Bullies

I don’t know if I can really look back at this objectively, but I’m going to try.

Growing up, I had one parent out of four who really, really didn’t approve of me. I was always too fat. It made him really upset that my hair fell out in perfectly round circles – what was up with that? I must have been doing something to myself, I should just stop it! (But it was my body attacking itself.) He told me that he loved my sister more than me because she was the first born, and my brother more than me because he was the boy he always wanted.

While I was still in elementary school, we moved from a large city to a very tiny town of 300. This was right in the middle of my awkward years when I couldn’t figure out what to wear on my strange new body and my teeth were still crooked like I could eat a carrot through a fence because the dentist wanted to wait a few more years before recommending braces. Fifth grade was brutal. I had almost no friends the entire year because a girl from my class (who was tall, also awkward, with blond frizzy hair and shifty eyes) gave me a horrible nickname and meanly declared that no one could be friends with me or come near me. She got one of the boys in our class to write me love letters as a joke. He then made a big deal of “breaking up” with me, or as much as you can break up with someone after a few badly written letters, and their little group passed around what I wrote to him. (Imagine my surprise when I visited my step-cousin’s cousin’s house and it was HER house a few years later. I thought she was going to shit her pants. I had no idea where my step-aunt was taking us, I was just riding with everyone.)

I also had bullies on my bus. They didn’t just pick on me, my sister was a target too. Our bus ride was a long one, nearly an hour in the mornings and about 40 minutes in the afternoons. The worst of them was the stop immediately before ours but still quite a distance from our house because we’re talking farm country. She was MEAN. ROTTEN. The others were further along the route. One was a girl in my class who has always been very mean spirited. Her whole family has taken on the same persona as her mom; her dad busted his ass, but it seems that her mom was never happy with that and was always focused on appearances and putting her dad down. So that’s what she embraced. So I was an easy target. Fat, awkward, and crooked teeth. There was a scrawny boy, I think he may have been a year younger than me, also part of their little group, that my sister ended up punching because he lifted her skirt. It’s too bad she didn’t break his nose. And then the last regular in that group was another girl, who, again, was spiteful. She was good friends with the girl with the nasty mom and she seemed to thrive on the nastiness herself. (As a side note, I have become friends with some of these people on Facebook to see if anything has changed. It hasn’t.)

I’m just going to skip way ahead here, to the bullies online. First there’s the guys who have dating profiles on the various dating websites. After a few decades of doing online dating between being in relationships, I have decided to not use online dating anymore as a means to find connections, because it can be pretty brutal. In my 20s and into my 30s, there were times when I would take things that were said to me very personally. It was really tough to let stuff go. This was also the time when I was in the process of losing all of my hair, so I was really self-conscious of my appearance and didn’t really know how to initiate the conversation about looking like Mr. Clean to prospective dates (or guys that I had already been out with a bunch of times). But everything nasty that was said to me was excused by the guys as being in the interest of not wanting to waste time. They HAD to say it. They couldn’t wait. They couldn’t filter. I had to take it or they would move on. They had to be shitty. If I couldn’t handle it, then it was my problem and not theirs. How can you reason with that anyway?

Now of course we’re in the era of Facebook. We thought this would be a fad that lasted maybe 5 years, maybe a bit more. But they keep changing the algorithms so we stay hooked. I try to take breaks, but they usually only last 4 of my waking hours. Facebook is filled with all kinds of ills. I belong to some rare disease patient groups because I know it’s likely I will hear something I’m not aware of, and it’s also a good way for me to keep track of doctors and medications. I don’t often comment, though. I will see the same people posting – sometimes daily. I know that some people need to find any reason to connect. It drives me a little batty because sometimes they ask, “Has anyone tried ______?” and of course there was just a long discussion about it the day before. If I have something different and useful to say, I will add to the discussion.

Recently in one of the groups, a guy posted that he was taking hydroxychloroquine for our condition, the same as what “cures the virus.” That really upset me, because first of all, no one takes that medication for our condition. It’s the wrong medication. Second, that medication also does not treat COVID-19. So I posted that along with scientific journal articles, plus the CDC directive stating that that med should not be used because it has caused people to die. Suddenly 4 guys jumped on and said all kinds of personal things about me, including one who said he hoped I didn’t have children – as if that related to me correcting this misinformation that this guy put up in the first place. So a few days later he came back on and said he did indeed put the wrong medicine up, that he was actually given an antibiotic of a completely (not even close) name. No one apologized to me for being shitty to me. Then two days ago from today, a woman jumped on and was shitty to me, telling me I was off topic and I should apologize for that. I wrote back and told her that ignoring all of the other posts and focusing on me for correcting misinformation, misinformation that the original guy admitted he was responsible for, was shitty. Then she just wrote another line saying, “Well, it was off topic.” Yep, it sure was, initiated by the original guy. But I’m going to correct it with science every time if someone else is going to put the wrong info out there.

Just yesterday, I was in another patient group for another rare disease. It’s a little more difficult for me to describe everything that happened or is happening with my brain and cerebrospinal fluid in a short enough paragraph that will make sense. Part of that is conveying this understanding that my symptoms are unusual and disarming to the doctors, to say the least. A fellow patient basically called me a liar. My fuse is pretty short these days, so I tend to stomp and snort once as warning, and that’s all you get. After that I will cut a bitch. I explained how many doctors I had encountered (over 100 in 10 years) and being banned from the Mayo in writing, and added that Barrow had just told me to go to a “neighborhood neurologist” because they didn’t know who to send me to in their own organization. This other patient continued on her crusade to tell me that I didn’t know what I was talking about and there was no way I could guess that doctors hadn’t seen my symptoms before. So I told her congratulations on deciding to be a bully to a fellow patient. In fact, all of the doctors were stumped by my symptoms, their words.

Also not too long ago was the issue with my cousin who lives on the east coast. He told me to get off my lazy ass when I became disabled after the ten failed brain surgeries (but before the issues with my vertebrae and the bones in my hands starting to fuse together). I did mention this before, but I didn’t hesitate to tell him to eat a bag of dicks. He is a drunk bully, and I just kind of feel sorry for his wife and daughters.

I’m 46 years of age now. There’s certain things you stop caring about, I suppose, but I think my thing is bullies. I mean, really, I think I’ve experienced them all. My feelings just aren’t getting hurt anymore. After the most recent exchanges, I did a temperature check and I felt nothing. That parental bullying is gone. My cousin hasn’t ever really been in my life. Elementary school is long done. I haven’t ridden a school bus since 10th grade. I’m definitely not doing online dating anymore, I think I gave that the old college try and then some. And those patient groups…well, now I can just scroll past them. Sometimes I get random comments online because of articles that have been posted that I respond to. Those are usually the lowest of the low. I think I remember one lady telling me to “get that thing in the middle of your forehead fixed.” I still have no idea what she was trying to say. It seems no one else did either because she didn’t get any responses or reactions.

I think one of the truest tests was after an exchange with complete strangers in a comment section, a stranger sent me a message that said, “Have you been drinking? You must be lol” and I was thinking, wow, he came all the way over here just to say that. No imagination. He’s the laziest bully ever.

It’s Hard Out Here For A Crip

[This isn’t a plea for more help. I try to spread my requests out, because everyone has their own lives. I have actually had certain friends get mad at me because I asked for help more than once in a year. So in the spirit of friendship no, I don’t need anyone to get my groceries or prescriptions.]

Facebook is great until it’s not. Just hang with me as I explain this.

I’ve got so many medical conditions, allergies, prescriptions, over-the-counter medications and supplements that I have everything alphabetized on a sheet that I keep updating and printing every time I go to appointments. I can’t remember everything. I’ve got two injections that I give myself every week in my stomach and thighs, and it’s possible I’ll be getting a third. One of them really hurts and it takes a long time to push the syringe down; my hands cramp up and a few times I didn’t go long enough and have shot the solution all over myself when I pulled the needle out. (I hate wasting that precious medication.)

Nothing is simple with my healthcare. I just got done coordinating a treatment for hidradenitis suppurativa, which means I have to fly to Minnesota for two different lasers and get Pronox gas since Lidocaine doesn’t work on me topically. One of the issues we had to figure out was what to do about me breathing back OUT into the air – what if I was breathing out contaminated microbes and spreading COVID-19? So the office had to track down a device to add to the machine. It took me a week and a half to put everything together and find flights/hotel that I could afford that would also work with the office’s schedule.

At the same time, I was also scheduling surgery for some scarred areas with the hidradenitis suppurativa. Again, since I don’t get numb from Lidocaine, I have to be put under completely to get the spots removed. They are not going to be closed up but rather left open because of the nature of the condition; it’s better not to make a tunnel, that would just encourage the disease to start again in those spots. So now I have to also reschedule other doctor appointments because I will be uncomfortable for a couple of weeks, especially since I can’t take pain medications because of mast cell activation syndrome.

I met with a new cardiologist because I’ve been having major problems with pitting edema, despite being on a very high dose of spironolactone. He put me through a very thorough ECG and ultrasound of my heart and carotid artery, and wants me to have a tilt table test performed. I have a resting heart rate of 110+ now but a very normal blood pressure which sometimes dips low and have had the diagnosis of POTS since 2017 (but symptoms since 2000), but he wants to be sure that that is what I’m still dealing with. When it gets into the summer months here in Phoenix, it gets a lot harder for me to deal with the heat, and I get closer to blacking out frequently, even in my apartment with air conditioning.

I saw my OB/GYN because I still have cysts in my breasts. I get checked every six months. So far they haven’t changed in size, so I might be able to go once a year.

I was being lectured by my primary care doctor and rheumatologist about being on steroids long term for ankylosing spondylitis. I told them that going off for even a day is very impactful, but of course, they didn’t believe me, so I had to demonstrate it. I went off for 7 days and then went in to my rheumatologist’s nurse practitioner. She saw my hands twisted, red and inflamed to three times the size of what is normal, and also observed the spasms in my back that also severely affected my breathing. I’m allergic to all NSAIDs including ibuprofin and naproxen sodium because of mast cell activation syndrome, so I’m not able to take anything besides Tylenol at this point, which is absolutely unhelpful. After seeing for herself, she agreed to continue the steroids. (Side note: the cardiologist told me that I obviously gained weight on the steroids because I was eating more. Wrong. I eat about 1,000-1,2000 calories a day. Doctors love to shame women. One of my fellow patients was told to lose weight when she only weighed 95 pounds at 5’4″.)

I went back in to Barrow to follow up on an EEG. I had reacted to the strobe light even though it hadn’t been noted on the report and the tech saw it happening and kept asking if I was okay. I also have been having issues with my tongue and mouth going numb, and my left arm has been having spasms. I know that my brain has had changes that are different from the last two MRIs. This appointment was set up with a nurse practitioner because the neurologist I previously had left Barrow (yes!!! he was horrible), so we had never met. It seemed like she understood what I was explaining about my history. She left the room, came back, and said, “We’re really specific here, and no one knows what to do with you. Can you just go to a neighborhood neurologist? Maybe they will know what to do with you.” Seriously. When I go to a neurologist who is outside of a big organization like Barrow, they throw up their hands and say, “But I’m just a neighborhood neurologist!! What do you want from me?” The NP gave me two names as a suggestion, but since I saw a different doctor in the same office already, I can’t see anyone else.

My thyroid stopped working at optimal, which explains why I was feeling extra tired and achy, and looking even more like a defensive tackle. Whenever that happens my cholesterol also goes through the roof. So I had to adjust all those meds again.

I’m being monitored for clotting by an oncologist/hematologist, so I had to go in for more tests. Right now it looks like my factor IV and fibrinogen are high. The fibrinogen makes sense because of what has happened to all of my shunts.

I need to have a laser treatment on my gums and one of my molars pulled but that has to be put off indefinitely because of the current situation. These are complications in my mouth because of mast cell activation syndrome. I can’t ever get dental implants, also because of mast cell activation syndrome – I’m allergic to metal, cement and glue/bonding.

Throughout all of this, I’m also trying to coordinate all of my meds. Some are traditional meds that I can get through a place like Walgreen’s. However, I’ve encountered some shortages. So it’s been left up to me to follow up to try to figure out how to get them. One of my meds I couldn’t get for FOUR months. Some of my medications have to be compounded because they aren’t available in the form I need to take them on the regular market. For instance, one is available as an eye drop, but I need to be able to take it as a pill. But the prescribing doctor is in Minnesota, and I’m overdue to see him, and he can’t do a televisit because I’m not physically in MN. None of my other doctors will write the script. See how this shit gets complicated? Besides that, I also had to go through the approval process multiple times for the shots because I failed out of multiple medications. I talked, I faxed, I talked some more, I faxed some more, I scanned, I talked, I waited on hold, I faxed, I scanned, I faxed…you get the idea. Oh, and they also ran credit checks on me. That’s something new all of them are doing. They are saying it’s because they want to make sure I’m getting all the benefits I can get, but obviously that’s a big fat lie. I’m wondering who they are withholding medication from. Drug manufacturers have a lot of power.

That sums up everything I have been dealing with for the past couple of months.

I’m on Social Security Disability Income (SSDI), which means I worked before I became disabled. In fact, the judge that decided my case said I truly worked as much as I possibly could before I really couldn’t work anymore. I now fall into the category of having a very low income, but it’s not low enough to receive any additional help. I don’t get any assistance with housing/rent, food, utilities or transportation. Some people get discounts but I don’t. The last time I had this income was 1993.

With this income, I have to pay for my monthly medical premiums. The premiums alone add up to $438.20. One of the plans I have isn’t from the state I live in. The state of Arizona doesn’t believe that someone could exist who is below the age of 65 and receives income above poverty level, who is also disabled. That’s me. They don’t have any policies for anyone under 65 who isn’t poverty. The craziest thing happened, though. I was actually living in another state when my case was decided, and the state had one – only ONE – policy that I could buy that could travel to any of the other 49 states no matter where I lived. I just can’t miss a payment for the next 22 years, ever. If I do it could mean hundreds of thousands of dollars of extra costs for me because of all of my crazy health stuff. This dollar amount does not include the money I spend on prescriptions, OTC meds or supplements. The supplements are absolutely necessary because they help to treat mast cell activation syndrome.

I spend something in the neighborhood of $100-150 on transportation a month because of having to go to doctor appointments, labs, scans and to the pharmacy. For about a month and a half Medicare was allowing our medications to be delivered, but they stopped allowing that, so I have to go and get my meds now. We can’t do mailing here in AZ because the heat degrades medications. (There have been a few times when the ice packs have been barely cold on my shots that have been delivered to me.)

I am signed up on two different transportation programs for disability, and I’m supposed to wait outside and be visible to the drivers. This is fucking hell in AZ in the summer. My heart condition makes it so much harder for me to be up and out in the heat.

So let’s talk masks, and COVID-19.

I have 8 masks now, with vents. My very first mask a few years ago was a Vogmask. I started wearing it on flights because I wanted to avoid breathing in the shit everyone was passing around in the cabin, because I was sure to catch whatever they were dishing out. So far it’s worked. And let me tell you, those vents make all the difference. Right now I’m on a list for the backordered masks from England for the fanciest of fancy vented Cambridge masks; I’m in for 2.

I’m up on COVID-19. I’m comfortable with the science, been correcting misinformation. One of my drivers tried to tell me the 19 stood for it being the 19th version of the virus. Ha. Ha. Nope. I think the people who walk around saying their freedom is being taken away are complete assholes and deserve what they get. I think the people who say they will make themselves sick with bronchitis or other lung infections by wearing a mask are assholes.

So when I’m going around to all of these appointments, seeing my doctors, getting labs and scans done, I have my mask on. There have been a few times where there blackness has been closing in on me because transportation has insisted I be outside in 100+ heat, my wig is dripping hot, I’m gasping for air, and I have to pull the mask off because I can tell my pulse is through the roof and my BP is dropping.  It will happen at the grocery store too. I’ll be walking around and suddenly my body will just crash. I have to take the mask off for a few so I don’t end up on the floor. I do my best to stay masked up unless my body rebels. When the episode is done, the mask goes back on.

Last night, a friend posted on Facebook that if someone didn’t mask up, he was going to cut that person or people off (with an exception for some medical situations). I saw some people posting, including comments about how there was no way there should even be exceptions for medical. So I raised my hand and said hey wait a second, there has to be exceptions, and we still need to go out. And one guy lectured me about how I needed to have my groceries and prescriptions delivered and my doctor visits should be telemed. I told him to fuck off.

I don’t know this guy. He doesn’t know my shit. But groceries cost me at least $30 extra delivered because of the delivery fee and tip, and they NEVER get what I need and they never do substitutions when I ask for them, which would result in another run to the grocery store. Do I have tons of extra money to spend? Do I have $30, or $60, or $120 a month to throw away on delivery fees? Prescriptions were only allowed to be delivered by Medicare for a short amount of time. Now I have to go and get them again. As far as the doctor visits go, my shit is so complicated that I am required to go in. The docs don’t give me a choice.

This guy’s response was that he thought I would want to not spread the virus and be responsible, and if I didn’t wear a mask, I should just at least pull my shirt up over my mouth and nose. So I told him that I’m not a bottomless pit of wealth, and he’s telling someone who uses a cane and two arm braces and whose face is also partially paralyzed to walk and pull her shirt up. He then offered to “get my groceries” and I told him to stop talking. His response was “Damn.” A particularly dumb broad piped in about how rude I was to refuse his help by telling him to fuck off.

Being a disabled, middle-aged, single, adult female is a fucking challenge. There was that time when a complete stranger grabbed me by the arm and dragged me into an elevator because I was waiting for someone to turn around their power scooter and he assumed I couldn’t handle the elevator on my own. So here’s this guy on Facebook telling me that I have to pay for delivery and get only half of what I need, get my prescriptions delivered (even though Medicare doesn’t allow it) and just see my doctors on video (even though they won’t allow it). Yes, I’m going to tell him to fuck off. He offered to get my groceries AFTER I told him to fuck off. He wanted to feel better about being an asshole and making HUGE assumptions. I would never, ever, ever let someone near my groceries, my medications or my living space who would try to ridicule me like that and then try to strap on the hero cape. “No, really, I’m a good guy.” Don’t ever trust a guy who tells you he’s a good guy right after he does something shitty. And I’m still masking up.

 

 

Sayonara, Senor Shorty

Have you ever dated one of those people who blamed everyone else when something bad happened?

The last time we were naked together, all Senor Shorty (height: best guess is 5’1″, I’m 5’5.5″) did was complain about his first long-term girlfriend, and why he was justified in cheating on her. The son they had together is now 12 years old. I tried to steer him away from that topic, because 1. (and I said this): I didn’t want to talk about another woman while we were doing what we were doing, and 2. He has never taken responsibility for cheating. It’s a choice.

Senor Shorty was angry with her because she didn’t service him enough. She was staying at home to take care of their kid, who was born with cystic fibrosis and a host of developmental disabilities, and she also takes care of this guy’s mom, whose house they lived in (and she and the kid still live there). So this woman is taking care of a child and an elderly woman all day, every day. Senor Shorty gets home and demands that she make herself more available for sex. She doesn’t make it happen, and he starts screwing around on her. He also controls her money and transportation. Classic abusive move right there.

Besides being a shit to his ex, Senor Shorty also bullies his 12-year-old. Because the kid has sensory issues, he has a hard time standing and peeing. So I found out this guy has been calling him a mama’s boy and telling the ex she’s doing a bad job of raising him. But this guy lives in my state, and these two live in New York. He tells everyone else this kid is his mini version, but he’s a total dick to the kid and the ex. I can’t convince Senor Shorty to stop bullying his kid. He thinks that he’s a great dad because he says he is. Of course, his actions say otherwise.

He says he “fell in love” with another woman and he got her pregnant while he was still with girlfriend #1, which resulted in his second son. He definitely favors Kid #2, 5 years old, because the little one misses him terribly and tells him so. Kid #2 is also in New York, though far away from Kid #1. Senor Shorty has given him very expensive gifts to make up for his absence, which Kid #2 really doesn’t want any part of. He just wants his dad. Of course, Senor Shorty cheated on this woman too, and punished her by taking away her transportation and controlling her money. It’s a common theme.

So, this guy. Within a week and a half of agreeing to date exclusively, he cheated on me. He tried to blame me for being hurt, saying it was my imagination, and he never said anything about dating me. I’m just gonna leave this screen shot right here.
Cheating1

I swear like a truck driver on the regular anyway, but I tore him a new asshole.

After a while, because when he’s not lying or manipulating, we can get along decently well, we decided to try friendship. The lines got blurred a few times and we did have sex, but it wasn’t a regular thing – maybe two more times at most over the span of five months? Anyway, I told Senor Shorty that I would help him get his life on track, and it would be better for the next woman. I meant it too. And his life is better, when he does things the right way.

But it always drove me fucking nuts whenever I’d catch him in a lie (which was every day, big and small). Like when he insisted he didn’t watch TV. We were talking about his budget, and he has this very fancy laptop that he only knows how to turn on and off. He doesn’t even know what an address bar is. I was telling him he didn’t need to buy a TV for his little studio apartment, he could just watch his laptop, and after I explained everything he agreed. Trust me when I say that he didn’t even have enough money to buy toilet paper. A couple of months later he was complaining about the fact that he was still paying off a TV that he didn’t even have for a week. I asked him to repeat himself and then told him I didn’t understand. I realized that he had been lying and that he had in fact gotten a TV and he immediately broke it – but it wasn’t his fault!!!! Oh god, just wait. He had put up a little shelf over his head and the bed, and put a 55″ TV on the shelf, that he bought on installment payments. But he just put it the shelf in the drywall. He didn’t look for studs in the wall. Basically, the shelf just peeled off the wall like an orange peel. So it was the shelf’s fault, it was the TV’s fault, how was he supposed to know that there was a right way to put it up? Now he’s going to be paying those installments for forever, because he doesn’t have enough cash to pay off what he owes. 

This guy decided he needed to sell this brand new iPhone he had no business buying in the first place because he couldn’t afford it. He told me he was going to be paying off the bill. Of course, he didn’t. He texted me in a panic saying that he got a notice stating that the phone was going to be disconnected and the buyers were upset. So I was concerned. I said, “So you sold the phone, and you had no intention of paying off the phone?” He said he didn’t know the phone company was going to expect to be paid. It was their fault the phone was cut off. Now he had to hurry and figure something out. He was looking for sympathy, but I shut that shit down real quick.

This guy. Senor Shorty goes through jobs like candy. It’s always the employer’s fault. He was getting one new job a month, or so it seemed, all the way through 2019.  His jobs are based on road and highway travel, and he some has very specific skills. It’s their fault that he can’t stay on budget if they pay every other week instead of every week, though. Nevermind that it’s the same pay, and the taxes work out the same. He doesn’t know how to budget. He blows the money if it is in his account for too long. He has told me this is the first time in his life he has been in financial trouble, but I think that’s a lie too. He’s only a year older than me, so he’s been old enough to work for 28 years. He’s been fucking up his bills for decades.

The lying is exhausting. Whenever I caught him lying, he would tell me it was just his personality flaw and I had to be okay with it. 

Last week, I had enough. He was posting high school, feeling-bad-for-himself-shit. We’re smack in the middle of this virus and he’s whining and crying on Facebook about how lonely he is and he wants to “find a woman he can trust, who is beautiful, who will cook and clean for him and make him feel special.” First of all, no one should be dating right now. Second of all, no woman should be signing up to be his slave. He just wants someone to control. Boy, did that post ever put me over the edge. And why the fuck would he demand someone he can trust, when absolutely no one can trust him? He has cheated on every single woman he has dated for the last two decades.

My response was, “All a woman wants is a guy who won’t fuck around or expect her to be a sex slave, have no life, and perform like a porno star while he lays back like a lazy ass pillow princess.” Which, by the way, describes him nearly perfectly. The other parts I haven’t told you is that he’s the worst kisser ever (he just sticks his tongue out like a dead fish), he’s a premature ejaculator, he doesn’t know anything about female anatomy, and he’s very rough in a not-fun way (he tore the skin under my boobs, took about 10 days for me to heal). This relationship was not destined for long term anyway. I tried to get him to discuss with me what he enjoyed about sex, and he couldn’t say one word. Then he said that I clammed up and it was funny. Talk about gaslighting! He was unable to tell me one single thing he liked. The last time that happened, the guy ended up coming out as gay a short time later. 

I finally told him to clean up his shit and stop claiming to be a good guy while he was cheating on everyone he dated. I knew there were other women after me and he was screwing around on them too. One of his jerky friends piped up and said he should “run, because it was obvious [I] was bitter.” Not about him dating other women, believe me. I just want him to not keep doing this shit and then feeling sorry for himself, so that was my response. So that got me unfriended on Facebook. Boo hoo. Good luck to whomever is next. He loves to dump his shit on you and then say that you won’t ever get close to him – meaning he doesn’t want to hear about you or support you, he only wants to talk about himself. (Pro tip: at least you don’t have to do a marathon BJ session ever.) 

Also, he wants to get a penis implant to make his penis larger. He thinks it will make sex better for him. He doesn’t care if it will for whomever is having sex with him. I asked him if he thought it would change his sensation, and he said no, but he still wanted it. And if it isn’t happening to his penis, he isn’t interested. 

I definitely should have vetted him better before jumping into a relationship. That’s on me. Sometimes I am blinded by the promise of fun and adventure. I’ve changed from my 20’s, though, and don’t let things drag on for years.

Why I Won’t Do Internet Dating Anymore

I’m a veteran. I was in the trenches for 20 years, on and off. But I retired in 2016, when the last one turned out to be a binge alcoholic-hoarder-gambler.

My first exposure to the internet was when my father had his brother-in-law set it up at his house around 1991; back then it looked like a bunch of links to articles that talked about space exploration, and it took forever to connect. It was boring as fuck. But as we know, technology doubles every 18 months, so by 1996 I was set up with chat room names and “meeting people.” Then everyone figured out how to meet in person besides meeting virtually.

Then came the dating sites. Oh, Lavalife. You were my gateway to my Saturday night sugar daddy. (Don’t judge; I only let him buy me dinner. But he was so much fun.) Lavalife gave us the option to just look for friends, look for serious relationships, or look for casual hookups. We were all kind of winging it. Some people had very strict rules. If you were on the casual hookups, then no way did you have a chance in the serious relationships. I also met the sweetest man in Atlanta who used to write me actual literature, but because I had to stop traveling to his area because of work, it killed our relationship. The curse of the internet. I know I can’t survive long on long distance. I can barely survive someone living 15 or more miles away.

I went through the quizzes on eHarmony. The response I got was, “Only 3% of the population would be interested in dating you. It might take a while for us to find a match for you.” The internet will either make you or break you.

And then of course later came Match.com, OKCupid.com and PlentyofFish.com. To pay or not to pay, that was the question. Then very specific sites got in on the action, like dating farmers, dating millionaires, dating BBWs, dating amputees…

There was a guy that I met through OKCupid and very briefly dated in Minnesota who I seemed to have a lot in common with and we had fun when we were together…or so I thought. But then he started acting like a total loser. He couldn’t even talk to me like a human. He would just send me a message that said, “Anal?” Not even hello. Or, “Bukake?” Or, “Swallow?” No other words, no other conversation. It was like he was having an entire exchange in his head and he would just send the end of it to me and expect me to say yes. When I called him out on it, all he did was send me more single words, and then change his profile to say that he needed someone to “keep up with him.” Except that isn’t keeping up with him. That isn’t even interesting. What did he need me for? Just to finish his sentences? He’d do fine with one of those real dolls, created just for jizz. It won’t talk back. It certainly won’t tell him to take care of the nasty stripe of fungal infection running along his waist and balls.

And now instant gratification is the preferred experience. Or is it? Because fuck these guys. Reporting women so they are forever banned from Tinder because they aren’t interested? And no one can dispute being banned? Where is the option for “I turned down his laziness, so I call bullshit”?

Guys Are Reporting Women on Tinder for the Crime of Not Being Into Them

 

Are You Being Served?

in·ter·sec·tion·al·i·ty
ˌin(t)ərsekSHəˈnalədē/
noun
  1. the interconnected nature of social categorizations such as race, class, and gender as they apply to a given individual or group, regarded as creating overlapping and interdependent systems of discrimination or disadvantage.
    “through an awareness of intersectionality, we can better acknowledge and ground the differences among us”

    The state of Arizona doesn’t believe that I exist. I’m a woman with a bachelor’s degree, but I also have some rare diseases that have disabled me to the point that I am unable to work. I really had worked my ass off until I had my last shunt failure and surgery, when my neurosurgeon threw in the towel and gave up on me. The judge that I sat in front of for six minutes in March of this year noted in my paperwork that I had an exceptional work history. So my monthly pay is above the poverty level, because it’s based on the amount of take-home pay for the past 10-15 years (at the judge’s and state’s discrimination and calculation).

    Let me back up a little. I got my official judgement saying I’m disabled. Yay. Then my attorney told me that I might have to wait a number of months to see any money. But on May 24th, I got a call from the federal office saying that my money would be released on May 27th. I asked how it would be paid. They said it would be sent how I asked it to be sent. I asked how that was possible, since I hadn’t specified. They said, oh, it looks like we have info from Arizona. (Instant panic, since I haven’t lived there for 3 years.) I said no, absolutely not, I have all of my info updated for Minnesota, there’s no reason for it to be sent to Arizona. They said too bad, if you want it sent to Minnesota, you have to go to your local Minnesota office.

    So I did, on the morning of Friday, May 25th. I was a little worried because it was right before the holiday weekend. Luckily it wasn’t a long wait. But I found out that the money was already sent to Arizona – they didn’t wait until May 27th. It was sent on May 22nd. My former bank in Arizona reopened my account, accepted this rather large amount of money, and just sat on it. They didn’t tell me, and didn’t send the money back. For days. I was able to work it out so they could send the money to my current bank so it wasn’t lost. Anyway…

    So, while at the Social Security office making sure they didn’t send anything else to Arizona, I mentioned Medicare. The man helping me said, oh, didn’t you know, you’ve had it since January of this year? Another panic. I knew just from reading some info and talking to others that meant that I had a deadline coming up in just a few days. I had to sign up for a supplemental insurance policy and medication policy or I could lose out on tens of thousands of dollars. And Monday was a holiday. That meant that I had Tuesday, Wednesday and Thursday to make phone calls and sign up.

    This is no small task. I take 19 prescription medications, one of which is a weekly injection. The doctor that prescribes that had actually been working on getting an exception because my condition has been worsening. I reached out to the Minnesota SHIP office to talk about supplemental plans and medication plans. We found a supplemental plan that costs hundreds a month but could possibly transfer if I moved out of state. For the meds, I plugged in all of the names and we found out the injectable is not covered. It costs $37,000. Welcome to the world of rare diseases! So I had to call the manufacturer and talk to them about a patient assistance program, which might also allow me to get on a higher dose.

    So now back to Arizona. When I talked to their local office that helps seniors find supplemental plans for Medicare, they couldn’t believe that a disabled person under 65 had a disability check that was above poverty level. It isn’t a huge amount, mind you, but it doesn’t meet the standards for poverty. So I can’t qualify for medical assistance as my supplement, which is their only option in Arizona. I also can’t qualify for utilities assistance, transportation assistance or food assistance. The woman on the phone had very little experience but offered to find out more info and call me back. When she did, she told me to buy the policy in Minnesota and take it with me, as there was no hope for me in Arizona. 

    So Wednesday afternoon, I purchased the supplemental plan for Medicare and verified it could come with me (in writing) if I moved out of state. It’s possible it’s going to become much more expensive, but not nearly as expensive as having nothing.

    Thursday I finished sifting through all of the medication plans and tried to pick the best one. It was the least restrictive with the medications that I currently take (most of them wanted to restrict my Singulair, for some reason, of which I need double the normal dose). So I managed to get everything signed up before my June 1st deadline.

    However, while all of this is going on, there’s something else that’s been cooking in the month of May.

    Actually, this started in March. I had a crown fall off. A bunch of decay was discovered – first on that tooth with the crown, then the tooth next to it, then two teeth above it, then a bunch of cavities all over my mouth and it’s painful to eat or drink. I actually had to file a complaint against my dentist that I was seeing for about 2.5 years because he was physically abusive. When he was examining or treating me, he would pull my mouth roughly – so much so that the last time he left bloody fingerprints all over my exam napkin, and I had a swollen face for five days after. It was only after my massage therapist asked me who had been abusive with me that I filed the complaint.

    The complaint was supposed to have been anonymous, according to my insurance. However, they revealed all of my info, and the dentist counter-complained (like I was the asshole, because I was the one sitting in the chair with my mouth open). Then my insurance told me to go to two other dentists, which I did, and then they told me to go to my original dentist, and he refused (DUH), all to get this decay and a root canal taken care of. The two new dentists told me that they wanted me to go fully under and to be in an oral surgeon’s office or hospital because of my anaphylaxis history as well as my inability to numb with Novocaine. They referred me either to the U of MN or to Hennepin County Medical Center (HCMC).

    I called the U of MN for five days straight, and got different answers each day. They would say they didn’t do sedation, or didn’t take care of complicated patients like me, or were too booked. In the end, I got nowhere. So I turned my attention to HCMC, which happens to be a trauma 1 hospital. They told me they weren’t taking new patients (a huge lie). Then they told me to get a note from my doctor specifying which medications I’m taking – but that was only after they refused to answer my messages for 3 weeks. They wanted to see if my medical assistance would run out before they had to do anything.

    Well, ta da! First day of no medical assistance, June 1st! That means I get absolutely no dental coverage. So even though they have been aware of this issue for a few months and I’ve done everything they told me to do, I got zero help. By the way, it’s likely I’m having the trouble with the decay in my mouth because the abusive dentist put metal back in my mouth even though I told him in writing and verbally many times I’m allergic. I found out after the two other dentists examined me that he put metal-based crowns in my mouth after I paid thousands to remove all the metal in my mouth because of my allergies.

    I’ve already talked to my dental office that I used to go to in Chandler, Arizona for 11 years, and they have an in-house plan. For $100 a year I can have my cleanings, checkups and x-rays, and then 20% off of fillings and other stuff. So that’s the route I’m going to have to take. Plus I like them and I know they’re not going to rip me up and make me bleed on purpose.

    If there was ever a time that I have felt the impact of being poor and being female and being ignored completely, this is certainly one of those times. I’m sure I’ll have many more opportunities.

Exhaling

April 10, 2015, was the last day I commuted home from a paying job. It was the last day I was on a dreaded conference call with a bunch of frustrated staff members. It was a Friday, and only three weeks into a contracting job after being laid off from a place where I had worked for over twelve years. I was already nervous about surviving because work had been interrupted by so many shunt surgeries prior to that time, but April 10th was the final straw.

I remember driving home during rush hour and having the familiar “lights out” sensation cloud my vision. I was only working about 8 miles from home, but since it was rush hour, it would take at least 45 minutes, and the darkness squeezed in almost right after I got behind the wheel. It took all my energy to focus on my lane and not crash into anyone else. I don’t even remember how I made it to the hospital after that, which was another 7 miles in the opposite direction. But I remember having to call my boss the next day to tell him that I would never be coming back in; they wouldn’t hold a short contract position indefinitely.

I wasn’t even sure my neurosurgeon would do surgery #10 in less than 4 years at that point. He had already said after #9 back in November that if I failed again, he was not willing to operate. But he did – sort of. He only did half of the surgery. And of course it failed. And then he sent me away, telling me I had to figure out what was the source of the problem, because he wasn’t going to continue doing something that was going to keep failing. It was all being put on me.

I did figure it out. It took me from 2010 to 2017 and 65 doctors to put all of the pieces together, not to mention the fact that I am one person, not even an entire lab or radiology department. I got zero support from the NIH’s Undiagnosed Diseases Network. The Minnesota Board of Health decided not to discipline 3 doctors (among many) who falsified information to get out of treating me. The Mayo Clinic banned me so I wouldn’t hurt their success statistics and change their #1 in the nation status in 21+ areas.

I lost everything: my car, my house, my ability to earn a livable wage, my confidence, my sense of security and self-worth, friendships, independence, and every last penny of my financial reserves. Thank goodness I already lost my hair over 15 years ago because if I had to go through that right now I’d absolutely lose my shit.

After filing three years ago, I finally had my disability hearing on Wednesday the 28th of March. I didn’t know what to expect. My attorney pulled me into a small conference room prior to the hearing and prepped me, telling me that if the judge asked me questions, to not take longer than 15-20 seconds to answer, and to speak up because he was older and may be hard of hearing. I was also told it may go as long as an hour.

But five minutes, and we were done. Long enough to read my name, and say that it was obvious I was disabled and not making anything up. The letters I asked Dr. Afrin and my current immunologist write for me were key for my case and noted in the judgment. The judge also specifically said that the way I was treated by the majority of the 65 doctors was appalling.

What’s next? I have to wait for Social Security to process the judge’s ruling, and then enter my info for payment, and like the Kool-Aid man, all you’ll see is my silhouette – I’m busting outta here. I gave Minnesota a fair shake for three years, but the fact that so many doctors lied in my medical records and refused to treat me has made my decision an easy one. I’ve decided to head back to Arizona where I will pick up again with 8 of the doctors I previously had; only a few will be switched out, including getting in with a neurologist who specializes in MCAS and Ehlers-Danlos. (Minnesota is a great place to be employed as a nurse, because they are paid relatively well, but it’s a horrible place to be a patient, and I’m far from being the only person who feels this way.)

I want to be clear about what this disability status means for me: 1) It doesn’t change any day-to-day abilities that I have. I still have to lay down and rest for the majority of my day, about 20 hours every day. 2) The actual status of disability is not permanent; I’ll be reviewed and my medical records will be combed through every few years by Social Security to make sure my health and abilities haven’t changed. 3) I still have to take the short bus everywhere, especially now since I’ll be making “too much” to get medical assistance (which is more than $0.00). 4) I still can’t get a motorized scooter – do you really want a half-blind person driving one of those??

My prediction is that this is all going to go down by the end of May, but I’m at the mercy of Social Security.

The Great Debate

When I was 14, I was visiting my dad’s house for the weekend and sleeping on the couch, which was the normal – I didn’t have a bedroom there. I’m a light sleeper. So it was a surprise that somehow between 12:30 a.m., when I fell asleep, and 7:00 a.m., when my stepmom answered a phone call from a stranger alerting her to the fact that her purse was scattered on the stranger’s front lawn, that the house had been robbed – and the burglar had somehow gotten past me. Three hunting rifles had been taken off of the wall along with a video camera and tripod, and of course, the purse.

The next night my dad took my place on the couch with his handgun in case anyone decided to come back. We used all of my babysitting cash to re-key the locks. But this story demonstrates many points: I grew up around guns (that were never locked up), the hunting rifles made it somewhere into the wide world to be used for who knows what, and that we are a violent society. The cops were surprised I was still alive and unharmed.

Not many years later, when my brother was five and a half, he was given his first gun for Christmas. His first few minutes alone with it and he shot out his bedroom light. I was never given a gun because I was a girl. Mind you, I never felt as if I missed out. But my dad and my brother perpetuated craving violence and guns. Even though I was the one who was on the couch, exposed, they were the ones who wanted to kill, kill, kill. At least, that’s what they projected.

My dad’s own father died of a self-inflicted gunshot wound. In fact, Dad was the one who found him. Included in the three rifles that were stolen was the one that Grandpa used to do the deed. It had a strange sort of sentimental value that I couldn’t relate to. Who would want to cradle that weapon, and use it over and over, knowing its history?

Fast forward a few decades to when I lived with violent men. One was the guy who grew up in Manhattan in a household whose own siblings stabbed each other. The last day I saw him was the last time I called the cops on him, when he was supposed to be gone at work while I moved my things out of the house we were renting. Instead he was hiding in one of the back rooms and came out when I set down some moving boxes and attacked me. I struggled to get back out to my car in my stocking feet and he was restraining me and pinning my arms, telling me that if I would just do what he told me to do, we would be happy. I finally wrestled free and got in my car and called 911. The responding police officers bought his big-eyed innocent act and told me that if I called them again that I would be arrested.

Then there was the live-in boyfriend who threatened to shoot me – twice. He also talked about taking his guns to work to shoot all of his co-workers constantly. The cops reassured me there was absolutely nothing I could do until he actually followed through and hurt one or all of us. 

Most recently of course was my downstairs neighbor who moved out the last weekend of July, 2017. He used to beat his wife and abuse their cat. Whenever I had visitors I was a nervous wreck, because I had no idea if he would pound down the door while they were here, falsely claiming that we were too loud, or take it out on me later, screaming and raging and dreaming up reasons to call the cops on me. Worse yet he could of course physically pulverize his wife and cat for revenge, just for existing. He was ex-military so I knew it was likely there was a gun or two or seven in his apartment.

So here we are in the U.S. with our easy access to the worst kinds of weapons and ammunition. I am the one who was laying on a couch while a stranger or two crept past me to rob our house; you would think I would fall into the category of wanting a gun for home protection. I grew up around them; you would think I would relax around them. I’ve lived with and around plenty of assholes who have wanted me dead; you would think that I would feel safer armed.

Fuck that.

First of all, we have over 7 billion people on the planet. We are no longer hunting strictly for food supply. Anyone who claims that is an outright liar. And hunting season is so abbreviated that there’s no need to keep guns out for the entire year to make them accessible to every man, woman and child on the planet. Second, home invasions do not happen with the regularity that the NRA has somehow convinced the gun lovers they do. I remember reading from one guy a quote last week that Texas experiences 800,000 home invasions a year. My answer was, “Are you talking about bugs?” I mean, c’mon. If that were true, Texas would be experiencing a mass exodus.

The biggest and hottest debate that has resurfaced is the arming of school staff. I cannot stress this enough, but there are so, SO many reasons why this is a bad idea. Right now I live in the city where Philando Castille was shot. He had a permit to carry a concealed weapon and told the cops, and was shot and killed anyway. If for some reason some idiots decided arming school staff members would be a good idea, the staff members had better be lily white, because we Americans cannot be trusted to be color blind. Even black cops have proven to have prejudice against black suspects without meaning to.

I posted this article on Facebook regarding an armed officer who never engaged in the shootout that was happening in Florida. He simply hung back while all of those kids were getting shot. I pointed out that if an officer did this, why would we expect teachers to uniformly charge without fear or hesitation, and to act correctly? A friend of 27 years, whom I considered a decently good friend, didn’t like that I used this as an example of why we shouldn’t arm teachers and staff. He also didn’t like that I proposed that we have stricter gun laws regarding background checks, wait times, amount of ammunition sold, amount of ammunition guns could fire, types of guns that could be sold on the market, and age of buyers/operators. He resorted to calling me an idiot. Finally, he just outright blocked me. 

But am I an idiot? I’ve just been trying to stay alive. I have all of this violence swirling around me, and all of these men are insisting that they have a right to violate me. I’m saying no. I will continue to say no. I’m good with saying no.

Lastly, here is a comprehensive list from a woman named Karen Nichols in Ottawa Center, Michigan; she had many questions regarding arming teachers and staff, and did a great job of articulating them:

Which teachers get guns?
Where will the guns be stored?
Who decides when guns can be brandished?
What penalties will apply if teachers mishandle a weapon?
Will teachers volunteer for gun duty?
Can teachers refuse it?
Who will audit their adherence to regulations?
Will students know which teachers have weapons?
Who will be liable if the teacher with the gun becomes the shooter?
What will be the consequences when students are accidentally shot by a teacher?
How will armed teachers communicate in a tactical situation?
Will teachers with a history of mental illness be allowed to use weapons?
Will teachers be required to disclose any history of mental illness?
Will teachers be issued a weapon? Reimbursed for purchase? For ammunition?
How will administrators conduct non-weapon-related discipline against a teacher?
Will there be armed assistance available to deter workplace shootings?
Who will shepherd the armed teacher’s classroom while the teacher is attempting to locate the active shooter?
What happens when a teacher misidentifies a student as a threat in good faith?
Will teachers who do not carry lethal weapons be offered non lethal alternatives?
If an armed teacher is shot, can another teacher employ his or her weapon?
How will armed teachers identify themselves to arriving first responders?
Will armed teachers be required to learn how to give first-response medicine?
Will armed teachers be required to attempt an arrest before using lethal force? Under what circumstances?
Will proficiency training on weapons count for teachers’ continuing education and professional development?
How will insurers adjust health and other rates to account for the presence of armed employees?
Will teachers receive additional pay for being armed?
how often will armed teachers be re-evaluated for licensing purposes?
Will armed teachers leading field trips deposit their weapons in a personally owned vehicle or school-owned transport?
Will one teacher per wing of a school building receive weapons? Two? Three?
Exactly which standards will count for proficiency—greater than a big-city police department, State Police, FBI, hobbyist, marksman?
In training scenarios, how will using force against innocents be penalized?
Will racial sensitivity courses be required?
Do parents have a right to refuse to send their kids to schools with guns?
Will students have to sign waivers? Will parents? What if a parent signs a waiver for a minor student who, when that student turns 18, refuses to abide by its provisions?
Will teachers on probation be allowed to carry weapons?
What about teachers with active union grievances? Complaints about sexual harassment? Anger management? Divorce proceedings?
Will armed teachers wear holsters?
Will they be stationed strategically during pep rallies or other gatherings?
Will they participate in lockdown drills as if they were armed or unarmed?
Will funding for the policies outlined above be distributed according to local budgets, statewide formulas, or national formulas?
Will schools in high-risk neighborhoods receive more or less funding? Suburban schools?
What is the right ratio of armed:unarmed teachers by grade level?
What is the procedure for debriefing and assessing armed teachers’ performance during a crisis?
Can an armed teacher who flinches be fired? Can an armed teacher who breaks protocol be rewarded?
Will preschool teachers have guns?
Will teachers in “juvie” (high risk) schools have guns?
Will the teacher or the school be liable if their gun is stolen?
Can administrators carry weapons? Can they do so in disciplinary situations?

Think about this: I quit playing clarinet after 8th grade because my band teacher was an outright asshole. After I quit, he was fired for punching a student. But let’s give him a gun, right?

Unhooked Generation – The Book

Originally published in my MySpace Blog, 2/10/2008.

Unhooked Generation by Jillian Straus

The woman that wrote the book was not a clinical psychologist; she was only a woman in her 30’s wondering why it seemed so much more difficult for people in our generation to find lasting love.  She traveled to different locations around the U.S. to interview random people that responded to her ads posted in free newspapers and Craigslist.  Some points really hit home for me.

1.  Do you make a list?  I know a man who has listed 42 qualities his future partner must have.  I even have a list myself, though it doesn’t go up to 42:  must pay his own bills and not try to steal my money; must bathe at least daily; must brush teeth 1+ times a day; must be nice to me.  Some standards are reasonable, I think, and some absolutely no one can live up to.  I don’t even think I can list 42 qualities about myself, so how do I know if I fit that manifest my friend created?  Oh, and once you have your grocery list made, then you can go shopping on eHarmony or Match or Plenty of Fish to make your selection.  Like a piece of meat.  What ends up happening is that we reject everything, which leads to….

2.  Why suffer?  If I don’t like something, or if it isn’t working for me, why not just cut it off and be done with it instead of beating myself up trying to make it work?  Relationships ARE work.  Or at least they require effort.  Expecting for things to just fall into place is unrealistic, and bailing is the easy way out.  I have absolutely been quick to jump ship but can honestly say that I’ve never regretted doing so.  I just don’t put up with any juvenile bullshit anymore.  Of course, the “why suffer” mentality is one of the main reasons that couples get divorced; think about it:  how many marriages do you know about that have lasted for less than a year?  I can think of 7 of my friends right at this moment.  Is it that they’re picking the wrong partners, or just giving up too easily?

3.   Fear of making the wrong choice:  let’s talk about the guy with the 42 requirements again.  He repeatedly says that he never wants to commit, because what if the next person that comes along is a better match for him?  He’ll never, ever be happy, I guarantee you that.

4.  Never allowing yourself to connect because you are afraid to fail at marriage.  Wow, this is a big one – I have always said that if I’m crazy enough to get married, it will be only once.  Half of the interviewees said they were afraid of failing by not living up to the seemingly seamless relationship their parents have, or failing by turning out just like their divorced parents.  I’m afraid of the second one myself.  No one goes into a relationship thinking that it’s going to fail, but it’s another thing to think that you’re not even going to allow someone to get close so there is no opportunity to fail.

5.  Losing our gender identities.  Yes, women’s lib was a blessing, I will bang the drum about that one all day long.  It’s what allows me to be a single woman in my 30’s [now 40’s] with a career and the ability to stand on my own.  But……..I could really use a mate who knows how to work on cars.  And by the way, can he also like going to art museums, and cry at mushy movies too?  But I don’t want him to open the freaking door for me, I have two arms and two legs and can manage on my own.  But can he still pay for dinner, because he’s the man?  I can say that I want a really strong, stoic man who can build a house but still tear up over “Love, Actually”, but how realistic is that?  It’s a bunch of mixed messages that lead to misunderstanding because one person gets pissed off that the other one didn’t pick up the check.  It is every man for himself, I tell ya – because there are no boundaries on the gender roles anymore.  Better brush up on your communication skills.

6.  Technology.  How easy is it to erase someone from your cell phone, and therefore your life?  How easy is it to send e-mails and instant messages, but never talk on the phone or see each other face to face?  We’re definitely disconnected and our spelling skills are becoming atrocious – because we are lazy.  And scared.

This is one of the few relationship/self-help books that I’ve read from cover to cover – usually I get bored pretty easily or can’t relate to what the message is.  This one is fascinating because I have so many single friends, just like me, wondering what in the hell is going on.  If you recognize any of these factors within yourself, this may be an interesting read for you too.
[Disclaimer: Since it’s now 10 years old, some references are going to be outdated, but the ideas are still relevant.]

 

Invading MySpace

Remember MySpace? I kept a blog up there too. In fact, I also dated some men through MySpace. The following is a story about one of those men, and knowing what I know now, he has exactly what I have: mast cell activation syndrome. I have thought about him often only because I wonder if he has actually been able to find the correct and comprehensive medical care. But hands down, he is a fucking lunatic. There is no way I could be around him for even five minutes ever again.
* * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * *

I debated about posting these, but the whole incident is classically surreal, like when the main character in “Swingers” calls a girl named Nicki that he just met at a club that night.

I went out with this guy for one date in November of 2005, where we met up at a bar and he was too cheap to even buy me a drink after he asked me what I was having (the woman sitting next to me was so pissed, SHE bought me a drink).  Afterwards I drove him to his apartment because he had taken a cab, and we ended up working on some of his original music together. While we were there, he got into a screaming match over the phone with his mother, and they were calling back and forth and hanging up on each other, and he was stomping and slamming doors.  Some other background:  he own(ed) his own business that manufactures DVDs and CDs.  He also has horrendous food allergies where if he deviates from eating six specific foods he can go into anaphylaxis, much like most of us with this disease.

We talked on the phone the Monday after that date, and I timed him talking non-stop about himself for 20 minutes.  He repeatedly said that he wanted to have children, so after the sixth time of hearing that I stated that I probably wasn’t the person to do that for him and tried to explain why (this was before I had my hysterectomy). He blew up.  He went on for another 10 minutes solid and accused me of criticizing him.  I told him I was getting frustrated because he wouldn’t let me finish my sentences, then he said I was being hurtful because I was accusing him of being rude, and he was completely insulted.  Anyway, after he hung up on me, I found this string of e-mails sent overnight.  I have blanked out his name for semi-privacy and included the times for your reading pleasure (all of his typing mistakes were left in):

11:58 pm:
Chelsea!

You know, you opened up the other night, and I was very, very, kind about it. I opened up tonight to you and you were VERY tough. Very not fair.

The items I discussed are not definite ever. But you had pre-ideas and canned my personally as to what I felt about you the other day and what you disapproved of me tonight. I had the HIGHEST FEELINGS, THEN TONIGHT YOU CAN MY FEELINGS. Hope your happy. If you want to call, go ahead. I don’t care if we are exact or not, but the words were very harsh.

12:09 am:
Chelsea,

I am only willing to love. Email never does justice. We just hit it off, something was up the other night, just want the one I met that night. Sincerely,
P

3:04 am:
[blank]

3:08 am:
I thought your were happy I was in to you. So there are differences, I was very insulted because you refused them last night. I can’t believe you would immediately be that way. We had a nice night the other day. You told me you had a great time. Something I’m missing?
P

3:20 am:
Not fair.

The decrisption of the “PERFECT” man was wrong. If that is exactyly what you want, you tell me, and tell me upfront and all! NO ONE EVER CUTS ME DOWN

I told you about the possibilitiles, and how I actually can handle the differences. But I still can handle the differences. And let my partner know.

3:23 am:
Not fair.

The decrisption of the “PERFECT” man was wrong. If that is exactyly what you want, you tell me, and tell me upfront and all! NO ONE EVER CUTS ME DOWN because I have the ability to raise a kid. Anyone who does cuts them self down. I just want to know who can.

I told you about the possibilitiles, and how I actually can handle the differences. But I still can handle the differences. And let my partner know. Kids are tough, but not 100fficial in a new relationship. But anyone who cuts me down about that…I can be the best dad.

I just only wanted to meet and go out. With no big deal.

Sincerely.

P

3:50 am:
Chealseal

OK. here it goes. I really like talking and hanigng with you. I almost died this weekend. I’m sorry.
I lost almost 10 pounds. I;m not having fun. I am just doing what I can. It is too much too handle by myself. I really like you, you just caught me in a time where I may or maynot have much time. PLEASE FORGIVE.

3:55 am:
Chelsea,

Please hang on. I did not mean to hang up.

It is hard to be myself with what is going on.

LOL…I’d really like a pizza! Can’t have it though.

All the things on the phone, just take them as friendly. You are great. Just know that.

Sincerely,

4:00 am (titled “RUDE”):
yes,, me,

I really hope you call me. I am not very happy with my self. It is hard, just please forgive and talk with me again. Sincerly,

P

5:22 am:
Chelsea.

I was about to Bankrutcy the business. I am not mysellf. You know, you are beautiful. I have words on the phone, and email. But they are just my venting that I might/might not loose everything I worked for. I am not my self at the moment. I apologize completely. I have a funny habbit of calling my friends in the middle of the night if I drink a bit. You caught me in a time of my life where everything is on the line.

I am totally sorry for anything I said wrong. I am really stressed. And, maybe wrong. I am sorry. I had the best time talking with you. You just met a guy who is “got it together” on the outside, but not on the inside.

I have done my best, but, I have now to realize the way it is.

Sincerely,

P

PS – anything I said in a voicemail is just me venting. I hope to hear from you, venting or what.

5:32 am:
Chelsea,

I had a rough night, obviously. But, just so you know, and whether you contact me again or not, you are very pretty. Your eyes and your smile are the best thing.

I had a really bad weekend. My food allergy thing is lethal. No one understands. My mom, well, she took about 5 phone calls to calm down and realize, and help me find a potential solution.

I am not myself. I just want to run the bus and play guitar/sing, and even sing with you.

I may have blown it. My bad. Then it is my fault and I must deal with it. I have these stupid health things that make me not myself. But if i was out of line, I apologize. Very sorry. Most Sincerely, and just not myself tonight, P

This was posted after I went to work, 9:05 am:
Chelsea,

Hi. In summary, I went overboard last night.

When I asked you if you were real, I was meaning a real person. I have been screwed over the last few times I met someone.

You are not only real, but again, have the prettiest eyes and smile. The first thing I noticed. So, anyway, I had one too many last night, and will NOT DO THAT again. I was very emotional and you just happened to be there.

So, I really like you. And everything you said was fine. I really enjoy looking at you the way you are. And/or the way I don’t yet know, but either way, you are good with me. Your eyes and smile are fantastic.

P. has some inside issues obviously of stress, probably from the business. They come out once in a while. I just need someone to slap me in the face if they come out again. Because I do not want them around. I just want me and….well…you….at least when I’m talking with you.

So, please forgive, I am just a human. I take things too personally sometimes, but understand.

So call me please. Anything wrong I did I apologize, I just had a bad night after being very sick for three straight days. I lost 6 pounds since you saw me. That bad. I was in a lot of pain.

But anyway, I am here. Most very sincerely,

P.

After much time and consideration, this is how I replied:
P,
I remember trying to explain the reasons why I have decided not to bear or raise children, and during the first point (of three) I was attempting to make, you interrupted me to talk about you again.  I remember thinking “What in the world do his allergic reactions have to do with MY ability to bear and birth children???”, but I let you continue talking.  Then somehow you turned it into me criticizing you for wanting to be a daddy, when no words of criticism or judgment (and in fact no words at all) came out of my mouth.  Then you got pissed because I said I was getting frustrated about not being able to finish my sentences.  You ended the call by talking for another 10 minutes non-stop and then saying “Maybe we’ll talk again, have a nice life, talk to you soon” and proceeded to hang up on me.

To top it all off, when I wake up this morning and check my e-mails, I have ELEVEN messages from you that are barely coherent and alternatingly rude, apologetic and complementary.

If ever there was a time that you needed someone special in your life, it is now.  However:  no matter how sick you are, no matter how drunk you are and no matter how stressed you are, if you treat me like crap, I’m not going to stick around.  I don’t let anyone else treat me this way, and I’m not going to start with you.

I have a hell of a lot more to say, but let’s just leave it at agreeing not to contact each other again.

I Know You Don’t Mean It

After I told the Go Stand In The Corner guy that I didn’t want to be his fantasy chat friend on Fet, he still tried to draw me in with more messages. So in the vein of Lin-Manuel, no means no means no means no means no…….well, anyway.

[Break for making arrangements to get the compounded medication to control my hives. I have to try one week of pills to see if I’m going to be allergic to the vegetable-based capsule they use for the powder. Total for 14 pills: $38. Not covered by Medicaid.]

Then I get another gem in my FetLife inbox, completely out of the blue, from a guy I’ve never had any contact with before in a town that is about an hour and a half south of Minneapolis:

Hey there beautiful. I just thought I would send you a text and tell you that you’re one great looking woman. In my eyes bald women are beautiful as I am bald myself. I know you say that you have health problems right now but I still wish that we could talk and hopefully meet as I will come to you as long as you let me. You seem like the type of woman that knows what she wants and I’m the type of guy that also knows what I want and that is you. I’m a gentleman that works too much but also enjoys beautiful women As You Are. I’m serious about meeting you as I would like to meet you now today tomorrow Sunday soon as possible as I don’t want no one else to steal you away from me. Give me a shout out if you’re interested in talking and we can go from there.

So, this is what my profile says:

I relocated from Phoenix back to my home state to be closer to family so they can take care of me during a serious health crisis. Feel free to message me but be aware that I cannot do any socializing of any variety right now. Respect my boundaries.

Now, is there anything in there that says, “Except you, guy. You know absolutely nothing about me including whether I even drink coffee but you know you’re going to make me happy for the rest of my life because you want to do dirty things to my bald head.”????