help in uk

[mecresci]

anyone know if any research done in uk or any doctors here who are willing to try treating it . i had self treated for 8 years without even knowing what was wrong. i have never heard anything about morgellons in uk until i chanced on recently it while watching discovery channel xxx

[EvDownJr]

Well I looked around. Couldn't find much: However, I did find a UK Lyme physician who advertises through his website. I don't know if he has ever treated Morgellons Syndrome patients. If you phone his office, perhaps he could point you in the right direction. Also I have given you a link to Eurolyme and ILADS.

What I would do if the first guy doesn't know anything is post on the other organization sites asking for UK Lyme physicians. Continue to phone whomever is provided until you reach someone who has treated Morgellons clients or interested in following the Vanderbilt Antibiotic protocol.

Good Luck

http://www.drowen4lyme.co.uk/index.htm

http://www.ilads.org/index.html

http://health.groups.yahoo.com/group/EuroLyme/

[carla]

There are only two lyme docs in the uk worth seeing .This guy and the one I went to see iwho is in Bolton. If you want his number Pm me .He is the medical advisor for the british lyme disease association. A chronic fatique sufferer who cured himself. I would recommend him to anyone. carla xxx

[mecresci]

thanks both of you
bolton is a long way from home but id like to have number
xxxxxxxx

[carla]

merc, HE also does does consultations over the phone and they are cheaper. It only takes a few weeks to get one of these. I ll pm you his details in a minute carla

[EvDownJr]

Seems like we have enough self-identified cases in UK. I'm just glad someone else has enough specific knowledge to recommend a physician more specifically.

Good luck with that.

[mecresci]

any idea how many of us there are over here so far xxxxx

[carla]

I only know of about twelve merc .I bet theres hundreds who dont know they have it yet.
carla

[mecresci]

agree with you 150% carla i havnt heard it mentioned in the media at all over here . thing is always been a head strong sort of girl i knew everything happening to me was too real so no doctor or person was going to tell me i was nuts I tried for 7 years to find others with symptoms and when i did it was by chance , so there must be so many more xxxxxxxx

[carla]

Merc, Only this week i have found that a new member here lives less than 2 miles away from me . We both had it for 4 years as well. We must have got it from the same source but we have not figured it out yet. At this rate we will be having our own rally soon in the uk. carla xx