LymeNet Flash: Need LDLD near Indianapolis, IN

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

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.

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 » Questions and Discussion » Seeking a Doctor » Need LDLD near Indianapolis, IN

UBBFriend: Email this page to someone!

Author

Topic: Need LDLD near Indianapolis, IN

PsychNurse
Junior Member
Member # 12130

posted

I need to locate a doctor familiar with Lyme Disease in the Indianapolis, Indiana area or in the surrounding states (Ohio, Kentucky, Illinois). Anyone have any referrals?

Thanks in advance for any help.

Posts: 1 | From Indianapolis, Indiana | Registered: Jun 2007 | IP: Logged |

bettyg
Unregistered

posted

welcome psych to board!

Please go to SUPPORT GROUPS, left-hand side column by state.
Click on the nearest group leader for advise. Read if they want emails or phone calls per THEIR request
Do NOT email; many are too sick to reply; thanks!

welcome! since this is your 1st post, please tell me more. The reason is we have trolls and spies from IDAS, infectious disease associated society trying to get names, phone nos/addresses so MORE of our LLMD, lyme literate mds can be brought up on charges from that state's health dept. like:

Dr. Jemsek in NC, and Dr. Charles Roy Jones, Conn; almost 2 years of hearings over $250,000+ OUT OF POCKET for lawyer's fee to defend him. Now I hope you understand. If you don't, go to activism and read the posts there about specific drs., especially Dr. Jones where he has a 5-31-07 hearing in conn. again! thanks [Smile]

now please tell us about yourself:
***********************************
is this for yourself or a child; what age?

how long have you been sick?

did you have an imbedded tick? a bulls-eye rash?

symptoms?

have you had testing done: western blot igm and igg blood test by:

igenex in calif; md labs in nj; or stoneybrook in ny ... they are the best USA has!

please show all this in your NEW post, and we will help you.

i just sent you privately my 57 pages newbie links/advise!

be sure to sign BOTH LYME PETITIONS, and ask family, friends, co-workers, church members, orgs, and all you know OVER 18 sign this too.

we desperately need your help/others http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=1;t=051205
to meet the 50,000 signatures for LDA's petition, and there's over 5200 on lynn's going to congress.

i'm pretty sure the UNDER THE SKIN LYME DOCUMENTARY is in there, but if not, check right now in ACTIVISM BY KRIS KROFT, one of the folks involved in this important lyme project!

they have a "trailer" to view IF YOU HAVE HIGH-SPEED INTERNET; folk like me with dial-up can NOT view it.

it's 20 minutes long and will give your family/friends extra knowledge what it is like to have lyme and all the political implications plus health insurance NOT paying our lyme bills, appts., labs, blood tests, etc

IP: Logged |

Printer-friendly view of this topic

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
http://www.lymenet.org/