posted
i am moving to sunrise florida to be closer to family and am in need of a lyme dr THAT TAKES INSURANCE..i cannot stress this enough...i cannot see a true llmd because i went broke and bankrupt and had to stop treatment and am now unable to care for myself and have to move closer to family to florida.
I did a search on the LDA site, which is ridiculous that they limit you to 3 searches at a time, but anyways...
I so wish I could mention names here so we all know who I am talking about......i don't know if these drs take insurance and i have to call but so far i have
dr P Sunrise (female) Dr C (boca raton) male and hispanic name Dr. LaP.... also south florida(male) Dr. C...tampa bay (male)
The lda rep gave me the last name and he does takeinsurance but is 4 hrs from where i will be and i have no way of getting there...i know beggers can't be choosers but if I cannot get there, it is pointless to get a referral...the only family i have there will be working and already told me all my drs need to be very close because they will not be able to take much time off.
And as much as I know everyone loves to share good drs...PLEASE do not flood this thread with names of drs who do not take insurance...yes...nothing more worth it than health but money doesn't fall from trees and flooding me with drs who don't take insurance would be like putting chocolate cake in front of someone who cannot eat sugar ever again
Thanks for any info and feel free to email me privately if you have any info on any of these drs...if they take ins, do iv, are stricly conventional, etc etc.
-------------------- Sick for 20 yrs+,dx'd 10 yrs ago fibro/cfs & hashimotos.dx 4 yrs ago w/neurolyme,recent adrenal failure, recurrent spinal cord injury,probable ankylosing spondylitis. Unable to get treatment & severe Cognitive, psych & physical symptoms progressing. Posts: 82 | From az but moving to ft lauderdale, florida= plantation. fl | Registered: Aug 2009
| IP: Logged |
Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936
posted
I'm very sorry to hear about your current situation. I can only offer you the Florida LLMD list. I hope you can find someone on the list to help you. Perhaps someone else will stop by with some ideas and information.
Also contact your local Lyme support group, which can be found on the left hand side of this site. I hope you will get further help there.
Posts: 5191 | From Lyme Zone | Registered: Jan 2009
| IP: Logged |
TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
Sorry but there is only one good lyme doc in Florida. Most people in Florida have to go out of state for their treatment.
The one doc is mentioned in the Burrascano guidelines on page 16:
posted
umm...thanks for the warning about florida but that is where my family is.
is is the humidity? rain?
-------------------- Sick for 20 yrs+,dx'd 10 yrs ago fibro/cfs & hashimotos.dx 4 yrs ago w/neurolyme,recent adrenal failure, recurrent spinal cord injury,probable ankylosing spondylitis. Unable to get treatment & severe Cognitive, psych & physical symptoms progressing. Posts: 82 | From az but moving to ft lauderdale, florida= plantation. fl | Registered: Aug 2009
| IP: Logged |
TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
Florida is a bad choice because there is only one good lyme doctor in the entire state.
Posts: 9931 | From Maryland | Registered: Dec 2007
| IP: Logged |
posted
oh well...that is the same with az but at least florida is on the east coast.
are ther4e others who aren't as good but takes insurance??
-------------------- Sick for 20 yrs+,dx'd 10 yrs ago fibro/cfs & hashimotos.dx 4 yrs ago w/neurolyme,recent adrenal failure, recurrent spinal cord injury,probable ankylosing spondylitis. Unable to get treatment & severe Cognitive, psych & physical symptoms progressing. Posts: 82 | From az but moving to ft lauderdale, florida= plantation. fl | Registered: Aug 2009
| IP: Logged |
posted
help.. i see that you ere looking for a dr too. i am in west palm beach. has anyone heard of dr k in orlando? i would prefer a natural approach but am having a lot of neuro problems such as constant tremors, mild convulsions-seizure like activity (on klonopin)and body wide nerve burning pain that makes me bed bound. who is the dr somebody mentioned in sout fla--which dr is that?
Posts: 1 | From s. Florida | Registered: Aug 2009
| IP: Logged |
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/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic