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 » need info on IV abx legwork

 - UBBFriend: Email this page to someone!    
Author Topic: need info on IV abx legwork
hodologica
Member
Member # 6408

Icon 1 posted      Profile for hodologica     Send New Private Message       Edit/Delete Post   Reply With Quote 
hello,
After 9 months oral treatment I am greatly improved, but still have many sx especially in the brain. I am considering seeking IV rocephin/ceftriaxone and will be reading all the pertinent refs in the latest ILADS guidelines, plus a few others, to help me decide.

So, exactly how many 10,000s of dollars does 3 months treatment cost, if I administer it myself at home? (I am told I would still need nursing services once a week for PICC care). And is it possible to pick out a good insurance plan that will cover it? How is that done?

Many many thanks if anyone can help.


Posts: 62 | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
valymemom
Frequent Contributor (1K+ posts)
Member # 7076

Icon 1 posted      Profile for valymemom     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't know the answer but would like to know myself.

I guess we just ask our insurance company.


Posts: 1240 | From Centreville,VA | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
Deb
LymeNet Contributor
Member # 4393

Icon 1 posted      Profile for Deb     Send New Private Message       Edit/Delete Post   Reply With Quote 
I recently completed 22 weeks of Rocephin to a tune of about $30,000. I did use a home nursing company that was recommended by my insurance company to do dressing changes and to supply me with meds/supplies. I did my own infusions twice daily, seven days a week. By using this company, we were able to keep medical expences lower.

The company that I selected from an approved list by my insurance company worked out well. I first ran the list of companies by both my doctor and his nurse to see what track record they had with any of the companies listed. Since they gave me glowing reports, I opted to use the services of the company I ended up with. It seemed to make most sense to me to do it this way than to randomly make a selection.

I realize that there are individuals who do their own dressing changes. However, I felt more secure having a nurse come into my home and change the dressing as well as do blood draws. She also checked my vital signs and we went over any questions I had or difficulties that she was able to advise me with.

I was on antibiotics for fourteen months before we had my picc line installed and started me on rocephin. I too had made some progress, but I then started to back slide.

The Rocephin did not "cure" me. However, it brought me to a point that the orals couldn't seem to achieve. We had to stop the Rocephin due to my developing a serious reaction to it. After the Rocephin, we switched me over to orals. I still have a ways to go, but overall I am at a better point then prior to being treated with Rocephin. At least now I am seeing progress with the orals. If I had to do it again, I would still opt for using the Rocephin...just my personal experience.

Wishing you all the best in your quest for wellnes.

Debbie-RI

[This message has been edited by Deb (edited 13 July 2005).]


Posts: 162 | From RI | Registered: Aug 2003  |  IP: Logged | Report this post to a Moderator
valymemom
Frequent Contributor (1K+ posts)
Member # 7076

Icon 1 posted      Profile for valymemom     Send New Private Message       Edit/Delete Post   Reply With Quote 
Debbie

Thanks for the thorough information!


Posts: 1240 | From Centreville,VA | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
Deb
LymeNet Contributor
Member # 4393

Icon 1 posted      Profile for Deb     Send New Private Message       Edit/Delete Post   Reply With Quote 
Happy to be of help hodologica.

Debbie-RI


Posts: 162 | From RI | Registered: Aug 2003  |  IP: Logged | Report this post to a Moderator
no2lyme
LymeNet Contributor
Member # 6978

Icon 1 posted      Profile for no2lyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was on Rocephin for 11 months, cefotaxime for 5 months and zithro thrown in every once in awhile.

I had a great insurance covered home nursing service once a week for the picc line. Although, I developed staph in my line twice, something to watch out for.

Over a year later I am still fighting/appealing for my insurance to cover the meds over the normal "30 days". I have won most of it and consider myself lucky.

Rocephin really did not seem to do much for me, and if you search the posts you will see a lot of info on that. Cefto did help a lot - along with orals and bicillin shots.

Beware, most companies that deal with lyme disease, i.e. the company that sends you the drugs and supplies, know that insurance will not pay for more than 30 days. They make you sign a contract that you will be a certain amount a day. Although it is less, it still adds up. I think my total was over $50,000.

But the nurses were amazing and would give me extra supplies they had, so I saved a lot.

Good luck and good health.


Posts: 152 | From On Horseback | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
Deb
LymeNet Contributor
Member # 4393

Icon 1 posted      Profile for Deb     Send New Private Message       Edit/Delete Post   Reply With Quote 
no2lyme - I am sorry to hear of the insurance difficulties you experieinced and hope it all gets resolved in the near future.

I was fortunate that my medical bill was resolved within two months after stopping the IV treatment. It was pretty straight forward in that I knew what costs I would be responsible for and what the insurance company would cover prior to starting IV treatment.

My insurance company honored my doctor's orders without question and my total out of pocket expences were only $1,500.00. I feel very lucky that we have the insurance coverage we have and the state laws to support long term antibiotic treatment for Lyme Disease.

Debbie-RI


Posts: 162 | From RI | Registered: Aug 2003  |  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.