LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » CA Residents-Best Insurance for Lyme?

 - UBBFriend: Email this page to someone!    
Author Topic: CA Residents-Best Insurance for Lyme?
gambler
LymeNet Contributor
Member # 8441

Icon 1 posted      Profile for gambler     Send New Private Message       Edit/Delete Post   Reply With Quote 
Looks like I have to move to CA.

The new job offers these options:

HMOs
PacifiCare
Kaiser Permanente
Blue Shield of California

PPO
United Healthcare

Even with a deductible of $1500 I can't imagine that an HMO would be a better option. I am figuring on paying my out of network LLMD and SPECT scan (back East) out of pocket, either way.

I have checked out CALDA's website and no info. My insurance now has been AWESOME at not questioning LD and paying what they are supposed to.

Thanks,

gambler

Posts: 243 | From chicago | Registered: Dec 2005  |  IP: Logged | Report this post to a Moderator
soleil16
LymeNet Contributor
Member # 16326

Icon 1 posted      Profile for soleil16     Send New Private Message       Edit/Delete Post   Reply With Quote 
We have Blue Shield HMO and it is ok for oral antibiotics, Diflucan, pretty much anything you want, except IV. They denied that within 12 hours of my doctor asking for approval and aren't budging on appeals.

They are not very good at covering lab tests (blood, CT, etc) and we end up paying a lot out of pocket. Much more than when I had United Healthcare PPO. That insurance seemed to cover a lot more without questions... but I wasn't treating Lyme then.

Posts: 236 | From Washington | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
Jill E.
Frequent Contributor (1K+ posts)
Member # 9121

Icon 1 posted      Profile for Jill E.     Send New Private Message       Edit/Delete Post   Reply With Quote 
From what I can tell when I compare notes with my other California Lyme friends, most of us have to pay out of pocket for the majority of physician visits and medications, particularly IM or IV. Even with oral antibiotics, many insurance companies will not authorize the number of days or number of pills of a prescription.

However, a Lyme friend of mine in the same city as me, with the same insurance company, gets almost everything paid for. The difference is that hers is a group plan and mine is an individual plan. So you may do better because your plan will be through an employer

I personally would stay away from the HMOs because I cannot think of a single Lyme doctor who is part of one. However you can use the HMO to do ongoing bloodwork such as liver enzyme tests, etc.

Most of the Kaiser Lyme patients have had terrible trouble and had to go out of network and pay completely out of pocket. Perhaps there is an exception but I think it's rare.

Congratulations on finding a job in California! Many of us who live here are in the economic doldrums!

Good luck!
Jill

--------------------
If laughter is the best medicine, why hasn't stand-up comedy cured me?

Posts: 1773 | From San Diego | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
eagle
Member
Member # 19278

Icon 1 posted      Profile for eagle     Send New Private Message       Edit/Delete Post   Reply With Quote 
Definitely go with the PPO!
Posts: 29 | From USA | Registered: Feb 2009  |  IP: Logged | Report this post to a Moderator
gambler
LymeNet Contributor
Member # 8441

Icon 1 posted      Profile for gambler     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the feedback.

I never forget how lucky we are to have found LLMDs.

But if Lyme hadn't put me on the verge of bankruptcy, I wouldn't have to move to CA to work off my medical bills. And now I can't afford to make the wrong insurance decision, for my health or my finances.

I appreciate the insight,

gambler

Posts: 243 | From chicago | Registered: Dec 2005  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.