I apologize if this isn't proper internet ediquette, but I'll put myself "out there" if it'll help our son. Troutscout, I see that you're from Northeast Iowa. How do I e-mail you? We are near there and have a lot of family in that area. We would appreciate any insight you may have. Who's your llmd, etc... Thanks.
Posted by bg (Member # 46416) on :
up for Trout to read/respond to.
fyi - in Iowa, we do NOT have any full-time LLMD. Most of us if we got lucky, go to 1 of a handful of MDs who are learning to be lyme literate who max lyme patients to 20 ! ONE PER WEEK!!
------------------ Now is the time in your life to find the "tiger" within. Let the claws be bared, and Lyme BEWARE!!! Iowa Lyme Disease Assoc. www.ildf.info
Posted by NP40 (Member # 6711) on :
Just a heads-up on the WI. groups. Please contact [email protected] for WI/IL info. The other group run by Jeanette is somewhat incorporated into Sewill.
Jeanette is currently too ill to respond to e-mails. She has done phenomenol work regarding lyme and assisting folks throughout the midwest for a very long time. Many folks owe their very lives to her. We owe our son's life to her. We're all trying to pitch in and take up the slack. She's in our prayers.
Please use the [email protected] addy or website. Additionally, click on the envelope above my name for e-mailing as well. Thanks. - Mike
[This message has been edited by NP40 (edited 30 July 2005).]
