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Lyme Disease ForumsGeneral & SupportDoes your insurance know you have lyme?
10/24/2011 08:56 PM
Kramberry
KramberryPosts: 116
Member

Is it ok for them to know?
Starting our lyme journey as a family... a new chapter in life is about to unfold.
Reply

10/24/2011 09:43 PM  Top
healinginprocess
 
Posts: 159
Member

Some insurance companies cover Lyme. Others don't.

Post edited by: healinginprocess, at: 10/24/2011 09:45 PM


10/24/2011 11:40 PM  Top
Bettyg
 
Posts: 27222
VIP Member
I'm an Advocate

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.

10/25/2011 04:16 AM  Top
shorelinelyme
shorelinelymePosts: 1252
Senior Member

One good thing for those of us who live in CT- They passed legislation where insurance companies CANNOT deny long-term antibiotic coverage to patients diagnosed with Lyme disease.

This passed in our state legislature with 100% support from both dems and republicans...unheard of!

Jackie


10/25/2011 04:27 AM  Top
Ramilin
Ramilin  
Posts: 442
Member

My insurance covered much of my 15 months of treatment, but nothing was coded with Lyme. For lyme specific things (testing, doctor visits, etc), I paid cash and did not submit the claim. I do have steep bills from it, but I am in remission. I didn't think the risk of submitting and them finding out and forcing me to stop the picc line treatment was worth it because I couldn't have afforded the picc treatment. The picc was what saved me and I knew I needed long term treatment.
24/7 headache started: 7-14-08
Dx myself -Lyme Disease- treatment started: March 2009
24/7 Headache resolved: June 2009
Treatment ended June 2010 (about 15-1/2 months)

Lyme Disease, Bartonella, and BLO's. Son confirmed with Bartonella and Lyme at 14 months old (he is now 3yrs old).

10/25/2011 04:33 AM  Top
shorelinelyme
shorelinelymePosts: 1252
Senior Member

Ramilin,

Just curious- what did they say was the reason you needed a PICC line- if it wasn't for Lyme?

Jackie


10/25/2011 04:45 AM  Top
lymeinmich
 
Posts: 1075
Member

I submit my receipts myself as my LLMD does not participate with insurance companies.

These receipts are clearly coded as Lyme Disease.

My BCBS has been covering it since January 2011. They reimburse me.

I have not had a PICC line or IV.


10/25/2011 12:36 PM  Top
Polkahero
Polkahero  
Posts: 225
Member

I'm not about to let them find out. I have private insurance. I don't submit my LLMD invoices as it would be out of network coverage (little to no reimbursement) and wouldn't meet my yearly deductible anyway. As long as they're covering my px, I'm find with that.
I got screwed by Lyme Disease!
Reply

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