Lenny17019
12-05-2003, 11:44 AM
If there are any people with P out there who are in the military, I thought I'd add my 2 cents of advice.
I retired a couple of years ago from the Army after 20 years. I was diagnosed with P at 28 and spent about 13 years seeing military docs (including Walter Reed) concerning it. I have a moderate to severe case of it - no P arthritis, though. I suppose you could find lesions on just about every part of my body.
Anyway, after retiring, I went to the VA to be evaluated. They were very curious and did an extensive interview. They then took pictures and sent me home. I later got a letter in the mail saying I had 60% disability for P!
When I tell people about the disability, they are amazed since most people don't see the P on my arms, legs, back, nails . . . It does make me proud of the Army, though, still taking care of me even though I'm retired. Who knows, maybe the stress of the Pentagon, always wearing a hat or helmet, hanging around the motor pool, or sleeping in the woods aggravated the P.
Bottom line is:
1) Make sure your medical records are well documented as to when you got diagnosed with P and all the treatments.
2) Get pictures when you get evaluated for disability - they communicate much better than words to the board.
3) Don't be shy at the evaluation. Usually I'm embarrassed to tell, must less show, people about how bad I have P. I was open and honest with the VA docs. (I suppose you could blow them away by not using any meds or lotions prior to your evaluation, but I think they are smarter than that).
I retired a couple of years ago from the Army after 20 years. I was diagnosed with P at 28 and spent about 13 years seeing military docs (including Walter Reed) concerning it. I have a moderate to severe case of it - no P arthritis, though. I suppose you could find lesions on just about every part of my body.
Anyway, after retiring, I went to the VA to be evaluated. They were very curious and did an extensive interview. They then took pictures and sent me home. I later got a letter in the mail saying I had 60% disability for P!
When I tell people about the disability, they are amazed since most people don't see the P on my arms, legs, back, nails . . . It does make me proud of the Army, though, still taking care of me even though I'm retired. Who knows, maybe the stress of the Pentagon, always wearing a hat or helmet, hanging around the motor pool, or sleeping in the woods aggravated the P.
Bottom line is:
1) Make sure your medical records are well documented as to when you got diagnosed with P and all the treatments.
2) Get pictures when you get evaluated for disability - they communicate much better than words to the board.
3) Don't be shy at the evaluation. Usually I'm embarrassed to tell, must less show, people about how bad I have P. I was open and honest with the VA docs. (I suppose you could blow them away by not using any meds or lotions prior to your evaluation, but I think they are smarter than that).