Guest guest Posted June 10, 2004 Report Share Posted June 10, 2004 This is the first time I am posting here. My husband was diagnosed in February with PSC and cholangiocarcinoma at the same time. It was found by accident when he showed up with elevated liver enzymes when getting a physical. Our local hospital wanted to resect part of his liver. We went to Mayo clinic for a second opinion. They disagreed with this plan and suggested Mike have radiation tx followed by transplant. They have done this protocol for a decade or so, only in cases of very early detection of the ca. We went with the Mayo protocol. Mike has completed the radiation. His sister is being evaluated as a donor. But our insurance is denying the whole protocol on the grounds that they say it is experimental. So amoung all this we must battle the insurance company. If anybody has any thoughts or suggestions on how to approach this or how to apply for financial assistance I would greatly appreciate it. Bonnie (44), wife of Mike (43) parents of Sam (4) Mike's PSC dx 2/04 Virginia Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 10, 2004 Report Share Posted June 10, 2004 Bonnie, I understand how frustrating this must be in such a time of stress. Sometimes it seems this is when insurance companies can be at their worst. It is almost as if they know the family is under such stress that they will not have the energy to fight. I have a couple of suggestions but I hope others will weigh in as well. I am not sure based on your e-mail what you have done so far so I will just give you all my thoughts. 1. My first reaction is how can they view this as experimental. Break down the procedures into their parts and what do you have? A) Radiation treatment of cancer cells (that is certainly not experimental and Liver transplantation. (No one can argue that as experimental either). What part of the equation here is experimental? In my opinion nothing. Perhaps by breaking it down that way you might talk some sense into them. 2. All insurance companies of an appeal and review process and this is probably where you should start. Be prepared for the run around but you have to keep working up the chain of command until you get to the person that will think outside the canned response. Before you can really go to the next level you probably need to work within the insurance company first until no one else will listen. This will take some time and patience. 3. Can the mayo doctor write a letter in support of the history and proven results of this protocol? I am sure he will be willing to help in that regard. 4. If contact with the insurance company fails then does your state have an insurance commissioner. I think a call to that office would be the next course of action in getting someone to put pressure on the insurance company. 5. Finally, if all else fails then often a call to your local investigative newspaper or televeision reporter can do wonders for getting a slow mule in gear. Keep fighting and persistence usually brings the insurance company around in a short periord of time. ANother resource you may hear from soon is Liz in Virginia who had I believe the same procedure done at Mayo and is in your home state. She may be a good resource to answer some of your medical questions. Good luck and keep us posted. in Seattle UC 1991, PSC 2001 > This is the first time I am posting here. My husband was diagnosed > in February with PSC and cholangiocarcinoma at the same time. It > was found by accident when he showed up with elevated liver enzymes > when getting a physical. Our local hospital wanted to resect part > of his liver. We went to Mayo clinic for a second opinion. They > disagreed with this plan and suggested Mike have radiation tx > followed by transplant. They have done this protocol for a decade > or so, only in cases of very early detection of the ca. We went > with the Mayo protocol. Mike has completed the radiation. His > sister is being evaluated as a donor. But our insurance is denying > the whole protocol on the grounds that they say it is experimental. > So amoung all this we must battle the insurance company. If anybody > has any thoughts or suggestions on how to approach this or how to > apply for financial assistance I would greatly appreciate it. > > Bonnie (44), wife of Mike (43) parents of Sam (4) Mike's PSC dx 2/04 > Virginia Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 10, 2004 Report Share Posted June 10, 2004 Dear Bonnie, I was so sorry to read of your insurance nightmare. On the top of the shock of the diagnosis and the effects of the radiation treatment, I am sure that this is quite a heavy burden for your family. It seems that has provided some excellent suggestions on dealing with your insurance company. Since you also asked about financial assistance, I thought that I would direct you to the Financial Support section of the TIGER (Transplant Information Gathering for Education and Research) webpage: <http://www.tigerfund.org/support.htm> Two programs which may be of relevance to you are the National Transplant Assistance Fund <http://www.transplantfund.org/> and the TIGER Family Aid Program <http://www.tigerfund.org/program2.htm> I would hope that the staff at either of these programs might be able to direct you to other resources. May I ask if you have discussed this with the financial coordinator or social worker on your transplant team? It was my social worker who provided me with the TIGER reference when I was first evaluated for transplant, along with references for transplant travel and medication support programs. Best Wishes, Shauna (29, AIH'86, Crohns'95, PSC'99, listed @ Duke, MELD = 17) ------- Think you're an ORGAN DONOR? Click here to find out: http://www.shareyourlife.org/become.asp Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 11, 2004 Report Share Posted June 11, 2004 Bonnie, I'm in VA and would like to offer whatever support I can. I'm sorry your insurance company is giving you such a hard time. I've been through the HMO nightmare in the past (though not on the level you describe). Now we pay almost $300 a month for a PPO. My husband maintains that job, driving nearly 1 1/2 hours to work so we can maintain this insurance. So far, we've had little trouble there - except over prescriptions. Liz is right - keep after them and document everything - who you speak with the date and time, etc. That helped immensely when I would try to get them to pay for things. I also asked to speak to supervisors quite frequently. Some insurance companies offer a " case manager " of sorts, so at least you're dealing with the same person over time. Sometimes you have to ask for that, though. Feel free to email me privately, too. I'm in Northern VA - Take care, Deb in VA AIH 1997, PSC 1998, UC 1999, Listed LTX 2001, MELD 18 > So amoung all this we must battle the insurance company. If anybody > has any thoughts or suggestions on how to approach this or how to > apply for financial assistance I would greatly appreciate it. > > Bonnie (44), wife of Mike (43) parents of Sam (4) Mike's PSC dx 2/04 > Virginia Quote Link to comment Share on other sites More sharing options...
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