LymeNet Flash: anyone see Dr W in CT?

This is topic anyone see Dr W in CT? in forum Seeking a Doctor at LymeNet Flash.

To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/2/8356

Posted by sman (Member # 15225) on :

Anyone see Dr. W in CT?

I am currently seeing Dr K in CT and am considering the possibility of changing doctors & would like to make an informed decision.

I heard Dr W follow Dr Burrascano's Guidleines- but does he really get into diet, supplements, etc?? How is he overall?

(I'm going for my 8th Rife today & can't wait to kill the little *&*%% inside me!!!) GOOD HEALTH TO ALL [woohoo]

THANK YOU!!!

[ 10-28-2009, 06:29 PM: Message edited by: Jenifer ]

Posted by dmc (Member # 5102) on :

sent PM

Posted by Tracy9 (Member # 7521) on :

Good and smart DR, no follow up from office staff. After spending $1,000 to see him they NEVER set up my IV Abx. Office staff would not follow through.

I had to change LLDs just to get them. What a waster.

Posted by mj1979 (Member # 22905) on :

sman,

How did you make out? I'm now in same boat as you - seeing Dr. K thinking of seeing Dr. W b/c he follows ILADS guidelines supposedly.

curious to hear any feedback you have.

Posted by Abxnomore (Member # 18936) on :

Please conduct these discussions via PM to protect our doctors. If you have patient comments about any of these doctors, you can send them to me to add to the LLMD list, so that others can benefit from your experiences.

Much Thanks [Smile]