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  • #1

    Question!

    I applied for disability in August. Today I got a letter saying that they are sending me to a physician to get more info about my medical issues. He is a general practice guy in the next town over. So, has anyone had to do this? I'm not sure what to think. Are these guys paid to just say we are all not disabled? Or is this a good thing that now I can tell my story personally and he can see for himself how bad off I really am?

    Any ideas of advice would be appreciated!
    Live life to the fullest day to day. The best way to eat an elephant is one bite at a time!
    _____________________________

    DX: IC - November 2002 after hysterectomy
    Interstim implanted March 2006 - died May 2011
    Interstim replacement June 2011
    Meds: Pain meds, muscle relaxer, cystex, and marcaine bladder instills as needed.
    Docs: Pain management doc, urologist, family practice
    Tags: None
  • #2
    It's not unusual to have to have to be seen by "their" doctor.

    Donna
    Stay safe


    Elmiron Eye Disease Information Center - https://www.ic-network.com/elmiron-p...mation-center/
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    Have you checked the ICN Shop?
    Click on ICN Shop at the top of this page. You'll find Bladder Builder and Bladder Rest, both of which we are finding have excellent results.

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    I am not a medical authority nor do I offer medical advice. In all cases, I strongly encourage you to discuss your medical treatment with your personal medical care provider. Only they can, and should, give medical recommendations to you.     [3MG]

    Anyone who says something is foolproof hasn't met a determined fool

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    • #3
      When I first applied 2 years ago I also had to go to their doctor. As Donna says, it's standard. I had an attorney from the beginning who advised me it would take at least 2 years to go through this process, largely in part due to my age. I was 38 at the time. So, I expected my application and appeal to be denied and that I would have to go to a hearing. Somehow though, it still stings when you get the denial letters. I am finally going for my hearing on Thursday. This process is very stressful, so the best I can suggest is to get an attorney if you don't already have one. Many attorneys don't take the cases until you are initially denied, but I found one who took me from the start.

      All my best,
      Deb

      Comment

      • #4
        Thanks! I have an attorney who has my info but won't take my case until I get denied. I haven't found anyone who will take a case before that. I'm trying not to get stressed about it and just take it all as it comes. They could have just denied me up front so that is a good thing I guess!
        Live life to the fullest day to day. The best way to eat an elephant is one bite at a time!
        _____________________________

        DX: IC - November 2002 after hysterectomy
        Interstim implanted March 2006 - died May 2011
        Interstim replacement June 2011
        Meds: Pain meds, muscle relaxer, cystex, and marcaine bladder instills as needed.
        Docs: Pain management doc, urologist, family practice

        Comment

        • #5
          It is never fun going through the process, but IC is a recognized disability. Document your "pees" and what you go through on a daily basis, it may help, and any other health issues. Don't get discouraged, it takes time. And you are right, lawyers usually do not take your case until you have been denied. Most do a really good job, they don't get paid until your settelement, so there is incentive. Never even met ours face to face, but he was real compassionate. Went with a lawyer "in state" rather than a national firm and had a better connection with him, but it is a personal choice. Wish you much luck, and don't get depressed and give up. You may go through a couple of denials. Don't ever let it stress you out, it's just the way it goes. Take care of yourself. Jill, wife of Bob

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