posted
Can't believe our luck. After dogging the medical folks here in our little town & plastering the paper with articles & appearing on two local t.v. stations with interviews, we are getting a new LLMD in my own town. He knows the controversy & is still willing to tackle it. He's heading out for ILADS training early this month, but is already seeing patients. I could kiss him! This is the 2nd doc we have had treating Lyme long-term in town - the last one moved to Illinois. Publicity CAN be effective!!! I wish I could do cartwheels!
Posts: 81 | From Iowa | Registered: May 2007
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Leelee
Frequent Contributor (1K+ posts)
Member # 19112
posted
This is wonderful news! There probably could never be enough LLMDs to go around.
What a wonderful person he is to help those with TBIs.
-------------------- The ultimate measure of a man is not where he stands in moments of comfort and convenience, but where he stands at times of challenge and controversy. Martin Luther King,Jr Posts: 1573 | From Maryland | Registered: Feb 2009
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bettyg
Unregistered
posted
mary,
would you send me this info so i can add to our nationwide llmd list? i'll forward to the rest who help sending out llmd lists to folks for states! i coordinate this.
mary in order to do this, you must ENABLE private messages.
it's easy to do; just click on YOUR PROFILE above and chose UPDATE MY PROFILE.
go to bottom and chose YES to enable private messages to folks.
then you can send me this info please. then if you chose to go back to NO ONE sending you a pm, you can.
as an iowan, i'm overjoyed hearing you got one in your home town! how many do we have now? i have no idea...
thanks for posting mary! how was your turnout for UNDER OUR SKIN in your city?
how was eldora's turnout? i heard it advertised on a local radio station.
i can see your husband jumping on a pogo stick explaining things at a lyme meeting, and being a boy scout leader.
the boy scouts chose to use my updated/revised LDA brochure type for the support group i once belonged too; 8000 copies if i remember right!
mary, this is the info i need IF you have it all please: *********************************************************
we need full name SPECIALTY street addy city, state
phone no. fax no. web site or email if possible
cost per hour for 1st visit and length of visit cost for follow-ups and length of visit
do they take insurance? what kind? treat by IV or ORAL?
thanks for helping us add to our drs. of around 300 nationwide who are LLMD!
thanks mary!
great tv interview using UOS alot in it, and newspaper article on you 3 !!
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Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936
posted
Hi Betty,
Can you PM me. I can help also in "SEEKING DR. FORUM", but need some additional info.
Thanks.
Posts: 5191 | From Lyme Zone | Registered: Jan 2009
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bettyg
Unregistered
posted
mary,
got your pm tonight now; since you DISABLED your pms i can not reply to you, so i'll just do it here.
hi mary,
sure i'll help you out and also tell you how to reply back and using our directory to reply to pms too ok
1. if she private messaged, pm, you; just click on the link sent which shows what she wrote you ... click REPLY and your note with info goes back PRIVATELY to her.
2. if you had a PM and deleted it by accident, click on DIRECTORY at top.
go to 1st line on left side, type name in aiden424 and click search
it will pop up with names or spellings like that
click on correct name shown in list; that will show her profile and you can send her a PM from there; upper right hand corner ok.
mary, i'll get the info to aiden since i'm just coming on and i do have her HOME email also
but try the suggestions above so you have a feel of what to do; 1st time is awkward; after that it feels comfortable.
thanks for the $350 figure; i'll forward that info to those of us w/nationwide llmd lists hugs
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bettyg
Unregistered
posted
i also pmed lakes/ann with this info also
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