Revere Beach is the first public beach in the United States (1896) and it’s absolutely gorgeous. Every year, since 2004, people from all over the world come to the area for a three day competition to design the creations before you, and it’s estimated that roughly one million people flock in to see these designs.
I was disappointed by this year’s winner, but I think it’s safe to say these are all pretty unique. If you’re ever in Boston, this is a place worth a few hours of your time. It’s a five mile long beach. 🌊🐚🌅🏄🌞
I may have shared the quote below last year around this time, or not. If it’s repetitive, it’s not intentional.
My mind has been focused a lot these days on home and my deceased loved ones.
Some people leave their hometowns and eventually feel no ties to wherever it is they’re from. I’m not one of them.
Home is deeply engrained in my soul. Going back is painful. And yet, the streets know my name and my blood feels calmer there. It’s more than a place, more than memories, and more than one particular moment. It simply IS.
When asked where I’m from, it’s an automatic reply. In Massachusetts, they ask because I, “talk funny”. It rarely occurs to them that I simply don’t have a Boston accent. Having filmed periodically over the last few months, I have noticed that, on film, I don’t sound the way I do in my daily life. I have, however, noticed that my accent (Which is one of many. Polyglots can often find themselves “stuck” in an accent if they’ve been thinking in a language and actively using it. I regularly take on an accent if I’ve talked to someone who isn’t American and speaks a language I know, or am extremely familiar with. In regular conversation with a friend, he jokingly noticed my “perfect London accent.” As I type this, I can hear his voice and in turn, my brain switches into the accent he mentioned. I’ve been doing it a lot lately without realizing it. 🤷 He refers to it as “Star Bird Lisa”. That’s a compliment.) is this overly perfected, “middle of nowhere” American English. I NEVER noticed the gradual change until my best friend pointed it out. But when I’m exhausted beyond words, I hear my accent completely change. Inevitably, each one will end up on film. Hopefully I’ll amuse someone besides myself.
Where was I going with this? Home. It’s not just a place. It’s my heart.
Sleep well, mes amis. 😗
“The tears I feel today
I’ll wait to shed tomorrow.
Though I’ll not sleep this night
Nor find surcease from sorrow.
My eyes must keep their sight:
I dare not be tear-blinded.
I must be free to talk
Not choked with grief, clear-minded.
My mouth cannot betray
The anguish that I know.
Yes, I’ll keep my tears til later:
But my grief will never go.”
*In Memory Of My Grandfather…Великою людиною дійсно ніколи не може бути втрачено або забуто- A great man can never truly be lost or forgotten.*
This day is emblazoned within my mind. I would learn so much within a forty-eight hour span of time, and I would be permanently changed. But no one tells you that when you’re a child. No. They try to keep you “innocent”. Except in my family. My mother decided I was not going to be lied to or be told nonsensical stories. I’ve been treated like an adult, with free thoughts and a free spirit, my entire life. There’s much to be said for this methodology because, even today, people do try to shield their children from many things. There’s no perfect way to be a parent. Did you just shake your head? You can disagree. That’s fine.
There are so many moments in life, but as someone with extreme intuition, this one still gets me.
I remember a full day of fun, spent with my mother, brother, and Grandparents. I remember exactly where we were, and that we had been in a specific store just minutes before the tension began. I remember feeling confused when some form of visibly silent arguing began, which is when my mother and her parents would switch languages in front of my brother and I. My brother probably doesn’t have any recollection of this, but I do. Whenever another language was spoken around me, I paid attention. I still do.
I remember my mother becoming frustrated, bordering on furious. The plans had changed and she was hurt, trying to rein in her temper. She was trying to put on a brave face in front of her children, but I felt the shift in emotions immediately. Once again, my Great-Aunt and Great-Uncle would get their way, and my mother was not pleased. She was not manipulative and didn’t appreciate manipulative people. She was never fake by nature, but in those final moments, she was putting on a show.
Me, always questioning everything, precisely as she taught me, demanded to know what was going on. “Where are they going? Why are they leaving? I have to say goodbye to Grandpa.” At that point in my life, my entire world revolved around my mother, Grandfather, Aunt (my mother’s sister), and brother.
My mother, of the softly spoken everything, of her calm, easy-going nature, would reply with a tone better suited for a teenager that arrived home at four a.m. drunk, without a phone call. “You don’t need to say goodbye. You’ll see him tomorrow.” I remember trying to get one final hug and kiss, and being forcibly taken away from him. I was angry. He and my Grandmother waved, promising me tomorrow. Tomorrow didn’t happen the way any of them expected, I am sure.
It was extremely early in the morning. Ever the night owl, I left the room I shared with my younger brother to find out what was going on. I remember facing my Grandmother, her always stoic expression conveying something was wrong. I had never seen her so quiet, so sad, so lost.
“Where is Grandpa?” I demanded. You rarely saw one Grandparent without the other, even though my Grandfather was the predominant force between the two. She looked up at me with a blatantly sad expression on her normally expressionless face. “He’s gone.” was the answer I received.
Gone. What did that mean to me? It made no sense. “Then we have to go and find him.” was my reply. I was adamant. I knew he would not leave without me, without talking to me, without saying goodbye. The fiercest part of me knew that he would never leave by choice. Never. She shook her head and waited for my mother to explain to me that the single most important man in my life was “in heaven”.
I quickly learned that NO ONE understood this concept. They would look at me sadly, point up to the sky, and tell me my Grandfather had “gone to heaven”. I did not believe them. I had already extensively searched the clouds and he was not there. Because they all pointed up, I believed he had gone to a castle in the clouds. He would always study the sky with me and show me things, so this made sense in my mind at the time.
I remember his funeral. The entire chapel was filled beyond capacity. People were huddled in to make additional room. Hundreds of people had come to pay their respects. My Grandfather was beloved, respected, admired. I remember looking at all the people, so many of them strangers to me, and everyone looked back at me sadly.
I remember the cemetery. The line of cars was unreal. Again, a testament to this great man. I remember my Great-Aunt Minnie and Great-Uncle Charlie wanting to dote on me from the funeral home to the burial site. I remember my cousins, Gloria and Lenny, trying to lighten the mood in the car. Lenny was known for his sense of humor. My Aunt Minnie tried distracting me with cookies. I was not to be distracted, though. I was this man’s only Granddaughter and I knew I had a purpose on this day. After all, I fought to be there. No one thought I should be “subjected to death”. I’d heard this stated quite a bit in the previous day, and knowing myself, I was paying exceptional attention to who said what and how they said it. I’ve always been a keen observer.
My mother sat down with me and explained everything and asked what I wanted to do. I remember her friend Ellen saying “Don’t you want to stay home and play with me and your baby brother?” I remember looking up at her coldly and saying “No. He is MY Grandfather and I AM GOING.” My mother actually stared at me, shocked by the tone of voice I had used. Before that moment, I had always been described as the “little girl with the ancient eyes”, even as a baby, but in that moment my mother knew I was the fierce warrior she had prayed for. There would be no further argument. I had stood my ground.
Cemeteries are for the living. It’s how we remember those we’ve lost and try to honor them. There is nothing more final than seeing someone’s name and the dates of their birth and death etched into granite or marble. Is it bizarre that my Grandparents’ headstone is the same as my parents’ stone? Not really. I remember asking my mother what she wanted for my father and she said “Just bury us together. Get one stone. Something similar to the one for my Mom and Dad, okay?” Her only concession was that her side have a specific design. I custom-designed that stone with the help of someone who does that sort of work. The final result was startling, same as it was to see my Grandparents’ names etched in finality.
After my Grandfather’s death, I remember heated discussions. My Great-Aunt, my Grandfather’s only sister, asked my Grandmother if she could still go on her vacation, despite the traditional 3-7 days where Jews sit Shiva. My Grandmother acquiesced, as she always did in situations such as this. My mother didn’t speak to my Great-Aunt for YEARS after the fact, and my own anger would become part of the mix as I got older and heard the entire story. If, G-d forbid, anything ever happened to my brother, I would not be on a plane the day after his funeral to go anywhere. I would never show his life such disrespect. It’s nonnegotiable. How the hell does someone claim to be in mourning and then get on a plane to go anywhere to enjoy themselves?! I will forever feel haunted by that move. In reverse, I can assure you my Grandfather would not have done something so despicable.
My Grandmother never spoke about it. She had friends, family, tons of well-wishers, and her children and grandchildren by her side. She became a prominent, front-and-center Grandmother in the wake of my Grandfather’s death, whereas she was very much in the background most of the time before his passing. There was NOTHING she did not do for us, take care of, or handle if my father refused. If my brother or I ever needed something, it did not matter what it is, she was there. She went to all of my gymnastic competitions, every drama performance, every Glee club performance, every Graduation. If it was during the day and my parents had to work, she was the face we saw in every crowd. She loved us, she helped raise us, and she was always right across the street. With her, we would get extra time before cancer came and took her from us. The insidiousness of that disease, coming along and taking someone who stayed out of the sun (I always remember her being under an umbrella or sitting in the shade.), never smoked, rarely drank, was devastating. It just goes to show you that no one is immune.
For roughly the next three years, after things had settled down, I would openly discuss suicide, a word that had NEVER been used in my home or in my life. My family did not discuss such things, EVER. My parents would stare at each other in dismay, and I know what they were thinking. “Where did she get that word from?” I had never been exposed to it, but it was constant. I was determined to be wherever my Grandfather REALLY was, and I made this clear. Every time I would talk about it, my brother would become hysterical, clutching me and telling my parents “She’s my sister. She can’t leave. Don’t let her leave me.” His face would turn red and he’d cry himself into an asthma attack at times. We were incredibly adult for kids, I now realize, but back then, I thought all people had similar family lives and discussions. They did not. They do not.
It’s important to discuss loss, grief, death, and every aspect of mental health with your children. I have suffered the majority of my life because my mother was afraid for me and my father was in denial. But as someone recently said to me “You could have harmed yourself so many times by now, and you’re still here. You’re still in one piece.” Only, I’m not truly in “one piece”. I’m very much a broken, pretty mess, but people only focus on the visual on front of them. They are sitting across from someone who is dressed appropriately, someone who is clean, hair done, makeup on, and they think that someplace, somewhere, I have it all “together”. Sometimes I do, but mostly, I do not. I don’t pretend. I am as imperfect as the amethyst I wear around my neck nearly all the time, except during a Full Moon.
To this day, I still suffer. I still hurt, wondering how different life might have been if he had lived another ten or fifteen years. I miss him terribly. But most importantly, I remember. I remember it all.
copyright © 2018 Lisa Marino & Blackbird Serenity, LLC. ALL RIGHTS RESERVED.
“The tears I feel today
I’ll wait to shed tomorrow.
Though I’ll not sleep this night
Nor find surcease from sorrow.
My eyes must keep their sight:
I dare not be tear-blinded.
I must be free to talk
Not choked with grief, clear-minded.
My mouth cannot betray
The anguish that I know.
Yes, I’ll keep my tears til later:
But my grief will never go.”
It’s hard to be patriotic today, at least for me. Perhaps others are struggling with it, too. Regardless, I hope everyone is having a safe, happy, and healthy time.
If you saw the look on my face when I say the word “July”, you would know precisely how disgusted I am during the summer. I have never enjoyed the heat and humidity, but it’s even worse when the heat can easily trigger a migraine for you. I’ve been experiencing them on and off with so much regularity, I have reached the point where I wonder if ANY treatment method is going to be helpful when I have so many environmental triggers.
July is a difficult month for me from an emotional standpoint, too, but it doesn’t have it be. I am doing my best, and we;ll leave it at that for now.
Stay safe and comfortable.
P.S. Happy Canada Day to all of our neighbors to the North. 🙂
Tonight is the New Moon in Leo. We welcome this shift of creative and passionate energy that this New Moon will brings us.
The Leo New Moon is about power. It is about taking control of our lives and pushing ourselves further than we thought we could go. True power is living and acting from who we really are and what we really want. When we express our passions and our joys without apology or fear, we are being our true self and this is where happiness comes from; don’t hold back. Be creative and let your creative juices flow. Take a walk on the wild side of life and get out of your comfort zone. If you stay in the same place and keep doing the same things, you will never move on or improve where you are.
All the inner work you have focused on this year will now be the foundation for bringing more power, love, and energy into your life in this forward-moving period. When the Moon is in this constellation sign it means standing in the center and receiving all the universe is ready to gift you, so you can then open your hands and your heart and take your universal gifts. This is a particularly lucky New Moon, so don’t be afraid to go for the things you want. Lady luck is shining on you right now.
Leo is the sign of ambition, so think big and dream big as this New Moon is going to give you much needed energy and a boost of luck. Go for things you may not have had the courage to go for before. Push your boundaries a little and ask for more.
This New Moon we will be feeling emotional as fiery Leo brings its strong passion and intense feelings. Our smallest emotions can feel magnified, don’t repress these emotions; let them out and use them to guide you as our emotions are also our truths.
On this New Moon we can truly bring in change and transform ourselves into who we want to be. We will feel braver and more confident than usual. Luck will be on your side. We will have renewed energy to complete tasks and get things done. The fire of Leo is burning brightly now, let the flames cleanse your spirit and burn away any negativity. Be positive and open yourself up to allow the good to come in to your life.
Have a blessed New Moon & may the Goddess watch over you.
Written & photo credit: Wicca Teachings
Edited by: Lisa Marino
I promised myself certain aspects of this year would be better, and they have been, but the rest of the year, thus far, has been a shit-show of epic proportions. I am so thrown by it all, I probably say “What the fuck?!” fifty times a day, if not more.
I’ve talked about it, so by now (unless you’re one of my newer subscribers) you’ve probably heard me say I’m blacking out/losing time. It’s been going on for over a year. I FINALLY go to the appointment with the new neurologist and instead of allowing to me speak and elaborate on this, he barely grunts about it. It was completely dismissed, as was a lot of what I said. He has all the personality of a wet mop someone has recently disposed of. Before I could finish speaking, he was out the door. Does he sound like someone you’d want as your doctor?
Obviously as a migrainuer, this was not my first rodeo with a neurologist. It is, however, my first time seeing one I’m completely unfamiliar with. I do NOT like him. I had such a solid relationship with my previous neurologist; he was like family. He always treated me with respect, he always listened to my concerns, and to this day, I still recommend people to him because I think he’s one of the best migraine specialists. The first two neurologists I was subjected to were complete jackasses I wouldn’t refer anyone to, be they human or animal. Reptile? Maybe.
I had no idea what to expect from this doctor. I read his reviews and they were not the least bit stellar, but I read them too late to cancel my appointment. Many of them stated he should have his license revoked, most people stated he was a highly dismissive, rude “physician”, and one or two said he’s an amazing doctor and they didn’t understand all the negative reviews. He must drink coffee on the days he meets the five-star review folks because grunting and muttering and being dismissive only pissed me off. It’s difficult for me to wrap my mind around the list of reviews because people don’t normally write reviews unless they’re motivated by positive or truly negative experiences. My experience left me with no feeling at all. I cannot deal with someone who does the bare minimum, doesn’t answer my questions, and then puts me on medication I’ve already been on. The pharmacist, at least, answered my questions. Don’t tell me generic names and expect me to know what the hell you’re giving me; tell me the brand name like you’re an actual doctor, regardless of what the insurance company pays for. Spend more than ten minutes in the room (The waiting room was empty, I have NO idea where they’re hiding his patients.), and please, do NOT think you’re doing me the biggest favor in the world by saying you’ll put in for prior authorization for treatment you had no idea my insurance even covers. I called them, despite already knowing the answer, and it’s covered, but I’m not 100% sure I trust you to do it because it involves a lot of fucking needles. I might ask a local tattoo artist instead. 😦 At least they work with needles every day.
After openly declaring I have “chronic migraines”, to which I wanted to say “Where the hell did YOU go to medical school, Sherlock?”, but refrained, he provided no rescue medication and no abortive medication, claiming my insurance doesn’t pay for it. I was only too happy to call him and inform him that they do pay for it, and to please contact them immediately for prior authorization for Relpax. If my insurance will pay for twelve pills a month, why shouldn’t I have it on hand? He merely put me on a beta-blocker and an anti-nausea drug that’s about as old as he is. To say I’m not happy is a gross understatement. That’s not effort. He was truly out of the room and down the hall before I could finish blinking. That’s not efficient; that’s half-assed.
To be fair to myself, I am writing up my concussion, migraine, and Fibromylagia history moving forward because I refuse to leave the diagnosis out ever again. My primary blew it off when I used the words “Physical pain from my neck to my toes.” She didn’t even look at me, she focused solely on the migraines and pretended like I hadn’t just explained something requiring a Rheumatology consult, though many rheumatologists are now passing Fibromyalgia off to neurologists. I am NOT dumbing myself down for another doctor. Let her diagnose it properly. The doctor who did diagnose it over a decade ago never put it in my chart. Mind you, when he put me on Cymbalta, at my request, because I had researched it extensively before it was even in pharmacies, I told him how much it helped with the Fibromylagia pain, exhaustion, and physical weakness. He allowed me to take 360 mgs of it for eight years, yet when I said “How is this diagnosis NOT in my chart, he replied “I don’t recall us ever having this conversation.” Dude, in what world would I take 360 mgs of Cymbalta that does NOT work for most people?! In what world does my insurance company approve that much medicine each month when the highest dose most people take is 120 mgs? It angers me greatly to feel jerked around like that. If my primary refuses to listen and/or refer me out, she still needs to know about the original diagnosis and that it was omitted from my chart. If she’s not happy that I didn’t tell her the first time, well, I’m not happy that she chose to ignore me, my blood work, and other things, but conveniently billed me $627 for what should have been an office visit, but actually looks like insurance fraud from where I’m sitting. I’m more than happy to tell her this to her face next month when I see her. She is overbooked, her office staff is negligent, and cannot get a proper message to her to save their life. I NEVER want to be subjected to her Physician’s Assistant again. That woman needs a brain. I shouldn’t have to wait two and a half months to see my primary care physician, who is, quite frankly, minutes away, for ANY reason. She’s not a brain surgeon.
To add insult to injury, when I called her office to ask for a referral for a second opinion after the neuro consult, she refused. “I went over his notes and he’s trying to get you the treatment, so you have to go to every follow-up and do what he says.” Um, who the fuck is the patient here? I can confirm that she has already lost me as a patient for the duration. I will say what I need to say and follow-up, but I am on a waiting list for a new primary care doctor for November, at the earliest. She made the blondest brunette mistake of sending an e-mail to me instead of her assistant. It wasn’t meant for me to read, clearly, but I did read it, and she cannot take back that sort of “mistake”. Once again, she blew me off. After constantly saying I needed to be assessed by her, her e-mail stated I should “go to the emergency room” during paralytic attacks. Apparently she doesn’t seem to grasp the fact that when you experience temporary paralysis, you are unable to move and unable to dial the fucking phone. I’m also ALONE when it happens, and it is TERRIFYING. It is almost always from the neck up or it’s the entire left side of my body, and the fear you feel is gut-wrenching because you never know if this is the next thirty minutes of your life, the next three hours, or if you turned wrong and this is now permanent. How would she like me to get to the ER? Via flying carpet?
If she blows me off at my appointment in any way, shape, or form, I will be on the phone to the state licensing board in a New York Minute. I’ve witnessed some heinous crap regarding my treatment in this state and I am NOT going to tolerate another second of bullshit from ANYONE.
I talked about not liking the whole “temporary” situation and I have to say I was disgusted when “Ms. Temporary” had her office call and cancel on me. My doctor called later on the same day because when he heard about it, he knew I was going to react badly. Despite planning on canceling myself because I simply don’t want to waste my time, or hers, I felt like it was a terrible first impression to force me to make an appointment in the first place and then cancel on me without an explanation. He assured me she’s the most reliable person in the world, and that he wasn’t sure what had happened, but he wanted me to know it was more than okay for me to feel justified in not wanting a temporary situation with anyone. Unlike most people, he genuinely gets me, and the affirmation of that was good to hear. Most doctors would NOT have called to check in with me over anything, but he did, and it meant so much to me because we were on the phone a long time. He was touching base and we went over a lot of different things. I know he was concerned based on what we were discussing, but he also said he trusted me. He probably shouldn’t, but I’m also very careful in how I speak to doctors. I’d never put them in the situation of not being able to trust me. I’m not stupid. The choices I make generally have no bearing on the doctors I am seeing.
I left him a message on his last day to thank him for talking me down, because he didn’t have to do that, but he did, and when I thanked him, he said “I’m here for you. My biggest regret is that I was not able to do more to help you.” There are doctors twice his age who would NEVER admit that to a patient.
When I checked earlier, one of the reviews I’d written for him had finally posted. At least he gets to move forward as a doctor with a five-star review. It is the only review he has. Most doctors don’t have them, for obvious reasons. I still have many more to write for him, but each one is the truth.
I did make an appointment with the doctor he recommended, but I told him not to expect anything out of it because I don’t have any trust to offer her. He said “That’s understandable. Either she’ll earn it, or she won’t.” I see why he chose her, but I reserve the right the judge her for myself. I don’t think I said that to him out loud, but he probably knows I’m not going to make it easy on her. She could be lovely and I’ll still find fault with something because she’s not who I want to work with, period.
He is the person who was disgusted by how my primary blew off the pain I’m in; he thinks it’s wrong that I should be suffering so much and be ignored by anyone. He is also the person who was mortified that my blood work and a high fever were blown off, as though they were no big deal, when in fact he agreed with me that neither of them are normal. I’m almost certain he wanted to ask where the Physician’s Assistant went to school, because he’s a very calm, laid-back person, and his voice is always even, but his entire tone changed when I told him what happened. Technically, despite being out of med school and having his license to practice, he’s still completing his residency, but his professionalism outshines people twice his age because he dots his i’s and crosses his t’s. He asks the right questions and doesn’t blow you off. Aside from clearly having the right kind of mind for this sort of work, he obviously had excellent teachers, as well. But ultimately, it comes down to being the right kind of person to be a doctor. Everyone’s mind works differently. His works from a “How can I understand this?” perspective, which, to me, is interesting because I had to answer some of his questions from a “How does he NOT understand this?” position, where I answered him, but tried not to roll my eyes, and sometimes, I flat-out DID roll my eyes at him.
A lot of people meet me and don’t know what to make out of me. I completely baffle the fuck out of them, and I openly admit I get a kick out of that. In six weeks, this person grasped me fully, appreciated my honesty and sense of humor, and made me feel a lot less damaged than I probably deserve to feel. Between our meetings and every single conversation we had in between, I don’t think I’ve ever felt more comfortable or at ease with someone. And it dawned on me that the ease of the doctor/patient relationship felt more comfortable because he felt like a brother or a close friend. I didn’t tiptoe around him, walk on eggshells, or pretend. I was always myself, and ultimately, I was accepted for that completely. It IS rare, so I have every right to say that I respect him and appreciate everything he did for me. I’m also unashamed to admit that I will track him down like a dog with a bone if I’m not able to find someone better who is fully able to do what he was able to do.
I am fighting for my life, my health, and for proper treatment. I REFUSE to dumb myself down for another doctor or ANYONE in the medical field ever again. I may be a pretty mess, but I’m also smarter than I let on, and it’s time to break all of that out and give doctors a run for their money. But I’m also not going to trust people simply because they think it’s a given. It isn’t. I trusted ONE person this year to take care of me properly because he earned that trust the second he introduced himself. Some people have positive energy, and others I don’t get the same vibe from. Being able to read people is a gift not everyone possesses, but it’s a gift I have. I can tell you a lot about someone just by sitting down with them for an hour or two. Often times, people think they’re getting to know me, but in actuality, I’m the one getting all of the information. People don’t realize how much their behavior, speech, and physicality gives them away. You can obverse a lot if you’re paying attention, just don’t expect to be able to read me. I’m not the “open book” type.
I’d forgotten how dishonest people actually are, at times, with their physicians. I don’t think you need to tell them every single detail of your life, but I do think they need to know what’s going on in order to help you. Set realistic goals and say what you mean, as opposed to what you think they want to hear.
Being told that I “know myself really well” and that I “did not come in asking for the magic pill that solves everything” were two of the greatest compliments a person could give me this year. Yes, I’m realistic, but I’ve also been through hell. I know that certain types of medication can help certain types of people, based on where they stand health-wise, but I also know there’s nothing that will help me moving forward for one specific thing, and as sad as that is, it’s life. There’s nothing I can do about it. You keep going until you can no longer go on, and you don’t listen to external “noise” telling you what you should or shouldn’t do, or what you should or shouldn’t “live for”. Unless you live inside my mind, suffer the way I suffer, experience my pain daily, struggle through the inability to sleep, function, react, and can while you’re going through all that, still be able to hard enough each month to pay all of my bills, you simply don’t get a say in how I live my life. I sit in judgment of no one on this front. I don’t say meaningless shit to people in order to make myself feel better. If I’m concerned about someone, I think about THEM and I say what they TRULY need to be told, not what they want to hear. No matter how hard I struggle sometimes just to get through the next five minutes, I still listen to others with compassion, care, concern, and genuine love. I’ve never turned a friend away. I have loved people and I have lost people, and I don’t ever want to question if I could have said more, or if I could have worded things better.
I’m looking to find out how to manage my migraines better, and find the best way possible to manage the chronic pain I am in, so I will be pushing for an MRI and x-rays of my brain, neck, and spine, even if it means a trip to the emergency room. Not being able to move my neck properly and being afraid that every turn could mean permanent paralysis is scary. My current doctor refused to have my back, so her “reward” is losing me as a patient. A new doctor gets me as her patient in a few months and her reviews are really good (This time, I looked immediately. No more surprises.), so I hope it’s a more promising situation despite the fact that she’s further away. There’s absolutely no reason that well over one hundred primary care doctors and internists in the Boston area aren’t taking on new patients. I thought I was losing my mind making phone calls until I finally found a doctor in another doctor’s office who just happened to be accepting new patients. I can switch to someone else immediately if something is wrong, which is good to know, but I feel like I’ve given this other doctor enough chances at this point. She has one efficient person in her office; her assistant. I cannot stay there just because I like her, nor should I.
So here I sit, on a muggy July morning, and honestly, the pain I am in is intense (I took two Aleve for it hours ago…an absolute JOKE.) and all I want to do is scream and cry. A huge part of me wants to go to the emergency room and demand they help me, but a larger part is afraid they’ll do nothing at all for me. As many times as I’ve fallen since moving here, I KNOW my back isn’t okay. I can feel it. I’m too young to have this much damage and this much pain. As many times as I’ve banged my head into the wall in my sleep (100% unintentionally. I’m restless, fitful, and I throw my body around a lot. I’ve also thrown pillows across the room and accidentally kicked Kitten off the bed a few times because I had no idea she was even here.), I know my head probably isn’t okay, either. I’ve failed two baseline tests, one in May and the other this month, and a Physician’s Assistant and a neurologist both ignored these facts. The brain doesn’t lie, and my poor back and neck aren’t amused by my having to use a heating pad when it’s 90+ degrees outside. Alternating between heat and ice only helps for short periods of time when you’re in excruciating pain. It lets you know it’s not a muscle spasm, but something serious.
I hope and pray doctors start taking me seriously, and SOON. I don’t know how much longer I can hold on without some serious intervention.
copyright © 2017 Lisa Marino & Blackbird Serenity, LLC. ALL RIGHTS RESERVED.