Medical Monday- Changing Insurance Carriers

I find it important to share the trials and struggles of dealing with insurance companies and doctor bills. It can become a job in and of itself. For those in chronic pain, we only have so much energy to deal with this crap. I feel like they assume you’re not going to fight them and just give in. While I don’t want to spend endless hours on the phone, I am not going to be taken advantage of or stuck in the red tape.

I’m sharing a two-party series on an insurance issue from 2015 that took 10 months to resolve. Just know that you are not the only one who gets bogged down in the bureaucracy.

In 2015, I switched insurance carriers through the Healthcare Exchange. I didn’t receive my insurance card or any type of member ID until late March. I can’t begin to tell you how many hours I spent on the phone trying to get this resolved. If I didn’t get the answer I needed, I kept telling the agent to get me someone higher. Eventually it worked and I had proof of insurance coverage three months after making the change. Estimated amount of time spent trying to get proof of coverage: 20 hours over 3 months.

During those three months, I couldn’t go without my medications and I had doctor appointments. I had to pay for everything out of pocket. The new insurance company assured me that once my paperwork was processed, I just needed to submit my receipts and I would get reimbursed. Total amount spent out of pocket $784.08.

After submitting three months worth of reimbursements, I received a letter saying they needed an explanation as to how many days each medicine covered. The form I filled out says 30 pills, wouldn’t one assume that it was a one-month supply? Anyway, I gave them what they asked for and sent the info back. Estimated amount of time spent on reimbursement: 3 hours.

July, 2015- I get a check in the mail for $65.33. The total that I had paid out of pocket for those three months was $784.08. $784.08! That’s only 8% of what I had paid out of pocket.

Where’s the rest of it?

There’s a difference between the cost of a medication, your copay, and the price the insurance company and the pharmacy has agreed upon. So one medication cost me $396, but if it had gone through insurance, the insurance company would have only paid $19.24 to the pharmacy for that medication and I would have had a $5 copay. But since I had to fight to get proof of coverage, I paid the full price. Not my fault. The insurance company owes me what I paid, not the price they had negotiated with the pharmacy-I am not a party to that contract.

So, after spending 13 minutes on the phone, the representative said the claim would be reprocessed within three business days and I would receive a call-back with the outcome. Let’s see how this review goes and if I see any more money. I did confirm that the measly check for $65.33 was ok to cash. Great, thanks.

Next week, I’ll tell you how the rest of it unfolded. Feel free to ask me to explain further any of these terms that can be extremely confusing!

 

Posted in

Why Being “Disabled” is a Full-Time Job

July 26, 2017

*************************SEEKING APPLICANTS************************* Job Title Chief Medical Officer of Personal Health Affairs (AKA Social Security Disability Beneficiary) Job Description Full-time position, flexible hours. Prerequisite: Ideal candidate would have a background in all of the following areas: analytics, accounting, patient advocacy, medical billing, insurance underwriting, legalese, pharmacology, healthcare administration, Social Security Disability, Medicare & Medicaid. Preference for…

Creative Corner – Out of Chaos

June 2, 2017

This beautiful piece of art was created by my friend Terah. I personally gravitate towards images of trees and roots I think because it represents grounding and growth for me. I’m so excited to share her creative work. After many years in a successful career with Coca-Cola, Terah was forced to go on disability in…

Creative Corner: Raising Awareness of Cluster Through Arte Cluster#2

May 19, 2017

Arte Cluster is a project founded to raise awareness of cluster headache through art. Arte Cluster Project is an independent project founded and managed by Claudio Geraci, a chronic sufferer, and Francisca Mesa, a supporter.

Leave a Comment

You must be logged in to post a comment.