Nursing Is Not for the Weak

Submitted on May 8, 2024 by  Red40something
Image

Flowers.

Becoming a nurse taught me how to live with HIV

Nursing is not for the weak, and nursing school is the epitome of that. There are two major things I didn't learn in nursing school. The first is how to be a nurse. You don't actually learn to be a nurse until you are a nurse. Nursing school teaches you how to be safe. Basic stuff like how to take a blood pressure, and the body's physiology. In fact, I learned more about what kind of nurse I didn't want to be while in school. Rotations through clinical sites gave me examples of nurses with bad habits I couldn't wait to forget. One of my worst experiences in HIV stigma happened in nursing school from an instructor, and it made me question if a person with HIV could be a nurse. Yet here I am.

The second thing I didn't learn was how to lose a patient to death. In thinking back, the only conversation about death was an abstract kind of idea that people die as part of the natural life process. Professionalism and distance make that easier. Or so they said. We didn't talk about what it would feel like to walk into a patient's room and find them and all of their things gone. My instructors never discussed navigating the talks with a patient's family about what active dying looks like. During one of my rotations at an assisted living facility, I walked in to find the patient who had been there the day before had passed away. We had only been there a short time, but this particular patient was cranky and had dementia which made her loud, demanding and at the same time hilariously funny. I had to say, she made an impression. While it was a shock to find she had passed, I remember saying a prayer for her, and noting mentally that we didn't discuss it beyond learning the cause of death. That bothered me, but there were things to learn and people to care for. Professionalism? Disconnection? Maybe a bit of both.

When I began nursing at the AIDS service health clinic I worked at, the idea of death and dying became more than an abstract idea. By that time,
I had (mostly) given up the idea that
I was going to die of AIDS. I was better educated, taking my meds like my life depended on it (she said tongue in cheek), and applying the wills and wonts of being a good nurse. It was a journey of navigating not only not dying but relearning how to live.

I was also listening to patients tell me about a time before meds when friends died every day. They spoke of stigma and about attending weekly memorials and funerals and forming a community. I witnessed PTSD and the flawed, but understandable guilt of being alive to talk about life when folks they loved were not. I honestly thought I had faced my personal mortality early on when I was diagnosed with HIV.
I realized through their stories, I had only glanced at it in the mirror. Those stories, and the path from diagnosis to nursing in AIDS care, to now aging with HIV gave, and still give, me my own dose of irrational guilt every time I struggle to take my meds or skip doses because I'm burnt out on taking them. Not so long ago, at diagnosis they told people to prepare to die in three months or in a year. Now they say you aren't going to die. The amount of living to be done that flows between those times and words is partially what makes death less abstract and more concrete.

I lost three patients to either comorbidities from, or complications of, an AIDS diagnosis. Three white, gay men
I had zero in common with except three letters and some medication. Men whose visits I looked forward to, and whom I daresay felt that way about me. It could be arrogant to say I lost them. Certainly, they had families and lives outside the clinic. Yet, they were mine.
I took care of them, knew their spouses and pet's names. I gave them shots, helped them with questions and gave out hugs. We laughed and cried during visits. I was the nurse they asked for when they needed help. What is also true is, sometimes, they nursed the nurse without even knowing it.

In my head, the fact that I don't remain disconnected or "professional" is one of my nursing superpowers.
I learned how to be a nurse by practicing nursing. I learned about the reality of losing a patient the same way. Nursing is not for the weak, but neither is life with HIV.

This blog was originally posted on Positively Aware's "Being Bridgette".

Submitted by Destiny1995
1

Thank you for sharing this experience. It's crazy how other aspects of our lives compare to the way we deal and or live with HIV. 

Submitted by MariaHIVMejia
3

Dear sis, 

Thankyou for this blog <3 I always say that nurses are like mY mothers and have played a very important role in my survival!! 
Thankyou for the work that you do and for being so transparent 

love and light,

Maria 

Submitted by KatieAdsila
2

Wow, thank you for sharing this, I find you so inspiring in so many ways, you are an amazing woman 💯🫶🏼

Submitted by Marig2016
2

Thank you for sharing sis and I’m so glad the way that teacher made you feel didn’t stop your from proceeding on. I sometimes think caregivers have better relationships with their patients than family members. Loss is never easy. Hugging you from afar 

Red40something 's recent blog posts

Image

Members of The Well Project community at USCHA 2022.

Become a Member

Join our community and become a member to find support and connect to other women living with HIV.

Join now >

banner

Do you get our newsletter?

¿Recibe nuestro boletín?

Sign up for our monthly Newsletter and get the latest info in your inbox.

Suscríbase a nuestro boletín mensual y reciba la información más reciente en su bandeja de entrada.

Browse Blogs by Theme

Recent Blog Posts

Our Bloggers