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So, yesterday I got diagnosed with IgA Nephropathy. If you can't remember the details from pathology (I didn't), it's the autoimmune disorder also known as Berger's.
The diagnosis was based on a renal biopsy. I chose to go without sedation, so I can tell you that the procedure wasn't that bad. Unfortunately, the next two days felt like someone moved my testicles to just underneath my ribscage, then used a nailgun to make sure they would stay in place while they were kicked repeatedly.
In regards to the disease, I can look forward to hematuria and proteinuria associated with every URI or gastroenteritis I ever get. With each of these episodes I will have to take 6 weeks to 3 months of steroids in an attempt to reduce the scarring and permenant renal damage from IgA deposition that leads to ESRD/dialysis/transplant listing in up to 40% of patients. At the ripe age of 31 I'll be placed on lisinopril to reduce proteinuria and control hypertension that also results from renal scarring/decreased GFR. Lipitor will keep my cholesterol under control, as this may have some protective effect. It also gives me a chance to damage my liver as well, since my other waste elimination system was feeling left out.
Background: I am finishing up my first year of EM residency. EM is what I've wanted to do for the last 10 years--since well before medical school. Recently (before this diagnosis) I have been thinking about a critical care fellowship, cause I really dig that too--all of your patients are really sick, the drunks are already intubated, and I just like the environment.
Concerns:
1. I have never been sick as often or as bad as I have in the last year. If every URI/gastroenteritis is moving me one step closer to dialysis, is the ER really the best place for me to be? Some have told me (again, before this diagnosis) that they essentially stopped getting sick after their intern year, but can I trust this anecdotal info?
2. Even if I stop catching every URI that walks in the door, what about being on steroids while being exposed to every bizzare, virulent bug that walks in the door? What about the serious infections that occur in immunocompromised states? Again, seems like the ED may not be the ideal environment.
3. If I decide to do something else, what specialty do I move to? IM/FP would be no improvement (and I've never been interested). Radiology certainly has the least contact with sick people, but how difficult is it to transfer into? Anesthesia would be another option with the same question. Also PM&R seems like a good lifestyle, probably easy to find a spot (speculation), but would I be bored out of my skull (again, speculation based on ignorance)?
I know this sounds like a big pity-party, and I am kind of overwhelmed, but I'm serious about these questions, so I'd appreciate any advice or suggestions.
SF
The diagnosis was based on a renal biopsy. I chose to go without sedation, so I can tell you that the procedure wasn't that bad. Unfortunately, the next two days felt like someone moved my testicles to just underneath my ribscage, then used a nailgun to make sure they would stay in place while they were kicked repeatedly.
In regards to the disease, I can look forward to hematuria and proteinuria associated with every URI or gastroenteritis I ever get. With each of these episodes I will have to take 6 weeks to 3 months of steroids in an attempt to reduce the scarring and permenant renal damage from IgA deposition that leads to ESRD/dialysis/transplant listing in up to 40% of patients. At the ripe age of 31 I'll be placed on lisinopril to reduce proteinuria and control hypertension that also results from renal scarring/decreased GFR. Lipitor will keep my cholesterol under control, as this may have some protective effect. It also gives me a chance to damage my liver as well, since my other waste elimination system was feeling left out.
Background: I am finishing up my first year of EM residency. EM is what I've wanted to do for the last 10 years--since well before medical school. Recently (before this diagnosis) I have been thinking about a critical care fellowship, cause I really dig that too--all of your patients are really sick, the drunks are already intubated, and I just like the environment.
Concerns:
1. I have never been sick as often or as bad as I have in the last year. If every URI/gastroenteritis is moving me one step closer to dialysis, is the ER really the best place for me to be? Some have told me (again, before this diagnosis) that they essentially stopped getting sick after their intern year, but can I trust this anecdotal info?
2. Even if I stop catching every URI that walks in the door, what about being on steroids while being exposed to every bizzare, virulent bug that walks in the door? What about the serious infections that occur in immunocompromised states? Again, seems like the ED may not be the ideal environment.
3. If I decide to do something else, what specialty do I move to? IM/FP would be no improvement (and I've never been interested). Radiology certainly has the least contact with sick people, but how difficult is it to transfer into? Anesthesia would be another option with the same question. Also PM&R seems like a good lifestyle, probably easy to find a spot (speculation), but would I be bored out of my skull (again, speculation based on ignorance)?
I know this sounds like a big pity-party, and I am kind of overwhelmed, but I'm serious about these questions, so I'd appreciate any advice or suggestions.
SF