LymeNet Flash: A GOOD ALTERNATIVE DOCTOR IN SOUTH FLORIDA?

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 » Medical Questions » A GOOD ALTERNATIVE DOCTOR IN SOUTH FLORIDA?

UBBFriend: Email this page to someone!

Author

Topic: A GOOD ALTERNATIVE DOCTOR IN SOUTH FLORIDA?

Angie
Member
Member # 6996

posted

Last year I got the names of two llmd's from this board, but I really want someone alternative to work with too. Does anyone here know of someone they think is good in South Florida?

Thanks!

Posts: 29 | Registered: Mar 2005 | IP: Logged |

lhm312
Unregistered

posted

I was writing an email to you but first looked up your email address which didn't seem to be a person but a resource website.

I didn't want to give you info. and have it appear on a website. Is this for you personally, or are you collecting data?

Btw, lovely website, and I firmly believe nothing is a coincidence. I plan to read more of it, it really resonated with me spiritually.

IP: Logged |

Angie
Member
Member # 6996

posted

Thank you so much - I hope it's useful for you.

I just recently got diagnosed with lyme after 20 years of being told it was cfs/fibromyalgia. I am asking for myself and wasn't thinking of the site.

Once I get going on my own research and start on my treatment, I will be most likely be adding to the site with lyme resources. If I found a great doc,I would only put his info up if he/she wanted me to, but you can see there are no names of any docs I use in Florida on the site. I tend to stay away from that, and would only do it with a doctors permission - if I thought the doc was outstanding.

I would be most grateful for any info you can share!

Angie

Posts: 29 | Registered: Mar 2005 | IP: Logged |

Angie
Member
Member # 6996

posted

Bump

Posts: 29 | Registered: Mar 2005 | 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/