Warrior. 

while speaking to one of my close friends, I took a look back at my condition.
I always hear how strong I can be, how amazing it is that I let nothing get in my way, how I never stop living my life to the fullest. It’s great to hear don’t get me wrong but just with those statements bring me back to the main reasonings why I have to be so strong, why nothing can get in my way, why I have to be insanely obsessed with what brings me peace and also how selfish with my own time I have to be. I will be completely honest, any day I can wake up sicker and back in the hospital, any day this sickness can turn into my worst enemy and become something that can be worse for my body. I always have to keep that in mind and no one wants to wake up feeling like they are a burden on themselves or anyone else. What I have noticed over time is that my parents take the worst of my burden. When your child is born, you just want them to be healthy and grow up healthy. My parents ended up with a sick child. Endless doctors’ visits, endless hospital visits, medication that you cannot even pronounce half of the damn time, needles, surgeries and whatever else you can name. I cannot even explain how much both of my parents have gone through just with me being sick. I admire them so much and nothing would ever change that in my mind. From long nights in the hospital to unexpected calls begging to go to the hospital, my parents always put me first. But it can take a toll on them, it can be overwhelming. When you’re sick, you don’t just worry about yourself but you also worry about everyone around you and how they accept it. Some accept it perfectly and some think you’re lying half of the time when you have to cancel plans or when you have no energy to even get out of bed. Those are the kinds of people I hate, no I’m not lying but then again I have nothing to prove to those people because they don’t know how I’m feeling on the inside and they don’t carry this burden with them. Even as I sit here writing this, I look back on every trial and tribulation I’ve had to go through at such a young age and it is exhausting. Some days I have breakdowns in which I wish my life was never like this and other days I feel like a warrior princess who can take on any battle if I can handle it. Living with any disease is like being on a roller coaster ride with a blindfold on half of the time. You never know what’s coming and you don’t know whether you’ll go up or drop down. I applaud people with chronical illnesses, with diseases, with any little tricky thing going on in their body because all of us are stronger then we could ever imagine being. 

 

With Strength & Concentration,

N. Rarity
*image does not belong to me. Found on geniusquote.org*

New & Exciting!

I know it’s been way too long and I apologize! I finally started my new job and I’m slowly getting used to it! I love it here and even though it’s only my third day I am obsessed :). I would go into more detail but there’s never a need for more detail regarding my job and what I do. I’m just in a better environment ❤️😁🙌🏼 . This is a short post, nothing long because life is currently hectic and I have so much that I want to do that there is not enough hours in the day! 😂 But don’t worry! More and new exciting things will come! 
Anywho,

I thought this week I’d be even more vulnerable *yikes* and put up one of my old poems. Yes, I write but I NEVER EVER show anyone because I’m too scared. I hope you guys enjoy and definitely leave me feedback 😊

Depression

Depression: feelings of severe despondency and dejection. 

Depression is an extremely sensitive subject. Most people brush it off, most people deny that they even have it, and others…. take the situation into their own hands. Depression is not a game. It is not something you can just push to the back of your mind and act as if it is not there. It’s real and it’s dark.

 

For me, depression is a dark cloud that just covers my judgment and I try to swat it away with always going out. It does not help what so ever. Being alone, with depression can lead you into deep memories or deep thoughts that send you into a breakdown. Luckily for me, I have severe anxiety, I get emotional breakdowns and when I’m depressed… it ends up feeling as if the entire world is against me and I won’t be able to break out of it. You can fight, fight, fight, but what good is the fighting if it leads you nowhere? The same thing happens when you try to avoid it all together and you just end up running yourself into a corner, staring it straight into the face and eventually giving in to the dark cloud. I’ve seen people actually be judged for being depressed and I have also been one of them that have been judged and it’s another kick me while I’m already down feeling. For me, I am lucky to have family and friends by my side doing no matter what it is to keep me going. Even though I am a huge loner when I am in one of my funks, no one ever leaves my side.

 

Depression is definitely a real thing to talk about. It’s a real thing to deal with in general because the person who is going through it just feels like they are in quicksand and there is no way out. But, from experience, there are ways out. There are so many other options and hobbies to dive into that you end up experiencing life. My biggest depression fixer is my little guy. It must have been fate that brought him and I together but every day I come home to his face and I know that I’m always perfect in his little eyes.

Dis-Nerd Cali Takeover

HEY EVERYONE!

 

yeah, I know I have been completely M.I.A. but packing, finishing costumes and getting everything settled for Cali was no joke.  I’m back and better than ever!  So now let’s get to the juicy details!

If you really know me, you know I am obsessed with Disney and it’s not a bad thing.  I used to be completely shy about it, hide it, and I used to believe it was only for kids.  Well, not anymore.  I’m pretty open about my Disney nerd-ness and I don’t really care the opinions of others anyway but it did take me a lot of steps to actually be upfront with this.

California is totally different then New York.  It’s a slow steady, yet speed racer kind of place.  I did not really like California as a state but that’s my opinion on it.  I like fast beat, uplifting places *coughFLORIDAcough*  but it all just stands on how you do it and how you take that state on.  I don’t even like New York all that much but once again, solely my opinion.fe9c276a-0789-47fc-84cd-9f82af98bd93

Now, DISNEYLAND.  Yes, I was entirely happy to experience another Disney Park.  But we finished both the parks within the morning portion of the day.  So let’s just say, it’s pretty easy to get through the parks if you manage time wisely.  We woke up at 6 am each day, to get to the parks by rope drop and get our fast passes and head on to smaller rides while waiting.  The one thing I adored about Disneyland was that they still have paper fast passes.  In Disneyworld, they have magic bands which leaves you no choice BUT to book fast passes 160 days in advance. *facepalm*  I adored meeting new characters that I have not met and also meeting my “father.”  I am a huge Star Wars nerd so as soon as I saw Darth Vader I fan-girled.

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“But I’m the child that actually EMBRACES the dark side”

 

 

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Disney’s California Adventure – Paradise Pier!

Disney’s California Adventure was an amazing park!  I got to ride the new Guardians of The Galaxy – Mission: BREAKOUT and I was not disappointed.  When I first heard of Disneyland changing over Tower of Terror to GotG, I have to admit I was a little shocked on how they would take out one of their best rides.  But I stand corrected when Disney went even further with a good ride and made it an amazing ride.  My friend Halie, then got us a dinner package which included World of Color tickets to be right up front.  Watching World of Color, I started crying like a baby.  Just being surrounded by Disney fans, hearing everyone oh and ah, hearing fans singing along to the best Disney tunes, really makes you wonder why can’t life always be like this?

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End of World of Color
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Princess Kida (Atlantis)

 

D23 is the biggest Disney fan conventions.  Hosted in California every other year, this is definitely a convention to do at least once.  We went in with the expectation of just walking around and seeing cosplayers because this girl is NOT camping outside of a convention center from 3 a.m. just to see a panel which I’ll see online ANYWAY. Day one I was Padme Amidala from the Star Wars prequels, Day two I was Princess Kida from Atlantis and day three I was just my regular self.  It took me months to put together these costumes and it took me about a week or so to sow together my entire Kida costume.  Big props to full time cosplayers because I was exhausted but I loved every minute of it!  I got to be close to Stan Lee, Mark Hamil, and my previous boss, Mr. Mickey Mouse blew me a kiss walking down the convention!  I was able to meet the voice of young Bambi and get his autograph, I was able to meet Tinkerbell. I got a Pixar Luxo Ball (which is extremely rare), I got to be in the same building as Oprah… (yeah, I know this is a long shot but c’mon SAME BLDG!), I was able to meet new people, buy a ton of new pin grails that I have and just experience being surrounded by people who love Disney as much as I do!  I was semi-bummed that I wasn’t able to be in some of the panels in which they announced Kingdom Hearts new world addition, the Marvel panel, or the Lion King panel but all in all, I could honestly do it again in a couple years on a Friday only. (because those lines O_O)

Thanks for reading

  • N.Rarity

“Disneyland is dedicated to the ideals, the dreams, and the hard facts that have created America, with the hope that it will be a source of joy and inspiration to all the world” — Walt Disney

Rave Tingssss

There’s no better feeling then when you walk into a music festival for the first time. My first festival was in 2013 during my Disney College Program. I loved the music but I never knew about such festivals until one of my close DCP friends asked me to go. I was doing all new things, living in a new state so of course I said why the hell not. Now, you would think after all I have told you about my condition, I wouldn’t and shouldn’t go. It’s standing up all day for about 10+ hours, being in packed crowds, some people pushing and shoving, and dealing with people that you probably do not want to come into contact with. Most people believe that raves and ravers are just people who go to do drugs and just get wasted. Let me break that stereotype right now. I go to raves sober. Completely and utterly sober. I go for the music, not to forget everything that happened plus with my condition I cannot do any of those things so I take it how it is. It’s funny because some people I have come across have literally told me they do not know how I can do a 10+ hour festival sober but it’s actually wonderful. The vibes are amazing and the people I go with are even better. I have made so many memories, so many friends, and it’s a great experience. Of course, with my condition there are limits as well. I have to sit down at times because not enough blood runs through to my legs. I’ve been in unbearable pain on day two of three day festivals. Then there’s also post-festival flu. Once you finish with a festival you either go into post-festival depression or you get sick. I unfortunately get both. My body ends up shutting down and I can barely move for a couple days, but it is well worth it. Listening to your favorite DJ play the one song that got you into EDM makes everything so unreal. Each time I see Afrojack and he plays Take Over Control, everything just stops for a second and then I remember who I am with and where I am and then life just feels perfect in that one moment. My rave stats aren’t as great or as high as some of my rave friends but soon enough it’ll start growing. From Life in Color to EDC Orlando to EDC New York to EZoo and just recently Ultra, raving keeps my spirits up. A lot of people do not understand why I do it or they tell me I’m getting too old to continue doing this, but they do not have to understand why I rave. It makes me happy. In a life where things can be out of control I know under the Electric Sky is where I need to be and all my worries and fears can just go away for that short amount of time and I just enjoy where I am in life, at that moment.

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ULTRA Miami 2017 – Afrojack

 

 

To all the ravers I have come across and raved with, thank you for bringing me further and deeper into this life that we love and we all have in common. Thank you for always inviting me to those weekend raves and all the amazing memories I have with you and the memories that we will soon create

 

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EDC Orlando 2013

 

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EDC New York 2014

 

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EDC New York 2015

 

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Electric Zoo 2015
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Electric Zoo 2016

Defective.

Inadequate. Unloved. Hurt. Hopeless. Deficient. Incompetent. These are words that while you’re going through a rough patch in life you go back and think about.  You think about how this could happen to you and how much you wish things were different but they aren’t and you have to suck it up, put on your big girl pants and just deal with it.  Remember how my last post was speaking on my flare-up?  This week it got worse. Way worse than I expected it to get.

So of course it starts off with a minor cold. A minor flu. I knew I was sick but I thought it would go away on its own and then I would be fine.  Monday through Wednesday I was functioning normally.  Yes, I was sick and I noticed it started progressively getting worse but I thought nothing of it.  I was going to be fine and nothing was going to happen.  Wrong as usual.

I wake up Thursday morning to my mother slamming our front door leaving while I’m hunched over my bed on the verge of tears. I call my boss, letting her know I cannot go into work and then call my mother telling her I’m going to go to Urgent Care.  I start getting ready slowly as each part of my body aches in pain and I head out to urgent care.  I’m there for about two hours and they say I have an infection in my body and they prescribe me some kind of nonsense.  I say nonsense because those pills actually made me worse.  I went back home with my prescription, tons of pedialyte and a couple bottles of ensure because I did not feel like eating.  I got into bed, took those pills and then fell asleep.  I woke up about 2 hours later with sharp pains in my stomach that I only remember so well.  I began freaking out and praying that it wouldn’t last.  I was praying it was just a spasm that my body was having and I was going to be okay.  I decided to fall back asleep just to check but once I woke up again the pain was even stronger.  I called my primary doctor and he told me to go to the hospital ASAP.  I knew something had to be wrong because I was not having stomach pains prior to that medication and I looked it up.  The medicine clearly states do not take if you have a liver disease. I wanted to flip out because a doctor who clearly knew I had blood clots in my liver and I had complications of my liver, gave me a medication in which affects my liver.  I called my mother and my father and told them to hold off on the hospital because I knew it was the medication making me feel horrible.  I didn’t go to work on Friday either and I was on bed-rest minus the hour I went to my job doctor to get actual antibiotics.

The whole time this was going on, I was having emotional breakdowns which I haven’t had lately. All you do is think about how much pain you are in, how you wonder why this happened to you, why you are so defective and imperfect and how any one would ever be able to handle you.  These are the lows of having a disease.  Somedays you feel like giving up and Thursday was that day for me.  I felt like giving up, I hated this sickness and I just let it take over my body and I gave into it.  I wasn’t positive and I was incredibly rude to people who just wanted to help me feel better.   I gave into thinking I wasn’t enough nor would I ever be enough trailing around with this sickness.

It’s just the highs and the lows.

N. Rarity.

 

Flare-Up

Let’s discuss the term “flare-up.” The definition of a flare-up is a sudden outburst of something, especially violence or a medical condition and in this case, I believe we know which is mine. I often get flare-ups if I do not get enough sleep, if the weather changes drastically, if I continuously go out, if I take an airplane, or if I just breathe the wrong way. The worst part about it is that I could go to sleep one day perfectly fine and the next day I feel like my body has been run over with an 18 wheeler. It’s hard to function throughout the day while you’re going through a flare-up because honestly all you want to do is stay in bed and not move throughout the whole day.

Currently, I’m going through a really tough flare-up. If you look at the main picture, you would think I look fine and there is no chance that I could be sick! WRONG! I was in so much pain and felt so sick but I managed to get through it. I do not know how it started, it could be the fact that I have barely had a day to rest in my bed curled up into a cocoon, but this is a hard flare-up. Remember the spoonie theory I introduced a couple posts back? Well counting spoons is a no go because I wake up in the morning with zero spoons at all, which means I have zero energy and zero will to even get up out of bed. That is the worst thing about having a condition and/or a flare-up. You wake up in the morning with no motivation and even when you find a little tiny bit of it; it’s gone as fast as you found it. With me, I wake up around 6:30 am to feed my puppy, go back to sleep for about an hour or so, get ready for work to leave my house by 9 am, to work from 11-7 and to get back home at 8 pm. So basically, I am dragging myself throughout the day to be out of my comfort zone for about 9-10 hours and even when I get home I either go out to enjoy my life or just go right to bed because my body cannot handle the pressure. What I am going through now is constant back aches, migraines, weakness, throwing up, stuffy nose with constant nose bleeds, chills, looking like I haven’t slept since 2016 and the list goes on and on. This is one of the worst flare-ups I’ve had in a while and all I want to do is sleep when I cannot even do that as much as I want to because weekends are my only free time for me. While you’re reading this you are probably wondering why I don’t just take pain medication and call it a day. Well, I can’t, it’s not as easy for me as it could be for someone else. Tylenol does not work anymore due to the years of using it and I am not allowed to take any other medication at all which leaves me with the only choice: Deal with it. So while you sit there, just remember everyone who LOOKS healthy may not be and everyone is going through their own struggles that sometimes can’t be easily fixed.

Thanks for reading.

– N. Rarity