LymeNet Flash: Arizona California or Soutwest Doctors requesting info

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 » Arizona California or Soutwest Doctors requesting info

UBBFriend: Email this page to someone!

Author

Topic: Arizona California or Soutwest Doctors requesting info

springshowers
Frequent Contributor (1K+ posts)
Member # 19863

posted

i am looking for a lyme doctor in Arizona who treats Lyme disease and can do IV treatments and intensive therapies.
I have not found one in AZ. As well I am open to going to California or anywhere in the Southwest or West coast if I need to.
Please let me know what you know.
Thank you

Posts: 2747 | From Unites States Of America | Registered: Apr 2009 | IP: Logged |

Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936

posted

Sent lists for AZ, CO & CA.

Posts: 5191 | From Lyme Zone | Registered: Jan 2009 | IP: Logged |

Siciliano
Frequent Contributor (1K+ posts)
Member # 15920

posted

Welcome

springshowers! We're happy that you have come to our site. You can learn alot about this disease here.

If you go to the left of the screen, 3rd one down, click on "support groups" and you will find some groups in the States you are interested in, they have alot of first hand experience with many llmds--this could help guide you in the right direction also.

Good luck to you springshowers. [Smile]

--------------------
I'm sorry but I am no longer accepting any private messages due to my own battle with lyme.

Posts: 3897 | From New Hampshire | Registered: Jun 2008 | IP: Logged |

Haley
Frequent Contributor (1K+ posts)
Member # 22008

posted

Please let me know what you find out. I am in California and I am willing to go anywhere but would prefer somewhere on the west side. I also would like to find someone that takes insurance.

Thanks,

Debi

Posts: 2232 | From USA | Registered: Aug 2009 | IP: Logged |

bettyg
Unregistered

posted

debi started her own post; she was sent llmd info [Smile]

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/