Diana M. Maulding v. Louis W. Sullivan, Secretary

961 F.2d 694
CourtCourt of Appeals for the Eighth Circuit
DecidedMay 5, 1992
Docket91-2747
StatusPublished
Cited by51 cases

This text of 961 F.2d 694 (Diana M. Maulding v. Louis W. Sullivan, Secretary) is published on Counsel Stack Legal Research, covering Court of Appeals for the Eighth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Diana M. Maulding v. Louis W. Sullivan, Secretary, 961 F.2d 694 (8th Cir. 1992).

Opinion

WELLFORD, Senior Circuit Judge.

Plaintiff, Diana Maulding, filed a complaint with the Merit Systems Protection Board (MSPB) alleging that she was constructively discharged from her agency job at the National Center for Toxicological Research (NCTR), Food and Drug Administration (FDA), United States Public Health Service, based on adverse agency actions as well as charging sex and handicap discrimination. 1 The administrative law judge (ALJ) found in her favor on the handicap discrimination claim, but found for the defendant on all other claims. The agency appealed the ALJ’s decision to the MSPB which reversed the rulings on handicap discrimination that were favorable to the plaintiff. 42 M.S.P.R. 605 The district court, on appeal, affirmed and dismissed all of plaintiff’s claims for relief. We AFFIRM.

The plaintiff began her employment with the Public Health Service, a division of the Department of Health and Human Services, in 1976. From 1976 to late 1980, she worked as a chemist in a laboratory, first in the Teratology Division and then in the Chemistry Division. She made no complaints to her superiors about breathing or pulmonary problems during the time. In December, 1980, the plaintiff was reassigned to a position as a pharmacologist in the Office of Scientific Intelligence, which later became part of the Division of Comparative Toxology, working in an office rather than in the laboratory.

When Dr. Lionell Poirier became Director of the Division of Comparative Tox-ology in early 1987, he began undergoing a long planned reorientation from “paper” research to bench or laboratory research in the area of nutritional toxology, the area in which plaintiff worked. Dr. Poirier spoke with each member of his staff regarding the proposed transition to laboratory research. At that time, Maulding informed him that she would not work in the laboratory due to a claimed allergy to certain chemicals which would be utilized in the laboratory.

In early 1988, persisting in her claims that she could not safely work in the laboratory, Maulding requested part-time work at NCTR so that she could obtain an outside position as a part-time law clerk to support herself. She reiterated her claim that health considerations precluded her from participating in lab work. In February of 1988, Dr. Poirier denied her request for part-time work. Insisting that the Division would be doing primarily lab work, Dr. Poirier asked the plaintiff to produce specific and current information about her alleged allergies or sensitivities to various substances to support her request to be excused from lab work. Dr. Poirier informed the plaintiff that her request would be submitted and reviewed by Dr. George Smith, the agency’s medical advisor, pursuant to OPM regulations.

In response to Dr. Poirier’s request, the plaintiff submitted a letter from Dr. Alvin Strauss, dated April 18, 1985, recommend *696 ing that she not be assigned to the lab. 2 Dr. Strauss’ letter indicated that the plaintiffs “further exposure to noxious fumes” is detrimental to her health based on adverse asthmatic reactions from Maulding’s claimed exposure to phosgene some ten years earlier. Along with Dr. Strauss’ letter, the plaintiff submitted a copy of Dr. Poirier’s request for medical documentation and a memorandum dated March 11, 1988, prepared by Dr. Poirier and addressed to Dr. Smith, which listed the chemical compounds that might be present in the lab. A proposed position description was also presented which indicated that the plaintiff would be conducting in vitro cell culture experiments in the lab.

Dr. Smith reviewed the documents submitted by the plaintiff to ensure that (a) the diagnosis or clinical impression was justified in accordance with established diagnostic criteria; and (b) the conclusion and recommendation were not inconsistent with generally accepted medical principles and practices according to 5 CFR § 339.-102, the applicable regulation. On March 25, 1988, Dr. Smith wrote a memorandum to Mary Long, an employee relations specialist, FDA, stating that “without clinical records to document the existence of a medical condition that warrants restriction from specific chemical exposure, and documentation that such exposures are likely to occur ...,” and “because no information exists that the plaintiff would be exposed to allergens in the laboratory to which she would not be exposed elsewhere, there is no medical basis upon which to recommend approval of her request.”

On April 8,1988, Dr. Poirier assigned the plaintiff to work in the laboratory. Because she did not come to work as ordered, Dr. Poirier next directed the plaintiff to report to the assigned laboratory job on April 13. On that day, she reported to NCTR for about two hours, without going to the laboratory. Dr. Poirier then charged the plaintiff with absence without leave for two days because she did not report to the laboratory without any approved excuse for her absence. 3

Upon request, the plaintiff was granted more time to supply Dr. Smith with additional medical documentation supporting her health claims. Maulding then submitted the following additional documents: (1) copies of office records from March and April of 1988 from an Arkansas family clinic; (2) a letter, dated April 13, 1988, from Dr. Forrest B. Miller recommending that plaintiff refrain from lab work; (3) a copy of a medical record from Dr. Strauss’ clinic; (4) a note to Dr. Smith from plaintiff dated April 22, 1988; (5) a copy of a page from the Dictionary of Chemical Producers showing that plaintiff’s former employer (prior to 1976) utilized phosgene; and (6) a memorandum from St. Vincent’s Infirmary dated April 15, 1988. After reviewing this additional information, Dr. Smith determined that the records did not sufficiently indicate that the plaintiff had a disease of the lungs or respiratory system except for allergies that the plaintiff has had all her life. In summary, Dr. Smith concluded that Maulding failed to carry her burden of persuasion in this regard.

Dr. Poirier accordingly directed the plaintiff to report to the laboratory on May 11, 1988, and the plaintiff again refused to report for this work. Beginning May 16, 1988, the plaintiff neither reported for duty nor requested leave. On June 21,1988, Dr. Poirier wrote to Maulding directing her to notify him by June 28, 1988, of her intentions with respect to her assigned job. On July 15, 1988, in the absence of any response, Dr. Poirier notified the plaintiff that he proposed to remove her from feder *697 al service as a pharmacologist. Defendant asserts that Maulding was notified of her right to respond, but failed to do so. We are furnished no contrary information in this respect.

The deputy director of NCTR notified the plaintiff of her removal, effective August 27, 1988, for failure to follow a written direction and because of her absence without leave. There was no response.

On September 20, 1988, however, Mauld-ing appealed her removal to the MSPB, alleging that the agency constructively and impermissibly discharged her.

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Bluebook (online)
961 F.2d 694, Counsel Stack Legal Research, https://law.counselstack.com/opinion/diana-m-maulding-v-louis-w-sullivan-secretary-ca8-1992.