The Board denied the claims for service connection for the cause of the veteran's death and for DIC benefits, pursuant to 38 U.S.C.A. § 1318, as there was no evidence that any of the veteran's service-connected disabilities caused or contributed substantially or materially to his death.
The deciding factor: The most probative medical opinion weighed against a finding that the veteran's service-connected disabilities caused or contributed substantially or materially to his death.
- Claimed conditions
- multiple myeloma with bone metastases, renal failure, peripheral vascular disease
- How they argued it
- Direct service connection
- Exposure basis
- None
- Rating assigned
- None in this decision
- Decision date
- May 5, 2008
- Citation
- 0814744
What this means for you
A denial is a starting point, not the end of the road. You can see why this claim fell short — and, if you are still inside the one-year window, the appeal lanes that may remain open to you.
What you can do next
Related decisions
Other Board decisions on a similar condition or argued the same way.
- Remanded (sent back)
The Board remands the claim for a VA medical opinion to determine if the Veteran's service-connected disabilities, including medications taken therefor, were a substantial or contributing factor in his death.
- Remanded (sent back)
The Board remands the claim for service connection for blood clots to afford the Veteran a VA examination and obtain a medical opinion regarding the etiology of his condition, as he has a history of lower extremity blood clots and participated in toxic exposure risk activities during service.
- Partly granted
The Board denied service connection for Parkinson's disease, emphysema, muscle cramps, bilateral shoulder disability, and neck disability. However, it granted service connection for peripheral vascular disease and asthma.
- Denied
The Board denied service connection for various conditions, including renal failure, sleep apnea, erectile dysfunction, blackout spells, swelling of the eyelids, diminished eyesight, sleep deprivation, and bladder incontinence. The Board also denied a rating in excess of 10 percent for left ankle tendonitis associated with residual scar.
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