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    Default please give me advices for an apeal about disability

    Hi,
    Ok, so I got an answer from the committee, the one that I requested recognition for disability from. The one with the ignorant, full of himself, disrespectful doc, who checked me only 5 min, with dismissive gestures, I wrote about it here http://www.wegeners-granulomatosis.c...k-sick-10.html
    as expected, they didn't give me the 90% I aksed for, only 50% which means nothing. I was not surprised, they are known as ***** still I was angry and started to write my appeal, which I can submit in 60 days.
    In their answer they didn’t give any argument why I shouldn’t get more. They wrote only one line: "suffering from temporary vasculitis".
    What ? since when is vasculitis temporary ?
    I will be glad to get any advice as to what to include in my letter to them.
    Thank you for being here. I couldn’t have made it without you
    Alysia
    dx 2008


    Here, in this forum, I have found my sweet eternal love, my beautiful Phil.. :
    https://www.wegeners-granulomatosis.com/forum/threads/4238-pberggren-memorial-thread
    "You are my sunshine", he used to sing to me... "you make me happy, when skies are grey" I still answer him.
    Rest in Peace, my brave Batman and take care of your weggies from heaven, until we meet again.

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    Quote Originally Posted by Alysia View Post
    They wrote only one line: "suffering from temporary vasculitis". What ? since when is vasculitis temporary ?
    Boy, I wish it was temporary! Wouldn't that be GRAND?!?!?

    Quote Originally Posted by Alysia View Post
    I will be glad to get any advice as to what to include in my letter to them.
    Perhaps you could send them a link to the VASCULITIS FOUNDATION website and maybe a couple PDFs from major university/teaching hospitals to EDUCATE them about the disease--since they obviously know NOTHING about it!

    I wish you all the best Alysia!!
    MikeG-2012

    "You never know how strong you are until being strong is the only choice you have"


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    yes, they know nothing. thanks Mike. diabetes here got 100%. they don't know what is wg so they gave me only 50%. are we less severe then diabetes ?
    Alysia
    dx 2008


    Here, in this forum, I have found my sweet eternal love, my beautiful Phil.. :
    https://www.wegeners-granulomatosis.com/forum/threads/4238-pberggren-memorial-thread
    "You are my sunshine", he used to sing to me... "you make me happy, when skies are grey" I still answer him.
    Rest in Peace, my brave Batman and take care of your weggies from heaven, until we meet again.

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    What did your doctor send them? Is this federal disability from the state or private insurance? You may need to get a lawyer.
    Phil Berggren, dx 2003

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    it is from the gov. the institute for national insurence. my doc send them an opinion over 5 pages with about 20 papers added and claimed for 90%. they didn't read it ! in their letter they write that I gave only 3 papers !
    Alysia
    dx 2008


    Here, in this forum, I have found my sweet eternal love, my beautiful Phil.. :
    https://www.wegeners-granulomatosis.com/forum/threads/4238-pberggren-memorial-thread
    "You are my sunshine", he used to sing to me... "you make me happy, when skies are grey" I still answer him.
    Rest in Peace, my brave Batman and take care of your weggies from heaven, until we meet again.

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    Good luck, Alysia. I wish I had something helpful to say. Here, if you are working full time or beyond a certain amount, you can't get the federal disability because they see that you are able to work. I don't know how much you are working, or how it is done there. Phil may be right that you need to get a lawyer. I wonder if cutting back on your hours voluntarily would help, too. A lawyer could advise you on that.
    Anne, dx'ed April 2011

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    Quote Originally Posted by Alysia View Post
    yes, they know nothing. thanks Mike. diabetes here got 100%. they don't know what is wg so they gave me only 50%. are we less severe then diabetes ?
    Diabetes can often be reversed with diet and weight loss. Everything i have read about WG says it is incurable! However, there is treatment for Wegeners. Sadly, for this disrespectful doctor, there is no treatment or cure for stupid!!

    I am SO sorry that you are going through this, but I know you will be able to assemble a rousing appeal. I suspect that some statements from your doctors, hospital records etc will help. I would include quotes and links from the most well regarded hospital and research facilities. In this country, I would suggest Johns Hopkins, The Mayo Clinic, and of course The Cleveland Clinic. I know there are many more. YOU GO GIRL!!!
    Jacquie (aka Lifelong Booknut)

    Updated status: "Honorary Weggie"

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    I would just add, give very specific details of what you can and can't do and for how long, eg, sleeping x number of hours plus napping in the afternoon, routines required for managing your symptoms (example tell them if you need to rinse your sinuses and use a nebulizer twice daily for total two hours), sitting in a warm bath or going for physio or whatever else takes your time and energy to manage your disease, how frequent are your appointments etc. they look at functional abilities and daily routine... When they see that after adding up everything the disease 'takes' from your day, there's not much of it left, it is harder for them to deny. I don't know how the system works in Israel, but here many people are initially denied and then succeed on appeal. In addition to sending the reading material you could tell them clearly that vasculitis is not temporary and you can expect to deal with it for life. In case they don't read the attachments. Sorry you have to go through this! It's stressful having to try to prove your illness... I hate it. You feel guilty as though you're making bit up or being lazy. They should feel guilty for causing ill people more stress.
    Last edited by LisaT; 06-04-2014 at 12:52 PM.
    Just when the caterpillar thought the world was over, she became a butterfly.
    - English proverb.

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    Quote Originally Posted by BookNut View Post
    I would include quotes and links from the most well regarded hospital and research facilities. In this country, I would suggest Johns Hopkins, The Mayo Clinic, and of course The Cleveland Clinic. I know there are many more. YOU GO GIRL!!!
    good idea. like Mike also said ! I will ! thanks !!!
    Alysia
    dx 2008


    Here, in this forum, I have found my sweet eternal love, my beautiful Phil.. :
    https://www.wegeners-granulomatosis.com/forum/threads/4238-pberggren-memorial-thread
    "You are my sunshine", he used to sing to me... "you make me happy, when skies are grey" I still answer him.
    Rest in Peace, my brave Batman and take care of your weggies from heaven, until we meet again.

  10. #10
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    WOW, thanks everyone, also those that I didn't thank by relating specific to their replies
    I love you all very much I knew I can count on you.
    so I need to make a big file, and to include, all my complaints, with exagerating (thanks Titus), and with all the papers from the docs (I have more then 20 from alll kinds of docs) and also links or articels about wg, because prob they are so ignorant
    I don't know if I will take an attorney, but I will check about it.
    after all, I can be my best advocate. I hope.
    thank you so much for your support and good words and excelent advices.
    I am so blessed to have my weggie family
    weggies are not only kind, sweet, and good looking but also so wise
    Alysia
    dx 2008


    Here, in this forum, I have found my sweet eternal love, my beautiful Phil.. :
    https://www.wegeners-granulomatosis.com/forum/threads/4238-pberggren-memorial-thread
    "You are my sunshine", he used to sing to me... "you make me happy, when skies are grey" I still answer him.
    Rest in Peace, my brave Batman and take care of your weggies from heaven, until we meet again.

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