Superman and Superwoman

Growing up, I always believed my grandparents were Superman and Superwoman. It was sort of hard not to believe that… since my grandmother had a “fly button” in her car, was eternally 24 years old, and both of my grandparents stayed up way later than anyone else’s. They were also ALWAYS there when anyone needed them, just like superheros.

Since they lived about two blocks away from us, their home was my second home. I stayed over there so often that I called one of the bedrooms “my room” and the last time I was there, I took pictures of every inch of “my room”. I took those pictures because my superheros are moving. They have a new penthouse to call their new “Fortress of [Anything But] Solitude”.

The move came as a huge blow to me. I tried to fake happiness... I tried to pretend it wasn’t happening... I got massively depressed... The works. What I neglected to think about until today when my mother mentioned it was that the house was where my mom and her siblings grew up and while I feel like I grew up there, I didn’t. I have tons of memories and I spent a lot of time there, but it wasn’t my home like it was their home.

So now I’m sitting here in my room (no quotation marks) in my apartment about to embark on the same journey that I did when my parents told me they were selling our house. I am sitting here letting memories wash over me, and hoping that by recording them in this heightened state of emotion, the emotions of the memories will be captured in such a way that I will still feel them even though I can no longer return to where they were made.

Forget being a superhero for a minute; my Grammy would also have made a great private investigator. When I was still in elementary school, I began walking home to her house by myself after my brother and older cousin went on to middle school. I didn’t go there every day, but when I needed to, my Grammy clearly wanted to ensure my safety. The first day I was walking there, I felt like I was being followed. After awhile I caught a glimpse of my Grammy in her car. She was driving as slow as a turtle behind me, making sure I was safe. She did that for the first several times I made the walk alone. I never let her know that I knew she was there, but I always felt better knowing that I wasn’t going to be alone until she felt I was ready. Soon after my Grammy felt I was ready, my friend Jenny and I started walking together when I was going to Grammy’s house, and I think that made both of us feel better.

Then there was the time I decided I wanted to ride my bike to my grandparents house, where I was staying while my parents were away. In the car, it always seemed like such a short ride. My Grammy once again trailed behind me in the car and said nothing when three quarters of the way there, I fell off my bike and asked to get in the car. She helped me load the bike in and that was that. I am so thankful that she was never the type to say “I told you so”.

When I would stay with Grammy and Papa, they stayed up late and Grammy always slept in. Papa on the other hand, used to be a pharmacist. When I was younger, I’d watch as he got himself ready to go to work. I’d be eating my cereal and watching tv and he would sit down on the couch behind me, change the channel, and start to put on his socks and shoes. I’d always give him a hard time about changing the channel on me, but it was our routine and I loved it. I knew that when he was done, we would go out to the car together and he would drive me to school. It was a short drive but I loved every minute I got to spend in the car with my Papa (and I still do).

My cousins and I had wild imaginations. We used to think there was a “snake hole” in the backyard and we would terrify each other by yelling “there’s a snake behind you!” We also had a secret game called “Camp”. The game had to be a secret because we weren’t allowed to be mean to one another but for some reason, I was given the role of the mean counselor… and of course, since I was one of the older grandkids, it would have been my fault for being a bad influence if we were caught… I guess the secret’s out now, but we all turned out okay.

Another rule of “Camp” was that we could only play when at least 4 of the 8 grandchildren were there. Although a seemingly arbitrary rule, it made sense as two lived out of state and two lived over two hours away. Due to this rule, when my little cousins Avery and Jordan and I were alone, we would play a game that had no name. The point of the game was for them to call up a “store” and be rich little girls who wanted very specific things (I have finally realized that a Lou Baton Backpack was meant to be a Louie Vitton Backpack) and my job was to make them laugh… typically by saying “WAZZUP????????????” The game never seemed to get very far, but we always had fun.

One of my favorite things growing up with younger cousins had to have been how we used to get them to take naps. They would go lie down in one of the bedrooms and I would be sent to lie down in Grammy and Papa’s room. Once they were sleeping, I was allowed to turn the tv on really low and just before they were woken up, we’d turn the tv back off. I’m sure the same was done to make me go to sleep when I was younger, but it was a defining moment. For me, it was the moment that I became a “big girl”.

Of course… that “big girl” still slept in the crib sometimes if there were too many people sleeping over at once, but that was because I was tiny NOT because I was a baby!

Being part of a large Jewish family meant lots of holidays with lots of people and we always gathered at Grammy and Papa’s. There were parts about preparation for the holidays that I always loved. I loved crushing corn flakes for the Noodle Kugel. I enjoyed setting the table and LOVED making place cards for everyone. I also liked helping out in the kitchen, although I often tired of it long before the work was done. While I’ve never done well in large groups of people, I always tried with my family. Unfortunately, more often than not I became overwhelmed and had to leave the table, but family has always been my top priority and so I always would return. Another step into being a “big kid” was when we got to move from the picnic bench to a real chair and so I always anxiously awaited that moment. I would put my place card in front of a real chair every time and somehow, I was still relegated to the bench more often than I would care to admit… but even if these memories aren’t the brightest and shiniest, I treasure every holiday and occassion I got to spend with my family, especially now when I spend most, if not all of my holidays alone.  

There is one memory though that stands out so well in my mind and is one that I feel the emotions for even now, even here in Texas, even just as I start to think about it. My Great Nana’s 90th birthday party was an amazing night. It might just have been the happiest I ever got to see her. Her old boss, Michael I think, was able to come and he not only presented her with an award, but he spent the entire night flirting with her. His face was bright red all night long. She was so tickled to have him there. She wore a crown made of tinsel and there was a HUGE  sheet cake with every name anyone called her. The look on her face that night is forever burned into my memory and that is one of my most favorite memories of all.

Let It Go... Not Elsa's Song

“Let it go.” Those words strike terror in my very soul. “Get over it.” That’s something I’ve never been able to do and never foresee myself being able to do. “Just push it out of your mind.” ...Sure, I’ll just try to mute the memories. That shouldn’t be too hard. Just kidding… It’s IMPOSSIBLE!

I have never been able to let things go. As a child it manifested in several ways. The first and most common for children was for me to determine that “so and so hated me” after one incident. I would recall that incident for years to come. It would happen over and over again. That certainly didn’t help my social problems.

The second way it manifested was in my hoarding. I’ve been a hoarder ever since I was a little girl. I kept everything. If my mother came up to help me clean my room, I was miserable because she came in with a trash bag. As a child I wasn’t able to explain, but as an adult, I have a little more understanding. I felt that each item could someday be important. A card may be the last card I ever received from someone; a note that seemingly meant nothing could become a theme for a novel I would write down the road; a piece of clothing that didn’t fit anymore had too many memories in it to let go of. My hoarding has only grown with my age.

The third way it manifested was in my obsession with death. No, I wasn’t one of those people… I am TERRIFIED of death BUT carry those who have passed on with me. I always have. When I was just a little girl, I used to go outside and play with bubbles. I always blew my bubbles towards the sky. Inside each bubble, I’d whisper a wish. It was a wish for my great grandfather and my grandfather to find the bubble and play with it. Those I’d lost were on my mind always… even when I was too young to comprehend what it all meant.

I used to have a nightly routine. I had a glow in the dark tic-tac-toe grid. Each night, I would speak to someone I had lost then I would take the grid and, placing my finger in each space, say goodnight to the eight people I had loved and lost. The center square was reserved for G-d. Interestingly enough, two of the people, my Bubbe and Zayde, were people whom I had never met (but I talked to them anyways). Another one of the people was my neighbor’s husband (I was very close with my neighbor but really didn’t know him at all). When I look at it that way, I realize that I mourned people that I didn’t even know.  

...A hazard of having a big heart I guess…

Looking at my life today, it still revolves around those I’ve lost.

My car and my computer are both named Lil Carol(e) 2. The Lil is for my great grandmother Lillian. The Carole is for my grandmother. The Carol is for my Carol who passed away a year and two days ago.

I have a picture frame in my room (in the shape of a ballerina). It has 6 photos in it. One has both my nana and my papa. Two more contain my nana but my papa is conspicuously missing. The last 3 don’t contain either of them. By the time those were taken, they were both in heaven. I call that frame my “If they could” wish. The other 3 photos are from events that I wish with all my heart they had been able to attend.

In my bed with me are many comfort objects, each tied to a particular person. I have my great nana’s blanket (which I sleep with every night). I also have my Relay for Life blanket (which I have slept with every night since Carol was diagnosed with Cancer). Beside my pillow lies a photo of myself and Carol. The doll my nana gave me, affectionately known as Pink Baby, lies on top of the photo. A square of blanket that my favorite neighbor crocheted for me covers Pink Baby to keep her warm.  Then there are the animals. My sock monkey family had not been complete without a Grammy and a Papa monkey, so I got full sized monkeys for them. They both sleep in the bed with me. Then I have Rosie, the pink orca named after Auntie Rozie. I also have my hospital bear which my parents gave me and my tigger pillow pet which my brother gave me. I also have my white tigger which my uncle whom I almost never get to see got for me on one of his visits.

...and those are just the ones in my bed… the couch is full too!

The thing is, as much as I want for these weights to be lifted off my heart, I will never be able to let go. I strive every day to make my loved ones proud. I strive to be as loving as my Great Nana and as courageous as Carol. I strive to be as big of a role model as Dr. Marcus and as tough as my Nana. I strive to be as romantic as my Papa seemed to have been (I may have read my Nana’s diary 10 or so times…) and as creative as my Great Papa. I strive to be as determined (and Awesome) as my friend RJ. I strive to be as good of a listener as Mrs. Vaughn. Without carrying these people in my heart, I’m afraid I wouldn’t know who I am anymore. I am a conglomeration of them.

I don’t mean to say that I don’t have my own identity. I just know that each had unfinished business to do and that my goals align in some way with each of theirs.

...Not to mention, here I am alone. Now I like being alone, but I like being alone on my own terms… not all the time. I was thinking of getting an emotional support dog or a trained Aspie service dog (trained to calm, read your emotions and react accordingly, and be a constant companion. also trained to be hypersensitive so loud barking etc is decreased), but have been told now’s not the time. I don’t have the money to support a dog and I certainly don’t have the money to pay to train a service dog.

I understand completely why my mom feels that I need to let things go and move on with my life. I hope that someday I can… I know that I am not intentionally ignoring the suggestion. For me, the mere suggestion simply seems impossible.

The Rollercoaster That Was My Trip Home

Part 1: Getting There

For the past several months, I had been getting ready for my trip home. Finally it was almost time to depart. Being me, I had made several lists detailing things I needed to do, things I needed to pack, and things I needed to accomplish before traveling on the 11th. Unfortunately… I am me…

What I mean by that is that common sense was not always on my side. I ran 3 loads of laundry but can only reach the bottom dryer in the laundry room, so I removed what needed to be hung and placed the rest of the laundry in the dryer. At the end of the cycle, most of the clothing was still wet and I wound up having to hang it dry… HOWEVER I didn’t have nearly enough room on the drying rack in my apartment, so I had to empty all of my wire hangers and hang the wet clothes on the hangers in my front closet. I left the door open and the light on so mold wouldn’t grow, but obviously, this was not ideal.

Furthermore; when I was putting my pills together, I realized that the remaining bottles of one of my medications were not filled with the proper medication (I had always gone by size of bottle on those ones because it was the only medicine that came in a bottle that big)... oops…

Knowing that I would more than likely not hear from my doctor before I left for the airport, I sent a message asking for the medicine to be called in to the pharmacy back home… then the new insurance company refused to fill it; but that’s a story for another time.

On Thursday night when I was supposed to be packing, my friend Jason had posted on facebook that he was uploading a new video of the abandoned Six Flags New Orleans. I call it my “Aspie Obsession”. I am obsessed with all abandoned amusement parks, but my true passion lies in SFNO. Anyhow, he posted that the video had been posted so I stopped packing and immediately started hitting the refresh button… Two hours later, I was still hitting the refresh button and was somewhat horrified that I hadn’t spent the last two hours packing. Around midnight, the video finally finished rendering and appeared on my computer screen. I spent a half hour watching it with a grin on my face. I felt that I had satisfied my obsession but I’d done nothing to prepare for my trip!

After my series of unfortunate events (many more than these three, but I hate to make myself look dumb), I was ready to travel. I worked both of my jobs on Friday night and returned home completely exhausted. I finished packing my carry-on, fitting my teddy in and my Tigger Pillow-pet in my suitcase, and climbed into bed.

I didn’t sleep… I was too excited (and anxious… but mostly excited)...

The next morning, I had some cereal, packed the car, and headed to the airport. I HATE flying! I don’t like airports, planes, and I definitely don’t like being out of control of the situation. Since my diagnosis, I have been able to receive accommodations at the airports and on the planes. Sometimes the help is great and sometimes it leaves something to be desired, but I am definitely grateful for it!

My local airport is very small. I don’t mind it so much. I still enter wide-eyed and “snap-necked” ( a phrase I coined to describe the quick jerking movements my head and neck make when I’m anxiously looking around) but don’t need any help navigating the airport. I do make sure to get there early so I don’t get stuck in a throng of people, but even if I did, there’s only about 50 people in my airport at a time.

About an hour before takeoff, I took my dramamine and zanex. As the waiting area filled, my headphones went on (although I sometimes look rather silly with the cord not plugged in to anything). Boarding was not as smooth as it normally is… they boarded all priority boarding with military (and I live in a town with an air force base) and AA Advantage members (that’s most of the town… AA is the only airline to fly in and out of our airport). Fortunately, once on the plane, I was in a single seat and the zanex sent me off to dreamland before takeoff (which for me is the best way to fly).

I HATE takeoff and landing. Nothing is ever perfect, and this time, I was asleep for take off but was awake for landing. My teddy was squeezed extra tightly but I survived. When I got off the plane, I stopped on the jet bridge and asked where I was supposed to meet my escort. Just my luck, the escort wasn’t there. I was brought to the gate and left while the gate attendant tried to get someone to escort me.

Because of the mixup, the special escort who was supposed to have training working with Autism and other special needs (as opposed to mobility needs) never came and I was escorted by a regular mobility assistant (someone who pushes the wheelchairs). He walked about 10 feet in front of me. When we were on the tram, I sat in the handicap seating and he stood on the other side of the tram. If I hadn’t been paying attention or if I’d been lower functioning, I can only imagine what could have happened because he was so far away. I told him I have a phobia of escalators and he walked right onto the escalator and proceeded down it like it was no big deal. I finally got onto the escalator and he was already off it and disappearing around the corner. The escort did not make things easier for me and other than showing me the way, it was almost like he was never there.

The second plane boarded much like the first, but instead of AA Advantage members, they boarded first class along with military and priority boarding. Again, I was surrounded by more people than I was comfortable with. I fell asleep before takeoff again and woke up to find that Paddington was on. I enjoyed the movie then watched one of my own on my tablet. Landing was once again a source of anxiety but I knew that my mother was waiting at the gate for me.

Once we landed and I released my grip on my teddy, my legs started bouncing up and down with joy. I was home and almost in my mom and dad’s arms.

Sometimes Aspergers Just Sucks

I love my new (second) job! It's perfect for someone with Aspergers. I roll silverware at one of my favorite restaurants.  It's great for me because I don't have to worry about talking to other people. At this job, as opposed to my full time job, I can sit and get my work done in a relatively relaxed manner. Even better, I get to sit and listen to movies on my phone while I'm rolling and I'm surrounded by the comforting smells of some of my favorite foods.

I follow a routine. Knife under fork, ridges on the knife face right, straw wrapper facing left and tucked underneath the knife's ridges, bottom corner folded up, left side crosses over, then roll and place napkin ring in a clockwise fashion with the sticky side at 12 o-clock. I make sure that every roll is neat and tidy. I make sure that no knives are sticking out, no napkins are coming undone, and the silverware is clean. It may take me a little longer than other employees to roll the silverware, but mine is OCD approved.

So if I'm loving my new job and it's so great for a person with Aspergers, why does Aspergers suck?

I got to work this morning and it was like any other. I made my way around the dining area with a spray bottle and a rag. I cleaned each table, booth, and seat. I said hello to the dishwasher and went into my "area" to get started. The dishwasher had already brought one tray of silverware into the room for me and proceeded to bring two more in.

Because I'm so small in stature, I rely on the dishwashers to bring the silverware to me, as it is typically washed in large trays that are very wide and very heavy when wet. I didn't really pay attention to where the dishwasher put the silverware; I just set about drying it off and sorting it so I would be able to quickly roll it.

I should have paid attention. The trays were on the floor. Okay... well they've been there before... no biggie...

BIGGIE!

As I was sorting the silverware, a man came into the room, looked around, and asked me if I could fit the silverware trays on the table. The table was overflowing with restaurant supplies. In my mind, it was comical that he would even ask. I didn't know this man from Adam and I replied that there wasn't room and thought nothing more of it. Employees come in all the time and tell me the silverware is in their way. I was working quickly to move it, but couldn't move any faster than I already was.

Then the man came back... the general manager was with him. He wasn't happy. He said something about the area not being right and they left. When one of my co-workers came in, I asked who the man was. He was the FREAKING HEALTH INSPECTOR! While I realize that we should be able to pass an inspection whether or not we know the inspector is there, I was very upset that no one had warned me that he was there. No one had come in to make sure that everything was okay for the inspection. In my mind, it was poorly handled...

But that didn't stop me from feeling horrible about it. All day, I kept replaying the interaction in my mind, trying to find clues that the man was the health inspector. He was not in a restaurant uniform. He carried a clipboard. He was wearing a jacket with an insignia on it, although I didn't focus on the insignia closely enough to remember it. I also kept replaying my response. If I was asked a question that didn't make sense to me (in this case because it seemed the answer was obvious) perhaps the better answer would have been: "let me get one of the guys to help move this large bag of sugar that's taking up half the table space and then the silverware trays will fit." Of course, hindsight is 20/20, but I am still obsessing.

In fact, my manager told me that if the inspector comes back and sees the silverware trays on the ground again, she will lose her job. WHICH MAKES ME FEEL HORRIBLE! And although the dishwasher was the one who placed the silverware trays in the offending spot, I still allowed them to stay put.

Sometimes I really wish I could pick up on subtleties...

Sometimes, Aspergers just sucks.

Unanswered Prayers?

I should be writing this entry from my room back home in MA... but I’m still here in Texas.

This was supposed to be the year that everything changed. On New Year’s Eve, I got the most amazing phone call. Funny enough, because of my literal take on language, I didn’t understand the call right away.

Since the day my dad started dialysis, every time my mom called and said she had news, my response was: “tell me we got a kidney”. After awhile, she stopped answering, but I would unfailingly ask every time just the same. During December, my dad was not doing well. He was back in the hospital and there were worries about his heart in addition to the usual worries about his kidneys. He had a blood clot. Thankfully, they found it and were able to remove it.

My dad was supposed to come to visit me here in Texas for the first time, but with the decline in his health, I began to worry about his impending trip. On December 30, I called my mother and suggested that I make the trip home rather than my father traveling here. She said there would be no need for that, but I was terrified that if he came down, he would get sick and I wouldn’t be able to take care of him.

That’s why I was so confused the next morning when I answered my phone.

My mom called and said she had some good news. I of course responded: “tell me we got a kidney!” She didn’t. She said that my dad would not be making the trip to Texas, but that I would be coming home in February for a week and that my aunt was a donor. Now to understand my confusion, you should first understand that my aunt (my MOTHER’S SISTER- never on my radar as a match) works for a travel agency and often is the recipient of free plane tickets. I assumed that she was donating a ticket for me to travel home to celebrate my father’s birthday. My response was a very underwhelming “okay”.

...About a minute passed...

Then my mom asked me if I was still breathing. ALL AT ONCE IT HIT ME! I started crying, I was speaking nonsense, attempting to explain that I had misunderstood, and attempting to confirm that my dream come true was actually happening. IT WAS! The transplant was set for February 17.

I couldn't be with my family, but I took a photo of my "happy face" and sent it to them.

We celebrated! We weren’t allowed to post anything online about the transplant or finding a match, but boy did we celebrate... and I just started calling people. I called my best friend, I called my old boss, I called anyone who would pick up the phone. I was on cloud 9!

Then the uncertainty came. First I was warned that the surgery date may change. Then I was told that the transplant team needed to meet to determine if the blood clot would require the date to be pushed back... but there was almost no chance of that happening.

For the first time in a very long time, I set my mind to one result: this was happening and it was happening on February 17. I believed that if I thought the thought hard enough I could wish it into being. I didn’t believe that G-d would dangle a happily ever after in front of us like this, only to rip it away.

I started having nightmares again. I called my grandmother and cried on the phone for a long time while I explained how scared I was that the surgery wouldn’t work or that I wouldn’t make it for the surgery due to weather/travel problems/etc. My nights were plagued by anxiety-ridden thoughts. I wasn’t sleeping. Selfishly, I said to my grandmother that I couldn’t take another month of this.

The next day, I discovered I wouldn’t have to.

The transplant team finally made up their minds. They want my dad on at least six months of blood thinners for the clot before they will do the surgery. My world came crashing down.

(Thank you to my grandmother who just spent 29 minutes on the phone with me, as I’ve been keeping these emotions bottled up inside for the last month and I just needed a good cry... now back to our regularly scheduled blog post).

I withdrew. I didn’t even call my grandmother. Not until tonight. I’ve never done that before.

I lied. I acted like everything was okay when inside I was torn up, feeling like I had somehow wished it into not happening instead of willing it into happening like I was trying so hard to do.

I avoided. Every time my mom talked to me about scheduling a trip home, I changed the subject.

I planned to see my therapist on the day that originally was meant to be so life-changing. I tried not to think about the date. I tried to be grateful that I wasn’t going home to the endless blizzard that they were experiencing. I even got excited about an anticipated movie night with people from work.

Unfortunately, the movie night was cancelled and, as my brain does, a little depression grew and burrowed and unleashed everything that’s been bottled up for the last month.

In a way, I’m glad it happened tonight. I was able to get some soothing words from my grandmother and greatest ally. I will probably sleep better tonight than I have in a long time. I have time to process my feelings before the day arrives and I will still see my therapist that day.

But I made my biggest decision of the night just now as I was typing my last sentence. After my appointment, I will go to dance class because our dream still is coming true, just not as soon as we hoped, and I want to celebrate again. I want to celebrate a hero. I want to celebrate my father.

...And I think I will plan that trip home...

Green Glass Love

I spent today alone. That’s not exactly true. I spent today surrounded by people... but I was alone.

“Just an ordinary day” I told myself as I got dressed for work. “Nothing special” I thought as I brushed my hair. “It’s not even a real holiday” I argued as I drove myself to work. Ok, I’ll say it: “I hate Valentine’s Day!”

I didn’t always hate Valentine’s Day. I used to be a girl who dreamed of a once in a lifetime love. I wanted nothing more than to have someone who loved me more than anything. Someone to laugh with and cry with. Someone to grow old with. Someone to be mine. Someone to have a family with. Someone who would be there beside me unconditionally.

I grew up listening to show-tunes. One of my favorite concepts was the “green glass love” from Thoroughly Modern Millie: a love that would be the same whether he were a prince or a pauper. I used to dream of the day that I would find my green glass love.

Over the past several weeks, I’ve become a part of, well I guess you could call it a “fandom”... It’s a daily vlog channel called The Frey Life. It features a husband and wife duo, my age, named Peter and Mary. They have the most beautiful green glass love I have ever seen. Mary has CF and Peter is with her through the good, the bad, and the ugly (or in Mary’s case pukey). I have to admit that when I watched the first vlog, I fell in love with Peter. Not that way! I fell in love with the idea of him. I fell BACK in love with the idea that someone existed who would be loyal and true in all instances, not just when it suited him. I loved seeing a love that saw beyond health problems. I love that every vlog ends with Peter and Mary’s smiling faces, even if it’s not the best time. I want a Peter of my own.

That’s where life gets tricky. You see, I’d kind of already given up on that...

DAD IF YOU’RE READING THIS BLOG POST, PLEASE STOP RIGHT NOW.

Four years ago today, I thought I was in love. I was having dinner with the man of my dreams. The ring of my dreams was on my finger. I thought life was perfect. I truly thought I’d found the man I was going to marry.

Unfortunately, my Aspergers (then undiagnosed) presented a serious problem.

I lost that love because I couldn’t be intimate. I can’t be intimate. Just thinking about the act makes my skin crawl and my heart race and I get all nauseas. I wanted things to work with my love; I really did. I tried to convince myself that it would be worth it; that I needed to give him what he needed so that I could keep him. I don’t know whether it was fortunately or unfortunately, but no matter what, I couldn’t convince myself. The last weekend we spent together he gave me a back massage. All at once I got nauseas and raced for the bathroom. I hid out there until we had to leave the room. Later that night he and I fought. He accused me of leading him on and playing with him and I had no real defense because I didn’t understand what was happening any better than he did. I will NEVER forget being on the phone with my mother (while in a hotel room with him), being screamed at to the point that I was afraid.

With that said, I didn’t give up on love because I was afraid or even because of him. I gave up because I AM afraid that it will become a recurring situation.

My history with men leaves much to be desired. My first boyfriend was gay. We dated for TWO YEARS! He came out on prom night. YEOW! My next boyfriend was NOT boyfriend material. He was a liar, a bad-boy, and he hurt me in a way that I will never recover from. Then there was the boy I mentioned; my lost love... and for a lovely bookend, one more gay boyfriend.

So I began to wonder: am I setting myself up to fail at love? The question makes sense. How many bad choices do you need to make before you wonder if you’re anticipating the outcome? The idea of being intimate has been such a locked off topic in my mind for so long that I wonder if I am purposely getting into relationships with people who I KNOW I won’t become intimate with. If I am, I’m my own biggest obstacle.

I question all of this because I’ve begun to wonder if my life has to be this way. I have a friend with Aspergers who has a husband and a son and she’s truly happy. At the same time, my Aspergers is preventing me from having a husband and a child; two things that would make me very happy. I’m not a desperate woman sitting at my computer writing this in the hopes that someone will read it and decide to go out with me. I’m writing this as an open letter to the Aspergers community. I need help. I want to change my future. I want to believe that love can come my way. Any helpful comments would be most appreciated.