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Monday, November, 09, 2009
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Guide for Uninsured Multiple Sclerosis Patients

Mandy Crest
Mandy Crest
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Mandy Crest is How are you doing?
MS Blogger and Freelance Writer

Currently residing in northern Virginia with my

Mandy Crest

Thursday, March 26, 2009
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The financial impact of multiple sclerosis cannot be overstated, whether you have medical insurance coverage or not, it becomes a large part of your struggle with the disease. Like it or not, MS and money are go hand in hand.   Obviously, the best scenario is employer provided group coverage. ...
  1. Insurance and Assistance
    Lisa Emrich
    Thursday, March 26, 2009 at 09:36 AM

    Great article Mandy.  Steve Tucker was kind enough to try to assist me (through Twitter) in finding a more affordable option for insurance.  However, we determined that what I currently have IS my best option at this time.  The Individual Insurance world is tough.

     

    Patients looking for prescription assistance programs specific to MS drugs can also read Beginner's Guide to MS: Need Help Paying Drug Bills?

     

    Reply
    re: Insurance and Assistance
    Mandy Crest
    Friday, March 27, 2009 at 02:39 PM

    Lisa,

     

    Thanks for the additional info. Readers -- any additional resources you have are welcome as well.

     

    By the way, I also found Steve through Twitter. Smile

    Reply
  2. Untitled Comment
    ladygraycloud
    Friday, March 27, 2009 at 09:58 AM

    Boy is this the truth, if you have no insurance it is a job alone trying to get any help. I'm in this process right now and have been since being diagnosed in Oct of 08 and still in the process of trying to get some kind of help to get into the MS clinic at Shands in Florida.  There was a nurse there that turned me onto a program they have it is the Outpatient Charity Care  program for people that have no insurance and low income.So if your in Florida and trying to get help-ask for it- there nothing to be ashamed for asking-unfortunately there are people that abuse these programs and it really makes it difficult for the ones like us that need it.

    Hope this info helps someone I know it has me.

    Good luck to all

    Ladygraycloud

    Reply
    re: Untitled Comment
    Mandy Crest
    Friday, March 27, 2009 at 02:45 PM

    It is almost mindboggling what a person has to go through in order to access proper medical services -- and a sad commentary on the state of health care in this country. I totally agree that those who abuse the system make it much harder for honest people to get help.

     

    I strongly encourage readers to share whatever resources they have found.

    Reply
  3. best place to be?
    CenteredNow
    Friday, March 27, 2009 at 11:39 PM

    Where are the "best" states to live with MS with regard to insurance?

    Reply
    re: best place to be?
    Mandy Crest
    Sunday, March 29, 2009 at 11:31 AM

    There are too many variables involved to answer that question. Your income level, your ability to access group insurance, and the availability of services in the local area would all be contributing factors.

     

    The American Diabetes Association has a wonderful resource, "Health Insurance in Your State," where they list the specifics of insurance laws by state.That would be a good starting point for anyone with MS who is thinking about moving.

     

    On a personal level, I have MS, no access to group insurance, and want to move out of state -- it is the insurance issue which has kept us from being able to make that move.

     

    I'm holding out hope for health care reform that would provide those of us living with chronic illness a few more options.

     

    Reply
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