posted
There is a young mom in our RI Support Group that has Lyme but does not have insurance.
Could anyone direct me to a source that I could give her that could help her out.
She is being seen by a doctor and paid out of pocket for the visit and the meds, but she cannot continue to do that financially.
Posts: 63 | From RI | Registered: Sep 2007
| IP: Logged |
bettyg
Unregistered
posted
anne,
click on my newbie package link below,
copy it all to ms word and paste there where you can use the wonderful search features.
go to FIND, upper right corner, click on it,
type in FINANCIAL BURDENS by melanie reber, and hit enter.
it will show up 1st in my table of contents, and 2nd time will be 20-25 pages of DETAILED info galore from melanie and others w/updated info!
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,
NJ08534USA http://www.lymenet.org/