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» LymeNet Flash » Questions and Discussion » General Support » IBM - BCBS

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Author Topic: IBM - BCBS
LPurdy1040
LymeNet Contributor
Member # 6543

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Hi

I'm looking for anyone who has IBM-Blue Cross Blue Shield Insurance and was able to get treatment with IV's for longer then 28 days.

I have a family with a child who is currently on IV's and could use some assistance.

Hugs
Linda

Posts: 107 | From Michigan | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
Tincup
Honored Contributor (10K+ posts)
Member # 5829

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I think BG has a copy of some documents I wrote up.

If she will share them with you (email documents) they should help.

I am on my way out of town and am shutting down... but don't want any child suffering.

Good luck!

BG- Can you help here? Thanks!

[Big Grin]

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www.TreatTheBite.com
www.DrJonesKids.org
www.MarylandLyme.org
www.LymeDoc.org

Posts: 20353 | From The Moon | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
tdtid
Frequent Contributor (1K+ posts)
Member # 10276

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My husband works for IBM and we have Blue Cross Blue Shield.

I had been treated for Lyme and co-infections orally for 20 months and they were covering all meds. As soon as I was referred to an LLMD that felt I needed IV, the brakes went on over the summer.

We paid out of pocket monthly for the IV since waiting for IBM BC/BS was not really an option.

The documents Tincup is discussing have been sent to IBM BCBS, but they still REFUSED to budge and said that 28 days and you are cured and didn't care what we sent as an appeal.

It was frustrating because we also sent all that documentation to politicians and although many would either send us canned letters or else when we talked to them on the phone, they informed us that they could do nothing because

IBM is PRIVATELY insured so they do not need to stick by any state rules or guidelines and can choose to cover what they will.

So......the way we were FINALLY able to get around it is that once my LLMD started treating me for Bartonella or Babsiosis, IBM started covering again.

We still have not gotten anything back for all the IV months on Lyme treatment and they still stand by their ground, BUT if you can get your LLMD to code it as a co-infection, it may get some help.

Good luck and if you need any other information, feel free to PM me. I haven't found anyone getting covered for IV for "LYME" so far. Would love some of that money back too, but think it's gone forever.

Cathy

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"To Dream The Impossible Dream" Man of La Mancha

Posts: 2638 | From New Hampshire | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
jt345
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Hi Linda

I have PM ed You. I have Bluecross and Bluesheild. I have not used it for IV's as of late but about 4 years ago they did not even blink. Just pd. But I was being treated for babs also.

It was good too see Your post.

appleseed

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bettyg
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linda,

please send me a PM with your home email and i'll send the 2 things to you tomorrow providing my pc is working .
ran into some glitches today... thanks.

tc, came across this and will handle for you...

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LPurdy1040
LymeNet Contributor
Member # 6543

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Hi Everyone

Thank you for your replies and information. I will pass this along to the family.

Hugs
Linda

Posts: 107 | From Michigan | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


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sent linda as requested above...
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