[Robert]

At first, I wondered if I would ever be able to get insurance after having cancer. My social worker warned me that it might be difficult, but I was encouraged just to know that it was not impossible. I started by exploring the laws in my state that determine what kind of health plans are offered. I called the state insurance department for information and spelled out my specific insurance needs. These laws can be different in each state. I found that my state has a government-sponsored insurance program that has a high-risk pool for people in my situation. It offers me the chance to get into an insurance program even though I don't qualify for other kinds of insurance. I found out that I would be eligible for what they call an "open enrollment period" - that's when everyone, no matter what kind of medical history they have, can sign up for an insurance plan.
 
[Social Worker]

Cancer survivors have to deal with a lot of change and upheaval in their lives, so the idea of changing to a job that provides health insurance may be too much to think about for a while. But, after things settle down, that is something that might make sense to think about. Certain types of jobs or companies are more likely to offer insurance as an employment benefit. Usually, the larger the company and the more employees, the easier it is to get insurance. Jobs in companies where employees belong to labor unions usually offer insurance as part of the job benefits package. Group insurance plans offered by companies often include an "open enrollment" period - a designated time during the year when employees select or change their health plans. When people enroll during this open enrollment time, they are usually not asked for information about their health history that has prevented them from getting insurance in the past. Government jobs offer a certain amount of protection since Federal and some state laws help protect cancer survivors against employment discrimination. Government employees have some very good advantages: their insurance goes with them when whey change government jobs, and they do have the right to sue their Health Maintenance Organization - or "HMO" - a right that is not always there for people with other kinds of insurance or HMO plans. Government jobs also extend benefits like insurance to a spouse who might be unable to get his or her own insurance.

[Robert]

I am young, and I hope that I have a long and healthy life ahead of me. I realize that I will probably see many doctors for different things throughout my life. I used to wonder IF I should tell my new doctors about my cancer even when I was seeing them for a non-cancer reason. Then, in a group meeting I went to, a nurse who is also a cancer survivor said that it will always be important for any doctor or nurse who provides me care to know about my cancer and the specific treatment I received. This way, they can order the right tests and make sure that I am not having any problems related to my past therapy. Then I thought, wow - my therapy was so complicated - I had surgery, then chemotherapy, and then radiation. How would I ever remember all I was supposed to tell the new doctors? We talked about this in my group, and together, we came up with a plan that everyone there seemed to think is a pretty good one. The plan goes like this: First, talk to your cancer doctors and ask for copies of your medical records. Second, make a notebook - maybe use a 3-ring binder that can be added to as time goes on. Test reports can go into pockets in the binder. Because of the insurance problems I have had, I suggested that the notebook should have a section especially for all the letters back and forth between me and any insurance company or Medicaid or Medicare. It would include information about what was paid for, what was not, letters, responses, contacts, and all the resources that have been used. Since other people in the group had insurance problems like mine, they liked this idea a lot. We decided it would be a good idea to take this notebook to any new doctor or clinic we might go to, whether it is an office, a free clinic, a county or government facility, a community hospital, or a university medical center. This information will also help social service agencies help us find the best resources for our particular needs. My nurse-friend also advised me not to let anyone else keep the binder. Sure, I can let doctors or clinics make copies of the information I have in the binder but to be sure to get it - and all that it contains - back. I can understand - it would be very difficult, or impossible, to replace the information I had gathered. Sometimes I felt frustrated by how hard it was for me to find and get good cancer care. I had to rely on a couple of friends, my family, and the doctors, nurses and social workers a lot of the time - especially to help guide me to the right places. But, it was worth it. I know I can keep getting the follow-up care I need for my cancer - that any problems I might develop will be picked up early, and the right kind of treatment will be started. Of course, I hope that won't be necessary! I was able to get insurance during an open enrollment period. And, if someday I get another job or move, I know what to do to take care of myself and stay healthy. I am a survivor - and all the work has been worth it. 

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