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Shadow boxing mis-hap #Fitness #adaptiveboxing #Ataxia

So…I’m nerding & refining my adaptive boxing routine…I’m experimenting with mirror work because you can’t see yourself punching

I’m thinking I’m gonna look muscular (OK forget that I have 2 coats on…this is how my thinking works) with 3 boxing classes and practice.

I don’t have a ring camera or anything so I was like “Let me just try it.”

So I start with the PunchLab & Heavy Bag Pro app…I hit “Record” on the iPhone…

Self-conscious but I do 1 or 2 rounds

Feeling a little confident, I get some of the food (I’m bulking so I keep food around).

I bend down for something….Somehow my other arm hit a fork perfectly so that it could last whiplash spaghetti on the side of my face

This startled my brain, ego, and spirit.

Welcome to life! 🤣

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Dr visit #GeneralizedAnxietyDisorder #OppositionalDefiantDisorder #CheckInWithMe #BorderlinePersonalityDisorder #BipolarIIDisorder

Ok so I saw 👀 my psychiatrist this morning and she is nothing but predictable she 🛑 my Xanax and gave me colonopin instead stopped my Zoloft and gave me Prozac. Then she sent me to have lab work done. I’m catching it rough and I’m at a job I hate I actually pray for someone to rear end my car every time I drive to work so I don’t have to go in. Like that’s how bad I hate my job! I don’t want to get paralyzed or anything but whiplash will work I can sue the person who hit me and it gives me a few days if not two weeks out of work. I know it’s wrong but I really wish I could utilize intimidation or threats to control the disability judges decision and force a approval for my disability so I don’t have to deal with people in a work environment. I am not a bad person I am just so sick of how life is going even though I’m severely afraid of dying I wish I was in heaven right now and not here because of all the 💩 I have to deal with. I’m scheduled to go to vocational rehabilitation services on April 3rd I pray they can help me find another job that’s not fast paced like my current one is and I know I sound like a jerk but I just can’t keep dealing with crap man I just can’t and people truly wonder why I have such a issue with authority figures gee I wonder why?

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It’s the kind of day where one pain runs into another. #Whiplash from a near miss, #TrigeminalNeuralgia and #Sarcoidosis #LupusPernio in my sinuses. Tea, rest, rX and lavender oil head massages.

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Let’s talk about CPTSD

It’s a lonely condition—not being able to share what you go through with your friends because they see your struggles as having a bad day or going through a phase or a response to a specific thing that happened that week. What they don’t understand is that #ComplexPTSD is lifelong and can be triggered by a myriad of seemingly small things to other people, e.g. someone raising their voice with you. They don’t understand that because of auto-responses baked in your brain from childhood trauma, you can’t just meditate it away. A yoga class, while relaxing, doesn’t stop your amygdala from smacking you in the face with emotional whiplash. So you keep your bad days to yourself or your journal or communities like this where you hope your words will be heard by someone.

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My Not So Mighty Moment

When I was in high school, a middle aged teacher showed up to class with her hand in a cast, courtesy of a wild bowls incident. Being an all-girls school, naturely this was a source of gossip. After some discussion, we crowned it the 'Most Geriatric Injury Ever Conceived by Teenage Minds'.

Fast forward to the present, and here I am, ready to steal her crown!

Enter Taryn, the Yoga Clown 🤡

Last week, while channeling my inner 'Warrior Pose' at my local MS Centre, I felt a small pop in my
chest that definitely wasn't my inner peace bursting forth. By the end of the session, my neck was brewing with what felt like the beginnings of a migraine that could rival a Shakespearean tragedy. So I did the logical things—a hot bath with lots of magnesium, dinner, and an early night with dreams of being a yoga guru.

Clearly, the Universe had other plans...

I woke up feeling like I'd been rear-ended by an invisible truck. It was like the whiplash injury I got in a car accident a few years back, but with a hefty dash of facial acrobatics. Pain in the left side of my neck, ear, sinuses, and teeth—because apparently, you can sprain your face doing beginner yoga.

As I start to feel less like a human pretzel, I can't help but chuckle about the absurdity of it all. So, to anyone needing a laugh: if you ever feel silly about an injury, just remember me – the person who went full Cirque du Soleil with her face in yoga class 🤗

#DistractMe #CheerMeOn #ChronicFatigue #ChronicFatigueSyndrome #MyalgicEncephalomyelitis #Fibromyalgia #Headache #Migraine #Endometriosis #PolycysticOvarySyndrome #MultipleSclerosis #BackPain #Laugh #Meme #BruisedEgo

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Fybro in car accident #cronicpain

So I suffer from fibromyalgia, I was rear ended on Thursday (no one was really hurt but I have a serious case of whiplash i have been in so much pain even with my management meds I just want to scream at every touch. #Fibromyalgia

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What are the 9 symptoms of BPD? Explained in great details.

Fear of abandonment. People with BPD are often terrified of being abandoned or left alone. Even something as innocuous as a loved one arriving home late from work or going away for the weekend may trigger intense fear. This can prompt frantic efforts to keep the other person close. You may beg, cling, start fights, track your loved one's movements, or even physically block the person from leaving. Unfortunately, this behavior tends to have the opposite effect—driving others away.

Unstable relationships. People with BPD tend to have relationships that are intense and short-lived. You may fall in love quickly, believing that each new person is the one who will make you feel whole, only to be quickly disappointed. Your relationships either seem perfect or horrible, without any middle ground. Your lovers, friends, or family members may feel like they have emotional whiplash as a result of your rapid swings from idealization to devaluation, anger, and hate.

Unclear or shifting self-image. When you have BPD, your sense of self is typically unstable. Sometimes you may feel good about yourself, but other times you hate yourself, or even view yourself as evil. You probably don't have a clear idea of who you are or what you want in life. As a result, you may frequently change jobs, friends, lovers, religion, values, goals,

Impulsive, self-destructive behaviors. If you have BPD, you may engage in harmful, sensation-seeking behaviors, especially when you're upset. You may impulsively spend money you can't afford, binge eat, drive recklessly, shoplift or overdo it with drugs or alcohol. These risky behaviors may help you feel better in the moment, but they hurt you and those around you over the long-term.

Self-harm. Suicidal behavior and deliberate self-harm is common in people with BPD. Suicidal behavior includes thinking about suicide, making suicidal gestures or threats, or actually carrying out a suicide attempt. Self-harm encompasses all other attempts to hurt yourself without suicidal intent. Common forms of self-harm include cutting and burning.

Extreme emotional swings. Unstable emotions and moods are common with BPD. One moment, you may feel happy, and the next, despondent. Little things that other people brush off can send you into an emotional tailspin. These mood swings are intense, but they tend to pass fairly quickly (unlike the emotional swings of depression or bipolar disorder), usually lasting just a few minutes or hours.

Chronic feelings of emptiness. People with BPD often talk about feeling empty, as if there's a hole or a void inside them. At the extreme, you may feel as if you're “nothing” or “nobody.” This feeling is uncomfortable, so you may try to fill the void. But no attempts to feel the void are long lasting... only temporary.

Explosive anger. If you have BPD, you may struggle with intense anger and a short temper. You may also have trouble controlling yourself once the fuse is lit—yelling, throwing things, or becoming completely consumed by rage. It's important to note that this anger isn't always directed outwards. You may spend a lot of time feeling angry at yourself.

Feeling suspicious or out of touch with reality. People with BPD often struggle with paranoia or suspicious thoughts about others' motives. When under stress, you may even lose touch with reality—an experience known as dissociation. You may feel foggy, spaced out, or as if you're outside your own body.

#ADHD #Autism #bpdworld #BorderlinePersonalityDisorder #PTSD #mentalthealth #BipolarDisorder #Bipolar2Disorder #Bipolar1Disorder

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Pacing, Creative Coping and How Small Things can be done in Great Ways.

My name is Mita. I am a 42-year-old multidisciplinary artist and podcast hostess; a mother and a wife. I focus a lot on Pacing and Creative Coping strategies to get through my days with various chronic conditions.

Following a whiplash injury in 2015, is when my chronic pain/illness journey started. I’ve been diagnosed with whiplash, fibromyalgia, orthostatic intolerance/dysautonomia, chronic fatigue syndrome, occipital neuralgia and chronic migraines.

I am in pain every day. Some days my cognitive function is severely hampered due to Brain Fog. And P.E.M (Post-Exertional Malaise) can be a real stick in the wheel.

My baseline, on a good day, is a headache pain level 2-3, occipital neuralgia at a 2 and fibromyalgia pain level 4-5 (on the ‘In Office Doctor’s Pain Scale’) with migraine attacks every few days.

Since developing a chemical sensitivity, it makes the pain hard to control, as I cannot take most medications.

I experience Vertigo, muscle weakness and extreme fatigue on top of all the other crazy symptoms these conditions come with, and I am at a fall/faint risk if I am not careful.

Late fall, winter and early spring are the roughest months to get through, living in the Midwest as I am. But once the weather stabilizes and becomes warmer and if I have been prudent with my energy supply during the winter, then I can find myself living it up a little more during summer which is invigorating for the soul.

So, I am limited. Physically. This is my reality. I only have so much energy to go around and every day I need to pick and choose what I spend it on. I always have to keep in mind that I cannot overdraw my account. I need to balance my ‘checkbook’, if you will, to make sure I do not go down to zero, because I may not have enough to go around for the next day, or even the next couple of weeks if I do. But with Pacing I can lead a somewhat decent life.

ME-pedia describes Pacing as such: “…an activity management strategy to help ME/CFS patients limit the number and severity of relapses while remaining as active as possible…”

(Obviously, I am not perfect at Pacing as I find myself doing too much on occasions, due to getting impatient with my limitations. Overall, I’d say I do pretty well with it though.)

So, what do I choose to spend it on?  Well, some mundane tasks need to be done, like laundry or light cleaning, so I spread it out over a few days. I work within my boundaries which I have somewhat figured out via trial and error. This is part of Pacing. Ups and downs til you figure what You can handle.

I am a very lucky gal to have an extremely supportive husband and three children that help me with some of the heavier chores. The house would be in utter chaos if this was not the case.

When the mundane, pragmatic things have been taken care of, I choose to use my energy on the activities that fill me with contentment, keeps my anxiety levels down and overall contributes to a better state of mind. Whether they are Creative Coping Strategies, like painting, drawing, forest bathing, expressive writing, or just being with my family in the moment, or listening/making music (the latter depends fully on headache pain levels and brain fog but within my capacity, music will always have a part in my life).

I am also half of a duo in a podcast we have named Creative Copes where we talk about these exact things – A labor of love for ourselves and what we hope becomes an aid to others in similar situations. I save some extra energy for research and general podcast prep so I can co-host it, because the idealistic compassionate part of myself wants desperately for other people to feel less alone: a constant state of mind when stuck at home, in a body that does not compute anymore.

This is what I spend my energy on. Things that matter to me; that settle my body and mind and make my heart soar.

I am not all knowing and cannot be worldly with how limited I am: I am clearly not meant to be a main figure in changing the world!

But I can do Small Things in a Great Way, for myself, my family and others, and hopefully someone can feel less alone because of my story and be more inspired to get up each morning and meet the day head on. Love and light ❤️

I can be found on Instagram handle MitaMu.Art and/or Creative.Copes

www.instagram.com/creative.copes

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If my loving hubby (34yrs married )doesn't recognize my distress, how the heck do I ever get my arrogant, know-it-all dr.s to see my distress

17 years ago I had 2 bad(on the inside) recreational accidents. I got thrown onto a lava outcropping by 2 hard rogue waves...two months later while sledding in the snow, we hit a deep divet, hard, the whiplash was a 20 on the pain scale of 10. But very little damage showed up on my body, rock cuts and bruises, all the rest was inside my body. Fast forward... I am a completely useless mass of bones, blood vessels, etc; I hardly qualify for the definition of a human.
My hubby has always been supportive and caring, truly I know I am the luckiest to have him.
BUT.... I am definitely getting weaker and the MDD, PDD are dragging me closer to the edge. We went to my neurologist yesterday for Botox, he went in with me,for the specific reason to get the dr to ok contrast in my next MRI. Today I found a passage that was pretty accurate at describing me.... I read it to my hubby and he replied that he didn't think it describes me, now.
WHAT THE 🤬🤯🤬 heck do I do, if he doesn't really "see me", the drs that never have, never will. I only have one answer...the one where no one will need to see me 🤯😱🤮💤💤💤💤permanent sleep. #NothingLeftInTheTank #63Feel93 #EFTH #🙏ForReliefOrDeath

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