Amanda81
Active member
- Joined
- Nov 1, 2012
- Messages
- 57
- Reason
- Loved one DX
- Diagnosis
- 12/2012
- Country
- US
- State
- IL
- City
- Central IL
This is confusing, so try to keep up
On 11/12/2012 my mom had a Complete ALS Evaluation (lab panel) done by Athena Diagnostics, ordered by her local neurologist after he made the diagnosis of ALS, but before she saw a specialist in St. Louis who made the official diagnosis.
At the time of the test, she had Blue Cross Blue Sheild as her primary and only insurance.
After the official diagnosis in St. Louis, she applied for and was approved for Medicare. They back-dated Part A to 8/1/12 and gave us the option to pay the premium for Part B. We opted not to pay because we didn't see the need, so Part B was not effective until 2/1/13.
After paying the claim in full, but sending it to the neurologist instead of Athena Diagnostics, BCBS has decided they don't owe the full amount of the lab test, they only owe a portion (10%) and we need to bill Medicare. After explaining that Medicare wasn't active, they stated that she was *eligible* she just chose not to accept the coverage, so they're still not going to pay it in full.
This test was $5895 and BCBS is only paying $589.51. Medicare isn't paying anything b/c she didn't have Part B at the time. So my mom is stuck with a bill for over $5,000.
The test was never explained to us by the doctor. It only detects 75% of familial ALS and 15% of other ALS. So the test was pointless anyway. But we live in a society where we are taught to trust our medical professionals. She had the blood work done just like she had the MRI done to rule out other things before we settled on the diagnosis of ALS.
Is there ANYTHING we can do? Shouldn't the doctor have explained the test to us? And the cost of it? I know it is ultimately our responsibility to be informed and ask questions, but this is a hard pill to swallow. Any suggestions would be appreciated.
On 11/12/2012 my mom had a Complete ALS Evaluation (lab panel) done by Athena Diagnostics, ordered by her local neurologist after he made the diagnosis of ALS, but before she saw a specialist in St. Louis who made the official diagnosis.
At the time of the test, she had Blue Cross Blue Sheild as her primary and only insurance.
After the official diagnosis in St. Louis, she applied for and was approved for Medicare. They back-dated Part A to 8/1/12 and gave us the option to pay the premium for Part B. We opted not to pay because we didn't see the need, so Part B was not effective until 2/1/13.
After paying the claim in full, but sending it to the neurologist instead of Athena Diagnostics, BCBS has decided they don't owe the full amount of the lab test, they only owe a portion (10%) and we need to bill Medicare. After explaining that Medicare wasn't active, they stated that she was *eligible* she just chose not to accept the coverage, so they're still not going to pay it in full.
This test was $5895 and BCBS is only paying $589.51. Medicare isn't paying anything b/c she didn't have Part B at the time. So my mom is stuck with a bill for over $5,000.
The test was never explained to us by the doctor. It only detects 75% of familial ALS and 15% of other ALS. So the test was pointless anyway. But we live in a society where we are taught to trust our medical professionals. She had the blood work done just like she had the MRI done to rule out other things before we settled on the diagnosis of ALS.
Is there ANYTHING we can do? Shouldn't the doctor have explained the test to us? And the cost of it? I know it is ultimately our responsibility to be informed and ask questions, but this is a hard pill to swallow. Any suggestions would be appreciated.