The Board has determined that the veteran's claims for service connection for scleroderma, a stomach disorder (including ulcers) and an esophagus disorder, a lung disorder, and a nervous disorder are not well-grounded.
The deciding factor: The medical evidence does not support a link between these conditions and service.
- Claimed conditions
- scleroderma, stomach disorder (including ulcers) and an esophagus disorder, lung disorder, nervous disorder
- How they argued it
- Direct service connection
- Exposure basis
- None
- Rating assigned
- None in this decision
- Decision date
- June 5, 2000
- Citation
- 0014653
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 0014653.
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.
- Partly granted
The Board denied an earlier effective date for the grant of a 70 percent rating for PTSD and granted an effective date of May 31, 2004, but no earlier, for the award of a total disability rating based on individual unemployability due to service-connected disabilities (TDIU).
- Dismissed
The appeal was dismissed due to a claims processing error, as there was no adjudicative determination from which the Veteran could file a notice of disagreement.
- Denied
The Board denied the Veteran's claims for service connection for a lung disorder and scoliosis, finding that the evidence did not support the existence of separate and distinct conditions from his already service-connected disabilities.
- Remanded (sent back)
The Board remands the claim for service connection for scleroderma to schedule a VA examination and address the Veteran's reported symptoms during active duty and periods of ACDUTRA.
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