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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD in London?

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Author Topic: LLMD in London?
mamalicious
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Member # 43611

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Trying to help a friend find a Lyme doctor in or near London. They

travel between the US and their home in London.

Her 4 year old is having a second episode of neuro symptoms that look Parkinsons like...ataxia.

The first episode they said post infectious..viral. This time the symptoms were triggerd by their flight back from the US to London.

Not sure if there is another site for Europe?

Thanks
Posts: 97 | From Rockwall,TX | Registered: Apr 2014  |  IP: Logged | Report this post to a Moderator
hopingandpraying
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I don't know of any LLMDs in the UK. From what I've read, it is much worse over there than here in finding one! Most UK patients come to the US for treatment if they are able to.

If your friend needs names of LLMDs who treat children in the U.S.A., please let me know & for what state(s).

Have your friend check the online UK Lyme Support Groups at:
https://groups.yahoo.com/neo/groups/UnitedKingdom/info

Maybe they can help.

Here are some more links from the Support Groups in the UK from the upper-left-hand side of the Lymenet page for her to also contact:

FOR THE UK

http://www.lymenet.org/SupportGroups/Europe/UnitedKingdom/BLDF.shtml

http://www.lymenet.org/SupportGroups/Europe/UnitedKingdom/Action/shtml

Note: BADA no longer exists, per one of its founding members.

There are a couple of posters on Lymenet who are from the UK that she could contact.
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