Insurance Coverage

I am interested in information anybody has regarding issues with their insurance carriers.  So far I have not had a problem.  I asked my PCP for a referral to a dermatologist.  He talked to me about some treatment options and which ones my carrier would cover.  But if we need to speak with a united voice since this is an experience that impacts the mental health of those with Vit.

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  • I posted the information regarding NVF info, because I had the same question years ago in one of the discussion forums.  I never realized there was a national voice for us.  Hope this information is helpful!
  • The National Vitiligo Foundation offers a wealth of current, accurate, and easy to understand information about vitiligo.  We strive to enable people with this disease to make the best choices for themselves and their families, and to serve as a one-stop resource for both the medical and scientific community.

    Why become a member of the Foundation?  Your membership empowers us to serve as a collective voice to implement our mission of increasing awareness, patient services, and research for vitiligo.  When we stand united as thousands, we become a powerful force for change.


    Why donate to the Foundation?  Your tax-deductable contribution is needed to support research focused on treating vitiligo and on finding a cure, to help with development of educational materials for the public and the medical profession, and to help the Foundation advocate for changes in government funding and insurance coverage. During its 24 year history, the Foundation has awarded nearly 1.5 million dollars in research grants because of the generosity of its members.  Please consider making a donation so that the NVF can continue making a difference in the fight against this disease.
    Click on this link to take you to the National Vitiligo Foundation
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