Looking for LLMD in Swindon UK, 1 hr west of London

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Mark FW
Regular Member

Date Joined Dec 2017
Total Posts : 131
   Posted 1/23/2018 11:29 AM (GMT -6)   
Found out a former coworker is on disability and in pretty bad shape. UN-diagnosed but sounds like it's a possible Lyme or co-infection.

Not sure how it works in UK but wanted to pass a LLMD to him.

I should be able to get direct emails so any info is appreciated.

Elite Member

Date Joined May 2007
Total Posts : 36310
   Posted 1/23/2018 12:42 PM (GMT -6)   
I'm having a rough day (did too much yesterday), so I'm not up to figuring out how far anything is from anything today (lol) - but if you don't get enough responses, if you would send me an email, I can take a look to see what I have listed. Just remember, I do not have any personal experience with these doctors as I live in the US.
Herb only treatment for Lyme & Bart ended 12/11 - no active symptoms for 2 yrs -Herb only treatment for Babesia ended 12/12
Had Lyme, Bart, Babs, RMSF, Ehrlichia, Myco, Anaplasmosis, EBV
New set of infections 8/2014 - still treating.
Come visit me: dogwoodtraditionals.freeforums.net/

Veteran Member

Date Joined Sep 2017
Total Posts : 505
   Posted 1/23/2018 1:08 PM (GMT -6)   
Hi Mark i have a reccomendation if you email me I will send you the info

Mark FW
Regular Member

Date Joined Dec 2017
Total Posts : 131
   Posted 1/23/2018 3:02 PM (GMT -6)   
Thanks, just sent email
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