For all, but especially those who may be lucky enough to have LTD (Long  Term 
Disability) insurance.
 
Come of you may have heard this before and for that I apologize, but not  all 
have, so I will repeat this story.  I worked for a company for 13 years  
prior to my TM, almost all of my time in Human Resources.  I started  my time 
there working in the Benefits department, and one of my responsibilities  was 
to 
do the new hire benefits orientations.  I learned about  our plans, and sat in 
on a couple of orientations done by another employee and  when she got to the 
LTD section I was really surprised by what she would  say.  She said "it is 
much more expensive to  become disabled than to die" and encouraged them to 
seriously  consider applying for the coverage, as well as the medical and life, 
etc.   I worked for a retail clothing chain and this was not easy to get our 
young  population to understand in those days, unless they knew somebody with 
AIDS,  which was just starting to really surface.   
 
Of course I applied for LTD, as I saw the benefit in it.  I was 37 at  the 
time, and knew that if something happened to me, I had children to provide  
for. 
  I am so glad that I did, as it did come in handy.
 
The disability company can ask about whether or not you are getting SSDI,  
and if you are recently approved and your plan allows them to recover it from  
you, they will ask you to repay it to them.  If you have been getting SSDI  for 
some time, they are only asking for informational purposes, as it cannot  
have any bearing on your case.  Your LTD benefits  are based on your earnings 
while you were working and is not reflective on any  SSDI money that you 
receive, 
whether increased or not.
 
The LTD companies try to get people to just back down and not fight for  
their rights.  They hope that those who aren't really disabled will back  down 
as 
the may not be able to prove their case.  They hope that the sick  don't have 
the energy to fight.  They count on this.  This is why  we have to fight so 
hard to get and keep the benefits that we have.  It's  not easy when the meds 
scramble our brains and make it hard to  concentrate.  
 
I was actually very careful during my appeal when I was out of the  house, in 
my yard, in front of the house and shopping, etc.  as I was  afraid that 
there may be somebody trying to film me doing something that could  be used 
against me.  Sometimes I am able to do more than other times and  didn't want 
to 
have to fight about that too.
 
When my claim was reinstated, I got all pay retroactive to the date it had  
been denied.  They have to do that, and it was a nice chunk, but it was a  
drastic cut in our money until then.  My husband had still been working so  it 
wasn't as bad as it could have been.  The bad part is that we got  it in 
December 
for 18 months worth and all taxable for that year.  Bummer  to be all taxable 
without no where near enough taxes taken.  But, nice to  be able to catch up 
on everything and have a nice Christmas then.
 
So far for medical insurance we are in good shape as we still have with  
Pete's ex-employer until he turns 65.  The good thing is that the coverage  
stays 
the same, which was good coverage, and we pay less than we could get for  good 
coverage on our own, if we could get good coverage with my  pre-existing.
 
Take care all and hope you are able to stay warm as well.
 
Hugs, Barbara A
 
 
 
 
 
\ssage dated 12/8/2008 3:16:39 P.M. Pacific Standard Time,  
[EMAIL PROTECTED] writes:
 
 
Barbara, 
Thank you for your kind words and advice. 
I have hired a lawyer to handle the case.  I worked for the county  
government and ERISA laws don't apply to government employees so I will be  
able to sue 
the company for her fees which under ERISA you can't do.  
I know that I will win eventually.  I hae gone through the small  savings I 
had, maxed out 2 credit cards and now, when the stock market is down  60%, I 
sell stocks from time to time.  I talked to my lawyer and she  said that we 
could bring a civil suit against the LTD compnay for the  total amount that I 
have 
lost as well as mental and physcial  anquish.  SO guess what, they should 
have continued to pay me because  they have really ticked me off!  Too many 
companies do this and it  is not humanly nor morally correct. 
Yes, I know there are people that take advantage of insurance companies but  
those people that really need LTD should not be punished - aren't we suppose  
to be innocent untl proven quilty - OH THAT"S FOR THE RICH - I keep forgetting 
 that!   
What really gets me is the way the insurance company went around everything  
and basically tricked me and my neuro - there should be laws against  that.  I 
always thought that ERSIA was suppose to protect employees BUT  in reality 
ERSIA protects employers and insurance companies and allow lawyers  to make 
more 
money!   
I don't know if you noticed but I really get upset regarding this  problem.  
I thought before TM that I was doing everything correct  financially to 
protect my future but I didn't count on insurance companies  bucking their 
responsibilities! 
I know that I am so much luckier than most.  I do have a home that's  paid 
for along with an older car that's paid for.  But there's the doctor  bills, 
meds, food, electricity, taxes, insurance and everything else adds up  to 
greater 
dollars than SSDI. I'm in the class that I'm too well off to get  help and 
yet not enough to make ends meet - a rock and a hard place that seems  to be 
our 
life!  I just hope that Obama can help us all in ways that we  can only dream 
of! 
Thank you for letting me boil over!   Everytime I think about  this, I get 
upset and I know that I shouldn't because all it does is harm  me!  Since July, 
I've had more attacks of spasms, headaches, and  more pain.  I know it is 
because of the stress!   
I need to follow my advice - let go let God!  Some days its easier  than 
others. 

Life is short! Break the rules! Forgive quickly! Kiss slowly! 
Love truly, Laugh uncontrollably . 
And never regret anything that made you smile.


Prayers and thoughts for you and yours,

Candy K.


-----  Original Message -----
From: [EMAIL PROTECTED]
To:  [EMAIL PROTECTED], tmic-list@eskimo.com
Sent: Monday, December 8,  2008 12:15:39 AM (GMT-0500) America/New_York
Subject: Re: [TMIC] your  thoughts?


Hi Candi,
    I wish you the best of luck with your LTD  hearing.  You have a right to 
all the paperwork out of your file at the  insurance co. and should order it 
if you do not already have it.  The  insurance companies have no conscience at 
all.  Their job is to get  people off the disability roles, and I understand 
that they need to get the  ones off that aren't really disabled, but not the 
ones that are.  
    My LTD provider (Prudential) did the same as  yours regarding sending a 
letter to my doctor requesting that he complete a  form about my condition and 
what my capabilities were.  They also stated  on the letter to him that I had 
been working on a part-time basis and  requested the stand, sit, walk, etc. 
questions.  Now, my policy states  that I am entitled to benefits if I am able 
to work on a full-time basis  based on my training or what I can be trained to 
do, something like that, and  on and on.  I haven't worked at all since Dec. 
2000, and they know it or  they would not have been paying me.
    This was sent to my Neuro, and all previous  correspondence was sent to 
PCP.  The Neuro hadn't even asked me to come  into his office for a visit 
before sending back the form to the insurance  company stating that since I had 
been working part-time that I could work  full-time now, after listing 
capabilities that don't match me at  all.  
    In the meantime, I had gone to a Physiatrist that  the insurance co. set 
up for a review of my condition.  This doc stated  that I was not able to 
work.  Then, since the insurance co. got the form  back from my Neuro stating I 
could work full-time, they contacted their doc  and asked him to reverse his 
decision and state that I could work, telling him  that my doc must know my 
condition better than he does, and he did it.  I  was denied my coverage at 
that 
point.
    It took a couple of visits to the Neuro to  get everything squared away 
with his paperwork and re-submitted.  It also  took me requesting copies of all 
my paperwork from the insurance co. in order  to have ammunition for my 
appeal.  There were about 3 reams of paper  worth of copies they sent me, and 
most 
were triplicates of my early TM years,  including hospital info.  That was 
very depressing looking back at that  stuff.  I had to submit 2 appeals.  They 
were tough, but I'm glad  that I stuck with it and finally noticed what they 
did 
with the doc they  hired.  That was very underhanded and let them know it was 
wrong and not  proper business practice.  When I later told my husband he was 
really  angry and felt we could have sued them for what they did, but I don't 
 know.  Especially since I may not have caught what they did, and could  have 
possibly lost again and had the expense of a lawyer.  If it went to  a lawyer 
and I would win, they pay the lawyer.  If I lose, I pay the  lawyer.
    This was about 3 years ago, and I just got  another letter with a form 
for a doctor's statement.  I now have a new  PCP and Neuro, so I hope all goes 
well.  I have a HMO and the process is  that I drop off the forms to the 
medical secretaries and they go back and  forth to docs to be filled out, 
transcribed, approved, distributed and  filed.  I sent emails to them letting 
them know 
I am available for  questions and the trouble that I had last time.  I hope 
this works out  without any snags. If we don't fight for our rights, who will 
do 
it for  us??     
 
Hugs to all, Barbara A
   



 
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