LymeNet Flash: Dr. S in Louisville, KY

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 » Dr. S in Louisville, KY - Neurology

UBBFriend: Email this page to someone!

Author

Topic: Dr. S in Louisville, KY - Neurology

Alias24
Member
Member # 9365

posted

Does anyone have any info on this doctor?

He is listed in the doctor referral list about half way down in the following site on the right side: www.chroniclymedisease.com You will have to click on the link in the red sentence.

He is also listed on this site www.walyme.org.
Go down and then click on Medical Resources link and then click on Lyme Literat/Lyme Friendly Doctors (US).

Has anyone been to see him? How did he respond to Lyme?

Thanks.

Posts: 59 | From Indiana | Registered: Jun 2006 | IP: Logged |

seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

posted

Pretty sure I called this docs office about a year ago -- was told he did not treat Lyme patients. Did not get the impression he would be Lyme literate.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004 | IP: Logged |

Alias24
Member
Member # 9365

posted

Update:
I called his office last week and the receptionist ended up telling me that this doctor does not treat Lyme patients. My question was probably framed incorrectly.

I then emailed the Washington group and they said this doctor is a member of ILADS. I then emailed ILADS and they confirmed that this doctor is a member of ILADS.

My thoughts are that one probably can not call his office and ask if he treats Lyme; however, if he is a member of ILADS then he should be familiar with Lyme. One would think he would be more helpful than a neurologist who is not familiar with Lyme.

I guess I can try to see if my local PCP would get me an appointment with him and find out.

Posts: 59 | From Indiana | Registered: Jun 2006 | 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/