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  When the time comes to think about disability, maybe something in  
this article I printed in the HAPS newsletter a few years ago may be  
helpful:


  Parkinson’s disease (PD) is a particularly difficult disease for  
Social Security Administration (SSA) personnel to understand and  
evaluate because of the varied symptoms which manifest differently in  
everyone.  Therefore, the crux of a PD disability case is built around  
the need to emphasize over and over again, in writing and in your  
doctor visits and interviews throughout the process, that no matter  
what your physical, mental or psychological problems the nature of  
your illness is such that you never know what your body will do or  
when your medicines will control your symptoms.  You don’t know when  
you can perform and you never know how long or how well you can  
perform. Your attendance is unpredictable and your work product is  
unreliable – therefore you are unemployable.

How to survive the Social Security Disability Process:

1)         Keep in mind that Social Security Disability Income (SSDI)  
is not welfare.  It is an earned benefit.  You have paid into the  
system and you are entitled to benefits if you meet the criteria.
2)         For a person with PD to qualify for SSDI benefits you must  
meet the requirements listed in section 11.06 of the SS Listing of  
Impairments:  “Significant rigidity, bradykinesia or tremor in two  
extremities which, singly or in combination, result in sustained  
disturbance of gross and dexterous movements, or gait and station.”
3)         The process is not a difficult one, but it does take  
organizational skills, patience and perseverance.
4)         Buy a notebook and take notes on every phone conversation  
you have with doctors, nurses, insurance companies, pharmacists, and  
especially with any SSA representatives.  Include the day, date, time,  
the person’s name, title, phone number and extension.  Write down the  
gist of your conservation and quote verbatim anything they told you  
that directly affects your case, or seems to contradict something else.
5)         Start right now - TODAY - to collect all records pertaining  
to your illness.  Buy a 3-ring binder and organize everything in  
chronological order.  If you don’t already have written reports of  
past doctor visits, call his/her administrative assistant or nurse and  
request them.  Include past and future written reports of each doctor  
visit, a dated list of your medications each time they change, any  
yearly evaluations from work that indicate you are regressing, all  
insurance reports, reports from any other physicians, including  
therapists, foot doctors, back doctors, your ob/gyn, internist–any  
medical professionals who observe your condition and can attest that  
you are disabled and/or that your physical condition is deteriorating.
6)         Send everything by registered mail and get a receipt.  If  
an SSA office is near you, deliver the forms in person and have them  
time stamped, dated and signed.
7)         Fill out the form completely and attach extra sheets if  
necessary.  Don’t limit yourself to the space provided.  Emphasize  
what you CAN’T do, not what you can do.  If asked if you can dress  
yourself, do not say yes or no.  Tell them how difficult it is to  
dress yourself and how long it takes compared to your pre-PD life.
8)         Be ready to describe a typical day and how you occupy your  
time.  You will almost certainly be asked this.  Remember to again  
emphasize what you CAN’T do, not what you can do. This web site can  
help you:  www.disabilty.com  Go to their home page and click on SS  
Disability Online for a wealth of information.  Ask family and friends  
what they notice different about you – what you appear to be  
struggling with, how you are getting worse.  Take notes.  Sometimes  
they have insights you might miss or might be denying.
9)         Describe special tools you need to accomplish tasks. Take  
note of the time it takes you to accomplish everyday tasks, compared  
to how long it used to take before PD.  Be specific.  For instance,  
with optimal conditions you may be able to get out of bed and be ready  
to leave the house in one and one-half hours, but on the other hand,  
you may never know when you wake up how well your medications or  
muscles are functioning, so this could take as long as 3-4 hours.
10)      You may be asked to see a doctor that they have chosen.  They  
give independent examinations but do not make recommendations or give  
advice on your case.
11)      Don’t worry about losing money if the process takes longer  
than you anticipated.  If you are approved you will receive back pay.
12)      If you are over 50 it helps, and if you are over 55 it helps  
even more.  Your age and education are also factors used to determine  
if you still can work.
13)      Sometimes when you call the SSA you will get different  
answers to the same questions.  Be sure to keep track of who told you  
what in your notebook.  Call back and talk to another representative  
or a supervisor if you have been given conflicting information.
14)      Include all your medical records with your initial  
application.  This could help shorten your processing time.  Also,  
retain a copy of everything sent to the SSA by doctors and anyone else  
communicating with them on your behalf so there are no  
misunderstandings about what is and is not in your file.
15)      Check periodically with your case worker to be sure that they  
are receiving all the information you and they are requesting from  
doctors, etc.  Be sure to do this in the spirit of helping the  
caseworker, not demanding to know what is going on with your case.
16)      Meet all the deadlines you are given.
17)      You may be asked to get statements from relatives, co-workers  
or friends.  Ask them to be honest and emphasize what you CAN’T do.  
This is not the time for them to be diplomatic.
18)      If you end up having an administrative hearing, do not worry,  
it’s not that bad.
19)      Wear business or business casual clothes.
20)      Do not drive to any appointments or hearings.  You will be  
asked if you did.
21)      If your handwriting is shaky, have someone else fill out your  
forms.  This illustrated that you cannot perform the basic tasks  
required in most jobs.
22)      DO NOT BE DISCOURAGED if you are turned down on your initial  
application and on “reconsideration”.  The process becomes abruptly  
fairer when you make it to the Hearings level.  Below the Hearings  
level, the SSA staff is overloaded and bogged down with paper work.  
However, at the Office of Hearings and Appeals (OHA) there is both  
time and competence, medical expertise, concern, compassion and in  
general, fairness.  Hearings are typically low key, always private,  
relatively informal and non-adversarial – nothing to fear.
23)      If your case goes to a hearing you are allowed to go before  
the date of your hearing and make copies of your file.  You will  
probably be surprised at how large and inclusive it is.
24)      If your doctor is uncooperative or doesn’t seem to get around  
to sending reports or information you request, offer to write them for  
him, pending his approval and signature.  Some doctors welcome you  
doing the work for them.
25)      When you make the decision to file for SSDI, do so at the  
earliest possible date.  Your case calendar won’t be retroactive  
earlier than the date you filed, even if you were ill or missed work.

Nina Brown
  "Circumstances determine our lives, but we shape our lives by what  
we make of our circumstances."

Secretary/Founding Board Member, The Alliance for Medical Research
(http://www.tamr-ed.org)
Founding Board Member, Texans for Advancement of Medical Research
(http://www.txamr.org)
Vice President, Houston Area Parkinson Society
  (http://www.hapsonline.org)
State Coordinator, Parkinson's Action Network
(http://www.parkinsonsaction.org)


On Feb 19, 2008, at 5:02 PM, [log in to unmask] wrote:

> I need to ask the group a question. I have Parkinsons and am 56 been
> diagnosed since 2001 and am doing fairly well.  I am still working.   
> I am a New York
> Ctiy Special Education teacher.  My question is:  when the time  
> comes that I
> need to go on SS disability, can I collect ssd and my full teacher's  
> disability
> pension?  I have heard Ray mention a few times that this is double  
> dipping
> from the Reagan era.  I am counting on the 2 sources of money when  
> the time
> comes.  Is it a federal law or just unique to certain states?  I  
> would appreciate
> if anyone could advise.
>
> Janet

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