The Veteran's heart disease is not service connected, and his peripheral neuropathy ratings are upheld at 10% each for both legs.
The deciding factor: The VA medical opinion determined that the Veteran's heart disease predated his diabetes, thus denying secondary service connection. The peripheral neuropathy was rated based on its mild sensory nature.
- Claimed conditions
- Congestive Heart Failure, Peripheral Neuropathy
- How they argued it
- Direct service connection
- Exposure basis
- None
- Rating assigned
- 10%
- Decision date
- April 5, 2010
- Citation
- 1012676
This is a plain-language summary generated by AI from a public Board of Veterans’ Appeals decision. It can contain errors — always verify against the original. Look up the original decision on VA.gov (opens in a new tab) using citation 1012676.
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 Veteran's appeal is remanded due to the need for a new VA examination focusing on his service-connected disabilities and their impact on his eligibility for benefits, as well as his need for aid and attendance.
- Granted
The Veteran's claim for an increased rating of 100 percent for CAD was granted effective November 28, 2023. The effective date is based on the date of a VA examination showing the increase in disability.
- Denied
The Board denied the Veteran's claims for service connection for Congestive Heart Failure with Atrial Fibrillation with AICD and Hypertension (High Blood Pressure), finding that there was no evidence of direct service connection, and that the conditions were not caused or aggravated by service-connected OSA.
- Granted
The Board granted separate 20% disability ratings for moderate neuralgia of the left and right lower extremity popliteal nerves (LLE and RLE neuralgia) effective from December 4, 2021.
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