Hi All,
I keep hearing and reading about many MS patients across the country currently receiving Rituxan and it has been improved through their insurance company.
Those of you who are receiving Rituxan for MS and it is approved through your insurance company, how have you been able to get this to happen?
I have failed on all other therapies, and my neuro believes I need a b-cell depleter. The clinical argument is solid. It is the FDA language that has become the greatest issue. How are others getting around this with their insurance company?
Any help would be appreciated, I am in the middle of writing my appeal letter to the insurance company.
txs much!!
P.S.-I am very familiar with the compassionate use program through Genetech.
I keep hearing and reading about many MS patients across the country currently receiving Rituxan and it has been improved through their insurance company.
Those of you who are receiving Rituxan for MS and it is approved through your insurance company, how have you been able to get this to happen?
I have failed on all other therapies, and my neuro believes I need a b-cell depleter. The clinical argument is solid. It is the FDA language that has become the greatest issue. How are others getting around this with their insurance company?
Any help would be appreciated, I am in the middle of writing my appeal letter to the insurance company.
txs much!!
P.S.-I am very familiar with the compassionate use program through Genetech.
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