Has anyone been denied Health Insurance because of being diagnosed with MS? This applies to buying Individual insurance only, not group insurance. Thanks
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I was rejected by three large companies before I even got a diagnosis. All it took was a few episodes of optic neuritis to make me too high risk to meet the underwriting guidelines. A diagnosis isn't required -- all it takes is the hint of an illness or chronic condition to classify someone as high risk. The only way I got health insurance was by being accepted into my state's high-risk insurance pool.
This happened in the mid-90s. The recent health reform act will likely change the guidelines for acceptance/rejection for health insurance, such as forbidding exclusions for pre-existing conditions. However, just because a company accepts a person for an individual policy, it doesn't mean that the policy is going to be affordable. In my area, single-person coverage for an individual policy can cost $700 per month.
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I was approved, but they said there will be changes. I'm assuming my rate will go up. I applied for Blue Cross/Blue Shield.
I found out that in Maryland there is a state based program called MHIP that is for people who have been denied health insurance OR have a qualifying disease/disorder. MS is on the list. It is a program run by Blue Cross/Blue Shield as well.
I will weigh both options. The state program may be a little cheaper than purchasing it as an individual policy.
I am not working right now and therefore can't take advantage of a group insurance plan
But I am thankful to have options!!
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I was denied by several insurance companies. I think it was three but don't remember for sure. The last one told me my only option would be a "high risk" pool. It was three times as expensive as the one DH got. He is the "healthy" one.
This is one of the main reasons I decided to apply for SSDI. I couldn't get a full time job with my symptoms and so no group insurance was available to me.
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I switched from one insurance company to another, before my diagnosis but after two MRIs showed lesions. There was no trouble switching, but as I say, at the time I switched, I was covered by insurance.
I was denied around that time for *disability* insurance (I am not currently disabled).RRMS dx 2/2010, Copaxone since 4/2010
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I had the same problem because when i moved over from florida to tn, they told me i had to wait a year before i can be eligible for state benefits or the risk pool, i recently got approved for a policy by health-insurance-buyer dot com, but the doctor had to fax over a lot of paperwork, hopefully in 2014 things will change.
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