Willis v. Callahan

979 F. Supp. 1299, 1997 WL 627058
CourtDistrict Court, D. Oregon
DecidedOctober 6, 1997
DocketCIV. 97-237-FR
StatusPublished
Cited by6 cases

This text of 979 F. Supp. 1299 (Willis v. Callahan) is published on Counsel Stack Legal Research, covering District Court, D. Oregon primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Willis v. Callahan, 979 F. Supp. 1299, 1997 WL 627058 (D. Or. 1997).

Opinion

OPINION

FRYE, District Judge:

The plaintiff, Jeanne Willis, brings this action pursuant to section 205(g) of the Social Security Act (the Act), as amended, 42 U.S.C. § 405(g), to obtain judicial review of a final decision of the Commissioner denying her application for disability insurance benefits.

*1302 BACKGROUND

Jeanne Willis filed applications for a period of disability and disability insurance benefits (DIB) on January 31, 1994, with a protective filing date of January 13, 1994, alleging that she became disabled within the meaning of the Act on June 25, 1993. The applications were denied initially and upon reconsideration. After a timely request for a hearing, Willis, represented by her lawyer, appeared and testified before an Administrative Law Judge (ALJ) on July 6,1995, and on September 28, 1995, as did several other witnesses.

On January 24, 1996, the ALJ issued a decision finding that Willis was not disabled within the meaning of the Act and therefore not entitled to DIB. This decision became the final decision of the Commissioner when the Appeals Council declined to review the decision of the ALJ.

FACTS

1. Willis’Background

Willis was forty-four years old at the time of the hearing. She has a bachelor’s degree in education and has completed two-thirds of the course work necessary for a master’s degree in psychology. Willis is a certified vocational consultant and has worked in vocational rehabilitation. She has supervised a group of sixty employees within the Workers’ Compensation Division of the State of Oregon. Her last job was Director of Education and Development of Staff at Dammasch State Hospital. She left that position on June 25, 1993 due to the symptoms of fibromyalgia. 2 Before leaving that job, Willis had reduced her hours to three-quarter time and later to half-time.

Willis completed a six-month program at the Oregon Health Sciences University (OHSU) for patients with fibromyalgia. The program includes education, support groups, and monitored exercise therapy. There is no cure for fibromyalgia. While in the program, Willis walked for exercise; however, she found walking so exhausting that she would have to go home and sleep. She has since discontinued the walking program.

Before her illness, Willis jogged, took ballet classes, exercised at a club, met at least weekly with friends to socialize, attended church every week, and worked in a job which included travel around the State of Oregon. At the time of the hearing, Willis was not employed. She testified that she was unable to exercise, rarely saw her friends, and went to church only on major religious holidays. Even when she went to church, she testified that she was unable to sit through the entire service. Her seventy-eight year old mother-in-law cleans the family home, and her husband and teenage daughter do the grocery shopping.

Willis, who is familiar with the concept of secondary gain from her rehabilitation work, denies that she is using her illness in any way. She contends that it is humiliating and embarrassing to have people think that secondary gain is a possible reason for her illness. She testified that work is 100% easier than fatigue and pain.

Willis takes five prescribed medications: one for restless legs, 3 a sleeping pill, an antidepressant, a thyroid medication which she has taken since she was a teenager, and pain medication. She has constant pain in most areas of her body for the entire day. Her muscles alternate between burning pain and deep, throbbing pain. Willis feels sleepy all of the time, no matter how much sleep she gets. Her concentration and memory have been affected; she is unable to comprehend information in the morning hours, to the point that she cannot read a morning newspaper and understand it. Cold weather or air conditioning cause the pain in her neck and shoulders to worsen. To combat cold, Willis frequently uses heating pads.

On most days, Willis engages in little activity before noon or one o’clock, when she showers and dresses. On her better days, she is able to be active on a limited basis for *1303 two to three hours out of her best eight hours of the day. She then has to take a nap. The rest of the day she sits, lies on the couch, or sleeps. Two or three days a month, she is so sleepy that she is unable to get out of bed at all. Willis has had to cancel social engagements at the last minute so often that her friends do not try to make advance plans with her. On the few occasions that friends have come to Willis’ home to visit, she has had to leave the group in order to lie down, or her friends have left early so that she could lie down.

Willis’ husband testified that for the first twenty years of their marriage, Willis was a very driven, high-energy person who worked full time, raised two children, engaged in many activities, and took full care of their home. He stated that she has changed from a woman who would chastise him for taking a nap to a woman who naps and watches television and does little else. According to her husband, during the best eight hours of a typical day, Willis is in bed half of the time.

2. Medical Evidence

Dr. John Garvey, Willis’ internist, first diagnosed fibromyalgia as the disease from which Willis suffered in the spring of 1992. She was referred by Dr. Garvey to Dr. Robert M. Bennett, Director of the Division of Arthritis and Rheumatic Diseases at the OHSU, who agreed with the diagnosis of Dr. Garvey. Dr. Bennett told Willis to reduce her work load to three-quarter time, and later to half-time, before concluding that Willis was totally disabled.

Dr. Bennett reexamined Willis on September 12, 1995. He concluded from her high score on an internationally used fibromyalgia impact questionnaire that Willis had “fairly severe fibromyalgia.” Tr. at 284. To test Willis for malingering, Dr. Bennett examined trigger points that are not widely published in medical literature and are not “known by the average doctor, not specializing in this area, let alone the non-medically trained patient.” Tr. at 285. Willis had tenderness at nine of these trigger points. Dr. Bennett concluded:

The patient’s degree of fibromyalgia severity is compounded by the restless leg symptoms and dysthymia. She could not be employed on a competitive basis. The problem with disability in fibromyalgia is not so much one of not being able to physically do a specific task, but rather the effects of activity in exacerbating the pain and increasing fatigue. Patients with fibromyaglia [sic] typically have flares of these symptoms precipitated by their work which leads to frequent leaves of medical absence. The bottom line is that patients with severe fibromyalgia, such as Jeanne, cannot be employed on a regular basis with any reliability.

Id. In a letter dated October 3, 1995, Dr. Bennett reported that Willis’ IGF-1 level had dropped by 90 ng/ml over three years. The normal age-related decline for Willis over three years would have been 10 ng/ml. Dr.

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Bluebook (online)
979 F. Supp. 1299, 1997 WL 627058, Counsel Stack Legal Research, https://law.counselstack.com/opinion/willis-v-callahan-ord-1997.