The C&P I recently had was for the A&A. The report states 5/200 or worse on eyesight, that functional impairments are permanent, self-care skills unable to perform include:dressing and undressing, bathing, grooming, toileting. I did not receive a C&P for the SLE, I guess since they had already dxd me with it, and it is incurable...the only decision will be the percentage, IF they do grant it service connected. I believe I submitted enough evidence to show that it should be presumptive, but the VA didn't diagnose it until 1 year 1 month AFTER my discharge, and presumption is within 1 year from discharge. Evidence I submitted shows Raynaud's, GERD, rashes, unexplained swelling of lymph nodes, joint pain, etc., all within 2 months of discharge, The VA hospitalization that occurred 1 year 1 month after discharged, showed polyclonal gammopathy, which indicates autoimmune disease, with SLE right up there on the list..... Had the VA performed such tests with my first hospitalization, when it was first reported that I had Raynaud's, my diagnosis would have come within 2 months of discharge! I know.. we are talking VA, and even though I may have supplied evidence to support my contention, the powers that be can still deny the SLE as SC, due to the time frame.
I know some of you will understand that having to go through all of this is not only a royal pain, but the constant reminder that I am not the person I "should" be, is very difficult to accept. Each year when the VA would send out that paper for TDIU asking if you are employed, was a cold smack of reality of who I no longer am. Other then an accident, chances are high (ok, certain) that I will die from one of these lovely disabilities, and it's getting more and more difficult to lie to myself (but I give it a great try!). Maybe fighting the VA, is my little way of holding onto the person I once was! Old soldiers never die.... we just find new wars to fight!