This is topic ENGLAND (UK) LLMD NEEDED in forum Seeking a Doctor at LymeNet Flash.


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Posted by ocdmark (Member # 8884) on :
 
is there a LLMD in the house?
pref London/Home Counties.

i live in Surrey.

i'm now 40. health's been in slow decline since 1999. have improved somewhat through qi gong & acupuncture. but my neuro symptoms - dysarthria, micrographia, balance - have worsened. it's now extremely difficult to understand a word i'm saying. the words are in here (taps head), but i can't speak them.

in 2005, i tested -ve under Western Blot, ditto a CSF test, but ELISA showed up something (my Doc wrote i had an outer surface protein C1 and C2, which in her words proved "an infectious agent is present").

pretending i don't have LD doesn't seem to have worked, so it's time to confront this... assuming i can find a LLMD!

many thanks,
mark
 
Posted by Siciliano (Member # 15920) on :
 
Hi, [hi] Mark and welcome to our site. We're happy that you found us!

I sent you information that you needed. I sent it through a private message. Click on the flashing envelope.

Also, please go to our "Medical" forum and ask any questions you may have--there are some very experienced and knowledgeable members that are eager and happy to help you during your journey. Just reading the postings is an education all in its self!! I know you will really like that forum!
 
Posted by 22dreams (Member # 17846) on :
 
Hi Mark,

Sorry to hear that your functionality has degenerated over the years.

I Pmd you the name of a couple UK organisations as perhaps additional resources to what Siciliano provided you.

Hope this information helps.
 
Posted by ticksickfamily (Member # 22786) on :
 
I am in the UK and currently seeing an LLMD in Hertfordshire.
I will post you details privately
 
Posted by Meg (Member # 22) on :
 
My suggestion is to contact those organizations above, as some of the Drs in England have a heavy workload or or not treating any longer, Good luck in your search.
 


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