Navigating Healthcare Obstacles On The Road

The Lady is a Tramp Blog: The Constant Companion

I have excellent health insurance coverage. I pay a lot for it. A whole lot. And it’s a good thing I have good health insurance, because I have a chronic disease. The infusion appointments I get every two months cost the equivalent of a decent used car.

But, having insurance does not mean having peace of mind. Those pesky exclusions and limitations can leave you holding a very expensive bag. My insurance will not pay for infusions administered at a hospital. I understand that hospital infusions might cost a lot more money than, say, outpatient infusion centers, so I get the reason for the exclusion. But in practice, it’s asinine.

My G.I. doctor practices at the University of Washington. In March he performed my colonoscopy. I also needed an infusion around that time, and our plan was to do the infusion immediately after the colonoscopy. But, the University of Washington has a medical center – a hospital. Even though I was at a satellite clinic, the University of Washington Medical Center would bill the insurance company for the infusion. My insurance company refused preauthorization. I had to schedule another appointment for a different day at the offices of a home healthcare visiting nurse service in an industrial park in Tukwila.

That’s because, while my insurance will not pay for a hospital infusion, it will pay for a home infusion. This I find the most curious, as a home infusion is very expensive. In theory, at a hospital that also performs home health care services, I could park the rig at the hospital, a nurse could administer the infusion in the parking lot in my home, and my insurance would cover that.

Fucking ridiculous.

The reason I’m writing about all of this now is the immense difficulty I had scheduling my last infusion. Granted, not all of it was due to insurance exclusions. For example, while I was in Tennessee, where there are plenty of non-hospital based infusion centers and visiting nurses, they would not accept my Seattle doctor’s standing order for Entyvio. Tennessee requires that I first see a Tennessee gastroenterologist, which could take weeks for an appointment, get a new order, then schedule the infusion, which could also take weeks.

Why? Entyvio is a prescription drug. My doctor has prescribed that drug. As I travel the country I can go to any Walgreens or CVS Pharmacy and get my prescriptions filled, as long as there is a doctor somewhere who ordered them. Why should Entyvio be any different?

Getting the infusion in Tennessee was going to be difficult and time-consuming given these hoops. I decided to get the treatment in Mississippi.

And here’s where the insurance exclusion came in to kick my ass. In small, rural communities, the only place to get an infusion, if at all, is in a hospital! In Tupelo, Mississippi, I thought I finally hit the jackpot when I found The Outpatient Infusion and Specialty Pharmacy at North Mississippi Medical Center. But, no. Even though it was outpatient and even though it was a specialty pharmacy, the fact that the bill would come from a hospital meant that my insurance would not pay for it.

Finally, I was able to get treatment in Meridian, Mississippi, at Vital Care Home Infusion Services,  and it was a really nice place, too!

image

I was thankful, as my symptoms have doubled since May. Yup, I’m back up to six or so events every other day or so, and those Canasa suppositories didn’t do jack shit. Now we’re trying corticosteroid suppositories.

The good news is I have two months between every appointment to figure out where I am going to be, and to find an infusion center that will be acceptable to my insurance company. I can also alter my plans to be somewhere else if necessary.

I will. not. let. this. disease. derail. my. life. or. my. dreams!

Facebook
Twitter
Pinterest
Email
Print

This Post Has 7 Comments

  1. Nancy S

    Love your positive attitude???

    Keep hanging in there Tammy

    Nancy S

  2. Velda

    I am glad you have been able to find solutions. There certainly are rules that need fixing in our medical system! A person cared for at home saves thousands yet instead of supporting family to care for loved ones at home they get put in a skilled nursing at $6000 a month and more. Hope in next few years we can fix the mess. Many RVers have trouble like you do.

  3. vyvyn lazonga

    You are such an inspiration Tammy, I would have been so frustrated and angry. You just keep pushing forward with your loving attitude and then sure enough something meets your need. You are my hero.
    Vyvyn

  4. elizabeth

    Way to go. Where there is will there is a way.

  5. Daphne Phelps

    Inspiring to read about all your travels considering extra health issues! Fell upon your site and have been enjoying the rv tips. Would love to pack up and travel more and with more than just a tent! Noticed you are heading to Eau Claire, where I grew up. Welcome and have a Leinenkugel’s while you are in Chippewa!

  6. Renee mejia

    Wow! I stumbled upon yr site and blogs looking for insight info hope somewhere!! I’ve had crohns since 8 yrs old was diagnosed at 15, I’m will be 56 this month, been in and out of hospitals, one bowel resection in’96 crohns return 2 months later, my faithful friend.. Lol anyway been getting remicade every 4 weeks at an infusion center and it is working on the complicated fistula problems and inflammation I have. My crappy insurance has now cancelled infusions and GI dr and referred me to someone they will now pay for. I missed last remicade because they wouldn’t pay and the earliest I can get in is 5 months from now.. Of course I’m having a flare up now, stress is not helping! This comment is very long sorry but wanted to say yr stories made me smile and relate and trying to keep my head up and moving forward! Have fun on yr many adventures and would love to follow along.. Thanx

    1. RoadTripTammy

      Renee, I’m glad you took the time to say hello! Glad to hear that Remicade is helping to combat your “faithful friend;” it’s frustrating to say the least when you find the right drug and then the insurance doesn’t cover it. But you are right – we must keep our heads up and move forward. Thanks for checking in!

Leave a Reply

recent Posts

WHERE IS TAMMY TODAY?

Upcoming: