>:O

[thejunipertree]

AN IMPORTANT MESSAGE TO OUR PATIENTS FROM THE CENTER FOR CANCER AND HEMATOLOGIC DISEASE- JANUARY 2004


Last month, the Federal Government passed the Medicare Prescription Drug Bill. The primary purpose of this bill was to provide assistance to our elderly and disabled in obtaining and affording prescription drugs. While the plan is designed to help the neediest of patients in giving them the access they need to necessary medications, the method of payment chosen by this new government entitlement is less than desirable for cancer care. The "Bill" significantly decreases payments to community cancer care clinics such as The Center.

As a result of the passage of this Bill, oncologists all over the country have been scrambling to find a way to make ends meet in 2004. In many instances, the payment we receive from CMS (The Center for Medicare and Medicaid) is less than our actual cost to purchase the drugs. As a participating provider in the Medicare program, we are obligated to accept Medicare rates as payment in full. In almost all instance, failure to collect the 20% copay from you, the Medicare patient, will result in a significant loss to this practice; one which we cannot afford to continually sustain and yet remain a viable community oncology clinic.

Additionally, some of the Medicare Managed Care Programs, such as Aetna US Healthcare Medicare, have added additional financial burdens to both physician and patient alike. A new injectable program has been instituted whereby many of the drugs administered to you, such as Procrit, Aranesp, Neupogen, Neulasta, and several others, will now carry an additional $45 copay over and above the normal office visit copay. This amount will be deducted directly from our Aetna reimbursement and now becomes an additional financial burden for you, our patient.

These facts and many other distress us greatly, as we feel that we are being hampered from providing you with the many services that have become the standard of care at The Center. The environment that we created was one of going the extra mile for each and every patient, meeting the needs of all with whom we come in contact. We have genuine concerns about our ability to continue that tradition in light of the serious cuts that are being thrust upon us in the years ahead.

You will be asked for copay and deductible payments at the time of your visit. No patient will be seen without a referral if you are part of a managed care plan. All patients without a medigap or secondary insurance will be expected to remit any and all balances due. While we realise that this practice is somewhat different than what you have been accustomed to, it is, in fact, a change we find imperative in order to continue providing you with the best in care without interruption.

Please be assured that we will do everything within our power to continue to provide all of our patients with excellent care, utilizing prescription plans, pharmaceutical assistance programs, clinical trials, and state and federal programs. Realise, however, that we cannot do this without your help.

What can you do to help? Please ask at our front door for a legislative contact sheet. Your voice can and will make change happen.

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What does all of this mean?

I'll break it down for you:

Basically, it's a bunch of bullshit that has been masqueraded as an effort to help the elderly and disabled get the medication they need. I'd really like to know who wrote this bill and why they thought it was a good fucking idea.

To pay for the medications, this Bill has deemed it necessary to decrease payments from Medicare and Medicaid to places like the Center. Because of this decrease, places like the Center are now receiving payments from Medicare and Medicaid that are actually LESS than the money they are putting out for drugs. And because they are participating provider in Medicare, they have to accept the rates as payment in full.

Places like the Center used to allow patients to not pay their copay, if they couldn't. They were billed for it and this was frequently used in the decision making process of whether or not the patient could go on permanent disability. Now however, because of this bill, places like the Center CAN'T bill for a copay. They have to have it up front, unless they want to incur a serious financial loss. And serious financial loss will result in being unable to run their practice the way it needs to be run.

Not only all of this, but because of this bill, patients receiving specific injectable drugs are now subject to an additional payment of $45 because the Aetna reimbursement to the practice for these drugs has been taken away.

What does all of this mean to me (other then a scathing round of profanity that I am currently holding in)?

It means that my mother, who needs to go back for a second round of chemotherapy, will most likely NOT BE ABLE TO RECEIVE HER TREATMENT because she can't afford to pay the copay. She received a treatment today, but is probably not going to be able to get any more of them because before all of this, she was just being billed for the copay. $15 an office visit.

Doesn't sound like much, does it?

Now take into account that she's unable to even pay her FUCKING RENT RIGHT NOW because her STUPID GODDAMN EMPLOYER FORGOT TO SEND IN THE DISABILITY PAPERWORK LAST MONTH. And we have NO IDEA when she's going to start receiving disability checks. Even after she starts to receive her disability checks, this is going to severely fuck up her finances because $15 every single office visit when you're visiting the office SEVERAL TIMES IN A MONTH is going to add right the fuck up.

In other news, I received an email from a potential job opportunity telling me that the salary is $10 an hour. I wrote back and told them this was acceptable (even though it actually really isn't) because since the sixth of November, I have put in 23 online job applications [**EDIT** actually it was way more than 23 because I just realised I deleted everything from my sent folder in my email program in the beginning of November] and barely heard back from ANY of them (this does not include the amount of job applications and resumes I have sent out in meatspace, I'm not sure of that total at the moment but it's comparable). I also asked them in the same email if they would be interested in setting up an appointment for an interview, but I've yet to hear back about that.

I'm trying very hard to not be negative about this, because if I succumb to that temptation I will most likely jinx the fuck out of myself. And with things getting as desperate as they are, I can't afford to do that (literally and metaphorically).

I wish I had a slingshot.

Comments

Re: ARRRRRRRRR!

[meetzemonsta.livejournal.com]

i didn't understand most of that, but that doesn't stop me from being angry.

That comment gave me my first smile of the day. :)