Mrs. Ram's Jams

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    • A Teacher Tale: The English Teacher Who Hates to Read Aloud

      Posted at 12:31 pm by Jeddarae, on January 23, 2021

      If I were to open my MyChart app for you, you’d see a scary list of my illnesses:  ulcerative colitis, fibromyalgia, Ménière’s, and IBS–to name a few. And while they sucketh harder than all marathons ever run collectively, most of my chronic issues are hidden beneath my cracked wide-open and bleeding (thanks visible psoriasis), painful to the touch most days (thanks invisible fibromyalgia), and purple-then-blue-then-white-then-red (thanks visible Raynaud’s) epidermis. 

      But if you were to open my classroom door and stay for a while, you’d see another of my afflictions (and I’m not talking about my very visible llama problem). While it doesn’t cause me any physical pain, the emotional distress it inflicts upon me makes me feel embarrassed and like a failure.

      You’d expect this funny, vibrant, spunky, whimsical (if I do say so myself) English teacher to be downright eloquent, a blonde version of John Keating in Dead Poet’s Society, but, y’all–I. Hate. To. Read. Aloud. In. Class. Because. I. Fuck. It. Up—-so hard. 

      Why?

      1. I read ALL the time but–to myself. And while my dad read the funnies out loud to me as a child, I don’t remember other adults consistently reading texts aloud to me. I might be misremembering, because my brain is fickle, but I’m fairly certain that by middle school, we did most of our reading for English class by ourselves. What does this boil down to? I haven’t heard a shit-ton of words that I would recognize in print ever pronounced. So throughout the years, I made up my own pronunciations. Yeah, I used to sit with a dictionary to look up a word’s meaning, but I never bothered with the pronunciation. It’s a whole hell of a lot easier now to stop and have Google’s online dictionary pronounce schadenfreude for you than it was in the 90s because a hardcover Webster’s Dictionary lacked that feature. I’ve blundered through words like caste, propitious, and scythe because I’d never heard them spoken only to have students correct me. That shit’s embarrassing. And it happens all the time. Once I even had a parent call to complain that I didn’t pronounce yeoman correctly while teaching The Canterbury Tales for the first time. Sorry that I’m not fluent in Middle English? How often is that word used in casual conversation? Also, get over yourself. I can’t ever get ahead of myself either because the curriculum is always changing. Next year? I get a brand-new curriculum (woohoo?), meaning new literature and an unexplored minefield of words I’ve never heard spoken.
      2. Y’all. The amount of Greek, Hebrew, Latin, French, and Spanish that is embedded in the texts that we read throws me for a loop as well. This Midwesterner who relocated to the deep Cajun French South only knows how to say bonjour in French. I can read some Greek, from studying abroad, and am even better at reading Russian (thanks college), but pronouncing Greek and Russian words? Nope. I bombed every Russian oral exam. Last year I taught The Odyssey, and I told the students, hey, I’ve never taught this before, there’s a lot of Greek, let’s work through this together. And it took us several rounds to remember how to say Telemachus, Antinous, Aeaea, etc., correctly. We just finished Elie Wiesel’s Nobel Peace Prize Lecture “Hope, Despair, and Memory” last week, and I know I mispronounced every single thing in Hebrew and several allusions–despite looking up how to say them beforehand. It takes time to commit how to say previously unknown words to memory. 
      3. There are just some words I can’t say. Like magnanimity. Despite listening to how to say this word on repeat, I can’t say it. I go all Nemo trying to say anemone and start thinking about magma and then the Magna Carta, and now I’ve exposed you to the rabbit hole that is my brain. Sorry!!!!
      4. Fibromyalgia. Most of the time, my fibro is invisible, but I struggle with cognitive function and brain fog if I’m in a flare, making my fibro finally visible. It’s worse in the morning and at night. What’s it like? Not being able to pronounce words that you know how to say. Slurring your words when you’re reading or talking when you are dead sober. The inability to find the word you want to use, even when it’s staring you dead in the face. Transposing letters in words. Saying one word when you meant to use a different one. Not being able to form a sentence period in the morning when you’re supposed to get students excited about literature and the kids look at you like you’re stupid when language fails you. And now that I’ve written this, I wonder just how much my fibro prevents me from mastering numbers 2-3.

      So how does this English teacher who hates to read aloud because she can’t spoken-word well cope? She relies heavily on audio versions of texts, and when she can’t find audio, she explains herself and asks for a little grace. 

      As a teacher, talk about your own struggles, issues, illnesses, etc., to normalize that it’s okay to discuss things that society would rather see swept under the rug. There’s nothing wrong with saying, “Hey, Mrs. Ram Jam is struggling today due to a fibro flare, so please excuse her as she tortures your eardrums while she reads this aloud to you.”

      And answer their questions if they have any, and move on. Some of them will judge you, no matter what you say (or in my case how you say it), but you’d be surprised how forgiving students (and people in general) can be when you’re honest about your own limitations and invisible battles you might be fighting. 

      Posted in education, fibromyalgia, meniere's disease, teaching, ulcerative colitis, Uncategorized | 0 Comments | Tagged english teacher, fibromyalgia, invisible illness, reading aloud, teachers who curse
    • Chronic Illness: My Bad Experience with Plaquenil

      Posted at 1:43 am by Jeddarae, on February 23, 2019

      At my biannual rheumatologist appointment in December, my doctor suggested I try the drug Plaquenil. Not only does it treat malaria, it also helps rheumatoid arthritis and Lupus. I have none of the aforementioned diseases but have positive ANA and other autoimmune red flags (sans a diagnosis). He warned it’s a well-tolerated drug but slow acting, taking about three months to kick in.

      At our visit’s end, he handed me informational printouts about it for homework and told me to call him when I made a decision.

      When I got home, I skimmed and scanned the side effects and the standard fare was presented: upset stomach, headache, rash, etc. One of its terrifying side effects is it can cause serious eye damage if taken for long periods of time. I conducted further research via Google, but concluded it didn’t seem overwhelmingly scary besides that whole hey-you-might-lose-your-vision thing.

      I talked to a friend who has Lupus and another who has RA who both take it. They said it mildly agitated their stomachs but overall had positive results.

      I deliberated over my decision. In general, I don’t tolerate medicines well, which is a lesser known fibromyalgia symptom. I don’t even take fibromyalgia medicine because it makes my muscle pain worse, causes extreme gastrointestinal distress, or gives me the spins.  

      But I trust my rheumatologist, and I gave him the go ahead to send in the prescription. I started popping my 200 mg pill daily.

      A mean a girl can dream that there’s a miracle drug for her, right?

      Five weeks into treatment, the backs of my arms started itching. Normally this isn’t too concerning. I have a tendency to get an I-inadvertently-consumed-something-with-wheat-in-it-rash in that exact spot. By Saturday though, my knees were bright red with clustered, itchy bumps. It kept me up Saturday night, and Sunday morning it spread to the back of my legs.

      When I pulled out my pill bottle that morning, it clicked. The Plaquenil had to be causing the rash.

      I sent a message to my doctor. Apparently because it’s a slow acting drug, it can take weeks for side effects to kick in–ughhhhhhh.

      Goober that I am, I thought as soon as I stopped taking the medicine the rash would go away.  Hahahahahahahahahahaha. It continued to get worse all week. Benadryl didn’t help.

      Friday morning, the rash had transmogrified into full blown hives up the back of my right leg. Lucky me! An allergic reaction!

      I hauled myself to a step-in clinic at the local hospital where the nurse practitioner explained that since I took the drug for six weeks it would take six weeks for it to get out. She gave me steroids for the hives and told me they could come back, which they did. Two days ago. So much ugh.

      Look, I realize I’m lucky; I had a mild allergic reaction. But now, I’m even warier of starting new medications–particularly if labeled as slow acting. Who wants side effects, let alone delayed ones, or even delayed allergic reactions? Who wants to be dealing with hives for six weeks (especially when there’s no honey and nary a queen bee)?

      I’m aware that was a bad joke. Deal with it. It made me forget I have hives for a split second. At this point, I’ll take what I can get.

      honeycomb close up detail honey bee

      Photo by Pixabay on Pexels.com

       

       

       

       

      Posted in chronic pain, fibromyalgia, Uncategorized, writing | 3 Comments | Tagged allergic reaction, blogging, blogs, chronic illness, fibromyalgia, hives, invisible illness, plaquenil, positive ana, writing
    • September is Pain Awareness Month

      Posted at 11:24 am by Jeddarae, on September 22, 2018

      It’s that time of year again.

      Back to school supplies have been replaced with Halloween decorations in Target’s seasonal aisles. Basic girls in their twenties, pretending they’re professional photographers, are staging pumpkin spice lattes on tables, snapping pictures of their overpriced coffees, swiping right until landing on the perfect filter, and then posting their faux artwork on their Instastories. Football fans are gorging themselves on a smorgasbord of touchdowns, tailgates, and tallboys, an all-American weekend buffet.

      But it’s also the time of year for Mrs.Ram’s Jam to write a pain awareness post because September is Pain Awareness Month.

      Because while the shelf stocker at Target was swapping out the display of Ticonderoga #2 pencils for skeleton wreaths, he was suffering from a migraine.

      Because even though sorority girl Sally’s posts seem overbearing, she was crippled with a fibromyalgia flare all week and is celebrating its end with an expensive coffee and Instagram.

      Because while the biggest Saint’s fan in New Orleans hollers “Who Dat”  in the Superdome on Sunday at noon, he’s masking the pain of the pinched nerve in his lower back that’s causing him to consider going on disability.

      Because one in three Americans suffer from pain.

      Because pain sufferers suck it up and trudge on when they can and deserve to be heard.

      Because pain sufferers deserve to be heard when it gets to be too much. 

      And because, as always, pain only remains invisible if isn’t discussed.


      For more information about Pain Awareness Month, visit the American Chronic Pain Association’s website.

      For more information about pain, visit the American Academy of Pain Medicine’s website.

      Here are links to other posts about pain and chronic illness by Mrs. Ram’s Jams:

      Chronic Pain Awareness

      A Poem: Invisible Illness Idioms

      My New Normal: Meniere’s Disease

      Is That My Invisible Illness, Am I Dying, or Is It Something Less Drastic Than Death but Still Needs To Be Treated?

      Chronic Illness: Playing Phone Tag with Doctors’ Offices

      Fibromyalgia Flare Friday

       


       

      Posted in chronic pain, fibromyalgia, Uncategorized | 2 Comments | Tagged blogging, chronic illness, chronic pain, fibromyalgia, ibs, meniere's disease, pain awareness month, raynauds
    • Is That My Invisible Illness, Am I Dying, or Is It Something Less Drastic Than Death but Still Needs To Be Treated?

      Posted at 6:35 pm by Jeddarae, on August 3, 2018

      It’s three days before the new school year starts, and I have E. coli. For real. The bad E. coli–where antibiotics are necessary.

      Want to know what floors me? I was oblivious to the severity of the matter until Wednesday evening when my doctor’s office called and informed me.

      You’re probably thinking to yourself, Mrs. Ram Jam, how in the French toast were you unaware when you experienced the classic symptoms: nausea, abdominal pain, fatigue, diarrhea, and malaise? Are you also one of those women who didn’t know she was pregnant until she sneezed and a baby came out?

      To answer the latter question–no. But to answer the former–these symptoms are a mere fraction of my normal. I just thought my IBS was flaring with the fire of a thousand suns.

      I’m going to be honest; 85 percent of the time, I’m in a shit ton of pain. It could be fibromyalgia, IBS, Raynaud’s, or Meniere’s Disease induced. I’m not looking for sympathy or to complain. It’s my truth, and as always, invisible illness remains invisible if its sufferers remain silent.

      Because I’m in pain most days, it’s pretty damn tricky to determine if new or increased intensity pain is due to chronic illness or if it has a different cause.

      Overwhelming fatigue? Is that my fibro flaring because of a midsummer cold front storming across Louisiana or a vitamin B12 deficiency, anemia, or strep throat? OR DO I HAVE THE PLAGUE???

      Radiating tender point hip pain? Is that fibro induced too or a vitamin D deficiency and a case of weak hips that needs three months of physical therapy? OR ARE MY BUTT CHEEKS GOING TO FALL OFF WHILE I SLUMBER???

      Bowel habit shifts and abdominal pain? Is my IBS pitching a hissy fit because it’s impossible to control while traveling or could it be small intestine bacterial overgrowth or E. coli? OR DO I NEED AN EMERGENCY COLOSTOMY???

      Most of the time my pain is due to chronic disease, but occasionally it’s something else. For example within the past six years, I’ve dealt with all of the diseases, physical therapy, and deficiencies listed above (excusing the all capped crazy thoughts of course). I initially chalked all these maladies up to my chronic illnesses.

      I’m lucky this bout of E. coli coincided with a regularly scheduled trip to the gastroenterologist; otherwise, it could have gotten awful before I convinced myself I needed a doctor.

      So how do I tell the difference?

      I can’t. When the pain gets different, unbearable, or alarming for too long, I schedule an appointment, describe my symptoms to my doctor, and try to convince myself I haven’t contracted botulism in the interim.

      And that’s part of what’s terrifying for invisible illness sufferers. We live in a habitual game show entitled: Is That My Invisible Illness, Am I Dying, or Is It Something Less Drastic Than Death but Still Needs To Be Treated?

      Unfortunately, I didn’t win a new car this episode, just E. coli. Which might be the worst thanks-for-playing parting gift ever. Who’s producing this game show anyway? You’re the suckiest. I hope the network drops you midseason and you get E. coli too.

      (P.S. How the hell did I get E. coli? *shudders violently* Okay, universe, you can keep that secret for eternity.)

       

      Posted in chronic pain, fibromyalgia, meniere's disease, Uncategorized, writing | 3 Comments | Tagged blogging, blogs, chronic illness, chronic pain, fibromyalgia, ibs, invisible illness, meniere's disease, writing
    • Chronic Illness: Playing Phone Tag with Doctors’ Offices

      Posted at 5:32 pm by Jeddarae, on June 8, 2018

      Because of chronic illnesses (fibromyalgia, Meniere’s disease, Raynaud’s, and IBS), I frequently contact my general practitioner, rheumatologist, ENT, and gastroenterologist.  Unfortunately, talking to someone alive the first go-round never happens.

      My doctors work for large hospital systems. For patients, no direct lines to a specific doctor’s office exist. I call the main hospital phone, listen to an automated message, press a bunch of numbers, get transferred to the doctor’s nurse’s line, and leave a message.  

      I completely sympathize. Medical professionals are overloaded just like teachers and can’t be constantly available therefore they use technology to filter and take messages.

      Also, I’m not calling to get free medical advice over the phone. I see my gastroenterologist every six weeks and my rheumatologist and ENT every six months. I schedule these appointments weeks or months in advance because it takes weeks or months to actually get an appointment. When my health suddenly shifts and I need specialist care, I call to make an appointment and often none are available. That’s when I resort to phone tag with doctors’ nurses because my doctors have expressly stated I can call and they will help via phone.    

      During the school year, it’s even harder to get in contact with doctors because I’m at work and in class before doctors’ offices open, I can’t call while I’m teaching, and my first break isn’t until 12:45 p.m. Then it normally takes an hour or two (or 24) for a return call.  (Again, I don’t expect an instantaneous return call. It’s like students expecting me to grade 100 five paragraph essays magically as soon as they get handed in. Not happening.)

      And if I miss the return call, then it’s necessary to repeat the aforementioned process because 98 percent of the time my call is returned when:

      • I’m using the bathroom, and my phone is on the kitchen counter, halfway across the house;
      • I’m driving through a school zone (No I don’t have bluetooth in my car, and yes it is still legal in Louisiana to be on a handheld device while driving–but not in school zones.);
      • I’m in class, and answering phones while teaching is severely frowned upon. #TeacherProblems;  
      • It’s my off period, and I could answer my phone, but I don’t get service in my classroom so by the time I sprint to an area with service, I’ve missed the call.  
      • I’m speaking with a different doctor’s nurse, and it’s rude to say, “Can you hold on for a sec?”;
      • Little Thing, watching Youtube Kids, has my phone and hangs up purposely instead of answering;
      • I’ve accidentally left my phone in the car for two minutes;  
      • I’ve forgotten to switch my phone off silent after the workday ends or after I wake up;

      OR

      • It’s 3:58 on a Friday afternoon, any bullet from above (except number three) conspires against me, and the doctor’s office closes at four–so I’m shit out of luck until Monday and the whole vicious cycle repeats.     

      I hate playing phone tag with the doctor’s office. The whole process is a colossal fiasco.  

      It’s 2018 people. I challenge the world to figure out a better way for doctors’ offices to communicate with patients.  A three or four phone call interaction per individual instance is comically ineffective.

      (I’ve even tried direct messaging doctors’ offices through apps like MyChart, but I’ve never gotten a written message back. The nurse calls in response to the emailed message. Go figure.)

      Surely the doctors’ nurses find themselves frustrated, too. Returning patient phone calls can’t be their only professional responsibility.

      How much time and money are wasted per salaried professional because of calling the same patient repeatedly over the same issue?

      Maybe it’s minimal, but the notion nags me–just like the fact that they’re never available when I am.    

      Posted in chronic pain, fibromyalgia, meniere's disease, Uncategorized, writing | 2 Comments | Tagged blogging, calling the doctor, chronic illness, chronic pain, fibromyalgia, meniere's disease, teacher problems, teaching, writing
    • Fibromyalgia Flare Friday

      Posted at 10:18 pm by Jeddarae, on April 27, 2018

      I’ve spent most of this week in fibromyalgia flare denial. But the tell-tale roaming muscle aches and spasms, the stabbing take my breath away jabs, the unable to form sentences or the inability to find the words I want to say attacks, and the overwhelming fatigue can’t be denied.

      Today, I’m on the downward slope of a five day flare.  

      I’ve managed to keep my fibro under control for two years, and I’m fairly successful containing it with exercise and diet.

      However, I’ve had right foot ailments, sesamoiditis and bursitis, since February, and I’m three weeks out of an orthopedic walking boot. My body is a wreck from walking misaligned for two months. My back is so stiff that a surfer could ride a gnarly wave with it. My left hip, a rusted shut nut and bolt, feels like Tim the Toolman Taylor is ratchet socket wrenching it unsuccessfully and brutally every time I take a step. My foot is mending, thank God, but my altered gait and the accompanying out-of-whack pain is definitely a flare-up offender.

      The second offender is the hit to my mobility. Normally, I can walk to keep the fibro pain at bay, but that’s impossible with a swollen big toe and an inflamed bone and fluid sac in the bottom of my foot. I normally average about 11,000 steps a day, but I rarely topped 5,000 during my boot stint–sometimes only hitting the 2,000 step mark. It seems counterintuitive, but the less fibromyalgia sufferers move, the more they hurt. And my body has declared anarchy because its walking rights have been violated. I’m hitting my average again, but the struggle and the pain sidecar has me feeling like I’m taking two steps forward and three steps back literally and figuratively.  

      Thirdly, my stomach is a disaster because of two rounds of prednisone and sundry anti-inflammatory drugs. Both are hard on tummies anyway, and often fibromyalgia sufferers don’t tolerate medicines well, experiencing side effects from them more strongly than other people do. I am no exception. My body abhorred every single prescription NSAID I swallowed and a couple locked my gut up tighter than Fort Knox. Ultimately, too many meds scalped my digestive track raw. When my stomach gets pissed for longer than a week, I know a fibromyalgia flare is in the future. The medicine has aggravated my IBS, too.  As a matter of fact, about 70 percent of fibromyalgia sufferers also have IBS (citation here). A parasitic symbiotic relationship, the two chronic illnesses are inextricable in my case.

      To finish, the previous three factors make sleeping challenging, and with fibro, lack of sleep makes everything: So. Much. Worse.

      I haven’t had to take a fibro day off from work in years. But twice this week, I didn’t know if I could physically make it to work, but I did.  I only sucked it up because we’re in the middle of state testing.

      I am feeling more myself today, and eventually all flares end.   

      Like I’ve said previously, I’m not writing to complain. I’m just writing to vent.

      And as always, it only remains invisible if we don’t discuss its existence.  

      fibromyalgia banner

      Posted in chronic pain, fibromyalgia, Uncategorized, writing | 11 Comments | Tagged blogging, blogs, chronic pain, fibro, fibro flare, fibromyalgia, invisible illness, writing
    • A Mrs. Ram’s Jams Tale: Death of a Pair of Skinny Jeans

      Posted at 10:23 pm by Jeddarae, on February 8, 2018

      Before bed last night, I had to cut my skinny jeans off my body.

      IMG_0107

      Why, you might ask?  

      My only other option was to drive home from the emergency room pantless.

      While I support the anti-pants movement more devotedly than any political movement, driving home partially naked in the wet, chilly weather with a cumbersome semi-permanent splint on my right foot sounded like a surefire way to cause an accident. Or an awkward arrest for indecent exposure.

      So after navigating home, I murdered my dark blue skinny jeans with cheetah handled kitchen shears.

      What exactly led me to the emergency room and first degree denim homicide?

      I wish someone could tell me because the events leading to the crime are fuzzy in my mind.  

      Does that mean I can plead temporary insanity?  

      Or at least get dropped to negligent pantslaughter?

      Here’s my confession through self examined blog deposition.

      The exposition of this murder thriller begins with a book . . . honestly.

      After blowing bubbles with Little Thing and picking up palm tree debris from the yard on Sunday afternoon, I cozied into my bed for a book date with Leigh Bardugo’s Crooked Kingdom.  

      When I reached a good breaking point, I stood to stretch. The ball of my right foot twinged upon contact with the hardwood floor. It felt like a Cheerio or sticker were stuck to the bottom of my foot.

      I sat back down on my bed to remove the unwanted hitchhiker and flipped my foot.

      Instead of seeing the expected trash attached, I saw a bubble of my skin ballooning into a tiny island on my foot’s sole.  

      That’s weird, I thought.

      Then the swelling began with gusto, and it oddly didn’t hurt.  

      I vacillated between icing it and hauling my booty to Urgent Care.

      I didn’t want to hobble in and come off as a dumb blonde, but that’s what happened.

      After X-rays, I left Urgent Care with a contusion diagnosis and a pat on the back from the nurse practitioner that said,  “You poor stupid thing; thanks for wasting my time.”

      As the bruise blossomed and kaleidoscoped my foot’s side into an aurora borealis of blacks and purples, I limped through Monday with the swelling receding by Tuesday. The pain felt no worse than the normal constant static of fibro pain.

      Yesterday in misguided brazenness, I sported low heeled black booties to work. By day’s end, my foot’s left side reached hobbit foot level ugliness. It throbbed, and nausea hit me with every step. It felt twelve different kinds of stabby stabby throbby throbby.  

      I googled my symptoms. Irrationally, I convinced myself I had a blood clot.  

      When six o’clock hit, I gave into the pain.  

      Fearing pulmonary embolism, I drove myself to the emergency room. The x-ray technician there assuaged my blood clot fears by assuring me deadly ones cannot develop in feet. She admirably held a straight face through the duration of our conversation.     

      My temporary mollification transfigured into mortification when another ER tech entered with fittings for a splint.

      I looked at my skinny jeans and side-eyed the slab of malleable bulky plastic thingy she was saturating with water.  

      “Is that permanent?” I asked.

      “No, but it’s permanent until you see the orthopedic surgeon.” She shrugged.

      “What about my pants?”

      “Unless you want to drive home naked, I suggest you cut them off when you get home.”

      To add further insult to injury, the ER doctor returned with his diagnosis:  a sprained foot with a possible tendon tear.

      sprain

      How could I sprain my foot and tear my tendon BY DOING NOTHING?

      He explained that when muscles are relaxed it’s not unheard of to damage them by simply stepping down.  

      So there you have it folks.

      I’m probably the only person on the planet to have ever sprained her foot because she was so relaxed from reading, ending with the denouement of skinny jean assassination.

      But is this the resolution, or merely the ending of blog one in a series of posts?  

      This lovely turn of events coincide with a pre-planned solo trip to Chicago over the Mardi Gras holiday. I fly out Saturday. Chiberia is supposed to get a foot of snow on Friday, and I’ll more than likely be rocking crutches during the duration.  

      What could go wrong?

      WHO CARES?  THIS GIRL HAS HAMILTON TICKETS!!!

      (P.S. Little Thing can’t be bothered with saying crutches. She’s deemed mine “those squeaky things.”)

      Also, think happy thoughts for me tomorrow while I’m at the orthopedic surgeon.

      Posted in reading, Uncategorized, writing | 7 Comments | Tagged blogging, blogs, fibro, fibromyalgia, jeans, reading, sprains, writing
    • Mrs. Ram’s Jams New Year’s Resolutions

      Posted at 9:06 pm by Jeddarae, on January 11, 2018

      Because my birthday falls on January seventh, my New Year’s resolutions never appear prior to January’s second full week. I’m a firm believer of birthday indulgences. I refuse to let my birthday get in the way of resolutions; therefore, I wait to avoid failure.

      Because intentional failure is stupid.

      But unexpected failure happens all the time for me.

      For example in a moment of lice inspired weakness before Christmas break, I lamented to my principal that I’m an idiot, relinquished all knowledge, and begged her to be my life coach. In the hallway. Loudly. With students and other teachers around.  

      That, my friends, is failing at life.

      As is catching lice at nearly 35. 

      (For my lice debacles, check out these posts: A Little Thing Tale: Merry Licemas and A Mrs. Ram’s Jams Tale: Happy Lice-a-Days)

      And I’m disconcertingly at peace with my spectacular fails.       

      Anyway, here are my resolutions.

        1. Read less. Write more. Instead of inhaling books at an alarming rate, I’m stepping back a notch. I’ll be just fine if I read 60 books instead of 119, allowing me more writing time. I’ve posted weekly since starting the blog, but often I’m scrounging around at the last minute trying to post something before my weekly Saturday self-imposed cutoff (because I’m caught up in a book). Writing is greater than reading in 2018.  
        2. Break the bad habit of spacing twice after a period. WHO KNEW THAT THIS IS NO LONGER A THING, AND HOW COME NO ONE HAS ALERTED THE MASSES??? Or were the masses alerted, and I missed it? Again, another life fail.  
        3. Do yoga everyday (barring contracting bubonic plague, botulism, or whatever more plausible virus is contaminating my middle school). I’ve done yoga everyday since November 13–that’s 60 days in a row! Might as well see if I can keep it up. I can already see the difference, and my back has NEVER felt better. My muscle inflammation is essentially nonexistent. On days that I know I can’t handle 30 minutes, I try to do a gentle 15 minute practice. On top of daily practice, I want to learn about yoga’s history, too.
        4. Brush up on my Russian. I was three classes short of graduating with a minor in Russian from the U of I. The department head, who I loved, left after my sophomore year and was replaced with a scary lady. By junior year, I was one of the few non Russian students. Feeling overwhelmed, I said dosvedanya and left the foreign language building’s basement. Fast forward a decade and I’ve forgotten everything I was taught except how to read it. (Okay that’s not true. The first full sentence from the Russian 101 textbook was лифт никогда не работает, which means “The elevator never works.” Why? Why was this the first thing I learned. Do elevators consistently refuse to work in Russia??? Also the Russian word for water is вода, pronounced voda. It’s. Only. One. Letter. Away. From. Vodka. Can I start calling water “wineter”? Do you think I can pull it off? Or is this a Gretchen Weiners-esque fetch pipe dream?) I dilly-dallied over relearning Russian last summer but was unwilling to fully commit. Rosetta Stone’s new best friend will be Mrs. Ram Jam this year. (Again, life fail. I’d like you to meet my future summer time best friend, Rosetta. I bought her for $179. She’s reteaching me Russian, and she’s not a real person.)
        5. Secret Resolution. Sorry! I’m being that girl.  

      Are these difficult resolutions to keep? Heck no! If I read 119 books, started a blog, mommed hard, taught hard, had a septoplasty, and visited four different doctors regularly in 2017, then 2018’s resolutions should be easy peasy lemon squeezy.

      (P.S. teaching a tiny Little Thing how to say easy peasy lemon squeezy was hilarious. I caught it on video circa three years ago. You’re welcome.)  

       

       

       

       

       

      Posted in books, chronic pain, fibromyalgia, fitness, reading, Uncategorized, writing, yoga | 0 Comments | Tagged books, chronic pain, fibromyalgia, lice, little thing, new year, new year's resolutions, reading, reading goals, writing, yoga
    • A Poem: Invisible Illness Idioms

      Posted at 10:57 pm by Jeddarae, on December 8, 2017

      Because sometimes you need to vent when you have invisible pain.  Because sometimes haters are going to hate.  And because it remains invisible if you don’t talk about it.


      I’m a pain in the ass, full of shit, lend me your ear, and put a sock on it
      because of fibromyalgia, IBS, Meniere’s, and Raynaud’s chronic disease fits.

      I’m a pain in the ass,
      a daily debacle that will never pass.
      No matter how much I tweedle and wheedle,
      I smell something fishy and am on pins and needles.
      I carry the weight of the world on my shoulders
      and my body betrays me as it twitches and smolders.
      I’m a taste of my own medicine,
      but I can’t take any because it glues my innards together and turns my muscles to gelatin.
      I’m a pain in the ass
      that will never pass.

      And full of shit
      that’s hard to pass,
      leaving me feeling like a twit.
      I’ve got a gut feeling that sends me reeling.
      I can’t have my cake and eat it too
      without a flare up coming out of the blue.
      I don’t have a cast iron stomach.
      Most culinary delights leave my digestive track flummoxed.
      I feel like I’m eighty-six,
      and I’ve had to eighty-six Cajun concoctions in cast iron pots because of my tummy.
      Gone are all the foods that are satisfying and yummy,

      including salt,
      but that’s my inner ear’s fault.
      Go ahead, lend me your ear.
      I’ve got loads to tell you about my diseases that you don’t want to hear.
      Don’t get bent out of shape
      because I am bent out of shape.
      I’ll take your ears and attach them to my own with tape,
      so I can hear what you have to say dear.
      I’d love you to lend me your ear.  
      But I’m just a dizzy dame
      who is going slowly lame.

      I’d bend over backwards
      to be able to bend over forwards.

      And I’ll put a sock on it
      as well as gloves
      to get my hands and feet to stop it,
      my loves,
      from looking like they’re from a cadaver.

      But people still can’t figure out what is the matter.

      They say I’m full of shit and a pain in the ass
      and to stop being so crass.
      They don’t want to lend me their ears 
      because of their own piddling fears.
      They’d rather I’d put a sock on it.  
      It’s been listed first on my “how do I make my diseases easier for you” docket
      for years because you’d rather I’d wear your rose colored glasses.
      But now I’ll wear my rose colored glasses for fashion and call you a fascist.

      Because you think I’m a pain in the ass and full of shit.
      Because you won’t lend me your ear.
      And because I’m tired
      of putting a sock on it.

      Posted in chronic pain, fibromyalgia, meniere's disease, poetry, Uncategorized | 2 Comments | Tagged chronic pain, dizzy, fibromyalgia, ibs, idioms, invisible illness, meniere's disease, poems, poetry, raynauds
    • Reading Goal Achieved: 100 Books Read

      Posted at 11:02 pm by Jeddarae, on November 2, 2017

      When I set a goal for myself to read 100 books this year, I didn’t know if I would succeed. But ta da! With two months to spare, I reached my goal on Sunday. Can I get a whoop whoop?

      How did I read 100 books before the end of October? I’m a bit mystified myself as to how I achieved this milestone, but the following list helped me achieve my goal (some might sound familiar from this previous post– Thirty Seven More to Go).

      1. For the most part, I don’t watch TV–except for Sunday morning NBC programming. I adore Willie Geist and Chuck Todd.
      2. My phone stays on silent. I have never been a phone talker. I was even slow to come around to the idea of texting during its advent and subsequent rise to ubiquity. And while I do peruse Facebook, Pinterest, and WordPress daily, I don’t spend hours on social media.  
      3. Although it took some coaxing, Little Thing is fairly independent, and I encourage her autonomy.  Yes, I stop and have dance parties, play games, craft, or bake with her. However, I refuse to stimulate her constantly.  
      4. I read when I can. When Little Thing has tumbling on Tuesdays, I read during her 45 minute class. I read while I’m waiting in primary school carpool, walking in circles around my kitchen, and waiting at the doctor’s office.  
      5. Fibromyalgia and Meniere’s disease has kicked my booty this year. Because of both diseases, my activity level has plummeted in comparison to previous years. If I can’t handle keeping myself upright anymore, I’m flat on my back with a book in my hand to dull the pain.
      6. I made a commitment by putting it in writing; therefore, I made it a point to carve out time.

      In hindsight, I probably could have read more if I hadn’t decided to start this blog. But this blog’s been fun and provided me with a place to vent, reflect, and grow.  

      Thank you to my friends who suggested books the past couple of months. I adored the books recommended to me, and because of them, October ended on a sweet note.  

      Now excuse me while I go bask in my goal achievement glory, resonating in imagined rainbows, sparkles, and cheers erupting firework style in the confines of my overactive imagination . . . and celebrate with another book and Thursday night wine.  

      Here’s my full list of 100 books. 

      (Once again, please forgive my formatting issue in May like in this previous post–Books Read: First Half of 2017; I cannot figure out how to fix it.)  

      January

      1. The Glass Magician (Book 2)–Charlie N. Holmberg
      2. Beautiful Ruins–Jess Walter
      3. The Probable Future–Alice Hoffman
      4. Here on Earth–Alice Hoffman
      5. Beautiful People (accidental reread)–Wendy Holden
      6. What She Knew–Gilly Macmillan
      7. The Girls–Emma Cline
      8. Commonwealth--Ann Patchett

      February

      1.  Mr. Mercedes (Bill Hodges Trilogy Book One)–Stephen King
      2.  Atonement–Ian McEwan
      3.  The Red Garden–Alice Hoffman
      4.  Finders Keepers (Bill Hodges Trilogy Book Two)–Stephen King
      5.  The Couple Next Door–Shari Lapena
      6.  A Man Called Ove–Fredrik Backman
      7.  Is Everyone Hanging Out Without Me–Mindy Kaling
      8.  The Curious Charms of Arthur Pepper–Phaedra Patrick

      March

      1.  End of Watch (Bill Hodges Trilogy Book Three)–Stephen King
      2.  It Ends with Us–Colleen Hoover
      3.  The Vacationers— Emma Straub
      4.  Dark Matter-Blake Crouch
      5.  The Road–Cormac McCarthy
      6.  The Woman in Cabin 10–Ruth Ware
      7.  Why Not Me–Mindy Kaling
      8.  Yes Please–Amy Poehler
      9.  Red Queen–Victoria Aveyard
      10.  Today Will Be Different–Maria Semple
      11.  Pretty Girls–Karin Slaughter

      April

      1.  Heartburn–Nora Ephron
      2.  Glass Sword–Victoria Aveyard
      3.  We Need to Talk about Kevin–Lionel Shriver (accidental reread)
      4.  Big Magic–Elizabeth Gilbert
      5.  Modern Lovers–Emma Straub
      6. King’s Cage–Victoria Aveyard
      7.  The Underground Railroad--Colson Whitehead
      8.  The Sellout–Paul Beatty
      9. On Writing–Stephen King
      10.  Eligible–Curtis Sittenfield

      May

      38  Shotgun Lovesongs–Nickolas Butler

      1. The Color Purple–Alice Walker
      2.  Before the Fall–Noah Howley
      3.  You–Caroline Kepnes
      4. The Magicians–Lev Grossman
      5.  Nine Women, One Dress–Jane L. Rosen
      6.  The Forgetting Time–Sharon Guskin
      7.  Talking as Fast as I Can–Lauren Graham
      8.  Caraval–Stephanie Garber
      9.  The Expats–Chris Pavone
      10. Rich and Pretty–Rumaan Alam
      11.  Saving Grace–Jane Green
      12.  See Jane Run–Joy Fielding
      13.  The Sympathizer–Viet Thanh Nguyen

      June

      1.  Here’s to Us–Elin Hilderbrand
      2. Perfect–Rachel Joyce
      3.  Bittersweet–Miranda Beverly-Whitemore
      4.  Snobs–Julian Fellowes
      5.  The Fifth Petal–Brunonia Barry
      6.  Someday, Someday, Maybe–Lauren Graham
      7.  The Girl You Left Behind–Jojo Moyes
      8. The Lace Reader–Brunonia Barry
      9. The Avenue of Mysteries–John Irving
      10.  Vampires in the Lemon Grove–Karen Russell
      11.  One Plus One–Jojo Moyes
      12.  This Is How It Always Is–Laurie Frankel

      July

      1.  It Was Me All Along–Andie Mitchell
      2. Between the World and Me–Ta-Nehisi Coates
      3.  Annihilation–Jeff Vandermeer
      4.  In the Dark, Dark, Wood–Ruth Ware
      5.  Beartown–Fredrik Backman
      6.  Neverwhere–Neil Gaiman
      7.  The Uncommon Reader–Alan Bennett
      8.  I am Malala–Malala Yousafzai
      9. Bone Gap–Laura Ruby
      10. Crazy Rich Asians–Kevin Kwan
      11. The Shadow of the Wind--Carlos Ruiz Zafron

      August

      1.  Nutshell–Ian McEwan
      2. The Wonder–Emma Donoghue
      3.  The Solitary House–Lynn Shepherd
      4.  American Gods–Neil Gaiman
      5. A Conjuring of Light–V.E. Schwab
      6.  Are You Sleeping–Kathleen Barber
      7. It Happens All the Time–Amy Hatvany
      8. Bossypants–Tina Fey
      9. Pretty Little Liars–Sara Shepard
      10. The Wednesday Wars–Gary D. Schmidt
      11.  Flawless–Sara Shepard

      September

      1. Life After Life–Kate Atkinson
      2.  Perfect–Sara Shepard
      3.  Unbelievable–Sara Shepard
      4.  Rich People Problems–Kevin Kwan
      5. Into the Water–Paula Hawkins
      6. The Muse–Jessie Burton
      7. The Girls in the Garden–Lisa Jewell

      October:

      1. Every Fifteen Minutes–Lisa Scottoline
      2. The Devil in the White City–Erik Larson
      3. The Keeper of Lost Things–Ruth Hogan
      4. Every Last Lie–Mary Kubica
      5. Saints for All Occasions–J. Courtney Sullivan
      6.  The Keepers of the House–Shirley Ann Grau
      7. All Over but the Shoutin’—Rick Bragg
      8. The Lonely Hearts Hotel—Heather O’Neill
      Posted in books, chronic pain, fibromyalgia, reading, Uncategorized, writing | 5 Comments | Tagged 100 books, books, fibromyalgia, meniere's disease, reading, reading goals, writing
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