1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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Lessons from ME/CFS: Finding Meaning in the Suffering
If you're aware of my previous articles here at Phoenix Rising then it's pretty clear that I don't generally spend my time musing upon the philosophy of the disease. I find it better to spend my time reading research and trying my best to break it down to its core elements and write...
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Looking for (private) disability claim stories.

Discussion in 'Action Alerts and Advocacy' started by Kati, Feb 28, 2013.

  1. Kati

    Kati Patient in training

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    Disability specialist, and former UNUM employee Linda Nee is looking for stories for a book about disability case stories that patients have . Take a look at her blogpost here:

    http://lindanee.wordpress.com/2013/02/28/a-book-in-the-making-disability-claim-case-stories/

    i have been a fan of Linda's blog for over a year now. She is on our side! she mentions ME and fibromyalgia when it comes to problems with private disability insurance, and has a lot of great tips and information about how to deal with the insurer, and what are the current trends in disability insurance (and it's not pretty)

    You can read more about Linda here: http://lindanee.wordpress.

    Telling our stories publicly (with key ID details withheld) may just be an important way to fight the isurance companies.
    ahimsa and Valentijn like this.

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