The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

US Marketplace Insurance questions

Forums General Melanoma Community US Marketplace Insurance questions

  • Post
    Anonymous
    Inactive

    Hello, fellow warriors. I am an American living in Hong Kong. I was diagnosed Stage IV in June, 2016 and have been on Nivo since July, 2016. It looks like we'll be required to move back to the US due to my job loss here. Is there anyone participating in the ACA Individual Marketplace insurance out there that is being treated with immunotherapy? What difficulties in coverage have you experienced? So far it's a bit of a nightmare trying to match network providers with plans on the Marketplace website. Telephone calls with Marketplace representatives have proven fruitless. Any info would be greatly appreciated. Keep fighting!

    Regards,

    Cary

     

     

Viewing 1 reply thread
  • Replies
      jennunicorn
      Participant

      My least favorite thing to do is deal with the dang marketplace! But, yes, I have individual insurance through Covered California (the CA version of the marketplace). I have Blue Shield Silver plan. Have not had much hassle with them going through multiple treatments and many scans and what not. I also have an awesome oncology team who takes care of any push back the insurance might try to give before I even know anything. So, with a good medical team and a PPO, you shouldn't have much trouble. The worst part is getting through the process of signing up!

        Anonymous
        Inactive

        Thanks for the quick reply, Jenn. If I may ask, has the insurance covered the cost of the meds? I suppose that's one of our big concerns, since the cost of the drug is astronomical. Have you ever had to seek treatment in another state? Thanks again,

        jennunicorn
        Participant

        100% of the drugs have been covered, never paid a penny for drugs. I have never had to go to another state for treatment, I consider myself very lucky to only be an hour away from one of the best places for melanoma treatment.

        Hriggenbach
        Participant

        I have Cigna and they have this awesome thing where they say what the price should be and it always seems like it's under what the actual cost is and I'm forced to pay the difference that is on top of my $2500 yearly deductible 

      TexMelanomex
      Participant

      Cary,

      This info might be a little late but worthwhile nonetheless. When I was diagnosed in January I quickly found out that MD Anderson no longer accepted BlueCros BlueShield of Texas HMO. In Texas, unfortunately, you cannot purchase PPO unless you belong to a group, HMOs are all that are available in the marketplace or otherwise. I quickly formed a small group (I'm a small business owner and found that you can reasonably purchase a really good plan) and bought a "Gold" PPO that is accepted almost anywhere (I'm no longer with BCBS). This actually turned out to be cheaper than my "Silver" HMO plan as far as montly premium, lower deducitble, and lower out of pocket expense. If you have an LLC, S-Corp, Partnership, or a business even with only indpendent contractors you might qualify for a much better plan than you can find in the open market. You can explore this with group health insurance brokers in your state and you might be surprised at what you find. I think it stinks that we have to do this in order to get to decent care but without talking politics, it appears to be a direct result of health care legislation…that being said, without the "pre-existing condition clause" I'd be up a creek.

       

      B

Viewing 1 reply thread
  • You must be logged in to reply to this topic.
About the MRF Patient Forum

The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.