I found out last week that my LTD Appeal was denied. I knew that the decision was pending and that I should have an answer shortly before XMAS.
When I didn't hear anything I started emailing my attorney who I found on the Yahoo Disinissues group site. You can imagine how antsy I was. I had a high paying salary and paid into a really good LTD policy and they cut me off with no warning last April at the 2 yr mark.
They had me under video surveillance for 2 weeks and I left the house once during that time to go to the doctor, the ATM machine to deposit a check and stopped at the grocery store for some grub. They said if I was able to do those things that I could work. Then they sent the video and their interpretation of it and sent it to every doctor I've seen in the last 2 yrs asking if after viewing it if they thought I was so disabled I couldn't work. They got a bite from my podiatrist who said I may be able to do sedentary work and walla! That's all they needed to deny my claim.
The attorney said I had a really good case. I had 5 letters from doctors that said I was disabled. The last was a physical capacity evaluation completed by a Rhuematologist. I won my SSD case in June. And the video shows me limping and using a cane and never lifting any groceries.
So over the Holiday I went into an old email account that I haven't used for 6 months and there was the email from my attorney saying that my case was denied on Dec 11. I don't rate a phone call, perhaps a letter? They suddenly forgot my current email address? Here it is Jan 7 and I still have not talked to them in person. They are avoiding me like I have the plague. Today I received my case file in a large box from Fed Ex with a letter saying that they have decided not to litigate the denial because I can't afford them. The appeal they did was on contingency. If I won they would take half of my monthly payments. Since I lost, there is no incentive for them.
Because I can't work and I'm poor I guess I can't fight this.
I'm pretty down. Any suggestions?
So sorry for what happened to you. I got mine long long time ago. I live East Coast, and got a private lawyer (he and other guy only did SSA disability claims). He was terrific, and my fee would only be a % of what I got from SSA - long story - I was on my work's disability, so I didn't apply for SSA disability. And it was past 2 years when I realized I had to - my work disability insurance company requested this.
Everyone is turned down multiple times because they just can, which is why a disability Social Security lawyer is needed to represent you. They request Zero payment - SSA must pay them money when you are awarded the SSA disability - so you can have no money at all.
You already did the PCE testing which I wasn't allowed to do, and 5 dr letters - so let the Insurance company send you to a Hospital for further testing or to be diagnosed. Most all drs/hospitals where I am told Paul Revere NO - they won't be part of this, but Johns Hopkins gets federal funding so had to say yes.
You have to take all the Dr files, and test results to 3rd party so they can tell whoever that you are too sick to work.
I just don't get if you are getting disability from work from Harford Insurance?
I understand you were turned down, but so is everyone else.
My private Disability lawyer went before a Federal Judge with all my records - and he wrote long brief
on how I can't work - I was the first one in my State that got awarded Disability only on CFS, not on mental disorder - this is main key.
My point being - I got my Disability from work from Paul Revere Ins CO - they are huge. I found out on disinissues site to be very careful - they film everyone - they hire guys to watch you come out, go to car, etc.
I was much too ill to shop, or drive, or go anywhere - so I didn't have this problem.
I had a Dr who called the leading disability drs in US - at time they were pretty famous. He studied CFS/ME.
He would yell at Paul Revere when they wanted to test me themselves - he said NO - it would ruin me to have 2 days of testing which was basically physical tasks.
I was harrased by phone for couple years by Paul Revere, not Social Security - they were sending man to my place - my home - to see I guess anything they could cut me off on. Again I threatened them - due to me living alone, and cannot let anyone in here, especially a lone male.
This was a full time job for me - and I slept 12 hrs a day for 1st 5 yrs, and lost 20 lbs too.
I would never go to huge Insurance Co to represent me - not criticizing - but they are most likely to get you denied - or is this the Ins Co that would give you disability?
As long as you are sick, and can't work - and this is big one - you must be assessed as having CFS/ME - not just by your dr, but this ins company sent me to Johns Hopkins who didn't believe in this disease, but after I took them huge file folders by my Internist - they had to agree I had it, plus I had extensive testing by Johns Hopkins themselves - which eliminated Lyme Disease, AIDS, Leukemia, MS, and one other.
It is a huge long fight to get disability for CFS/ME - I would have thought by now - it would not be, due to proof that this is real. NIH - gives 5 million a year grants to famous Drs to study this disease, and so far they have definitively seen something in our blood that non CFS people don't have, could be not causal but it's a start.
So unclear if Harford Insurance was trying to get you disability - or representing you.
One has to use private Social Security disability lawyer for this - and be very careful, you are being filmed all the time, just assume this.
Starlily88