In 1995 Unum’s Atlanta Southern Region Benefits (SRB) put together what it called a “collaborative strategy” to “manage CFS files more aggressively” and in a “proactive rather than a reactive fashion.” The so-called strategy was called the Chronic Fatigue Syndrome Management Program (CFSMP) and involved members of Unum’s management such as Dr. Carolyn Jackson, Sally Fowler, Dr. Don Abbott and potentially Susan Steele and Anne Dinsmore.
The 1995 document specifies that in part the role and responsibility of those involved will be to “engage in open and objective discussion on interpretation of results from IMEs and FCEs.” Unum’s objective regarding the CFS project states the following, ” The CFSMP is based on the premise that CFS impacts more than just UNUM employers, attending physicians, and claimant are at risk. Many attending physicians are having a difficult time managing through the subjective nature of CFS. Group policy holders (employers) are paying higher premiums and losing valued employees. Many highly educated and trained professions are losing motivation and slipping into self-imposed oblivion because of CFS.”
Unum claimants and insureds with CFS should not walk over the last statement….”slipping into self-imposed oblivion!” If the statement truly represents the philosophy of Unum in reviewing disability claims, then insureds certainly are being subjected to a deliberate prejudicial review process in which the claim doesn’t have a chance of being paid. Although the CFSMP project documents are old, there is sufficient file evidence to suggest CFS claim applicants today are subjected to the same highly discriminative view documented by management years before.
The document itself contains a page titled Chronic Fatigue Syndrome, Current Thinking at Unum. Quoting directly from that document here’s Unum’s Diagnosis, Claimant Profile, Condition Profile, and Treatment.
Diagnosis – “Neurosis with a new banner.”
Claimant Profile – “Professional working women ages 30-50; Susceptible to doctor’s power of suggestion; Self-reports symptoms; Longer Claim Duration; and Difficult return to work (recovery claims).”
Condition Profile – “Burnout: loss of concentration, memory, sleep; Sensitive immune system; CFS is a symptom, not a cause; Cause involves other psychological, psychosomatic issues; Often linked to soft tissue conditions (fibromyalgia).”
Treatment – “Eliminate all other conditions before giving CFS diagnosis.”
In its conclusion Unum outlines its final objective called Executive Summary as follows:
“The objective of the Chronic Fatigue Syndrome Management Program (CFSMP) is to effectively address the growing number of Chronic Fatigue Syndrome claims through collaboration with attending physicians, claimants, employers, and internal Unum groups thereby reducing Unum’s financial exposure while simultaneously motivating claimants to gradually and willingly return to work.”
As CFS insureds you need to be careful of what is called UNUMSPEAK when reading its literature. What this paragraph is directing to those who understand the lingo is this:
“The objective of the Chronic Fatigue Syndrome Management Program (CFSMP) is to effectively target and “risk manage” the growing number of Chronic Fatigue Syndrome claims by contacting physicians, claimants, and employers using a “collaborative strategy” to return CFS patients to work, thereby reducing Unum’s financial reserves by limiting the number of CFS claims that are paid.“
Amazing how different the message from management is when UNUMSPEAK is appropriately translated. As a former employee of both Unum Life Insurance and UNUMProvident I can accurately state I’ve sat through many “pilot projects” given by management where the objective is to target certain groups of claims intended to “reduce Unum’s financial exposure.” Great term for “deny more claims.”
Currently as evidence suggests from Unum claim files, CFS remains a “compilation of subjective complaints” by individuals who are “highly educated professionals slipping into self-imposed oblivion.” On occasion, Unum’s medical department appears to have some difficulty distinguishing chronic fatigue as a symptom of fibromyalgia as compared to chronic fatigue syndrome which is diagnosed using a set of diagnostic criteria published by the CDC.
Although there is a great deal of research going on in the medical community linking CFS to an identified virus, it is, of course, advantageous to Unum to claim results have not yet resulted in solid evidence. CFS claimants and insureds need to be careful what they wish for. If it should happen the medical community approves a blood test to identify a virus present in CFS patients, Unum and other disability insurers will no doubt look for results of that blood test in every CFS patient and will consistently eliminate all CFS claims with negative results. This is consistent with how UNUM currently manages Lyme patients in the absence of a positive Western Blot or CD-57 blood test.
Bottom line the existence of Unum’s CFS “collaborative project” report, even though the document dates back to 1995, is that it suggests the company had internal strategies to target certain impairments and occupational groups for the intended purpose of reducing its “financial exposure”. (Not paying claims.) Of course when asked about the project Unum alleges it never implemented the CFSMP program and didn’t promote it, although one might also argue Provident didn’t really know WHAT was going on at the time of 1999 merger.
In reviewing Unum Group’s CFS claims today, there is documented evidence suggesting the company: 1) still targets CFS claims; 2) considers the impairment to be “subjective”; 3) rejects physician’s medical reporting for CFS as over-restrictive; and 4) denies a disproportionate number of CFS claims as compared to other impairments. (Fibromyalgia also fits conveniently into this category.)
Once again those CFS insureds and claimants with Unum policies may not be getting a fair shake when the disability is described by the insurer as “highly educated professionals who are slipping into self-imposed oblivion.” The philosophy behind such statements suggests a claims process that isn’t fair or objective.
all the insurance companies do this – not just unum – and so does social security – we need doctors with some cojones who will shout the jerks down
You are exactly right – all disability insurers do basically the same thing. However, it’s been my observation Unum is the master of it. Thanks for posting.
This sounds like what they also do with Fibromyalgia. I’m dealing with The Standard right now and it’s the same story. We’ve been going through this for 2 years! Self-imposed oblivion…that says it all!
Very interesting Lindanee, especially that yesterday I got this letter from my insurance company, and they noted that there were no objective signs to my illness:
“In June 2010 the findings indicated your skin, hair and nails were normal. It also indicated your head eyes, ears nose, throat and neck were all normal. No abnormalities were found on your cardiac, abdomen, musculoskeletal and extremities and neurological assessments. ”
Awww shucks!
I’m not sure I really get the gist of your point of view, but there are no objective evidence provisions in disability insurance policies. In other words, there are no requirements for objective evidence in order to be paid a disability benefit. Sounds to me your insurance company is claiming your illness as self-reported which is what they usually do for chronic fatigue….Thanks for posting.
My point was, they are trying to get out of paying me disability, trying to find that nothing is wrong with me. If my nose, my skin and my ears are fine, well I must be fit to work, right?
Disability insurers often use outlandish comments and reasons to deny claims. Yours is certainly right up there.
I think I stopped reading this about halfway through, honestly. We all know it happens and to be reminded of it again is just.. well, depressing. And CONTRARY TO POPULAR BELIEF we really do try to avoid that, don’t we!
The purpose and philosophy of this Blog is to communicate knowledge to insureds at least equal to that of the insurance company. For insureds, knowledge is power and the more insureds know about how things work, the less likely they are to be cheated. The worst thing insureds and claimants can do is to lend a blind eye or a deaf ear to the egregious claims practices which deprive insureds of much needed benefits. Certainly, we aren’t trying to depress our readers, but rather give them the tools they need to challenge a system stacked against them. Even though many, many insureds know the insurance companies engage in bad faith, policies are still sold and benefits are unjustly denied without challenge from anyone. We seek to give insureds the knowledge to know when they are being deprived of legitimate benefits and potentially what to do about it. In this sense it is better to know, then not know. Thanks for posting.
Of course, of course. Blogs like this with such information need to exist. I myself was denied before finally allowed my benefits two years later. In no way was I trying to insinuate that this information was redundant or needlessly depressing. I’m sorry if it seemed that way. Perhaps my comment made more sense in my head before I actually posted it. I was just stating that, personally, I’ve already read it many times before: Just the sporadic thoughts of a passing illness-veteran.
There are many insureds who contact me actually defending insurance companys because of feeling guilty they have to go out on disability. We want to make sure all insureds know they are not to blame and that remaining in control of the process is the way to protect themselves from insurance abuse. Thanks for posting….truly. It’s people such as yourself who take the initiate to post opinions that is so helpful to others. Not surprisingly, insureds are often too afraid to comment which is why I’m so grateful to those who do.
Ahhhhhh, UNUM!!!! Just for the record I challenged them and Liberty as well … truly a battle and the stress of it all most likely made me feel worse, however, it had to be done!!! The people I worked with knew how sick I was – the insurance companies had to be challenged and I am very glad that I did!!! After hiring an attorney, I won . . . Patricia
We assist claimants who also win their claims and appeals. Congrats! Patricia you are one of the few who fight interestingly enough. Many are too afraid or do not have the money to fight back- a very sad testament to the insurance industry as a whole. Thanks for posting.
Hi Lindanee, I do know that most people do not fight back for many reasons. I truly didn’t have the money, but I managed a way to take a withdrawal from my 401K and that helped me. If not, I would have borrowed it. I was so upset with those insurance companies – they followed me everywhere (when I did get to go out) most times I was in the house and they would be walking by my front window or hiding up the street, etc. etc. I almost always knew when they were around. I had such an instinct for that!! Drove me so crazy, though . . . but it is all over with. Truly an intrusion of your privacy! Thanks for listening. xo
I think you are great. Please keep in touch.
http://biomedicalmecfs.blogspot.com/2011/01/unum-is-still-doing-it-to-disabled.html
A reader of my blog just alerted me to this post on your blog.
I think it’s time for another class action lawsuit against Unum.
Unum has conspired with psychiatrists in UK to have ME/CFS morphed into a mental illness, just as they have done in the US. They have been more successful in UK, but they are bringing their methods to the US. Those UK “psychobabblers”, as we who have ME/CFS call them, have captured the CDC when it comes to CFS.
I’m glad I found your blog. I think you’ll enjoy at least some of mine. See also: http://biomedicalmecfs.blogspot.com/2011/01/hysteria-as-misdiagnosis-then-and-now.html
Right now Unum is operating totally unregulated. And…the attorneys I’ve spoken to have no interest in pursuing Unum except in wealthy bad faith cases where there is a great deal of money to be had. What we need is another round of whistleblowers to provide incentive to all those attorneys who called me everyday in 2002 to obtain more and more information. Whistleblowing is a very lonely place after a while, but that’s what we need to wake up attorneys again.
I am aware of the activity going on in the UK spurned by Unum physicians who claim CFS and FMS are somatized creations of imagination. I have tried to warn recipients in the UK about Unum but have received very little response. Unfortunately for those in the UK their futures on the welfare system are identical to those here in the US. Apparently Unum’s philosophy is the same everywhere.
There is a test for Post Exertional Malaise being done in Stockton, CA that may be used to prove disability beyond any doubt. It will be like torture on the CFS person to do as it is two days of stress tests, but proves physical abnormalities that preclude ongoing employment.
See website links for more info:
http://web.pacific.edu/x31823.xml
http://forums.aboutmecfs.org/content.php?277-Lannie-at-the-Pacific-Fatigue-Lab-Part-IV-The-Report-is-In!
Thank you for this fabulous information. Fibromyalgia sufferers everywhere will benefit from your article. I hope that you continue to write good informative articles to help people with fibromyalgia, and I will be back to check often! Thanks!
I read this once a month to remember not to let my awareness, of all that is around me, change from what Ms Nee has taught me it need be.
Thank you for your blog and the valuable information and support you provide through it. As an individual who contracted with UNUM for both STD & LTD it is reassuring, however ironic, that the runaround, contradictory statements, and just plain piss poor customer service is not a singular experience. If an individual is not showing signs of depression or anxiety before they begin working with UNUM and their claims process it is nothing short of a miracle for them to get through the relationship without it. One more way for UNUM to deny or shorten the timespan for which benefits are, if ever, paid. Just beginning my initial appeal process…. I will be sure to check the site regularly as I have already found valuable information and acknowledgement around my concerns regarding EIRSA, IME, contractual semantics/legal applications, etc. and dealing with UNUM.
Good luck on your appeal. Those who read the blog regularly know I do not advocate attempting an ERISA appeal on your own. 95% of ERISA appeals attempted by claimants aren’t successful. Whether you hire an attorney, consultant or other paralegal is up to you, but you do need help to achieve a successful result. I know this is probably not what you want to hear, albeit it is accurate.
I have recently been accepted by a lawyer to take my claim against Unum for CFS and Fibro. I resent the knowledge that an “erissa” lawsuit means that I can only recover past payments and can not claim “bad faith” or any punitive damages for the stress they have caused. I see a top NY specialist and yet they equate their inside “Doctors”, IME D.O. Doctor and Job specialist as equal to her opinion. I resent that if the lawyer is unsuccessful I get nothing and that if he is successful I will pay him a chunk of what was owed to me by Unum in the first place. I thank you for having a blog with this discussion as this is all new to me and I feel very alone. I wish there was a new class action suit in play as there was in 2002. I wish someone would put together the multitude of CFS sufferers who are going through this so that there can be strength in numbers. While I would never wish this illness on any person, I wish that someday it could happen to a big celebrity who would draw more attention in one press release than all of us “non-celebrities” can as we cry in our beds. Thanks for listening – any and all advise is welcome and appreciated as I amble forward into this new and sad adventure.
I am also seeing a top ny specialist and need an attorney to fight unum. can you share with me the name of your attorney?Thanks
This was definitely my experience. I was told by a UNUM rep that my ‘unwiilingness to go back to work’ was part of the reason the claim was denied. I was so floored, I didn’t know what to say. I contacted 3 different law firms, none would take my case. At that point I decided to drop it, since the stress was too draining. It’s not right, but when the injured parties are too sick to do much about it, the bad guys win.
Thank you very much for making this post. Insurance companies (Unum included) all count on the fact that most ERISA claimants just fold up and go away when their claim is denied. In fact, ERISA claims are targeted by Unum because it is presumed most claimants cannot afford to litigate. It is also known by Unum most attorneys refuse ERISA cases, or at least the poorer ones.
And, you are exactly right. Those who are disabled just don’t have the stamina or power to fight back. Disability insurance cannot be relied upon to secure the future. It really is too bad.