Dear Nurse Beth Advice Column - The following letter submitted anonymously in search for answers. Join the conversation!
Published
I recently graduated from nursing school and passed my NCLEX. But I have not began job searching due to my recent diagnosis for lupus. I'm worried whether or not I can do nursing. I plan to work part time and avoid working big hospitals and pursue mental health facilities, hospice, or skilled nursing care.
However nursing is known to be physically and mentally stressful. I'm worried because I'm struggling to tolerate the symptoms. I get mild to moderate flare ups pretty frequently. My symptoms are nausea, vomiting, muscle aches, fatigue, brain fog, headache, skin rashes, swelling, nerve pain, itching. Nausea and vomiting is moderately frequent so I struggle to eat and keep food in, which affects my energy levels.
From clinical experience, I noticed that whenever I work, I'll be physically fine but in a few weeks to months, my symptoms will get severe and I am so fatigued, cannot concentrate, and my immune system will start attacking a body system. Then I get hospitalized.
I literally do not know what strategies to use to cope with lupus as a future nurse? I started on plaquenil and I'm giving it some time for the effects to kick in. My plan to work part time and avoid hospitals is a start. But other than that I do not know how to avoid flare ups esp since they're so common. I feel so lost on what to do. I get so tired and either cannot concentrate and/or slowed thinking. I'm worried I wouldn't be able to give my patients the best attention.
It's hard for me to sustain any job because of this. Im hoping part time work and medications will help.
Im even debating if I should stop nursing all together because I'd earn too much money to qualify for low income medi-cal insurance. But I won't be able to sustain a job and pay for medical expenses. And part time positions generally do not offer health insurance or benefits. Should I even bother to work?
Any advice on how to cope would be helpful! Or any insight on my situation and whether mental health, hospice, or skilled nursing is a a good choice for lupus
Published
I recently graduated from nursing school and passed my NCLEX. But I have not began job searching due to my recent diagnosis for lupus. I'm worried whether or not I can do nursing. I plan to work part time and avoid working big hospitals and pursue mental health facilities, hospice, or skilled nursing care.
However nursing is known to be physically and mentally stressful. I'm worried because I'm struggling to tolerate the symptoms. I get mild to moderate flare ups pretty frequently. My symptoms are nausea, vomiting, muscle aches, fatigue, brain fog, headache, skin rashes, swelling, nerve pain, itching. Nausea and vomiting is moderately frequent so I struggle to eat and keep food in, which affects my energy levels.
From clinical experience, I noticed that whenever I work, I'll be physically fine but in a few weeks to months, my symptoms will get severe and I am so fatigued, cannot concentrate, and my immune system will start attacking a body system. Then I get hospitalized.
I literally do not know what strategies to use to cope with lupus as a future nurse? I started on plaquenil and I'm giving it some time for the effects to kick in. My plan to work part time and avoid hospitals is a start. But other than that I do not know how to avoid flare ups esp since they're so common. I feel so lost on what to do. I get so tired and either cannot concentrate and/or slowed thinking. I'm worried I wouldn't be able to give my patients the best attention.
It's hard for me to sustain any job because of this. Im hoping part time work and medications will help.
Im even debating if I should stop nursing all together because I'd earn too much money to qualify for low income medi-cal insurance. But I won't be able to sustain a job and pay for medical expenses. And part time positions generally do not offer health insurance or benefits. Should I even bother to work?
Any advice on how to cope would be helpful! Or any insight on my situation and whether mental health, hospice, or skilled nursing is a a good choice for lupus
Share this post