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Turning down invitations

Post-COVID Recovery & COVID-19 | Last Active: Sep 2 7:10pm | Replies (32)

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Profile picture for RMS @rinadbq

I've had this since Nov. 2020-an ER nurse in a pandemic, go figure. For me, I call them 'crash episodes' because I have crashed head on into a semi, at 100mph, hauling military missiles...then they go off and I am on fire.
I am only seen when I feel good and able to leave the house and I look perfectly fine-I am not hauling oxygen, a cane, wheelchair, missing body parts. I describe it to others as profound, incapacitating, overwhelming, leaden exhaustion-loosing days at a time. I wait as long as I can to get up to walk to the bathroom. Shower and hair puts me out. Food is microwave or Door Dash-when I feel like eating. I have groceries delivered, my bills are on autopay, my body has aged 20 years.
My life is divided into before and after. I used to be an ER nurse, at a Level I trauma center who not only prevented death, but sent electricity through the human heart and brought people back to life, ran 15 units of blood over 20 minutes into a trauma patient. I ran a half marathon for my 60th birthday. I was one of the top weight lifters at the gym, maintained a 1/2 acre garden, cooked for and hosted family events like Martha Stewart, traveled internationally. In short, I was Wonder Woman.
Now I decline concerts that I have waited a lifetime for, Cubs game over the dugout, Blackhawk games, anything social after 1:00 (if it is a 'good' day), dinner and a movie. sex knocks me out for 2 days, is it really worth it? I lost a 40year career due to stamina and cognitive loss-I am not safe. I'm stuck at home looking like Nick Nolte's mug shot. I am a mere shadow of myself. The only thing that has stayed the same is my social security number and color of my hair. I'm in counseling for grief from loss of what used to be my life, anger when I forget and do something that turns out to be overwhelming, lost a committed relationship and fear/dread of the next crash episode.
It takes what little I have to remind myself that I can take care of bathing, toileting, nutrition, dressing myself, shelter-the absolute basics of living. I could have had that truck hit me, had a serious stroke, be in hospice for caner, be in line for a lung transplant (like a woman I worked with), unable to walk, unable to live independently in my own home . I have worked with countless patients who can not. It is hard to remember gratitude-something I am working on.
What really got to me was media coverage of 5 years since the pandemic, no one talked about the lives left behind, especially the emergency providers who were out there 24/7 and what became of us-the physical and emotional toll 5 years later. Only a small handful of fellow ER workers are still there in my hospital; the experienced nurses are gone. The pandemic wiped us out, one way or another which frightens me for the future when I need help.

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Replies to "I've had this since Nov. 2020-an ER nurse in a pandemic, go figure. For me, I..."

I consider you miraculous. What I find with all of us is a remarkable push to live and that's what is amazing to me esp on days when I just don't wanna and then figure out how to do what I can. when I can.

I so hope you get the transplant and that it gives you more stamina.

And there ARE those of us who talk about the many health professionals who are lost to this. An article recently wrote about the nurse shortage has lead to "fake" nurses - that is people pretending to be and not vetted - practicing. THAT alone should be a wake up call to WHY so many nurses in particular are gone.

The emotional toll of giving up a loved career can be as painful as the physical toll. Here's to you - to others - and to healing and doing what we can.
Joan

@rinadbq - Yours and others medical service during those awful times was very much noticed and appreciated by many I’m sure, despite all the political insanity. I remember taking my husband to our ER for an unrelated medical emergency during the worst part of it and feeling so badly for all the ER nurses. They all looked so completely weary and battle worn. Our son lives in LA and his friend was an ER nurse there during the pandemic- she described the hospitals there as war zones. She eventually quit and did something else.

I’m so sorry you’re suffering and that life has taken such a dramatic turn. I relate! I became totally disabled with ME/CFS at 36 - (I’m 73 now) and life as I knew it came to a screeching halt. But humans are more resilient than we realize. Miserable and disappointing as living with chronic illness is, we are still us with character qualities and interests that can be developed around our limitations.

I hope you can achieve some level of improvement over time. It can happen. I was able to get to about 70% after several years and it lasted for quite a few years. During that time I was able to travel some and do concerts.

Wishing you all the best!