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#theres like multiple side order things that go FAR too perfectly with it and
localsolverhost · 6 months
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why do splatoon and md go so fucking well together
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bakugohoex · 4 years
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I know we all love the monkey man and hes sexy and everything...but maybe Zeke for number 1 or your 1k fluff prompts? Theres never anything for him that's fluff...🥺🙏
“you’ll be mine one day”
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pairing: zeke yeager x female reader
cw: language, mentions of weed and alcohol, fluff, reader cheating with zeke, mutual pining
word count: ​2500+
a/n: yes i all monkey man sm and of course this fluff has a bit of a weird theme to it but i hope you still liked it
summary: in which after meeting zeke multiple times throughout the month, every time saying the same thing, the only problem being that you have a drunken boyfriend in his way
1k event masterlist
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Zeke loved coffee, everyday for the past month he’d walk right into the coffee shop right before work started, ordering his favourite coffee and waiting in the seat right beside the window. The atmosphere smelled of crushed coffee beans, the cakes and desserts that were behind glass. Zeke loved coffee especially when the pretty barista with locks that framed her face perfectly was the one to take his order and give him the coffee cup with the perfect heart in it. He loved coffee like an addict does opium, he loved the way it sat on his tongue, the way it looked at him with such lust. The way it’d be gone in a matter of seconds in one rash blink.
You knew the man’s routine so often that when he’d be running late a hurt was felt through your body. Zeke and you both knew that the constant glances in the half an hour he stayed at the window seat, the lingering touches as you grabbed the empty coffee cup to get him another was wrong. But even then how could he resist you, the way your eyes spoke so much in just a mere glance. He felt infatuated beyond belief but there was one thing in his way of pursuing anything with you, your boyfriend.
With his unkempt hair and smell of weed always around him, Zeke didn’t understand why someone as delightful and pretty as you would go for someone who looked off his head. He was unemployed from what Zeke had gathered; he knew if you were with him you wouldn’t have to work this job. You could stay at home and be his, you wouldn’t have to worry about making ends meet as long as you stayed by his side.
Even with your boyfriend being a minor factor in his mission to get you, he left the same words on the napkin each day, he always left as soon as you went into the back to restock the cupcakes and savoury desserts. The napkin placed on top of the empty mug, you hated how much influence the man had on you.
You had had many conversations with him when work got slow which occurred a lot when he came in the early mornings. But even then his insistence that you’d come to him was prevalent, maybe you did have a crush on the man, he was older by a couple years, established in life, had the stability and security you and your boyfriend never had and worst of all. He had the ability to flirt with you so easily even with the risk of your boyfriend around, Zeke may have respected the position of your relationship with another, but he would never give up on you as easily as you had expected him too.
It was another early morning, you stood behind the counter, watching Zeke in his tight suit, the white shirt unbuttoned as his suit jacket swayed with the wind. The cigarette that he had in his mouth being chucked to the ground as he stepped on it putting it out. The sound of the door jingling made you plaster on a smile at the blond boy who came with a small smirk on his face. “Hello, what can I get for you today, Zeke?” The place was pretty much empty, it hadn’t hit the morning shifts yet and you assumed Zeke started working a lot earlier than the rest of the city. You were the only one at the counter as your colleague had gone to make some food for when the breakfast rush came.
“Morning Y/n, can I have a white coffee and your number on the side?” He spoke the last part confidently with his lip twitching upwards at how you shook your head.
“Nice try Zeke, anything else you need?”
He paused thinking as he stared at you, you looked so delicate and pretty, all the things he could do to you flashed through his head. Maybe it was sleazy to think such crude thoughts but what you didn’t know didn’t harm you, right? “You, if possible.”
“I’ll have your drink made in a couple minutes, Zeke.” You chuckled out, he loved the way you said his name, the way you gave that soft touch as he passed you the money. Your fingers gliding against his own, he took his normal seat watching you pour the hot liquid into the cup, he knew you’d give him another heart like you normally did. You always did concentrate too much on the finer details, you took the cup and plate that went under it bringing it to the man. Placing it down, Zeke saw the heart as you gave him a soft smile, “what you working on now?” You questioned knowing nobody else was going to come in.
You took the seat opposite him, the papers in his hand that looked really important, “foreign affairs, all hush hush, but for a pretty girl like you I could tell you the details.”
“Wouldn’t that be a national security issue?” You folded your arms raising an eye at the man, he gave off this presence of confidence and knew exactly what he was doing with his life. A stability that seemed ever so far away from you, you had often imagined what dating a man like Zeke would be like, how you could work full time at university instead of part time, how you could come home to warmth rather than weed. “Tell me more about what you do.”
You leant your head against your arm as you often spent mornings listening to him ramble on about his career, nodding and humming along whenever the time came. He seemed to enjoy speaking about his work, you could listen to it forever, you nodded almost love struck as the man spoke. Your work colleagues often saying you looked like a girl who was talking to her first crush. “One day I’ll show you what we’re working on.” You nodded at the false promise, one day he’d forget about the barista, he'd become too big, too important for a girl who had nothing going for her than an alcoholic weed smoking loser.
“Promise.” You hadn’t meant to whisper the words, but Zeke gave a soft smile.
He watched how you put your hands out, away from your chin as you leant backwards, grabbing your hands he looked you dead in the eye, “I don’t lie to pretty girls.”
You gave another chuckle, seeing how your eyes went to the arriving customers, the rush about to occur. “I’ll see you tomorrow.” You walked away without another word, he watched you go into the back to help bring some of the new produce. Quickly bringing his pen out as he wrote the words onto the napkin, you’ll be mine one day, in his cursive handwriting, his initials were underneath before leaving it beside the empty coffee. Grabbing his stuff as he left just as customers began to barge past to get their morning fix, he took one last look inside seeing you happily smile and take their money, before finally walking away.
You had managed to hand out the coffee cups to those in a hurry before starting to clear tables, taking the napkin Zeke left, the same words every day. Maybe if you had outright told him to stop he would, but the excitement each day you got from the romantic gesture filled your heart. You didn’t know what had gone wrong in your relationship with your boyfriend, maybe it was the drugs or his loss of job. Maybe you had fallen out of love and he had notices, his lying and pleas to make you stay by him. The manipulation and deceit something you wouldn’t get from Zeke; you stuffed the napkin in your pocket ready to put it with the 28 other napkins you had.
Keeping all safe within a box in your bedroom, the fear that arose from being caught with it all. Maybe it was emotional cheating but in a relationship like your own maybe you deserved better, you wiped your hands on your apron. Everything has subsided as you and your colleague went on your break as your manager took over.
“I see how you look at Zeke, just break up with your shitty boyfriend.” She said taking a sip of her coffee, you had your own in your hand thinking about the man.
“I can’t, he needs me.”
She raised her eyebrow at the comment, “he needs a fix and therapy, Y/n, I might sound like an ass right now, but all your boyfriend thinks about is getting his dick wet, getting high and getting drunk.”
There was truth in your friends words and as your break ended, you gripped the napkin tighter than you had imagined. Staring at the eloquent writing, the way he wrote Z and Y, even his handwriting seemed perfect. You took a sharp breath realising that in the 29 days you had known Zeke, he had provided more love and warmth than the man you had been dating for years now. You needed to break up with him, needed to confess to Zeke that his crush wasn’t one sided.
Just as the café closed up, you nimbly parted ways from your friend as you began to walk to your apartment. You knew what was to occur, your boyfriend on the couch high with his friends beside him, you really didn’t want to go back. You felt your phone begin to ring as you answered it to hear the drunken shouting of your boyfriend, you didn’t even bother with the words instead hanging up. Clinging the napkin between your fingers, you walked a different direction, towards the offices that Zeke had so often told you about.
You didn’t know what you would do once you arrived but the glass doors with the frosted words of Marley led you to walk inside. The yellow lights bringing warmth as you walked towards the front desk, you didn’t look like you belonged, looked like some stray. You tapped your fingers against the white marble as the woman finally turned to meet you, “hi, what can I help you with?”
She smiled at you as you really had no idea what to say, “Zeke.”
“Zeke?” She paused, “like Mr. Yeager, one of the partners here.” You nodded as she gave a confused look at you. “Who are you?”
“I’m a friend of his, do you know where I…I can find him.” She looked at you hesitantly.
She tapped on the keyboard, the only sound being her taps, “I can call him down if he’s a friend, we have a security measure so I can’t send you up, but if you wait on those chairs he’ll be down shortly.”
You nodded quickly turning on your heels as you moved to the white chairs, it looked empty, the staff probably having left hours ago. You hadn’t realised Zeke to have been a partner of this place, it seemed way above your standards. You felt the need to leave and never come back, to apologise for wasting the woman’s time but just as you were about to get up. The ding of the elevator made you stop, Zeke coming out with a brunette-haired woman, she smiled at the man as he walked beside her speaking on some matters.
He went to the front office lady and he pointed to you as both him and the woman looked at you. Zeke confused before beginning to walk up to you, “Y/n, what happened?”
“I…I…don’t know why I came here?” You paused taking a sharp breath, “so…sorry I should go, I…” You were ready to run away, embarrassment across your face at the fear of feeling vulnerable in front of this man.
He grabs your wrist stopping you from leaving, bringing you to face him again, “Pieck, I’ll see you tomorrow.” The woman he had been with nodded saying a goodbye before she left herself, “come on, you can explain everything in my office.”
You didn’t know how you had agreed to go with him, your other hand had been clutching the napkin out of instinct, he guided you up the elevator, his taller frame against your own as his hand was on your back. He shuffled you along past the many smaller offices before his name was frosted onto the door, opening the glass as he let you into the much larger area.
“Take a seat.” He gestured to the couch that had a coffee table in front of it, he got out some alcohol putting it on the table as he poured two glasses out for the two of you. “What happened?”
“I…I…I’m sorry, I interrupted your meeting, and I shouldn’t have come here.” You were ready to get up again, but Zeke moved to sit beside you. His discarded suit jacket on his desk as he had rolled up his sleeves, his glasses sitting perfectly across his face.
He brought his hands to your one shaky ones, it seemed to have calmed you down, but he noticed the napkin scrunched up in your hands. “Shoosh it’s okay, take your time.”
You nodded taking a sharp breath as you explained how your boyfriend had shouted at you and how you really didn’t want to go back to your apartment. “I just can’t do this anymore Zeke, I…I deserve happiness right, I do don’t I?”
Zeke had noticed the tears form in your eyes, it cascaded down your perfect face as he wiped them away softly. He was frustrated, frustrated at your arrogant dickhead of a boyfriend, frustrated at the world for making his girl cry.
“You deserve happiness.” You didn’t know what had gotten into you, but at his tender sweet words you moved your hand onto his thigh, crashing your lips onto his own. You felt no guilt, nothing as you kissed the man, your other man moving to his blonde beard as you cupped his face. He knew it was wrong, you had a boyfriend, you were cheating but he couldn’t resist you. He felt you crawl onto his lap, pushing him against the couch as you deepened the kiss. His tongue gliding inside your own as you gave a soft moan of his name, it sent him into an overload as he gripped your waist with one hand and the other to caress your cheek.
He watched as a string of saliva stayed between the two mouths as you both parted, “I…shouldn’t have done that.”
“Don’t go back on me now, doll.” He teased, laying underneath you, he brought his hand to touch your hair, his touch making you go soft inside. “I told you…”
“Told me what?” You questioned still on his lap; he brought his head closer again to your mouth.
Through every kiss he gave you, he said the four words, “that you’d be mine someday” In a matter of seconds you realised the implications of his words, you were his, you were everything he had dreamt about. You would leave that disgusting man and be Zeke’s forever.
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zeravmeta · 5 years
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Ok so, my thoughts on the VR ending and VR overall as the 6th entry.
Also because most of my thoughts aren't...complimentary im editing the names so they dont appear in the general tag. This also got LONG so readmore.
The Good:
- A//i's character still managed to be the one thing that saves VR as a show for me. Even with all the weird...contradictory plot issues, A//i still manages to be a compelling character who brings up the question of the right to live. I actually do like how he made it so itd be an ultimatum that he loses in either way, even if the ending kinda ruins the weight behind the action (which I will get to in a bit).
The meh:
-the ending was left somewhat open to interpretation which for a show as...empty as this was works out but honestly it was so vague as to A//is fate is that it may as well not exist.
The Bad:
-The main conflict behind the entire show is...simulations. No joke. Every conflict in the show can be traced back to someone doing a simulation and deciding to lose it. Even if they gave the (rather stupid) explanation that AI experience simulations like actual life (which btw the first villain wasnt an AI so this reason doesnt work), the fact that Yu//sa//ku took a bullet for one of A//is robot bodies that he literally has millions of is...just stupid and there solely for the "uwu drama".
-They actually killed A//i off but wait hes actually alive, so like the final duel literally had no purpose aside from...drama??? The episode is called Compromise and yet A//i had to lose just to keep Yu//sa///kus win streak and theres no compromise whatsoever. Yu//sa//ku litetally destroys the CompromA.I.se card so its just, no comrpomise in any way.
-This....wasn't a happy ending??? I have no idea why both the show and the fanbase frame this as a happy ending bc think about it in context: A//i pretty much loses everything, so does Yu//sa//ku who just isolated himself from everyone else for 3 months in order to comb the network for whatever remnants of A//i exist.
- So many of the supporting characters are just...there. Like, there is no side/supporting character who actually has a character arc in this show. Lets go through the list: Ao//i is pretty much the same character as when she started and goes through 2 unnecessary costume changes for a character growth that isnt there because she has literally ONE victory against an opponent that was stated multiple times to be weak and faulty and have her lose and tortured multiple times for no reason whatsoever, G//o had this weird deterioration that may have lead to something but ultimately didn't, Ak//ira is pretty much the same, J//in has ALL HIS TRAUMA ERASED SO THERES THAT, literally the only side characters who have some sembalnce of an arc are Sho//ichi (the best one anyways) from his "betrayal" in S2, and E//ma with her reconciliation with her brother. Outside of that, nothing. Yu//sa//ku, Re//volv//er and Ho//mu//ra are pretty much the only characters with an arc and even then they're not too solid? Which brings me to-
- Yu//sa//ku has been so wildly ooc since the end of S1. Ive seen so many say that his enphasis on bonds and friendship are character growth but actually looking at the sequence of events he suddenly just like. changes completely around his first duel with Ea//rth. Plus, the message of "revenge is good" was always so weird? Like, he got his revenge so all his trauma is ok now and never brought up or explored again aside from within the first 20 episodes. Theres nothing about it after that and its never built upon. The whole point of a revenge arc is to show that its BAD and yet he starts preaching that revenge is wrong AFTER he successfully gets revenge??? And even then its not exactly a revenge as it is more lashing out since it was Ko//ga//mi who was behind it all. Yu//sa/ku was definitely at his strongest characterization in S1 where we see how badly the Lo//st Incid//ent hurt him but S1 had its own share of problems that led into S2 and so many random plot threads that never went anywhere (such as the Anot//her Incid//ents, the Cy//berse deck being irl despite that A//i didnt have a physical body before then, The Bl//ue Mai//den meetup that was repeated by Nao//ki like 10 times in S2 which seemed to be leading up to something but never did, and the fact that theres 4 recap episodes in S1 already spelled some early problems). So much of the supporting cast function to just say "he turned this whole situation around...with ONE card..." i kid you not watch back every Yu//sa//ku duel I GUARANTEE you'll see someone saying hes a great duelist and serve only that purpose. ALSO THE END OF THE SHOW IS JUST MORE DRAMA?? They make him suffer for no reason other than that they can??? What purpose does his suffering at the end serve aside from just "uwu...poor baby..."???
-Re//volv//er is not a good rival. At all. He's so incredibly bland because much like Yu//sa//ku he was at his strongest characterization in S1 where he actually had some solid motivation in continuing his fathers work and being unable to accept that his dad was evil, yet most of that just flies out the window with all the collateral he's willing to inflict with the K//O//H?? All his character amounts too post S1 is "yeah i told you robots are evil and YOU didnt believe me". The most we got of him growing out of this mindset was calling A//i by his name exactly one time and nothing ever again. Also the fact that in the end we see him and his crew working for S//O//L despite the fact that they were gonna turn themselves in for their crimes just. leaves a rotten taste in my mouth. hes not a good rival at all. All he proves to me is that a good design can get anyone to like a character.
- Ho//mu//ra is...there. I literally cant say anything about him because he absolutely has the strongest motivations of the three but then the show jumps through hoops to push him to the back of the other two. He also has a bunch of early victories I do feel are undeserved (ESPECIALLY the A//oi duel that one pissed me off so much). Also the fact that the show just made him Yu//sa//kus friend immediately whereas it took Sho//ichi several months to get Yu//sa//ku to warm up to him just had me :/.
-The speed duels were a cool concept but they just became these huge cheat fests? Seriously Play//Maker uses StAccess literally every speed duel to pull out a new monster from whatever plot holes the writers need to patch up. I am not kidding. You can go back to every single speed duel Yu//sa//ku was in and youll see this. Skills just werent a good mechanic because when a protag pulls a new card its supposed to be representative of some growth/characterization but he stays the same pretty much throughout the entire show up until S2 where he wildly just switches personality. Plus the fact that Que//en could literally use a skill whenever just shows that it was cheating???
- The villains were overall lackluster. Boh//man was the best because Re//volv//er is just flat whereas A//i struck me more as an anti hero. And again: simulations are the enemy. Light//ning ran one and decided to go ham. Kog//ami ran one and decided to go ham. A//i ran one and decided to go ham. The conflicts are all the same and it just makes things happen rather than following a consistent plot thread? I will say that Boh//mans characterization of a hive mind to become perfect does strike my tastes but thats more my personal preference in villains rather than any merit he has.
- This is a bit of a personal pet peeve but I've seen some of the praise to this show about being the "darkest Y//G//O to date so therefore its good" and im just...no? Edge does not make a good show and just because they lightly focused on the tragedy in Yu//sa//kus life (and it IS lightly because its barely touched upon after mid S1) most of the stuff that happens in this show is pretty tame in comparison? The most that happened here was an attempted global hack of everyones minds from S2 and destroying the internet in S1, with a few references to the torture that happened during the Lo//st incid//ent. To compare: the previous series had this huge interdimensional war that, even if they could reverse the carding of people (which makes Den//nis' attempted suicide even more tragic), ended with an entire dimensions full of brainwashed soldier children, a dimension with huge class inequality that was still being heavily worked upon since there were canonically slaves, and a dimension that was savaged by a genocide and total global destruction. Hell, the series before that had a huge war where the arc actually did focus on the tragedys the characters faced and held consequence (even if they pulled a dbz revive everyone at the end). And as far back into the very first series there were even more graphic depictions of war and death? Idk i feel like people are overplaying the edge here just to find a way to complement this show.
Overall:
I'm...genuinely dissappointed. VR really had so many strong starting points but it all just fell apart at execution. Really the only reason I even bothered to watch it as kong as I did was because Im a longtime fan of the series and wanted to give it a chance rather than jump on whatever love/hate train the show has. Its been rated poorly on the JP side and most of the approval is a vocal minority. Just to be clear: this isnt me bashing the show, my opinions are mine and you can agree or disagree to any capacity, and even if a show isnt well written you can still find a reason to enjoy it despite the flaws.
But if Im being perfectly honest? I do not like this show. It's rushed, choppy, has no consistent or clear plot threads, most of the genuinely interesting characters are wasted for the protagonist to look better and he never really does because he ALSO has an interesting idea behind him but it never goes anywhere. It started strong but ended so poorly. Id be angry but im more dissappointed because Ive watched this show from day 1 and wanted to see the good things it has rather than focus on the negatibes but. yeah. This show really had potential and yet it just fell flat.
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apsbicepstraining · 7 years
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What it’s like to be diagnosed with multiple sclerosis at age 25
In February of 2015, after a busy weekend, I began feeling some tingling in the bottom of my feet. I thought that I was just sore from wearing heels, but within a few days, the numbness and tingling proceeded to go up my shins and into my knees and through my thighs. Id compare the feeling to when your foot falls asleep.
Although the sensation was getting more and more intense over the course of two or three days, I wasn’t super concerned. I thought that maybe my diet had played a role. I’m a very active person and I work in health and fitness PR, so I was just thinking, “Oh, maybe I’m not getting enough magnesium or something.”
After about five days of this feeling traveling inch by inch up my legs, I went to see my primary-care physician thanks to the advice of my sister, who’s a surgical nurse. My doctor quickly ordered an electromagnetic test (EMG) and an MRI to rule out meningitis, ALS, multiple sclerosis, and lymphoma. That’s when I started to get a little nervous.
The next day I went and got those tests done. By then, the numbness and tingling had become so severe that I almost couldn’t walkI could feel the pressure of the ground beneath me, but I was forcing my leg to move. By day seven, it was almost a state of complete paralysis.
The EMG was the first test and it began with them sticking needles all over my legs and then sending electromagnetic shocks through those needles to see how my nerves reacted. I’ll never forget it. The neurologist said I had severe swelling in my spinal cord, and ordered an immediate brain and spinal cord MRI.
When I was done with the MRI they said, “Go home, get some food because you’ve been in testing all day. Your doctor will likely call you and go over the results tomorrow or they’ll bring you in. Just relax.”
But within 10 minutes of me walking out of that place, my doctor called me and said, “I don’t mean to scare you but you need to stop whatever you’re doing right now and go into the ER. I just got your preliminary images and there’s a major, major area of swelling in your spinal cord. You need to seek treatment right away.” That was exceptionally terrifying. I thought that I was going to be able to relax and see what happens, but instead it was back to the ER, where they whisked me into a wheelchair right away.
That’s when the series of diagnostic tests took place. I had two spinal taps, blood work, etc. I had four different neurologists come down to put me through strength tests, like the sharp-soft test, where they break a toothpick in half and they ask you if you can tell the sharp side from the soft side. At this point, they were trying to diagnose me through a process of elimination. 
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At first, they said, “Oh, you definitely have to spend the night”, then it was two nights, then three. Every day they would come back and say, “Oh, you don’t have AIDS”, and I’d think, “Great, this is wonderful. Wasn’t hoping for AIDS.”
But in all seriousness, AIDS is an autoimmune disease, which is what MS is, so its not too far off. They would say, “Oh, you don’t have lupus. We can rule out Lyme disease.” And so on, and so on
In the meantime, my doctors were trying to reduce my spinal swelling. Every day I got a little bit more feeling back, but there was still a lot I couldn’t feel.
Then after day four or five, doctors told me that I had transverse myelitis. A neurological disorder caused by inflammation of the spinal cord, transverse myelitis can be an initial indicator of multiple sclerosis, according to Kathleen Costello, vice president of healthcare access for the National MS Society. 
There’s no one test that can determine whether or not you have MS. It was the combined results from the MRI, the spinal tap, blood work, electrical tests, etc. (not to mention, my symptoms) that led my neurologists to that conclusion. By the time I got my diagnosis, I had already figured it would be something severe based on my symptoms. Despite that, I don’t think any young woman is ready to hear that she has MS.
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I’ve been told the paralysis I experienced is one of the worst ways that MS can initially present itself. To put it in perspective, when some people are diagnosed with MS, their first symptoms are blurred vision or a lack of coordination or they have a little bit of numbness in their pinky finger, says Costello.
At the worst point, the paralysis had gone all the way up to the top of my ribcage, right below my bra line, and I felt a tightness, like someone was squeezing my ribs together, making it hard to breathe and hard to walk. That, I later found out, is called the MS hug, which is a common first symptom. For me to go from a person who is boxing and doing Crossfit and yoga classes seven days a week to not knowing if Id be able to walk again, was quite shocking.
Of those who suffer transverse myelitis, around 30 percent of them are never able to walk again, another 30 percent can walk with limited mobility and residual symptoms such as spastic gait and urinary urgency, and the last 30 percent get back, for the most part, full mobility. Thankfully, at the end of my recovery, I was in that last 30 percent, and now I’m walking and moving and working out and doing most of the things I used to be able to do.
However, I now live with permanent nerve damagea common side-effect of MS. Any time it gets above 75 degrees or there’s humidity in the air, I have tingling all up and down the back of my legs and my spinal cord. I have this thing called LHermitte. It’s this weird, residual effect that happens when you put your chin to your chest, like if I’m looking down at my phone or if I’m tying my shoe. I get a weird electronic sensation from my nerves misfiring down my back. The way that I best can describe the sensation is that it feels like there’s a vibrator on your back.
Today, I tire much more quickly and I can’t do workouts that are as strenuous as what I used to do. Sometimes I can’t wear heels for too long because Ill begin feeling numbness and tingling. Im still navigating the waters of my mobility, but Im just thankful to not be confined to a wheelchair and have feeling in both my legs.
I had another attack recently, which was much less severe and less traumatizing. I lost feeling in my left arm, but this time I knew what it was and I got on steroid treatment right away. Now I have most of my feeling back with minimal permanent damage. Today, I manage my disease by adhering to a very strict, clean diet, going for MRIs every few months and blood tests every couple weeks, and taking medication and/or seeing my doctor when another attack comes on.
Theres a common misconception that MS is like ALS or that it’s this degenerative, terminal thing, that I’m just going to keep getting worse and worse and there’s nothing to stop it. It seems so much worse than it is. What I’m learning is that you can have an attack and then not have another attack for 30 years; that’s very common. On the other hand, you can have five attacks in two years, which could be really bad and result in a lot of permanent nerve damage. There is a chance that I could be in a wheelchair five or 10 years from now, but that chance is very slim. My youth and the fact that Ive led such a healthy lifestyle have both helped me recover from attacks quickly so far.
For me, the hardest part of all this is the unknown. There is no cure, so I’m waking up every morning wondering if Im going to have another attack, or if today is going to be the day where five lesions pop up into my brain and I wont walk again.
Eighty percent of people diagnosed with MS are Caucasian females in their childbearing years. Learning that statistic was shocking, but in a way, I was comforted by itI feel less alone.
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The one thing I want everyone to know is that I can still live my life with this disease. A lot of people dont realize thateven my own friends.
I’ve had friends talk badly about me, saying things like, Well, if shes so sick, hows she drinking on Saturday at a rooftop brunch? and wondering why I look perfectly normal.
Its hard to be open with people because I can see how they might think Im using my disease as an excuse when its convenient. But the reality is I have bad days and I have good dayssometimes I feel ready to take on the world and other days I cant physically get out of bed.
I think thats been one of the more difficult parts for me, dealing with other peoples perceptions and judgments. Whether they think Im dying or being dramatic, its impossible for them to understand what I and other people with MS go through, which leads to misconceptions.
I dont blame people for being confused, but at the same time, I’m not going to lie down and not do things. I’m still a 25-year-old living in New York City. I’m going to have fun. I still want to date and try to find a good guyeven though that situation now comes with a plethora of complications.
At the end of the day, Im learning to appreciate every moment. Yes, it would be great to not have MS, but Im very aware of how lucky I am that my case isnt more severe. Thats been my greatest take away from this experience: Dont take anything for granted.
This article originally appeared on WomensHealthMag.com.
The post What it’s like to be diagnosed with multiple sclerosis at age 25 appeared first on apsbicepstraining.com.
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xenonmonster · 7 years
Text
A Disney Song List To Make Life A Musical
Disney Song List for your Life As you may guess, I love Disney with all my heart. If a Genie would grant me a wish, I would wish for life to be a musical, and Disney makes that crazy dream come true. So without further a due, here is a list of Disney songs matched with moods and themes, for your daily life! First and foremost - How to listen to a Disney song: Of course you can just enjoy the song! But here are some things that just bring them to life: 1. Listen to the lyrics. Although ANYONE can enjoy a good disney song, we must remember that disney movies essentially are made for a younger audience, and are all about the moral of the story. That’s why disney songs tend to have deep meaning within them, and these are told by their beautiful lyrics. Sometimes listening to the words being sung brings a new light to the song, and sometimes even your mind! 2. Memorize! Theres nothing more satisfying than knowing every word to a song you love. Disney songs are a great way to bring back nostalgia too, and what better way to do it to jam and sing it out loud? 3. Act it out! This is basically a one up of point nr.2, for us lovers of theatre. Once you take on the character, their intention and start feeling the emotions the songs bring out, is when you really start to feel Disney work it’s magic on you. It’s not rare to have you jamming and dancing to a fun number when you’re in a good mood, and it’s even less rare to burst out into tears when listening to an emotional song that perfectly fits your situation. Alright, enjoy the list! They are in no particular order, and some songs are repeated since they fit multiple categories. All songs on the list are linked to the song itself, so have fun! The Dance-ability Scale: This is a scale to show how dance-able the song is. So for example, if you feel like listening to a 'Chasing dreams’ category song, but you’re feeling happy, you can make sure it’s a fun song that lifts your spirits rather than accidentally picking a slow musical number. 1: Quiet listening and appreciating the music 2: Head bobbing; Tapping feet 3: Shimmy Shoulders 4: Intense Jazz Hands 5: Go wild! Songs about Chasing Dreams: Out There - The Hunchback Of Notre (2.5) Almost There - The Princess And The Frog (3.5) I Can Go The Distance - Hercules (1.5) When Will My Life Begin - Tangled (3.5) For The First Time In Forever - Frozen (3.5) Touch the Sky - Brave (2) I Just Can’t Wait To Be King - The Lion King (5) After Today - A Goofy Movie (3.5) How Far I’ll Go - Moana (3) Part Of Your World - The Little Mermaid (2) I Wanna Be Like You - The Jungle Book (4.5) I’m wishing / One Song - Snow White And The Seven Dwarfs (1) Little Town / Belle - Beauty And The Beast (3) One Last Hope - Hercules (3) I’ve got a Dream - Tangled (4) Someday My Prince Will Come - Snow White And The Seven Dwarfs (1) Just Around The Riverbend - Pocahontas (3) Like Other Girls - Mulan II (3.5) Lava - Lava (2) A Girl Worth Fighting For - Mulan (3) True Love’s Kiss - Enchanted (3) A Dream Is A Wish Your Heart Makes - Cinderella (1) When We’re Human - The Princess And The Frog (4) Strangers Like Me - Tarzan (3.5) When You Wish Upon A Star - Pinocchio (1) Jack’s Lament - Nightmare before Christmas (3) Perfectly Perfect - Cinderella III (3) How To Believe - Tinker Bell And The Great Fairy Rescue (2) In A World Of My Own - Alice In Wonderland (2) Beautiful Love Songs: Can You Feel The Love Tonight - The Lion King (1) If I Never Knew You - Pocahontas (1) So Close - Enchanted (1) One Song - Snow White and The Seven Dwarfs (1) Tale As Old As Time - Beauty And The Beast (1) A Whole New World - Aladdin (3) I See The Light - Tangled (1) Evermore - Beauty And The Beast (2017) (1) Heaven’s Light - The Hunchback of Notre Dame (1) Love Will Find A Way - The Lion King II (1) I Wonder - Sleeping Beauty (1) So This Is Love - Cinderella (1) Bella Notte - Lady And The Tramp (1.5) Fun Love Songs: Once Upon A Dream - Sleeping Beauty (2) Love Is An Open Door - Frozen (4) I Won’t Say I’m Love - Hercules (4) Something There - Beauty And The Beast (2.5) He’s a Tramp - Lady And The Tramp (3) Kiss The Girl - The Little Mermaid (4) That’s How You Know - Enchanted (4) True Love’s Kiss - Enchanted (3) Evil Love Song - Phineas And Ferb (3.5) Gitchi Gitchi Goo - Phineas And Ferb (4) A Guy Like You - The Hunchback Of Notre Dame (4) A Whole New World - Aladdin (3) Upendi - The Lion King II (4) Ma Belle Evangeline - The Princess And The Frog (2) Bella Notte - Lady And The Tramp (1.5) Journeys: Son Of A Man - Tarzan (3.5) One Last Hope - Hercules (3) I’ll Make A Man Out Of You - Mulan (4) On My Way - Brother Bear (3.5) On The Open Road - A Goofy Movie (4) What’s This - The Nightmare Before Christmas (4) Good Doggy, No Bone - The Fox And The Hound (3) Beyond The Sea - Finding Nemo (3) Put That Thing Back Where It Came From, Or So Help Me - Monsters Inc. (5) I’m Still Here - Treasure Planet (2) Gonna Take You There - The Princess And The Frog (3) Cultural, Themed Honour To Us All - Mulan (2) Colors Of The Wind - Pocahontas (2.5) Where You Are - Moana (4) We Know The Way - Moana (4) Hawaiian Rollercoaster Ride - Lilo & Stitch  (4) He Mele No Lilo - Lilo & Stitch (3) Circle Of Life - The Lion King (2.5) Gospel Truth I,II,II - Hercules (4.5) Topsy Turvy - Hunchback of Notre Dame (4) We Are One - The Lion King II (2) Two Worlds - Tarzan (3) Touch The Sky - Brave (2) Steady As The Beating Drum - Pocahontas (3) He Lives In You - The Lion King II (2) This is Halloween - The Nightmare before Christmas (4.5) Savages - Pocahontas (1) Arabian Nights - Aladdin (3) The Court Of Miracles - The Hunchback Of Notre Dame (4)                           Down In New Orleans - The Princess and The Frog (3) All In The Golden Afternoon - Alice In Wonderland (2) Be Our Guest - Beauty And The Beast (4)
Magical, Fun Lifestyle Songs: Hakuna Matata - The Lion King (4) The Bare Necessities - The Jungle Book (3.5) Thomas O’ Malley - Aristrocats (2.5) Under The Sea - The Little Mermaid (5) Prince Ali - Aladdin (5) Why Should I Worry - Oliver And Company (5) Streets Of Gold - Oliver And Company (4) A Spoonful Of Sugar - Marry Poppins (3) You Can Fly - Peter Pan (2) Heigh Ho - Snow White And The Seven Dwarfs (3) Life Is A Highway - Cars (4) Dig A Little Deeper - Princess and The Frog (4) Everybody Wants To Be A Cat - Aristrocats (3) The Wonderful Thing About Tiggers - Winnie The Pooh (4) Today Is Gonna Be A Great Day - Phineas and Ferb (5) Whistle While You Work - Snow White And The Seven Dwarfs (3.5) Happy Working Song - Enchanted (3.5) The Silly Song - Snow White And The Seven Dwarfs (4) Perfect World - The Emperors New Groove (5) A Very Merry Unbirthday To You - Alice In Wonderland (4) Le Festin - Ratatouille (2) I’ve Got No Strings - Pinocchio (3) Supercalifragilisticexpialidocious - Marry Poppins (4) Bibbidi Bobbidi Boo - Cinderella (3) Perfect Isn’t Easy - Oliver And Company (3.5) The Work Song - Cinderella (3) Let Me Be Good To You - The Great Mouse Detective (3) Oo-De-Lally - Robin Hood (2)                                                                           Chim Chim Cheree - Marry Poppins (3)                                                            One Jump Ahead - Aladdin (3.5)
Empowering Songs: Zero To Hero - Hercules (5) Let It Go - Frozen (3.5) I am Moana - Moana (1) You’re Welcome - Moana (4) Try Everything - Zootopia (4) A Star Is Born - Hercules (5) Perfect Isn’t Easy - Oliver And Company (3.5) Stand Out - A Goofy Movie (5) For A Moment - The Little Mermaid II (3) Almost There - The Princess And The Frog (3.5) Friendship And Family: You’ve Got A Friend In Me - Toy Story (2) Friend Like Me - Aladdin (5) We Are One - The Lion King II (2) You’ll Be In My Heart - Tarzan (2) Two Worlds - Tarzan (3) He Lives In You - The Lion King II (2) Nobody Else But You - A Goofy Movie (3) I’m Still Here - Treasure Planet (2) Best Of Friends - The Fox And The Hound (2) If I Didn’t Have You - Monsters Inc. (3 You And Me - Oliver And Company (1) Little Wonders - Meet The Robinsons (2.5)                                                       Eye to Eye - A Goofy Movie (5) Beautiful Sad Songs: Our Town - Cars (1) Reflection - Mulan (1) God Help The Outcasts - The Hunchback Of Notre Dame (1) Not One Of Us - The Lion King II (2) Villain Songs: Be Prepared - The Lion King (4) Prince Ali Reprise - Aladdin (3) Poor Unfortunate Souls - The Little Mermaid (3.5) Gospel Truth II - Hercules (1) Shiny - Moana (4) Hellfire - The Hunchback Of Notre Dame (1.5) Oogie Boogie’s Song - The Nightmare Before Christmas (4) Friend’s On The Other Side - The Princess And The Frog (3) Mother Knows Best - Tangled (4) My Lullaby - The Lion King II (2) Savages - Pocahontas (1) Gaston - Beauty And The Beast (5) Mine Mine Mine - Pocahontas (3) Cruella De Vil - 101 Dalmatians (3) The Mob Song - Beauty And The Beast (3.5) The World’s Greatest Criminal Mind - The Great Mouse Detective (3.5) Trust In Me - Jungle Book (0.2)                                                                    Siamese Cat Song - Lady And The Tramp (1) It’s Our House Now - Disney Villains (3)
Hope you Enjoy! Feel free to message me, if you find a song you love missing :)
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apsbicepstraining · 7 years
Text
What it’s like to be diagnosed with multiple sclerosis at age 25
In February of 2015, after a busy weekend, I began feeling some tingling in the bottom of my feet. I thought that I was just sore from wearing heels, but within a few days, the numbness and tingling proceeded to go up my shins and into my knees and through my thighs. Id compare the feeling to when your foot falls asleep.
Although the sensation was getting more and more intense over the course of two or three days, I wasn’t super concerned. I thought that maybe my diet had played a role. I’m a very active person and I work in health and fitness PR, so I was just thinking, “Oh, maybe I’m not getting enough magnesium or something.”
After about five days of this feeling traveling inch by inch up my legs, I went to see my primary-care physician thanks to the advice of my sister, who’s a surgical nurse. My doctor quickly ordered an electromagnetic test (EMG) and an MRI to rule out meningitis, ALS, multiple sclerosis, and lymphoma. That’s when I started to get a little nervous.
The next day I went and got those tests done. By then, the numbness and tingling had become so severe that I almost couldn’t walkI could feel the pressure of the ground beneath me, but I was forcing my leg to move. By day seven, it was almost a state of complete paralysis.
The EMG was the first test and it began with them sticking needles all over my legs and then sending electromagnetic shocks through those needles to see how my nerves reacted. I’ll never forget it. The neurologist said I had severe swelling in my spinal cord, and ordered an immediate brain and spinal cord MRI.
When I was done with the MRI they said, “Go home, get some food because you’ve been in testing all day. Your doctor will likely call you and go over the results tomorrow or they’ll bring you in. Just relax.”
But within 10 minutes of me walking out of that place, my doctor called me and said, “I don’t mean to scare you but you need to stop whatever you’re doing right now and go into the ER. I just got your preliminary images and there’s a major, major area of swelling in your spinal cord. You need to seek treatment right away.” That was exceptionally terrifying. I thought that I was going to be able to relax and see what happens, but instead it was back to the ER, where they whisked me into a wheelchair right away.
That’s when the series of diagnostic tests took place. I had two spinal taps, blood work, etc. I had four different neurologists come down to put me through strength tests, like the sharp-soft test, where they break a toothpick in half and they ask you if you can tell the sharp side from the soft side. At this point, they were trying to diagnose me through a process of elimination. 
RELATED: THE SURPRISING REASON MOST PEOPLE GET CANCER
At first, they said, “Oh, you definitely have to spend the night”, then it was two nights, then three. Every day they would come back and say, “Oh, you don’t have AIDS”, and I’d think, “Great, this is wonderful. Wasn’t hoping for AIDS.”
But in all seriousness, AIDS is an autoimmune disease, which is what MS is, so its not too far off. They would say, “Oh, you don’t have lupus. We can rule out Lyme disease.” And so on, and so on
In the meantime, my doctors were trying to reduce my spinal swelling. Every day I got a little bit more feeling back, but there was still a lot I couldn’t feel.
Then after day four or five, doctors told me that I had transverse myelitis. A neurological disorder caused by inflammation of the spinal cord, transverse myelitis can be an initial indicator of multiple sclerosis, according to Kathleen Costello, vice president of healthcare access for the National MS Society. 
There’s no one test that can determine whether or not you have MS. It was the combined results from the MRI, the spinal tap, blood work, electrical tests, etc. (not to mention, my symptoms) that led my neurologists to that conclusion. By the time I got my diagnosis, I had already figured it would be something severe based on my symptoms. Despite that, I don’t think any young woman is ready to hear that she has MS.
RELATED: DO YOU HAVE A VITAMIN B12 DEFICIENCY? ANSWER THESE 5 QUESTIONS TO FIND OUT
I’ve been told the paralysis I experienced is one of the worst ways that MS can initially present itself. To put it in perspective, when some people are diagnosed with MS, their first symptoms are blurred vision or a lack of coordination or they have a little bit of numbness in their pinky finger, says Costello.
At the worst point, the paralysis had gone all the way up to the top of my ribcage, right below my bra line, and I felt a tightness, like someone was squeezing my ribs together, making it hard to breathe and hard to walk. That, I later found out, is called the MS hug, which is a common first symptom. For me to go from a person who is boxing and doing Crossfit and yoga classes seven days a week to not knowing if Id be able to walk again, was quite shocking.
Of those who suffer transverse myelitis, around 30 percent of them are never able to walk again, another 30 percent can walk with limited mobility and residual symptoms such as spastic gait and urinary urgency, and the last 30 percent get back, for the most part, full mobility. Thankfully, at the end of my recovery, I was in that last 30 percent, and now I’m walking and moving and working out and doing most of the things I used to be able to do.
However, I now live with permanent nerve damagea common side-effect of MS. Any time it gets above 75 degrees or there’s humidity in the air, I have tingling all up and down the back of my legs and my spinal cord. I have this thing called LHermitte. It’s this weird, residual effect that happens when you put your chin to your chest, like if I’m looking down at my phone or if I’m tying my shoe. I get a weird electronic sensation from my nerves misfiring down my back. The way that I best can describe the sensation is that it feels like there’s a vibrator on your back.
Today, I tire much more quickly and I can’t do workouts that are as strenuous as what I used to do. Sometimes I can’t wear heels for too long because Ill begin feeling numbness and tingling. Im still navigating the waters of my mobility, but Im just thankful to not be confined to a wheelchair and have feeling in both my legs.
I had another attack recently, which was much less severe and less traumatizing. I lost feeling in my left arm, but this time I knew what it was and I got on steroid treatment right away. Now I have most of my feeling back with minimal permanent damage. Today, I manage my disease by adhering to a very strict, clean diet, going for MRIs every few months and blood tests every couple weeks, and taking medication and/or seeing my doctor when another attack comes on.
Theres a common misconception that MS is like ALS or that it’s this degenerative, terminal thing, that I’m just going to keep getting worse and worse and there’s nothing to stop it. It seems so much worse than it is. What I’m learning is that you can have an attack and then not have another attack for 30 years; that’s very common. On the other hand, you can have five attacks in two years, which could be really bad and result in a lot of permanent nerve damage. There is a chance that I could be in a wheelchair five or 10 years from now, but that chance is very slim. My youth and the fact that Ive led such a healthy lifestyle have both helped me recover from attacks quickly so far.
For me, the hardest part of all this is the unknown. There is no cure, so I’m waking up every morning wondering if Im going to have another attack, or if today is going to be the day where five lesions pop up into my brain and I wont walk again.
Eighty percent of people diagnosed with MS are Caucasian females in their childbearing years. Learning that statistic was shocking, but in a way, I was comforted by itI feel less alone.
RELATED: ARE YOUR PERIODS IRREGULAR? YOU COULD HAVE THIS SYNDROME AND NOT EVEN KNOW IT
The one thing I want everyone to know is that I can still live my life with this disease. A lot of people dont realize thateven my own friends.
I’ve had friends talk badly about me, saying things like, Well, if shes so sick, hows she drinking on Saturday at a rooftop brunch? and wondering why I look perfectly normal.
Its hard to be open with people because I can see how they might think Im using my disease as an excuse when its convenient. But the reality is I have bad days and I have good dayssometimes I feel ready to take on the world and other days I cant physically get out of bed.
I think thats been one of the more difficult parts for me, dealing with other peoples perceptions and judgments. Whether they think Im dying or being dramatic, its impossible for them to understand what I and other people with MS go through, which leads to misconceptions.
I dont blame people for being confused, but at the same time, I’m not going to lie down and not do things. I’m still a 25-year-old living in New York City. I’m going to have fun. I still want to date and try to find a good guyeven though that situation now comes with a plethora of complications.
At the end of the day, Im learning to appreciate every moment. Yes, it would be great to not have MS, but Im very aware of how lucky I am that my case isnt more severe. Thats been my greatest take away from this experience: Dont take anything for granted.
This article originally appeared on WomensHealthMag.com.
The post What it’s like to be diagnosed with multiple sclerosis at age 25 appeared first on apsbicepstraining.com.
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0 notes
apsbicepstraining · 7 years
Text
What it’s like to be diagnosed with multiple sclerosis at age 25
In February of 2015, after a busy weekend, I began feeling some tingling in the bottom of my feet. I thought that I was just sore from wearing heels, but within a few days, the numbness and tingling proceeded to go up my shins and into my knees and through my thighs. Id compare the feeling to when your foot falls asleep.
Although the sensation was getting more and more intense over the course of two or three days, I wasn’t super concerned. I thought that maybe my diet had played a role. I’m a very active person and I work in health and fitness PR, so I was just thinking, “Oh, maybe I’m not getting enough magnesium or something.”
After about five days of this feeling traveling inch by inch up my legs, I went to see my primary-care physician thanks to the advice of my sister, who’s a surgical nurse. My doctor quickly ordered an electromagnetic test (EMG) and an MRI to rule out meningitis, ALS, multiple sclerosis, and lymphoma. That’s when I started to get a little nervous.
The next day I went and got those tests done. By then, the numbness and tingling had become so severe that I almost couldn’t walkI could feel the pressure of the ground beneath me, but I was forcing my leg to move. By day seven, it was almost a state of complete paralysis.
The EMG was the first test and it began with them sticking needles all over my legs and then sending electromagnetic shocks through those needles to see how my nerves reacted. I’ll never forget it. The neurologist said I had severe swelling in my spinal cord, and ordered an immediate brain and spinal cord MRI.
When I was done with the MRI they said, “Go home, get some food because you’ve been in testing all day. Your doctor will likely call you and go over the results tomorrow or they’ll bring you in. Just relax.”
But within 10 minutes of me walking out of that place, my doctor called me and said, “I don’t mean to scare you but you need to stop whatever you’re doing right now and go into the ER. I just got your preliminary images and there’s a major, major area of swelling in your spinal cord. You need to seek treatment right away.” That was exceptionally terrifying. I thought that I was going to be able to relax and see what happens, but instead it was back to the ER, where they whisked me into a wheelchair right away.
That’s when the series of diagnostic tests took place. I had two spinal taps, blood work, etc. I had four different neurologists come down to put me through strength tests, like the sharp-soft test, where they break a toothpick in half and they ask you if you can tell the sharp side from the soft side. At this point, they were trying to diagnose me through a process of elimination. 
RELATED: THE SURPRISING REASON MOST PEOPLE GET CANCER
At first, they said, “Oh, you definitely have to spend the night”, then it was two nights, then three. Every day they would come back and say, “Oh, you don’t have AIDS”, and I’d think, “Great, this is wonderful. Wasn’t hoping for AIDS.”
But in all seriousness, AIDS is an autoimmune disease, which is what MS is, so its not too far off. They would say, “Oh, you don’t have lupus. We can rule out Lyme disease.” And so on, and so on
In the meantime, my doctors were trying to reduce my spinal swelling. Every day I got a little bit more feeling back, but there was still a lot I couldn’t feel.
Then after day four or five, doctors told me that I had transverse myelitis. A neurological disorder caused by inflammation of the spinal cord, transverse myelitis can be an initial indicator of multiple sclerosis, according to Kathleen Costello, vice president of healthcare access for the National MS Society. 
There’s no one test that can determine whether or not you have MS. It was the combined results from the MRI, the spinal tap, blood work, electrical tests, etc. (not to mention, my symptoms) that led my neurologists to that conclusion. By the time I got my diagnosis, I had already figured it would be something severe based on my symptoms. Despite that, I don’t think any young woman is ready to hear that she has MS.
RELATED: DO YOU HAVE A VITAMIN B12 DEFICIENCY? ANSWER THESE 5 QUESTIONS TO FIND OUT
I’ve been told the paralysis I experienced is one of the worst ways that MS can initially present itself. To put it in perspective, when some people are diagnosed with MS, their first symptoms are blurred vision or a lack of coordination or they have a little bit of numbness in their pinky finger, says Costello.
At the worst point, the paralysis had gone all the way up to the top of my ribcage, right below my bra line, and I felt a tightness, like someone was squeezing my ribs together, making it hard to breathe and hard to walk. That, I later found out, is called the MS hug, which is a common first symptom. For me to go from a person who is boxing and doing Crossfit and yoga classes seven days a week to not knowing if Id be able to walk again, was quite shocking.
Of those who suffer transverse myelitis, around 30 percent of them are never able to walk again, another 30 percent can walk with limited mobility and residual symptoms such as spastic gait and urinary urgency, and the last 30 percent get back, for the most part, full mobility. Thankfully, at the end of my recovery, I was in that last 30 percent, and now I’m walking and moving and working out and doing most of the things I used to be able to do.
However, I now live with permanent nerve damagea common side-effect of MS. Any time it gets above 75 degrees or there’s humidity in the air, I have tingling all up and down the back of my legs and my spinal cord. I have this thing called LHermitte. It’s this weird, residual effect that happens when you put your chin to your chest, like if I’m looking down at my phone or if I’m tying my shoe. I get a weird electronic sensation from my nerves misfiring down my back. The way that I best can describe the sensation is that it feels like there’s a vibrator on your back.
Today, I tire much more quickly and I can’t do workouts that are as strenuous as what I used to do. Sometimes I can’t wear heels for too long because Ill begin feeling numbness and tingling. Im still navigating the waters of my mobility, but Im just thankful to not be confined to a wheelchair and have feeling in both my legs.
I had another attack recently, which was much less severe and less traumatizing. I lost feeling in my left arm, but this time I knew what it was and I got on steroid treatment right away. Now I have most of my feeling back with minimal permanent damage. Today, I manage my disease by adhering to a very strict, clean diet, going for MRIs every few months and blood tests every couple weeks, and taking medication and/or seeing my doctor when another attack comes on.
Theres a common misconception that MS is like ALS or that it’s this degenerative, terminal thing, that I’m just going to keep getting worse and worse and there’s nothing to stop it. It seems so much worse than it is. What I’m learning is that you can have an attack and then not have another attack for 30 years; that’s very common. On the other hand, you can have five attacks in two years, which could be really bad and result in a lot of permanent nerve damage. There is a chance that I could be in a wheelchair five or 10 years from now, but that chance is very slim. My youth and the fact that Ive led such a healthy lifestyle have both helped me recover from attacks quickly so far.
For me, the hardest part of all this is the unknown. There is no cure, so I’m waking up every morning wondering if Im going to have another attack, or if today is going to be the day where five lesions pop up into my brain and I wont walk again.
Eighty percent of people diagnosed with MS are Caucasian females in their childbearing years. Learning that statistic was shocking, but in a way, I was comforted by itI feel less alone.
RELATED: ARE YOUR PERIODS IRREGULAR? YOU COULD HAVE THIS SYNDROME AND NOT EVEN KNOW IT
The one thing I want everyone to know is that I can still live my life with this disease. A lot of people dont realize thateven my own friends.
I’ve had friends talk badly about me, saying things like, Well, if shes so sick, hows she drinking on Saturday at a rooftop brunch? and wondering why I look perfectly normal.
Its hard to be open with people because I can see how they might think Im using my disease as an excuse when its convenient. But the reality is I have bad days and I have good dayssometimes I feel ready to take on the world and other days I cant physically get out of bed.
I think thats been one of the more difficult parts for me, dealing with other peoples perceptions and judgments. Whether they think Im dying or being dramatic, its impossible for them to understand what I and other people with MS go through, which leads to misconceptions.
I dont blame people for being confused, but at the same time, I’m not going to lie down and not do things. I’m still a 25-year-old living in New York City. I’m going to have fun. I still want to date and try to find a good guyeven though that situation now comes with a plethora of complications.
At the end of the day, Im learning to appreciate every moment. Yes, it would be great to not have MS, but Im very aware of how lucky I am that my case isnt more severe. Thats been my greatest take away from this experience: Dont take anything for granted.
This article originally appeared on WomensHealthMag.com.
The post What it’s like to be diagnosed with multiple sclerosis at age 25 appeared first on apsbicepstraining.com.
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0 notes