Chronic Illness Bloggers

Sleep and Counting Sheep

Posted on by akiwifreund

What are the two most common symptoms of just about any chronic disease under the sun? Pain and fatigue. Sometimes pain interferes with my sleep, leading to even more fatigue. It’s a never-ending cycle. I jumped on the opportunity to try this product from ProHealth called FibroSleep, because let’s face it – even the best bubble baths, candles, teas and essential oils can’t fix everything every time. Specifically, I was given this product as part of a product review opportunity through the Chronic Illness Network. This item was a gift and I have been encouraged to give an honest opinion and review without any influence by the company. If you have read anything else I’ve written, you know I don’t hold back.

One of the problems that I run into with my additional strange, undiagnosed rare disease is that because of the increased pressure in my cranium, I get anxiety. Sometimes it feels like it comes out of nowhere. Sometimes I can blame it on specific events – like doctors who tell me that I am imagining my symptoms, or that my cluster of symptoms are actually unrelated to each other (even though the majority occur in my brain), or that there’s nothing that can be done and to never come back, etc. About every ten days I will have an entire night pass where my anxiety simply rules my entire body and I cannot fall asleep.

I received this product just in time for a particularly bad run of insomnia thanks to some discouraging appointments:
2016-05-05 08.02.56
I always, always check labels to see what’s going to be invading my body, so here’s the ingredients:
2016-05-05 08.02.42
This particular beef has come up for me before with me and labeling, but I would like to point out that if you have a camera on your phone that has a high pixel setting and can adequately blow up a picture so that you can read tiny writing, you may not see this as a problem. However, if you don’t, and you don’t carry a magnifying glass, you will not be able to read this label and figure out the ingredients. I’ve been told before that it’s a space issue – they simply don’t have enough – but here’s some blank space that’s not being used:
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The size of the capsules are pretty standard:
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I tried the capsules for three nights in a row and nearly gave up completely. I have had previous experience with 5-HTP and melatonin (both included in this product) and figured that it would be a slam-dunk, but anxiety that was prompted by doctors with big egos and closed minds completely overruled any compounds I was consuming, so I got zero sleep. I didn’t even get a weird, loopy feeling that I sometimes get with those two ingredients the morning after.

Which brings me to an important point: with both 5-HTP and melatonin, you will give yourself the best chance at getting good sleep if you cut out ALL light because light messes with your REM patterns. Look around your sleeping area and address all sources of light, including your phone, your laptop/tablet, your router/modem and your TV. Okay, so I just named off everything in my sleeping area – because it’s my bedroom and also my living room since I have a studio apartment. Even my sun therapy lamp has a bright red light that glows when I turn off my room light at night that would otherwise mess with my sleep if I didn’t somehow cover it up (I used black electrical tape).

I put FibroSleep in a drawer for a week and a half and resigned myself to terrible nights (and days) while I struggled with the politics of navigating the good ol’ boys’ club of male doctors. When I felt like I had put enough space between them and me, I tried again. Boy, did I sleep – like a rock. I did have some funky dreams because apparently my brain had a lot to work out. Also, each night I took the FibroSleep I dreamed that I was physically going through the motions of going to the bathroom, which I have learned over the years that that is my own personal signal to wake up pronto because my bladder is full and no joke, IT’S TIME TO GO. It conked me out so fast that I forgot to use the facilities before falling asleep. Most of the times I woke up to use the bathroom I also could not fall back asleep, so I only clocked about 4-5 hours of sleep total. On those nights I was loopy. This is definitely not the fault of FibroSleep. I have always had a hard time falling asleep after waking up to do things like running to the bathroom, so I broke the cardinal rule of not interrupting the sleep so that I could reap the benefits fully. I have always envied those people who can easily go right back to where they left off.

I have had fibromyalgia for about 18 years, and sleep is always a big challenge. Even if you don’t have fibromyalgia but you are like about 70% of the adult population at any given time and you are going through an especially extended and rough patch of chronic insomnia, FibroSleep may be worth checking out. Currently (May 2016) they are offering a 20% discount on FibroSleep orders here: https://www.prohealth.com/shop/product.cfm?product__code=PH311FB&B1=BLGGPH311

Also, if you are interested, they are giving you the opportunity to enter in a chance to win on their giveaway: http://fibrosleep-giveaway-bloggers.instapage.com/

Lastly, ProHealth offers a number of products. They actually have done something quite handy with their site and divided it up by conditions and topics, so you can read articles and shop for products specific to your condition: http://www.ProHealth.com

The Remains Of The Day

Posted on by akiwifreund

Yesterday I was picked up by the short bus for back-to-back appointments at the health crisis center. I was the only one on the bus and so I felt comfortable chatting with the driver, unhindered by eavesdroppers or joiners. First I asked if he was a Prince fan. Hey, why not? He didn’t look to be much younger than me, and it’s still big news around here since it’s Prince’s home base. Rumors are still flying and spreading like wildfire. How did he actually die? How will his estate be handled? Will his family completely melt down and will it get ugly like it so often does when there is money involved?

The guy admitted he wasn’t much of a Prince fan. Our conversation wandered around the world of entertainment, and he talked about how dissatisfied he was with staying hooked up with satellite TV, but he kept it for sports. But then he said that he really didn’t enjoy watching any sports either. I asked him if he liked to see games in person as opposed to seeing them on TV and he said he kind of did, but he couldn’t afford to go to games. I asked him if he liked to go to shows like theater or dance, and he said he’d rather be burned alive. He also didn’t really “get into” movies or music.

A 20-minute bus ride isn’t really the place to offer life coaching. I also can’t make people feel what I feel, which can’t necessarily be put into words. A sense of urgency, maybe, or finality? It could be that my bullshit meter goes off a lot more than it ever has before. What I wanted to tell him is that he needs to find his joy. I cannot say this loudly enough, though, but this cannot be confused with finding his next fix. So many men are stuck in this cycle of seeking thrills and the adrenaline wears off and they are onto the next conquest while constantly feeling empty and wondering why they do. Where is their humanity?

Before connecting with The Saint Paul, I talked to a few men through OKCupid by text and/or phone who made excuses to play stupid games with me or not respect boundaries. I changed their identifiers in my phone to start with “Asshole ______” and programmed my phone to automatically send their calls and messages into my spam folders. I don’t even think about these folders unless I get weird calls like I have been for the past three days from recruiters based on resumes I put out in the universe over a year ago when I got laid off of my job in Phoenix before I had my last surgery. I went to update the blocks and thought to myself, “I should check my spam folder.” Lo and behold, there were some messages.

The first was from the Christian asshole who had no respect for my boundaries, and who previously tried to bait me into talking to him again by randomly telling me he had arrived at his hotel room. This time he just said, “Hey stranger how are you?” Of course, it’s been almost three months since we’ve texted, and we never even talked on the phone – but by God, he’s not gonna give up!!!! Answer, bitch!!!

The other two were from the last guy I talked to on the phone and texted with before I met The Saint Paul who abruptly said he met someone and cut off all communication after he tried to sext, which I guessed to be a lie since he was constantly logging into OKCupid still when I had an account before mine was deactivated. After two months of silence, he sent texts saying, “How have you been? Just wanted to say hi.” Gawd, please – I am not new. He didn’t “just” want to say hi. We were not casually keeping in contact and staying friends. He’s trying to keep his options open in case whomever he is currently trying to bang doesn’t work out.

I resisted the urge to reply to both of these messages because really, neither one of them deserve a response. I really, really like this phone I purchased on New Year’s just for this blocking feature alone.

There are a couple of great lines in this song by Sean Rowe that I think applies to these guys (and really, listen to the whole song because it fucking rocks): “I’m a man, I am the world, I’m a man, I am the Lord” and “He puts out the lights and jerks off alone.”

I can’t save everyone. They need to figure this shit out.

Le Petit Mort

Posted on by akiwifreund

I cried a lot yesterday. I never used to – it was a bragging point for me, that I would shed tears once a year, tops. But yesterday I started by spending an hour on my counselor’s couch recounting my dehumanizing neurologist’s appointment on Tuesday with big, fat tears rolling down my cheeks the entire time. It actually took me days to process what happened in the visit, and is the reason why I still have to write part two now.

I barely got five words out before the tears started. They were angry tears. I’m pissed. It’s not just that the doctor was a dick – because he was – but it’s that his actions could affect my life for the next few years to come. It’s not an exaggeration. I’ve been through this before too. When I had my very first shunt placed and experienced abdominal pains from day one, the neurosurgeon and general surgeon passed me back and forth for a couple of months and blamed each other for causing me pain before finally throwing up their hands and telling me that it was my imagination and there was nothing wrong with me before they had to do a large cut on me two and a half years later and discovered my abdomen was grossly inflamed from an allergic reaction to the shunt. Two and a half years before they admitted there was a problem.

The problem with this neurologist now is that he is saying that I have spasms in my face, and that I just need to stretch my muscles. He’s going to put that on my records too – and the records are going to the NIH and Vanderbilt. Vanderbilt will either take his word as gospel or dismiss his diagnosis and study me, and I have no idea which way they will tilt, but if they decide not to accept my case, it could mean YEARS of more testing before they will consider my case again.

The most insulting part of the visit with this douchebag is that he spent more time demanding to know why I wasn’t on antipsychotic meds. I am having some issues with word recall, which apparently he views as a clear sign of being psychotic. Well, that and I have this condition that no one can seem to name up to this point. He performed physical tests including forcing me to fall, all the while holding onto my hips to assist me to the next starting point because my legs shudder and I list to the right during any physical activity and I wasn’t allowed to use my cane. Then he had the balls to tell me that I was just having facial spasms. I couldn’t believe it. I said, “But you were holding me up because I couldn’t stand!” He acted as if I didn’t say anything.

This neurologist gave me the standard statement on my discharge papers saying basically “don’t come back.” I don’t make this up, people – it was there in writing. The list of doctors who will let me through their doors is tiny at this point. I would have to go through the effort of finding all new doctors to try this all over again if I wanted to get another referral to the rare diseases unit if Vanderbilt denies me this time.

I’m not crazy. I just need doctors to set aside their preconceived notions and overinflated egos and listen to me, because I have had six years of this, compared to their one hour with me and my pages of documentation that they won’t read anyway.

I sat down on Thursday night and wrote this to the doctor and his nurse. I don’t think it will change what goes in my chart but I wanted to say it anyway:

“Regarding Dx of Facial Spasm:
Just to be clear, my primary dx should NOT be functional facial spasm. I am preparing documentation to submit to the NIH through Vanderbilt and I would like it to be accurate. My symptoms have always followed the same pattern, in this order: vertigo, fatigue, slurred speech, uncoordinated walking and then ptosis. Every shunt revision has been performed after all of the symptoms have presented indicating that the shunt has clogged or broken. My shunt has been clogged since it was placed on May 11, 2015. The symptoms resolve when I lie flat, which is why I don’t have permanent damage on an EMG (and why the test was unnecessary). When I lie flat, I can feel the fluid move away from the area that it’s pressing on, as if an orange peel is slowly being removed, and the pressure is relieved from my brain. That is why my eyes open and all of the other symptoms resolve. When I am upright, the fluid pools and the symptoms return. I demonstrated this in person on Tuesday, including laying flat as well as turning my head to the far left to open the shunt to drain off fluid so I could open my eyes fully.

The printout regarding functional facial spasm does not address CSF pooling in the brain or how doing stretching of facial muscles is going to help pooling of CSF in the brain. Since I have to travel hundreds of miles in the near future to continue research on my medical mystery, it would be helpful if my records were as accurate as possible and did not contain information that does not apply to me.

Thank you.”

Next week I’ll see my primary doc and will find out if I stirred up any shit or if I have been completely ignored.

What a difference having someone who loves me and who is in my corner makes in my life, though! The Saint Paul is like my hallelujah clouds during a shit storm. I promised not to spill all of our personal details, but there are things that I feel are safe to share. The Saint Paul has a big brain and is humble, which makes me weak in the knees. He’s also a good listener. I mean this in a very specific context: If I say that I need to be touched in a certain way, he doesn’t try to correct me and say that “every woman likes” what he’s doing and he’s not going to change it. Instead, he listens and makes the adjustment, and the reward is that I don’t have to fake anything and do the crab crawl backward.

I don’t know if he noticed last night but my eyes were leaking. It was for a much different reason than 12 hours prior when I was parked on my counselor’s couch, but it felt infinitely better.

Me and Prince

Posted on by akiwifreund

This morning after I took my bath, I wrestled into my purple bra and underwear, shoved my purple long-sleeved shirt over my head and torso and slipped my phone with its purple case into my pocket before heading out the door. I briefly considered taking my purple cane but decided against it because I knew I would be gone for about 20 minutes tops, which is the high end of how long it takes for the CSF to start pressing on my brain and making me wobbly.

Then the news started to trickle in: A dead body was reported at Paisley Park, Prince’s residence here in Minnesota. Just a week ago or less, there was a report that Prince’s plane had to make an emergency landing because he was experiencing some sort of health crisis, but he was resting at home comfortably. It was not a huge leap to assume the body was Prince’s, and it’s also not a huge leap to know that many of us locals are just plain sad about it. Of course he has a large following outside of Minnesota, but he was OUR guy.

Back when my dad was working on making a name for himself as a top-rate hair stylist in the very early 1980’s, he met Prince. My dad loved to name drop. He also thought Prince was a spoiled brat and didn’t hold back on saying so. Prince always traveled with an entourage (read: there was never a time he wasn’t a star). I later bragged to my classmates that my dad talked to Prince. I wasn’t afraid to name drop either.

The movie “Purple Rain” came out and the residents of Minneapolis/St. Paul (commonly referred to as the Twin Cities) were absolutely thrilled to be featured in a movie. First Avenue – “First Ave” if you’re cool – was forever galvanized as THE stage to play on thanks to “Purple Rain,” and who cares that the script was weak? The soundtrack was to die for! I mean, “Darling Nikki”?? Prince was so dirty! He actually talked about masturbation in a song and if any stations played it, the word had to be altered. How could such a short little guy get so many women to throw their panties at him?

When I went to the arts high school for my junior and senior year, I remember a boy who was trying to get into my pants saying to me, “Just give me a dark room and a Sam Cooke album.” I had no idea he was quoting a line from “Under the Cherry Moon,” another low-budget Prince movie that also starred Kristin Scott Thomas, at that point an actress largely unknown to American audiences in a film that didn’t have the commercial or musical success that “Purple Rain” did. I laughed when I finally did see the movie (on VHS tape!) because Prince found a way to infiltrate my love life as I’m sure was his intention all along.

In my senior year at the arts high school, I had a roommate who only played three albums: Nirvana’s “Smells Like Teen Spirit,” Weird Al (I can’t remember the name) and Prince’s “Diamonds and Pearls.”

I don’t remember which album the rumors were flying around for, but supposedly Prince actually recorded a woman getting off and put her “sounds” on a track. This was well before we could actually research anything on the internet. He is well-known for pushing artistic and cultural boundaries. I mean, who else would have a top 40 song called “Cream (Get On Top)”?

In 1996, my boyfriend at the time and I road tripped back from Albuquerque to Minneapolis and after a night of drinking with a friend and my sister, decided to check out Paisley Park. My friend had worked there previously as a security guard and offered to guide us with him driving his car and me driving my car just to show us where it was. Well, my boyfriend told me to pull into the driveway where the guard was stationed; when my friend saw what we were doing, he took off. My sister was pretty drunk in the back seat and pulled a blanket over her head, saying, “If I can’t see them, they can’t see me.” The guard greeted us, saying, “Can I help you?” My boyfriend leaned over me from the passenger seat and slurred, “Is this where Prince lives??” The guard straightened up and said, “I’m going to have to ask you to leave.” My boyfriend persisted, saying, “Can we take your picture??” The guard said again, “I’m going to have to ask you to leave.” In the meantime, my sister Heidi is quietly saying, “Oh god, oh god” in the back seat under the blanket. I backed up and managed to find our way out of the back roads of wherever we were; this was well before GPS and it was around 1:00 a.m. in a very rural area, and my friend was long gone, so it was no cake walk. Thank goodness I have a pretty good internal compass.

The same boyfriend and I relocated to Cincinnati and worked for a box office that was also a Ticketmaster outlet and managed to score tickets to two very different Prince shows. One was in Columbus, Ohio; the entire show started two hours later than it should have and we were already an hour away from home. Start time was supposed to be 8 but it was more like 10 and it was an opening act, then Prince came on at around midnight and played “Purple Rain” and we thought well shit, that’s it – but NO, he played for two more hours!!! The next day was hell because of course we had to work after taking an hour to drive home, but we got to see it. The next show we saw was very different, which was Prince playing with no opening act and playing all of his hit songs, but it was like one 2-hour medley – he had so many hits that he couldn’t play any of them all the way through. I was sitting behind Peter Frampton for that show.

After I moved here from Phoenix last summer, I saw something I never thought I would see, and that is Prince opening Paisley Park up to the public for parties. He has always been notoriously private. I hope that holding those parties brought him some joy. I never thought they would be his final act.

I feel like those of us (and yes, I say “us” because I count myself in this bunch) who do as much as we can as soon as we can somehow have a sense that our time on this earth will end at a much younger age than those who are much more methodical about how they spend their time. The moral of this story is to get your purple on and party like it’s 1999. We will miss this magical man and all of the soundtracks that he has provided for our lives.

https://youtu.be/-ZCiHsIfrOg

I’m Just The Patient

Posted on by akiwifreund

Today was my big appointment with the movement disorder neurologist at the U of Minnesota, and it was decidedly anti-climactic. My first impression was that he was a young version of Derek Jacobi, pictured here:
Derek Jacobi
All of the doctors seemed to be excited that I was scheduled to see this particular one and told me repeatedly how thorough he was. In fact, I was supposed to see him over a month ago, but he looked over my file a few days before I was due in and instead insisted I get my face tased (with an EMG) before seeing me, which pushed my appointment back so that he could rule out myasthenia gravis (a second time). I knew I didn’t have it as of 2010 and I still don’t.

This doctor was short on bedside manner, so I immediately shortened my answers and didn’t elaborate on anything. We went over my family’s extensive history of autoimmune diseases. He made me walk and do things with my eyes closed to deliberately make me fall (which made me sweat and because I was under so much stress, the tremors started up almost immediately). He shook my shoulders, sending white hot pain through my left shoulder that I’ve been going through PT for but am going to get an MRI for after next Friday because I’m not healing – I spent three years laying on that shoulder because all of my surgeries were done on the right side for that length of time, and the pressure really messed up the tendons and ligaments.

After all of that, the doctor told me that his nurse gave me the website in December that I should have checked out on movement disorders. He must have seen my eyes glaze over and the stubborn set in my chin because he left the room and returned with screenshots of the website. I politely folded them into squares and stuffed them into a pocket in my purse. He said that a doctor from July of 2015 believed that I have a facial movement disorder. I told him it was news to me, since the only thing that was said to my face was that I wasn’t a good candidate to have surgery to relieve the pressure on my optic nerves. This doctor said that the other doctor may have chosen not to tell me that I have a movement disorder because there’s “nothing that can be done about it anyway.”

This entire conversation is deeply flawed. First, I don’t have a facial movement disorder. I have a problem with CSF pooling in my cranium while I’m upright and it presses on some of the nerves leading to my face as well as my cerebellum; as soon as I lay flat, the fluid moves away from the area and I get full functionality back. Second, I have plenty of issues in which “nothing can be done” for them – including alopecia universalis, though he was quick to point out that someone was doing a study. I told him that it was low on my list of priorities. Third, I’m the motherfucking patient. Doesn’t it stand to reason that if this is one or more of the thought process of the doctors that it should be discussed with me?

When it was time to go home, the cab driver that got the dispatch to take me home pretended to come and pick me up but then acted like I didn’t show up – even though I was outside sitting on a bench in between approaching every cab that rolled up asking if they were there to pick me up, so it took me an extra hour to get home after I had to call dispatch to bitch.

I really could have just stayed home.

In fact, I would have benefited from a day in bed. I predicted that I would be laid out for a good week after last Saturday, but I think that it was an accurate call. Now that I have an honest to goodness boyfriend, we’ve been trying to do activities that I can actually handle for a few hours. There was a flea market/antiques expo at the state fairgrounds and I thought we could just take the bus because it stops right outside my building and seemed to spit us out right at the fairgrounds gate. I was not a good planner for this trip and we ended up doing a lot more walking than we thought – and it wasn’t like we had a choice, no one could do the walking for us. My phone tracks my walking automatically and I wasn’t surprised when I saw 2.5 miles for the day rather than my usual high of 0.5 miles. By the time I climbed the steps to my building, I was visibly shaking and was fighting fatigue tears.

But damn, this boyfriend rocks. The Saint Paul is loving and affectionate, and goes on food runs and lets me stay behind so I don’t have to get out of bed. I have begun meeting his family and friends, and he is in the process of meeting my people.

Most importantly, we have said the “L” word, and meant it, and will continue to say it. When someone great comes along, you absolutely can’t take for granted that they just automatically know how much they mean to you or how much you appreciate them. I’m infinitely grateful to the universe for nudging me in his direction.

And then there were two.

Grief and Acceptance

Posted on by akiwifreund

Every other week I am in my counselor’s office, and there seems to be something new that brings me to tears, which drives me crazy. I can’t figure out why I am crying so much. I mean yeah, I have experienced loss on a major scale in the last nine months – my sister, my friend, my uncle, moving states, losing my job, losing all of my doctors, losing my option for more surgeries – but I keep thinking that I should be adjusted by now. But reading this post by my fellow blogger reminds me that I keep experiencing loss and that I still have a sense of instability. Since my U of MN doctors insist that I don’t have Lyme, I have to go through the long process of getting set up through the NIH rare diseases unit and make arrangements through Vanderbilt University to be studied there, as they have locations designated throughout the country for patients to be screened. In the meantime, I have to continue with my treatments with my naturopath, even though I have NO IDEA if it’s the right thing to do.

In addition, I’ve been given the option of getting a TAP block in my abdomen with the hope that it will relieve some of the nerve pain that I’m having from being allergic to the drainage catheter from the shunt. The doc is going to numb nerves on both sides of my abdomen leading to my lower belly. The kicker? I have no idea if it’s going to affect my sexual functionality. And I’ve got a brand new boyfriend. And I really like said new boyfriend and I want to jump him every time I see him. And I don’t think it will be fair to lose what little functionality I do have, because who knows how much longer these good years of responsiveness are going to last? It’s asking a lot of a new boyfriend to possibly give up intimacy for an unknown period of time (forever???); I mean, I call him The Saint Paul, but Jesus H…I don’t know, is there something that is a step above sainthood? If I lose my ability to orgasm, that’s gonna take a LOT of mourning. Maybe some booze and mood stabilizers. I’m already stressed out about possibly taking out the shunt permanently because it’s clogged and I’m allergic to all of the shunts, which means that I may be stuck laying down forever and can’t be up for even an hour.

In closing: Send kittens and puppies and rainbows.

+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +

Wendy's avatarPicnic with Ants

When people think of grief they often think of death, they don’t think about grieving over other significant losses.  Those of us who have had major losses due to chronic illness know all too well that we grieve those losses.

The five stages of normal grief that were first proposed by Elisabeth Kübler-Ross in her 1969 book “On Death and Dying” are: Denial, Bargaining, Depression, Anger, and Acceptance.  Kübler-Ross describes these stages as being progressive, you needed to resolve one stage before moving on to the next.  This is no longer thought to be true.  It is accepted that most people who have loss go through states of grief but it is not linear nor is it finite.

The The British Journal of Psychiatry Nov 2008, published a study on grief and acceptance.  The authors note that “disbelief, yearning, anger and sadness may represent aspects of a single underlying psychological construct – grief.”…

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Careful, Your Old Is Showing

Posted on by akiwifreund

This afternoon I had the opportunity to spend time with my cousin’s daughter. We connected at my uncle’s funeral; the last time I saw her was when she was 3 or 4, and now she’s 24.

Over and over, this meme flashed in my head:
40Now

Here are some of the milestones I hit by the age of 24:
– Moved out at age 16
– Worked two jobs since age 18- Moved to Michigan, New Mexico, Kentucky and Ohio
– Road tripped around the U.S.
– Lived with my first boyfriend

I found myself saying those dreaded words, “When I was your age…” and I cringed every time.

In contrast, this young lady has been living with relatives and doesn’t work or currently attend school. We spoke about what she envisioned for her future, which included dreams of working at a bookstore or a movie theater. I prodded her into thinking bigger – after all, bookstores are becoming obsolete, and movie theater jobs are really more for high schoolers. She admitted that what she really wanted to do was travel the world and learn as much as she can. Thank goodness! That I can work with. I told her about how The Professor works at a law library on a college campus, and we agreed that a library would be a perfect environment for her. She would be surrounded by academics and wouldn’t be required to ask patrons if they would like to upsize their sippy cups for another $0.50.

Another area that I thought would be great for her (before she and I even had a chance to sit down and talk, but she brought up this afternoon) is the tech field. There is still a huge disparity of ratio of male vs. female tech employees and it’s a field that does not often require customer service interaction with the exception of level one support. There are so, so many degrees and specialties in the tech area that she could go into that really, she just needs to pick one and it should not be difficult to make a living.

So again, here is the whole closing a door/opening a window business being demonstrated in real life: I can’t work, but that doesn’t mean I have completely lost my value in this universe. I think I can successfully mentor this young woman and hopefully send her off into the world with some practical skills so she can do the things she thought were only a dream previously.

My Adolescent Heart Is Cured

Posted on by akiwifreund

Right at the cusp of my childhood and the beginning of the time when I became self-conscious and awkward, we moved from a large metropolitan area with a population of 1.5 million people to a town of 300. My bus ride to school was long and filled with strange faces; it took an hour to get to a town of 700, where people rarely moved to or away from and were all largely related. In fact, I had a couple of classmates who were the offspring of first cousins, sentenced to lifelong special ed classes thanks to genes that were far too similar to have been considered safe to pair up.

I was bullied terribly my first year at the farm town school. It really wasn’t until the next year, 6th grade for me, that I started making friends. I also became a little more comfortable expressing myself – including being vocal about crushes on boys. One boy in particular held my attention for ten whole years. I’ll nickname him C. C. Deville, because he played guitar and wanted to be a rock star just like the guys in Poison and Motley Crue.

I made Valentine’s Day cards for everyone in my class. However, for C. C.’s card, I did exactly what I read about in a book, which was write a little poem without signing it:
“You can’t be my Valentine, you look too much like Frankenstein!”
He was intrigued! It worked, just like in the book! Except when he thought another girl wrote it for him, and he started making eyes at her. That wasn’t supposed to happen.

Two years later a friend from Minneapolis stayed with me for a couple of days and came with me to school. C. C. Deville was doing everything he could to charm her, and she flirted right back, even though she knew I liked him. She liked him too and thought he was very cute. Later that year he got suspended for smoking pot under the bleachers in the gym, so obviously he was a little bit of a bad boy. No wonder all of the ladies were flocking to him like bees to honey.

When I was in 9th grade, I tried out for and made the cheerleading squad for boys’ JV basketball…which meant that I would be cheering for HIM. Oh, sure, there were a few other boys who were cute too. But there was one time on an away game that I was floating on cloud nine because we had to drive two hours through a snow storm on the bus and I was sitting in front of him, and he let me borrow his leather jacket to sleep on it. I could smell his cologne. I thought maybe he might eventually warm up to me since he lent me this article of clothing. Instead, he started talking to one of the other girls on my squad and eventually started dating her. I had confessed to her that I had had a long-term crush on him and I’m pretty sure she spilled the beans to him if he hadn’t already figured out that I had been throwing myself at him for years at that point.

(2 years break to attend arts high school.)
(2 years pass while I move back and forth between Michigan and Minnesota.)

When I was 20, I discovered that a former classmate was living in my apartment complex. She said, “Oh, did you know that C. C. Deville also lives here?” I just about shit my pants. It turned out that he lived above me. Shortly after that I ran into him, said hi, exchanged pleasantries, talked him into putting my new license plate on my car for me. (“Oh, C. C., you’re so manly, thank you!” Okay, no, I didn’t say that, not really.) Sadly, I didn’t see him after his dad and my aunt died and I left on my big trip around the U.S. to find a new place to live.

Facebook has directed us back into each others’ lives many years later. However, he posts maybe 6 times a year, and my average is maybe 6 times a day – mostly goofy stuff, sometimes political stuff, and occasionally medical updates. As far as I can tell he hasn’t moved much, he doesn’t have children, may or may not play in a cover band, may or may not have a girlfriend, and may or may not work in a bank. In other words, we are really only peripheral observers. All that we have in common is that we have been in the same place at the same time in the distant past.

Today, for instance, he posted something on Facebook that really weirded me out – mainly because it didn’t seem like he wrote it (though he was taking credit for it, but its rhythm and spelling and punctuation didn’t match the rest of his writing in other posts), and because it’s some sort of rambling message about “God.”

It starts out nice enough: “Most of the time, our biggest obstacle is us. Maybe we’ve stopped dreaming.” True enough. Then: “Or, maybe we’re refusing to share our dreams out loud because we fear that God’s reputation might be at stake. God’s reputation is fine. It’s our reputation as leaders that we fear taking a hit. The dreams in our hearts were planted by God who loves us!”

“God’s reputation”? That, my friends, is anthropomorphism – assigning human qualities to non-human entities.

He goes on: “The day we stop following the dreams God has put in us is the day we allow ourselves to go into cruise control. When our biggest desire starts to shift from seeing God do great things to making everyone as comfortable as possible, we know we’re losing sight of how big God is.

“Fight the urge to maintain the status quo. Instead, do everything possible to advance the cause God placed in your heart. Stay focused on what could be rather than what has been.”

This is what has cured my heart once and for all: I feel like C. C. Deville deliberately lived a small life, looking for hero worship in a small town, and is now turning to “God” to try to make his life feel expansive and limitless. A classmate said that she was surprised at his preacher-like post (hell, I was too), but he replied that he wasn’t trying to be a preacher, he was just coming to his senses. I think it’s more like he realized that he’s middle aged and he hasn’t done anything he said he said he was going to do when he first reached adulthood.

For the longest time I felt inadequate and undesirable while he chose girls around me. Now I feel as if I have run circles around him with my life experiences and we would have nothing to talk about.

 

Pat, I’d Like to Solve the Puzzle — Patient Worthy

Posted on by akiwifreund

One Thursday night, I was completely emotionally wiped out. There was something that went down in my family and I spent that evening on the phone and in tears. I’m not going to go into detail; I feel like it’s not my story to tell. I had as much pep as a wrung-out washcloth. I…

via Pat, I’d Like to Solve the Puzzle — Patient Worthy

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Posted on by akiwifreund

I got accustomed to living in my house in Phoenix; I had a large lot, the walls were brick, and not many sounds penetrated from the outside with the exception of the neighborhood roaming illegal roosters crowing day and night. Conversely, I could make as much noise as I wanted to like singing loudly, and I didn’t really have to worry about disturbing my neighbors. In true Phoenix fashion the curtains were always drawn to keep the sun from heating the house up too much.

Now I’m in an apartment in an old building in Minnesota that is less than 1/6 the size of my house, and besides being aware of the size, I’m aware of touching space. Specifically I know what my neighbor upstairs has for breakfast on weekends, or when her kitten is playing with a toy. I also always wince whenever I drop something on the floor in case there happens to be an apartment below me in the basement (which I still can’t figure out but have heard noises come from that area from time to time like someone is doing prep work in a kitchen).

All winter long I have had a fan going because even though this is an ancient building, the radiators work like ancient screaming, steaming beasts, and I sweat like crazy. I don’t even get under the covers. I also wear my summer pajamas, which are usually big t-shirts or chemises.

Today, however, the radiators are not on, so neither is my fan. It’s just chilly enough for me to be under my covers and for my electric bed pad to be on. I decided to dissemble my fan and wash all the parts because they have been caked with dust like fans are wont to do. In the quiet, I have become aware of certain things.

First, just because my fan has drowned out outside noises to me, doesn’t mean my fan has drowned out my noises to other people. I mean sure – I’m a decent singer. You’re welcome, neighbors. Second, I could hear my upstairs neighbor and a few of her friends giggling. This was not loud giggling. If this was not loud giggling, then what could she hear from ME? I really, really need to work on my whisper-scream, if you know what I mean. Pretty sure I need to stuff the space around my door with towels too. What the other tenants must hear when they pass by my door…! I can see it now: “Hang on, honey, I need to do some soundproofing. Hold that thought.” I just saw the movie “Room.” I wonder if I could soundproof my little sweat box just like the psycho did the shed where he kept the girl imprisoned? I would only use my powers for good and never for evil. I sure would love the luxury of screaming loudly without summoning the cops. Of course, that would work against me too. I have wiped out a few times in the tub and it would be just my luck that I will have to holler for help at some point and not a soul will hear me just because I want to set up my apartment to have noisy sex.

Speaking of sweat box, I tend to dress down when I’m in my apartment and it’s about 80-85 degrees F when the radiators are blasting away. My windows face a business that doesn’t have any windows facing mine and the alley doesn’t get any foot traffic because it’s fenced off on both ends…except for today. When I got up this morning I raised my blinds about a foot so I could see some sunshine. However, at around 9 am, two heads came floating by my windows about 7 feet from where I lay in bed next to the windows – I’m on the first floor, but I’m up a half flight of stairs, so my floor is not exactly flush with the ground floor. Apparently the business was experiencing problems with its ventilation system and a bunch of guys had scaled the fence to work on the wires.

I didn’t make any sudden movements, just laid in bed in my not-safe-for-public-consumption t-shirt and undies, no makeup and no wig. I slowly raised my body pillow so that it blocked me from their sight and when they left the alley temporarily, I jumped out of bed to put my shades back down. I honestly don’t know if they were being polite or unaware by not looking in my windows. Really, I was doing them a favor by sparing them of the full effect of me in all of my glory because it can be quite startling if one isn’t at all prepared.
This is the ultimate dilemma. If spotted, do I flash them my saggy 40+-year-old boobs so they know I’m really a woman and not a dude with a bald head? I mean, if I were transsexual, there is no way I would pay money to have this body. <sigh> I guess this was a good reminder that I shouldn’t run around in my skivvies with the blinds up even a little bit.