Disability Denial Upheld – MS, Fibromyalgia, Lyme Disease Diagnosed

In Hamilton v. Standard Insurance Company, the Fifth Circuit Court of Appeal upheld the insurer’s decision to deny long-term disability benefits to a disabled worker.  In this case, a phone company employee submitted a claim for long-term disability benefits alleging MS, fibromyalgia, and Lyme disease.  The long-term disability insurer denied the claim and the Court’s upheld the decision.  Based on my reading of the case, I would have to agree that the Court made the correct decision in this case.

This case illustrates a number of issues that you should be aware of if you need to apply for long-term disability benefits.  We will discuss each issue here.

Objective medical tests are required to support your doctor’s opinion

Ms. Hamilton’s family doctor diagnosed her with MS (multiple sclerosis), fibromyalgia, and possibly Lyme disease.  The only medical test performed by the family doctor came back negative for Lyme disease.

The family doctor did not perform diagnostic testing for fibromyalgia and MRI’s came back negative for MS.  In short, the file submitted to the insurance company for review did not contain any evidence which could minimally support the family physician’s diagnosis.

So what should you take away from this – a doctor’s opinion/diagnosis is not sufficient by itself to convince the insurer that you are disabled.  The opinion/diagnosis must be supported by recognized and appropriate tests to confirm/support the diagnosis.

A medical specialist should be utilized where possible

Ms. Hamilton’s family doctor diagnosed her with MS, fibromyalgia and Lyme disease.  While such diagnoses are well within the ability of the family doctor, these disabilities are better diagnosed and treated by specialists in the field.  A specialist’s opinion will hold more weight with both the insurance company and the court.

In this case, when the insurance company had the claim reviewed, it turned to specialists in the respective field to determine if the necessary testing was performed and if the results supported the diagnosis.  A rheumatologist evaluated the fibromyalgia claim for the insurance company and a neurologist evaluated the MS claim.  Both were board certified according to the opinion.

I take away from this that the court found it important enough to mention the board certification that you should find it important.  Plus, if you have a board certified doctor on your side, the court’s decision may be a little more difficult.

Pay attention to Appeal Deadlines

Here, the appeal was not submitted for over 2-years after the initial denial.  Luckily for Ms. Hamilton, the insurance company agreed to evaluate her appeal even though it was late.  The insurance company would have been well within its rights and the law to refuse to review the appeal due to its lateness.  And there would have been nothing that Ms. Hamilton could have done about it other than take the case to court.

Also, the court notes the lateness and so it did not go unnoticed.  By ignoring the deadlines and not requesting extensions in writing (and receiving a response in writing), you are giving the court an impression about your credibility and reliability.  Do you think it’s a good impression?

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One of your goals in appealing a denial to the insurance company is to provide them with enough sufficient and objective evidence to make it difficult for their doctors/consultants to rationalize a determination that you are not disabled.  Ms. Hamilton did not do that unfortunately.

I do feel bad for her because it does seem she was disabled and truly could have used her long-term disability benefits.  An attorney familiar with long-term disability claims and the process could have helped her make her appeal timely, provide more necessary information to support her diagnosis, and maybe helped her win her case.

This post was created by Greater New Orleans SSDI attorney and long-term disability lawyer Loyd J. Bourgeois on Louisiana Disability Law and is for educational purposes only. The social security disability or long-term disability information provided here is no substitute for speaking with or seeking assistance from a Louisiana lawyer familiar with social security disability claims or long-term disability claims.
2 Responses to Disability Denial Upheld – MS, Fibromyalgia, Lyme Disease Diagnosed
  1. Karen
    January 6, 2011 | 1:53 PM

    This is horrible we need to give these people this for couple months or have someone come in & see how we live. Took me 6 yrs. in that time got so much worse I also gave up & tried to work until 2X picked up off floor so weak could not get up. Guess you know what happened asked to leave. DUH, tried over & over could not make it in AM had to make things later.
    I am soooo sorry I am outraged how we are treated, FM,Cfids,MS,Parkinson’s(RLS IS),ALS,RA. All 1 of same just co-infections according to many Drs.
    Auto Immune is now being looked at as Lyme, You just do not wake up 1 day body turns on you. Cause & effect for everything. Lies by Govt. to hide their part, That Jesse Ventura, even opened up truth on Lyme. Open your eyes folks. I am in late stage & have many ALS signs. Was dxed with FM,Cfids,Lyme,MS,Parkinson all part of 1 co-infections & FM,as 1 of most painful parts being this is linked to brain so it is all in our heads, so to speak. Keep up finding all info you can I work hard for Lymies. Went from Jock,business,owner, to blob. Who would want that life????? Get honest to yourselves, Dr.s,Govt.++++>People in general no 1 could make this up///Please find some compassion people!!!!! Hugggggssss, To all in need, Karen

  2. Dr. Jan Hogle
    May 8, 2012 | 3:49 PM

    This is frustrating to read on many counts. Lyme is well-documented to trigger MS in at least 1/3 of MS cases, and doctors who are literate in Lyme believe Fibromyalgia is not a separate disease at all but undiagnosed Lyme. The fact that this person failed to file an appeal in a timely manner is classic Lyme behavior, as time and memory–as well as attention to detail and ability to complete tasks–suffers in many, if not most, Lyme patients. Lacking sympathy for these failings is akin to being annoyed at someone for limping with a broken leg. And, it should be noted that it is common for Lyme NOT to show on the first or the second test, or to never show up at all, due to the extraordinarily poor tests available for Lyme. My father nearly died of Lyme, and yet never showed a positive test for Lyme itself. Tests did show confirmation of bacterial die-off months after he was treated for it with heavy antibiotics, but many MDs refuse to treat until a test shows positive. Lyme is an example of where our medical and court systems are seriously behind in understanding and dealing with a more-common-than-most-realize disease.

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