, too convinced I’d receive only rejections and too emotionally fragile to deal with that outcome in any way more than in my own head.

It was essentially a dream come true to receive my acceptance into the University of Hartford’s graduate program. It felt like not only my chance to change my life, but actually my chance to “redo” and get back into what I had actually wanted to do, years before my lack of confidence and challenges became impossible obstacles. This was my opportunity to run from the trauma, to free myself from the chains of my current job, and to have a career I was proud of.

The program was fantastic. It was full-time for twenty-three months with some of the best faculty and curriculum I’ve ever had the privilege of experiencing. I learned all about many of the things I had always wondered about and I was busy in such a different and new way, my day taking on entirely fresh activities and people. It commanded significant mental energy and I threw myself into my studies, which distracted me from my trauma pain. It also got me off the couch, where I wallowed in paralyzing fear, disgust, and depression for six months. I met bright peers who distracted me from my reality and made me remember what it’s like to see the world as one of opportunity instead of one of violence and threat.

Most importantly, in the end, the program led me to hold up a metaphorical mirror to myself long enough to really face what was going on and seek the help, and eventual diagnosis, I needed. Unfortunately, it took 22.5 of the 23 months to get me there, but I choose to think that the challenges and experiences I encountered throughout the program were brewing in my brain and sorting themselves into discernible categories with sufficient evidence so that I could make necessary connections to seek the steps toward the help I needed. It is because of this program that I learned of my sensory processing disorder and autism.

Ultimately, not being able to pursue the path of prosthetics and orthotics and engage in this career is a painful pill to swallow, both for my pride and self-esteem but also for my heart, as it’s a job I’d love to do. I was ripe with shame when I had to tell the professors I so respected, the friends and acquaintances still in my life, my peers at school, and even my own family, that I wasn’t going to be able to embark on the next stage—the residency (which I will explain below)—despite my sustained and honorable efforts during the program. It was embarrassing as well because I had been accepted as a resident at several prestigious sites, thanks not only to my achievements in school but to the support and connections from our esteemed faculty. I felt like I was letting them down as I turned down amazing opportunities, like someone declining an admissions offer from Harvard outright, not even to attend a different program. I was saying no to the profession.

I think that was one of my greatest frustrations with the field is the inflexibility of the residency requirement; it was a deal breaker for me. The required hours mandated a schedule that I just can’t contend with, especially in such a sensory assaulting environment. In all honesty, the only aspect of school that I didn’t like was the internship placements each semester. We had to accrue a certain number of hours of direct supervised clinical experience each semester, which took the form of one full eight-hour workday per week and one six-week full-time placement and an affiliated site in the summer between the two school years. The clinicians were all wonderful people and I loved interacting with the patients, but invariably, I found that nearly every single Tuesday (my usual clinical day), I was stricken with nausea, migraines, unmanageable fatigue, throbbing joint pain, and low-grade fevers a mere hour or two into the morning. These symptoms were particularly apparent on days I had to work in the lab, surrounded by loud power tools and machines, giant ovens melting plastic, the offensive and strong odor of carbon fiber lamination and my most hated offended, Siegleharts, a tacky adhesive used to sure up test sockets that must be stirred and stirred to create the correct consistency, all while the toxic fumes are inhaled. It seems that every preceptor’s favorite ask to task me with was, “can you go mix up the Siegleharts?” It was a miracle that I made it through the graduate program’s internship requirement. I had to make up a lot of hours and days for each placement and it took an unfortunate toll on my health and wellness. It started to become so stressful and physically damaging to me that the symptoms would linger into Wednesday and then Thursday and I’d be tossing and turning Monday night in anticipation of the inevitable pain. Instead of being relieved when I’d finally be checked out and back into my car at the end of a full Tuesday, I’d begin immediately dreading the next Tuesday, disappointed that it was now less than a week away. The irony was, as sick as internship day made me feel each week, I was unable to really identify the pattern accurately enough to determine earlier in the program that there was a striking discordance with my health and happiness and the profession’s work environment. For a long time, I was convinced, it seemed to be just a coincidence to me that I was always sick on Tuesdays. In hindsight, I think overtime, part of me was aware, but did not want to admit the issue, lest it become more of tangible truth that it already was. It was safer and more agreeable to try and ignore the glaring issue, offering a wide array of excuses to myself and my questioning friends and family.

Anyway, it’s virtually unheard of for a facility to offer a part-time schedule and compensate by extending the duration of the residency. Even if this were offered, the governing body of the profession’s accrediting agency sets limits on this accommodation and it was barely a shorter day. After the mental and physical exhaustion of the school program, my doctors said it would be wise to take a break and they cautioned me to seriously consider abandoning the path of residency was the only option to certification, which it is. It’s a behemoth of a gatekeeper—an incompatibility with my physical and emotional health needs. The sensory processing problems and the autism fatigue are the greatest offenders that render this impossible.

Then there’s the problem of support. One of the enticing but also apparently unfortunate aspects of prosthetics is that it is a unique and niche profession. There aren’t prosthetists’ offices in every town and even fewer that are certified to accept and train hopeful residents. In fact, in New England, there are just a handful of possible residency sites, which is one of the reasons that landing a good placement is an honor and a highly competitive process. The residency for which I was selected was many states away from the family I so desperately need for emotional support, especially at the burgeoning awareness of my sensory problems. Instead of moving closer to home after graduation, which both my husband and I felt was an important and necessary decision, accepting the residency would have landed us a plane ride away, in Virginia, for a minimum of two to five years.

I initially accepted the offer without hesitation: it was a pretty unbeatable opportunity and the culmination of my work and dreams during my studies. I was certainly disappointed that it was so far away, but I understood this was a definite possibility when I signed up for school, knowing full well, through research, that the scarcity of sites would certainly increase the chance that I’d need to travel for residency. Sitting at home on a computer imagining my life post-degree, two years down the road was so far removed from reality that I couldn’t gauge my discomfort and repulsion to this idea. I was still living in fear of death from the trauma, and picturing a week or month into the future in any realistic sense was virtually unthinkable. I was still unsure if I’d wake up the next morning, and more seriously, if I’d even want to. Every little thing I did each day felt like a major achievement and a surprising accomplishment, and I thought in abstract ideas rather than concrete realistic plans. My whole self-concept and identity was entirely lost in my trauma; I felt like I not only occupied a foreign body, but had a new mind. What felt unknown, I feared. I hated the changes and I longed for my old self, but that’s the thing about some monumentally devastating traumas: to survive them, you have to change. The “old you” had a coveted innocence and peace that is forever lost; at the same time, I’ve learned that with overcoming such a horrific challenge, comes deep and unparalleled strength and courage: the “new me” is braver, tougher, and more appreciative of seemingly small victories and gifts because she needed to be. I used to hate her, but I’m starting to admire her and give her a chance.

As the “doomsday” of my residency start date drew nearer, I started to panic. Words that were initially filled with promise began to form a faint picture of what my residency life would actually look like, nearly one thousand miles from home. It even became clear that Ben would be unable to join me there for “several months,” while we determined if it was a good fit and he could find a job. Even in that less informed stage, we were building in contingency plans, as the track record for my health and robustness has been marred over the past several years, and my ability to successfully withstand the physical demands of a more-than-full-time job were called into question. The sheer utterance of the word “residency” became enough to send me into complete chaos, crumbling into an emotional wreck. I would have full-blown meltdowns when we tried to plan out or talk through the coming months. I have faced many uncomfortable or even dreaded transitions in my life; it’s one of my guaranteed struggles (which is not uncommon for those on the spectrum), but for many of them, despite the disproportionate and overwhelming anxiety that characterized their lead up, in my heart I was excited enough or sure enough that it was the right decision, that I was confident I’d be okay. Not with residency. The notion of it filled my body with a sweeping wave of stifling heat, suffocating not only my physical ease of breathing but my emotional outlook and mood. I’d become diabolically irritable, moody, and despondent. I’d cry so hard that I would choke on my breath or unintentionally throw up my last meal. My sleep, while undeniably restless and problematic since my attack, became punctuated with even more nightmares: a messy blend of flashbacks from my trauma with creepy fantasy scenes from a prosthetic lab in which I had never been. In this way, we discovered my insomnia and my post-attack PTSD were significantly exacerbated with the increased anxiety imposed by the impending residency. Deep in my heart, I kept asking myself: Am I just afraid of change or being away from Ben? Am I afraid to fail? It wasn’t difficult for me to know the answer with conviction. It was difficult to admit that that (failure) was the answer because I so wanted it to not be. I wasn’t afraid of failing in the sense that I thought anything bad would necessarily happen if I did, and it wasn’t a matter of “if” I did, because I knew, without a shadow of a doubt, that I would “fail.” And that’s the operant word here. Fail didn’t necessarily mean I wouldn’t do well at the residency; it meant my body and my mind would break, maybe not literally, but certainly by all measures of practicality. The happiness, improved sense of physical and emotional well-being, and semblance of progress that I had fought and clawed so hard for were still so fragile, yet intensely important for my survival. I didn’t want to risk shaking them off and I was positive that the challenges imposed by the residency would not catapult my growth to even greater heights but would be immensely counterproductive.

As soon as I was brave enough to admit this to Ben, I started feeling like I could breathe again. I was gripped with fear of letting him down; after all, we had moved to Connecticut for me to do the program, sacrificed income and quality of life, and I had been unemployed or otherwise a non-contributing member to our financial state since the attack. School represented the promise of a successful career and a life of less penny-pinching and more affluence. I felt indebted to him and responsible for completing the loop on our investment in a better future by pushing through the residency and beyond to a career as a clinician.

So, I tried to troubleshoot the problem and seek as many alternative arrangements as possible in typical Amber fashion. I’m almost always cooking up some kind of plan or seeking any number of opportunities. As I say, you never know what may work out so it’s good to cast a wide net.

As painful and embarrassing as it was to turn down the one residency, I was fueled with motivation to reconcile the situation. I figured arranging a placement closer to home would negate some of the challenges and make the situation more plausible: a workable battle. My good fortune and hard work landed me another opportunity closer to home, about a two-hour drive and within striking distance of a reasonable commute for Ben’s job, meaning that we could live together. This had all the makings of a more feasible solution, so I again agreed and was temporarily filled with such a gulp of relief that the remaining obvious problems were muted to me. It wasn’t in Virginia and it wasn’t to be tackled in complete isolation, so I was blindly hopeful. At least for a week or two.

The elimination of my paralyzing shame of telling Ben that I needed to amend the plan restored enough courage and self-esteem that I was able to confess to my professors that I had to withdraw my commitment to the one residency for another. I was still filled with guilt, driven by my desire to repay their servitude and legwork to facilitate my success during my tenure in the program, I was disappointing them by not jumping at the chance afforded by the first position. Apologetically, I assured them that I would still work hard and make them proud, bestowing as much honor as I could to the program that so well-equipped me for a bright future in the field. I was eager to progress through the remainder of the required steps to become a board-certified clinician and excited to have an impactful change on the lives of my future patients. The initial relief that my problem-solving plan afforded wore off as quickly as the days before graduating were passing. It was only a matter of weeks before I was to move and begin my exhausting residency. Once again, I was filled with panic at the thought of my impending life. It wasn’t what I wanted because it wasn’t what felt right for me.

I asked my therapist to help me evaluate and understand what was going on. She strongly encouraged me to see my physician and request medical accommodations at the site for some of my health issues. I figured she was right; I had long since tried to force myself to meet all requirements and expectations “normally,” but I had some real and serious hindrances. It was through that process of determining what accommodations would be beneficial yet not incompatible with the job requirements that the sensory processing issues and autism were diagnosed, after a trail of appointments, testing, and specialists were seen. That journey is best saved for another day, but the outcome is the same: I suddenly was given access to the more complete picture of what was going on with me, both at that time, and throughout my life. All of the challenges and confusions began to be met with more clarity. It was both a relief and a burden at the same time. It had taken me nearly 30 years to be properly diagnosed, and when I finally was, it felt like my self-concept was significantly altered overnight. Like the moments of rising after my attack, I suddenly felt like I needed to get to re-know myself, only this time, unlike the attack, I didn’t initially hate the “new” self that was emerging. I realized she needed more compassion and credit for her achievements despite the numerous and clearer barriers to her success. It was the first time since becoming a teenager that instead of berating myself and tearing myself down, I paused and granted myself just the slightest bit of grace with the incredibly stringent expectations that I normally hold myself to. That perfectionist attitude isn’t lost overnight, but it was at least relaxed just enough to give me permission to make the right decision for my psychological and physical needs, and abide by the boundaries I needed to set to respect these needs. I had battled long and hard enough, particularly after surviving the attack, and I just needed to let myself choose the less popular or esteemed route. I had to walk away from prosthetics, at least for some time. My journey of emotional healing from my trauma was only just beginning and my journey towards cultivating an environment and life that supported the needs imposed by my neurodiversity had not yet begun.

Much of this came to a head the Tuesday before graduation. In light of everything going on, my husband and I decided that indeed a residency was not the right thing for me at the time, and I politely and supremely apologetically declined the second offer. I had no alternative plan. The future was a completely blank canvas, save for the dozens of occupational therapy and social/behavioral therapy appointments that were scheduled to begin helping me work on various challenges of the new diagnoses. I desperately wanted to cancel my plans to attend the graduation ceremony. First and foremost, I knew it would be long and boring, crowded and over-stimulating, a recipe for a very Amber-unfriendly event. I also hate attention so I didn’t want to walk across the stage. Most importantly, I seriously questioned whether I deserved to march and receive my diploma, both because I felt ashamed that I wasn’t going to be doing residency any time soon, if at all, and because as much as the new diagnosis helped me see myself in a new light, it also made me feel “disabled” and undeserving of success. I am not entirely sure why; I know that people with all sorts of challenges and abilities can achieve great feats, but it’s different for me somehow. My own self-esteem is so low, and has been for years, that I don’t naturally grant forgiveness for my own weaknesses or mistakes; and that’s a gross understatement to how I viewed my participation in the prosthetics program: a mistake. I felt so stupid for “wasting” two years of my life fully dedicated to a career that was not viable for me. I felt even more stupid for not knowing how to identify and then articulate my challenges. It was Ben who helped me see how short-sighted this blame was. After an emotionally painful conversation in which I was completely vulnerable in how I felt regarding everything going on, Ben helped me see that the program was not at all for naught. In fact, it had saved me. Before receiving my acceptance letter from the program, I had no desire to live and I certainly wasn’t engaging in a life that could be considered living, beyond the basic biological definition. For all intents and purposes, I was so broken and hopeless after the attack, so traumatized and disenfranchised, that I was often mad at myself that I had pulled my body up from the floor after the attack and ultimately saved my own life. In many post-attack moments, I figured it would have been preferable and easier to die. The prosthetics program completely changed that. I not only enjoyed my day-to-day life much more again, but I saw reason and relief for my survival. It renewed the sense that every human should have: that life, even when impossibly challenging, is worth living. When that basic operating premise disappears, it is so far beyond scary that I lack the vocabulary to convey it.

During the program, I re-learned to trust people, particularly men. Despite my social challenges that come part and parcel with the autism, I tried to make friends. Prior to that, I vowed that I never wanted another friend because the risk of a possible attack was not worth the reward, so the valiant effort to be social and make meaningful relationships was a big achievement. I learned to dream again, to love myself and others, and be grateful for my strength. The twenty-three months of hard work and focused studying may not have been leading me to the next logical step on the path, but it did pay me in dividends, just in a different form than most people would have assumed. Ben and I decided that needed to walk for me and for us. No contests are fought in solitude, and this one was no exception. My graduation was as much my own accomplishment as that of Ben’s (or my mom’s). After all, he had been the one I considered when deciding if my life was worth salvaging and he had been the sturdy rock above me, from which he offered an endless number of hands to pull me up and steady me when I stumbled in my physical and then emotional recovery.

As I sat under the large circus tent during my graduation ceremony, I was surrounded by twenty of the most interesting and hopeful peers. Moreover, there were hundreds of excited graduates from other departments, excited to take to the stage and receive their diplomas for all of their hard work. They couldn’t wait to embark on the careers for which they had so long been dreaming of and working towards. Parents, friends, and family surrounded the periphery of the huge tent in countless rows of chairs. There was a dizzying sea of people I had predicted and part of me really wished I had heeded to my wish not to come. Only two of them knew my secret. I didn’t know how to appropriately broach the subject with my peers who were all too excited to be taking the next big step and I didn’t want to rain on anyone’s parade, so I kept to myself, a familiar position anyway.

When my row was finally in queue to receive our diplomas, my heart was racing. I felt like a fraud and once again, I was flooded with feelings of “undeservedness” and shame. I looked to Ben and my mom, who were clearly talking quietly but excitedly that the boring ceremony was about to experience its five seconds of interesting air time. While everyone else’s fear was just that they would trip while walking across the stage, I was worried that someone would yell, “you wasted your degree!” (which, incidentally, is what one of the residency directors shamed me by commenting). When the dean called my name, all of this vanished. Suddenly, I stood tall and proud, as if endowed with the task of proudly receiving my diploma. There are pictures capturing the moments that I traversed the stage. My smile is so genuine and so rich that it appears my whole body is smiling. I shook the dean’s hand with conviction and as I posed for my photo at the far end of the stage, my sole thought was, “good job, kid”—an exceedingly rare self-directed compliment.

Nearly a year later, my life looks very different but I’m okay with that. In fact, I’m generally trending toward increased happiness. I am beyond grateful for the gifts in my life, both in terms of people, opportunities, and my own unwavering ability to eventually turn toxic lemons into the sweetest lemonade. I still have so much healing and growing to do, and that need is not lost on me. In fact, it becomes more clear to me that I bury some of the deepest and hardest parts of my trauma instead of working through them, but I’m getting there. It’s been the most trying and rewarding year in many ways.

I still feel a major loss regarding my prosthetics dream; it remains a devastating heartache. It is a loss; the acknowledgement and acceptance of the fact that it’s not compatible with my current (and likely future) means that that goal is unattainable and I have to re-envision a life that I will be happy with and proud of. And I’m doing just that, one day at a time, with my trusty companion, my copilot, the wind in my sails when my own winds are flagging. The other day Ben so astutely commented that marriage is largely about taking care of one another even when it’s hard. It feels like he’s been dealt an unfair hand, but if anyone or anything has the ability to restore my faith in humanity, it’s certainly Ben’s loyal and staunch support, patience, guidance, and love. Extending beyond ourselves as a cohesive unit, I am also learning to reach out to other family and friends for support and connection; some of the most meaningful relationships over time have their genesis in unfortunate or otherwise strange situations or between unlikely participants so it is good to cast a wide net and accept any and all love and connection offered.

Lastly, I am trying harder to respect and value the person that I am, the needs that I have, and the decisions that will bring me the most happiness, even if they are unpopular or confusing to others or otherwise feel like they are letting myself or someone else down. It seems that is the first requisite to improving my self-esteem and building a life that gives me fulfillment, happiness, meaning, and peace. As Steve Jobs so wisely stated: “Don’t let the noise of others’ opinions drown out your inner voice. And most important, have the courage to follow your heart and intuition.” Right now, I’m happy to be alive, I’m grateful for the life that I have and the people in it, I’m enjoying my job and exploring different hobbies and interests, and I’m hopeful that my growth and strength will continue to create a future that is healthy, meaningful, and rich in the things that truly matter.

Healing?

Good news! My body may be finally stepping in and trying to heal my foot. We are going to postpone the surgery until May 11th, to give it a few more weeks. I’m happy about this for two reasons: there’s the relief that the surgery isn’t tomorrow morning (which makes it feel less real because it is less imminent and there’s a chance I won’t need it at all) and it makes me feel like my body, even though weakened in many regards, may have some inherent healing ability hidden within it after all. I also started to be overcome with nervousness about the general anesthesia required for the procedure.  I had no idea that it meant I was not going to be breathing on my own and would have tubes down my throat. In the past 24 hours, I’ve done enough research to convince myself that logically, this is safe and would be uneventful, but emotionally, it still triggers fear.

So, here’s to hoping that my body decides to heal this thing up on its own. While that’s certainly far and above what I’d prefer, I will face whatever outcome we reach on the 11th with as much stoicism and positivity as I can muster.

Strength Training

I have been lifting weights again and strength training for exactly two months. Although this has nothing to do with autism, when I started my blog, I decided not to put constraints on myself regarding what I needed to think about or write about. This blog tends to be a space where I can simply mull over and express some of the many thoughts and experiences that confuse, frustrate, excite, scare, or otherwise impact me. As mentioned, strength training also has been a big bear I wanted to retackle, after going cold turkey post-attack for a couple years. Once a huge part of my identity and an integral source of joy in my life, it became one of many things I could no longer face. Except for running, I became a voyeur of the fitness world, as the mere thought of strength training made my stomach flip.

Not anymore. I’ve been training. I wouldn’t necessarily classify this training by tacking on any adjectives like “hard” or “serious,” because I’ve tried to take a low-key approach (and I have a broken foot!), but I would say my practice has been dedicated, courageous, and empowering. And fun. For as much as I’ve been trying to hold my ground above the depression abyss, any little source of happiness must be coveted like prized possession. Plus, it’s been effective. I’m actually back up to all of my old benchmarks and lifting at least as much—and in some cases even more—weight than in my prime strength training days in NYC as a full-time trainer. I never thought I’d get my body back up to that level of physical strength because it just hasn’t seemed as resilient anymore and I’ve had so many health problems, not to mention I was basically working out all day then through my job. 

It’s interesting because I have also mentioned that I avoid looking in the mirror. While I’ve gotten better and continue my daily practice of positive self-talk, this is just to the reflection of my face. My body is a different story: I don’t look at it. Until very recently, the weather had been cold enough that I was always bundled up anyway, so I never even really “accidentally” saw it. Sometimes I feel like this is actually healthier than it sounds for me personally, because I’ve hated my body unwaveringly for so long that it can be more beneficial to ignore its appearance altogether than risk critiquing it and hating it. I hope this is not the case for most people. I even shower in the dark. 

With all that said, I’ve looked at my arms lately. In fact, I not only looked casually at them, I decided to flex them. Boy there’s a lot of muscle trapped in a little arm! My scrawny atrophied arms of the past couple of years have reverted back to my healthy and muscular arms of my younger twenties. I’m not sure how it makes me feel, maybe surprised, maybe partly (ashamedly) nervous that my attacker’s words will ring true (that having muscles and a strong body made me attractive, and thus a target). Most of the time, my logical brain assures me this is not true, but I still have to fend off the occasional worries. The good news is that I’m not repulsed by my changing appearance, so that’s a start. I hope that confidence finds her way to quietly seep in, gathering a groundswell presence while I’m busy focusing on other things, until one day, she is big and loud enough for me to notice her secure hold in my mind. From there, she can slowly open the gates for the self-hatred, fear, and trauma to begin to recede and my mind, heart, and body will start finding more peace.

The Mighty

Exiting news! My first blog post—the one that bravely kicked off this blog (if I may step out of my normally modest shoes for a second and toot my own horn!)—was featured by The Mighty and is available on their website. The Mighty is a big, supportive online community for those with or affected by any variety of disease or disability. The community offers not only perspectives of afflicted individuals, but also their parents, siblings, friends, etc. One thing I really admire about The Mighty is that it not only provides great resources for those with or affected by a given condition, but it gives those same individuals a platform from which to share their experiences, triumphs, and concerns, which I think is powerfully influential in altering our stereotypes and rattling our contemptuousness. The Mighty gives voices to people who may not otherwise be heard and through such sharing, shortens the distance between things that seem blatantly different. Honestly, even before I had my autism and sensory processing diagnoses, I followed The Mighty and subscribed to their weekly digests of stories and articles because I marveled at the bravery of the storytellers and found that weekly messages of some people’s hidden or invisible struggles was a good reminder of the strength of humanity and the importance of constantly exercising compassion, even through my own hurt and battles. Some stories, even if about a disease I had never heard of and certainly didn’t face, made me feel understood, simply because many of the same challenges are faced by all of us, even if they come with different names or wear different costumes.

This now reads like an advertising spot for The Mighty, which certainly wasn’t at all my intention. I guess it’s just my honest one-minute appreciation speech for my new inclusion into the community as a contributing writer. In fact, they have asked me to add new content and posts overtime, so I’m really appreciative of the opportunity to share my perspective to hopefully help some readers understand and help others feel understood.

(it’s actually the featured story on the main page this morning!)

Prognosis

I’m crutching all around the hospital today. For some reason, they’ve designed it so that the orthopedist is in the basement in a small office that’s only reachable by snaking through several very long hallways. The radiology department—where he sends nearly every patient to get an X-ray after first seeing him—is upstairs at the opposite end of the building, in an entirely different wing, down another set of long, zig-zagging hallways. Thank goodness that I’ve been doing my strength training and have these triceps in gear!

After crutching for what feels like 30 minutes, I’m sitting back in his office waiting: waiting for him to come back in, waiting to hear why my foot is not getting better, waiting for an action plan. I start working myself up into an anxious state, flirting with a full-blown panic attack. I have my huge headphones on to drown out the rattling of the heating unit that seems to be situated in the wall behind his office rooms. I wear my noise-blocking headphones without exception when I go on most errands, unless I’m certain the place is very quiet or I’m accompanied by someone (in which case, it would be rude). I’ve also been wearing my winter beanie basically as part of my daily get-up since November (at least I have three!). It not only keeps me warm, but it tamps down my little flyaway curls that otherwise blow as I move—a guaranteed fast-track to throwing me into sensory overdrive.

The thick hat and the enormous headphones are quickly sending me into overheated territory. Thermoregulation and body temperature awareness are significant challenges for me with SPD. I seem to have to no idea if I’m trending towards becoming too hot or too cold until I’m beyond the point of easily reversing the situation and re-establishing comfort. This is one of those moments. It seems I am still dressing for January and it’s in the 60s outside. I begin to sweat. Anxiety is indubitably contributing to this heat flush, but my down coat isn’t helping. This doctor makes me nervous and so does this injury. I have a premonition it’s not going to be a favorable prognosis. My foot throbs as if to remind me, yes, I’m here and I really hurt. I don’t need the reminder but the throb won’t be silenced.

For some reason, once I’ve identified that I am, indeed, too hot, I do nothing to remedy it. I keep waiting.

I wish Ben was with me. He’s at work so I send him a text telling him I’m bored. I’m sure he knows to substitute in the word scared or lonely. I do multiplication problems in my head while I wait; over the years, I have found this to have a mild relaxant effect. 243×77

Finally, my doctor enters after reviewing my x-ray. Even though I struggle to interpret facial expressions appropriately, his is a clear tell.

It’s not good news.

I need surgery. He will insert an intermedullary screw, which is essentially a screw that gets drilled longitudinally into the metatarsal bone marrow. It will help my fracture heal.

The word surgery doesn’t jive well with runner or anxiety-riddled—both of which are equally understated adjectives to describe me.

So that’s where I am today: just wrapping my head around this next hurdle and working on convincing myself that I’ll be fine and this will ultimately be the best treatment. I will and it is.

I’m sure that I’ll have a lot of thinking and writing to help me digest this but I’m actually feeling like the depression might be lifting a little bit. Even though this is a scary proposition, it will ultimately help me heal. April 25th sounds like a good day to have surgery anyway, right?

 

Is the Sinkhole Escapable?

The beautiful weather this weekend helped wrap a strong rope around me and took me back a little further from the edge of my depression canyon. I can still see too easily for comfort over the edge into the sinkhole, but I’ve got at least one foot on some solid soil. Now I’ve got to harness all my physical and mental strength and pull the rest of my dangling body up onto the ledge.

At the risk of over-analyzing things and scaring this slightly elevated mood back into its shell, I want to consider what made this weekend a little better so that possibly I can identify strategies to keep things trending in this direction. Of course, weekends are always nice because I get to spend much more quality time with Ben and we had fun together this weekend. Unfortunately, the way that our schedules (don’t) line up during the week prevents this from transferring easily to a weekday luxury. The weather was great, and I thrive on sunshine. With the significant limitations of my injury, this is actually a positive and negative. It’s almost more emotionally painful to weather the tease when the warm weather and sunshine beckons me to be out walking, running, biking, or playing outside than suffer through the gloomy, rainy days we’ve had lately; at least in the latter, I don’t feel like I’m missing much. The weather will only get better as we enter spring and summer, so I guess this will be mostly good.

Ben and I had some difficult talks this weekend but they enabled us to make some big steps forward together so I think that feels good. It reminds me that I’m healing. Sometimes progress seems so stagnant and possibly even reversed, but then suddenly, an impressive step is taken and rewards the patience and toiling that was previously invisible.

What else? A few people reached out after my last post about depression and that helped me feel connected and understood. I’m quite socially isolated, so sometimes it can feel like my struggles fall in uncharted human territory: I’m the sole soldier in such battles. Even with others who are far away and whose lives have seemingly little parallel with mine, it feels validating and somewhat relieving to know the struggle is not only mine (not that I would ever wish an ounce of emotional or physical pain on anyone).

Not that much else this weekend was radically different. I just tried to ride on the coat tails of my own inertia and bounce between activities a bit to keep busy and distracted. I also made a list of things I’m grateful for as I strongly believe there’s nothing as powerful as gratitude (outside of love) that can elevate one’s mood. I’ve restarted my daily morning practice of jotting down three things for which I am grateful, even if they are ostensibly small; it’s remarkable how quickly a list of life’s beautiful gifts amasses and that bounty is plentiful enough to keep my head and heart reeling me away from depression’s cliff.

 

Is the Sinkhole Inevitable?

I’m in a tough place today and there’s not really any specific reason or excuse for it. I suffer from chronic clinical depression. Most days, I’m actually “fine” because I’ve become so accustomed to the depressed feeling that the bar against which I compare my emotional state has been permanently lowered. On these days, I grind through the motions, keeping busy with work and daily obligations, peppered with (hopefully) some leisure activities to lift my spirits. Other days, like today, for no obvious reason, I’m not fine. Everything feels like an emotionally draining chore and my resilience seems completely dried up. On these types of days, I may even cry with just the slightest frustration or discomfort because I’m in a perpetual state of straddling the precarious threshold between holding it together and completely falling apart.

On days like today, I feel deep and genuine loneliness. I am alone all day every weekday, but even if I was blessed with company today, I’d likely still feel loneliness in my heart. That’s one of the challenges of true clinical depression—it can be virtually impossible to ease the suffer during a low because the real things I’m depressed about are just that: they are real, they are heavy, and they are virtually impossible to change. Add those factors to a neurochemistry that predisposes me to emotional lows, and it’s more of a mystery as to why I (thankfully) have mostly “fine” days versus the more occasional bad days. (For the record, I’ve been doing therapy for several years and still actively do so and I don’t respond well to anti-depressants so I steer clear of those.)

Why is today worse than usual? Like I said, it’s unclear. The weather is awful and I’m in a lot of physical pain, so those two variables don’t lend themselves to the easiest of days, but honestly, I’m in pain most days and New England weather often graces us with less-than-ideal and erratic conditions. It’s probably somewhat of a chicken-and-egg situation. The more depressed I feel, the more I become aware of the reasons behind my depression and my powerlessness (coupled with impatience in some instances) to improve these. For example, when I’m really down, it helps me to get outside and run or take a walk with Comet. Right now, it’s pouring rain and I am on crutches so this is not going to happen. That makes me feel more trapped and takes away one of the few effective coping mechanisms I have. The frequency and severity of PTSD flashbacks is significantly magnified when I feel trapped and depressed. There’s an exponential relationship between the number of flashbacks I have in a day and my depressed mood, so as they come with increasing frequency on days like today, the emotional pain I feel skyrockets. It’s pretty impossible to have a good day when your brain will not bring you peace from violent memories. I think my PTSD has been particularly bad lately because of my broken foot. It just so happens that when I was attacked, I was also in a boot with a broken foot. The injury did not contribute to the traumatic event but my brain still relates “broken foot” with “attack” because in the weeks following the attack while I was healing, I was also painfully aware of my foot situation because again, it limited how well I felt I could cope. Now when my body sees “boot” it thinks, “attack.” (Pavlov was onto something…)

I’m depressed about things other than the attack and its aftermath (the ways it still affects me today), the foot, and the weather, but the other stuff feels even less topical and more stubborn or impossible to change. For instance, I’m upset that I have all the sensory processing challenges with autism because they are so limiting. Even with dedicated OT (occupational therapy), these aren’t going to go away. I can’t change my neurology. There’s an actual issue in my brain. The only thing that I can control is my attitude toward the issue and that forces me to abdicate the captain’s chair from which I’m a lot more comfortable. It puts me in more in the passenger’s seat: a less powerful, more hands-off role, with significant limitations in my ability to effectuate change. I’m not steering the ship and it’s not going where I want it to, yet I’m told to just take out my camera and enjoy the view. Sure, a bunch of pictures of glacial bays may be pretty, but if I actually want to be sailing by a coral reef, there’s only so much satisfaction that icy vistas will give me. One of the autistic brain’s modus operandi is ruminating on something and not being flexible to change course or stop fixating. When my brain decides or wants something, it’s all in and there’s virtually no way to convince it otherwise. This isn’t always a negative trait; in fact, I’m sure it’s helped me remain steadfast in many pursuits and goals, but such inflexibility can also be frustrating and annoying (to others for sure, but to me as well!). Even when I want to change course or focus or let go of something, I often can’t and no amount of logical or emotional convincing or targeted strategies will convince the rest of my brain otherwise. Of note, partly due to this reason, I find it nearly impossible for me to transition and switch tasks. Even if I physically move on to the next thing on my agenda, nine or more times out of ten, my brain is still analyzing, cogitating, and deliberating on my last task. I am much more productive if I only take on one or two things per day and do each for an extended bout of time because I don’t waste time trying to wrangle my brain to shift gears and catch up with the new activity.

*          *          *          *          *

Well, this post has been marinating for several days. I’m not doing any better. I’m findings myself clawing at the falling rubble at the edge of the cliff as a dangle and fight the to stay on the solid land above the abyss, above the sinkhole of deep depression below. I’ve been down there so many times and it is barren, dark, cold, and scary. It’s not where I want to be and it’s even harder to climb back out than it is to cling on and try to grab any solid rocks I can find, even though this position is also terrifying and exhausting. I’m trying to distract myself and also dedicate my energy to preventing the fall. Hopefully instead of avoiding writing as I have been for a few days, I will embrace it as a tool to help hold me up where the beauty, the light, and the stability reside. I’m surrounded by goodness when I am brave enough and strong enough to see it, so hopefully admitting my current struggle will help me face the pain and this problem and fight back with the tenacity and resolute that seems hardwired in my steadfast and stubborn ASD brain.