LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » General Support » SSDI Medical Exam

 - UBBFriend: Email this page to someone!    
Author Topic: SSDI Medical Exam
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 8 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
What are your experiences with this LOVELY process?

My daughter went in, had to walk a straight line, told she was too young to be disabled, couldn't be in pain she wasn't in a wheelchair or a stroke vicitm. She was told she could be cured, why isn't she doing anything about it?

I knew it would be a sham, but I didn't know how much.

Kelly

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 9 posted            Edit/Delete Post   Reply With Quote 
yes, that was my 1st one like that.

REMEMBER, YOUR DAUGHTER HAS A CHOICE TO GO TO HER PRIMARY DR/SPECIALIST. ASK IF THEY WILL DO THE TESTING OF "MEDICAL EVIDENCE" NOT IN HER FILE!

keep this in mind for future; reread my comments, minoucat's, conniemc, and the disinissues in the 25 pages of GOOD INFO! ok.

have she been denied on 1st step,

2nd step reconsideration

3rd step preparing for aljudge hearing? [confused]

HOW LONG WAS SHE IN W/DOC? mine wass 10-15 min. max

IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
This is our first time through the process.

The "exam" took 10-15 min.

This "doctor" was actually smiling (almost laughing) when she looked through my daughter's records.

I don't understand what you said about a choice, but I'll try to figure it out.

Kelly

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
Michelle M
Frequent Contributor (1K+ posts)
Member # 7200

Icon 1 posted      Profile for Michelle M   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Kelmo, I feel for your daughter.

I just had an SSDI exam a few weeks ago.

No, there is no way I could have substituted my own doctor's exam -- of which I have many. They decided they wanted a neurologist's evaluation.

I was asked to do a grip test. He hit me with a couple hammers to elicit reflexes. He ran a pin down my arms but did not even slow down enough for me to register my telling him that I couldn't feel it in certain places. (Bilateral radial nerve "dead" spots.)

He asked how often I have migraines.

He excused himself to browse through my file as it was clear he had not seen it before. I offered additional records but he refused.

As I was leaving, he said "Don't worry, I will make sure and tell SSDI about your headache pain." This was spoken in a reassuring manner, but who can be certain?

The whole thing was less than 10 minutes long.

I am choosing to believe he will report the truth, until and unless I hear otherwise. I have a plethora of positive tests and objective evidence. I made a respectful comment about my previous neuro, resisting the urge to mention that he was an idiot, because they are just down the street from one another.

He noted my dual diagnoses of MS and lyme. I said I guessed it didn't matter what you wanted to call it, the effect on me was the same.

Kelmo, I think you have good grounds for appeal if this doctor's findings are greatly at odds with your daughter's treating physician, whose opinion is given more weight.

Good luck and keep us posted.

Michelle

Posts: 3193 | From Northern California | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
cantgiveupyet
Frequent Contributor (1K+ posts)
Member # 8165

Icon 1 posted      Profile for cantgiveupyet     Send New Private Message       Edit/Delete Post   Reply With Quote 
I would start working on your appeal. My exam was just like that and they denied me.

My neck was horribly stiff that day, but he wrote I was fit to work. Also, i walked in with a water bottle,

so I wasnt sick since i could carry something. He also asked me if they found a cause for my IC (bladder) and I said no, they dont know what causes IC. He says everything has a cause.

He wished me luck, took a phone call during the appt to go over blood work with someone. sigh.

The whole process is a real joke in this country.

Hang in there.

Im fighting both ssi and my long term disability company right now.

--------------------
"Say it straight simple and with a smile."

"Thus the task is, not so much to see what no one has seen yet,
But to think what nobody has thought yet, About what everybody sees."

-Schopenhauer

pos babs, bart, igenex WB igm/igg

Posts: 3156 | From Lyme limbo | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Some drs are such Dippy Doodles!! [rant] [shake]

Don't give up!!!

=========

Cant...You should have said, Yeah, the LYME caused my IC! [you IDIOT!!]

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I told my daughter that she could've walked in blind and they would've told her that if Jose Feliciano could work, so can you.

The woman ended it by saying "You don't have chronic pain, but that doesn't mean you are disqualified".

How could she even say my daughter didn't have chronic pain, who's to judge by looking?!

I don't even know how to begin to start an appeal. We didn't do this for the check, we did this to get a letter of disability to take to my husband's HR Dept. so she could stay on our insurance. We want NOTHING from the STATE!!!

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
lymedad
LymeNet Contributor
Member # 8074

Icon 1 posted      Profile for lymedad     Send New Private Message       Edit/Delete Post   Reply With Quote 
GET A LAWYER !!!!

Having been through the process once without a lawyer (unsuccessful) and once with a lawyer (successfully), it's the only way to go.

If your dealing with company provided long term disability payments, you might get some financial help from the insurance carrier.

Good Luck to all.

Posts: 681 | From California | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
fatigued15
LymeNet Contributor
Member # 6437

Icon 1 posted      Profile for fatigued15     Send New Private Message       Edit/Delete Post   Reply With Quote 
My daughter was one of the fortunate ones when it came to ssd/ssi. She was approved thefirst time. She was seen by 2 doctors. We were very surprised she was approved that quick.
Posts: 488 | From NY | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
ConnieMc
Frequent Contributor (1K+ posts)
Member # 191

Icon 1 posted      Profile for ConnieMc     Send New Private Message       Edit/Delete Post   Reply With Quote 
Consultative exams (CEs) ordered by DDS (disability determination) or an ALJ (judge) are typically short and sweet. These doctors are paid very little for these exams and most take very little time.

The CE doctor does not make decisions on claims. What they do is determine if there is objective evidence that DDS can use when evaluating the claim.

I have seen many CEs which were very favorable to the claimant, and the claimant was still denied benefits.

Likewise, I have seen CEs which were not particularly favorable, and the claimant was allowed benefits.

An ALJ cannot use a CE to make a denial decision and disregard documentation from the primary treating physician and other evidence in the file as a whole.

Any time an ALJ cherry-picks evidence to suit his particular decision, he is generally leaving himself open for an Appeals Council remand or reversal.

An attorney or advocate can point out SSA rulings which state controlling weight goes to the treating physicians. And generate just that from the treating physician.

I always think it is best to have your own physician complete a letter to document specific reasons you cannot work.

Bettyg has a sample letter I wrote and many have used it to work toward successful claims. I have used it quite a few times successfully.

Remember, with SSA, it has nothing to do with the actual diagnosis and everything to do with your inability to function as a result of your medically determinable impairment.

With someone who is young, it is best to focus on residual functional capacity, and show that the claimant cannot sustain competitive employment. The SSA medical-vocational rules can be helpful. As long as a claimant has good longitudinal evidence that is fairly consistent, a claim can be won.

As far as CEs are concerned, go, take a page long summary with pertinent facts about your illness (date you became ill, tests with positive findings, what a typical day is like for you - don't leave out the neuropsychological symptoms) and leave it with him, and be cooperative and pleasant. He won't take much time out so be short and sweet to give him some overall understanding of what you have been through.

Good luck...

Posts: 2276 | From NC | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
RoadRunner
Frequent Contributor (1K+ posts)
Member # 380

Icon 6 posted      Profile for RoadRunner     Send New Private Message       Edit/Delete Post   Reply With Quote 
get a Lawyer at all cost.
make sure they are good also.

RR

--------------------
"Beep Beep"

Posts: 2630 | From ct | Registered: Nov 2000  |  IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Both her LLMD and her psychiatrist have completed and sent in their evaluations. Daughter has been a patient of her psychiatrist for five years, and her LLMD for almost two.

Thank you for your help.

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
AZURE WISH
Frequent Contributor (1K+ posts)
Member # 804

Icon 1 posted      Profile for AZURE WISH     Send New Private Message       Edit/Delete Post   Reply With Quote 
Definetely get a lawyer.

there is no way I would have been able to keep tract of all the paperwork and file things in a timely fashion myself.

If there is a local lyme support group I would ask to see who people reccomend.

--------------------
multiple chemical sensitvity group:
http://www.lymefriends.com/group/multiplechemicalsensitivities

Group for artists. All media welcome:
http://www.lymefriends.com/group/creativecorner


http://groups.yahoo.com/group/Lyme_Artist

Posts: 3860 | From nj,usa | Registered: Mar 2001  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 10 posted            Edit/Delete Post   Reply With Quote 
thx connie for contributing your background and your being a SSDI advocate/NON-lawyer expertise in this.

in my newbie package is connie mc's letter she mentioned toward the very end of ALL 25 pages of ssdi info; it's already in there and has been since she shared it on this board.

if you HAVE a good neuro psych presently, YES, you can ask that they do SSDI evaluation if that doc agrees to do this vs. their LOW-PAID mds they get.


if you are getting, make sure they can go to CIVIL/FEDERAL COURT if appeals council DENIES YOU TOO! i had my lawyer for almost 4 years until he quit me saying, i could not take your 1st one any further; he didn't have what it takes to represent me there!

so make sure that's one question you ask. if you go to federal court, the entire process can take between 6-9 years to get there and a decision made! my 2 apps took 5 full years.

after lawyer quit me, i represented myself since i was doing all the work and i was very dissatisfied with lawyer/his staff; many incompetents were fired during this time.

it took a LONG TIME TO DO THINGs, and this was noted for everything i was doing giving amount of hours etc. good luck!

also as you go along, you are going to want to read your file or disinissues web site says it's now put on CDS and you can get them.

just make sure you get the SSDI MDS/PHYSICHIATRIST'S REPORTS TOO so you can use what they are holding against you, and have proof showing they are WRONG! [Eek!]

IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks Betty, she goes for her psyche exam next week.

I'm having all her SSDI/MDS exam notes sent to our respective doctors.

My daughter is hoping to be well before any process concludes. I would shutter to think that she would have to go another 6-9 years like this.

She is going to venture from the home this semester and take ONE class at the community college.

We have arranged for Dial-a-Ride. It's a 50 minute class of sign language. She took an 8-wk summer class and found her brain could retain it.

This is a big step for her. No...it's HUGE!

It's been over two years since she has been in a classroom.

Kelly

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
Chaya
Member
Member # 12880

Icon 1 posted      Profile for Chaya     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by kelmo:
What are your experiences with this LOVELY process?


I am on SSDI and have been for several years. This is what I learned: SSA workers are pressured to turn down all apps the first time, no matter what.

The ones after that--the appeals--are given as short shrift as possible.

The philosophy appears to be that those who REALLY need it will keep trying. That is not true, of course.

I could tell that I was just being played with because the responses to each appeal were simplistic and beyond absurd.

I had gone to a lawyer, and she had warned me that that was going to happen: I was to just live through it (without having to pay her), then at a certain point, when it was time for an actual hearing, I was to return to her.

Then what happened? I got a court date with an alcoholic judge that hates women and most especially my lawyer. He throws out all her cases.

So she transferred my case to a partner, which forced a change of docket so I could appear in front of a different judge. This time I was assigned a "hangin' judge" who turns everyone down.

What to my wondering eyes--especially since I usually have routinely bad luck--this judge had developed a bad back and a sudden case of compassion for others' pain. She questioned hard, but my lawyer had prepared me well: she awarded me disability.

The lesson learned? Never even try to do this alone. You need the best SSDI lawyer in town.

Do it. It's CHEAP. [Smile]

Posts: 13 | From Santa Fe, NM | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.